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Codling moth

The codling moth (Cydia pomonella L.), a small species in the family Tortricidae (Lepidoptera), is a cosmopolitan insect pest primarily affecting pome fruits such as apples and pears.^[1] Native to Eurasia, it features adults that are approximately 10–12 mm long with grayish forewings marked by coppery or bronze tips and irregular bands.^[2] Its larvae, the damaging stage, are creamy white to pinkish, reaching 12–20 mm in length with a brown head and dark plates, and they bore tunnels into fruit cores, feeding on seeds and flesh while leaving behind frass-filled exit holes.^[3] This behavior renders infested fruits unmarketable and can lead to secondary infections by fungi or bacteria.^[4] The life cycle of the codling moth typically spans 1–4 generations per year, depending on climate and latitude, with overwintering occurring as mature diapausing larvae in silken cocoons under tree bark, in leaf litter, or in soil.^[2] Pupation begins in spring as temperatures rise, requiring about 100 degree-days above a base of 10°C, leading to adult emergence around apple full bloom (often April–May in temperate zones).^[5] Females lay up to 100 flat, white eggs singly on leaves or fruit near calyces, which hatch in 6–20 days; neonate larvae then spin silken threads to reach and penetrate the fruit, developing through five instars over 3–4 weeks before exiting to pupate.^[4] Adults are active during warm evenings above 15–16°C, mating within hours of emergence, and a single generation requires roughly 610 degree-days.^[1] Ecologically, the codling moth thrives in temperate regions worldwide, having spread from its Eurasian origins to North and South America, Australia, New Zealand, South Africa, and most apple-growing areas, but it is absent from Japan and certain Asian locales due to unsuitable conditions.^[2] It prefers apples as its primary host but also infests pears, quince, hawthorns, crabapples, and in some regions, walnuts or stone fruits like apricots and plums.^[5] Behaviorally, larvae cause "stings"—shallow feeding marks from failed entries—while successful ones create deep galleries that promote rot; populations are monitored using pheromone traps, and natural enemies include parasitoids, predators, and entomopathogens.^[3] As one of the most economically significant orchard pests, the codling moth can infest up to 95% of untreated apples, reducing yields by 30–50% and necessitating intensive management to keep damage below 0.5–1%.^[1]^[3] Control relies on integrated pest management (IPM) strategies, including degree-day modeling for timing, mating disruption with pheromones, targeted insecticides against eggs and neonates, and biological agents like granulosis virus, though challenges include insecticide resistance and varying regional climates.^[4]^[5]

Taxonomy and Description

Taxonomy and Classification

The codling moth is scientifically classified as Cydia pomonella (Linnaeus, 1758), belonging to the kingdom Animalia, phylum Arthropoda, class Insecta, order Lepidoptera, family Tortricidae, subfamily Olethreutinae, genus Cydia, and species pomonella.^[6]^[7] This placement situates it within the diverse Tortricidae family, which encompasses over 10,000 species of small moths commonly known as leafrollers or bell moths, many of which exhibit adaptations for rolling or webbing plant tissues.^[7] Originally described by Carl Linnaeus in the 10th edition of Systema Naturae published in 1758, the species was initially named Phalaena Tinea pomonella, reflecting its association with apple fruits (poma in Latin).^[8] The type locality was not precisely specified but indicated as occurring within European apple habitats ("Habitat intra Europae poma").^[8] Over time, the nomenclature evolved; an older generic synonym is Carpocapsa pomonella, frequently used in early 20th-century literature before taxonomic revisions established Cydia as the valid genus due to priority and homonymy rules.^[9]^[10] Common names for C. pomonella include codling moth (predominant in North America and Europe), codlin moth (especially in Australia), and apple worm, the latter emphasizing its larval stage's damage to fruit cores.^[11] As a member of the Olethreutinae subfamily, C. pomonella represents an evolutionary adaptation within Tortricidae toward internal fruit feeding, diverging from the more typical leaf-rolling behaviors of related taxa to specialize in infesting pome fruits like apples and pears.

Physical Description

The codling moth, Cydia pomonella, exhibits distinct morphological features across its life stages, characteristic of the family Tortricidae. The adult moth measures 9-12 mm in body length with a wingspan of 15-20 mm.^[5] The forewings are grayish-brown, mottled with darker scales, and feature a prominent coppery or bronze patch near the tip, while the hindwings are lighter, copper-brown, and fringed with long scales.^[5]^[4] The body is robust and covered in fine scales, with antennae that are filiform and held backward along the body. Sexual dimorphism is evident, particularly in males, which possess brush-like scale structures on the hind legs used for disseminating pheromones.^[12] The eggs are small, flat, and oval-shaped, measuring 0.8-1.0 mm in diameter.^[5] Initially translucent white when laid, they develop a reddish embryonic ring and become brownish before hatching, with the black head capsule of the larva visible through the chorion in the final stage.^[5]^[13] Larvae, or caterpillars, are the primary damaging stage, reaching up to 20 mm in length when fully grown.^[4] They have a pinkish-white to creamy body with a distinct brown head capsule and brown thoracic and anal shields; newly hatched larvae are smaller, about 2 mm long, and pale with a black head.^[5] The body is segmented, smooth, and equipped with eight pairs of legs: three pairs of true legs on the thorax and five pairs of prolegs on the abdomen.^[14] The pupa is 10-12 mm long, reddish-brown, and elongated, typically enclosed within a silken cocoon for protection.^[4]^[13] The coloration darkens as it matures, and the cremaster at the posterior end anchors it within the cocoon.^[14]

Distribution and Habitat

Global Distribution

The codling moth (Cydia pomonella) is native to southeastern Europe and parts of Asia Minor, where it has long been associated with pome fruit orchards.^[15]^[2] It was introduced to North America in the mid-18th century through international trade in infested fruits and plants, becoming a well-established pest in pome fruit regions by around 1750.^[16]^[17] This human-mediated dispersal marked the beginning of its expansion beyond its original range, transforming it from a regional threat to a global concern in temperate agriculture. The codling moth has a near-cosmopolitan distribution in temperate zones worldwide, present across Europe, Asia (its native Eurasian range), North America, southern parts of South America, Australia, New Zealand, South Africa, and most other apple-growing areas.^[18]^[19] Despite suitable climatic conditions in some regions, it is absent from Japan and certain Asian locales, likely due to historical lack of introduction or local ecological barriers.^[2]^[18] It thrives in areas with suitable climatic conditions, such as those supporting apple and pear cultivation, but is largely absent from tropical regions due to its physiological requirements for cold temperatures during diapause.^[18]^[20] Optimal developmental temperatures range from approximately 15°C to 30°C, limiting its establishment in consistently warm equatorial areas.^[20] Historically, the species' spread accelerated in the 19th and 20th centuries, with records of establishment in North America by the early 1800s and subsequent introductions to the Southern Hemisphere via colonial trade routes.^[21] Recent expansions continue through global fruit commerce, where larvae hidden in exported apples and pears facilitate long-distance movement.^[22] Key factors driving this dispersal include unintentional transport of infested produce and the alignment of its life cycle with temperate climates, enabling rapid population growth in new suitable habitats.^[23]^[18]

Habitat Preferences

The codling moth (Cydia pomonella) primarily inhabits temperate regions worldwide, favoring deciduous fruit orchards where apple and pear trees predominate, as these provide ideal conditions for survival and reproduction. These environments typically feature moderate annual temperatures and precipitation patterns, with high suitability in areas between 30° and 60° latitude, aligning with major apple-growing zones in Europe, North America, and Asia. The moth thrives in orchards that accumulate 500–1,500 chill hours (hours between 32°F and 45°F or 0°C and 7°C during winter dormancy), which support host plant phenology and enable effective diapause termination in overwintering larvae.^[18]^[24] Climate tolerances for the codling moth center on moderate temperatures conducive to development, with an optimal range of 15–27°C for most life stages, allowing efficient progression from egg to adult. Development halts below 10°C, facilitating overwintering diapause, while temperatures exceeding 30–34°C impose upper limits, reducing viability in prolonged heat. The species avoids extreme aridity, such as desert regions, and excessive humidity in tropical zones, preferring balanced conditions with annual mean temperatures around 10–20°C and low precipitation in the driest months to prevent desiccation or fungal issues.^[25]^[2]^[18] Within these orchards, the codling moth exploits specific microhabitats for protection and resource access. Larvae seek shelter inside fruit cores after boring entry, providing a nutrient-rich and shielded environment. Pupae form silken cocoons under loose bark scales on tree trunks or in ground litter and debris at the orchard base, offering insulation during overwintering. Adults remain in tree canopies during the day, resting with wings folded in a tent-like posture among foliage for camouflage and proximity to oviposition sites. Soil associations favor well-drained loamy types common in deciduous orchards, while dense vegetation layers, including leaf litter, enhance overwintering success by buffering against temperature fluctuations.^[2]^[26]^[27]

Life Cycle and Reproduction

Life Stages Overview

The codling moth (Cydia pomonella) undergoes holometabolous metamorphosis, consisting of four distinct life stages: egg, larva, pupa, and adult.^[5] The egg stage lasts 5-20 days, depending on temperature, followed by the larval stage, which is active for 3-4 weeks as the caterpillar feeds and grows through five instars.^[5]^[28] The pupal stage then occurs over 2-3 weeks within a cocoon, after which the adult moth emerges and lives for 2-3 weeks, during which mating and oviposition take place.^[28] The total cycle for one generation typically spans 6-10 weeks under favorable conditions.^[5] Development across all stages is highly temperature-dependent, with a lower developmental threshold of 10°C (50°F); activity ceases below this temperature.^[25] The accumulation of degree-days (DD), calculated as the integral of temperature above the base, drives progression, with approximately 500-600 DD required for the first generation from adult emergence to the next.^[25] Voltinism varies from 1-3 generations per year, influenced by latitude and climate; temperate regions often support two full generations, with a partial third in warmer areas. Due to ongoing climate change, voltinism is increasing in many regions, with projections indicating additional generations (up to 3-5 in warmer areas like California's Central Valley by mid-century).^[5]^[28]^[29] Overwintering occurs primarily as diapausing fifth-instar larvae in protective cocoons under tree bark or in ground litter, allowing survival through cold periods until pupation in spring.^[28]^[5] Details of each stage, including specific behaviors and morphological changes, are covered in subsequent sections.^[5]

Life Stage	Approximate Degree-Days (base 10°C)
Egg	80
Larva	345-350
Pupa	280
Total per Generation	610-700

Egg and Oviposition

Female codling moths, Cydia pomonella, typically lay 50–100 eggs over their adult lifespan, with fecundity ranging from approximately 60 to 120 eggs per female under optimal conditions.^[31] Eggs are deposited singly, primarily on the upper surfaces of leaves or directly on fruit, often within 10 cm of potential larval hosts to facilitate neonate dispersal.^[32] Oviposition commences 2–3 days after mating, peaking on the third day, and continues for 4–7 days until the female's death around 14 days post-emergence.^[33] The eggs are small, flattened, oval discs measuring about 1 mm in diameter, initially translucent white and developing a reddish embryonic ring as development progresses.^[5] A key feature is the micropylar region at the anterior pole, consisting of a rosette with 8–9 petal-like cells that serves as the entry point for sperm during fertilization.^[34] Embryonic development, or incubation, requires 80.1 degree-days above a lower threshold of 11.06°C, resulting in a period of 4–10 days at typical summer temperatures of 20–25°C.^[35] Hatching occurs when the first-instar larva chews through the chorion, the egg's outer membrane, typically in the early morning light phase.^[35] This process is influenced by host plant volatiles, which orient the emerging neonate toward suitable entry points on fruit.^[32] Site selection during oviposition favors young fruits measuring 4–5 cm in diameter, where females preferentially deposit eggs near the calyx or shaded leaf undersides to minimize exposure to predators and environmental stressors.^[32] Exposed sites, such as outer canopy wood or sunlit surfaces, are largely avoided, with over 90% of eggs placed in protected proximity to fruit clusters.^[32]

Larval Development

The codling moth, Cydia pomonella, undergoes larval development through five distinct instars, a process characterized by progressive increases in size and feeding activity within host fruits. Head capsule widths serve as a reliable indicator of instar progression, starting at approximately 0.31 mm for the first instar and increasing to 0.49 mm, 0.81 mm, 1.18 mm, and 1.61 mm for the subsequent instars, following Dyar's rule of geometric growth.^[33]^[36] The total feeding and development period typically spans 16 to 24 days under optimal temperatures around 25–30°C, though this can extend to 20–30 days in cooler conditions.^[37]^[38] Upon hatching, neonate larvae, weighing about 0.1 mg, exhibit limited dispersal by crawling on foliage or fruit surfaces, often within a few meters on the tree to locate a suitable host such as apple or pear fruit.^[5] They preferentially enter through the calyx end or stem cavity, mining shallowly before tunneling deeper toward the seed core, where they feed on pulp and seeds.^[28] As they burrow, larvae expel reddish-brown frass (excrement) through the entry hole, which enlarges over time and may function as an exit upon maturation.^[39] Throughout the instars, larvae experience rapid weight gain, from 0.1 mg in the first instar to 1.5 mg, 7.7 mg, 16.8 mg, and up to 49.8 mg in the fifth instar, driven by nutrient intake from the fruit interior.^[33] Molting between instars is triggered by reaching critical size thresholds, primarily determined by head capsule expansion, allowing the larva to accommodate further growth.^[36] This staged development ensures efficient resource utilization, with each instar dedicated to intensified feeding and tunnel expansion.^[40]

Pupal Stage

Following the final larval instar, the codling moth larva spins a silken cocoon and undergoes ecdysis to enter the pupal stage, during which it remains immobile while undergoing metamorphosis.^[41] This transition typically occurs after the larva has ceased feeding and seeks a protected site for pupation.^[5] The pupal stage lasts 7–30 days, with duration inversely related to temperature; at around 20°C, it commonly spans 10–20 days, while warmer conditions near 25°C can shorten it to 8–14 days.^[5]^[42] Pupae are reddish-brown, approximately 13 mm long, and encased within the tough silken cocoon formed by the larva.^[5] During this phase, significant morphological changes occur, including the development of wings, legs, and other adult appendages from imaginal discs, culminating in the formation of the adult body structure.^[42] Pupation sites vary by season: overwintering pupae form in more protected locations, such as deep under loose bark, in soil, or amid ground debris at the base of host trees, where they can endure cold; in contrast, summer pupae are often in more exposed positions, like leaf litter or directly within harvested fruit remnants.^[41]^[5] These cocoons provide mechanical protection and camouflage against environmental stresses and predators.^[41] Adult emergence is triggered by a combination of rising temperatures and photoperiod cues, with the moth slitting the cocoon and pupal case to exit; for non-diapausing pupae, this process aligns with warmer spring or summer conditions, often beginning around 175 degree-days (base 10°C) from January 1 in temperate regions.^[42]^[5] Overwintering pupae delay emergence until environmental signals indicate suitable conditions, typically mid-March to early April in many apple-growing areas.^[41]

Adult Emergence and Mating

Adult codling moths (Cydia pomonella) emerge primarily from pupae in the soil or under bark, with activity peaking at dusk when temperatures exceed 15°C (59°F), initiating their nocturnal flights for dispersal and mate location.^[43] Upon eclosion, adults exhibit limited feeding behavior, relying mainly on dew or nectar from flowers if available, though many remain non-feeding in orchard settings.^[44] Their lifespan typically ranges from 10 to 20 days under field conditions, influenced by temperature and generation, with females averaging around 12-18 days and males slightly longer at 16-21 days when provided minimal sustenance like sugar solution in laboratory studies.^[44]^[33] Flight patterns of emerging adults are characterized by low-altitude dispersal, often 1-2 meters above the tree canopy, assisted by wind currents that carry them up to several hundred meters from the emergence site.^[45] Males initiate mate-seeking flights shortly after sunset, navigating via optomotor anemotaxis toward pheromone plumes, while females remain more stationary, calling from perches on branches or foliage.^[46] Mating occurs soon after emergence, with females typically ready 2-3 days post-eclosion, often engaging in a single copulation that fertilizes their lifetime egg production of 30-100 eggs.^[33]^[47] Males detect female-emitted sex pheromones from distances up to 100-260 meters downwind, following intermittent plumes in a zigzag pattern guided by antennal receptors sensitive to nanogram quantities.^[48] The primary pheromone component, codlemone [(E,E)-8,10-hexadecadien-1-ol acetate], is released by calling females during a brief diel period in the early evening, eliciting upwind flight in responsive males.^[45] Courtship involves the male landing near the female, followed by wing fanning to disperse additional pheromones and tactile interactions, culminating in copulation lasting 1-2 hours if the female accepts the suitor.^[49]

Generations and Diapause

The number of generations, or voltinism, of the codling moth (Cydia pomonella) varies significantly with climate and growing season length. In cooler regions such as northern Europe, the species typically completes only one generation per year due to limited thermal accumulation.^[15] In warmer areas like California, two to three generations are common, with a partial fourth possible in exceptionally hot years.^[50] Climate change is driving an increase in voltinism, with studies projecting up to 3-5 generations in California's Central Valley by 2050 due to warmer temperatures extending the growing season.^[29] The potential for a second generation emerges when more than 800 degree-days (base 50°F) have accumulated since the first generation's biofix, allowing subsequent generations if sufficient heat units continue to build.^[51] Diapause in the codling moth occurs primarily in the fifth larval instar, where development halts to enable overwintering survival.^[52] Induction is triggered by environmental cues, including short photoperiods of less than 14 hours of daylight or low temperatures below 15°C during late summer and fall, prompting the majority of late-season larvae to enter this dormant state.^[53] This diapause phase typically lasts 6 to 9 months, spanning from late summer through winter until spring conditions resume development.^[52] Diapause termination is initiated by rising spring temperatures exceeding 10°C, which stimulates pupation and aligns emergence with host fruit availability.^[25] Hormonal regulation, particularly involving juvenile hormone, plays a key role in modulating this transition by influencing metabolic resumption and preventing premature pupation during dormancy.^[54] Overall, diapause synchronizes codling moth populations with host plant phenology, ensuring that post-diapause adults emerge when apple and pear fruits are suitable for oviposition and larval development.^[52]

Feeding Behavior and Host Interactions

Host Plants and Food Resources

The codling moth, Cydia pomonella, primarily infests pome fruits in the family Rosaceae, with apple (Malus domestica) and pear (Pyrus communis) serving as the principal host plants worldwide.^[28] These crops provide optimal conditions for larval development due to their nutritional composition and availability in temperate orchards. Secondary hosts include quince (Cydonia oblonga), walnut (Juglans regia), and stone fruits such as apricot (Prunus armeniaca) and prune (Prunus domestica), though infestations on these are less frequent and often regionally specific, such as walnut in California.^[5]^[28] Larvae target the seeds and adjacent pulp within the fruit core, which are rich in lipids and proteins that support rapid growth and preparation for pupation.^[28]^[55] In contrast, adult moths derive their nutrition primarily from floral nectar, feeding on blossoms from various plants to sustain energy for mating and oviposition.^[56] Host preferences are guided by volatile compounds emitted from fruits and foliage, with females showing stronger attraction to apple and pear volatiles compared to other Rosaceae species.^[57]^[58] Plants employ several defenses to resist codling moth infestation, including thick fruit skins that impede larval entry and high concentrations of tannins in unripe fruit that act as feeding deterrents through astringency and toxicity.^[59] Polyphenols, a class of secondary metabolites abundant in apple skin, pulp, and seeds, further contribute to resistance by disrupting larval digestion and development.^[60] Certain apple cultivars demonstrate genetic resistance linked to elevated phenolic diversity and content, reducing larval survival rates compared to susceptible varieties.^[60]^[61]

Larval Feeding Mechanisms

Newly hatched codling moth larvae (Cydia pomonella) employ chemotaxis and anemotaxis to locate suitable host fruit, primarily guided by kairomones such as pear ester (ethyl (2E,4Z)-2,4-decadienoate) and (E,E)-α-farnesene emitted from apples and pears. These volatiles act as attractants, increasing larval walking speed and directing movement toward point sources even in still air, with neonate larvae typically finding and penetrating fruit within approximately 2.5 hours of hatching, as eggs are often laid within 20 cm of the fruit. Early chemotactic studies confirmed that larvae respond positively to apple odors, achieving up to 65% success in locating food sources via olfaction when combined with other cues like touch and sight.^[62]^[63] Upon reaching the fruit surface, larvae select entry points preferentially at the calyx end, stem end, or side, where they rapidly bore through the skin using their mandibles to access internal tissues. This swift penetration, often completed within minutes, serves as an avoidance tactic against surface predators such as ants and spiders, isolating the larva within the protected fruit interior.^[28]^[39] Once inside, the larvae tunnel through the flesh toward the core, feeding primarily on seeds and surrounding pulp in a pattern that creates linear galleries lined with silk. During feeding, they expel frass—compact, sawdust-like pellets—in visible extrusions at entry or exit holes, which accumulate as external signs of infestation.^[28] The internal galleries produced by larval tunneling disrupt fruit integrity, facilitating secondary infections by fungi and bacteria that cause rot and premature drop, rendering affected fruits unmarketable. A single larva feeds on seeds and surrounding pulp, but the primary economic impact stems from the galleries promoting decay throughout the core and flesh. Economic thresholds for management are typically set at 1-2% infested fruit in apple orchards, as higher levels lead to significant harvest losses exceeding 30-50% without intervention.^[1]

Adult Feeding and Nutrition

Adult codling moths (Cydia pomonella) primarily obtain nutrition from nectar sourced from flowers in orchards, which provides essential carbohydrates for sustenance. They occasionally supplement this with water from dew droplets on foliage, but there are no confirmed observations of adults feeding directly on fruit in natural settings, despite attraction to ripe fruit odors that may signal potential nectar sources nearby.^[64]^[65] Foraging behavior in adults consists of short, localized flights, typically at dusk or night, to locate blooming plants or moist surfaces, enabling efficient access to these limited resources without extensive dispersal. This nectarivory supports basic metabolic needs, with carbohydrates fueling energy for activities such as locomotion and reproduction; without access to nectar, adult longevity drops sharply from around 20 days on sugar solutions to approximately 5 days under starvation conditions.^[64]^[65] The nutritional intake from nectar plays a critical role in female fecundity, as carbohydrates are allocated to oogenesis, resulting in significantly higher egg production when feeding occurs—moths provided with honey water or sucrose solutions laid roughly twice as many eggs as those given only water or none at all. This underscores nectar's importance for reproductive success, with deprived females exhibiting reduced fertility and viability in offspring. Nectar-derived energy also briefly sustains the demands of mating flights, linking adult nutrition to overall population dynamics.^[64]^[65]

Ecology and Natural Enemies

Predators

The codling moth, Cydia pomonella, faces predation from a range of vertebrate and invertebrate species that target various life stages, contributing to natural population regulation in orchards.^[1] These predators primarily consume eggs, larvae, pupae, and adults, with their effectiveness varying by habitat and management practices.^[66] Among vertebrates, birds are prominent predators, particularly targeting overwintering larvae and pupae embedded in tree bark. Species such as woodpeckers in eastern Canadian orchards exert the greatest mortality on pupae by foraging on trunks and branches during winter. In California apple orchards, bird predation can account for up to 83% of codling moth larvae mortality over winter, with rates increasing from 11% to 46% when birds have unimpeded access to cocoons.^[67] Bats also play a role by consuming adult moths at night, helping suppress emerging populations in fruit orchards.^[68] Invertebrate predators include ground beetles (Carabidae), which are effective against diapausing larvae and pupae near the soil surface or on tree trunks. Studies in apple orchards demonstrate that carabid species, such as Pterostichus melanarius, consume significant numbers of fifth-instar larvae and pupae.^[69] Spiders prey on eggs, small larvae, and adult moths, often ambushing them in foliage or on bark, and represent a diverse group contributing to overall mortality across life stages.^[1] Collectively, these predators can reduce codling moth larval populations in unsprayed orchards, primarily through foraging behaviors like bark pecking by birds and ground-level hunting by beetles. Bird predation alone can account for 11-46% mortality of overwintering larvae in such settings.^[70] Conservation strategies, such as planting hedgerows and maintaining semi-natural habitats around orchards, enhance predator density and activity; for instance, hedgerow proximity correlates with lower larval abundance, potentially due to habitat factors such as shadow and wind protection.^[71]

Parasitoids

Parasitoids play a significant role in the natural regulation of codling moth (Cydia pomonella) populations, with over 100 species recorded attacking various life stages of the pest.^[72] Among these, egg parasitoids of the genus Trichogramma (Hymenoptera: Trichogrammatidae), such as T. cacoeciae and T. evanescens, target codling moth eggs and can achieve parasitism rates leading to 50-80% reduction in fruit damage when released inundatively.^[73] Ascogaster quadridentata (Hymenoptera: Braconidae), a specialist larval endoparasitoid, is another key species, with parasitism rates typically ranging from 20-40% in natural settings, particularly on young larvae.^[74]^[75] The life cycle of these parasitoids is closely synchronized with that of the codling moth host. Trichogramma species are endoparasitoids that lay eggs inside host eggs, with their larvae developing internally and emerging as adults, often resulting in blackened, non-viable host eggs. A. quadridentata is an egg-larval koinobiont endoparasitoid, ovipositing in host eggs but allowing the codling moth to hatch and develop into a larva before the parasitoid larva emerges from the host's penultimate instar, typically exiting to spin a cocoon nearby. Larval endoparasitoids like A. quadridentata often emerge during the host's pupal stage if development aligns, though hyperparasitism by secondary parasitoids such as Perilampus spp. can reduce their effectiveness by up to 30% in some populations.^[72]^[75]^[76] Host specificity varies among codling moth parasitoids, with many showing preference for tortricid moths; A. quadridentata is highly specific to C. pomonella and related species, while Trichogramma spp. are more generalist but effective against lepidopteran eggs in orchards. Overall parasitoid complex effectiveness fluctuates by codling moth generation, with higher rates (up to 29% for young larvae) observed in summer cohorts due to increased host availability and favorable temperatures.^[77]^[75] These parasitoids can integrate with predators like ants and spiders to enhance overall biological control in integrated pest management systems.^[72] Augmentative releases are a common strategy for enhancing parasitoid impact, particularly with Trichogramma spp., where rates of 100,000 individuals per hectare, applied twice per generation at 7-10 day intervals, have demonstrated control efficacy in apple orchards.^[78] Such releases target early generations to suppress population buildup, though success depends on timing, release method (e.g., point sources), and minimizing pesticide interference.^[72]

Pathogens and Diseases

The codling moth, Cydia pomonella, is susceptible to a range of microbial pathogens, including fungi, bacteria, and viruses, which can significantly contribute to natural mortality in populations. These pathogens primarily infect larval and pupal stages, with efficacy influenced by environmental factors such as humidity and population density. Fungal and viral agents often lead to epizootics under favorable conditions, while bacterial pathogens target the gut epithelium upon ingestion.^[79] Fungal pathogens, particularly Beauveria bassiana, are among the most prevalent natural enemies of codling moth. This entomopathogenic fungus infects larvae and pupae topically through cuticle penetration after conidial attachment, leading to mycosis and death. Prevalence of B. bassiana infections in field populations ranges from 0.9% to 100%, with a mean of approximately 32%, and it is most common in late instars during autumn and diapausing stages in spring. High humidity enhances virulence, with studies showing 92-95% mortality in cocooned larvae under humid conditions compared to 46-57% in drier environments. Another fungal pathogen, Isaria farinosa, occurs frequently in mixed infections with B. bassiana, contributing to overall fungal-induced mortality in overwintering stages.^[79]^[72]^[79] Bacterial pathogens, notably Bacillus thuringiensis var. kurstaki (Btk), provide targeted control by producing crystal toxins that disrupt the midgut upon ingestion by neonate and early instar larvae. Btk is highly effective against newly hatched larvae, achieving up to 90% mortality in early instars when applied appropriately. This gut-specific action prevents further feeding and leads to septicemia, making it a key natural regulator in low-density populations.^[80]^[72] The most specific viral pathogen is the codling moth granulovirus (CpGV), a baculovirus that causes lethal infection via oral ingestion of occlusion bodies by larvae. CpGV disrupts host tissues, resulting in liquefied remains and up to 95% larval mortality across instars in susceptible populations. The Mexican isolate (CpGV-M) has been widely studied and used, though resistance has emerged in some field strains, including the first confirmed case in the USA in 2022, prompting ongoing monitoring and management strategies as of 2025. Recent studies (as of 2024) have identified viral genes like pe38 in CpGV isolates that help overcome resistance in codling moth populations.^[81]^[82]^[83]^[84]^[85] Transmission of these pathogens varies by type but is facilitated by environmental factors. Fungal conidia, such as those of B. bassiana, spread via rain splash and wind, with rain promoting dispersal and infection in humid microclimates. Epizootics occur predominantly in dense codling moth populations, where high host density amplifies pathogen cycling. CpGV transmits orally through contaminated fruit surfaces or frass, while Btk relies on larval contact with sprayed residues. These pathogens are also harnessed as bioinsecticides in integrated pest management.^[86]^[79]^[72]

Olfaction and Sensory Physiology

Olfactory System Structure

The olfactory system of the codling moth, Cydia pomonella, is primarily housed in the antennae, which serve as the main chemosensory organs located on the head and covered with specialized sensilla that detect volatile compounds.^[87] The antennae are filiform in structure for both males and females, consisting of a scape, pedicel, and flagellum divided into numerous flagellomeres, with males exhibiting longer antennae and a greater density of sensilla compared to females.^[88] These sensilla include six main morphological types—trichodea, basiconica, coeloconica, auricillica, chaetica, and styloconica—among which the multiporous sensilla trichodea, basiconica, coeloconica, and auricillica are primarily olfactory, housing olfactory receptor neurons (ORNs) that respond to pheromones and plant volatiles.^[88] Male antennae feature a higher abundance of long trichodea sensilla subtypes, contributing to enhanced sensitivity for detecting sex pheromones.^[88] At the molecular level, the codling moth expresses over 60 odorant receptor (OR) genes, with transcriptomic analyses identifying 58 candidate ORs in antennal tissue, including the obligatory co-receptor ORco that forms heteromers with tuning ORs to detect specific ligands.^[87] For instance, CpomOR1 is highly expressed in male antennae and tuned to the primary sex pheromone component codlemone ((E,E)-8,10-dodecadien-1-ol), while CpomOR3 responds to the kairomone pear ester (ethyl (E,Z)-2,4-decadienoate), a host plant volatile that aids in locating fruit.^[87]^[89] These ORs interact with soluble ligand-binding proteins, such as odorant-binding proteins (OBPs), which are abundantly transcribed in the antennal sensilla to solubilize and transport hydrophobic odorants across the sensillar lymph to the ORN dendrites.^[90] Olfactory signals are transduced through a neural pathway beginning in the sensilla, where ORN axons project via the antennal nerve to the antennal lobe (AL) in the brain, the primary olfactory processing center. Within the AL, inputs converge into approximately 50 glomeruli in males and 49 in females, forming discrete synaptic modules where pheromone and plant odor information is segregated and integrated. Glomerular organization shows sex-specific clustering, with males featuring a macroglomerular complex (MGC) comprising a large cumulus and associated ordinary glomeruli dedicated to pheromone processing, whereas females lack an MGC and process both pheromone and plant signals primarily through ordinary glomeruli near the antennal nerve entry. The system enables highly sensitive detection, with males responding to pheromones such as codlemone at picogram levels (10^{-12} g), allowing long-range orientation toward conspecific females. Similarly, plant kairomones like pear ester are detected at nanogram thresholds in heterologous systems, facilitating host plant location for oviposition and feeding.^[91] This structural and molecular architecture underpins the moth's ability to discriminate among complex odor blends in natural environments.^[87]

Sexual Dimorphism in Olfaction

Sexual dimorphism in olfaction is a key feature of the codling moth Cydia pomonella, enabling sex-specific adaptations in mate location and host selection. Males exhibit enhanced sensitivity to female-produced sex pheromones, primarily through antennae that are longer, have more segments, and bear a greater number of sensilla trichodea than those of females. These hair-like sensilla, particularly the long subtype exclusive to males, are multiporous structures specialized for long-range detection of pheromones such as codlemone ((E,E)-8,10-dodecadien-1-ol).^[88] This structural advantage correlates with a higher density of olfactory receptor neurons (ORNs) in male antennae, estimated to be over 10-fold greater for pheromone-responsive types due to increased sensilla abundance and biased gene expression. Several odorant receptor (OR) genes, including CpomOR5, CpomOR6, CpomOR7, and CpomOR31, show male-enriched expression levels exceeding 10-fold compared to females (FPKM <1 in females), tuning male ORNs specifically to sex pheromone components.^[87] In females, pheromone receptor expression is markedly lower, with fewer dedicated sensilla and ORNs responsive to these cues.^[92] Females, conversely, display a broader olfactory response profile geared toward plant volatiles essential for oviposition. Their antennae express elevated levels of OR genes such as CpomOR21, CpomOR22, CpomOR30, and CpomOR41 (over 10-fold female-biased, FPKM <1 in males), enabling detection of host-related kairomones like pear ester and α-farnesene from apple and pear trees.^[87] This dimorphism arises from sex-linked regulation of OR gene expression, an evolutionary adaptation that optimizes male pheromone tracking and female host assessment.^[87] These olfactory differences have functional implications for behavior: males can detect and orient to pheromones from greater distances, often flying several kilometers to locate mates, while females use plant scent gradients to select optimal egg-laying sites on developing fruits, ensuring larval survival.^[93]

Pest Status and Management

Economic Impact

The codling moth (Cydia pomonella) has been recognized as a major agricultural pest since the 19th century, originating in southeastern Europe and spreading globally with apple cultivation to regions including North America and beyond.^[94] Its larvae bore into developing fruit, causing direct damage that renders apples unmarketable and leads to substantial yield losses in pome fruit production. In untreated orchards, infestation can result in 20-50% yield reductions, with unmanaged cases reaching up to 90% damage in severe scenarios.^[22] Infestation rates typically range from 5-30% in commercial settings without adequate control, though peaks as high as 71% have been recorded in individual orchards.^[95] Apples are the primary crop affected, accounting for the bulk of economic impacts, though the pest also infests pears, walnuts, and other hosts. Globally, codling moth infestations contribute to annual losses in the hundreds of millions of dollars in apple production, encompassing direct fruit damage and associated management expenses.^[96] In key producing regions like Washington State, USA—responsible for over half of U.S. apple output—codling moth represents a major threat, with unmanaged infestations potentially destroying up to 80% of the crop.^[97] Control measures alone cost growers $500-1,000 per hectare yearly, driven by the need for repeated applications of insecticides or alternatives like mating disruption.^[98] Beyond direct feeding damage, codling moth larvae create entry wounds that facilitate secondary rots from fungi and bacteria, exacerbating fruit decay and further diminishing marketable yield.^[99] The pest's status as a quarantine organism imposes additional economic burdens through trade restrictions; for instance, detections in shipments have led to multimillion-dollar losses for exporters, as seen in disruptions to international apple markets during the 2010s. Regional outbreaks, such as increased populations in European orchards amid changing climate conditions, have compounded these challenges by necessitating intensified monitoring and interventions.^[47]

Preventive and Cultural Controls

Preventive and cultural controls for the codling moth (Cydia pomonella) emphasize proactive orchard management to suppress populations and limit damage to pome fruits like apples and pears, integrating practices that target the pest's life cycle without chemical inputs. These strategies focus on habitat disruption, life stage interruption, and regulatory measures to prevent establishment or spread, contributing to sustainable integrated pest management (IPM) systems.^[1] Sanitation remains a primary cultural practice, involving the systematic removal and destruction of fallen or infested fruit, as well as pruning and disposal of branches showing signs of larval entry or frass. These actions target overwintering sites, where up to 80-90% of diapausing larvae may reside in dropped fruit or debris under trees, thereby reducing the subsequent adult emergence the following spring. For instance, weekly collection and composting or burial of infested apples during the growing season prevents larval maturation and pupation, breaking the reproductive cycle. Proper bin sanitation, such as using plastic harvest containers and sterilizing them post-use, further minimizes larval refuge in storage, as wooden bins can harbor significant overwintering populations.^[26]^[100]^[39] Timing cultural interventions using degree-day models enhances efficacy by aligning practices with codling moth phenology. Accumulating heat units above a 50°F (10°C) base temperature from biofix—the first sustained moth flight detected in pheromone traps—allows growers to schedule intensified sanitation during peak larval drop periods, typically around 250-300 degree-days when eggs hatch and larvae exit fruit. This predictive approach ensures resources target vulnerable stages, optimizing labor without overlapping into chemical timing.^[66]^[39] Orchard design incorporates elements to deter codling moth establishment, such as wider tree spacing (e.g., 12-15 feet between trees) to improve canopy airflow and reduce shaded, humid refuges that favor larval survival and diapause. Interplanting cover crops like clover or vetch in alleyways not only suppresses weeds but also bolsters soil biodiversity, fostering ground-dwelling predators and parasitoids that indirectly regulate codling moth populations. These designs promote overall ecosystem resilience, minimizing pest hotspots while supporting fruit quality.^[101]^[102] Quarantine protocols prevent inadvertent spread through regulated fruit movement and certification programs enforced by agencies like USDA APHIS. Infested areas require inspection and documentation for interstate or international shipment, with treatments or origin certifications ensuring codling moth-free status, particularly for exports to markets like Japan where it is a prohibited pest. Compliance involves tracing host materials (apples, pears) and prohibiting unregulated transport from high-risk zones, safeguarding uninfested regions.^[103]

Mechanical and Physical Controls

Mechanical and physical controls for the codling moth (Cydia pomonella) rely on non-toxic barriers, traps, and environmental modifications to disrupt the pest's life cycle without relying on chemical agents. These methods target adult moths, eggs, and larvae, often integrated into broader integrated pest management (IPM) programs to monitor populations and suppress damage in apple and pear orchards. Pheromone-baited traps, utilizing synthetic codlemone (the female sex pheromone), are essential for monitoring male moth flights and determining biofix for timing other controls. Standard deployment involves 1 trap per 2.5 hectares, placed in the upper canopy, with weekly checks to assess catches against thresholds (e.g., 2-5 moths per trap for first-generation action). For mass trapping in low-density situations, higher densities of 10-20 traps per hectare can capture up to 50% of males, reducing mating success and larval production, though efficacy diminishes in high-population areas.^[28]^[104]^[105] Particle films, such as kaolin clay (e.g., Surround WP), form a protective coating on fruit and foliage when sprayed at 25-50 lb per acre, deterring oviposition by making surfaces less suitable for egg-laying and disorienting neonates. Applications begin around 100 degree-days after biofix, with reapplications every 7-14 days, achieving over 77% reduction in deep-entry fruit wounds in field trials. This method also mitigates sunburn but requires thorough coverage for optimal results.^[106]^[107] Sticky bands or trunk wraps, typically made of corrugated cardboard or burlap (1.5-2 inches wide), are applied around tree trunks at bark transitions to intercept larvae descending for pupation. Placed before the end of larval generations (e.g., mid-summer and fall), bands are checked biweekly and larvae destroyed by removal or crushing, capturing a portion of the population—though only a small percentage overall, as many larvae pupate elsewhere. This provides supplementary control, especially on smooth-barked trees.^[26]^[50] Reflective mulches, such as silver or aluminum polyethylene sheets laid around tree bases, disrupt adult moth orientation by scattering ultraviolet light, potentially reducing oviposition on nearby fruit. While primarily researched for other pests, preliminary trials indicate variable suppression of codling moth landings and egg-laying in young orchards.^[108] When combined with regular monitoring, these mechanical and physical approaches enable threshold-based decisions that can reduce reliance on spray applications by up to 50% in commercial settings, promoting sustainable orchard management.^[28]

Chemical Controls

Chemical control of the codling moth (Cydia pomonella) primarily relies on synthetic insecticides that target various life stages, particularly eggs and larvae, to prevent fruit infestation in pome fruits like apples and pears.^[1] Organophosphates, such as azinphos-methyl, were historically dominant for codling moth management since the late 1960s due to their broad-spectrum neurotoxic activity, but they have been largely phased out in many regions since the early 2010s because of environmental concerns, regulatory restrictions, and widespread resistance development.^[109] Neonicotinoids, including thiacloprid (marketed as Calypso), serve as alternatives by acting as nicotinic acetylcholine receptor agonists, providing effective control against codling moth larvae with reduced impact on beneficial insects when applied judiciously.^[110] Pheromone-based attractants, particularly synthetic codlemone (the sex pheromone of codling moth), are integral to mating disruption strategies within chemical control frameworks. These involve deploying hand-applied or aerosol dispensers at rates of 500–1000 units per hectare to flood the orchard with pheromone, confusing male moths and preventing successful mating, achieving 70–90% reduction in fruit injury under optimal conditions.^[46] Monitoring trap catches can guide dispenser density adjustments to maintain efficacy.^[47] Insect growth regulators like methoxyfenozide offer targeted control by mimicking the insect molting hormone ecdysone, binding to the ecdysone receptor complex to disrupt larval development and molting without immediate lethality, resulting in high mortality in codling moth neonate larvae.^[111]^[112] Insecticide resistance in codling moth populations has been documented globally since the 1990s, driven by mechanisms such as enhanced detoxification via glutathione S-transferase (GST) enzymes, which conjugate and neutralize organophosphates and other xenobiotics.^[113] To mitigate resistance, rotation among insecticide classes—alternating organophosphates, neonicotinoids, pyrethroids, and growth regulators—has been a standard practice since the mid-1990s, often integrated with resistance monitoring to sustain long-term efficacy.^[1]^[114]

Biological and Integrated Controls

Biological control strategies for the codling moth, Cydia pomonella, primarily involve the augmentation of natural enemies such as egg parasitoids from the genus Trichogramma. Inundative releases of Trichogramma cacoeciae at rates of 50,000 individuals per hectare, timed to coincide with peak egg-laying periods, have demonstrated efficacy in suppressing codling moth populations in organic apple orchards by parasitizing up to 30-50% of eggs and reducing fruit damage.^[115] These releases are most effective when integrated with monitoring to target vulnerable life stages, leveraging the parasitoids' rapid reproduction to establish temporary population suppression without persistent environmental residues.^[72] Biopesticides, particularly the codling moth granulovirus (CpGV), provide another cornerstone of biological management. Applications of CpGV at dosages of 10^13 occlusion bodies (OB) per hectare, applied weekly during the first generation egg hatch, infect and kill neonate larvae upon ingestion, achieving control levels comparable to conventional insecticides in low-to-moderate pressure scenarios.^[116] This virus exploits the codling moth's host specificity, minimizing non-target impacts while promoting natural pathogen cycles observed in unmanaged populations.^[83] Integrated pest management (IPM) for codling moth synthesizes these biological tactics with monitoring and non-chemical disruptions for sustainable suppression. Pheromone traps guide decision-making, with action thresholds such as 1 moth per trap per week prompting interventions like Bacillus thuringiensis (Bt) sprays or mating disruption via pheromone dispensers, which confuse male moths and reduce successful matings by over 90% in coordinated applications.^[47] Area-wide IPM programs in the United States, building on the foundational Codling Moth Areawide Management Program (CAMP) initiated in 1995 and expanded post-2000 across Washington, Oregon, and California, coordinate these elements across orchards to achieve population-level control.^[117] Such programs have reduced reliance on synthetic insecticides by approximately 70%, enhancing biodiversity and fruit quality while maintaining economic viability.^[118] As of 2025, sterile insect release programs continue to expand in regions like Washington State, offering sustainable alternatives amid rising insecticide resistance and climate variability.^[59]^[119] Despite these advances, challenges persist in IPM implementation, including climate variability that alters codling moth phenology and extends generations, potentially requiring adaptive timing of releases and sprays.^[25] The sterile insect technique (SIT) addresses this through trials releasing irradiated sterile males at rates of 2,000 per hectare weekly, which compete with wild males and suppress fertility in area-wide settings, though logistical demands for mass-rearing limit widespread adoption.^[120]

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Bats Are the Perfect Predator for Destructive Moths — If Farmers ...
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GROUND BEETLES (COLEOPTERA: CARABIDAE) AS ...
May 31, 2012 · GROUND BEETLES (COLEOPTERA: CARABIDAE) AS PREDATORS OF THE CODLING MOTH, CYDIA POMONELLA (L ... . Survival of mature larvae of codling moth ...
[68]
How to attract bug-eating birds to farms | Green Blog
Nov 18, 2019 · “Permitting bird access to cocoons during the wintertime increased codling moth predation from 11% to 46%, and predation increased with an ...
[69]
Effects of hedgerow characteristics on intra-orchard distribution of ...
Citation Excerpt : Over the study years, 72% of orchards were protected by a windbreak hedgerow (WbH), and 47% had a spontaneous hedgerow (SpH).
[70]
[PDF] biological control of codling moth (cydia pomonella - USDA ARS
Biological control of codling moth uses natural enemies like entomopathogens (CpGV, EPNs), predators, and parasitoids, and is part of IPM.
[71]
Natural enemies (Codling moth) - NIAB
Neoaplectana carpocapsae are significant natural enemies of overwintering larvae/pupae on tree trunks, especially close to the soil surface. Virus diseases
[72]
Biological Control of Codling Moth <cydia pomonella = carpocapsa ...
Ascogaster was accidentally introduced from Europe to North America, and is the most important larval parasitoid of codling moth, causing ca. 25% parasitism ...Missing: key | Show results with:key
[73]
Temporal dynamics of parasitoid assemblages parasitizing the ...
Parasitized codling moth larvae are only one-third of the size of non-parasitized larvae at the maximum of their development. The A. quadridentata larva emerges ...
[74]
Braconidae), a key parasitoid of codling moth - ScienceDirect.com
The key parasitoid of codling moth, Ascogaster quadridentata, consumes various sugars and concentrations, naturally occurring in plant nectar and aphid honeydew ...
[75]
(PDF) Parasitoids on codling moth Cydia pomonella (Lepidoptera
... Cydia pomonella ... The most abundant parasitoids included Ascogaster quadridentata, Bassus rufipes, Trichogramma cacoeciae, and Neoplectops pomonella.
[76]
[PDF] Efficacy of Trichogramma evanescens and Bacillus thuringiensis var ...
Apr 28, 2017 · In each generation of the egg stage,. 100,000 parasitoids per hectare were released twice (1440 parasitoids/plot), with an interval of 7–10 days ...
[77]
Occurrence and Prevalence of Insect Pathogens in Populations of ...
B. bassiana was identified as the major fungal pathogen, causing larval prevalences of 0.9% to 100% (mean, about 32%). During prognostic long-term ...Missing: humid | Show results with:humid
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[PDF] Eco-Friendly IPM Approaches for Codling Moth Management
Jun 3, 2025 · (50°F for codling moths). Insects like codling moths develop faster as temperatures increase. The formula: Degree Days = ((Max temp + Min temp) ...Missing: optimal | Show results with:optimal<|separator|>
[79]
Cross-Resistance of the Codling Moth against Different Isolates of ...
Sep 29, 2021 · The OB concentration normally causes mortality of >95% for all instars of CpS exposed to CpGV-M, CpGV-S, as it is expected for fully susceptible ...
[80]
Baculovirus resistance in codling moth is virus isolate ... - PNAS
Oct 20, 2014 · Since 2005, 38 codling moth field populations resistant to CpGV products containing the Mexican isolate (CpGV-M) were discovered in Europe ...
[81]
[PDF] Consensus document on Beauveria bassiana strains as microbial ...
transmitted to plants and the soil via rain splash (Meyling and Eilenberg ... rosa moth, codling moth, cabbage aphids, tabacco thrips, beet flea leaf.
[82]
The chemosensory receptors of codling moth Cydia pomonella ...
Mar 23, 2016 · The chemosensory system, through olfactory pathways, is involved in food, mate and host seeking behaviors, as well as predator and parasitoid ...
[83]
Morphology and distribution of antennal sensilla of two tortricid ...
Aug 18, 2016 · The olfactory sensilla in moths house specific neurons that respond electrophysiologically to sex pheromones and plant volatiles from host or ...
[84]
A predicted sex pheromone receptor of codling moth Cydia ...
The finding that a codling moth PR is tuned to pear ester is remarkable. It corroborates the interaction between pear ester and codlemone, which may play an ...
[85]
Putative Chemosensory Receptors of the Codling Moth, Cydia ...
Feb 20, 2012 · In this study, our aim was to identify chemosensory receptors in the codling moth as a means to uncover new targets for behavioral interference.
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Candidate pheromone receptors of codling moth Cydia pomonella ...
Jan 24, 2017 · Olfaction plays a dominant role in the mate-finding and host selection behaviours of the codling moth (Cydia pomonella), an important pest of apple, pear and ...Missing: review | Show results with:review
[87]
Physiology and morphology of pheromone-specific sensilla on the ...
The sensitivity of the pheromone receptors to their respective stimuli was the same in the sexes, while the number of pheromone-specific sensilla was much lower ...
[88]
Coding and interaction of sex pheromone and plant volatile signals ...
Dec 15, 2010 · The number of glomeruli found in the codling moth is slightly lower than in other moths; 50–55 glomeruli were found in the silk moth Bombyx mori ...
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Codling Moth One Of World's Most 'Historic' Pests — King City ...
The native home of the codling moth was southeastern Europe, but early in the 19th century it set out to see the world. Within that century it spread over ...
[90]
Top-down and bottom-up regulation of codling moth populations in ...
Apple damage in individual orchards reached 71%, but decreased with apple production, indicating codling moth satiation. Seven parasitoid species were recorded ...
[91]
Prospects of Codling Moth Management on Apples with Botanical ...
Jan 28, 2023 · To be effective, Bacillus thuringiensis or Carpocapsa pomonella must be ingested in large quantities, and the fruit is damaged before the larvae ...Missing: kurstaki | Show results with:kurstaki
[92]
Economic Impact of a Potential Expansion of Pest Infestation: Apple ...
It was found that the losses for the Washington apple industry's range from $510 million to $557 million, depending on the codling moth pressure.Missing: global | Show results with:global
[93]
Codling Moth Control: Why Mating Is the Hardest Part
At a cost of about $400 per acre, the technology would not be practical to the growers in his state, Gut says. “We need to make this program economical if ...<|control11|><|separator|>
[94]
[PDF] Biology and control of the codling moth in the Pacific Northwest.
Apr 11, 1985 · A 15-hour photoperiod at 24OC causes larvae to develop normally, while a 12-hour photoperiod at 24OC causes all larvae to enter diapause (74).
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Cultural Control | WSU Tree Fruit | Washington State University
First, using plastic bins for harvest will greatly mitigate bin infestation by codling moths. Second, sterilize bins before they go back out to orchards. While ...
[96]
Orchard Establishment - WSU Tree Fruit - Washington State University
The irrigation system, tree support system, alleyway grass or cover crop, and understory weed strip areas are all design considerations. ... Codling Moth ...
[97]
Organic Farming and Cover-Crop Management Reduce Pest ...
Mar 4, 2021 · The aim of this study was to investigate the combined effects of organic farming, cover-crop management, and landscape composition on natural ...
[98]
https://www.growingproduce.com/fruits/codling-moth-control-why-mating-is-the-hardest-part/
[99]
[PDF] Final Report - Hort Innovation
Delta traps baited with the best performing lure could be used at 8 traps/ ha to produce reliable estimates of codling moth population density. Damage levels ...
[100]
[PDF] Optimization of pheromone trap densities and impact of insecticides ...
Feb 18, 2019 · The present study observed that 20 traps/acre was the optimum trap density required to ensure maximum catches and integration of ...<|separator|>
[101]
Codling Moth - Pear - UC IPM
Codling moth has two generations, and maybe a partial third generation, each season in the pear-growing regions of California. Pears are exposed to only one ...
[102]
Organic Control Strategies for Use in IPM of Invertebrate Pests in ...
Pheromones can also be deployed without trapping devices for effective pest control. Codling moth is one of the most damaging insects in apple and pear crops, ...
[103]
[PDF] Integrated Pest Management Strategic Plan - OSU Extension Service
Codling moth larvae feed directly on the fruit, either by making a shallow feeing cavity (sting), or boring into it and feeding within on flesh and seeds (entry) ...
[104]
Incorporating Organophosphate Alternative Insecticides Into Codling ...
Azinphos-methyl (AZM) has been the most used insecticide in apple production in the United States since the late 1960s, primarily as a control for the key ...
[105]
[PDF] Calypso® 480 SC Insecticide - Resources
Calypso 480 SC is a unique chloronicotinyl insecticide (CNI) which provides excellent control of codling moth, oriental fruit moth and apple dimpling bug when ...
[106]
Toxicity and Residual Activity of Methoxyfenozide and Tebufenozide ...
A series of studies were conducted to examine the residual activity and toxicity of the ecdysone agonists tebufenozide and methoxyfenozide to codling moth, ...
[107]
Effects of ecdysone agonists on the expression of EcR, USP and ...
In our previous studies, both tebufenozide and methoxyfenozide have been shown to significantly reduce fecundity of the coding moth Cydia pomonella, an ...
[108]
(PDF) Worldwide variability of insecticide resistance mechanisms in ...
Aug 10, 2025 · The activity of detoxifying enzymes (glutathione-S-transferases (GST), mixed-function oxidases (MFO), and esterases (EST)) and the presence ...Missing: rotation | Show results with:rotation
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Chemical Control | WSU Tree Fruit | Washington State University
Its residue is short – only about 1 day, however, because it kills eggs that have already been laid, it has an effective residue of 150 DD (the length of the ...
[110]
Trichogrammatidae) against the codling moth, Cydia pomonella ...
Nov 16, 2024 · Various management strategies have been applied to manage this pest including releases of parasitoids. Trichogramma wasps are known as efficient ...
[111]
[PDF] Evaluation of efficacy of Cydia pomonella granulovirus (CpGV) to ...
The rates of CpGV were from 0.5 × 1013 gran./ha to 1.00 × 1013 gran./ha. The higher rate (1.00 × 1013 gran./ha) was used for the first treatment, and further ...
[112]
First Evidence of CpGV Resistance of Codling Moth in the USA - NIH
Jun 10, 2022 · Cydia pomonella granulovirus (CpGV) is used to control codling moth in organic and conventional production. Due to increasing codling moth ...
[113]
[PDF] Codling Moth Areawide Integrated Pest Management
Neonate larvae do not generally feed before entering the fruit, which significantly reduces the effectiveness of many of the selective insecticides that require ...
[114]
[PDF] Bigger Areas Are Better - USDA ARS
“The principal way we control the moth is through the use of synthetic female sex pheromone that growers place in orchards at a rate of 120 to. 400 dispensers ...
[115]
Twenty-five Years of Research Experience with the Sterile Insect ...
Sep 10, 2019 · The control of diapausing codling moth in wooden bins was attempted using entomopathogenic nematodes [140] or with glacial acetic acid [141] ...