Temporal range: Early Cretaceous–Recent
|False colour scanning electron micrograph of a flea. CDC image.|
Flea, the common name for the order Siphonaptera, includes 2,500 species of small flightless insects that survive as external parasites of mammals and birds. Fleas live by consuming blood, or hematophagy, from their hosts. Adult fleas grow to about 3 mm (0.12 in) long, are usually brown, and have bodies that are "flattened" sideways or narrow, enabling them to move through their host's fur or feathers. They lack wings, but have strong claws preventing them from being dislodged, mouthparts adapted for piercing skin and sucking blood, and hind legs extremely well adapted for jumping. They are able to leap a distance of some 50 times their body length, a feat second only to jumps made by another group of insects, the superfamily of froghoppers. Flea larvae are worm-like with no limbs; they have chewing mouthparts and feed on organic debris left on their host's skin.
The Siphonaptera are most closely related to the snow scorpionflies, or snow fleas in the UK, formally the Boreidae, placing them within the Endopterygote insect order Mecoptera. Fleas arose in the early Cretaceous, most likely as ectoparasites of mammals, before moving on to other groups, including birds. Each species of flea is more or less a specialist with respect to its host animal species: many species never breed on any other host, though some are less selective. Some families of fleas are exclusive to a single host group; for example, the Malacopsyllidae are found only on armadillos, the Ischnopsyllidae only on bats, and the Chimaeropsyllidae only on elephant shrews.
The oriental rat flea, Xenopsylla cheopis, is a vector of Yersinia pestis, the bacterium which causes bubonic plague. The disease was spread to humans by rodents such as the black rat, which were bitten by infected fleas. Major outbreaks included the Plague of Justinian, c. 540 and the Black Death, c. 1350, both of which killed a sizeable fraction of the world's population.
- 1 Morphology and behavior
- 2 Life cycle and development
- 3 Taxonomy and phylogeny
- 4 Relationship with host
- 5 Relationship with humans
- 6 See also
- 7 References
- 8 External links
Morphology and behavior
Fleas are wingless insects, 1/16 to 1/8-inch (1.5 to 3.3 mm) long, that are agile, usually dark colored (for example, the reddish-brown of the cat flea), with a proboscis, or stylet, adapted to feeding by piercing the skin and sucking their host's blood through their epipharynx. Flea legs end in strong claws that are adapted to grasp a host.
Unlike other insects, fleas do not possess compound eyes but instead only have simple eyespots with a single biconvex lens; some species lack eyes altogether. Their bodies are laterally compressed, permitting easy movement through the hairs or feathers on the host's body (or in the case of humans, under clothing). The flea body is covered with hard plates called sclerites. These sclerites are covered with many hairs and short spines directed backward, which also assist its movements on the host. The tough body is able to withstand great pressure, likely an adaptation to survive attempts to eliminate them by scratching.
Fleas lay tiny, white, oval eggs. The larvae are small and pale, have bristles covering their worm-like bodies, lack eyes, and have mouth parts adapted to chewing. The larvae feed on organic matter, especially the feces of mature fleas, which contain dried blood. Adults feed only on fresh blood.
Their legs are long, the hind pair well adapted for jumping; a flea can jump vertically up to 7 in (18 cm) and horizontally up to 13 in (33 cm), making the flea one of the best jumpers of all known animals (relative to body size), second only to the froghopper. The flea jump is so rapid and forceful that it exceeds the capabilities of muscle, and instead of relying on direct muscle power, fleas store muscle energy in a pad of the elastic protein named resilin before releasing it rapidly (like a human using a bow and arrow). Immediately before the jump, muscles contract and deform the resilin pad, slowly storing energy which can then be released extremely rapidly to power leg extension for propulsion. To prevent premature release of energy or motions of the leg, the flea employs a "catch mechanism". Early in the jump, the tendon of the primary jumping muscle passes slightly behind the coxa-trochanter joint, generating a torque which holds the joint closed with the leg close to the body. To trigger jumping, another muscle pulls the tendon forward until it passes the joint axis, generating the opposite torque to extend the leg and power the jump by release of stored energy. The actual take off has been shown by high-speed video to be from the tibiae and tarsi rather than from the trochantera (knees).
Life cycle and development
Fleas are holometabolous insects, going through the four lifecycle stages of egg, larva, pupa, and imago (adult). In most species, neither female nor male fleas are fully mature when they first emerge but must feed on blood before they become capable of reproduction. The first blood meal triggers the maturation of the ovaries in females and the dissolution of the testicular plug in males, and copulation soon follows. Some species breed all year round while others synchronise their activities with their hosts' life cycles or with local environmental factors and climatic conditions. Flea populations consist of roughly 50% eggs, 35% larvae, 10% pupae, and 5% adults.
The number of eggs laid depends on species, with batch sizes ranging from two to several dozen. The total number of eggs produced in a female's lifetime (fecundity) varies from around one hundred to several thousand. In some species, the flea lives in the host's nest or burrow and the eggs are deposited on the substrate, but in others, the eggs are laid on the host itself and can easily fall off onto the ground. Because of this, areas where the host rests and sleeps become one of the primary habitats of eggs and developing larvae. The eggs take around two days to two weeks to hatch. Experiments have shown that fleas lay more eggs on hosts which have limited food intakes, and that eggs and larvae survive better under these conditions, perhaps because the host's immune system is compromised.
Flea larvae emerge from the eggs to feed on any available organic material such as dead insects, faeces, conspecific eggs, and vegetable matter. In laboratory studies, some dietary diversity seems necessary for proper larval development. Blood-only diets allow only 12% of larvae to mature, whereas blood and yeast or dog chow diets allow almost all larvae to mature. Another study also showed that 90% of larvae matured into adults when the diet included nonviable eggs. They are blind and avoid sunlight, keeping to dark, humid places such as sand or soil, cracks and crevices, under carpets and in bedding. The entire larval stage lasts between four and 18 days.
Given an adequate supply of food, larvae pupate and weave silken cocoons after three larval stages. Within the cocoon, the larva molts for a final time and undergoes metamorphosis into the adult form. This can take just four days, but may take much longer under adverse conditions, and there follows a variable-length stage during which the pre-emergent adult awaits a suitable opportunity to emerge. Trigger factors for emergence include vibrations (including sound), heat (in warm-blooded hosts), and increased levels of carbon dioxide, all of which stimuli may indicate the presence of a suitable host. Large numbers of pre-emergent fleas may be present in otherwise flea-free environments, and the introduction of a suitable host may trigger a mass emergence.
Once the flea reaches adulthood, its primary goal is to find blood and then to reproduce. Female fleas can lay 5000 or more eggs over their life, permitting rapid increase in numbers. Generally speaking, an adult flea only lives for 2 or 3 months. Without a host to provide a blood meal, a flea's life can be as short as a few days. Under ideal conditions of temperature, food supply, and humidity, adult fleas can live for up to a year and a half. Completely developed adult fleas can live for several months without eating, so long as they do not emerge from their puparia. Optimum temperatures for the flea's life cycle are 21 °C to 30 °C (70 °F to 85 °F) and optimum humidity is 70%.
Adult female rabbit fleas, Spilopsyllus cuniculi, can detect the changing levels of cortisol and corticosterone hormones in the rabbit's blood that indicate it is getting close to giving birth. This triggers sexual maturity in the fleas and they start producing eggs. As soon as the baby rabbits are born, the fleas make their way down to them and once on board they start feeding, mating, and laying eggs. After 12 days, the adult fleas make their way back to the mother. They complete this mini-migration every time she gives birth.
Taxonomy and phylogeny
Between 1735 and 1758, the Swedish naturalist Carl Linnaeus first classified insects, doing so on the basis of their wing structure. One of the seven orders into which he divided them was "Aptera", meaning wingless, a group in which as well as fleas, he included spiders, woodlice and myriapods. It wasn't until 1810 that the French zoologist Pierre André Latreille reclassified the insects on the basis of their mouthparts as well as their wings, splitting Aptera into Thysanura (silverfish), Anoplura (sucking lice) and Siphonaptera (fleas), at the same time separating off the arachnids and crustaceans into their own subphyla. The group's name, Siphonaptera, is zoological Latin from the Greek siphon (a tube) and aptera (wingless).
Fleas are related to the Diptera (true flies) and the Mecoptera (scorpion flies) as shown in the cladogram, based on a 2008 analysis of four loci (18S and 28S ribosomal DNA, cytochrome oxidase II, and elongation factor 1-alpha) for 128 flea taxa from around the world. The Boreidae (snow scorpionflies) are the sister clade to the Siphonaptera.
|part of Endopterygota||
- Amphies. = Amphiesmenoptera
Fossils of wingless "pre-fleas" with siphonate (sucking) mouthparts from the middle Jurassic to early Cretaceous have been found in northeastern China. These belonged to three proposed extinct families, the Pseudopulicidae, the Saurophthiridae, and the Tarwiniidae. The last common ancestor of modern Siphonaptera separated from the Mecoptera during the early Cretaceous. Most flea families formed after the end of the Cretaceous (in the Paleogene and onwards). Fleas probably arose in the southern continental area of Gondwana, and migrated rapidly northwards from there. They most likely evolved with mammal hosts, only later moving to birds.
Siphonaptera is a relatively small order of insects: members of the order undergo complete metamorphosis and are secondarily wingless (their ancestors had wings which modern forms have lost). In 2005, Medvedev listed 2005 species in 242 genera, and despite subsequent descriptions of new species, bringing the total up to around 2500 species, this is the most complete database available. The order is divided into four infraorders and eighteen families. Some families are exclusive to a single host group; these include the Malacopsyllidae (armadillos), Ischnopsyllidae (bats) and Chimaeropsyllidae (elephant shrews).
Many of the known species are little studied. Some 600 species (a quarter of the total) are known from a single record from a single host. Over 94% of species are associated with mammalian hosts, and only about 3% of species can be considered to be specific parasites of birds. The fleas on birds are thought to have originated from mammalian fleas; at least sixteen separate groups of fleas switched to avian hosts during the evolutionary history of the Siphonaptera. Occurrences of fleas on reptiles is accidental, and fleas have been known to feed on the hemolymph (bloodlike body fluid) of ticks.
Flea phylogeny was long neglected, the discovery of homologies with the parts of other insects being made difficult by their extreme specialization. Whiting and colleagues prepared a detailed molecular phylogeny in 2008, with the basic structure shown in the cladogram. The Tungidae, including the harmful chigoe flea or jigger, is sister to the rest of the Siphonaptera.
Boreidae (snow scorpionflies)
Relationship with host
Fleas feed on a wide variety of warm-blooded vertebrates including humans, dogs, cats, rabbits, squirrels, ferrets, rats, mice and birds. Fleas normally specialise in one host species or group of species, but can often feed but not reproduce on other species. Ceratophyllus gallinae affects poultry as well as wild birds. As well as the degree of relatedness of a potential host to the flea's original host, it has been shown that avian fleas that exploit a range of hosts, only parasitise species with low immune responses. In general, host specificity decreases as the size of the host species decreases. Another factor is the opportunities available to the flea to change host species; this is smaller in colonially nesting birds, where the flea may never encounter another species, than it is in solitary nesting birds. A large, long-lived host provides a stable environment that favours host-specific parasites.
One theory of human hairlessness is that the loss of hair helped humans to reduce their burden of fleas and other ectoparasites.
Direct effects of bites
In many species, fleas are principally a nuisance to their hosts, causing an itching sensation which in turn causes the host to try to remove the pest by biting, pecking or scratching. Fleas are not simply a source of annoyance, however. Flea bites cause a slightly raised, swollen, irritating nodule to form on the epidermis at the site of each bite, with a single puncture point at the centre, like a mosquito bite.:126 This can lead to an eczematous itchy skin disease called flea allergy dermatitis, which is common in many host species, including dogs and cats. The bites often appear in clusters or lines of two bites, and can remain itchy and inflamed for up to several weeks afterwards. Fleas can lead to secondary hair loss as a result of frequent scratching and biting by the animal. They can also cause anemia in extreme cases.:126
As a vector
Fleas are vectors for viral, bacterial and rickettsial diseases of humans and other animals, as well as of protozoan and helminth parasites. Bacterial diseases carried by fleas include murine or endemic typhus:124 and bubonic plague. Fleas can transmit Rickettsia typhi, Rickettsia felis, Bartonella henselae, and the myxomatosis virus.:73 They can carry Hymenolepiasis tapeworms and Trypanosome protozoans.:74 The chigoe flea or jigger (Tunga penetrans) causes the disease tungiasis, a major public health problem around the world. Fleas that specialize as parasites on specific mammals may use other mammals as hosts; thus, humans may be bitten by cat and dog fleas.
Relationship with humans
In literature and art
Fleas have appeared in poetry, literature, music and art; these include Robert Hooke's drawing of a flea under the microscope in his pioneering book Micrographia published in 1665, poems by Donne and Jonathan Swift, works of music by Giorgio Federico Ghedini and Modest Mussorgsky, a play by Georges Feydeau, a film by Charlie Chaplin, and paintings by artists such as Giuseppe Crespi, Giovanni Battista Piazzetta, and Georges de La Tour.
John Donne's erotic metaphysical poem "The Flea", published in 1633 after his death, uses the conceit of a flea, which has sucked blood from the male speaker and his female lover, as an extended metaphor for their sexual relationship. The speaker tries to convince a lady to sleep with him, arguing that if the mingling of their blood in the flea is innocent, then sex would be also.
Flea circuses provided entertainment to nineteenth century audiences. These circuses, extremely popular in Europe from 1830 onwards, featured fleas dressed as humans or towing miniature carts, chariots, rollers or cannon. These devices were originally made by watchmakers or jewellers to show off their skill at miniaturization. A ringmaster called a "professor" accompanied their performance with a rapid circus patter.
Carriers of plague
Oriental rat fleas, Xenopsylla cheopis, can carry the coccobacillus Yersinia pestis. The infected fleas feed on rodent vectors of this bacterium, such as the black rat, Rattus rattus, and then infect human populations with the plague, as has happened repeatedly from ancient times, as in the Plague of Justinian in 541–542. Outbreaks killed up to 200 million people across Europe between 1346 and 1671. The Black Death pandemic between 1346 and 1353 likely killed over a third of the population of Europe.
Because fleas carry plague, they have seen service as a biological weapon. During World War II, the Japanese army dropped fleas infested with Y. pestis in China. The bubonic and septicaemic plagues are the most probable form of the plague that would spread as a result of a bioterrorism attack that used fleas as a vector.
The Rothschild Collection
The banker Charles Rothschild devoted much of his time to entomology, creating a large collection of fleas now in the Rothschild Collection at the Natural History Museum, London. He discovered and named the plague vector flea, Xenopsylla cheopis, also known as the oriental rat flea, in 1903. Using what was probably the world's most complete collection of fleas of about 260,000 specimens (representing some 73% of the 2,587 species and subspecies so far described), he described around 500 species and subspecies of Siphonaptera. He was followed in this interest by his daughter Miriam Rothschild, who helped to catalogue his enormous collection of the insects in seven volumes.
Fleas have a significant economic impact. In America alone, approximately $2.8 billion is spent annually on flea-related veterinary bills and another $1.6 billion annually for flea treatment with pet groomers. Four billion dollars is spent annually for prescription flea treatment and $348 million for flea pest control.
- "Wiley: The Insects: An Outline of Entomology, 5th Edition – Gullan, P.J.; Cranston, P.S." www.wiley.com. Retrieved 11 November 2016.
- Taylor, Sean D.; Cruz, Katharina Dittmar de la; Porter, Megan L.; Whiting, Michael F. (May 2005). "Characterization of the Long-Wavelength Opsin from Mecoptera and Siphonaptera: Does a Flea See?". Molecular Biology and Evolution. 22 (5): 1165–1174. doi:10.1093/molbev/msi110. ISSN 0737-4038. PMID 15703237.
- Fleas. Koehler, P.G.; Oi, F.M. Printed July 1993, revised February 2003. Provided by the University of Florida
- "Order Siphonaptera – Fleas". BugGuide.Net. Retrieved 11 November 2016.
- Crosby, J.T. "What is the Life Cycle of the Flea?". Veterinary Parasites. About Home. Retrieved 4 November 2016.
- "Fleas leap from feet, not knees". Science News. 2 October 2011. Retrieved 11 November 2016.
- Burrows, M. (2009). "How Fleas Jump". Journal of Experimental Biology. 212 (18): 2881–2883. doi:10.1242/jeb.022855. PMID 19717668.
- Krasnov, Boris R. (2008). Functional and Evolutionary Ecology of Fleas: A Model for Ecological Parasitology. Cambridge University Press. pp. 44–54. ISBN 978-1-139-47266-1.
- Krasnov, Boris R. (2008). Functional and Evolutionary Ecology of Fleas: A Model for Ecological Parasitology. Cambridge University Press. pp. 64–67. ISBN 978-1-139-47266-1.
- Krasnov, Boris R. (2008). Functional and Evolutionary Ecology of Fleas: A Model for Ecological Parasitology. Cambridge University Press. p. 194. ISBN 978-1-139-47266-1.
- Silverman, Jules; Appel, Arthur (March 1994). "Adult Cat Flea (Siphonaptera: Pulicidae) Excretion of Host Blood Proteins in Relation to Larval Nutrition" (PDF). Journal of Medical Entomology. 31 (2): 265–271. doi:10.1093/jmedent/31.2.265. Retrieved 18 July 2014.
- Shryock, J. (2006). "Time Spent by Ctenocephalides felis (Siphonaptera: Pulicidae) Larvae in Food Patches of Varying Quality". Environmental Entomology. 35 (2): 401–404. doi:10.1603/0046-225x-35.2.401.
- Hinkle, Nancy C.; Koehler, Philip G. (2008). Capinera, John L. (ed.). Cat Flea, Ctenocephalides felis felis Bouché (Siphonaptera: Pulicidae). Springer Netherlands. pp. 797–801. doi:10.1007/978-1-4020-6359-6_536. ISBN 978-1-4020-6242-1.
- "Flea Life Cycle: Eggs, Larvae, etc". Orkin.com. Retrieved 13 September 2019.
- Koehler, P.G.; Pereira, R.M.; Diclaro, J.W. "Fleas". Edis.ifas.ufl.edu. Retrieved 11 November 2016.
- "How long is the life span of a flea?". Everyday Mysteries: Fun Science Facts from the Library of Congress. Loc.gov. 2 July 2013. Retrieved 11 November 2016.
- Piper, Ross (2007), Extraordinary Animals: An Encyclopedia of Curious and Unusual Animals, Greenwood Press.
- Gillott, Cedric (2005). Entomology. Springer Science & Business Media. p. 97. ISBN 978-1-4020-3183-0.
- Meyer, John R. (28 March 2016). "Siphonaptera". North Carolina State University. Retrieved 3 December 2016.
- Whiting, Michael F.; Whiting, Alison S.; Hastriter, Michael W.; Dittmar, Katharina (2008). "A molecular phylogeny of fleas (Insecta: Siphonaptera): origins and host associations". Cladistics. 24 (5): 677–707. CiteSeerX 10.1.1.731.5211. doi:10.1111/j.1096-0031.2008.00211.x.
- Yeates, David K.; Wiegmann, Brian. "Endopterygota Insects with complete metamorphosis". Tree of Life. Retrieved 24 May 2016.
- Whiting, M. F. (2002). "Mecoptera is paraphyletic: multiple genes and phylogeny of Mecoptera and Siphonaptera". Zoologica Scripta. 31 (1): 93–104. doi:10.1046/j.0300-3256.2001.00095.x.
- Wiegmann, Brian; Yeates, David K. (2012). The Evolutionary Biology of Flies. Columbia University Press. p. 5. ISBN 978-0-231-50170-5.
Recently, a close affinity between Siphonaptera and Mecoptera has been convincingly demonstrated via morphology (Bilinski et al. 1998) and molecular data (Whiting 2002), rendering Mecoptera paraphyletic, but making the clade including Mecoptera and Siphonaptera monophyletic ... there is a general consensus among entomologists that the relationships described above are relatively well established.
- Huang, D.; Engel, M.S.; Cai, C.; Wu, H.; Nel, A. (8 March 2012). "Diverse transitional giant fleas from the Mesozoic era of China". Nature. 483 (7388): 201–204. doi:10.1038/nature10839. PMID 22388812.
- Zhu, Qiyun; Hastriter, Michael; Whiting, Michael; Dittmar, Katherina (September 2015). "Fleas (Siphonaptera) are Cretaceous, and Evolved with Theria". Molecular Phylogenetics and Evolution. 90: 129–139. bioRxiv 014308. doi:10.1016/j.ympev.2015.04.027.
- Krasnov, Boris R. (2008). Functional and Evolutionary Ecology of Fleas: A Model for Ecological Parasitology. Cambridge University Press. pp. 3–9. ISBN 978-1-139-47266-1.
- Krasnov, Boris R. (2008). Functional and Evolutionary Ecology of Fleas: A Model for Ecological Parasitology. Cambridge University Press. pp. 72–74. ISBN 978-1-139-47266-1.
- Poulin, Robert (2011). Evolutionary Ecology of Parasites (Second ed.). Princeton University Press. p. 68. ISBN 978-1-4008-4080-9.
- Rantala, M.J. (2006). "Evolution of nakedness in Homo sapiens" (PDF). Journal of Zoology. 273: 1–7. doi:10.1111/j.1469-7998.2007.00295.x. ISSN 0952-8369.
- Mullen, Gary R.; Mullen, Gary; Durden, Lance (2009). Medical and Veterinary Entomology. Academic Press. p. 637. ISBN 978-0-12-372500-4.
- Krasnov, Boris R. (2008). Functional and evolutionary ecology of fleas: a model for ecological parasitology. Cambridge University Press. p. 593. ISBN 978-0-521-88277-4.
- Sherman, David M. (2002). Tending animals in the global village: a guide to international veterinary medicine. Wiley-Blackwell. p. 209. ISBN 978-0-683-18051-0.
- Stein, Ernst (2003). Anorectal and colon diseases: textbook and color atlas of proctology. Springer. p. 478. ISBN 978-3-540-43039-1.
- Smith, Darvin Scott. "Tungiasis". Medscape. Retrieved 11 November 2016.
- Barnes, Ethne (2007). Diseases and Human Evolution. UNM Press. p. 253. ISBN 978-0-8263-3066-6.
- Neri, Janice (2008). "Between Observation and Image: Representations of Insects in Robert Hooke's Micrographia". In O'Malley, Therese; Meyers, Amy R. W. (eds.). The Art of Natural History. National Gallery of Art. pp. 83–107. ISBN 978-0-300-16024-6.
- Roncalli, Amici R. (June 2004). "La storia della pulce nell'arte e nella letteratura" [The history of the flea in art and literature]. Parasitologia (in Italian). 46 (1): 15–18. PMID 15305680. See also the 2009 version.
- Black, Joseph, ed. (2010). The Broadview Anthology of British Literature, Volume 2 (2nd ed.). Broadview Press. ISBN 978-1-55481-290-5.
- "The Project Gutenberg eBook of A Budget of Paradoxes, Volume II (of II), by Augustus de Morgan". www.gutenberg.org. Retrieved 30 October 2019.
- Schmäschke, R. (1 April 2000). "The flea in cultural history and first effects of its control". Berliner und Münchener Tierärztliche Wochenschrift. 113 (4): 152–160. ISSN 0005-9366. PMID 10816916.
- "The rise and demise of the flea circus". BBC Radio 4 Natural Histories. Retrieved 2 November 2016.
- Rosen, William (2007). Justinian's Flea: Plague, Empire, and the Birth of Europe. Viking Adult. p. 3. ISBN 978-0-670-03855-8.
- Hays, J. N. (1998). The Burdens of Disease: Epidemics and Human Response in Western History. Rutgers University Press. pp. 58 and following. ISBN 978-0-8135-2528-0.
- Austin Alchon, Suzanne (2003). A pest in the land: new world epidemics in a global perspective. University of New Mexico Press. p. 21. ISBN 978-0-8263-2871-7.
- Bossi, P.; et al. (2004). "Bichat guidelines for the clinical management of plague and bioterrorism-related plague". Eurosurveillance. 9 (12): Article 12.
- "Charles Rothschild". The Wildlife Trusts. Retrieved 1 November 2016.
- Sullivan, Walter (10 April 1984). "Miriam Rothschild Talks of Fleas". The New York Times. Retrieved 1 November 2016.
- "Siphonaptera collections". Natural History Museum, London. Retrieved 1 November 2016.
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