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Euroleon nostras

Euroleon nostras is a of in the family Myrmeleontidae, native to much of where it inhabits dry, sandy soils in wooded or open areas. The larvae are specialized ambush predators that construct conical pit traps in loose substrates to capture small arthropods such as and woodlice, using sickle-shaped to pierce and liquefy prey before consuming it. Adults emerge in summer, resemble damselflies with brown bodies up to 30 mm long and wingspans reaching 70 mm, and primarily feed on and during their short lifespan of about one month, during which they mate and lay eggs. First described by Geoffroy in 1785, the binomial name translates to "our European lion," reflecting its predatory nature and regional prevalence. The is common but locally distributed, with larvae requiring fine, loose for pit-building, often under overhangs or near , and densities varying from 44 to 543 pits per square meter depending on conditions. Larval development spans approximately two years across three instars, during which they exhibit cannibalistic behavior under high densities, leading to significant mortality rates. Upon maturation, larvae pupate in silk-lined cocoons, emerging as adults active from to that perch in and rarely descend to the . While widespread in from to western and extending to parts of and the , it is rarer in , confined to specific sandy regions like the Suffolk . The strength of the larval mouthparts, with up to 1.98 GPa and elasticity ranging from 3.47 to 20.88 GPa, enables efficient prey puncture and withstands from sandy environments.

Taxonomy and Etymology

Classification

Euroleon nostras belongs to the kingdom Animalia, phylum Arthropoda, class Insecta, order Neuroptera, family Myrmeleontidae, subfamily Myrmeleontinae, tribe Myrmeleontini, genus Euroleon, and species E. nostras. The family Myrmeleontidae, commonly known as antlions, encompasses approximately 2,000 species worldwide and is characterized by predatory larvae, many of which construct pit traps to capture prey. Within this family, the genus Euroleon is recognized as a pit-building antlion, with species typically associated with the tribe Myrmeleontini, which includes other European antlions known for similar ambush predation strategies. Originally described as Formicaleo nostras by Geoffroy in Fourcroy in 1785, the species has undergone taxonomic revisions, with subsequent placements in genera such as Myrmeleon before its current assignment to Euroleon established by Esben-Petersen in 1918. No major synonymy disputes persist in contemporary classifications, though historical names like Myrmeleon europaeus have been noted in older literature.

Naming

The scientific name of this species follows the binomial nomenclature system established by Carl Linnaeus, designated as Euroleon nostras (Geoffroy in Fourcroy, 1785). Originally described as Formicaleo nostras in 1785, the name reflects its classification at the time within a genus combining Latin formica (ant) and leo (lion), alluding to the insect's predatory habits on ants and its fierce appearance. The current genus Euroleon, established by Esben-Petersen in 1918 with this as the type, derives its name from elements: "Euro-" referring to and "leon" meaning , thus evoking a "European lion" in recognition of its widespread occurrence and characteristics across the continent. The specific epithet nostras is Latin for "ours" or "native," emphasizing its familiarity and commonality as a native in the region where it was first documented. This was first described based on specimens collected in the vicinity of , , as detailed in Fourcroy's catalog of insects from the Parisian area.

Description

Larval Morphology

The third larvae of Euroleon nostras exhibit a robust form typical of pit-building antlions, with a broad that is not distinctly separated from the , and an overall length averaging 9.32 mm (range: approximately 8–10 mm based on multiple specimens). The head capsule is slightly longer than wide, measuring about 2.24 mm in length and 1.84 mm in width, while the mandibles are and nearly as long as the head (2.26 mm), adapted for grasping and subduing prey. Coloration in preserved specimens is reddish brown dorsally with dark markings, including a V-shaped pattern on the head capsule and lateral dark spots; the ventral side is paler, often mottled with brown elongated markings and spots, providing in sandy . The body is covered in black setae, including dolichasters (star-shaped setae) on the head and pronotum, which contribute to sensory . These setae, along with sensilla campaniformia distributed across the body, legs, and mandibles, function as mechanoreceptors sensitive to substrate vibrations, enabling prey detection from a distance. The are sickle-shaped, heavily sclerotized at the tips for piercing, and equipped with three ; the apical is slightly longer, and interdental setae number approximately (4)(2)(2)(1). A ventral , formed by the opposing and maxillae, allows injection of and into captured prey, with serrated edges on the and maxillae facilitating grip and penetration. The features specialized structures for locomotion and pit construction, including the eighth sternite with only hair-like setae on its posterior margin and the ninth sternite bearing two short rastra, each armed with four digging setae (the inner one shortest) for excavating .

Adult Morphology

The adult Euroleon nostras measures approximately 30 mm in body length with a of about 70 mm, featuring a slender, elongated that contributes to its overall form resembling a or . The body exhibits a brown coloration, which provides effective during its primarily nocturnal activities. The wings are translucent and held roof-like at rest, displaying a densely net-veined structure characteristic of , with several distinct dark spots that distinguish the species visually. These spots are absent in related Danish congeners, aiding in taxonomic identification. The head bears short, clubbed antennae that are curved and slightly swollen at the apex, along with large compound eyes for enhanced vision. Mouthparts consist of modified chewing structures adapted for liquid feeding on and , while the labial palps are four-segmented and the hind legs lack dark spots. The shows no bright spots, and neither sex possesses Eltringham's organ on the forewings.

Distribution and Habitat

Geographic Range

_Euroleon nostras exhibits a broad distribution across the Palearctic region, primarily spanning most of from the , including and , in the west to western in the east. Its range extends southward into , with records from , and eastward into western Asia, encompassing , , , and . This widespread presence reflects its adaptation to temperate and Mediterranean climates, though it favors drier conditions within its overall range. The species' northern boundary reaches southern , where it has been documented in , often in association with aeolian deposits. In contrast, it is absent or extremely rare further north, such as in , beyond the south, or the beyond specific locales. Within , E. nostras is common and well-established in central regions, such as parts of , , , and the , but becomes localized and vulnerable at the edges of its range. In , for instance, it is confined to two sites: the coastal area around Minsmere in and Holkham National Nature Reserve in , where breeding populations persist in sandy heathlands. Populations at these northern and western peripheries are declining due to and loss, driven by agricultural expansion and , which reduce suitable open sandy areas.

Habitat Preferences

_Euroleon nostras larvae primarily inhabit dry, loose sandy or friable soils that facilitate pit construction, with a strong preference for medium particle sizes ranging from 230 to 540 μm, as these allow for stable yet excavatable traps. They avoid compacted or fine cohesive substrates (e.g., 110–230 μm) that hinder digging and coarse gravels (>1540 μm) that prevent pit stability, tolerating a broad spectrum of medium sands incorporating finer or coarser fractions for optimal trap efficiency. Wet or high-density soils are unsuitable, prompting relocation to drier areas to minimize mortality and developmental delays. The species favors open, sandy settings such as dunes, riverbanks, heathlands, sand steppes, and disturbed areas like quarries or paths, often in low-vegetation grasslands where sparse cover provides minimal obstruction. Larvae select sheltered microhabitats protected from direct and , including forest edges, under fallen trunks, rocks, or shrubs, which offer partial and reduce environmental extremes. In experimental conditions, over 84% of larvae chose shaded over illuminated substrates, highlighting an intolerance for full exposure. Climate preferences align with warm, temperate conditions typical of Mediterranean-influenced , where larvae thrive in balanced thermal regimes around 25–28°C and low to support prolonged development. High disrupts pit maintenance and increases pupation risks, while excessive accelerates succession toward denser vegetation, threatening open sandy niches.

Life Cycle

Egg and Larval Stages

Females of Euroleon nostras deposit eggs individually in sandy soil, typically in sheltered, habitats suitable for larval construction. Using the at the tip of the , the female repeatedly taps the sand surface to create small depressions before inserting her to lay each , often completing about 20 such depositions in a localized patch of . In captivity, females lay an average of 20 , showing a preference for warmer during oviposition. The are small, though specific dimensions for this species are not well-documented in primary . The eggs hatch after 20–30 days, with the varying based on environmental ; warmer conditions accelerate , while cooler temperatures prolong it. Upon emergence, first-instar larvae are small and immediately begin constructing shallow pits, typically 1–2 cm in diameter, to ambush small arthropods such as . These early pits reflect the larva's limited size and mobility, serving as initial traps for minute prey that fall in and are captured by the larva's prominent mandibles. Larval development proceeds through three instars over 1–2 years, with the third instar being the longest and most resource-intensive . Pit dimensions increase non-linearly across instars, reaching up to 5–7 cm in diameter for later stages to accommodate larger prey and the growing larva's body size, which can exceed 9 mm in length by the final instar. Growth is influenced by food availability and temperature, with slower development in cooler climates leading to extended larval periods; larvae often overwinter in the , sometimes twice, remaining dormant to survive adverse conditions. During this time, they feed primarily on small arthropods, building and relocating as needed to optimize predation efficiency.

Pupal and Adult Stages

The mature of Euroleon nostras constructs a spherical within the , utilizing secreted by the Malpighian tubules and binding it with particles to form a protective chamber. This pupation process occurs after the larval stage reaches maturity, typically in late spring or summer, as the ceases feeding and prepares for . The remains non-feeding throughout this phase, relying on stored resources for the transformation into the adult form. The pupal stage lasts approximately 20–30 days, with duration influenced by environmental ; warmer conditions accelerate . , or eclosion, happens at night to minimize predation risk, allowing the adult to expand and harden its wings in relative safety before daylight. Adults of Euroleon nostras appear from to across their range, with peak activity in and . Their lifespan spans 2–4 weeks, a brief period dedicated primarily to and oviposition before . The exhibits a univoltine life cycle, completing one generation annually, though larvae may enter during unfavorable conditions to synchronize with optimal seasonal cues.

Ecology and Behavior

Predatory Strategies

The larvae of Euroleon nostras are predators that construct conical traps in loose, dry to capture prey. Using their head and powerful , the larva excavates the pit by tossing particles outward in a systematic manner, starting from the center and expanding the while sifting finer grains to maintain steep walls. These pits typically measure 2.5–7.5 in depth, with dimensions scaling to the larva's body size across instars, and the builder positions itself motionless at to avoid detection. Prey detection occurs through sensitive setae distributed across the 's body, which perceive vibrations generated by approaching arthropods, prompting the predator to orient toward the source. To hasten capture, the rapidly flicks sand from its body with jerking head movements, inducing minor landslides that destabilize struggling victims and direct them to the pit's steepest slope. Upon a prey item tumbling in, the lunges forward, seizing it with elongated, sickle-shaped equipped with hollow projections that pierce the and inject liquefying enzymes to externally digest the internals for fluid intake. Common prey encompass small ants (such as Lasius spp.), , and spiders, though experimental trials also confirm success with . In natural populations, pit densities vary widely from 44 to 543 per depending on quality and larval , influencing encounter rates with both prey and conspecifics. At elevated densities exceeding 1000 larvae per , intraspecific competition intensifies, often resulting in that imposes substantial mortality, such as up to 50% in experimental high-density setups.

Reproductive and Adult Activities

Adults of Euroleon nostras exhibit nocturnal behaviors in , where volatile compounds from males may function as aggregation pheromones to attract mates. Copulation is an acrobatic process in which the female grips a twig while the male attaches his to hers via specialized genital structures, suspending himself below her for approximately one to two hours. Following , the female consumes a nutrient-rich from the male, which provides additional energy, before descending to select oviposition sites in loose, sandy substrates suitable for egg deposition. As weak fliers, adult E. nostras undertake short, low-altitude flights primarily for dispersal and mate location, spending daylight hours concealed in vegetation to evade predation. Their active flight period spans to across much of their range, coinciding with peak reproductive opportunities and warmer conditions that facilitate emergence from pupation. In contrast to the carnivorous larvae, adults of E. nostras adopt a non-predatory lifestyle, sustaining themselves mainly on and . This dietary shift supplements the substantial reserves built up during the prolonged larval phase, supporting the brief adult lifespan dedicated to .

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