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Fly

Flies are insects of the order Diptera, characterized by a single pair of functional wings and a pair of halteres—modified hindwings that function as gyroscopic stabilizers during flight.^[1] This order encompasses approximately 160,000 described species worldwide, making it one of the most diverse groups of insects, second only to beetles in species richness.^[2] Dipterans exhibit complete metamorphosis, progressing through egg, larval (often maggot), pupal, and adult stages, with larvae typically inhabiting moist environments such as decaying organic matter, water, or animal tissues.^[3] Adults are renowned for their agile flight capabilities, including hovering, backward flight, and rapid maneuvers, facilitated by the halteres and specialized musculature.^[4] Ecologically, flies are vital as pollinators for numerous plants, decomposers that recycle nutrients from dead material, and predators in their larval stages, contributing significantly to biodiversity and ecosystem health.^[4]^[5] However, certain species, such as mosquitoes and houseflies, serve as vectors for diseases like malaria, dengue, and typhoid, posing major public health challenges.^[6]^[7]^[8] Economically, flies impact agriculture through pollination services and pest control via predatory species, while also causing losses as invaders of food sources and carriers of pathogens in human settlements.^[9]^[10] Found in nearly every terrestrial and aquatic habitat except extreme polar regions, flies demonstrate remarkable adaptability and evolutionary success spanning over 250 million years.^[11]

Taxonomy and Evolution

Higher Classification and Phylogeny

Flies, belonging to the order Diptera within the class Insecta and phylum Arthropoda, are defined by key synapomorphies including the transformation of the hind wings into club-shaped halteres for flight stabilization and the reduction or loss of the hind wings themselves, alongside specialized mouthparts adapted for liquid feeding.^[12] These traits distinguish Diptera from other insect orders and underscore their monophyly, as confirmed by morphological analyses.^[12] In higher-level phylogeny, Diptera form part of the Antliophora clade, which also includes Mecoptera (scorpionflies) and Siphonaptera (fleas), with Diptera positioned as the sister group to the Mecoptera + Siphonaptera lineage based on comprehensive phylogenomic datasets. Recent molecular studies from the 2020s, utilizing transcriptomic and genomic data, have robustly confirmed the monophyly of Diptera and resolved its internal structure into two primary suborders: the paraphyletic Nematocera (lower flies with long antennae, including basal lineages like Tipulomorpha and Culicomorpha) and the monophyletic Brachycera (higher flies with short antennae, encompassing groups such as Stratiomyomorpha, Tabanomorpha, and the derived Muscomorpha).^[13] These analyses, drawing on thousands of nuclear loci, have clarified relationships that were ambiguous in earlier morphology-based phylogenies.^[14] The evolutionary origin of Diptera traces to the Triassic period, approximately 240 million years ago, with the earliest definitive fossils appearing in Late Carnian deposits around 220 million years ago. Major radiations occurred during the Cretaceous, coinciding with the diversification of angiosperms, which provided new ecological niches and resources that drove increases in fly origination rates and overall biodiversity.^[15] This period saw the proliferation of brachyceran lineages, adapting to pollinator and herbivore roles in emerging flowering plant communities.^[16] Diptera encompasses over 150 families, with approximately 160,000 described species; among the most prominent are Tipulidae (crane flies, diverse in moist habitats), Culicidae (mosquitoes, known for blood-feeding vectors), Chironomidae (non-biting midges, abundant in aquatic environments), Ceratopogonidae (biting midges, small pests), Simuliidae (black flies, riverine breeders), Syrphidae (hoverflies, pollinators mimicking bees), Muscidae (house flies, synanthropic decomposers), Calliphoridae (blow flies, forensic indicators), Sarcophagidae (flesh flies, parasitoids and scavengers), and Tephritidae (fruit flies, agricultural pests).^[4] These families represent key ecological roles across the order, from aquatic larvae to terrestrial adults.

Diversification and Fossil Record

The fossil record of Diptera commences in the Triassic period, with the earliest definitive evidence consisting of a diverse assemblage of nematoceran flies from Late Carnian deposits (approximately 220 million years ago) in the Solite Quarry of Virginia, USA, including forms with primitive piercing mouthparts and wing structures suggestive of early aquatic or moist terrestrial adaptations.^[17] Additional early records include Middle Triassic representatives of Protorhyphidae from European localities, marking the initial diversification of basal lineages.^[18] Notable Jurassic fossils, such as species of Protorhyphus preserved in amber from Eurasian deposits, reveal primitive wing venation patterns with extensive crossveins and reduced discal cells, indicative of the transitional morphology between early nematocerans and more derived forms.^[19] Diptera underwent significant diversification events throughout the Mesozoic, with molecular clock analyses estimating the crown-group origin of the order around 250 million years ago in the early Triassic, followed by episodic radiations.^[20] A major burst of speciation occurred in the Lower Cretaceous (approximately 125 million years ago), particularly among lower brachycerans, coinciding with the rapid radiation of angiosperms that offered novel floral resources and habitats for larval development and adult feeding.^[21] In parasitoid lineages, such as the diverse family Tachinidae, host shifts to new insect prey have been a key driver of adaptive radiation, enabling exploitation of expanding ecological niches during this period.^[22] These patterns of diversification are informed by phylogenomic studies using transcriptome data, which calibrate divergence times across major clades like Nematocera and Brachycera, highlighting accelerated lineage splitting in the mid-Mesozoic.^[20] However, substantial gaps persist in the fossil record, especially for Nematocera, where preservation biases favor harder-bodied brachycerans, leading to underrepresentation of early larval and soft-bodied forms.^[23] Ongoing debates center on the early evolution of Brachyceran flies, including the precise timing and morphological transitions from nematoceran ancestors, with conflicting interpretations of Triassic and Jurassic fossils regarding the origins of discal cell reduction and proboscis elongation.^[23]

Species Diversity and Distribution

Flies (order Diptera) exhibit extraordinary species diversity, with approximately 160,000 species described worldwide, though estimates suggest the total could reach 1 million or more, highlighting the order's vast undescribed biodiversity.^[24] This richness is disproportionately concentrated within the suborder Brachycera, which accounts for the majority of described species—around 125,000—encompassing families such as Syrphidae (hoverflies) and Muscidae (house flies), while the more primitive Nematocera suborder contributes fewer, with about 35,000 species including mosquitoes and crane flies.^[25] Such disparity underscores Brachycera's evolutionary success in diverse habitats, driven by adaptations like advanced flight mechanisms.^[26] Distributionally, Diptera are cosmopolitan, inhabiting every continent except Antarctica, but their species richness peaks in tropical regions due to favorable climatic conditions supporting complex ecosystems.^[24] Endemic hotspots further accentuate this pattern; Australia hosts unique radiations within Tabanidae (horse flies), with over 230 species, most of which are endemic and adapted to arid and coastal environments, reflecting the continent's isolation.^[27] Similarly, Madagascar serves as a biodiversity refuge with high endemism rates, such as 55% in Muscidae and notable endemic genera in Hippoboscidae and Nemestrinidae, where island isolation has fostered specialized lineages.^[28]^[29] A significant portion of Dipteran diversity remains undescribed, particularly in "dark taxa" like Chironomidae (non-biting midges), which are morphologically cryptic and harbor thousands of unrecognized species, complicating traditional taxonomy.^[30] Recent initiatives, such as the International Barcode of Life (iBOL) projects in the 2020s, including Germany's GBOL III targeting dark taxa, employ DNA barcoding to uncover this hidden diversity, revealing unexpectedly high species counts in understudied groups through rapid genetic screening of specimens.^[31] Human activities have profoundly altered distributions, facilitating the global spread of synanthropic species like the house fly (Musca domestica) via international trade and transportation, originating from the Middle East but now ubiquitous in human-modified landscapes worldwide.^[32]

Morphology and Anatomy

External Structure

Flies, members of the order Diptera, exhibit a distinctive external morphology characterized by a body divided into three primary regions: the head, thorax, and abdomen. This structure is adapted for their diverse lifestyles, with key diagnostic features including a single pair of functional wings and a pair of halteres derived from the hind wings.^[33]^[4]^[34] The head is a prominent feature, bearing large compound eyes that provide a wide field of vision, often occupying much of the head's surface. Between the compound eyes, most species possess three simple eyes called ocelli, arranged in a triangle, which detect changes in light intensity.^[35] Antennae vary widely across families, ranging from filiform or stylate in nematocerans to aristate in brachycerans, serving sensory functions. The mouthparts are haustellate, forming a proboscis adapted for liquid feeding; variations include piercing-sucking types in mosquitoes (Culicidae) with needle-like stylets for blood meals, and sponging types in houseflies (Muscidae) for lapping up liquids.^[33]^[4]^[34] The thorax consists of three fused segments, with the mesothorax greatly enlarged to support the wings and legs. It bears three pairs of legs, each with five-segmented tarsi ending in claws and pulvilli for grasping. The diagnostic single pair of membranous forewings arises from the mesothorax, while the hind wings are reduced to clubbed halteres that function in flight balance.^[33]^[4]^[34] The abdomen is typically segmented into 7–10 visible parts, flexible and tapered, with females often possessing an ovipositor modified for egg-laying, varying from a simple tube to elaborate piercing structures.^[34]^[36] Adult flies range in size from as small as 0.4 mm in some phorid flies (Phoridae)^[37] to over 30 mm in certain robber flies (Asilidae).^[38] Coloration is diverse, often featuring metallic sheens, stripes, or spots; for instance, many hoverflies (Syrphidae) display yellow-and-black patterns mimicking bees or wasps as a form of Batesian mimicry to deter predators.^[39] Sexual dimorphism is evident in several traits, such as in fruit flies (Drosophilidae), where males possess relatively larger compound eyes compared to females, aiding in mate detection during courtship. In biting flies like mosquitoes, females have more developed piercing mouthparts for blood-feeding, absent or reduced in males.^[40]^[33]

Internal Organs and Systems

The circulatory system of flies, like other insects, is an open type that lacks true blood vessels and capillaries, instead relying on a hemocoel—a spacious body cavity—through which hemolymph circulates to bathe the organs directly.^[41] The primary pumping organ is the dorsal vessel, a longitudinal tube extending from the abdomen through the thorax to the head, functioning as a heart in its posterior region and an aorta anteriorly; it propels hemolymph anteriorly in pulsatile waves, while body movements and accessory pulsatile organs aid in its return posteriorly.^[42] In Diptera, this system efficiently distributes nutrients, hormones, and immune cells, with hemolymph comprising plasma and hemocytes but lacking respiratory pigments like hemoglobin.^[43] The respiratory system in flies consists of a branched tracheal network that delivers oxygen directly to tissues, bypassing the circulatory system for gas exchange.^[44] Air enters through ten pairs of spiracles—two thoracic and eight abdominal—valved openings that regulate airflow and prevent desiccation or pathogen entry; in many Diptera, these spiracles feature sieve plates or filters for added protection.^[45] The tracheae, reinforced with spiral taenidia, branch into finer tracheoles that permeate organs and end blindly near cells, where oxygen diffuses across thin cuticular linings; during flight, convective airflow enhances delivery to high-oxygen-demand muscles.^[44] The digestive system of flies includes a foregut with a crop—a thin-walled diverticulum of the esophagus—for temporary food storage, allowing rapid intake followed by controlled release into the midgut for enzymatic digestion.^[46] The midgut, the primary site of nutrient absorption, varies among Diptera; in blood-feeding species like mosquitoes, it expands dramatically to accommodate large meals, with specialized epithelial cells secreting digestive enzymes and absorbing proteins.^[47] Excretion occurs via Malpighian tubules, blind-ended tubes arising at the midgut-hindgut junction, which actively transport waste ions and water from hemolymph to form uric acid-rich urine, minimizing water loss in terrestrial environments.^[48] Reproductive organs in female flies consist of paired ovaries, each containing multiple ovarioles where oocytes develop and mature, connected by lateral oviducts to a common oviduct for egg passage.^[49] Accessory glands (colleterial glands) produce secretions for egg coating or lubrication, while one or more spermathecae—sclerotized sacs—store sperm post-mating, nourishing it via glandular cells for long-term viability and fertilization at egg-laying.^[49] In males, paired testes produce sperm packaged in follicles, with vasa deferentia leading to an ejaculatory duct; accessory glands secrete seminal fluids that activate sperm or influence female behavior, as seen in species like the Australian sheep blowfly Lucilia cuprina.^[49]

Adaptations for Flight

Flies have evolved a specialized wing structure that optimizes stability and maneuverability during flight. The functional wings are a single pair of membranous forewings, reinforced by a intricate network of veins that distribute mechanical stresses and maintain structural integrity against aerodynamic forces.^[50]^[51] The hindwings are modified into club-shaped halteres, which do not contribute to lift but serve as vibrational gyroscopes, oscillating at the same frequency as the forewings to sense body rotations in three dimensions.^[52]^[53] Arrays of campaniform sensilla, mechanosensory organs embedded at the haltere base, detect Coriolis forces and strains during oscillation, enabling rapid stabilization adjustments.^[54]^[55] Power for flight derives from the thorax's indirect flight muscles, which do not attach directly to the wings but instead deform the exoskeleton to drive wing motion. These include antagonistic sets of dorsal-longitudinal muscles, responsible for the power stroke (downstroke), and dorsal-ventral muscles, which facilitate the recovery stroke (upstroke).^[56]^[57] In Diptera, these muscles function asynchronously, where a single neural impulse triggers multiple contractions via stretch-activation, allowing wingbeat frequencies from approximately 200 Hz in medium-sized flies like Drosophila to over 1000 Hz in tiny species such as midges.^[58]^[59] This mechanism amplifies power output while minimizing neural demands, contrasting with synchronous muscles in many other insects that limit frequencies to below 100 Hz.^[60] Aerodynamic lift in flies relies on unsteady flow phenomena tailored to body size. In smaller species, the clap-and-fling mechanism enhances circulation: at the end of the upstroke, the wings clap together dorsally and then fling apart, generating a strong vortex in the gap that boosts leading-edge suction during the subsequent downstroke.^[61]^[62] Complementing this, a stable leading-edge vortex forms along the forewing during translation, creating low pressure above the wing and contributing up to 50% of the total lift, as demonstrated in fruit fly models.^[63] In larger flies, such as robber flies, analogous leading-edge vortices provide high lift coefficients similar to those in hawkmoths, though without the pronounced clap-and-fling due to scale effects on Reynolds numbers.^[64] These adaptations confer exceptional energy efficiency, with flies maintaining low overall mass—often under 1 mg in small species—and a high power-to-weight ratio in flight muscles exceeding 200 W/kg, enabling sustained hovering and evasion.^[65] Compared to butterflies or dragonflies with synchronous muscles, Dipteran asynchronous systems achieve greater mechanical efficiency at high frequencies, with muscle conversion efficiencies reaching 20-30% during optimal flight speeds, though this drops at extremes.^[66]^[67] The halteres' sensory feedback further optimizes energy use by minimizing corrective maneuvers, underscoring the integrated anatomical design for agile, low-cost flight.^[57]

Life Cycle and Reproduction

Egg and Larval Stages

The eggs of flies (order Diptera) exhibit considerable morphological variation adapted to their oviposition environments, typically measuring around 1 mm in length and featuring a micropyle for sperm entry and aeropyles for gas exchange. In many species, such as the house fly (Musca domestica), eggs are elongated and white, often described as banana- or boat-shaped with flattened sides, and are laid in clusters of 75–150 on moist, decaying organic substrates like feces or garbage to ensure rapid hatching and larval access to food.^[3] Females use a specialized ovipositor to deposit these eggs singly or in batches, with some species like fruit flies (Tephritidae) puncturing host fruits for internal placement.^[68] Hatching occurs within 8–24 hours under optimal conditions, triggered by moisture and warmth, releasing the first-instar larva.^[3] Fly larvae, commonly known as maggots, are vermiform (worm-like) and undergo three instars in most species, characterized by a soft, cylindrical body lacking true legs but equipped with hook-like mouthparts (cephalopharyngeal skeleton) for feeding and locomotion. The first instar is small (about 1–2 mm), progressing to larger sizes in subsequent stages, with the third instar reaching 7–12 mm in house flies and displaying a greasy, cream-colored appearance.^[3] Feeding strategies vary widely: terrestrial larvae like those of blow flies (Calliphoridae) are saprophagous, consuming protein-rich decaying matter, while aquatic larvae of black flies (Simuliidae, e.g., Simulium spp.) employ filter-feeding mechanisms using cephalic fans to capture microorganisms and detritus from water currents.^[68]^[69] Nutritional requirements emphasize essential amino acids (e.g., arginine, histidine) and proteins for growth, as demonstrated in blow fly larvae (Phormia regina), which fail to develop without these in defined diets.^[70] Growth occurs through ecdysis, where larvae shed their exoskeleton at the end of each instar to accommodate rapid size increases, a process regulated by hormones like ecdysone and influenced by nutrient availability. In house flies, the larval stage lasts 4–13 days at 35–38°C but extends to 14–30 days at cooler temperatures of 12–17°C, highlighting temperature's role in accelerating metabolic rates and shortening development time.^[3] Optimal development requires high-moisture environments (e.g., 60–70% for house fly maggots) and temperatures around 25–30°C, beyond which desiccation or heat stress can halt progression.^[3]^[68]

Pupal Stage

The pupal stage in flies (order Diptera) marks the transformative phase of holometabolous metamorphosis, bridging the larval and adult forms in a non-motile, non-feeding period that typically spans 3–20 days, with duration inversely related to temperature and varying by species.^[71] This stage follows the cessation of larval feeding and growth, initiating profound anatomical reorganization essential for adult functionality.^[72] Dipteran pupae assume one of two primary morphologies: coarctate or exposed (exarate). Coarctate pupae, prevalent in the series Cyclorrhapha within the suborder Brachycera (e.g., houseflies in Muscidae), develop within a rigid puparium—a barrel-shaped case derived from the hardened, tanned exoskeleton of the final larval instar, which conceals appendages and provides structural protection. Exposed pupae, characteristic of the series Orthorrhapha within the suborder Brachycera (e.g., robber flies in Asilidae), feature free, visible appendages such as wings and legs, emerging directly from the larval skin without a puparium, often in soil or litter habitats.^[73] Metamorphosis during pupation entails histolysis, the programmed breakdown of larval tissues via autophagy and phagocytosis, alongside the proliferation and differentiation of imaginal discs—pre-formed clusters of undifferentiated cells that evaginate to form adult appendages like wings, legs, and eyes.^[72] This process is orchestrated by pulses of the steroid hormone ecdysone, which induces pupariation behaviors including larval contraction and the sclerotization (hardening) of the puparium through phenolic tanning of the cuticle.^[74] Protective adaptations enhance pupal survival amid environmental hazards. The puparium in coarctate forms acts as a desiccation-resistant barrier, while many species bury pupae in soil or substrate for concealment; aquatic Diptera, such as black flies (Simuliidae), may enclose pupae in silken cases anchored to surfaces for stability and defense against currents.^[75] Nonetheless, this immobile stage incurs high mortality, primarily from desiccation in arid conditions or predation by soil invertebrates and parasitoids, underscoring its vulnerability in the life cycle.^[76]

Adult Stage and Mating

Adult flies emerge from the pupal case through eclosion, marking the transition to sexual maturity, which typically occurs within hours to days depending on species and environmental conditions. The lifespan of adult flies varies widely across Diptera, generally ranging from a few days to several weeks, influenced by factors such as nutrition, temperature, and predation. For instance, adult houseflies (Musca domestica) live 15 to 30 days under optimal conditions, with higher temperatures accelerating metabolic rates and shortening longevity while nutrient-rich diets, particularly proteins, extend survival by supporting reproductive and somatic maintenance. In black soldier flies (Hermetia illucens), adult longevity decreases with rising temperatures but increases with access to protein sources, highlighting the interplay between diet and thermal stress in modulating post-eclosion survival.^[77]^[78]^[79] Mating in adult flies involves complex courtship displays that ensure species recognition and mate selection, often mediated by pheromones and visual or acoustic signals. In Drosophila melanogaster, males initiate courtship by orienting toward females, followed by wing fanning to produce species-specific songs and release aggregation pheromones like cis-vaccenyl acetate, which stimulate female receptivity and inhibit male-male aggression. Some muscoid flies, such as those in the genus Lispe (Muscidae), exhibit lekking behaviors where males aggregate in display arenas on substrates like beaches, performing dances and territorial flights to attract females without providing resources, thereby intensifying sexual selection. These systems promote rapid mate location in dense populations, with successful copulation lasting seconds to minutes. Fertilization in Diptera is internal, occurring via spermatophore transfer during copulation, after which females store sperm in spermathecae for delayed use in egg fertilization. Oviposition follows, with females selecting suitable sites based on moisture and substrate; clutch sizes vary by species and nutritional status, such as approximately 100–300 eggs laid individually on damp substrates in female Aedes mosquitoes, enabling high reproductive output from a single blood meal.^[80] In semelparous Dipterans like the antler fly (Protopiophila litigata), post-reproductive senescence is pronounced, with males experiencing rapid physiological decline—including muscle degeneration and reduced mobility—immediately after mating, leading to death within days as resources are fully allocated to a single reproductive bout. This contrasts with iteroparous species, where multiple clutches are possible over extended adult lifespans.^[81]^[82]

Behavior and Physiology

Sensory Perception and Nervous System

The nervous system of the fruit fly Drosophila melanogaster comprises a supraesophageal ganglion that forms the brain and a ventral nerve cord extending through the thorax and abdomen to innervate the body segments.^[83] The supraesophageal ganglion arises from three embryonic neuromeres—the protocerebrum, deuterocerebrum, and tritocerebrum—and integrates sensory inputs for processing.^[83] The brain includes paired optic lobes, which are the largest structures by neuron count and primarily handle visual information, containing approximately 77,536 intrinsic neurons in the adult female.^[84] The entire central nervous system encompasses about 139,255 neurons in the brain, enabling compact yet sophisticated computation for behaviors like navigation and learning.^[84] Vision in flies relies on compound eyes, each composed of roughly 800 ommatidia that collectively provide a panoramic field of view exceeding 300 degrees.^[85] These ommatidia detect ultraviolet light with peak sensitivity around 350–370 nm, facilitating tasks such as foraging on UV-reflective flowers and polarotactic navigation using skylight cues.^[86] Motion perception occurs through a mechanism involving flicker fusion, where rapid changes in light intensity across ommatidia trigger neural responses at frequencies up to several hundred hertz, allowing flies to track fast-moving predators or prey effectively.^[87] Additional sensory modalities include mechanoreception via the aristae on the antennae, which house scolopidia that detect airflow and wind direction by measuring subtle antennal deflections during flight or locomotion.^[88] Chemoreceptors on the tarsi of the legs sense taste chemicals upon contact, with gustatory receptor neurons responding to sugars, bitters, and salts to evaluate potential food sources before extension of the proboscis.^[89] Vibration detection is mediated by chordotonal organs distributed across the body, including in the legs and antennae, where stretch-sensitive neurons transduce substrate-borne oscillations into proprioceptive or auditory signals for balance and communication.^[90] Neural processing integrates these inputs for adaptive behaviors, as seen in the optomotor response, where wide-field motion-sensitive neurons in the optic lobes detect rotating patterns and elicit compensatory turns, gated by central inputs from flight-related activity to enhance responsiveness during locomotion.^[91] In the mushroom bodies—a paired structure in the central brain—olfactory conditioning experiments demonstrate associative learning, where odors paired with unconditioned stimuli like electric shocks or sucrose rewards lead to synaptic plasticity in Kenyon cells, enabling memory formation and behavioral modification.^[92]

Feeding Mechanisms

Flies in the order Diptera exhibit a wide array of feeding adaptations in both adults and larvae, reflecting their diverse ecological roles and the order's evolutionary success. Adult mouthparts are highly modified for liquid or semi-liquid diets, forming a proboscis that facilitates sucking or lapping. In blood-feeding species like mosquitoes (family Culicidae), the mouthparts form a piercing-sucking apparatus, where the labium sheathes needle-like stylets that penetrate host skin to access blood vessels.^[25]^[93] In contrast, scavenging flies such as blowflies (family Calliphoridae) possess sponging or lapping mouthparts, consisting of pseudotracheae on labellar pads that absorb fluids like decaying matter or nectar through capillary action.^[94] Some nematoceran flies, including certain long-proboscid taxa, have elongated siphoning proboscides adapted for nectar uptake from deep flowers, analogous to lepidopteran mechanisms but evolved independently within Diptera.^[95]^[96] Larval feeding mechanisms are equally varied, often tied to specific habitats and resources. Many cyclorrhaphan larvae, such as maggots of blowflies and houseflies (family Muscidae), are scavengers that burrow into carrion or feces, using hook-like mouthparts to rasp and ingest liquefied tissues.^[97] Predatory larvae, exemplified by those of robber flies (family Asilidae), employ grasping mouthparts to capture and consume other arthropods, injecting enzymes to predigest prey externally before sucking up the resulting fluids.^[98] Aquatic larvae of non-biting midges (family Chironomidae) utilize filter-feeding strategies, with cephalic fans or brushes creating currents to trap suspended particles like algae and detritus from water columns.^[99] Digestion in Diptera primarily occurs in the midgut, where enzymatic hydrolysis breaks down ingested nutrients. Proteases, amylases, and lipases secreted by midgut cells facilitate the degradation of proteins, carbohydrates, and lipids from diverse sources.^[100] In specialized cases, such as blood-feeding tsetse flies (genus Glossina), symbiotic bacteria like Wigglesworthia glossinidia in the midgut aid digestion by supplementing nutrients, including vitamins and amino acids essential for metabolizing blood meals that lack certain compounds.^[101]^[102] Nutritionally, adult female flies prioritize protein intake to support egg production, often sourcing it from blood, pollen, or animal fluids, while carbohydrates from nectar provide energy for flight and longevity.^[103] In species like stable flies (Stomoxys calcitrans), supplementing blood diets with nectar enhances fertility and larval emergence rates by balancing macronutrients.^[104] This dietary strategy underscores the flies' reliance on complementary resources to optimize reproduction and survival.^[105]

Locomotion and Migration

Flies exhibit diverse non-aerial locomotion strategies adapted to their environments. In adult flies, such as those in the genus Drosophila, walking and crawling rely on specialized tarsal structures for traction and adhesion. The distal tarsi bear paired claws that grip rough surfaces, facilitating stable movement across uneven terrain, while pulvilli—hairy pads with spatula-like terminal contact zones—enable adhesion to smooth substrates through van der Waals forces and secretion-mediated attachment.^[106] These adaptations allow flies to navigate vertical or inverted surfaces effectively. Additionally, tarsal grooming behaviors maintain these structures' functionality; flies use forelegs to systematically clean tarsi, removing debris and contaminants in a periodic, coordinated manner that involves rapid leg sweeps and sensory-guided actions triggered by contact chemicals.^[107]^[108] Aquatic fly larvae, including those of certain crane fly species in the family Tipulidae, employ leg-based propulsion for locomotion in water. These larvae, often found in semi-aquatic or fully aquatic habitats, use their segmented legs in a paddling motion to maneuver through sediments or open water, supplemented by body undulations for steering and burrowing.^[109] This leg paddling enables efficient short-distance movement, such as foraging or escaping predators, in oxygen-poor environments where swimming enhances survival. Migration in flies involves large-scale, wind-assisted dispersal, particularly among nematoceran groups like midges (Chironomidae). Billions of individuals undertake seasonal high-altitude migrations annually, carried by prevailing winds over hundreds of kilometers to exploit new breeding sites or resources; radar studies reveal peaks in nocturnal flights reaching altitudes of several kilometers, with Diptera comprising the dominant taxa in these events.^[110] Some nematocerans form locust-like swarms during dispersal, exhibiting oriented collective flight where individuals align with wind currents and visual cues for coordinated movement, enhancing efficiency in mating and colonization.^[111] These patterns underscore flies' role in broad ecological connectivity. Diel activity rhythms influence locomotion, with many flies showing crepuscular peaks in movement to optimize foraging and reduce predation risk. Mosquitoes (Culex spp.), for instance, display bimodal flight activity at dawn and dusk, driven by circadian cues that synchronize take-off and dispersal.^[112] Escape responses further refine locomotion; threatened flies initiate rapid take-offs at specific angles—often 90–180 degrees opposite the stimulus—using visual processing to direct jumps away from predators, integrating body orientation for precise evasion.^[113]

Ecology

Habitats and Niches

Flies of the order Diptera occupy a broad spectrum of terrestrial habitats, where they play key roles in decomposition and nutrient recycling. In forest ecosystems, numerous species function as decomposers, with larvae of families such as Sciaridae and Mycetophilidae feeding on decaying plant material in leaf litter and soil, facilitating organic matter breakdown. Vertical stratification is a prominent feature in these environments; for instance, in temperate deciduous forests, Diptera abundance and diversity increase from the forest floor to the canopy, with canopy-dwelling species like certain Cecidomyiidae exploiting resources in upper strata. In urban settings, the house fly Musca domestica predominates, breeding in accumulations of organic waste such as refuse and animal manure, adapting well to human-altered landscapes with high nutrient availability.^[3] Aquatic niches are critical for many Diptera, particularly during larval stages. Black flies of the family Simuliidae develop exclusively in lotic habitats like streams and rivers, where their larvae attach to substrates in flowing, oxygenated waters using silk and posterior crochets, often reaching high densities in riffles. Mosquitoes (Culicidae) frequently exploit phytotelmata, small water bodies held within plants such as tree holes or bromeliad axils, providing isolated breeding sites; over 400 mosquito species worldwide utilize these micro-aquatic environments, with genera like Aedes and Wyeomyia being particularly specialized.^[114]^[115] Diptera also thrive in specialized microhabitats that support distinct life stages. Scatophagous flies, including those in the family Scathophagidae such as the yellow dung fly Scathophaga stercoraria, congregate around fresh dung pats in pastures and meadows, where females oviposit and larvae consume the nutrient-rich substrate, aiding in waste decomposition. Hoverflies (Syrphidae) occupy floral microhabitats, with adults visiting open flowers for nectar and pollen, thereby occupying a niche as generalist pollinators in meadows, gardens, and forest edges.^[116]^[117] Certain Diptera demonstrate remarkable abiotic tolerances, enabling occupation of extreme environments. Members of the family Psychodidae, such as Pericoma species, inhabit thermal springs, enduring elevated temperatures in these geothermal aquatic systems. Chironomidae (non-biting midges) extend into polar regions, with larvae adapted to cold, low-oxygen sediments in Arctic and Antarctic lakes and streams, representing a significant portion of benthic biomass in these harsh conditions.^[118]^[119]

Trophic Interactions

Flies occupy diverse trophic levels within food webs, functioning as primary consumers through herbivory and predation, secondary consumers via parasitism, and detritivores in decomposition processes, while also serving as prey for various predators and hosts for parasitoids.^[120] Their interactions contribute significantly to ecosystem dynamics, including nutrient cycling and biodiversity maintenance.^[121] In herbivorous roles, certain fly families engage in plant feeding that influences vegetation structure and reproduction. Syrphid flies (Syrphidae), often called hoverflies, act as effective pollinators by visiting flowers for nectar and pollen, contributing to the pollination of at least 72% of global food crops and supporting agricultural yields valued in billions annually.^[121] Meanwhile, Agromyzidae, known as leaf-miner flies, include herbivorous species whose larvae induce galls on plants, such as the poplar twiggall fly (Hexomyza schineri), which forms spherical galls on twigs, altering host plant growth and providing habitat for other organisms.^[122] Predatory flies exemplify carnivorous trophic positions, actively hunting other arthropods to regulate prey populations. Robber flies (Asilidae) are agile aerial predators that capture insects mid-flight, using spiny legs to seize prey like bees, wasps, and grasshoppers before injecting liquefying saliva to consume them, thereby exerting top-down control in insect communities.^[38] Additionally, some dipteran larvae function as internal parasitoids; for instance, Conopidae larvae develop within adult Hymenoptera hosts, such as bees and wasps, consuming host tissues and ultimately causing death, which impacts hymenopteran abundance in shared habitats.^[120] As decomposers, flies play a crucial role in breaking down organic matter and facilitating nutrient cycling. Blowflies (Calliphoridae) are primary colonizers of carrion, with their larvae (maggots) rapidly consuming soft tissues and accelerating decomposition; for example, maggot activity can lead to substantial mass loss, thereby releasing nutrients like nitrogen and phosphorus back into the soil.^[123] Flies also participate in symbiotic relationships that modify their trophic interactions. Certain pseudoscorpions engage in phoresy with flies, attaching to adult Diptera for dispersal to new habitats without harming the host, representing a commensal symbiosis that aids pseudoscorpion distribution while flies serve as vectors.^[124] Conversely, flies themselves are frequent targets of parasitoids, particularly from Hymenoptera; for instance, necrophagous dipterans like blowflies are parasitized by wasps in families such as Pteromalidae, whose larvae develop within fly pupae, reducing fly populations and influencing decomposition rates in food webs.^[125]

Predation and Defense Strategies

Flies utilize a range of morphological adaptations to evade predators, primarily through camouflage and physical barriers. Larval stages often feature cryptic coloration that blends seamlessly with their surroundings, such as patterns mimicking leaves or debris in species like certain syrphids, reducing detection by visual hunters.^[126] For instance, the larvae of Ocyptamus flies exhibit subdued hues and textures that enhance crypsis in foliage or soil environments.^[126] Hoverfly larvae, in particular, bear dorsal spines that serve as a mechanical deterrent, impeding predator bites and improving survival during encounters with conspecific or heterospecific attackers. Behavioral defenses further bolster fly survival by exploiting predator sensory limitations and decision-making. Adult flies frequently adopt erratic flight paths, characterized by rapid, unpredictable turns that thwart interception by pursuing threats. In Drosophila, this involves visually mediated maneuvers where flies dynamically adjust trajectories to anti-track approaching dangers, achieving high evasion rates in controlled settings.^[127] Among muscoid flies, such as blowflies (Calliphora spp.) and houseflies (Musca domestica), thanatosis—prolonged immobility resembling death—triggers upon disturbance, deterring further investigation by predators that prefer live prey. This tonic immobility response, documented across multiple dipteran species, enhances escape probability by exploiting predator foraging biases.^[128] Chemical mechanisms provide an additional layer of protection, often rendering flies unappealing or actively repellent. Fruit flies (Drosophila spp.) secrete pyrazines from specialized glands during alarm situations, producing odors that signal danger and deter approaching predators through irritation or aversion. These volatile compounds function as rapid-response defenses, conserved across insects for antipredator signaling.^[129] In Batesian mimics like hoverflies (Syrphidae), underlying unpalatability from such secretions reinforces visual resemblance to stinging models, amplifying protection; larvae, for example, release adhesive or distasteful fluids that discourage consumption.^[130] Empirical studies underscore the integrated efficacy of these strategies. Anti-predator experiments with Drosophila reveal high escape success attributable to swift visual processing and agile locomotion that outpace predator lunges. Such high success rates highlight how combined morphological, behavioral, and chemical traits enable flies to navigate intense predation pressures effectively.^[131]

Relation to Humans

Disease Vectors and Pests

Flies in the order Diptera play a significant role as vectors for numerous human and animal diseases, transmitting pathogens through bites or mechanical contact, which exacerbates global health challenges.^[132] Among the most notorious are mosquitoes, such as species in the genus Anopheles, which serve as biological vectors for malaria caused by Plasmodium parasites and dengue fever caused by arboviruses.^[133] Female Anopheles mosquitoes ingest the parasite during a blood meal from an infected host, allowing Plasmodium to develop within their bodies before being transmitted to humans via subsequent bites.^[132] Similarly, tsetse flies (Glossina spp.) act as biological vectors for human African trypanosomiasis, or sleeping sickness, caused by Trypanosoma brucei parasites; the parasites multiply in the fly's midgut and salivary glands, enabling injection during feeding.^[134] In contrast, houseflies (Musca domestica) primarily function as mechanical vectors, carrying pathogens like Salmonella typhi—the bacterium responsible for typhoid fever—on their legs, mouthparts, or bodies after contact with contaminated feces or waste, then depositing them onto food or surfaces.^[135] Transmission mechanisms differ fundamentally between biological and mechanical vectors, influencing disease dynamics and control strategies. In biological transmission, as seen with mosquitoes and tsetse flies, the pathogen undergoes essential development or replication within the vector, often requiring 7–21 days for maturation, which limits but sustains long-term spread.^[136] Mechanical transmission, exemplified by houseflies, involves passive transfer without pathogen alteration, allowing rapid dissemination in unsanitary environments but typically over shorter distances.^[137] These vectors contribute to a substantial global disease burden; for instance, malaria alone caused an estimated 263 million cases and 597,000 deaths worldwide in 2023, predominantly in sub-Saharan Africa, underscoring the persistent public health impact despite interventions.^[138] Beyond disease transmission, certain fly species inflict severe economic damage as agricultural pests and livestock parasites. The spotted-wing drosophila (Drosophila suzukii), an invasive fruit fly, infests ripening soft fruits like cherries, berries, and grapes by laying eggs directly into intact skin, leading to larval feeding that renders produce unmarketable and causes annual losses exceeding $500 million in North American crops.^[139] In livestock, flies induce myiasis—a condition where larvae infest living tissue—particularly through species like the New World screwworm (Cochliomyia hominivorax), whose maggots burrow into wounds, causing tissue destruction, secondary infections, and animal distress; untreated cases can result in animal death and economic losses of approximately $1.3 billion in Mexico over the past year as of 2025.^[140] Control of fly vectors and pests relies on integrated approaches, including insecticides and innovative biological methods. Insecticides such as pyrethroids and organophosphates provide rapid knockdown of adult flies through contact sprays or baits, targeting species like houseflies and mosquitoes in residential and agricultural settings.^[141] For obligate parasites like screwworm, the sterile insect technique (SIT) has proven highly effective; this method involves mass-rearing, sterilizing, and releasing male flies via radiation to mate with wild females, producing non-viable offspring and leading to population collapse—evidenced by successful eradications in the United States by 1966 and ongoing 2020s efforts in Mexico and Panama through expanded sterile fly production facilities. As of 2025, efforts continue amid rising cases in Mexico, with the USDA announcing sweeping plans in August to protect the US through enhanced sterile fly production.^[142]

Economic and Forensic Applications

Flies play a significant role in forensic entomology, where the predictable succession patterns of their larvae on decomposing remains help estimate the postmortem interval (PMI), or time since death. Blow flies (family Calliphoridae), such as Calliphora vicina and Lucilia sericata, are among the first insects to colonize a corpse, often arriving within minutes of death to lay eggs in natural orifices and wounds.^[143]^[144] The eggs typically hatch into first-instar larvae within 8-24 hours under temperate conditions, with the presence of small larvae indicating a PMI of 1-3 days at around 20°C, depending on species and environmental factors.^[143] As larvae develop through instars, feeding on soft tissues, their size and stage provide a biological clock for PMI estimation, often accurate to within hours when combined with temperature data.^[144] This succession—progressing from eggs to mature maggots and eventual pupation—follows observable waves influenced by local climate, enabling forensic experts to reconstruct timelines in criminal investigations.^[143] In medical applications, flies contribute through maggot debridement therapy (MDT), where sterile larvae of Lucilia sericata are applied to chronic wounds to remove necrotic tissue and promote healing. The U.S. Food and Drug Administration (FDA) cleared MDT as a medical device in January 2004 under 510(k) clearance #K033391, allowing the production and use of "Medical Maggots" for debridement in conditions like diabetic ulcers and venous stasis wounds.^[145] Beyond physical cleaning, maggot excretions and secretions (ES) exhibit antimicrobial properties, including compounds like lucifensin and phenylacetic acid, which inhibit bacteria such as Staphylococcus aureus (including MRSA) and Pseudomonas aeruginosa, reducing infection rates by up to 92% in clinical cases.^[145]^[146] These secretions also disrupt biofilms and stimulate tissue growth, making MDT a valuable alternative for antibiotic-resistant infections.^[146] Economically, certain fly species provide benefits in waste management and agriculture. Black soldier fly (Hermetia illucens) larvae efficiently convert organic waste into high-protein biomass, with dry larvae containing 40-50% crude protein and reducing substrate mass by 50-60%, offering a sustainable alternative to soy or fishmeal in animal feed.^[147] This bioconversion process supports circular economies by transforming food waste, manure, and brewery byproducts into feed for poultry, aquaculture, and livestock, while the larvae's frass serves as a nutrient-rich fertilizer.^[147] The global black soldier fly market has grown rapidly in the 2020s, projected to expand at a compound annual growth rate (CAGR) of 31% from 2024 to 2033, driven by demand for eco-friendly protein sources amid rising feed costs and sustainability goals.^[148] Additionally, flies contribute to pollination services, with species like hoverflies and bee flies aiding crop reproduction; their annual economic value is estimated at around $300 billion globally, supporting yields of fruits, vegetables, and nuts such as strawberries and carrots.^[149] In biological control, predatory and parasitoid flies help manage agricultural pests. Tachinid flies (family Tachinidae), for instance, are effective parasitoids of caterpillars, with larvae developing internally in hosts like those of cabbage loopers (Trichoplusia ni) and armyworms, ultimately killing the pest and regulating populations.^[150] Over 400 tachinid species in regions like California target moth and butterfly larvae, reducing the need for chemical pesticides and enhancing integrated pest management in crops such as brassicas and fruits.^[150] By laying eggs on or injecting larvae into caterpillars, tachinids achieve high parasitism rates, contributing to natural pest suppression without harming beneficial insects.^[150]

Cultural Symbolism and Conservation

In various cultural and religious contexts, flies have symbolized decay, evil, and transience. In the Bible, the fourth plague of Egypt described in Exodus 8:20-32 depicts swarms of flies infesting the land as a divine punishment, emphasizing God's sovereignty and the association of flies with filth and affliction. This negative portrayal extends to broader Judeo-Christian traditions, where flies often represent moral corruption or demonic forces, as seen in references to Beelzebub, meaning "lord of the flies."^[151] Conversely, in ancient Egyptian culture, flies symbolized resilience and military valor, with fly-shaped amulets awarded to warriors for bravery, reflecting their tenacity in harsh environments.^[152] In Native American lore, certain tribes view flies as agents of transformation, embodying adaptability and the cycle of life through their rapid reproduction and ecological roles, though interpretations vary across traditions.^[153] In Western art, particularly 17th-century vanitas still lifes, flies appear as emblems of mortality and the fleeting nature of earthly pleasures, often perched on skulls, wilted flowers, or rotting fruit to remind viewers of inevitable decay.^[154] Artists like Ambrosius Bosschaert the Younger incorporated flies in compositions such as Vanitas (Dead Frog with Flies) to underscore themes of vanity and the brevity of life, drawing from memento mori traditions.^[155] These depictions highlight flies' dual role in cultural symbolism: harbingers of ruin in some narratives, yet resilient survivors in others, mirroring their biological adaptability.^[153] Many fly species face conservation challenges, with dozens listed as threatened on the IUCN Red List due to habitat destruction and other pressures. For instance, Hawaiian picture-wing flies (genus Drosophila), endemic to the islands, are critically imperiled, with over a dozen species classified as endangered primarily from habitat loss caused by invasive plants, feral ungulates, and urbanization.^[156] These flies, once widespread across diverse ecosystems, now persist mainly in fragmented high-elevation forests, where their specialized breeding on native plants is disrupted.^[157] Key threats to fly biodiversity include climate change, which alters ranges and phenology; for example, warming temperatures enable mosquito species (Aedes and Anopheles) to expand into higher latitudes and elevations, potentially displacing native Diptera.^[158] Pesticides pose another major risk, reducing populations of pollinating hoverflies (Syrphidae) through direct toxicity and habitat degradation, with studies showing up to 40% declines in beneficial fly abundance in agricultural areas.^[159] Research from the 2020s documents broader Diptera declines, with insect biomass in protected ecosystems dropping by over 70% in some regions due to combined stressors like pollution and land-use change.^[160] Conservation efforts focus on habitat protection and genetic preservation. Reserves such as those in Hawaii's higher-elevation native forests safeguard endemic picture-wing flies by controlling invasives and restoring host plants, supporting population recovery for species like Drosophila silvestris.^[156] Genetic banking initiatives store strains of Diptera, including those with traits for pest resistance, to aid future breeding programs and maintain biodiversity against threats like insecticide resistance in agricultural pests.^[161] These strategies, informed by genomic studies, emphasize ex situ conservation to bolster resilience in vulnerable taxa.^[162]

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Jul 22, 2022 · By contrast, the protective functions of shelters occupied during the pupal stage have been little studied, despite their ubiquity and ...
[73]
What is the Lifespan of a Fly? - Orkin
The life expectancy of a housefly is generally 15 to 30 days and depends upon temperature and living conditions.
[74]
Effects of Feeding Adults of Hermetia illucens (Diptera ...
Feb 11, 2019 · We suggest using a protein-rich diet to maximize oviposition and longevity parameters as adults do benefit from feeding.
[75]
Influence of Temperature on Selected Life-History Traits of Black ...
Mar 2, 2019 · With increasing temperatures, the longevity of adult BSF decreased, while the fecundity of females increased. Thus, it is possible to take ...
[76]
Mosquito Biology
A raft of eggs looks like a speck of soot floating on the water and is about 1/4 inch long and 1/8 inch wide. Each raft may contain from 100 to 400 eggs.Missing: clutch | Show results with:clutch
[77]
Senescence: rapid and costly ageing in wild male flies - PubMed
Senescence: rapid and costly ageing in wild male flies. Nature. 2002 Nov 28;420(6914):377. doi: 10.1038/420377a. Authors.Missing: semelparous post- reproduction
[78]
Senescence: Rapid and costly ageing in wild male flies - ADS
Here we show that ageing is detectable in wild populations of a very short-lived insect, the antler fly (Protopiophila litigata), and causes debilitating and ...Missing: semelparous Diptera post-<|control11|><|separator|>
[79]
Drosophila tissue and organ development: Brain
The supraesophageal ganglia is made from three neuromeres, or neural segments. These neuromeres are formed during neurogenesis, coincident with the formation ...
[80]
Whole-brain annotation and multi-connectome cell typing of ... - Nature
Oct 2, 2024 · With 139,255 neurons, the newly completed full adult female brain (FAFB) connectome is intermediate in log scale between the first connectome of ...Missing: supraesophageal | Show results with:supraesophageal
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Contribution of photoreceptor subtypes to spectral wavelength ...
The Drosophila compound eye consists of about 750 ommatidia, each containing 8 photoreceptor cells (1). The six outer photoreceptors (R1–R6) contain a blue ...
[82]
The spectral sensitivity of Drosophila photoreceptors - PMC - NIH
Oct 26, 2020 · The Drosophila compound eye is formed from approximately 800 ommatidial units, each comprising 6 outer (R1–6) and 2 inner photoreceptors (R7 ...
[83]
The Drosophila visual system: From neural circuits to behavior - PMC
Linking Drosophila's visual motion input to its behavioral output, the optomotor response, has provided most of our knowledge on neural implementation of motion ...
[84]
Multisensory integration for active mechanosensation in Drosophila ...
Flies actively position their antennae in response to frontal airflow. To assess how mechanosensory and visual stimuli influence antennal movements and wingbeat ...
[85]
Recent advances in the genetic basis of taste detection in Drosophila
Oct 9, 2019 · In this review, we present the current knowledge of the molecular and cellular basis of taste detection of various categories of tastants.
[86]
Mechanosensation and adaptive motor control in insects - PMC
They function as proprioceptors, sensing movements of one joint segment relative to the adjoining segment. (E) Chordotonal organs are stretch-sensitive ...
[87]
Central gating of fly optomotor response - PNAS
We study the integration of multisensory and central input at the level of an identified fly motoneuron, the ventral cervical nerve motoneuron (VCNM) cell.
[88]
Olfactory Learning in Drosophila - PMC - PubMed Central - NIH
Most of the studies have shown that the integrity or synaptic output of the mushroom bodies (MB) is required for normal olfactory learning (16, 17, 42, 50).
[89]
A Review of Insect Mouthparts as a Tool Kit for Biomimetic Studies
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[90]
Dipteran - an overview | ScienceDirect Topics
These Diptera are characterized by spiracles on the first thoracic segment and also in the posterior body area (Fig. 16.1 B). Examples are Psychodidae, ...
[91]
Adaptations for nectar-feeding in the mouthparts of long-proboscid ...
Adaptations for nectar uptake through elongated proboscides. In anthophilous Diptera, the mouthparts form tubular sucking organs that take up nectar via the ...
[92]
One proboscis, two tasks: Adaptations to blood-feeding and nectar ...
Female Pangoniinae in the tabanid fly genus Philoliche can display remarkably elongated proboscis lengths, which are adapted for both blood- and nectar-feeding.Highlights · Abstract · 3.1. Mouthpart Morphology
[93]
Diverse mechanisms of feeding and movement in Cyclorrhaphan ...
Diverse mechanisms of feeding and movement in Cyclorrhaphan larvae (Diptera) ... mechanisms of larval feeding and movement in 20 species of Cyclorrhapha (Diptera).
[94]
Phylogeny and evolution of larval feeding mode in the megadiverse ...
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[95]
[PDF] FILTER-FEEDING ECOLOGY OF AQUATIC INSECTS
Studies of larval hydropsychid feeding habits indicate they are primarily omnivores; however, late instars of Arctopsychinae and some other hydrop- sychids ...<|control11|><|separator|>
[96]
Microbial symbioses in the midgut of insects - SpringerLink
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[97]
Tsetse fly microbiota: form and function - PMC - NIH
Oct 29, 2013 · These flies have also established symbiotic associations with bacterial and viral microorganisms. Laboratory-reared tsetse flies harbor up to ...
[98]
The Obligate Mutualist Wigglesworthia glossinidia Influences ...
The ability to rear adult tsetse that lack the obligate Wigglesworthia endosymbionts will now enable functional investigations into this ancient symbiosis.
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Flesh flies regulate the consumption of 3 macronutrients to maximize ...
Sep 22, 2015 · Protein is an important nutrient invested into eggs. But protein can only be invested in eggs if flies live long enough to produce eggs and ...Flesh Flies Regulate The... · Materials And Methods · Results
[100]
Supplementing Blood Diet With Plant Nectar Enhances Egg Fertility ...
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[101]
Protein- and Carbohydrate-Rich Supplements in Feeding Adult ...
Jan 28, 2023 · Feeding a 5% honey solution was shown to make females live 2.8 d longer, become more fecund (9 egg clutches per 10 females), lay more eggs.
[102]
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Hygienic grooming is induced by contact chemicals in Drosophila ...
Jul 23, 2014 · In order to induce this behavior, we gently brushed their wing margin or one of their leg with the tip of a toothpick. Flies which never ...
[104]
Behavioral evidence for nested central pattern generator control of ...
Here, we show that Drosophila grooming behavior contains periodic elements over several time scales of which we explore two: a fast repeat of individual leg ...
[105]
Massive seasonal high-altitude migrations of nocturnal insects ...
Apr 22, 2024 · High-altitude, windborne movements of insects occur on an enormous scale, and have significant impacts on ecosystem function, provision of ...
[106]
Collective Behaviour without Collective Order in Wild Swarms of ...
Collective behaviour is a widespread phenomenon in biology, cutting through a huge span of scales, from cell colonies up to bird flocks and fish schools.
[107]
QTL Determining Diel Flight Activity in Male Culex pipiens Mosquitoes
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[108]
Report Visually Mediated Motor Planning in the Escape Response ...
the escape behavior of the fruit fly, Drosophila, and found that flies can use visual information to plan a jump directly away from a looming threat. This ...
[109]
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[110]
Mosquito fauna (Diptera: Culicidae) in phytotelmata environments of ...
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Evolutionary insight from a humble fly: sperm competition and ... - NIH
Oct 19, 2020 · Yellow dungflies can be found associated with cattle throughout the cooler temperate regions of Europe, Asia and North America. The flies arrive ...
[112]
Hover Fly Biocontrol Fact Sheet - Cornell CALS
Because they often exhibit stripes of yellow they are often mistaken for wasps or bees, however they are harmless as they do not have a stinger. The legs, ...
[113]
[PDF] HABITAT CONSERVATION PLAN FOR WARM SPRINGS NATURAL ...
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Chironomid Midges (Diptera, Chironomidae) Show Extremely Small ...
Jun 1, 2015 · Chironomid midges (Diptera; Chironomidae) are found in various environments from the high Arctic to the Antarctic, including temperate and ...
[115]
DIPTERA AS PARASITOIDS - Annual Reviews
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Insect and mite galls - Agricultural Biology
Gall flies (Agromyzidae). In Colorado, the poplar twiggall fly (Hexomyza schineri) is a native insect in Colorado that produces smooth, spherical galls.Missing: herbivory | Show results with:herbivory
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[PDF] Phoresy in animals: review and synthesis of a common but ...
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[120]
The Community of Hymenoptera Parasitizing Necrophagous Diptera ...
A parasitoid larvae or pupae feed exclusively on other arthropods, mainly insects, resulting in the death of the host (Eggleton and Gaston 1990; Amendt et al.
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[122]
Spiny Prey, Fortunate Prey. Dorsal Spines Are an Asset in Intraguild ...
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[123]
Flies dynamically anti-track, rather than ballistically escape, aversive ...
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Biological roles of pyrazines in insect chemical communication
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Colour, shape and defence in aphidophagous syrphid larvae (Diptera)
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Malaria - World Health Organization (WHO)
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[129]
World Malaria Day 2024 - CDC
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[130]
DPDx - Trypanosomiasis, African - CDC
The only known vector for each is the tsetse fly (Glossina spp.). Geographic Distribution. T. b. gambiense is endemic in West and Central Africa. T. b.
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House Flies - Penn State Extension
Jun 19, 2023 · House flies are not the neatest of insects. They are suspected of transmitting at least 65 diseases to humans.
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Vector-borne diseases - EFSA
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[134]
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Economic Impacts and Management of Spotted Wing Drosophila ...
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[136]
Fly Control Around the Home - Extension Entomology
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[137]
USDA Announces Sweeping Plans to Protect the United States from ...
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[138]
Forensic Entomology - ENT 425 - NC State
Within minutes of death, blow flies (family Calliphoridae) ... In general, a fresh corpse (1-3 days) has many blow fly eggs and only a few small larvae.
[139]
Time Flies—Age Grading of Adult Flies for the Estimation of the Post ...
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[140]
Maggot Therapy - BioTherapeutics, Education & Research (BTER ...
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[141]
Mechanisms of Maggot-Induced Wound Healing: What Do We Know ...
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[142]
The nutritive value of black soldier fly larvae reared on common ...
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[143]
Black Soldier Fly Market Report: Trends, Forecast and Competitive ...
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[144]
Flies and Pollination: More than Just Aphid Slayers and Nuisances
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[145]
Tachinid flies - UC IPM
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[146]
The Strange Religious Meaning of Flies - Catholic 365
Jul 2, 2024 · Flies serve as symbols and signs of evil. Especially attracted to the smell of blood, death, trash and dung, they are a perfect symbol of evil.
[147]
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A Cultural and Natural History of the Fly - PMC - NIH
May 15, 2007 · For the same reasons for which they were demonized, flies were sometimes poetically elevated to a symbol of liberty because “Each fly is king ...
[149]
We Spy a Fly! Here Are 12 Artworks With Cameos by the Insect That ...
Oct 8, 2020 · Flies have a long history in Western art. Dating back to Medieval times, the bug's appearance in an artwork was used to symbolize death or rot ...
[150]
How Memento Mori and Vanitas Paintings Symbolized Death | Artsy
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Native Ecosystems Protection & Management | Picture-winged flies
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[152]
Endangered Species Act profile - Center for Biological Diversity
ENDANGERED SPECIES ACT PROFILE. PROTECTION STATUS: Eleven species of Hawaiian picture-wing flies are listed as endangered and one species as threatened.Missing: conservation | Show results with:conservation
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Explainer: How climate change is amplifying mosquito-borne diseases
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The Risks of Pesticides to Pollinators | Xerces Society
Their effects include removing important floral resources, causing subtle yet concerning effects on reproduction, navigation and memory and high-profile ...
[155]
Even untouched ecosystems are losing insects at alarming rates
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[156]
Gene drive strategies of pest control in agricultural systems
In this article, we identify issues associated with the potential use of gene drives in agricultural systems, to control pests and diseases that impose a ...
[157]
Using conservation genetics to prioritise management options for an ...
Apr 5, 2023 · Here, we use genomic data to investigate population parameters and genetic diversity of an endangered songbird to inform conservation management ...