Misplaced Pages

Scolopendra morsitans

Article snapshot taken from Wikipedia with creative commons attribution-sharealike license. Give it a read and then ask your questions in the chat. We can research this topic together.
Species of centipede

Scolopendra morsitans
Scientific classification Edit this classification
Domain: Eukaryota
Kingdom: Animalia
Phylum: Arthropoda
Subphylum: Myriapoda
Class: Chilopoda
Order: Scolopendromorpha
Family: Scolopendridae
Genus: Scolopendra
Species: S. morsitans
Binomial name
Scolopendra morsitans
Linnaeus, 1758

Scolopendra morsitans, also known as the Tanzanian blue ringleg or red-headed centipede, is a species of centipede in the family Scolopendridae. S. morsitans is the type species for the genus Scolopendra.

Adult Tanzanian blue ringlegs grow to around 13 centimetres (5.1 in) and are generally characterised by bright red heads and striated body segments; however, their colouration varies widely across regional populations. The species is found across all inhabited continents and is highly invasive. The centipede is an aggressive and opportunistic predator which hunts primarily at night and feeds on other arthropods and some small vertebrates, using a neurotoxic venom and its strong jaws to capture, incapacitate and digest its prey. The species prefers warm environments and is often found beneath leaves, bark and other substrate on the ground.

S. morsitans should not be confused with the giant red-headed centipede (Scolopendra heros), Chinese red-headed centipede (Scolopendra subspines), or the Tanzanian blue ring centipede (Ethmostigmus trignopdus), all of which have similar sounding common names to S. morsitans.

Taxonomy

Scolopendra morsitans was first described by Carl Linnaeus in his book 10th edition of Systema Naturae in 1758 and has since retained its original scientific name. The species was nominated as the type species of the centipede genus Scolopendra in a submission to the International Commission on Zoological Nomenclature in 1955 which was approved two years later. The name ‘Scolopendra’ is derived from a Greek term meaning ‘biting earthworms’ which was first used by Aristotle in his book Historia Animalium to refer to aquatic polychaetes and terrestrial centipedes. The word ‘morsitans’ means ‘that bites’ in Latin, a name that is shared with a species of tsetse fly (Glossina morsitans).

There are two recognised subspecies of S. morsitans—Scolopendra morsitans morsitans, which was first described by Linnaeus in 1758 to refer to a species locality in India, and Scolopendra morsitans coerulescens, which was described by Francis Cragin and refers to a species locality first found in Kansas in the United States. The species is monophyletic and occupies a clade with Scolopendra pinguis, which is the most closely related member of the genus Scolopendra to S. morsitans.

Description

Tanzanian blue ringlegs have been recorded to grow to lengths of up to 127 mm (5.0 in) in Australian populations, though in other regions, including Southeast Asia, they rarely exceed 100 mm (3.9 in). Because S. morsitans populations differ greatly in colouration, using colour alone to identify the species can be misleading. However, adults are generally characterised by a bright red head and brownish body with distinct striations between each body segment. Juveniles lack clear stripes and often have a head that is a similar colour to their body trunk. In field observations, the species can sometimes be distinguished from other Scolopendras by its relatively thick rear legs (known as ultimate legs).

Juvenile (A) and adult (B) Tanzanian blue ringlegs found in South-East Asia.

In north-western Thailand, adult Tanzanian blue ringlegs have dark blackish heads and ultimate legs, whilst in north-east Thailand and Cambodia the centipedes have bright red heads and ultimate legs. Similar variations in colour have been observed across Australia and Africa. The centipede's antennae typically have 18–20 segments (occasionally 17 or 21–23), with the 5–7 segments closest to the head having dorsally facing hairs and the next 5–8 having ventrally facing hairs. Their tooth plates contain 5–6 teeth. Body segments 7–20 contain visible lines (known as paramedian sutures) surrounding the centre of the trunk, while the final segment of the centipede has a central line known as a medial suture. The centipede does not display obvious sexual dimorphism so subtle differences between the lateral margins of the tergites of male and female individuals are used as a visible determinant of sex.

Distribution

The Tanzanian blue ringleg occupies a cosmopolitan distribution, and is found across all major continents; however, it has not been widely documented in Europe. It is thought to be native to the majority of continental Australia (with the exception of Victoria, South Australia, and south-western Western Australia), Africa (except for the Eritrean Highlands and Red Sea Hills), most of South and South East Asia, Madagascar and Sri Lanka. The centipede has been introduced to much of the Americas, with sightings outside its native range in Peru, Mexico, Argentina, the Bahamas and the Southern United States. It has been proposed that the preference of red-headed centipedes for habitats similar to the conditions on ships has resulted in their widespread invasion of inhabited areas.

The species occupies a diverse range of habitats, from the arid and semi-arid outback of Australia to the diverse tropics and temperate zones of India and tropical rainforests of Southeast Asia. Tanzanian blue ringlegs have a preference for warmer climates and the range of the centipede appears to be limited by this affinity. Additionally, the centipede requires sufficient air humidity to survive which limits its habitat choice and distribution. Individual populations of Tanzanian blue ringlegs are known to differ in physical characteristics based on their local geographical distributions, this has prompted the creation of over 50 synonyms for S. morsitans in scientific literature, largely due to misidentification of location specific populations of the species.

Tanzanian blue ringlegs are sometimes kept in captivity as pets and are traded and sold internationally for prices averaging around US$35 online.

Life cycle

A Tanzanian blue ringleg in a maternal double coil

Male centipedes produce sperm-containing packets known as spermatophores wrapped in a silk-like substance which they then deposit in the sexual organs of female centipedes. The sexual organs of male and female Tanzanian blue ringlegs are not visually distinct, and examination of an individual's tergites is required to reliably determine its sex. Female centipedes construct brood chambers under substrate in protected areas for their young, laying clutches of 22–86 eggs and displaying extended parental care by forming a double coil around their eggs, newly hatched instar embryos, and post embryonic young. When threatened, or otherwise stressed, mothers guarding their offspring are known to engage in filial cannibalism, consuming their own eggs or embryos in order to minimise the energetic loss associated with an attack or perilous situation.

Because the Tanzanian blue ringleg finds shelter beneath leaves, logs and other ground substrate and is primarily active at night, very little is known about the species' natural biology, including precise information relating to their lifespan or length to maturity. However, the closely related Scolopendra subspinipes is known to live for upwards of 10 years on average. In captivity, S. morsitans has been reported to live for around 4 years.

Behaviour

Centipedes of the family Scolopendridae are known to be opportunistic, generalist predators which primarily capture and kill live prey. They use their front facing fangs, known as forcipules, to both hold and envenomate their prey, which most commonly consists of small arthropods. Other species of the Scolopendra genus such as the Amazonian giant centipede (Scolopendra gigantea) and Scolopendra alternans have been observed feeding on large arachnids such as scorpions, toads, small snakes, and even mice and bats. Some Scolopendra are known to use their anterior walking legs or ultimate legs to catch and hold prey for envenomation. Blue ringleng forcipules are able to detect chemicals such as glucose and can act as sensory organs in the centipede, providing evidence that they play a role in its ability to taste and interact with its environment.

Tanzanian blue ringlegs, along with other centipedes of the genus Scolopendra, are known to use their ultimate legs in threat displays—raising the appendages aggressively when approached from behind. This behaviour is thought to be a form of automimicry, confusing potential predators by disguising their vulnerable flanks as their fang-bearing heads.

Toxicology

Tanzanian blue ringleg venom is neurotoxic and acts on the nervous systems of invertebrates, and autonomic nervous system of vertebrates, to rapidly paralyse and kill the centipede's prey. The centipede's venom contains serotonin, which causes a pain response, as well as a mix of proteins, enzymes, lipoproteins, cholesterol, triglycerides, cholesteryl esters, squalene, free fatty acids, and phospholipids. Although the exact action of the fatty components of the centipede's venom are unknown, removing the fatty portion of other venoms, such as that of the Indian cobra, is known to significantly reduce the lethality of the venom in vertebrates by a factor of 40–50%. The protein components of the centipede's venom bear close resemblance to the venom compositions of scorpions and spiders such as the Mexican scorpion Centruroides limpidus, the black widow spider, and the brown recluse spider.

Esterases in the venom of the Tanzanian blue ringleg were the first active enzymes to be found in the venom of any centipede, and were discovered by researchers at Ain Shams University in 1983. The presence of enzymes in the centipede's venom such as estirases, acid and alkaline phosphatases, and proteases, allows the Tanzanian blue ringleg to digest its prey outside of its body, sucking the broken down components of the animals that it captures out of their body cavities. This helps the centipedes consume the edible components of arthropods through their tough, chitinous exoskeletons.

A transferrin protein, a class of protein which plays a role in the mammalian circulatory system, has been found in the venom of the Tanzanian blue ringleng along with the Scutigerid centipede Thereuopoda longicornis and the Scolopendrid Ethmostigmus rubripes. Transferrins are thought to function in support of the blue ringleg's immunity as they are known to display antibacterial properties in invertebrates. Some components of centipede venom, including that of S. morsitans, are thought to result from bacterial and fungal genes that have been horizontally transferred by microorganisms throughout the evolutionary history of the chilopods. Centipedes are the only known animals with a venom resulting at least in part from the horizontal transfer of genes from several other families of organisms.

In cases of human bites, the venom of the Tanzanian blue ringleg is known to produce redness, swelling, and in some cases, severe pain. Although robust case studies of S. morsitans are limited, bites of the closely related Scolopendrid, Scolopendra subspinipes, can result in severe edema and pronounced localised swelling.

References

  1. "0208. Los ciempiés escutigeromorfos (Scutigeromorpha), escolopendromorfos (Scolopendromorpha) y geofilomorfos (Geophilomorpha) de la selva tropical caducifolia de la reserva de Chamela, Jalisco, México". Insecta Mundi: 1–17. 29 February 2012.
  2. "Scolopedra morsitans". Global Biodiversity Information Facility. Retrieved 5 May 2022.
  3. "Red-Headed Centipede (Species: Scolopendra Morsitans) in Taxonomy (Gaia Guide)". Gaia Guide. Retrieved 5 May 2022.
  4. "Scolopendra morsitans". Global Invasive Species Database. Invasive Species Specialist Group (ISSG) of the IUCN Species Survival Commission. 28 April 2009. Retrieved 2 March 2012.
  5. ^ Siriwut, Warut; Edgecombe, Gregory D.; Sutcharit, Chirasak; Panha, Somsak (2015). "The Centipede Genus Scolopendra in Mainland Southeast Asia: Molecular Phylogenetics, Geometric Morphometrics and External Morphology as Tools for Species Delimitation". PLOS ONE. 10 (8): e0135355. Bibcode:2015PLoSO..1035355S. doi:10.1371/journal.pone.0135355. PMC 4536039. PMID 26270342.
  6. ^ "Chilobase". University of Padua. Retrieved 5 May 2022.
  7. ^ Shelley, R; Edwards, G; Chagas Jr, Amazonas (2005). "Introduction of the Centipede Scolopendra Morsitans L., 1758, into Northeastern Florida, the First Authentic North American Record, and a Review of Its Global Occurrences (Scolopendromorpha: Scolopendridae: Scolopendrinae)". Entomological News. Vol. 116. pp. 39–58.
  8. ^ Koch, LE (1983). "Morphological Characters of Australian Scolopendrid Centipedes, and the Taxonomy and Distribution of Scolopendra Morsitans L. (Chilopoda:Scolopendridae:Scolopendrinae)". Australian Journal of Zoology. 31: 79. doi:10.1071/zo9830079.
  9. ^ Panha, Somsak; Siriwut, Warut; Edgecombe, Gregory; Sutcharit, Chirasak; Tongkerd, Piyoros (2016). "A taxonomic review of the centipede genus Scolopendra Linnaeus, 1758 (Scolopendromorpha, Scolopendridae) in mainland Southeast Asia, with description of a new species from Laos". ZooKeys (590): 1–124. doi:10.3897/zookeys.590.7950. PMC 4926625. PMID 27408540.
  10. ^ Hodges, Cameron W.; Goodyear, Jesse (2021). "Novel foraging behaviors of Scolopendra dehaani (Chilopoda: Scolopendridae) in Nakhon Ratchasima, Thailand". International Journal of Tropical Insect Science. 41 (4): 3257–3262. doi:10.1007/s42690-021-00431-9. S2CID 234097157.
  11. ^ Cupul-Magaña, Fabio G. (2020). "Cuidados Parentales en el Ciempiés Scolopendra morsitans1". Southwestern Entomologist. 45: 309. doi:10.3958/059.045.0135. S2CID 214718553.
  12. ^ Mohamed, A.H.; Abu-Sinna, G.; El-Shabaka, H.A.; Abd El-Aal, A. (1983). "Proteins, lipids, lipoproteins and some enzyme characterizations of the venom extract from the centipede Scolopendra morsitans". Toxicon. 21 (3): 371–377. doi:10.1016/0041-0101(83)90093-4. PMID 6623485.
  13. "Giant Red-Headed Centipede". Missouri Department of Conservation.
  14. Ali, Salwa Mansur; Khan, Naveed Ahmed; Sagathevan, K.; Anwar, Ayaz; Siddiqui, Ruqaiyyah (2019). "Biologically active metabolite(s) from haemolymph of red-headed centipede Scolopendra subspinipes possess broad spectrum antibacterial activity". AMB Express. 9 (1): 95. doi:10.1186/s13568-019-0816-3. PMC 6598926. PMID 31254123.
  15. ^ Winsor, Mary P. (1976). "The Development of Linnaean Insect Classification". Taxon. 25 (1): 57–67. doi:10.2307/1220406. JSTOR 1220406.
  16. Crabill, R. E. (1955). "Proposed use of the plenary powers to designate for the genus Scolopendra Linnaeus, 1758, (Class Myriapoda) a type species in harmony with accustomed usage". The Bulletin of Zoological Nomenclature. 11: 134–136. doi:10.5962/bhl.part.2832.
  17. Barber, A. (2014). "Early Records and Names of British & Irish Centipedes 'Scolopendra". Bulletin of the British Myriapod & Isopod Group. 27: 43–52.
  18. Fraumann, Robert. (2003). “Glossina Morsitans.” Animal Diversity Web. 2003. https://animaldiversity.org./accounts/Glossina_morsitans/ .
  19. ^ Elias, Scott A. (2021). "The International Trade in Insects and Terrestrial Arthropods". Reference Module in Earth Systems and Environmental Sciences. pp. 378–394. doi:10.1016/b978-0-12-821139-7.00195-1. ISBN 9780124095489. S2CID 244868866.
  20. ^ Jangi, B.S. (1955). "LXXI.—Some aspects of the morphology of the centipede Scolopendra morsitans Linn. (Scolopendridae)". Annals and Magazine of Natural History. 8 (92): 597–607. doi:10.1080/00222935508655671.
  21. ^ Dugon, Michel M.; Arthur, Wallace (2012). "Prey orientation and the role of venom availability in the predatory behaviour of the centipede Scolopendra subspinipes mutilans (Arthropoda: Chilopoda)". Journal of Insect Physiology. 58 (6): 874–880. doi:10.1016/j.jinsphys.2012.03.014. PMID 22490529.
  22. ^ Kronmüller, Christian; Lewis, John G. J. (30 June 2015). "On the function of the ultimate legs of some Scolopendridae (Chilopoda, Scolopendromorpha)". ZooKeys (510): 269–278. doi:10.3897/zookeys.510.8674. ISSN 1313-2970. PMC 4523778. PMID 26257548.
  23. Elzinga, Richard J. (1994). "The Use of Legs as Grasping Structures During Prey Capture and Feeding by the Centipede Scolopendra viridis Say (Chilopoda: Scolopendridae)". Journal of the Kansas Entomological Society. 67 (4): 369–372. JSTOR 25085542.
  24. Dass, C.M.S; Jangi, B.S (1977). "Chemoreceptive Function of the Poison Fang in the Centipede Scolopendra Morsitans L.". Indian Journal of Experimental Biology. 15: 803–4.
  25. Kabara, Jon J.; Fischer, George H. (1969). "Chemical composition of Naja naja: Extractable lipids". Toxicon. 7 (3): 223–227. doi:10.1016/0041-0101(69)90009-9. PMID 5358066.
  26. Fernández-Taboada, Guillermo; Riaño-Umbarila, Lidia; Olvera-Rodríguez, Alejandro; Gómez-Ramírez, Ilse Viridiana; Losoya-Uribe, Luis Fernando; Becerril, Baltazar (2021). "The venom of the scorpion Centruroides limpidus, which causes the highest number of stings in Mexico, is neutralized by two recombinant antibody fragments". Molecular Immunology. 137: 247–255. doi:10.1016/j.molimm.2021.07.010. PMID 34298407.
  27. Ornberg, Richard L.; Smyth, Thomas; Benton, Allen W. (1976). "Isolation of a neurotoxin with a presynaptic action from the venom of the black widow spider (Latrodectus mactans, Fabr.)". Toxicon. 14 (4): 329–330. doi:10.1016/0041-0101(76)90030-1. PMID 960115.
  28. Rekow, Mary A.; Civello, David J.; Geren, Collis R. (1983). "Enzymatic and hemolytic properties of brown recluse spider (Loxosceles reclusa) toxin and extracts of venom apparatus, cephalothorax and abdomen". Toxicon. 21 (3): 441–444. doi:10.1016/0041-0101(83)90102-2. PMID 6353666.
  29. ^ Undheim, Eivind; Fry, Bryan; King, Glenn (2015). "Centipede Venom: Recent Discoveries and Current State of Knowledge". Toxins. 7 (3): 679–704. doi:10.3390/toxins7030679. PMC 4379518. PMID 25723324.
  30. ^ Undheim, Eivind A. B.; Jenner, Ronald A. (2021). "Phylogenetic analyses suggest centipede venom arsenals were repeatedly stocked by horizontal gene transfer". Nature Communications. 12 (1): 818. Bibcode:2021NatCo..12..818U. doi:10.1038/s41467-021-21093-8. PMC 7864903. PMID 33547293.
  31. ^ Balit, Corrine R.; Harvey, Mark S.; Waldock, Julianne M.; Isbister, Geoffrey K. (2004). "Prospective Study of Centipede Bites in Australia". Journal of Toxicology: Clinical Toxicology. 42 (1): 41–48. doi:10.1081/clt-120028743. PMID 15083935. S2CID 24659920.
  32. Veraldi, Stefano; Çuka, Ermira; Gaiani, Francesca (2014). "Scolopendra bites: A report of two cases and review of the literature". International Journal of Dermatology. 53 (7): 869–872. doi:10.1111/ijd.12434. PMID 24673437. S2CID 23154815.
Taxon identifiers
Scolopendra morsitans
Categories: