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Musca (fly)
Musca (fly)
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Musca
Musca domestica (housefly)
Scientific classification Edit this classification
Kingdom: Animalia
Phylum: Arthropoda
Class: Insecta
Order: Diptera
Family: Muscidae
Tribe: Muscini
Genus: Musca
Linnaeus, 1758
Type species
M. domestica
Species

See text.

Synonyms

Musca is a genus of flies. It includes Musca domestica (the housefly), as well as Musca autumnalis (the face fly or autumn housefly). It is part of the family Muscidae.

Selected species

[edit]

Phylogeny

[edit]
Nematocera

Other Nematocera (crane flies, mosquitoes, etc.)

Brachycera

Tabanomorpha (horse flies, etc.)

Muscomorpha

Other Muscomorpha (robber flies, etc.)

Syrphoidea (hoverflies)

Schizophora

Acalyptratae (marsh flies, etc.)

Calyptratae

Hippoboscoidea (louse flies, bat flies, etc.)

Cladogram showing higher level classification[3][4][5] and position of Musca within the family Muscidae.[6]

References

[edit]
Revisions and contributorsEdit on WikipediaRead on Wikipedia
from Grokipedia
Musca is a of true in the family and order Diptera, encompassing approximately 60 that are predominantly distributed across the , with some having spread to temperate regions of the . These flies are characterized by their small to medium size (typically 5–10 mm in body length), grayish to black coloration, robust bodies covered in bristles, and a single pair of functional wings with calypters at the base. They exhibit complete , with larvae developing as maggots in moist, decaying such as animal feces, garbage, and . The genus is best known for Musca domestica, the common house fly, a cosmopolitan strongly associated with settlements and operations worldwide. M. domestica adults feed on liquids via a sponging , often regurgitating onto solid food to liquefy it, and can mechanically transmit over 100 bacterial, viral, and parasitic pathogens, including typhoid, , and , by carrying contaminants on their bodies and mouthparts. Females lay batches of 100–150 eggs, up to 500–900 total, in suitable breeding sites, completing a generation in as little as 7–10 days under warm conditions, leading to rapid population growth. Other notable species include Musca autumnalis, the face fly, which primarily affects and horses by feeding on ocular and nasal secretions, potentially spreading eye diseases like pinkeye, and Musca sorbens, the bazaar or eye fly, prevalent in tropical regions where it targets human eyes and open wounds, exacerbating conditions like . While most Musca species are non-biting, their proximity to humans and animals underscores their role as pests and disease vectors, prompting extensive research into control measures such as , insecticides, and biological agents. The genus's evolutionary adaptations, including diverse microbial communities in their guts that aid survival in varied habitats, highlight their ecological significance in and nutrient cycling.

Taxonomy

History and etymology

The genus name Musca derives from the Latin word for "fly," a term historically used as a broad descriptor for various flying before its formal adoption in scientific . Carl Linnaeus established the genus Musca in the 10th edition of Systema Naturae (1758), providing a diagnostic description—"Os proboscide carnosa: labiis lateralibus: Palpi nulli"—and listing approximately 100 species based primarily on European specimens, with Musca domestica serving as the type species by subsequent designation. This initial classification encompassed a diverse array of taxa now recognized in multiple dipteran families, leading to early confusions; for instance, species like Musca calcitrans Linnaeus, 1758 (now the type of Stomoxys Meigen, 1803) were included due to superficial similarities in morphology. Throughout the , taxonomic revisions progressively refined Musca within the emerging family , separating it from broader Diptera groups such as Syrphidae and ; key contributions included Johan Christian Fabricius's (1775–1805) generic splits and Johann Wilhelm Meigen's (1804–1838) use of wing vein M curvature to delineate muscid boundaries. Further advancements came from Camillo Rondani (1856), who defined Musca by the absence of ventral bristles on the mid-tibia and an angular bend in vein M, and the establishment of the tribe Muscini in the late 19th to early to unite Musca with morphologically allied genera within . In the , works by Paul Stein (1919), who cataloged 46 Palaearctic species, and subsequent efforts by W.S. Patton (1933), van Emden (1939, 1965), and Adrian C. Pont (1984, 1990) addressed lingering ambiguities through lectotype designations and reclassifications, solidifying Musca as a monophyletic entity. Notable modern synonymies include the resolution of Musca corvina Fabricius, —a junior of M. autumnalis De Geer, 1776—as confirmed by Stein (1919), reflecting improved understanding of limits through comparative morphology.

Classification

The Musca Linnaeus, 1758, is classified within the following taxonomic : Kingdom Animalia > Phylum Arthropoda > Class Insecta > Order Diptera > Family > Subfamily Muscinae > Tribe Muscini > Genus Musca. Members of the genus Musca are distinguished by several diagnostic morphological features shared with the tribe Muscini, including the presence of well-developed calypters covering the scutellar margin, a pubescent arista, and a frons bearing interfrontal setulae. Additional genus-specific synapomorphies encompass the mid tibia lacking an internal bristle and wing vein M exhibiting an angular forward curve. The type species of Musca is Musca domestica Linnaeus, 1758, originally described in Systema Naturae and formally designated by Westwood in 1840, with the designation ratified by International Commission on Zoological Nomenclature Opinion 82 in 1925; this species serves as the nomenclatural benchmark for the genus, defining its core characteristics in muscid taxonomy. The encompasses approximately 60 valid , primarily distributed in the , with subgeneric divisions including Musca (sensu stricto) and other groupings such as the domestica-group and sorbens-group, as recognized in early systematic revisions.

Description

Adult morphology

Adult Musca flies are medium-sized insects, typically measuring 4 to 10 mm in length, with a grayish body coloration that serves as in various environments. The is characterized by four prominent longitudinal dark stripes, a diagnostic feature of the , while the is generally gray or yellowish with irregular dark markings along the midline and sides. The legs are yellowish to blackish, adapted for walking on diverse surfaces, and the compound eyes are large and , providing a wide field of vision. The head features short antennae consisting of three segments, the third bearing a dorsal arista that aids in sensory perception. Mouthparts are of the sponging type, with a retractable comprising a haustellum and labellum equipped with pseudotracheae—fine, tube-like structures on the labellum's inner surface that facilitate the uptake of food by . These mouthparts include prestomal teeth that filter particles larger than approximately 45 µm, preventing ingestion of solids. Wings in adult Musca are translucent with a yellowish tinge at the base and exhibit characteristic Dipteran venation, including the R1 terminating before the wing's and the costal extending to the junction of M1 and M2. A key identifying trait is the sharp upward bend in the fourth longitudinal (M1), which distinguishes Musca from related genera. Sexual dimorphism is evident in several traits: males possess holoptic eyes that nearly meet at the vertex, enhancing for mate location, while females have dichoptic eyes with wider separation; females are generally larger than males, and males often exhibit a yellowish underside to the . Differences in setation, such as arrangement on the and legs, also vary subtly between sexes to support reproductive behaviors. Across the , morphological variations are subtle but notable; for instance, M. domestica adults have uniformly reddish eyes and a predominantly gray , whereas M. autumnalis (face fly) shows sexual differences in abdomen color—mottled gray-black in females and bright golden in males—and slightly larger body sizes up to 10 mm. These traits reflect adaptations to specific ecological niches within the genus.

Immature stages

The eggs of flies in the genus Musca are elongated and white, measuring approximately 1 mm in length, and are typically laid in clusters on decaying such as or garbage. The surface features longitudinal ridges that aid in to substrates and to each other within the cluster. These ridges, along with a sticky from the , ensure the eggs remain in place in moist environments suitable for . Larvae of Musca species undergo three instars, appearing as legless, maggot-like forms that are creamy white and cylindrical, tapering anteriorly toward the head. The first is small, about 3 mm long, with simple posterior spiracles featuring two straight slits; subsequent instars grow progressively, reaching up to 12 mm in the third instar. A prominent cephalopharyngeal skeleton, composed of sclerotized mouthhooks and supporting structures, enables feeding on liquefied and is characteristic of muscid larvae. Posterior spiracles in later instars are slightly raised, with sinuous slits bordered by a dark oval ring, a trait adapted for respiration in humid, decaying substrates; notably, Musca larvae lack prolegs, distinguishing them from some other fly genera and emphasizing their burrowing lifestyle in moist media. The spiracle arrangement foreshadows adult thoracic spiracles, maintaining continuity in respiratory morphology across life stages. The pupal stage in Musca is non-feeding and occurs within a barrel-shaped puparium, measuring 6–9 mm in length, formed by the hardened, darkened of the third-instar . This puparium is bluntly rounded at both ends, with color varying from pale yellow to reddish-brown or black as it matures, and includes respiratory structures like anterior and posterior spiracular plates for during . The enclosed undergoes internal reorganization, culminating in adult emergence through a split in the puparium.

Life cycle

Reproduction

Mating in the genus Musca, particularly Musca domestica, is initiated by males through a stereotyped sequence that includes orientation toward the female, landing nearby, extension of wings (wing fanning), and raising of forelegs to signal readiness. Males release aggregation pheromones to attract both sexes, leading to clusters on preferred vertical surfaces such as walls, fences, or piles where and copulation occur. Copulation typically lasts 15-30 minutes, during which the male transfers sperm via . Following mating, females store in specialized spermathecae within the reproductive tract, allowing fertilization of multiple batches over their lifespan without remating. does not occur in the genus Musca, requiring for viable development. Gravid females select oviposition sites based on olfactory cues from fermenting , such as decaying , , or waste, to ensure suitable conditions for larval survival. Each oviposition event involves laying a batch of 75-150 , with capable of producing up to five such batches over 3-4 days post-mating. Lifetime reaches 500-900 eggs per female, with peak production at temperatures of 25-30°C where egg output can exceed 700 eggs. Higher temperatures beyond this range reduce overall egg viability and female longevity, limiting total output.

Development stages

The development of Musca flies follows a holometabolous life cycle, progressing through , larval, and pupal stages before emergence, with the entire pre-imaginal period influenced primarily by environmental conditions such as and . of Musca domestica typically hatch within 8 to 20 hours under warm conditions (around 25–30°C), though this can extend to 24 hours at lower , with hatching requiring sufficient moisture to prevent . The larval stage lasts 3 to 7 days in total under optimal warm conditions (35–38°C), during which larvae feed voraciously on bacteria-rich organic substrates like ; they undergo three molts, progressing through instars that increase in size from approximately 3 mm to 12 mm. High moisture levels in the substrate (above 60% relative ) are essential for larval survival and growth, as drier conditions inhibit feeding and development. Mature larvae migrate to drier sites, such as or desiccated , to pupate, where the pupal endures 3 to 6 days at temperatures of 32–37°C; during this non-feeding phase, occurs as larval tissues reorganize into adult structures via histolysis and histogenesis. At cooler temperatures around 24°C, pupal development can extend to about 7 days. The complete generation time from to emergence ranges from 7 to 30 days, depending on conditions, with optimal development at 25–35°C; below 10°C, development halts, and flies become inactive. In some like Musca autumnalis, adults enter reproductive during cooler periods, characterized by halted and , induced by short photoperiods and low temperatures.

Distribution and habitat

Geographic distribution

The genus Musca encompasses species primarily of Old World origin, with many tracing their native ranges to Paleotropical regions, including tropical and . For instance, Musca domestica, the common house fly, is believed to have originated in the steppes of or the within the southern Palearctic. Other species, such as Musca sorbens, are native to tropical and subtropical areas of and . Currently, Musca species exhibit a , facilitated by human activities, and are present on all continents except . The genus shows highest species diversity in the Afrotropical and Oriental regions, where over 39 species have been documented in alone, reflecting adaptations to diverse tropical environments. In contrast, diversity is lower in temperate and polar zones. Species-specific ranges vary notably; M. domestica is now worldwide, thriving in both urban and rural settings across all climates. M. autumnalis, the face fly, is primarily found in temperate areas of the Holarctic region, including , and introduced populations in . M. sorbens remains largely restricted to tropical and , where it is associated with settlements. The spread of Musca species has been tied to trade and migration since ancient times, rendering many synanthropic and dependent on anthropogenic environments like farms and cities. This human-mediated dispersal has expanded their ranges dramatically over millennia, from original foci to global ubiquity for key like M. domestica.

Habitat preferences

Musca species, particularly the house fly Musca domestica, preferentially breed in decaying organic substrates rich in moisture and nutrients, such as animal , garbage, piles, and food waste. These sites provide the necessary fermenting material for larval development, with horse manure often cited as an optimal medium due to its consistent availability in areas. Adult flies, in contrast, favor warm, sunny surfaces for resting and activity, including walls, ceilings, and outdoor structures near human habitation, where they can bask and access food sources. Larval stages require moist, organic-rich microhabitats with temperatures ideally between 20°C and 40°C for optimal growth and survival, though development is fastest at 35–38°C. These conditions support rapid feeding on and decomposing matter, with pH levels around 6–8 in the substrate facilitating enzymatic breakdown. Prior to pupation, larvae migrate to drier, shaded edges of breeding sites to avoid direct and , pupating in protected crevices or . Musca flies exhibit notable adaptations to challenging environments, including high tolerance for urban pollution, high ammonia levels in manure, and contaminated organic waste, enabling persistence in densely populated or industrial areas. For instance, Musca vetustissima, the Australian bush fly, thrives in arid outback conditions by breeding primarily in livestock dung and human feces, exploiting ephemeral water sources from animal activity in otherwise dry landscapes. Seasonally, Musca populations peak during warm months when temperatures exceed 20°C, aligning with increased breeding and adult activity. In temperate regions, they overwinter as pupae or dormant adults in sheltered spots like manure piles or building cracks, resuming development with rising spring temperatures.

Behavior

Feeding and foraging

Adult Musca flies, particularly the house fly Musca domestica, possess sponging mouthparts adapted for imbibing liquids, consisting of a proboscis with a labellum that functions like a sponge to absorb fluids through capillary action. To consume solid foods, adults regurgitate digestive enzymes from their crop onto the material, liquefying it into a soluble form before sponging it up; this process allows them to feed on a variety of substrates without biting. The diet of adult Musca flies is omnivorous and opportunistic, comprising from flowers, fluids from wounds, , carrion, and decaying such as garbage or , though they avoid hard or dry substances unless pre-liquefied. This broad feeding repertoire supports their synanthropic lifestyle near human and habitats, where nutrient-rich, moist sources abound. Foraging in Musca species involves visual cues, with adults strongly attracted to moving objects, contrasting colors, and edges of resource patches, which guide them to food sources and help delineate rewarding areas during exploration. They often aggregate in swarms at discovered food sites, enhancing efficiency through collective detection, and can learn short-term associations between visual stimuli and food quality to refine their search patterns. Nutritionally, adult Musca flies require carbohydrates as their primary energy source for flight and general , while proteins are crucial for ovarian development and production in females; diets balancing both, such as milk-sugar mixtures, optimize and compared to carbohydrate-only sources. Feeding on contaminated substrates also results in incidental microbial intake, which may contribute to but is not a targeted nutritional strategy.

Locomotion and activity patterns

Adult house flies of the Musca, particularly M. domestica, exhibit flight capabilities that enable rapid and agile locomotion, with maximum speeds reaching approximately 8 km/h. This speed facilitates evasive maneuvers, such as dodging predators or obstacles through quick changes in direction, supported by their compound eyes and neural processing that detect motion with high . The wings beat at a frequency of around 200 Hz during flight, generating the characteristic buzzing sound and providing the thrust for sustained hovering or short bursts of speed. On the ground, Musca species walk using their tarsi, which feature paired claws and pulvilli covered in secretory hairs that enable attachment to vertical or inverted surfaces via forces and der Waals interactions. This allows them to traverse walls and ceilings effortlessly during or resting. Positive phototaxis influences their activity, as adults are attracted to sources, promoting movement toward illuminated areas during active periods. Activity in Musca follows diurnal circadian rhythms, with peak locomotion occurring midday under temperate conditions, though patterns shift with temperature—advancing in heat and broadening in cooler environments. Dispersal from breeding sites typically extends 1-5 km, often wind-assisted, while at night, flies rest in aggregations on walls, ceilings, or to conserve energy.

Ecology and human interactions

Ecological roles

The larvae of Musca species, particularly Musca domestica, serve as key decomposers in ecosystems by accelerating the breakdown of organic waste such as and carrion, thereby facilitating nutrient recycling and preventing the accumulation of decaying matter. This process enriches with essential nutrients like and , supporting plant growth and microbial activity in nutrient-poor environments. In human-associated habitats, where organic waste is abundant, Musca larvae contribute significantly to this , enhancing overall productivity. As prey items, Musca flies occupy an important position in food webs, with both larvae and adults serving as food sources for a diverse array of predators. Larvae are consumed by ground-dwelling organisms such as predatory beetles, , and small mammals, while adults form part of the aerial and are hunted by birds, spiders, amphibians, reptiles, and parasitic wasps. This predation helps regulate Musca populations and transfers energy across trophic levels, supporting in both terrestrial and aerial ecosystems. Musca adults play a minor role as pollinators by feeding on floral and inadvertently transferring between plants, particularly in open habitats where specialized pollinators are scarce. However, this benefit is limited because the flies often carry contaminants from organic waste on their bodies, potentially introducing pathogens to flowers and reducing the viability of for . In breeding sites like decaying , Musca engage in competition with other filth flies, such as black soldier flies (), for resources, which influences larval survival and . Additionally, Musca larvae impact microbial communities in waste substrates by grazing on and competing with predatory microbes, thereby shaping the process and altering nutrient availability.

Pest status and disease transmission

House flies in the genus Musca, particularly Musca domestica, are significant pests due to their synanthropic habits, thriving in close proximity to human settlements and operations, where they contaminate food, surfaces, and wounds. Their pest status stems primarily from mechanical vectoring of pathogens, as they lack the specialized mouthparts for biological transmission but readily transfer microbes on their bodies, legs, and mouthparts after contacting contaminated sources like or decaying matter. As mechanical vectors, Musca species carry a wide array of pathogens, with systematic reviews identifying over 100 bacterial, fungal, protozoan, and viral taxa associated with house flies alone, including Salmonella spp., Escherichia coli, and agents of typhoid (Salmonella Typhi) and cholera (Vibrio cholerae). These flies can harbor viable bacteria such as Salmonella enterica on their legs and bodies for up to 24 hours, facilitating transmission to human food and water supplies during feeding or landing. Their feeding behaviors, which involve regurgitation and defecation on surfaces, further exacerbate pathogen spread by depositing contaminated fluids. The economic burden of Musca pests is substantial, with control efforts and associated damages costing U.S. producers an estimated $700 million to $1 billion annually (as of 2025), driven by reduced animal productivity and veterinary treatments. For instance, the face fly (Musca autumnalis) inflicts direct harm to by feeding on ocular and nasal secretions, causing that leads to bacterial pinkeye (infectious bovine keratoconjunctivitis), which results in economic losses of $150 million annually (as of the early , with recent estimates suggesting higher adjusted values) in the U.S. due to treatment, , and . Certain Musca species pose species-specific threats; M. domestica is a ubiquitous pest in homes, farms, and urban areas, where it invades structures and spreads foodborne illnesses, while M. sorbens (the bazaar fly) predominates in tropical regions, targeting ocular and nasal discharges to transmit , the bacterium causing —a leading infectious cause of blindness affecting millions in endemic areas. Control of Musca pests relies on integrated approaches, including to eliminate breeding sites like and waste, chemical insecticides such as pyrethroids and organophosphates applied to adult flies or larvae, and biological agents like entomopathogenic fungi (), parasitic wasps (Muscidifurax spp.), and predatory mites to suppress populations without heavy reliance on pesticides.

Diversity

Number of species

The genus Musca comprises approximately 60 valid species, primarily distributed in the Old World, with the tribe Muscini encompassing about 350 species across 21 genera worldwide. Diversity within Musca is highest in the Afrotropical region, where 39 species have been recorded, and the Oriental region, which hosts a significant portion of the remaining species due to its tropical environments favoring muscid proliferation. In contrast, representation is low in the Nearctic region, limited to just a few introduced or adventive species such as Musca domestica. Taxonomic delineation in Musca faces ongoing challenges, including the recognition of cryptic that exhibit subtle morphological variations, necessitating revisions based on of structures like wing venation, chaetotaxy, and male genitalia. Historical nomenclatural issues, such as junior homonyms and synonyms, have complicated counts, with over 2,000 names proposed but only a fraction validated through systematic catalogs. Modern approaches integrate , particularly the COI gene region, with morphological data to resolve boundaries, as demonstrated in studies of Nearctic where genetic clusters aligned with morphological distinctions without uncovering hidden cryptic diversity. No species in the genus Musca are currently listed as endangered, reflecting their predominantly synanthropic lifestyles and widespread adaptability to human-modified habitats, which enhance their resilience against environmental pressures.

Selected species

Musca domestica, commonly known as the , is a cosmopolitan measuring 6–7 in length, characterized by a gray adorned with four dark longitudinal stripes. This fly is a significant global pest, breeding prolifically in decaying such as animal , garbage, and other , with females capable of laying up to 500 eggs per batch. As a mechanical vector, it transmits over 100 pathogens, including responsible for diseases like typhoid and , by carrying contaminants on its body and regurgitating fluids during feeding. Musca autumnalis, the face fly, inhabits temperate regions worldwide, particularly in areas with , and adults measure 6–10 mm long, resembling the but with a slightly larger size and similar thoracic striping. It preferentially feeds on secretions from the eyes and muzzle of and other animals, causing and potential spread of bacterial infections like pinkeye. Unlike many flies, M. autumnalis overwinters as reproductively inactive adults in sheltered locations such as buildings or woodpiles, emerging in spring to lay eggs in fresh cattle dung. Musca sorbens, known as the eye fly or bazaar fly, is a tropical species distributed across , , and the Pacific, with adults approximately 6–8 mm in length and a grayish body with four longitudinal dark stripes on the , similar to the . It targets human and animal ocular and nasal secretions for feeding, serving as a key vector for , a leading cause of infectious blindness, by mechanically transferring bacteria between hosts. Larvae develop in human and animal , contributing to challenges in endemic areas, though direct causation of is less documented compared to its role in bacterial transmission. Musca vetustissima, the Australian bush fly, is endemic to , especially arid and semi-arid zones, where adults reach 5–7 mm and exhibit a dull gray coloration similar to the but with more pronounced reddish eyes in males. This non-biting species swarms around humans and livestock, particularly during the warmer months, causing significant annoyance by landing on faces and wounds, though it does not feed on blood. It breeds exclusively in dung, with populations peaking in spring and summer, exacerbating irritation in and regions. Musca crassirostris stands out among congeners with its robust, thickened adapted for blood-feeding, making it one of the few haematophagous in the genus, and adults measure 5.5–7.5 mm. Distributed from through the to , it targets such as camels and , piercing skin to suck blood and potentially transmitting diseases like . Its biting behavior and preference for warm, environments underscore its veterinary importance in these regions.

Phylogeny

Evolutionary history

The genus Musca, belonging to the family within the suborder of Diptera, originated during the , with molecular estimates placing the divergence of Muscidae in the early Eocene around 51.6 million years ago (95% highest posterior density: 48.9–54.2 Ma), coinciding with the Eocene Climatic Optimum. Molecular analyses suggest the ancestral area of Muscidae was in the Neotropical region. This timing aligns with broader diversification events in calyptrate flies, driven by climatic warming that facilitated adaptive expansions from ancestral brachycera lineages. The cosmopolitan species M. domestica likely originated in the steppes of , adapting to human-associated environments before global radiation. Fossil evidence for Muscidae begins in the Eocene, with the oldest confirmed specimens including Acanthomyites aldrichi from Eocene deposits in the United States, providing direct insights into the family's early morphology and ecology. Although no fossils are definitively assigned to the genus Musca, the Eocene record of muscid-like flies supports inferences about the ancient origins of the tribe Muscini, to which Musca belongs, with shared traits such as calypters and larval saprophagy indicating continuity from these precursors. Miocene fossils, such as those from Dominican amber (dated 20–15 Ma), further document diversification, marking the Oligocene-Miocene transition as a period of increased speciation within Muscidae, though the family remains relatively young compared to other dipteran groups. Earlier estimates suggesting Permian origins lack supporting fossils and are considered unsubstantiated. A key in Musca involved the shift to synanthropy, where species like Musca domestica became closely tied to human habitats, exploiting resources from agriculture and waste beginning around the period approximately 10,000 years ago. This association with domesticated mammals and farming practices enabled rapid global dispersal from Central Asian origins, enhancing survival in anthropogenic environments. In more recent evolutionary history, M. domestica has demonstrated remarkable adaptability through the evolution of insecticide resistance, particularly to pyrethroids, driven by mutations in voltage-sensitive genes that confer target-site insensitivity, allowing populations to persist amid widespread chemical control efforts. Post-Pleistocene events further shaped Musca diversification, with analyses revealing widespread dispersal during the Pleistocene followed by regional clustering and limited (N_m ≈ 0.32), likely facilitated by and the expansion of livestock . This period saw increased and within the , as synanthropic species capitalized on post-glacial environmental changes and human-mediated introductions, solidifying their cosmopolitan distribution.

Phylogenetic relationships

The genus Musca is classified within the tribe of the subfamily , family , superfamily Muscoidea, which belongs to the section Calyptratae in the subsection Schizophora of the order Diptera. Within Muscidae, forms one of the basal subfamilies, with positioned as the to Stomoxyinae in both morphological and molecular phylogenies; this relationship is supported by cladograms derived from adult morphology and mitochondrial genome data. Phylogenetic analyses of the Muscini tribe, encompassing approximately 350 species across 18–21 genera, confirm its based on adult morphological characters such as the development of fronto-orbital setae in females, the forward bend of the M vein toward R4+5 in venation, and modifications to the cercal plate with median or marginal spined processes in the genitalia. At the genus level, Musca is monophyletic, with support from both morphological traits (e.g., specific genitalia structures distinguishing species groups) and molecular data including mitochondrial COI sequences and nuclear 28S rRNA genes, as well as whole mitogenome analyses. These studies integrate 50–80 morphological characters with sequence data from 15–43 taxa to reconstruct relationships, showing Musca as a cohesive within Muscini. Inter-species relationships within Musca reveal distinct clades, including the cosmopolitan domestica-group (e.g., M. domestica) and the tropical sorbens-group (e.g., M. sorbens), with the latter nested within or closely allied to the former; a third lusoria-group represents more basal divergences. Molecular evidence from mitochondrial genomes further corroborates these groupings, estimating divergences within Musca around 20–30 million years ago (mya) during the to early , consistent with broader Muscinae radiations following the split from Stomoxyinae at approximately 34 mya.

References

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