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Ten-lined June beetle

The Ten-lined June beetle (Polyphylla decemlineata), also known as the watermelon beetle, is a large scarab species characterized by its robust, brown body measuring 22–35 mm in length, featuring ten prominent white longitudinal stripes formed by scales on the elytra, pronotum, and head. Males possess large, fan-like antennal clubs for detecting pheromones, while females have shorter, more compact antennae; both sexes can produce a hissing when disturbed by expelling air from the spiracles. Native to western , including much of the west of the and parts of , this beetle thrives in sandy or loose soils within forests, orchards, grasslands, and agricultural areas such as groves and tree fruit plantations. Adults are primarily nocturnal, emerging from late to early (depending on and ) and are strongly attracted to lights, often swarming around outdoor fixtures during warm summer evenings. The species exhibits a 2–4 year , with females laying 60–70 eggs in near host plants; the creamy-white, C-shaped larvae (white grubs) develop over multiple instars, overwintering deeply in the soil and feeding on roots of grasses, shrubs, s, and crops like apples, s, corn, and potatoes, potentially causing significant damage by roots and leading to tree decline or death in heavy infestations. While adult feeding on foliage results in minor notching of leaves with negligible economic impact, the root-feeding larvae pose the primary concern in and , though infestations spread slowly and are often localized. Natural enemies such as parasitic wasps and nematodes provide some biological control, but management typically involves treatments or removal of infested plants. Despite their imposing size and occasional abundance, these beetles are harmless to humans and play a role in and through larval activity.

Taxonomy and nomenclature

Classification

The ten-lined June beetle, scientifically named Polyphylla decemlineata (Say, 1824), belongs to the order Coleoptera within the class Insecta. This species was originally described by naturalist in 1824 under the name Melolontha decemlineata, based on specimens collected during an expedition to the , with the description published in the Journal of the Academy of Natural Sciences of Philadelphia. Say's work marked one of the early systematic contributions to North American , establishing the binomial nomenclature for this beetle in the context of then-current classifications. The full taxonomic hierarchy of P. decemlineata places it within the following categories:
TaxonClassification
Kingdom
Phylum
Class
Order
Family
Subfamily
Genus
Species
This classification reflects its position as a scarab in the diverse subfamily Melolonthinae, known for root-feeding larvae and often robust adult forms. Within the genus Polyphylla, which encompasses around 30 of large scarab predominantly native to western , P. decemlineata is distinguished by its specific morphological traits that align with generic boundaries established in taxonomic revisions. The is characterized by shared features such as lamellate antennae and a preference for arid or semi-arid habitats.

Common names and etymology

The primary common name for Polyphylla decemlineata is the ten-lined June beetle, reflecting the ten pale longitudinal stripes on its elytra and the species' typical adult emergence in across much of its range. This name distinguishes it from other June beetles in the family, emphasizing its characteristic markings and seasonal activity. An alternative common name is the watermelon beetle, though it is used less frequently and regionally in agricultural contexts. The scientific name's genus Polyphylla derives from "poly" (many) and "phyllon" (), referring to the multiple leaf-like antennal lamellae in males that fan out for detection. The epithet "decemlineata" stems from the Latin "decem" (ten) and "lineata" (lined or striped), directly alluding to the ten stripes on the beetle's forewings.

Morphology and

Adult characteristics

The adult Ten-lined June beetle (Polyphylla decemlineata) measures 20 to 35 mm in length, ranking among the largest scarab beetles in western . Its body exhibits a mottled brown coloration accented by conspicuous pale longitudinal stripes: three on the pronotum and head, and five per elytra (typically four long and one short), which form the ten-lined pattern diagnostic for identification. These stripes consist of broad bands of white or yellow scales set within elytral punctures. Antennae are 11-segmented with a lamellate club; in males, this club is enlarged, comprising long, flat, tongue-shaped lamellae approximately 1.5 times the length of the remaining antennal segments, enabling detection from females. In females, the club is more compact, measuring about one-half to one-third the length of the other segments. The pronotum lacks discal setae but bears the characteristic white stripes. The legs are robust and structured for digging, consistent with adaptations in the for burrowing in . The elytra cover the hindwings, and the exposed terminal abdominal segment (pygidium) remains partially visible beyond their edges. When disturbed, adults emit a loud hissing or squealing sound by forcefully expelling air through their spiracles.

Larval and immature stages

The eggs of the ten-lined June beetle (Polyphylla decemlineata) are oval and dull creamy white, measuring up to 4 mm in length. They are laid singly or in small clusters within the , differing markedly from the robust, patterned form by their simple, unadorned suited for subsurface protection. Larvae, known as white grubs, exhibit a typical C-shaped body posture characteristic of scarab , with a creamy white , a distinct brown head capsule, and three pairs of thoracic legs. Mature third-instar larvae reach lengths of 25–50 mm, featuring a robust build stiffer than related species like , and a pronounced raster pattern on the terminal abdominal segment consisting of two short, parallel longitudinal palidia each bearing 7–12 sharp , along with forward-extending tegilla and numerous preseptular hamate setae for . The head lacks eye spots and includes a frons with 3–4 posterior setae per side, while the maxillae possess at least 14 conical stridulatory teeth and the lacinia bears 3 stout unci; the anal opening is transverse and angular with an uncleft ventral lobe. These larvae progress through three instars, with mouthparts adapted for consumption, contrasting the adults' and winged mobility. Pupae are of the exarate type, with appendages free from the body, measuring approximately 25 mm in length and initially creamy white before darkening to light tan. They feature external wing pads and form within earthen cells, rendering them non-mobile and highly vulnerable compared to the active adults.

Distribution and habitat

Geographic range

The Ten-lined June beetle (Polyphylla decemlineata) is native to , with a discontinuous spanning the , southwestern , and northern . Its distribution extends from southern and southern in southward through , , , and in , primarily west of the but with disjunct populations reaching eastern , central , northeastern , , and . In the United States, the species is widespread in western states including , , , , , , , , , and , with additional records in , , , and ; in Canada, it occurs in and . These populations are often localized in sandy or loamy soils suitable for larval development. The beetle inhabits elevations from near sea level, such as 190 feet in , up to 10,500 feet in high-elevation sites like Whitney Portal, California, and various mountainous areas across its range. Historically, P. decemlineata was first described by in 1824 from specimens collected in and along the near Pawnee villages, with a neotype later designated from , , reflecting its early documented presence in central plains regions before more extensive western records accumulated.

Habitat preferences

The ten-lined June beetle (Polyphylla decemlineata) prefers well-drained, sandy soils for egg-laying and larval development, as these provide suitable conditions for burrowing and root access. These soils often contain high content, which supports the processes that benefit early larval stages feeding on decaying matter. Loamy textures may also be tolerated where drainage remains adequate, though infestations are more common in lighter, sandier substrates across its range. This species is associated with a variety of vegetation types, including grasslands, shrublands, and pine-oak woodlands, where larvae can access root systems of grasses, forbs, and trees. It frequently occurs in agricultural settings such as orchards and vineyards, particularly those with established tree crops like almonds and pines, which offer both larval food sources and adult foliage. These habitats overlap with arid to semi-arid regions of the western United States, where the beetle's distribution is concentrated. The beetle thrives in climates with mild winters and hot summers, enabling a 2–4 year life cycle with overwintering larvae. Adults are most active during dry, warm evenings from late to September, aligning with low-humidity conditions that facilitate flight and mating. In microhabitats, larvae to depths of 10–35 cm (4–14 inches), particularly in fall to avoid , before returning nearer the surface in for feeding and pupation. They construct earthen cells near the soil surface for pupation in the final larval . Adults, being nocturnal, rest in tree canopies or under organic debris by day and are often found near lights or on foliage at night.

Life cycle

Developmental stages

The life cycle of the Ten-lined June beetle (Polyphylla decemlineata) follows a complete with four distinct developmental stages: , , , and . The entire cycle spans approximately 2–4 years from to . Females lay in and August, depositing them singly or in small clusters in moist soil rich in , often near the base of host plants. Each female produces 60–70 during her brief lifespan, burying them 5–10 cm deep. The are pearly white, oval, and about 4 mm long; they hatch in 2–3 weeks under suitable soil temperatures and moisture conditions. Upon hatching, first-instar larvae emerge and begin feeding at the soil surface on fine and decaying . The larval stage consists of three s and lasts 2–4 years overall, depending on . In the first year, small larvae remain near ; as they progress to second and third instars in subsequent years, they burrow deeper—up to 1.5 m—targeting larger woody of grasses, shrubs, and trees. Larvae, which adopt a characteristic C-shaped posture, overwinter in the twice, once after the first instar and again after the third, descending deeper to avoid freezing temperatures. In the spring of the third year, mature third-instar larvae construct earthen cells 15–20 cm below the surface and enter the pupal stage, which lasts 2–4 weeks. Pupae are initially whitish and gradually darken as the form develops within the protective cell. Adults eclose in mid-June to mid-October, with peak in early , though activity is concentrated from late June to July in many regions. The stage is short-lived, lasting 4–6 weeks, during which individuals focus primarily on and egg-laying rather than extensive feeding. Males typically eclose slightly earlier than females and exhibit crepuscular to locate pheromone-emitting females near sites or on .

Duration and environmental influences

The of the ten-lined June beetle (Polyphylla decemlineata) typically spans 2 to 4 years, with the vast majority of this duration spent in the larval stage underground. In warmer southern regions like , the complete cycle often completes in about 2 years, while in cooler northern areas such as the , it extends to 3 or 4 years due to slower development rates. and are primary environmental factors influencing this variability, as larvae require consistent conditions for feeding and growth on plant roots. Larval development, which dominates the , lasts 2 to 4 years depending on climate, with extended periods in cooler environments where lower temperatures slow metabolic processes and delay molting between the three instars. Optimal larval growth occurs in well-aerated, sandy soils with adequate moisture to support root-feeding activity, but prolonged cold reduces feeding efficiency and prolongs the stage. In unirrigated or dry conditions, larvae migrate deeper into the (often beyond 8 inches) to access residual moisture, potentially delaying progression to pupation. Adult beetles emerge in late spring to summer and typically live for several weeks to a few months, during which they focus on mating and minimal feeding before dying off by fall. Emergence timing is influenced by soil warming to around 60°F (15.6°C), with activity peaking on warm evenings above this threshold. Predation and environmental stress, such as , can shorten adult longevity by limiting access to foliage or increasing risk. Other stressors significantly impact cycle completion: excessive drought can halt larval feeding and delay pupation by restricting essential for survival, while flooding may drown immature stages in poorly drained areas. Agricultural disrupts the cycle by exposing larvae to predators and , often reducing populations in cultivated fields.

Ecology and behavior

Feeding habits

The larvae of the Ten-lined June beetle (Polyphylla decemlineata) are subterranean root herbivores, feeding primarily on the of grasses, forbs, perennials, , and shrubs. They exhibit a broad host range, including woody plants such as oaks, (particularly pines), and fruit trees like , where their chewing mouthparts sever and girdle , often leading to weakening or death. This underground rasping and consumption occurs in sandy or well-drained soils, up to several inches deep, with full-grown larvae capable of substantial damage despite their C-shaped, white grub form. In contrast, adult Ten-lined June beetles engage in minimal foliar feeding compared to their larval stage, primarily browsing on the leaves of various trees and shrubs at night. They notch the edges of foliage from species such as oaks and willows, as well as occasional flowers, though this activity rarely results in noticeable injury to plants. Adults are nocturnal feeders, using their maxillary palps to explore and select plant material, but their short adult lifespan limits overall consumption. Overall, P. decemlineata occupies a primarily herbivorous , with larvae functioning as destructive root herbivores that contribute disproportionately to ecological and agricultural impacts relative to the adults' superficial .

Reproductive and social behaviors

Adult females of the Polyphylla decemlineata, known as the ten-lined June beetle, emit sex pheromones upon from the to attract males, who detect these chemical signals using their large, fan-like antennae during evening patrols close to the ground. Mating typically occurs shortly after female , at or near the surface by the emergence hole, with copulation lasting approximately 2 minutes on average; polyandry has not been extensively documented. Following mating, females burrow back into the soil to oviposit, laying 60 to 70 eggs singly over several weeks in moist, sandy substrates near plant roots, preferring areas with decaying for subsequent larval development. Eggs are oval, creamy-white, and measure up to 4 mm in length, hatching after 3 to 4 weeks under suitable warm conditions. The species exhibits no , with eggs and early larvae left unguarded, resulting in high mortality rates primarily from soil-dwelling predators and environmental factors. Adults show limited , forming temporary loose aggregations or swarms around artificial lights post-emergence, particularly males in erratic flight patterns at dusk; when threatened, individuals produce a defensive hissing by expelling air from the spiracles, which may occur communally in groups but serves individual deterrence rather than coordinated social defense. Reproductive activity peaks from late June to July, aligning with adult emergence in mid-summer, though activity can extend into September depending on regional climate.

Interactions with humans

Pest status

The larvae of the Ten-lined June beetle (Polyphylla decemlineata) primarily damage agricultural crops by feeding on roots, leading to girdling, canopy decline, and eventual tree death, particularly in sandy soils where infestations are more severe. This root-feeding behavior weakens plant vascular systems, causing stunted growth and increased susceptibility to drought stress, with initial symptoms often remaining hidden until significant injury occurs. Affected crops include fruit orchards such as almonds, apples, and apricots in and , as well as turf grasses, field crops like corn, strawberries, cane fruits, potatoes, and ornamentals like roses. Localized infestations in these systems can result in substantial yield reductions, with thousands of almond trees removed in due to severe root injury causing decreased foliage and nut production. The beetle's economic significance has grown in western U.S. since the 1990s, with notable outbreaks in orchards and California's Central Valley contributing to replanting costs and lost productivity. Detection of infestations typically involves observing or declining patches in orchards, emergence holes in the from adult beetles, and clusters of adults attracted to lights near affected fields during evening hours from late to . While larvae pose the main threat, adults cause minor non-target defoliation by notching leaves, which rarely results in economic harm to fruit trees or other crops.

Management and control

Monitoring populations of the Ten-lined June beetle (Polyphylla decemlineata) involves using light traps, such as blacklight or tungsten sources, to detect adult male emergence in early to mid-June, providing an indication of infestation levels in orchards. Soil sampling by digging trenches or pits around tree roots in spring or fall can identify larvae, particularly in sandy soils where they feed on roots. Pheromone traps are under evaluation for adult monitoring but are not yet widely adopted for routine use. Cultural control strategies emphasize practices that disrupt the beetle's without chemicals. Deep in or summer exposes shallow-feeding larvae to natural predators like birds and , reducing their survival in affected areas. with non-host plants and selecting rootstocks resistant to root damage can limit larval establishment, though options are limited in orchards. Avoiding excessive in sandy soils prevents larvae from migrating upward toward roots, as influences their depth. Biological controls rely on natural enemies and augmented agents for suppression. Predators such as , , scoliid wasps, and tachinid flies target larvae and adults, respectively, though their impact is often insufficient for heavy infestations. Entomopathogenic nematodes (Steinernema riobrave and Heterorhabditis megidis) show promise against larvae but have variable efficacy, particularly against older instars protected by symbiotic mites. Chemical controls target larvae during vulnerable stages, integrated within an IPM framework to minimize environmental impact. Soil drenches with (e.g., Admire) applied post-egg hatch achieve high larval mortality when followed by irrigation to ensure penetration to depths of 14 inches or more. or similar insecticides can be used as soil treatments for young larvae, with applications timed for maximum efficacy after adult emergence. For severe cases, soil fumigation after tree removal is effective but reserved for pre-planting scenarios due to regulatory restrictions. Preventive measures focus on limiting spread in high-risk areas like nurseries. Quarantine protocols for and material help contain infestations, as larvae can be transported in root balls. in small plots during summer heats the to lethal temperatures for eggs and young larvae, offering a non-chemical option for site preparation. Overall, combining these approaches is recommended to manage populations sustainably in orchards affected by root damage.

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