Toxorhynchites rutilus

Last updated

Toxorhynchites rutilus
Toxorhynchites rutilus adult.jpg
Scientific classification OOjs UI icon edit-ltr.svg
Domain: Eukaryota
Kingdom: Animalia
Phylum: Arthropoda
Class: Insecta
Order: Diptera
Family: Culicidae
Genus: Toxorhynchites
Species:
T. rutilus
Binomial name
Toxorhynchites rutilus
(Coquillett, 1896)
Synonyms [1]
  • Megarhinus rutilaCoquillett, 1896

Toxorhynchites rutilus, also known as the elephant mosquito or treehole predatory mosquito, is a species of mosquito in the family Culicidae. [2] [3] [4] Unlike most species in the genus that populate the tropics, Tx. rutilus is endemic to temperate regions. [5] As their name suggests, these mosquitoes commonly lay their eggs in treeholes where their larvae are predators on a variety of arthropods. As with other mosquitoes, they also inhabit other bodies of stagnant water such as in a tire or artificial containers. but not large bodies of water like ponds and ground pools. [6] Females are able to strategically locate breeding sites that already contain prey to oviposit in.

Contents

Tx. rutilus feeding behaviors make them strikingly different from a typical mosquito. Both adult males and females are strictly nectar-feeding and so they do not have a role in the transmission of pathogens to animals as in other mosquitoes. [7] Instead, their larvae are predacious and could potentially help curb the spread of diseases via vector mosquitoes. While they commonly prey on copepods, rotifers, ostracods, and chironomids, they also generally have a preference for certain species of mosquito larvae including common disease vectors such as Aedes albopictus, Aedes aegypti, and Aedes polynesiensis . [8] [9] [10] If their habitat lacks food or is overcrowded, the larvae are known to succumb to cannibalism. Their larval feeding preferences make them of special interest to biological control scientists and entomologists. There have been few successful instances of using Tx. rutilus as biological control in regions such as Hawaii, Florida, Louisiana, and Japan. [11]

Taxonomy

Tx. rutilus is placed under subgenus Lynchiella . [12]

There are two subspecies under Tx. rutilus:

While the phylogenetics of the genus Toxorhynchites have not been completely studied, several phylogenetic studies using a variety of targets including the white gene, ribosomal DNA, and small subunit ribosomal DNA placed Toxorhynchites as its own subfamily sister to Culicinae . [13] However, other studies using mitochondrial DNA confidently places the genus within Culicinae. [14] It is worth continuing the investigation of the phylogenetics to help understand how herbivory arose in the genus.

The genome of Tx. r. septentrionalis is partially available on GenBank.

Description

Tx. rutilus is one of the largest species of mosquitoes. The adults can grow up to 7 mm in length and 12 mm in wingspan, and the fourth larval instar can grow to 20 mm, comparable to the diameter of a penny. [15] Unlike most other mosquitoes, adult males and females are roughly the same size. [16] Even though they have a global distribution, all 91 described species of Toxorhynchites have very similar morphological characters, making them hard to identify to species level. [5] [13]

Like most others in the genus, Tx. rutilus has a characteristically strongly recurved proboscis. [7] [12] [17] The adult mosquitoes have iridescent purple and golden scales on their abdomen, wings, and legs. [17] Their femur is mostly dark-scaled, while the tarsi are mostly white. [17] The larvae are generally dark brown or red, with conspicuous hairs on the abdomen. [6]

Natural history

Like all mosquitoes, Tx. rutilus is holometabolous, meaning they undergo complete metamorphosis over four life stages - egg, larva, pupa, adult.

Adult and egg

The adults of Tx. rutilus are strictly nectar-feeding, but there have been no studies on their nectar preferences or on their role in pollination. [13] Their salivary glands are morphologically different from those genus such as Aedes, Anopheles, and Culex mosquitoes. [13] This is interesting from an evolutionary and disease control perspective as the salivary glands in the later genus play an important role in disease transmission. Future studies could look into the development of transgenic mutants resistant to pathogens.

Since the adult mosquitoes do not feed on blood, all the proteins and fats required for successful oogenesis is acquired from the larval diet. [6] [13] Some amino acids are obtained from the nectar. [6] The adult female's reproductive follicles mature continuously over several days, allowing her to lay eggs over many days with an average of 1.0 to 3.2 eggs each day. [18] Eggs are laid in flight by launching or dropping them into a chosen suitable habitat. Before laying each egg, she flies in counterclockwise loops that progressively become smaller as she nears the water body until she is close enough to eject her egg. [5] [18] This process is repeated until she is done laying all her mature eggs. Because the eggs are hydrophobic, they float on the surface of the water where they incubate for 24 to 50 hours, depending on the subspecies and temperature. Tx. r. rutilus tends to have a longer hatch time than Tx. r. septentrionalis. The eggs are susceptible to desiccation, so the female chooses a oviposition site that is not exposed to strong winds that may blow her eggs away. [10] [19] Females have demonstrated preference to sheltered and dark colored oviposition sites (black, brown, blue, red) over bright colored ones (white, yellow, green). [20] This makes them a worse candidate for biological control than other Toxorhynchites species, especially in urban areas where common target breeding sites will be brightly colored man-made containers.

Larvae and pupae

Toxorhynchites rutilus larvae Toxorhynchites rutilus larvae.jpg
Toxorhynchites rutilus larvae

Tx. rutilus larvae are sensitive to temperature and humidity. The subspecies Tx. r. rutilus typically spend 12 to 18 days in their larval stage and pupate for about six days, while Tx. r. septentrionalis spend 11 to 16 days as larvae. [10] In warmer temperatures, they tend to go through their larval stages faster. Males pupate 1–2 days before females. [21]

Larvae use mechanoreceptors to detect and ambush moving prey and have modified mandibular mouthparts for predation. Tx. r. septentrionalis hunts more commonly at the surface of the water. [5] While it is thought that Tx. rutilus larvae have a diet preference, there is no strong data to support their preference. Still, it is commonly reported that they predate on anything, including their siblings. Especially in overcrowded habitats, the larvae commonly cannibalize each other to reduce competition. High rates of cannibalism are also attributed to the fact that the larvae often swim backwards. The accidental bumping into each other sees a higher rate of cannibalism than when they meet head-on. [5]

Natural prey of the larvae include the eastern treehole mosquito Aedes triseriatus . [22]

To survive the reduced prey available during the colder months, the larvae overwinter in their fourth instar and typically weigh more. [10] [17] [23] Diapause is induced when the first instar larvae experiences shorter periods of daylight, not from a decrease in temperature. [10] [6]

Certain Toxorhynchites species, including Tx. r. septentrionalis, exhibit an odd behavior called prepupal compulsive killing. [5] This is when the larvae kill prey but do not consume any of it. It is thought that this would help limit any harm that could be done to the vulnerable pupae. The behavior begins three to four days before pupation, and is most intense right before pupation. [5]

Biological control

Tx. rutilus have been successfully released into areas including Hawaii and Gainesville, Florida to significantly decrease the natural populations of vector mosquitoes including Aedes and Culex species. [11] Although it is thought that the larvae has preference for different species of mosquito prey, there has not been extensive studies on the hypothesis. A study showed that the larvae did not exhibit preference between Ae. aegypti and Cx. quinquefasciatus. [15] It is difficult to introduce the species to new areas because of their sensitivity to their environment and their behavior. Because of their low egg laying rate, long larval development, and tendency to cannibalize their siblings, not many adults exist at a single time. [13] This small population makes it difficult to produce enough larvae to prey on the much larger populations of vector mosquitoes. Tx. rutilus thus cannot single-handedly control mosquito populations, but must be used in combination to other mosquito control methods such as insecticides. Care must be taken in the timing of applying pesticides as the species are also susceptible to commonly used insecticides. [6]

A strategy to help boost the population of Toxorhynchites is to rear the species in the lab and release them to the field. This was successfully implemented in New Orleans, Louisiana in the 1980s. [11]

Rearing

The risk of cannibalism makes rearing in a lab inefficient and costly as each larva would have to be reared individually. [13] As such, a lab in Texas successfully reared each Tx. rutilus larvae in individual wells. [21] The hatchlings were fed with Panagrellus worms, and then later on switched to a mixture of worm and other mosquito and fly larvae. [21] For efficiency and productivity, the lab did not feed the Tx. rutilus larvae solely on live prey mosquitoes.

The geographical distribution of Toxorhynchites rutilus in the United States. Map is redrawn after Burkett-Cadena 2013. Credit: Abdullah A. Alomar, UF/IFAS The-geographical-distribution-of-Toxorhynchites-rutilus-in-the-United-States.png
The geographical distribution of Toxorhynchites rutilus in the United States. Map is redrawn after Burkett-Cadena 2013. Credit: Abdullah A. Alomar, UF/IFAS

Distribution

Species in the subgenera Lynchiella are present in the New World. [13] While most of its species are tropical, Tx. rutilus is one of its few temperate species. Tx. rutilus are native to the Southern United States, covering regions in Florida and South Carolina.

The subspecies Tx. r. septentrionalis has a wider distribution than Tx. r. rutilus. It is found as north as Southern Canada, and as West as Texas.

Related Research Articles

<span class="mw-page-title-main">Mosquito</span> Family of flies

Mosquitoes are a family, the Culicidae, of some 3,600 species of small flies. The word "mosquito" is Spanish for "little fly". Mosquitoes have a slender segmented body, one pair of wings, three pairs of long hair-like legs, and specialized, highly elongated, piercing-sucking mouthparts. All mosquitoes drink nectar from flowers; females of some species have in addition adapted to drink blood. Evolutionary biologists view mosquitoes as micropredators, small animals that parasitise larger ones by drinking their blood without immediately killing them. Medical parasitologists view mosquitoes instead as vectors of disease, carrying protozoan parasites or bacterial or viral pathogens from one host to another.

<i>Aedes albopictus</i> Species of mosquito

Aedes albopictus, from the mosquito (Culicidae) family, also known as the (Asian) tiger mosquito or forest mosquito, is a mosquito native to the tropical and subtropical areas of Southeast Asia. In the past few centuries, however, this species has spread to many countries through the transport of goods and international travel. It is characterized by the white bands on its legs and body.

<i>Anopheles</i> Genus of mosquito

Anopheles is a genus of mosquito first described by J. W. Meigen in 1818. Its members are sometimes called nail mosquitoes or marsh mosquitoes. Many are vectors of the parasite Plasmodium, which causes malaria in birds, reptiles, and mammals including humans. Anopheles gambiae is the best-known species, as it transmits one of the most dangerous human malarial parasites, Plasmodium falciparum. No other mosquito genus is a vector of human malaria.

<i>Toxorhynchites</i> Genus of flies

Toxorhynchites, also called elephant mosquito or mosquito eater, is a genus of diurnal and often relatively colorful mosquitoes, found worldwide between about 35° north and 35° south. Most species occur in forests. It includes the largest known species of mosquito, at up to 18 mm (0.71 in) in length and 24 mm (0.94 in) in wingspan. It is among the many kinds of mosquito that do not consume blood. The adults subsist on carbohydrate-rich materials, such as honeydew, or saps and juices from damaged plants, refuse, fruit, and nectar.

<span class="mw-page-title-main">Ceratopogonidae</span> Family of flies commonly known as no see ums, or biting midges

Ceratopogonidae is a family of flies commonly known as no-see-ums, or biting midges, generally 1–3 millimetres in length. The family includes more than 5,000 species, distributed worldwide, apart from the Antarctic and the Arctic.

<span class="mw-page-title-main">Culicinae</span> Subfamily of flies

The Culicinae are the most extensive subfamily of mosquitoes (Culicidae) and have species in every continent except Antarctica, but are highly concentrated in tropical areas. Mosquitoes are best known as parasites to many vertebrate animals and vectors for disease. They are holometabolous insects, and most species lay their eggs in stagnant water, to benefit their aquatic larval stage.

<i>Culex restuans</i> Species of fly

Culex restuans is a species of mosquito known to occur in Canada, the United States, Mexico, Guatemala, Honduras, and the Bahamas. It is a disease vector for St. Louis encephalitis and West Nile virus. In 2013 West Nile Virus positive specimens were collected in Southern California.

<i>Aedes triseriatus</i> Species of mosquito

Aedes triseriatus is a member of the true fly order. It is called the eastern tree hole mosquito due to its predilection towards breeding in stagnant water that is found in natural holding containers such as tree holes. It is native to the eastern United States and southern Canada and favors hardwood habitats. It has been found as far south as the Florida Keys, as far west as Idaho and Utah, and as far north as Quebec and Ontario. This species has not yet been found in Europe, but it has the potential to spread through international trade. In 2004, it was found in a shipment of tires travelling from Louisiana to France, but it was identified and targeted with insecticides that truncated its spread. It is a known vector of La Crosse encephalitis and canine heartworm disease. In the laboratory, it has been found to vector several other viruses including yellow fever, eastern encephalitis, Venezuelan encephalitis, and western encephalitis. Because of its potential for international spread and its proclivity for transmitting disease, monitoring the distribution of this species is essential.

<span class="mw-page-title-main">Hydrachnidia</span> Group of mites

Hydrachnidia, also known as "water mites", Hydrachnidiae, Hydracarina or Hydrachnellae, are among the most abundant and diverse groups of benthic arthropods, composed of 6,000 described species from 57 families. As water mites of Africa, Asia, and South America have not been well-studied, the numbers are likely to be far greater. Other taxa of parasitengone mites include species with semi-aquatic habits, but only the Hydracarina are properly subaquatic. Water mites follow the general Parasitengona life cycle: active larva, inactive (calyptostasic) protonymph, active deutonymph, inactive tritonymph and active adult. Usually, larvae are parasites, while deutonymphs and adults are predators.

Diptera is an order of winged insects commonly known as flies. Diptera, which are one of the most successful groups of organisms on Earth, are very diverse biologically. None are truly marine but they occupy virtually every terrestrial niche. Many have co-evolved in association with plants and animals. The Diptera are a very significant group in the decomposition and degeneration of plant and animal matter, are instrumental in the breakdown and release of nutrients back into the soil, and whose larvae supplement the diet of higher agrarian organisms. They are also an important component in food chains.

Aedes capensis is a species of mosquito primarily found in forests in sub-Saharan Africa.

<i>Aedes canadensis</i> Species of fly

Aedes canadensis, the woodland pool mosquito, is an aggressive, day biting mosquito that can be a vector of a number of diseases which is found mainly in eastern North America.

Aedes africanus is a species of mosquito that is found on the continent of Africa with the exclusion of Madagascar. Aedes aegypti and Aedes africanus are the two main yellow fever vector species in Zambia. Aedes africanus is mainly found in tropical forests not near wetlands.

Aedes luteocephalus is an African species that is a demonstrated or suspected vector of several important arboviral diseases of humans. First described in 1907 as Stegomyia luteocephala, the species is currently classified in the genus Aedes, subgenus Stegomyia.

<i>Aedes japonicus</i> Species of fly

Aedes japonicus, commonly known as the Asian bush mosquito or the Asian rock pool mosquito, was first described by Theobald in 1901 from Tokyo, Japan. They are competent arbovirus vectors known to transmit the West Nile virus as well as Japanese and St. Louis encephalitis. They are listed as an invasive species by the Global Invasive Species Database.

Lutzia fuscana is a mosquito that is predatory in its larval stages. It has been investigated as a possible biological control agent, showing some promise where vector species share limited or specific breeding habitat.

Toxorhynchites minimus is a species of zoophilic mosquito belonging to the genus Toxorhynchites. It is found in India, Sri Lanka Indonesia, Malaysia, Philippines and Sumatra. When under mass rearing conditions, the larvae show cannibalism.

<i>Toxorhynchites splendens</i> Species of fly

Toxorhynchites (Toxorhynchites) splendens is a species of non-hematophagous mosquito belonging to the genus Toxorhynchites. It is widely used as a predator to control dengue mosquitoes.

<i>Anopheles freeborni</i> Species of Mosquito

Anopheles freeborni, commonly known as the western malaria mosquito, is a species of mosquito in the family Culicidae. It is typically found in the western United States and Canada. Adults are brown to black, with yellow-brown hairs and gray-brown stripes on the thorax. Their scaly wings have four dark spots, which are less distinct in the male.

<i>Aedes taeniorhynchus</i> Species of fly

Aedes taeniorhynchus, or the black salt marsh mosquito, is a mosquito in the family Culicidae. It is a carrier for encephalitic viruses including Venezuelan equine encephalitis and can transmit Dirofilaria immitis. It resides in the Americas and is known to bite mammals, reptiles, and birds. Like other mosquitoes, Ae. taeniorhynchus adults survive on a combination diet of blood and sugar, with females generally requiring a blood meal before laying eggs.

References

  1. "Toxorhynchites rutilus (Coquillett, 1896)". Global Biodiversity Information Facility . Retrieved 24 January 2024.
  2. "Toxorhynchites rutilus Report". Integrated Taxonomic Information System. Retrieved 2019-09-23.
  3. "Toxorhynchites rutilus". GBIF. Retrieved 2019-09-23.
  4. 1 2 3 4 5 6 7 Steffan, W A; Evenhuis, N L (January 1981). "Biology of Toxorhynchites". Annual Review of Entomology. 26 (1): 159–181. doi:10.1146/annurev.en.26.010181.001111.
  5. 1 2 3 4 5 6 Jones, C; Schreiber, E (1994). "The carnivores". Toxorhynchites. 5 (4): 4.
  6. 1 2 APHC (2016). Mosquito Genera Identification Key United States and Alaska. Defense Centers for Public Health.[ page needed ][ ISBN missing ]
  7. Campos, Raúl E.; Lounibos, L. P. (1 November 2000). "Natural Prey and Digestion Times of Toxorhynchites rutilus (Diptera: Culicidae) in Southern Florida". Annals of the Entomological Society of America. 93 (6): 1280–1287. doi: 10.1603/0013-8746(2000)093[1280:npadto]2.0.co;2 . hdl: 11336/33910 . S2CID   85694680.
  8. Tyagi, B. K.; Munirathinam, A.; Krishnamoorthy, R.; Baskaran, G.; Govindarajan, R.; Krishnamoorthi, R.; Mariappan, T.; Dhananjeyan, K. J.; Venkatesh, A. (2015). "A revision of genus Toxorhynchites Theobald, 1901, in the South-East Asian countries, with description of a new species Toxorhynchites (Toxorhynchites) darjeelingensis from West Bengal, India (Diptera, Culicidae)". Halteres. 6: 13–32.
  9. 1 2 3 4 5 Gerberg, E. J. (1983). "Sequential biocontrol application in the use of Toxorhynchites spp". In Laird, Marshall; Miles, James W. (eds.). Integrated Mosquito Control Methodologies: Experience and components from conventional chemical control. Academic Press. ISBN   978-0-12-434002-2.[ page needed ]
  10. 1 2 3 Collins, Larissa E.; Blackwell, Alison Blackwell (2000). "The biology of Toxorhynchites mosquitoes and their potential as biocontrol agents". Biocontrol News and Information. 21: 105–116. S2CID   45541264.
  11. 1 2 Darsie, Richard F.; Ward, Ronald A. (2016). Identification and Geographical Distribution of the Mosquitoes of north America, North of Mexico. University Press of Florida. ISBN   978-0-8130-6233-4.[ page needed ]
  12. 1 2 3 4 5 6 7 8 Donald, Claire L.; Siriyasatien, Padet; Kohl, Alain (30 October 2020). "Toxorhynchites Species: A Review of Current Knowledge". Insects. 11 (11): 747. doi: 10.3390/insects11110747 . PMC   7693308 . PMID   33143104.
  13. Hickey, Donal A.; Mitchell, Andrew; Sperling, Felix A.H. (2002). "Higher-level phylogeny of mosquitoes (Diptera: Culicidae): mtDNA data support a derived placement for Toxorhynchites". Insect Systematics & Evolution. 33 (2): 163–174. doi:10.1163/187631202X00118.
  14. 1 2 Marshall, Daniel S (2020). The Preferred Prey of Toxorhynchites rutilus Between Two Common Vectors and Implications for Its Future Use as a Biocontrol (Thesis). ProQuest   2452544642.[ page needed ]
  15. Lounibos, L. P.; Escher, R. L.; Duzak, D.; Martin, E. A. (1996). "Body Size, Sexual Receptivity and Larval Cannibalism in Relation to Protandry among Toxorhynchites Mosquitoes". Oikos. 77 (2): 309–316. Bibcode:1996Oikos..77..309L. doi:10.2307/3546070. JSTOR   3546070.
  16. 1 2 3 4 Andreadis, Theodore G.; Thomas, Michael C.; Shepard, John J. (2005). Identification Guide to the Mosquitoes of Connecticut. Illustrations by Gale Ridge. New Haven: The Connecticut Agricultural Experiment Station. pp. 155–156. Bulletin No. 996. Retrieved 24 January 2024 via Internet Archive.
  17. 1 2 Alomar, Abdullah A.; Alto, Barry W. (1 November 2022). "Toxorhynchites rutilus Coquillett, 1896 (Insecta: Diptera: Culicidae): EENY-787/IN1380". EDIS. 2022 (5). doi: 10.32473/edis-in1380-2022 . S2CID   257599859.
  18. Focks, Dana A. (July 2007). "Toxorhynchites as Biocontrol Agents". Journal of the American Mosquito Control Association. 23 (sp2): 118–127. doi:10.2987/8756-971X(2007)23[118:TABA]2.0.CO;2. PMID   17853602.
  19. Jones, Carl J.; Schreiber, E. T. (1 February 1994). "Color and Height Affects Oviposition Site Preferences of Toxorhynchites splendens and Toxorhynchites rutilus rutilus (Diptera: Culicidae) in the Laboratory". Environmental Entomology. 23 (1): 130–135. doi:10.1093/ee/23.1.130.
  20. 1 2 3 Schiller, Anita; Allen, Mary; Coffey, Jewel; Fike, Arielle; Carballo, Franklin (1 March 2019). "Updated Methods for the Production of Toxorhynchites rutilus septentrionalis (Diptera, Culicidae) for Use as Biocontrol Agent Against Container Breeding Pest Mosquitoes in Harris County, Texas". Journal of Insect Science. 19 (2). doi:10.1093/jisesa/iez011. PMC   6407668 . PMID   30843583.
  21. Miner, Angela (2014). Martina, Leila Siciliano (ed.). "Aedes triseriatus". Animal Diversity Web. Retrieved 24 January 2024.
  22. Lounibos, L. P.; Escher, R. L.; Nishimura, N.; Juliano, S. A. (1997). "Long-Term Dynamics of a Predator Used for Biological Control and Decoupling from Mosquito Prey in a Subtropical Treehole Ecosystem". Oecologia. 111 (2): 189–200. Bibcode:1997Oecol.111..189L. doi:10.1007/s004420050225. JSTOR   4221679. PMID   28307994. S2CID   19436485.