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Chrysopa

Chrysopa is a genus of green lacewings belonging to the family Chrysopidae in the order Neuroptera, characterized by adults that are typically bright green with golden eyes, long antennae, and transparent wings featuring a distinctive venation pattern including an intramedian cell.^[1] The genus comprises approximately 75 species, primarily distributed in the Holarctic region, including North America, Europe, and Asia, where they are common in various habitats such as forests, gardens, and agricultural areas.^[2] Larvae of Chrysopa species are voracious predators of soft-bodied arthropods, particularly aphids, making them valuable in biological pest control, while adults may feed on pollen, nectar, or small insects.^[1] Taxonomically placed in the subfamily Chrysopinae and tribe Chrysopini, the genus was established by Leach in 1815 and is distinguished from related genera by features such as a face lacking prominent lines or with dark brown markings, small eyes, and broad wings.^[2]^[1] Notable North American species include C. incompleta, C. oculata, and C. quadripunctata, which contribute to natural pest regulation in ecosystems across the continent.^[1]

Taxonomy and Phylogeny

Taxonomic Classification

Chrysopa is a genus within the order Neuroptera, family Chrysopidae, subfamily Chrysopinae, and tribe Chrysopini.^[2] The genus was originally described by William Elford Leach in 1815 as part of Brewster's Edinburgh Encyclopædia.^[2] Approximately 75 species are currently recognized in Chrysopa, though this number varies with ongoing taxonomic revisions.^[2]

Evolutionary Relationships

Phylogenetic analyses place Chrysopa within the tribe Chrysopini of the subfamily Chrysopinae in the family Chrysopidae, part of the order Neuroptera. Recent studies combining molecular and morphological data have recovered Chrysopa as a well-supported clade, with close relations to other genera in Chrysopini, such as Chrysoperla and Chrysopodes. Notably, the monotypic genus Furcochrysa has been identified as sister to Chrysopa, leading to its synonymization with Chrysopa due to insufficient diagnostic characters to maintain separation. These analyses, based on multi-gene datasets including mitochondrial and nuclear markers, highlight the monophyly of Chrysopini and its position within the broader Chrysopidae phylogeny, where Chrysopinae emerges as a derived group relative to earlier-diverging subfamilies like Apochrysinae.^[3]^[4] The fossil record of Chrysopidae extends back to the Middle Jurassic, approximately 165 million years ago, with early representatives such as Mesypochrysa from Chinese deposits providing evidence of Chrysopa-like ancestors. These Jurassic fossils, including over 60 species across 26 genera, exhibit wing venation and body structures akin to modern chrysopines, suggesting that key neuropteran traits, including predatory adaptations, were established early in the family's evolution. Implications from this record indicate that the lineage leading to Chrysopa diversified during the Mesozoic, with crown-group Chrysopinae appearing in the Cenozoic, supported by amber inclusions from the Eocene.^[5]^[6] A defining evolutionary trait in Chrysopa and related genera is the development of specialized predatory larval forms, which are active hunters of soft-bodied prey like aphids. Larvae typically exhibit debris-carrying behavior, attaching plant material, prey remains, or exuviae to their bodies for camouflage, allowing stealthy approaches to aphids and other hemipterans without alerting them or their ant guardians. This adaptation, which evolved independently multiple times within Chrysopinae, enhances predation efficiency and survival, contributing to the ecological success of Chrysopa as natural aphid controllers. Fossil evidence of debris-carrying larvae from the Early Cretaceous further underscores its ancient origins in the family.^[7]^[8] Molecular studies, particularly DNA barcoding using the COI gene, have been instrumental in supporting genus boundaries and species delimitation within Chrysopa. Comprehensive barcode libraries from regions like China reveal distinct genetic divergence thresholds (around 1.87%) that align with morphological species, uncovering cryptic diversity and refining Chrysopa limits against closely related genera. These approaches, combined with multi-locus phylogenetics, confirm the integrity of Chrysopa while aiding in species delimitation, emphasizing its monophyly and evolutionary distinctness.^[9]^[10]

Morphology and Physiology

Adult Characteristics

Adult Chrysopa individuals are delicate, medium-sized insects characterized by a predominantly green body coloration that provides camouflage in foliage, complemented by conspicuous iridescent golden eyes that are a hallmark of the genus.^[11] These eyes are relatively small, with the greatest diameter much less than the interocular diameter.^[1] The body typically measures 10-15 mm in length.^[12] Some species exhibit subtle variations, such as darker markings on the head or thorax, but the green hue dominates across most taxa.^[13] Distinguishing features include a face lacking prominent lines or with dark brown markings, pronotum with red or orange marginal/submarginal bands, and hind wing pterostigma without a dark brown spot.^[1] The wings of adult Chrysopa are four in number, subequal in size, and membranous with a distinctive net-like venation pattern featuring a broad costal field and numerous cross-veins, which contributes to their delicate, lace-like appearance.^[14] Forewing length ranges from 6-35 mm, resulting in a wingspan of approximately 15-30 mm, enabling agile but somewhat fluttery flight.^[15]^[13] The wings are held roof-like over the body at rest and are typically transparent with green tinges matching the body.^[11] Antennae in adults are long, filiform (thread-like), and multisegmented, often exceeding the body length and serving sensory functions during nocturnal activity.^[15] Mouthparts are of the chewing type but modified for liquid feeding, consisting of mandibles and maxillae that allow lapping nectar, honeydew, pollen, or small prey fluids.^[16] Sexual dimorphism in Chrysopa adults is subtle and primarily evident in the genitalia and terminal abdominal segments, where males lack a distinct genital lip as sternites 8+9 are not fused, while females show variations in ovipositor structure.^[1] External differences, such as slight variations in antenna length or abdominal sclerite patterns, may occur but are not pronounced across the genus.^[15]

Larval and Pupal Stages

The larvae of Chrysopa species are elongate, flattened, and alligator-like in appearance, featuring distinct legs and prominent, paired, sickle-shaped mandibles that curve inward for grasping prey.^[11] These mandibles form a venom-injecting apparatus, a key physiological adaptation enabling efficient predation by immobilizing and liquefying prey tissues.^[17] Larvae are typically covered with short hairs, and the body coloration is often cream, tan, or yellowish, providing additional blending with plant surfaces. Chrysopa larvae are generally "naked" and do not carry debris for camouflage.^[1]^[7] Chrysopa larvae undergo three instars, with body length increasing progressively from less than 1 mm in the first instar to 6–10 mm or more in the third.^[12] The first instar lasts about 3–5 days, the second 4–6 days, and the third 7–10 days, depending on temperature and food availability, supporting rapid growth through voracious feeding that sustains high metabolic rates for energy-intensive predation activities.^[11] Physiological adaptations include specialized digestive enzymes and a robust circulatory system to process consumed prey quickly, allowing larvae to consume up to several dozen small arthropods daily.^[18] Upon reaching maturity, third-instar larvae spin a round, parchment-like silken cocoon, typically 3–6 mm in diameter, often attached to vegetation or concealed in leaf litter for protection during metamorphosis.^[11] Silk production occurs via modified labial glands, which secrete proteins forming the loosely woven, whitish cocoon structure.^[19] The pupal stage, including a brief prepupal period, lasts 10–15 days under typical conditions, during which the curled pupa undergoes internal reorganization, including the development of adult wings.^[12] This phase features reduced metabolic activity compared to the larval stage, focusing energy on histolysis and imaginal disc eversion for adult formation.^[20]

Life History and Biology

Reproduction and Development

Reproduction in the genus Chrysopa begins with complex courtship rituals that ensure species-specific mating. Males and females engage in duet-like acoustic signaling through substrate-borne vibrations produced by abdominal jerking, which facilitates mate recognition and attraction.^[15] In some species, such as Chrysopa perla, males additionally deploy pheromones from eversible vesicles on the abdomen during courtship, enhancing chemical communication.^[21] These behaviors, often lasting several minutes, culminate in copulation, after which females seek suitable oviposition sites. Recent research has shown that vertebrate-type testosterone plays a role in maintaining male longevity and supporting female reproduction in species like C. pallens.^[22] Oviposition typically occurs on vegetation near prey sources, with females laying individual eggs singly on elongated silken stalks approximately 0.5–1 cm long.^[11] This solitary placement reduces the risk of intraspecific cannibalism by newly hatched larvae, as first-instar larvae of species like Chrysopa oculata preferentially consume eggs lacking stalks when given the opportunity.^[23] The egg stage lasts 3–10 days, influenced by environmental temperature; for instance, incubation shortens to 2–4 days at 30–35°C but extends to 7–10 days at 15–20°C.^[20] Eggs are pale green or bluish-white, turning grayish before hatching, and the stalk elevates them above potential threats.^[11] Complete development from egg to adult spans 20–40 days under optimal conditions (20–25°C), encompassing three larval instars, pupation within a silken cocoon, and adult emergence.^[24] Warmer temperatures accelerate this timeline, while cooler ones prolong it; for example, Chrysopa harrisii requires about 566 degree-days above a 10–13°C threshold for full development. Many Chrysopa species enter facultative diapause as late-instar larvae or pupae in response to shortening photoperiods, allowing overwintering survival; this diapause can persist for months until terminated by prolonged cold exposure or increasing day length.^[25] Chrysopa species exhibit no post-ovipositional parental care, relying instead on the adaptive egg stalk for protection. The stalk's length and occasional adhesive fluid deter ant predation, as ants that tend aphids often consume accessible lacewing eggs but avoid stalked ones.^[11]

Feeding Behaviors

Chrysopa larvae are voracious polyphagous predators that primarily consume aphids but also feed on mites, thrips, small insects, lepidopteran eggs, and other soft-bodied arthropods.^[15] These larvae exhibit generalist feeding habits, targeting a variety of prey available in their habitats, though some species, such as Chrysopa slossonae, show specialization on particular hosts like the woolly alder aphid.^[26] Foraging tactics involve active searching across surfaces, with intensified short-turning movements upon encountering prey cues; larvae then use their sickle-shaped mandibles to grasp and pierce victims, injecting digestive enzymes to liquefy internal tissues for consumption.^[27] Protein-rich prey is essential for larval growth and development, as inadequate nutrition can prolong instars and reduce survival rates to the pupal stage.^[28] In contrast, adult Chrysopa individuals are often predaceous, feeding on aphids and other small insects, though many also consume pollen, nectar, and honeydew as supplemental carbohydrate sources.^[15] Some species display cannibalistic tendencies, particularly under prey scarcity, where adults may prey on conspecific eggs or larvae to meet nutritional needs.^[23] Foraging by adults includes hovering over flowers to access nectar and pollen, facilitated by their chewing mouthparts, while predatory encounters involve direct capture of mobile prey.^[26] Carbohydrates from these plant-derived foods are crucial for adult longevity and flight activity, whereas proteins support reproductive output, with symbiotic yeasts in the crop aiding amino acid assimilation in pollen-fed individuals.^[29] Food availability across stages can influence overall life cycle duration, with nutrient-poor conditions extending developmental times.

Ecology and Distribution

Habitats and Environmental Preferences

Species of the genus Chrysopa are predominantly found in temperate regions, favoring habitats such as deciduous forests, orchards, grasslands, and scrubby areas where vegetation supports aphid populations, their primary prey. These lacewings associate closely with diverse plant communities, including woodland edges, hedgerows, and agricultural borders, which provide shelter and foraging opportunities. For instance, Chrysopa perla thrives in cool, shady environments like wet forests and shrublands.^[30]^[13]^[31] Larvae of Chrysopa species select microhabitats on aphid-infested foliage, crawling across plant surfaces to hunt soft-bodied prey, often remaining concealed under leaves or in crevices for protection. Adults, in contrast, prefer floral-rich areas and pollen sources near crop edges or wildlands, where they feed on nectar, honeydew, pollen, and small insects to sustain energy for dispersal and reproduction. This habitat partitioning enhances their predatory impact on pest populations in agricultural settings.^[11] Chrysopa species exhibit optimal activity at temperatures between 20°C and 30°C and relative humidities of 50% to 80%, conditions common in temperate growing seasons that support rapid development and predation rates. They show sensitivity to pesticides, with larvae and adults often experiencing high mortality from insecticides like chlorantraniliprole and thiamethoxam, necessitating careful application in integrated pest management.^[32] Behaviorally, Chrysopa adults display crepuscular flight patterns, peaking in late afternoon to evening, which aids in avoiding diurnal predators while locating mates and food sources. Overwintering occurs primarily as third-instar larvae or prepupae within silken cocoons attached to bark, foliage, or leaf litter, allowing survival in sheltered microhabitats during cold periods.^[33]^[34]^[14]

Geographic Range and Biodiversity Hotspots

The genus Chrysopa is primarily native to the Holarctic region, encompassing North America, Europe, and Asia, where it exhibits a broad distribution across temperate and subtropical zones. In the Nearctic realm, species are widespread from southern Canada through the United States to northern Mexico, with records indicating presence in diverse landscapes such as forests and agricultural areas. The Palearctic distribution is similarly extensive, spanning from the Iberian Peninsula in the west to Japan in the east, including high-latitude regions in Scandinavia and Siberia. While the core range is Holarctic, a few species have been reported in Neotropical areas, such as northern South America, though their affinities to the genus remain debated and may represent extensions or distinct lineages.^[15]^[35]^[36] Efforts to introduce Chrysopa species beyond their native range have met with limited success. In the late 19th and early 20th centuries, consignments of Chrysopa larvae, pupae, adults, and eggs were imported from Australia to New Zealand for biological control of aphids and mealybugs, including shipments in 1890, 1921, 1925, and 1927. However, these introductions failed to establish self-sustaining populations, likely due to unsuitable climatic conditions or competition with native lacewings. No verified established populations of Chrysopa exist in Australasia, where other chrysopid genera like Mallada dominate.^[37]^[38]^[14] Biodiversity hotspots for Chrysopa are concentrated in regions of high species richness within the Holarctic. The western Palearctic, particularly Mediterranean Europe, hosts the greatest diversity with approximately 27 species, benefiting from varied habitats like shrublands and orchards that support specialized adaptations. Eastern Asia, including China and Japan, represents another key area with around 15 species, where elevational gradients in biodiversity hotspots like the Shaluli Mountains reveal patterns of species turnover and abundance peaks at mid-elevations. In North America, roughly 18-20 species occur, with concentrations in western states like California, though overall diversity is lower than in Eurasian hotspots.^[15]^[39]^[10] Migration in Chrysopa is generally limited, with adults engaging in dispersive flights rather than long-distance seasonal migrations characteristic of some congeners like Chrysoperla. Preoviposition flights by newly emerged females typically cover short to moderate distances of up to 10-40 km over 2-3 nights, influenced by wind and resource availability, facilitating local colonization of suitable habitats such as woodlands or fields. These patterns underscore the genus's reliance on regional dispersal for maintaining populations within its Holarctic range.^[40]^[41]^[32]

Species Diversity

Diversity and Endemism

The genus Chrysopa comprises approximately 75 valid species, primarily restricted to the Holarctic region, though taxonomic revisions continue to refine this estimate as new species are described and synonymies resolved. Recent discoveries, such as Chrysopa niki described from Syria in 2024, continue to expand the known diversity.^[42]^[43]^[44] Endemism within Chrysopa is notably high in the Palearctic realm, where the majority of the genus's diversity occurs, with roughly 42 species (27 in the western Palearctic and 15 in the eastern Palearctic according to a 1990 review), indicating strong regional specialization.^[42] In contrast, endemism is low in the Nearctic, with about 10 species documented, reflecting limited speciation and broader dispersal limitations across the region.^[42]^[44] Diversity patterns in Chrysopa are influenced by environmental pressures such as habitat fragmentation, which disrupts population connectivity and limits gene flow in forested and agricultural landscapes, potentially hindering speciation.^[45] Climate change further exacerbates these dynamics by altering elevational distributions and thermal tolerances, driving shifts in species ranges that may promote isolation and localized adaptation in vulnerable Palearctic populations.^[10] Most Chrysopa species are not currently considered threatened at a global scale, benefiting from their adaptability as generalist predators in diverse habitats. However, certain localized endemics, particularly those confined to fragmented Palearctic habitats, face vulnerability from ongoing environmental changes, warranting targeted monitoring to prevent declines.^[10]

Notable Species and Synonyms

Chrysopa oculata, commonly known as the golden-eyed lacewing, is a prominent species in North America, ranging from Canada to Mexico. Its larvae, often referred to as aphid lions, actively hunt aphids, mites, and small insects.^[46]^[29]^[46] Another notable species, Chrysopa formosa, is distributed across parts of Europe and Asia. Adults exhibit typical green lacewing morphology with delicately veined wings, and the species is frequently encountered in orchards, shrubs, and forest edges.^[47]^[48]^[47] Taxonomic history within the genus includes significant synonymy and reclassifications, particularly with the closely related genus Chrysoperla; for instance, Chrysopa carnea Stephens, 1836, a widespread European species once central to biological control studies, is now synonymized under Chrysoperla carnea (Stephens), reflecting morphological and genetic distinctions that separated the genera. Other transfers, such as certain Nearctic and Palearctic taxa moved from Chrysopa to Chrysoperla based on differences in adult venation and larval traits, highlight ongoing nomenclatural refinements to stabilize classification.^[49] Species-specific traits vary regionally; in C. oculata, adults display golden eyes, a dark ring on the frons, reddish markings on antennae, and four dark spots on the wings, with coloration shifting from bright green to yellowish-green or brownish tones depending on environmental factors and geographic location. This species overwinters in the third larval instar within silken cocoons, entering facultative diapause influenced by temperature cues.^[46]^[50]^[51] Recent taxonomic revisions in the genus, driven by detailed examinations of genitalia morphology, have redescribed numerous species since 2000 to resolve cryptic diversity and phylogenetic relationships; for example, molecular and morphological analyses have led to new generic placements, such as the erection of Kymachrysa for former Chrysopa species in the Nearctic region. These efforts, including phylogenetic studies incorporating DNA sequences, have clarified boundaries within Chrysopidae, affecting around 20 Holarctic species through redescriptions or reassignments.^[35]^[3]^[15]

Role in Biological Control

Predatory Impact on Pests

Larvae of Chrysopa species are voracious generalist predators primarily targeting aphids, with a single larva capable of consuming hundreds of aphids over its development.^[52] Secondary prey includes whiteflies (Bemisia tabaci), thrips, and mealybugs, which are also effectively targeted due to the larvae's preference for soft-bodied insects. This predatory behavior relies on the larvae's active foraging and piercing-sucking mouthparts to extract hemolymph from prey.^[53] In field studies, Chrysopa larvae have demonstrated significant pest suppression in various crops. Similar impacts have been observed on whitefly densities in treated plots compared to untreated controls. These metrics highlight the predators' role in maintaining low pest levels in orchards and row crops, often preventing economic damage without chemical interventions. Chrysopa larvae engage in intraguild predation with other natural enemies, such as ladybird beetles, but this interaction is minimized at higher extraguild prey densities, where aphid availability shifts focus to primary targets. Effects on non-target beneficial insects are generally low, as increased prey abundance reduces cannibalism and inter-predator attacks, preserving overall predator diversity. Studies indicate that competitive displacement of indigenous lacewing species occurs rarely under natural conditions with ample aphids. Field observations reveal greater predatory efficacy in diverse cropping systems versus monocultures, where landscape habitat diversity boosts Chrysopa abundance, enhancing sustained pest suppression. In olive groves integrated with semi-natural habitats, higher lacewing populations correlate with improved control of pests such as the olive moth (Prays oleae). This pattern underscores the value of polycultures in amplifying natural predation dynamics.^[54]

Commercial and Agricultural Applications

Commercial rearing of Chrysopa species focuses on mass production of eggs and larvae for augmentative biological control programs, with species such as C. oculata preferred due to their high fecundity and adaptability to laboratory conditions.^[55] Techniques involve rearing larvae on cost-effective factitious prey like prepupae of the alfalfa leafcutting bee (Megachile rotundata), achieving up to 91% survival to adulthood and an average of 424 eggs per female over 30 days.^[55] Similarly, C. pallens is mass-reared on artificial diets or live prey like pea aphids, with females producing around 1,000 eggs under optimal conditions of 25°C and 70% relative humidity.^[56] These methods enable scalable production in insectaries, supporting releases in agricultural settings while minimizing costs, such as less than 1.95 Canadian cents per larva for C. oculata.^[55] Application methods primarily involve inundative releases of eggs or larvae in greenhouses and field crops, integrated into broader integrated pest management (IPM) strategies to target soft-bodied pests.^[57] Typical rates range from 1,000 to 10,000 individuals per hectare, with multiple applications (e.g., 2–4 times per season) to establish populations and suppress outbreaks; for instance, 5,000–50,000 per acre (approximately 2,000–20,000 per hectare) is recommended for aphid control in vegetables and ornamentals.^[57] In greenhouses, releases of 2 larvae per square foot enhance predation without disrupting beneficial insect dynamics when combined with selective pesticides.^[58] Cold storage of pupae at 10°C for up to 20 days further facilitates shipping and timed releases, maintaining over 50% emergence rates.^[56] Success stories highlight Chrysopa species' effectiveness in aphid control on crops like citrus and cotton, where augmentative releases have reduced pest densities in field trials. In citrus orchards, releases have suppressed aphids, demonstrating practical viability in subtropical systems. For cotton, inundative applications in IPM programs have provided high levels of control against aphids and other sucking pests, contributing to sustainable production by lowering reliance on chemical inputs.^[59] These outcomes underscore Chrysopa's role in reducing crop damage and supporting economic viability through decreased pesticide expenditures. Key challenges in commercial rearing include larval cannibalism, which can reduce survival rates by 12% or more if not managed through isolated rearing units or protective cocoons, and the short shelf life of eggs, typically 7–10 days at low temperatures (e.g., 12°C) to preserve hatchability above 80%.^[23] For C. pallens pupae, prolonged cold storage beyond 20 days sharply declines emergence (to 10.7% at 60 days) and fecundity (up to 35.5% reduction), necessitating precise timing in production and distribution.^[56]

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BCANZ · Biological Control Agents introduced to New Zealand
Two consignments of Chrysopa sp. from Australia, comprised of 'many' larvae and pupae, together with jars of adults and eggs, arrived in New Zealand in 1921, ...Missing: populations | Show results with:populations
[44]
BCANZ · Biological Control Agents introduced to New Zealand
Biocontrol introduction. Target pest: Aphids (Hemiptera: Aphididae). Agent introduced: Chrysopa sp. 2 (Neuroptera: Chrysopidae). Imported: 1925, 1927.
[45]
[PDF] Chrysopidae of the Palearctic Region - a review - Zobodat
One genus with holarctic distribution is Chrysopa LEACH. At present we know in the. Palearctic Region 33 species with a rather remarkable pattern of ...
[46]
Preovipository migration flights in the green lacewing, Chrysopa ...
Average migration distance is 40 km per night. Even ... Duelli P (1980) Adaptive dispersal and appetitive flight in the green lacewing, Chrysopa carnea.
[47]
(PDF) Adaptive dispersal and appetitive flight in the green lacewing ...
Aug 6, 2025 · The flight behaviour of Chrysopa cornea Steph. (Neuroptera: Chrysopidae) with regard to dispersal activity has been investigated in field experiments.
[48]
The green lacewings of the world: a generic review (Neuroptera ...
The green lacewings of the world: a generic review (Neuroptera: Chrysopidae). By. Brooks ... 1990. Original Publication. Bulletin of the British Museum (Natural ...
[49]
(PDF) First Record of a New Species of Green Lacewings Chrysopa ...
Jul 2, 2024 · Thus, the discovery of a new morphologically distinct species of chrysopid belonging to the extensively studied genus Chrysopa, Chrysopa niki n.
[50]
Species richness and composition of Neuroptera in the forests ...
Forest fragmentation is a primary concern for landscape ecologists since it could represent an important threat to the preservation of biological diversity.
[51]
Species Chrysopa oculata - BugGuide.Net
May 3, 2008 · Family Chrysopidae (Green Lacewings). Subfamily Chrysopinae (Typical Green Lacewings). Tribe Chrysopini. Genus Chrysopa (Stink Lacewings).
[52]
The green lacewing Chrysopa formosa as a potential biocontrol ...
Jul 29, 2022 · The green lacewing Chrysopa formosa is a promising polyphagous predator that is widely used in the biocontrol of various pests in China, but ...
[53]
Chrysopa formosa Brauer, 1851 - GBIF
Clypeus yellow, lateral margins dark brown. Labrum yellow, covered with short yellow setae. Genae yellow, with a median transverse or round dark spot. Maxillary ...Missing: characteristics | Show results with:characteristics
[54]
Chrysoperla carnea (aphid lion) | CABI Compendium
aphid lion. Other Scientific Names: Anisochrysa carnea: Anysochrysa carnea: Chrysopa carnea Stephens: Chrysopa nipponensis: Chrysopa vulgaris Schneider ...Missing: synonym | Show results with:synonym
[55]
Green lacewing (Chrysopa oculata)
Oct 12, 2024 · They are typically bright green in color, although some species may exhibit variations in coloration, ranging from yellowish-green to brownish- ...
[56]
Diapause in the neuropteran Chrysopa oculata - ScienceDirect.com
Chrysopa oculata has a facultative diapause in the third instar within the cocoon. ... overwintering larvae is determined by the temperature requirements of the ...
[57]
Chrysopidae) Fed on Aphid, Myzus persicae (Sulzer) (Hemiptera
The larvae consumption rates were 379.2 aphids during their life span. ... Feeding potential and growth rate index of aphid lion, Chrysoperla carnea on different ...
[58]
Field evaluation of indigenous predacious insect, Chrysoperla ...
Mar 1, 2018 · On sweet pepper plants, reduction rates of the aphid and whitefly reached about 90 and 97%, after the second predator release of five and ten ...
[59]
Predation efficiency of the green lacewings Chrysoperla agilis and C ...
Sep 9, 2022 · The reduction in aphid populations achieved by C. agilis larvae was more pronounced when compared to C. mutata. This can be explained by species ...
[60]
Intraguild Predation between Chrysoperla carnea (Neuroptera
May 8, 2020 · Theoretically, it has been hypothesized that IGP occurrence can lead to different effects ranging from exclusion to coexistence of engaged ...Missing: non- | Show results with:non-
[61]
(PDF) Larval Cannibalism and Intraguild Predation Between the ...
Aug 7, 2025 · Increasing the availability of aphids tended to decrease both cannibalism and IGP levels. Nontarget effects such as competitive displacement ...
[62]
Habitat Diversity Increases Chrysoperla carnea s.l. (Stephens, 1836 ...
Feb 12, 2024 · This transformation has led to the depletion of natural habitats, resulting in a loss of biodiversity and a decline in associated ecosystem ...Missing: Chrysopa endemism<|separator|>
[63]
[PDF] Rearing Lacewings, Chrysoperla carnea and Chrysopa oculata ...
We describe here rearing techniques and bionomics of Chrysoperla carnea and. Chrysopa oculata Say fed as larvae on prepupae of the alfalfa leafcutting bee, Mega ...
[64]
Effects of cold storage on quality of Chrysopa pallens and recovery ...
Mar 29, 2019 · The C. pallens colony was fed with pea aphid (Acyrthosiphon pisum) and kept at 25 °C and 70% relative humidity (RH) under a 16 h light ...
[65]
Green Lacewing Technical Bulletin - Rincon-Vitova Insectaries
Ants: are attracted to the eggs on the card. They will eat all the eggs on the card. Ants generally interfere with biological control, and in particular ...Missing: parental | Show results with:parental
[66]
Greenhouse & Indoor - Biocultivation
Within about a week they start eating aphids. Release 2,000-3,000 eggs per acre every 2 weeks, 2-4 times OR 1 per 20 pests OR 2 per sq ft in greenhouses.
[67]
EFFICACY OF INUNDATIVE RELEASESl - Annual Reviews
However, combined releases of both Coccinella and Chrysopa produced reductions of 33-97% in the three aphid species with an average of 58% for all species (10' ...
[68]
(PDF) Evaluation of green lacewings, Chrysoperla plorabunda (Fitch ...
Aug 7, 2025 · The average pupation rate was 37.5%, but only 6.3% of pupae yielded adults. Developmental time and survival to pupation varied with the life ...
[69]
Beneficial Insects - Mid-Florida Research and Education Center
Development and reproduction of the mealybug destroyer occur most rapidly at temperatures between 22 and 25 degrees C (72 and 77F), and relative humidities of ...
[70]
storing eggs of chrysoperla externa (hagen, 1861) (neuroptera
Eggs of one, two and three days old can be stored at 12 °C, but must be removed from storage in up to 16, 11 and seven days respectively, in order to guarantee ...Missing: Chrysopa | Show results with:Chrysopa