Wikipedia

Phormia regina

(Redirected from Phormia)

Phormia regina, the black blow fly, belongs to the blow fly family Calliphoridae and was first described by Johann Wilhelm Meigen.[1]

Phormia regina
Scientific classification
Kingdom:
Animalia
Phylum:
Arthropoda
Class:
Insecta
Order:
Diptera
Family:
Calliphoridae
Genus:
Phormia

Species:
P. regina
Binomial name
Phormia regina
Meigen, 1826
Synonyms
  • Musca regina Meigen, 1826

The black blow fly's wings are specialized with a sharp bend. These flies also have well-developed calypters. Blow flies generally are about the size of a house fly or a little larger, and many are metallic blue or green in color. Key characteristics of this species include black gena, mostly white calypters, and anterior thoracic spiracles that appear to be orange yellow due to being surrounded by bright orange setae.[2][3]

P. regina is especially important to forensic entomology. Female P. regina, like other blow flies in the family Calliphoridae, oviposit their eggs on carrion, where they hatch. The larvae develop through three instar stages until pupation.[4] Adult black blow flies aggregate on feces in order to mate. The success of these mating interactions has been studied and appears to be related to size and diet of the adult flies. Following successful mating encounters, the adult females are then attracted to decaying material rather quickly for oviposition,[5] allowing forensic entomologists to use development stages of larvae as a clue in determining an approximate time of death. P. regina are extremely common in the United States and other areas in North America.[4] Combined with their importance in forensic entomology, these flies have been relatively well studied, particularly for variables affecting their development.

Taxonomy

edit

Phormia regina was described by the German entomologist Johann Wilhelm Meigen in 1826. Its specific epithet is derived from the Latin word regina meaning 'queen'.[1]

 
Sanitary entomology; the entomology of disease, hygiene and sanitation (1921)

Description

edit
 
Another phormia

Phormia regina adults are metallic blue or green in color and have a distinctive set of orange setae near the anterior thoracic spiracle.[2] They are also recognizable by their black gena (the side of the head below eye level), mostly white calypteres, and the distinctive bend in their wings.[2][3]

Distribution

edit

P. regina is commonly found across the entirety of the United States as well as across other regions in North America[4]

Habitat

edit

P. regina can be found on human corpses, animal carcasses, and feces. Researchers have observed these flies on a wide variety of animal excrement, but at least in the northwestern United States, they exhibit a preference for human, mink, and swine feces.[6] P. regina is predominantly found in the northern United States during spring and summer months, but in the winter they are localized to more southern regions.[7] This localization is tentatively linked to the importance of temperature on their development.[7] These flies prefer rural areas, especially near water sources, as opposed to urban spaces—at least in the San Francisco Bay Area.[8]

Life history

edit

The life cycle and development of Phormia regina is similar to that of most other Dipteran species, in which females oviposit their eggs onto a nutrient substrate. Then, after hatching, the larvae feed throughout three instar stages until they have stored up enough calories to commence pupation and finally emerge as adult blow flies. Each transition from first, second, and third instar is marked by a molt, and eventually the third-instar larvae develop sclerotized (hardened) casings which envelop and protect them throughout metamorphosis.[4]

Larval development

edit

Relatively few studies have been conducted on the adults of this species in comparison to those on larval development, mostly due to the importance of blow fly larvae in determining the post mortem interval (PMI) of corpses during investigations by forensic entomologists. For this reason, many researchers have conducted experiments to investigate the effect of various environmental factors on the duration time of larval development in this species (as well as many others).

Because the larval life cycle of this species is dependent on a climate with temperatures ranging from 12.7°C (55°F) to 35 °C (95 °F), it tends to inhabit the northern regions of the United States during summer months and southern regions in the winter. Researchers have discovered that at 40 to 45 °C, larval development occurs normally until the prepupal stage, at which point a majority of the larvae die. The few able to pupate at these high temperatures do not emerge as adults. The lowest temperature threshold for this species was found to be 12.5 °C below which females will not oviposit. The highest rate of development (with survival into adulthood) was seen at a constant temperature of 35 °C, where the average time of adult emergence was 265 hours (about 11 days). Flies at constant temperatures between 15 and 30 °C (at 5-degree increments) developed slower, with flies at the coolest temperatures taking the longest. Cyclic temperatures ranges of 25 to 35 °C and 15 to 25 °C proved to decrease the rate of development when compared to constant temperatures. (The cyclic temperature data were collected by placing specimens in an incubator which steadily alternated between the maximum and minimum temperatures of a particular 10-degree range (e.g. 25 to 35 °C). Each 10-degree fluctuation took place over a 12-hour span.)[4]

Also, studies have been conducted to assess the effects of light exposure on developmental variability in larvae. Larvae exposed to cyclic photoperiods (shifting intermittently between 12 hours of light to 12 hours of darkness) have higher rates of development than larvae exposed to constant photoperiods (24 hours of light per day). These findings suggest that darkness may be a stimulus for larval growth. However, these variations in light photoperiods failed to influence pupal duration times.[9]

Adult development

edit

While this species is in the wild, dung constitutes a majority of the nutritional intake used for sexual development in both male and female adults, but diets with higher protein intake better facilitate mating ability of both sexes. Female sexual maturity requires the completion of 10 stages of follicle development in the ovaries to produce eggs that are completely mature, and ovaries in females which have been deprived of a high-protein diet do not develop fully. Although it is possible for females on a diet of only dung to reach the final stage of sexual maturity, it takes much more time than if they were to feed exclusively on beef liver; even then, a lower percentage of those feeding on dung will have fully developed. An experiment by Stoffolano demonstrated this, revealing that 100% of females feeding exclusively on beef liver were able to reach the final stage of sexual development after 13 days, while only 78% of females were able to do so when feeding exclusively on pig dung over a 20-day period. Although some Dipteran species oviposit on dung, P. regina females exclusively deposit their eggs on carrion.[10]

The neuroendocrine system in adult males, which controls their mating behavior, must be stimulated before they will mate with a female. Protein in the male diet is not necessarily needed for this stimulation, but Stoffolano also saw that higher percentages of females were successfully inseminated by male specimens which had been fed either dung or beef liver versus specimens with a diet of only sugar. Protein is not generally necessary for spermatogenesis in male flies, but it is paramount for accessory reproductive gland development, higher rates of copulation, and the capability of impregnating females.[10] An additional study found a positive correlation between male head size and the size of the aedeagi (the external reproductive organs), which has been proposed as a possible reason for lower percentages of insemination between small males and large females within this species.[11]

Food sources

edit

Feeding habits vary greatly throughout the life cycle of P. regina. The feeding habits of adult flies depend both on sex and reproduction status of the fly. This is particularly important with respect to their protein intake, which literature suggests has an important role in sexual maturation and copulation ability in adult P. regina. [10][12] Like most other flies, the black blow fly feeds via sponging. Though adults require various types of nutrients, in the wild they are typically able to procure all their nutrition from feces.[13]

 
Decomposing possum

Larvae

edit

Adult females oviposit eggs on carrion. These eggs hatch into larvae that feed on the decaying tissue.[4]

Adult females

edit

Virgin adult females, when given access to protein and carbohydrate sources, utilize both for food. However, after their emergence as adults, they will gradually increase their protein intake until they are approximately 8 to 10 days old. From here they will continue to intake protein at a relatively constant rate that is lower than their required carbohydrate intake. Once a female has mated, either for the first time or all subsequent times, a spike in protein intake occurs following oviposition of her eggs.[12]

Adult males

edit

Protein intake in adult male black blow flies follows similar trends to that of virgin adult females; however, they require less total protein than females. The males will gradually increase their protein intake for the first 8–10 days of adulthood. They will then drop their protein intake to a relatively low and constant amount.[12]

Mating

edit

Adult black blow flies aggregate on feces, particularly animal dung pats, not only because they act as a food source, but also in order to mate. Some research has suggested a preference for settling on human, swine, and mink feces, but this may be localized to the northwestern region of the United States.[6] P. regina is a panmictic species.[14] Research supports mating success of adult males positively correlates to their size. Larger males have larger aedeagus which leads to more successful insemination of females. The mechanism of how and why larger aedeagus lead to better insemination is unknown.[11]

Female reproductive system

edit

Female black blow flies each have a pair of ovaries and lateral oviducts, one common oviduct, a vagina, and a bursa copulatrix, which is simply a sac-like cavity within the female that is roughly equivalent to a uterus. Each ovary has a lateral oviduct; these two lateral oviducts meet to form the common oviduct and connect the ovaries to the burs copulatrix. Three spermathecae are connected to the bursa copulatrix via spermathecal ducts, and two accessory glands attach to the bursa copulatrix near the spermathecae entries. The vagina is connected to the bursa copulatrix on the opposite end of the ovaries and allows the male aedeagus access to the bursa copulatrix and spermathecae.[15]

Male reproductive system

edit

Male black blow flies have an external phallus that is a tube-like structure with unique flaps centrally located. The phallus can be divided up into several different sections. There is the hypophallus, which protrudes from the abdomen of the fly. The cornua, which is the name given to the centrally located wing-like flaps on the phallus, protrude from the hypophallus. A pair of paraphallic bulbs are embedded in the cornua with only their tips jutting out. These bulbs are sclerotized, meaning they are hardened, as are a variety of spines on the outside of the cornua. From the cornua a narrower tube structure, the acrophallus, extends with a terminal fluted opening, referred to as the gonophore, from which sperm and accessory secretions flood.[15]

Copulation

edit

During mating the tip of the male's phallic structure is near the spermathecal ducts of the female's reproductive system. The wing-like flap structures on the male's phallus are situated in grooves within the bursa copulatrix of the female's reproductive system. The males also have appendages used to grasp and hold the female during copulation.[15]

Parental care

edit

Similarly to other flies in the family Calliphoridae, P. regina exhibit little or no parental care. Females, however, oviposit their eggs after mating on carrion, leaving the eggs to hatch and develop on their own.

Oviposition

edit

Mature P. regina females are known to oviposit their eggs on animal carcasses following copulation. Interestingly, it has been seen that the olfactory senses of female flies play some role in their decision of where and when to oviposit. Research suggests adult female P. regina will increase their ovipositing in the presence of a medium that provides odor stimuli to the fly.[16]

Social behavior

edit

Maggot mass effect

edit
 
Fly and beetle larvae on the 5-day old carcass of a South African porcupine

Black blow fly larvae, like many other blow flies, exhibit the maggot mass effect: a raise in temperature due to the aggregation of maggots. This rise in temperature may be beneficial to the larvae by aiding in feeding and development as well as protection from dangerously cold temperatures, predators, and parasites. Studies with other blow flies suggest that the change in temperature seen in the maggot mass effect functions well at a wide range of temperatures and that the larvae do not reduce their heat production at higher temperatures.[17]

Genetics

edit

The entire genome of P. regina has been sequenced so that it may serve as a reference genome that can be used in comparison with other Calliphoridae species. This fly has a chromosome number of 2n=12. The sex chromosomes of P. regina are a heteromorphic chromosome pair, meaning they have two morphologically distinct chromosomes that remain a homologous chromosome pair.[18]

Picard and Wells used amplified fragment length polymorphisms (AFLP) to create genetic profiles of P. regina flies collected from different regions to compare both within region and across region relatedness. They discovered adult flies take from the same corpse showed high relatedness, but between regions genetic variability was high. They suggest these findings may be especially important to forensic entomology with respect to determining if a recovered body has moved locations by comparing AFLP data across individual P. regina.[14]

Physiology

edit

P. regina, like other flies, is poikilothermic: the growth and development of the fly is dependent on temperature. At room temperature, the egg to pupal stage lasts about 6–11 hours. With an increase in temperature of the surrounding environment, metabolic rates of the blow fly typically increase, causing an increase in the rate of growth and development.[19] However, this species is intolerant to warmer temperatures, unlikely to survive to adulthood at temperatures of 40 °C or greater. This observation provides an explanation as to why the species cannot survive the summer months in southern regions of the US. The adult organism's activity becomes inhibited by temperatures lower than 12.5 °C.[4] In addition to an increase in the growth and development, temperature also has a profound impact on female oviposition.[20] It is key to note the fluctuations between diurnal and nocturnal temperatures.

It is important to note the larval stage of the blowfly, due to its importance in forensics. The larvae have posterior spiracles, small openings on the back used for the intake of oxygen. Larvae are also equipped with mouth hooks used for the physical breakdown of proteins when feeding, while proteolytic enzymes are used for chemical breakdown of these proteins.[21]

Interactions with humans

edit

Myiasis

edit

P. regina larvae have been shown to be an important organism in myiasis of both humans and animals, particularly in the southern region of the United States. Often in a myiatic infection where P. regina larvae are found, they are the only species involved; however, they had been found to be present in a wound with Cochliomyia hominivorax formerly C. americana as well.[22]

 
Severe myasis hen


Forensic importance

edit

P. regina is a very important species in medico-criminal entomology, an area in forensic entomology which uses entomologists to aid with arthropod evidence in criminal investigations.[23] This aspect of forensic science stresses using arthropod evidence in solving crimes, often of a violent nature, through two ideal approaches to estimate post mortem interval (PMI). The first approach accounts for the general succession of arthropod communities, and the second considers environmental influences on the development of arthropods.[23] With knowledge of the regional insect fauna and times of carrion colonization, the insect gathering associated with the remains can be analyzed to determine a window of time in which death took place. PMI is a critical aspect of criminal investigations following recovery of a corpse. PMI relies on an entomologist's ability to correlate the species or stage of development of arthropods, in this case P. regina, to an approximation of the elapsed period between a person's death and the discovery of his/her body.[23]

Blow flies are usually the first insects to colonize a body, frequently within minutes after death.[24] P. regina adults and larvae are attracted to the body because, during decomposition, the remains go through rapid physical, biological, and chemical changes. If a corpse is found, the presence of Dipteran larvae may be used to suggest PMI by estimating the time it would have taken for eggs to have been deposited and larvae to have developed to the stage they were collected, while taking into account environmental factors. Blow flies will lay their eggs on the corpse, usually in a wound, if present, or in any of the natural orifices, and the maggot age can give a date of death accurate to a day or less, and is used in the first few weeks after death.[5]

Research is being conducted to further perfect the dating of a PMI. One study suggests that P. regina occasionally oviposits on carrion at night only when certain conditions are met.[20] A similar study found a combination of artificial lighting, warm temperatures, and the onset of low-pressure atmospheric conditions encourages nocturnal oviposition in P. regina[19] Other studies suggest P. regina preferentially distribute their eggs during the day. Confirming the preference for daytime or nighttime oviposition in P. regina could aid in increasing the accuracy of PMI determination, and the disagreement necessitates more experimentation to investigate this environmental effect.[25]

 
Maggot debridement therapy on a diabetic foot

Medical Importance

edit

Phormia regina is a flesh-eating fly not usually used for medical gain. However, the maggots from the black blow fly are used in maggot therapy, a type of biotherapy involving the intentional introduction of live, disinfected maggots into the skin and soft tissue wound of a human or animal for the purpose of selectively cleaning out only the necrotic tissue to promote healing.[26]

References

edit
  1. ^ a b Simpson DP (1979). Cassell's Latin Dictionary (5 ed.). London: Cassell. ISBN 0-304-52257-0.[page needed]
  2. ^ a b c Whitworth, Terry (1 November 2010). "Keys to the genera and species of blow flies (Diptera: Calliphoridae) of the West Indies and description of a new species of Lucilia Robineau-Desvoidy". Zootaxa. 2663 (1): 1. doi:10.11646/zootaxa.2663.1.1.
  3. ^ a b Rognes, Knut (1991). Blowflies (Diptera, Calliphoridae) of Fennoscandia and Denmark. E.J. Brill/Scandinavian Science.[page needed]
  4. ^ a b c d e f g Byrd, Jason H.; Allen, Jon C. (August 2001). "The development of the black blow fly, Phormia regina (Meigen)". Forensic Science International. 120 (1–2): 79–88. doi:10.1016/S0379-0738(01)00431-5. PMID 11457615.
  5. ^ a b Anderson, G.S. Forensic Entomology: the use of insects in death investigations. [1]
  6. ^ a b Coffey, Marvin D. (1 January 1966). "Studies on the Association of Flies (Diptera) with Dung in Southeastern Washington1". Annals of the Entomological Society of America. 59 (1): 207–218. doi:10.1093/aesa/59.1.207.
  7. ^ a b Weidner, L. M.; Jennings, D. E.; Tomberlin, J. K.; Hamilton, G. C. (September 2015). "Seasonal and Geographic Variation in Biodiversity of Forensically Important Blow Flies (Diptera: Calliphoridae) in New Jersey, USA". Journal of Medical Entomology. 52 (5): 937–946. doi:10.1093/jme/tjv104. PMID 26336244.
  8. ^ Brundage, Adrienne; Bros, Shannon; Honda, Jeffrey Y. (October 2011). "Seasonal and habitat abundance and distribution of some forensically important blow flies (Diptera: Calliphoridae) in Central California". Forensic Science International. 212 (1–3): 115–120. doi:10.1016/j.forsciint.2011.05.023. PMID 21683536.
  9. ^ Nabity, P. D.; Higley, L. G.; Heng-Moss, T. M. (1 March 2007). "Light-Induced Variability in Development of Forensically Important Blow Fly Phormia regina (Diptera: Calliphoridae)". Journal of Medical Entomology. 44 (2): 351–358. doi:10.1093/jmedent/44.2.351. PMID 17427708.
  10. ^ a b c Stoffolano, John G.; Li, Mei-Fang; Sutton, James A.; Yin, Chih-Ming (October 1995). "Faeces feeding by adult Phormia regina (Diptera: Calliphoridae): impact on reproduction". Medical and Veterinary Entomology. 9 (4): 388–392. doi:10.1111/j.1365-2915.1995.tb00010.x. PMID 8541589. S2CID 46576978.
  11. ^ a b Stoffolano, John G.; Gonzalez, Elizabeth Y.; Sanchez, Marilyn; Kane, Joann; Velázquez, Kenneth; Oquendo, Aida L.; Sakolsky, Gabrielle; Schafer, Peter; Yin, Chih-Ming (1 May 2000). "Relationship Between Size and Mating Success in the Blow Fly Phormia regina (Diptera: Calliphoridae)". Annals of the Entomological Society of America. 93 (3): 673–677. doi:10.1603/0013-8746(2000)093[0673:RBSAMS]2.0.CO;2. S2CID 86641107.
  12. ^ a b c Yin, Chih-Ming; Qin, Wen-Hong; Stoffolano Jr, John G (September 1999). "Regulation of mating behavior by nutrition and the corpus allatum in both male and female Phormia regina (Meigen)". Journal of Insect Physiology. 45 (9): 815–822. doi:10.1016/S0022-1910(99)00047-5. PMID 12770294.
  13. ^ Stoffolano, John G.; Tobin, Edward N.; Wilson, James; Yin, Chih-Ming (1995). "Diet Affects Insemination and Sexual Activity in Male Phormia regina (Diptera: Calliphoridae)". Annals of the Entomological Society of America. 88 (2): 240–246. doi:10.1093/aesa/88.2.240.
  14. ^ a b Picard, C. J.; Wells, J. D. (2009). "Survey of the Genetic Diversity of Phormia regina (Diptera: Calliphoridae) Using Amplified Fragment Length Polymorphisms". Journal of Medical Entomology. 46 (3): 664–670. doi:10.1603/033.046.0334. PMID 19496440.
  15. ^ a b c Merritt, David J.; Yin, Chih-Ming; Stoffolano, John G. (1 January 1994). "Copulatory Apparatus and Deposition of Male Accessory Secretion in Phormia regina (Diptera: Calliphoridae)". Annals of the Entomological Society of America. 87 (1): 97–103. doi:10.1093/aesa/87.1.97.
  16. ^ Barton Browne, L. (October 1960). "The role of olfaction in the stimulation of oviposition in the blowfly, Phormia regina". Journal of Insect Physiology. 5 (1): 16–22. doi:10.1016/0022-1910(60)90019-6.
  17. ^ Johnson, Aidan P.; Wallman, James F. (August 2014). "Effect of massing on larval growth rate". Forensic Science International. 241: 141–149. doi:10.1016/j.forsciint.2014.05.006. PMID 24972255.
  18. ^ Andere, Anne A.; Platt, Roy N.; Ray, David A.; Picard, Christine J. (28 October 2016). "Genome sequence of Phormia regina Meigen (Diptera: Calliphoridae): implications for medical, veterinary and forensic research". BMC Genomics. 17 (1): 842. doi:10.1186/s12864-016-3187-z. PMC 5084420. PMID 27793085.
  19. ^ a b Kirkpatrick, Ryan S.; Olson, Jimmy K. (March 2007). "Nocturnal Light and Temperature Influences on Necrophagous, Carrion-Associating Blow Fly Species (Diptera:Calliphoridae) of Forensic Importance in Central Texas". Southwestern Entomologist. 32 (1): 31–36. doi:10.3958/0147-1724-32.1.31. hdl:1969.1/1104. S2CID 85762551.
  20. ^ a b Greenberg, Bernard (1 September 1990). "Nocturnal Oviposition Behavior of Blow Flies (Diptera: Calliphoridae)". Journal of Medical Entomology. 27 (5): 807–810. doi:10.1093/jmedent/27.5.807. PMID 2231617.
  21. ^ Fletcher, Fred Walker; Haub, James G. (March 1933). "Digestion in Blowfly Larvae, Phormia Regina Meigen, Used in the Treatment of Ostermyelitis". Medicine, Biology. hdl:1811/2619.
  22. ^ Knipling, E. F.; Rainwater, H. T. (October 1937). "Species and Incidence of Dipterous Larvae Concerned in Wound Myiasis". The Journal of Parasitology. 23 (5): 451. doi:10.2307/3272391. JSTOR 3272391.
  23. ^ a b c Byrd, J. H., and J. L. Castner. 2001. Forensic entomology : The utility of arthropods in legal investigations. CRC Press, New York.[page needed]
  24. ^ Catts, E P; Goff, M L (January 1992). "Forensic Entomology in Criminal Investigations". Annual Review of Entomology. 37 (1): 253–272. doi:10.1146/annurev.en.37.010192.001345. PMID 1539937.
  25. ^ Maureen C. Berg, M. Eric Benbow, Environmental Factors Associated With Phormia regina (Diptera: Calliphoridae) Oviposition, Journal of Medical Entomology, Volume 50, Issue 2, 1 March 2013, Pages 451–457, doi:10.1603/ME12188
  26. ^ Hays, A. History of Medicine Part 1: Maggot Therapy. 15 March 2007

Further reading

edit
Retrieved from "https://en.wikipedia.org/w/index.php?title=Phormia_regina&oldid=1237816577"