Overview
Brief Summary
- Sanchez-Arroyo, H. and J. L. Capinera, 2008. Housefly. University of Florida/IFAS Featured Creatures. Publication EENY-48. Retrieved January 2, 2012 from http://entomology.ifas.ufl.edu/creatures/urban/flies/house_fly.htm
- Wikipedia, The Free Encyclopedia. 14 December, 2011. “Housefly”. Retrieved January 2, 2012 from http://en.wikipedia.org/w/index.php?title=Housefly&oldid=465867645
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- Sanchez-Arroyo, H. and J. L. Capinera, 2008. Housefly. University of Florida/IFAS Featured Creatures. Publication EENY-48. Retrieved January 2, 2012 from http://entomology.ifas.ufl.edu/creatures/urban/flies/house_fly.htm
- Wikipedia, The Free Encyclopedia. 14 December, 2011. “Housefly”. Retrieved January 2, 2012 from http://en.wikipedia.org/w/index.php?title=Housefly&oldid=465867645
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Biology
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Description
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Distribution
National Distribution
Canada
Origin: Native
Regularity: Regularly occurring
Currently: Present
Confidence: Confident
Type of Residency: Year-round
United States
Origin: Native
Regularity: Regularly occurring
Currently: Present
Confidence: Confident
Type of Residency: Year-round
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Range
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Ecology
Habitat
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Associations
Flowering Plants Visited by Musca domestica in Illinois
(observations are from Robertson, Graenicher, and Anderson & Hill)
Anacardiaceae: Rhus copallina [pist sn] (Rb); Apiaceae: Cicuta maculata sn fq (Rb), Oxypolis rigidior sn (Rb), Pastinaca sativa sn (Rb), Sium suave sn (Rb); Asteraceae: Ageratina altissima sn/fp (Gr), Anthemis cotula sn/fp (Gr), Aster drummondii sn/fp (Gr), Aster laevis sn/fp (Gr), Aster lanceolatus sn/fp (Gr), Aster lateriflorus sn/fp (Gr), Aster pilosus sn (Rb), Aster puniceus sn/fp (Gr), Conyza canadensis sn (Rb), Eupatorium perfoliatum sn/fp (Gr), Eupatorium serotinum sn (Rb), Euthamia graminifolia sn/fp (Gr), Helianthus giganteus sn/fp (Gr), Leucanthemum vulgare sn/fp (Gr), Pseudognaphalium obtusifolium sn (Rb), Solidago juncea sn/fp (Gr), Solidago nemoralis sn (Rb); Bignoniaceae: Campsis radicans [exfl sn] (Rb); Caprifoliaceae: Sambucus canadensis fp (Rb); Caryophyllaceae: Stellaria media sn (Rb); Cucurbitaceae: Echinocystis lobata sn (Rb), Sicyos angulatus sn (Rb); Hamamelidaceae: Hamamelis virginiana sn/fp (Gr, AH); Hydrangeaceae: Hydrangea arborescens sn (Rb); Liliaceae: Melanthium virginicum sn (Rb); Parnassiaceae: Parnassia glauca sn/fp (Gr); Polygonaceae: Fallopia scandens sn (Rb); Ranunculaceae: Clematis virginiana [stam sn fq] (Rb); Rhamnaceae: Ceanothus americanus sn (Rb); Rubiaceae: Cephalanthus occidentalis sn (Rb)
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Hilty, J. Editor. 2013. Insect Visitors of Illinois Wildflowers. World Wide Web electronic publication. illinoiswildflowers.info, version (05/2013)
See: Abbreviations for Insect Activities, Abbreviations for Scientific Observers, References for behavioral observations
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larva of Musca domestica inhabits dung of Mammalia
Foodplant / debris feeder
larva of Musca domestica feeds on decaying debris of Magnoliopsida
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Known predators
Sinea complexa
Proctacanthella leucopogon
Silpha truncata
Necrophorus marginatus
Conomyrma bicolor
Pheidole
Novomessor cockerelli
Crematogaster clara
Iridomyrmex pruinosum
Saprinus discoidalis
Syspira longipes
Psilochorus utahensis
Creophilis maxillosus
Based on studies in:
USA: Texas, Hueco Mountains (Carrion substrate)
USA: Texas, Franklin Mtns (Carrion substrate)
This list may not be complete but is based on published studies.
- K. Schoenly and W. Reid, 1983. Community structure of carrion arthropods in the Chihuahuan Desert. J. Arid Environ. 6:253-263, from pp. 256-58 & unpub. material.
- M. McKinnerney, 1977. Carrion communities in the northern Chihuahuan Desert. M.S. thesis. University of Texas-El Paso, Texas; and 1978, Carrion communities in the northern Chihuahuan Desert. Southw. Nat. 23:563-576, from thesis and p. 571.
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Known prey organisms
carcass
Lepus californicus
Based on studies in:
USA: Texas, Hueco Mountains (Carrion substrate)
USA: Texas, Franklin Mtns (Carrion substrate)
This list may not be complete but is based on published studies.
- K. Schoenly and W. Reid, 1983. Community structure of carrion arthropods in the Chihuahuan Desert. J. Arid Environ. 6:253-263, from pp. 256-58 & unpub. material.
- M. McKinnerney, 1977. Carrion communities in the northern Chihuahuan Desert. M.S. thesis. University of Texas-El Paso, Texas; and 1978, Carrion communities in the northern Chihuahuan Desert. Southw. Nat. 23:563-576, from thesis and p. 571.
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Diseases and Parasites
House flies are the carriers of more than 100 human and animal intestinal diseases and are a vector for protozoan (amoebic dysentery), bacterial (shigellosis, salmonellosis, cholera, rickettsia) and helminthic (round worms, hookworms, pinworms and tapeworms) infections as well as viral infections (Malik et al. 2007). These diseases are contracted by flies from garbage, sewage, and other sources of waste. The flies can also transmit eye diseases such as trachoma and infect wounds and skin with diseases such as cutaneous diphtheria, mycoses, yaws and leprosy. Larvae swallowed in food material sometimes survive in the human gut, causing intestinal myiasis, with symptoms of pain, nausea and vomiting. About 60% of house flies carry bacteria, most commonly staphylococci (Malik et al., 2007).
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Evolution and Systematics
Functional Adaptations
Functional adaptation
House flies land on ceilings by approaching at a 45° and then cartwheeling into the landing.
"A fly lands on a ceiling by flying up at an angle of about 45° with its front feet extended; as soon as contact is made the fly cartwheels over onto its other four feet." (Foy and Oxford Scientific Films 1982:13)
Learn more about this functional adaptation.
- Foy, Sally; Oxford Scientific Films. 1982. The Grand Design: Form and Colour in Animals. Lingfield, Surrey, U.K.: BLA Publishing Limited for J.M.Dent & Sons Ltd, Aldine House, London. 238 p.
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Functional adaptation
The olfactory systems of some flies help them find food due to their extreme sensitivity to the smell of rotting meat.
"The sense of smell is vital to most insects for finding food. Flies are particularly sensitive to the chemical odour given off by rotting meat…" (Foy and Oxford Scientific Films 1982:129)
Learn more about this functional adaptation.
- Foy, Sally; Oxford Scientific Films. 1982. The Grand Design: Form and Colour in Animals. Lingfield, Surrey, U.K.: BLA Publishing Limited for J.M.Dent & Sons Ltd, Aldine House, London. 238 p.
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Molecular Biology and Genetics
Molecular Biology
Barcode data: Musca domestica
There are 91 barcode sequences available from BOLD and GenBank. Below is a sequence of the barcode region Cytochrome oxidase subunit 1 (COI or COX1) from a member of the species. See the BOLD taxonomy browser for more complete information about this specimen and other sequences.
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Download FASTA File
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Statistics of barcoding coverage: Musca domestica
Public Records: 48
Specimens with Barcodes: 88
Species With Barcodes: 1
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Conservation
Conservation Status
National NatureServe Conservation Status
Canada
Rounded National Status Rank: NNR - Unranked
United States
Rounded National Status Rank: NNR - Unranked
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Threats
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Management
Relevance to Humans and Ecosystems
Benefits
Despite the many negative aspect that house fly have on humans, there are however, some benefits to be derived. The first advantage is derived from its mode of nutrition and life cycle. Since digestion of food takes place outside of the body and its larval stage lives and feeds on organic matter, flies are significant decomposers, disposing of decaying matter and replacing nutrients back into the soil.
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Risks
Musca domestica is the most common species, among a multitude of houseflies. They carry pathogens, cause food spoilage, and are significant domestic, medical, and veterinary pests . Musca domestica, a synanthropic fly, has a close association with humans and their environment. Musca domestica can be found at every place where people live and they also associated with livestaock farming (e.g., poultry farms, cattle sheds, horse stables and pig farms). They feed on human food and wastes where they can pick up and transport various disease agents. Flies have proboscis that helps them suck up food because they lack teeth to chew and bite. After landing on a potential food source, the house fly first vomits its stomach contents on to the food. Digestive juices, enzymes, and saliva in the vomit breaks down and dissolve the food, making it possible for the fly to suck up the liquid food using its proboscis. If flies suck up food from any source containing pathogens or bacteria, some of these microorganisms stick to the fly’s mouth or body parts, and when the fly comes in contact with human food, these contaminating or pathogenic agents are transferred. (Malik et al., 2007).
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Wikipedia
Housefly
- Not to be confused with horsefly.
The housefly (also house fly, house-fly or common housefly), Musca domestica, is a fly of the suborder Cyclorrhapha. It is the most common of all domestic flies, accounting for about 91% of all flies in human habitations, and indeed one of the most widely distributed insects, found all over the world. It is considered a pest that can carry serious diseases.
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Physical description [edit]
| This section relies largely or entirely upon a single source. (April 2012) |
The adults are 2 cm long. Their thorax is gray, with four longitudinal dark lines on the back. The whole body is covered with hair-like projections. The females are slightly larger than the males, and have a much larger space between their red compound eyes. The mass of pupae can range from about 8 to 20 mg under different conditions.[1]
Like other Diptera (meaning "two-winged"), houseflies have only one pair of wings; the hind pair is reduced to small halteres that aid in flight stability. Characteristically, the media vein (M1+2 or fourth long vein of the wing) shows a sharp upward bend.
Species that appear similar to the housefly include:
- The lesser house fly, Fannia canicularis, is somewhat smaller, more slender, and the media vein is straight.
- The stable fly, Stomoxys calcitrans, has piercing mouthparts and the media vein is only slightly curved.
Life cycle [edit]
Each female fly can lay approximately 500 eggs in several batches of about 75 to 150.[2] The eggs are white and are about 1.2 mm in length. Within a day, larvae (maggots) hatch from the eggs; they live and feed on (usually dead and decaying) organic material, such as garbage or feces. They are pale-whitish, 3–9 mm long, thinner at the mouth end, and have no legs. Their average life cycle is from 14 hours to one week. At the end of their third instar, the maggots crawl to a dry, cool place and transform into pupae, colored reddish or brown and about 8 mm long. The adult flies then emerge from the pupae. (This whole cycle is known as complete metamorphosis.) The adults live from two weeks to a month in the wild, or longer in benign laboratory conditions. Having emerged from the pupae, the flies cease to grow; small flies are not necessarily young flies, but are instead the result of getting insufficient food during the larval stage.[3]
Some 36 hours after having emerged from the pupa, the female is receptive for mating. The male mounts her from behind to inject sperm. Copulation takes a few seconds to a couple of minutes.[3] Normally, the female mates only once, storing the sperm to use it repeatedly for laying several sets of eggs.
The flies depend on warm temperatures; generally, the warmer the temperature, the faster the flies will develop.
Sex determination [edit]
| This section relies largely or entirely upon a single source. (April 2012) |
The housefly is an object of biological research, mainly because of one remarkable quality: the sex determination mechanism. Although a wide variety of sex determination mechanisms exist in nature (e.g. male and female heterogamy, haplodiploidy, environmental factors), the way sex is determined is usually fixed within one species. However, the housefly exhibits many different mechanisms for sex determination, such as male heterogamy (like most insects and mammals), female heterogamy (like birds) and maternal control over offspring sex. This makes the housefly one of the most suitable species to study the evolution of sex determination.[4]
Evolution [edit]
Even though the order of flies (Diptera) is much older, true houseflies are believed to have evolved in the beginning of the Cenozoic era, some 65 million years ago.[5] They are thought to have originated in the southern Palearctic region, particularly the Middle East. Because of their close, commensal relationship with humans, they probably owe their worldwide dispersal to co-migration with humans.[3]
Flies and humans [edit]
| This section needs additional citations for verification. (April 2012) |
In colder climates, houseflies survive only with humans. They have a tendency to aggregate and are difficult to dispose of. They are capable of carrying over 100 pathogens, such as those causing typhoid, cholera, salmonellosis,[6] bacillary dysentery,[7] tuberculosis, anthrax, ophthalmia, and parasitic worms.[8] Some strains have become immune to most common insecticides.[9][10]
House flies feed on liquid or semiliquid substances beside solid material which has been softened by saliva or vomit. Because of their large intake of food, they deposit feces constantly, one of the factors that makes the insect a dangerous carrier of pathogens. Although they are domestic flies, usually confined to human habitations, they can fly for several miles from the breeding place.[11] They are active only in daytime, and rest at night, e.g., at the corners of rooms, ceiling hangings, cellars, and barns, where they can survive the coldest winters by hibernation, and when spring arrives, adult flies are seen only a few days after the first thaw.
Housefly as a transmitter of disease [edit]
Mechanical transmission of organisms on its hairs, mouthparts, vomitus and feces:
- parasitic diseases: cysts of protozoa e.g. Entamoeba histolytica, Giardia lamblia and eggs of helminths, e.g., Ascaris lumbricoides, Trichuris trichiura, Hymenolepis nana, Enterobius vermicularis.
- bacterial diseases: typhoid, cholera, dysentery, pyogenic cocci, etc. House flies have been demonstrated to be vectors of Campylobacter and E. coli O157:H7 using PCR.[12] House flies can be monitored for bacterial pathogens using filter paper spot cards and PCR [13]
- Viruses: enteroviruses: poliomyelitis, viral hepatitis (A & E)..etc.
Potential in waste management [edit]
The ability of housefly larvae to feed and develop in a wide range of decaying organic matter is important for recycling of nutrients in nature. Research suggests that this adaptation may be exploited to combat with ever-increasing amount of waste.[14] Housefly larvae can be mass-reared in a controlled manner in animal manure, thus reducing the bulk of waste and minimizing environmental risks of its disposal.[15][16] Harvested maggots may be used as feed for animal nutrition.[16][17]
References [edit]
- ^ Larraín, Patricia & Salas, Claudio (2008). "House fly (Musca domestica L.) (Diptera: Muscidae) development in different types of manure [Desarrollo de la Mosca Doméstica (Musca domestica L.) (Díptera: Muscidae) en Distintos Tipos de Estiércol]". Chilean Journal of Agricultural Research 68 (2): 192–197. doi:10.4067/S0718-58392008000200009. ISSN 0718-5839.
- ^ Stuart M. Bennett (2003). "Housefly".
- ^ a b c Anthony DeBartolo (June 5, 1986). "Buzz off! The housefly has made a pest of himself for 25 million years". Chicago Tribune.
- ^ Dübendorfer A, Hediger M, Burghardt G, Bopp D. (2002). "Musca domestica, a window on the evolution of sex-determining mechanisms in insects". International Journal of Developmental Biology 46 (1): 75–79. PMID 11902690.
- ^ Brian M. Wiegmann, David K. Yeates, Jeffrey L. Thorne, Hirohisa Kishino, a fly's head, showing compound eyes and hair[dead link]
- ^ Ostrolenk M. & Welch H. (1942). "The house fly as a vector of food poisoning organisms in food producing establishments". American Journal of Public Health 32 (5): 487–494.
- ^ Levine, O.S. & Levine M.M. (1991). "House flies (Musca domestica) as mechanical vectors of shigellosis". Reviews of Infectious Diseases 13 (4): 688–696. PMID 1925289.
- ^ Förster M., Klimpel S. & Sievert K. (2009). "The house fly (Musca domestica) as a potential vector of metazoan parazites caught in a pig-pen in Germany". Veterinary Parasitology 160 (1-2): 163–167. doi:10.1016/j.vetpar.2008.10.087.
- ^ Georghiou G.P. & Hawley M.K. (1971). "Insecticide resistance resulting from sequential selection of houseflies in the field by organophosphorus compounds". Bulletin of the World Health Organization 45 (1): 43–51.
- ^ Keiding J. (1975). "Problems of housefly (Musca domestica) control due to multiresistance to insecticides". Journal of Hygiene, Epidemiology, Microbiology and Immunology 19 (3): 340–355. PMID 52667.
- ^ Nazni W.A., Luke H., Wan Rozita W.M., Abdullah A.G., Sadiyah I., Azahari A.H., Zamree I., Tan S.B., Lee H.L. & Sofian A.M. (2005). "Determination of the flight range and despersal of the house fly, Musca domestica (L.) using mark release recapture technique". Tropical Biomedicine 22 (1): 53–61. PMID 16880754.
- ^ A. L. Szalanski, C. B. Owens, T. Mckay & C. D. Steelman (2004). "Detection of Campylobacter and Escherichia coli O157:H7 from filth flies by polymerase chain reaction". Medical and Entomology 18 (3): 241–246. doi:10.1111/j.0269-283X.2004.00502.x. PMID 15347391.
- ^ Sheri M. Brazil, C. Dayton Steelman & Allen L. Szalanski (2007). "Detection of pathogen DNA from filth flies (Diptera: Muscidae) using filter paper spot cards". Journal of Agricultural and Urban Entomology 24 (1): 13–18. doi:10.3954/1523-5475-24.1.13.
- ^ Miller B. F., Teotia J. S. & Thatcher T. O. (1974). "Digestion of poultry manure by Musca domestica". British Poultry Science 15 (2): 231. doi:10.1080/00071667408416100. PMID 4447887.
- ^ Cickova H., Pastor B., Kozanek M., Martinez-Sanchez A., Rojo S. & Takac P. (2012). "Biodegradation of pig manure by the housefly, Musca domestica: A viable ecological strategy for pig manure management". PLOS ONE 7 (3): e32798. doi:10.1371/journal.pone.0032798. PMID 22431982.
- ^ a b Zhu FX., Wang WP., Hong CL., Feng MG., Xue ZY., Chen XY., Yao YL. & Yu M. (2012). "Rapid production of maggots as feed supplement and organic fertilizer by the two-stage composting of pig manure". Bioresource Technology 116: 485–491. doi:10.1016/j.biortech.2012.04.008. PMID 22541952.
- ^ Hwangbo J., Hong E. C., Jang A., Kang H. K., Oh J. S., Kim B. W. & Park B. S. (2009). "Utilization of house fly-maggots, a feed supplement in the production of broiler chickens". Journal of Environmental Biology 30 (4): 609–614. PMID 20120505.
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