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Gryllidae

Gryllidae is a family of in the order , commonly known as true crickets, distinguished by their dorsoventrally flattened bodies, thread-like antennae equal to or longer than the body length, and enlarged hind femora adapted for . These also feature three-segmented tarsi, a tympanal organ on the front tibiae for hearing, and in females, a prominent cylindrical or needle-like for egg-laying. Males are notable for their stridulatory apparatus on the forewings, which they rub together to produce species-specific chirping sounds used in mating calls and territorial defense. With more than 2,400 described , Gryllidae represents one of the largest families within the superfamily Grylloidea and exhibits a across nearly all terrestrial habitats, from tropical forests and grasslands to urban environments and arid regions. The family is divided into several subfamilies, including Gryllinae (field crickets), Oecanthinae (tree crickets), Eneopterinae (bush crickets), and Trigonidiinae (sword-tailed crickets), encompassing diverse forms adapted to specific ecological niches. In alone, there are over 100 , though global diversity is highest in tropical areas. Gryllids are primarily nocturnal omnivores and , feeding on decaying material, fungi, seeds, and occasionally small or conspecifics, which positions them as key decomposers and prey items in food webs. Their involves incomplete metamorphosis, with eggs laid in batches via the into moist soil or tissues, hatching into nymphs that resemble wingless adults and undergo several molts over weeks to months depending on and environmental conditions. rates, produced only by males in most , vary with and serve as indicators of environmental conditions, while the family's acoustic communication has made certain , such as the (Acheta domesticus), valuable as model organisms in studies of neurobiology, behavior, and development. Some are agricultural pests, while others are commercially reared for bait, , or human consumption in various cultures.

Overview

Introduction

Gryllidae, commonly known as true crickets, is a family of within the order , suborder Ensifera, and superfamily Grylloidea. This family encompasses 1,996 valid extant species distributed across 230 genera, making it one of the most diverse groups among ensiferans. The family was established by Laicharting in 1781, with designated as the . True crickets are widely recognized for their nocturnal habits and distinctive chirping sounds, produced primarily by males through , which are iconic of summer evenings in many temperate and tropical regions. These are often found in grassy areas, forests, and human-modified habitats, contributing to their familiarity in both natural and urban environments. Ecologically, Gryllidae species play key roles as omnivorous consumers of matter, , and small , facilitating cycling in soils and layers. They also serve as important prey for a variety of predators, including birds, reptiles, amphibians, and mammals, thereby supporting dynamics and overall .

Key characteristics

Gryllidae, commonly known as true crickets, are distinguished by their long, filiform antennae that are thin, whip-like, and typically exceed the body length, serving primarily for sensory perception in navigating dark environments. Their body structure is robust and cylindrical, often described as stocky with a globular head and a smooth pronotum covering the , while the terminates in a pair of well-developed cerci—long, hairy appendages present in both sexes that aid in sensory detection. The hind legs are prominently adapted for jumping, featuring thickened femora and elongated tibiae armed with spines, enabling powerful leaps for escape or locomotion. Females possess a distinctive long, cylindrical or needle-shaped , which is used to deposit eggs into or substrates, contrasting with the more blade-like ovipositor found in related families such as (katydids). This ovipositor, along with the paired cerci, helps differentiate true from mimics or other orthopterans, as katydids have a broader, sword-like egg-laying structure. Unlike mole (Gryllotalpidae), which have forelegs for digging, Gryllidae exhibit a more generalized body form suited to surface-dwelling. Most Gryllidae species are primarily nocturnal, remaining concealed in leaf litter, under logs, or in vegetation during the day and becoming active at night, though some tropical species, such as those in the genus Nisitrus from , display diurnal behavior. This activity pattern aligns with their sensory reliance on long antennae and cerci for detecting predators and mates in low-light conditions.

Taxonomy and classification

Phylogenetic position

Gryllidae belongs to the kingdom Animalia, phylum Arthropoda, class Insecta, order , suborder Ensifera, and superfamily Grylloidea. The family name Gryllidae was established by Laicharting in 1781, with the type genus ; historical nomenclature has occasionally encompassed broader groupings of ensiferans under "Gryllidae" in older classifications, but modern restricts it to true crickets. Within , Gryllidae is nested in the suborder Ensifera, which also includes (katydids) and (wetas and allies), forming a characterized by long antennae and complex auditory systems. In Grylloidea, Gryllidae is the to Oecanthidae (tree crickets), with Gryllotalpidae () positioned in the closely related superfamily Gryllotalpoidea or sometimes included in an expanded Grylloidea; this arrangement reflects shared morphological traits like stridulatory structures but highlights ecological divergences. The of Gryllidae and Grylloidea is robustly supported by molecular phylogenies using nuclear ribosomal genes (18S and 28S rRNA) and mitochondrial markers (16S rRNA and complete mitogenomes), which resolve Ensifera as basal to and confirm Grylloidea's position within ensiferan diversification dating to the Permian. The fossil record of Gryllidae underscores its ancient origins, with the oldest known specimens attributed to Protogryllus grandis from the (approximately 237–201 million years ago), representing early Gryllidea and featuring primitive wing venation and morphology. Diversification accelerated in the , as evidenced by diverse amber-preserved fossils from and , including representatives of subfamilies like Oecanthinae and Nemobiinae, which document the radiation of acoustic signaling and habitat specialization amid angiosperm expansion. These fossils align with molecular divergence estimates placing Gryllidae's crown radiation around 150–100 million years ago.

Subfamilies and genera

The family Gryllidae encompasses eight extant subfamilies and one extinct subfamily, comprising 230 extant genera and 1,995 extant species worldwide. The extant subfamilies are Eneopterinae (tropical distribution), Gryllinae (cosmopolitan), Gryllomiminae (tropical), Gryllomorphinae (tropical), Itarinae (tropical), Landrevinae (tropical), Pentacentrinae (tropical, discontinuous in the Americas), and Hemigryllinae (revalidated in 2025, endemic to South America). Gryllinae represents the most diverse subfamily, containing approximately 125 genera and over 1,200 species/subspecies. Notable genera within Gryllidae include Gryllus, the type genus of Gryllinae, which is cosmopolitan and encompasses over 100 species of field crickets. Acheta, also in Gryllinae, includes the house cricket A. domesticus and several other species adapted to human environments. Teleogryllus, another Gryllinae genus, features around 52 species of black field crickets primarily distributed in Africa, Asia, Australia, and the Pacific. Extinct taxa are represented by the subfamily Gryllospeculinae, known from deposits, with additional Gryllidae fossils from the Eocene, such as those in . Examples include Cratogryllus species from the Lower Cretaceous Santana Formation in Brazil's Araripe . Recent taxonomic revisions have refined Gryllidae's classification, including the elevation of former subfamilies like Oecanthinae to family status (Oecanthidae), Phalangopsinae to Phalangopsidae, and Podoscirtinae to Podoscirtidae based on phylogenetic analyses. Ongoing updates in the Species File incorporate splits and new descriptions, particularly in subfamilies like Landrevinae and the revalidated Hemigryllinae, with new genera and species added from Indo-Malayan and Madagascan regions as of 2025.

Physical description

Morphology

Gryllidae, the family of true crickets, exhibit a typical orthopteran divided into three tagmata: head, , and , with adaptations suited to their terrestrial lifestyle. The is chitinous and segmented, providing protection and support, while allowing flexibility for movement. The head is hypognathous, featuring large compound eyes composed of numerous ommatidia for wide-angle vision and three ocelli arranged in a for detecting . Mouthparts are mandibulate, adapted for biting and chewing, enabling an omnivorous diet that includes plant material, fungi, and small . Antennae are long, filiform, and multisegmented, serving as primary sensory organs for touch and chemoreception. The consists of three segments, with the pronotum forming a prominent, shield-like plate that covers and protects the . Legs are specialized: forelegs, attached to the , are equipped with sensory structures including a tympanum on the for audition; middle legs on the mesothorax facilitate walking; and hind legs on the metathorax are elongated and powerful, with enlarged femora enabling jumps of up to 16 times the body length through rapid extension of the tibiae. The abdomen comprises 10 visible segments, cylindrical in shape, and terminates in a pair of long, sensory cerci. In females, segments 8 and 9 bear a prominent consisting of four valvulae—two and two ventral—for egg deposition into or substrates. Males possess clasping structures, including modified cerci and a subgenital plate, adapted for grasping during mating. Spiracles along the and abdomen connect to the internal . Sexual dimorphism is evident in these genital appendages, with females typically longer due to the ovipositor. Wings, when present, include leathery forewings known as tegmina that overlay and protect the fan-like hindwings; the tegmina in males feature specialized structures such as a file and scraper for , while hindwings enable flight in many for dispersal. Internally, occurs via a tracheal system of branching tubes that deliver oxygen directly to tissues from external spiracles, supported by taenidia to prevent collapse. Excretion is handled by Malpighian tubules, slender structures clustered at the hindgut junction that filter to remove nitrogenous wastes, which are then processed into for .

Variation in size and coloration

Gryllidae species display a wide range of body sizes, typically measuring 1–3 cm in length, though extremes span from under 1 cm in certain small tree crickets, such as some species reaching 12–13 mm, to over 5 cm in large burrowing forms like . Coloration in Gryllidae is predominantly brown, black, or green, adaptations that facilitate against , , and leaf litter in their terrestrial or semi-arboreal environments. Some species, such as Gryllodes sigillatus, feature distinctive yellow tones accented by black dorsal bands, providing subtle contrast while maintaining overall . Sexual dimorphism is prevalent, with females generally larger than males across the family, often by 9% on average, reflecting differences in reproductive investment; females possess notably longer ovipositors for egg-laying, while males in certain species, like , exhibit broader heads and larger mandibles suited to agonistic interactions. Intraspecific and interspecific variations align with distinctions: Gryllinae tend to have robust, stocky builds with dark brown to black integuments, emphasizing terrestrial adaptations, whereas Oecanthinae are more slender and pale green or yellowish, enhancing their arboreal among foliage.

Distribution and habitats

Global distribution

Gryllidae, the family of true crickets, display a across all continents except , with more than 2,400 described species recorded globally. This widespread presence reflects their adaptability to diverse terrestrial environments, though they are absent from polar regions due to climatic constraints. Fossil records dating back to the indicate an ancient lineage, with distributions of certain subfamilies, such as those in southern continents, consistent with origins linked to the fragmentation of the . The highest species diversity occurs in tropical regions, particularly in , , and the , where warm climates support prolific . Recent assessments suggest over 2,400 described species, with ongoing discoveries in tropical regions. In , the family boasts significant richness, with genera like exhibiting broad distributions extending into , where species such as are native and widespread across mainland habitats. similarly hosts substantial diversity, including unique assemblages in isolated areas like , where members of the subfamily Phalangopsinae show notable , contributing to regional biogeographic patterns. Human-mediated dispersal has facilitated the global spread of certain species, rendering them virtually cosmopolitan. The house cricket Acheta domesticus, originally from southwestern and , has been introduced worldwide through and , establishing populations in urban and agricultural settings across continents. In , for instance, A. domesticus was introduced from in the and now occurs widely, often associated with human structures. Such introductions highlight the role of activities in altering natural biogeographic ranges within the family.

Habitat preferences

Gryllidae species primarily inhabit terrestrial environments, including grasslands, forests, and even arid deserts, where they exploit a variety of vegetation layers for shelter and foraging. Many ground-dwelling members, such as those in the genus Gryllus, prefer open meadows and construct burrows in loose, sandy soil to evade environmental extremes and predators. Within these broader habitats, Gryllidae occupy specific microhabitats that provide moisture and cover, such as under rocks or logs, within leaf litter accumulations, and in arboreal settings for tree crickets in the Oecanthinae, which frequent shrubs and tree branches. A subset of are cavernicolous, adapted to interiors where stable humidity supports their survival, exhibiting troglomorphic traits like elongated appendages in some cases. These demonstrate adaptations to challenging conditions, particularly tolerance to through burrowing behaviors that maintain internal and protect against in dry grasslands and fringes. They generally favor warm and humid microclimates, with optimal developmental temperatures ranging from 26°C to 34°C for species like Gryllus bimaculatus and Acheta domesticus. Gryllidae exhibit a broad altitudinal distribution, occurring from up to moderate elevations around 3,000 m in some mountainous regions.

Biology and behavior

Life cycle and development

Gryllidae, like other orthopterans, undergo incomplete (hemimetabolous) , consisting of three primary life stages: , , and adult. The stage begins when females use their elongated to deposit eggs singly or in clusters into moist soil or decaying plant material, with varying widely by and environmental conditions, typically ranging from 200 to over 2,000 eggs per female; for example, in Gryllus bimaculatus, females produce 280 eggs at 20°C to 2,300 at 32°C. Incubation duration also varies by and temperature, e.g., 6–34 days in G. bimaculatus at 32–20°C, with higher temperatures accelerating hatching within the viable range of 20–37°C. Recent research indicates that rising temperatures due to may accelerate development but increase mortality risks beyond optimal ranges (e.g., above 37°C), affecting as of 2024. Upon hatching, nymphs emerge resembling miniature adults but lacking fully developed wings and reproductive structures; they pass through 5 to 12 s, with the number varying by species and environmental factors. Growth occurs through periodic molting, typically every 3 to 14 days depending on and instar stage, during which the exoskeleton is shed to allow for size increase and gradual development of features like wing pads in later instars. The entire nymphal period, encompassing multiple molts, lasts from 27 days at 32°C to over 180 days at cooler s like 20°C, resulting in a total development time from to adult of 1 to 3 months under favorable conditions (25–35°C), though it can extend to 7 months in cooler environments. Adult crickets, reached after the final molt, exhibit full and live for 1 to 3 months, with influenced by temperature—shorter at higher temperatures (e.g., 35–70 days at 32–36°C) and longer at cooler ones (up to 200+ days at 24°C). In temperate zones, many species overwinter as late-instar nymphs, entering to survive cold periods before completing development in spring, which allows univoltine or semivoltine life cycles in such regions.

Communication and sound production

Gryllidae, commonly known as true crickets, primarily communicate through acoustic signals produced via stridulation, a process in which males rub a file-like structure on one forewing (tegmen) against a hardened scraper on the opposing forewing to generate vibrational energy that radiates as sound. This mechanism acts as a frequency-multiplying system, converting the slow wing closure rate of approximately 20-30 Hz into audible chirps with carrier frequencies typically ranging from 2 to 8 kHz, though most species produce sounds around 4-5 kHz. The stridulatory files on the wings vary in tooth density and arrangement, influencing the temporal pattern and intensity of the resulting pulses. Crickets produce distinct song types that serve specific behavioral functions. The calling song, emitted by solitary males, functions in long-range attraction of females and territory advertisement, consisting of regular s with species-specific pulse rates and durations. songs are performed in close proximity to females, featuring softer, more variable trills or ticks to stimulate mating readiness. Aggressive songs, triggered by encounters with rival males, include longer s or trills to deter competitors and establish dominance. These songs are modulated by environmental factors such as , which can alter rates. Hearing in Gryllidae is facilitated by tympanal organs located on the proximal tibiae of the forelegs, consisting of thin membranes backed by air-filled cavities and innervated by sensory neurons (scolopidia) that detect vibrations from 100 Hz to over 100 kHz, including . These organs enable directional hearing through a four-channel system involving acoustic spiracles, allowing precise localization of sound sources. Females exhibit phonotaxis, orienting toward attractive male calls, while both sexes can detect aggressive or predatory sounds. Song patterns exhibit significant species-specific variations, aiding in mate recognition and reproductive isolation; for example, in Gryllus firmus, the calling song features chirps at approximately 2 per second with 3-5 pulses each, while Gryllus bimaculatus produces chirps at rates of 30-80 per minute depending on context. Some Gryllidae species, particularly in subterranean or cave habitats like certain Euscyrtinae, have reduced or absent stridulatory apparatus, resulting in silent communication reliant on alternative cues.

Reproduction and mating behaviors

Gryllidae typically exhibit a , where males defend territories using calling songs to attract multiple females while females often with several males to increase and sperm reserves. Males establish and maintain burrows or fixed locations as territorial centers, aggressively repelling rivals through physical confrontations involving clashes to secure opportunities. The courtship sequence begins with the male stridulating to lure a receptive female, who approaches and orients toward the sound source; upon contact, the male mounts the female, leading to copulation and the transfer of a containing sperm and nutritive material. In many species, such as Gryllodes sigillatus, the represents a substantial , comprising up to 20-26% of the male's weight, with the gelatinous spermatophylax portion serving to occupy the female during sperm transfer and providing nutritional benefits. Following transfer, males in species like G. sigillatus often engage in mate guarding, remaining mounted on the female for minutes to hours to prevent immediate remating and ensure paternity. Sexual selection in Gryllidae operates through both female choice and male-male competition; females preferentially select males based on the quality of their calling , which signal genetic , , and viability, often favoring longer or more complex chirps. Males compete directly via agonistic encounters, using their mandibles to grapple and subdue rivals, with winners gaining priority access to territories and females, thereby enhancing . Parental care is generally absent in Gryllidae after hatching, with adults providing no provisions or protection to nymphs; however, in some species like Anurogryllus muticus, females exhibit limited maternal care by guarding egg pods post-oviposition to protect against predators and environmental threats. This behavior is rare within the family and contrasts with the typical lack of post-hatching investment, emphasizing the reliance on high fecundity for reproductive success.

Diet and foraging

Gryllidae, commonly known as true crickets, exhibit an omnivorous diet in the wild, with a primary emphasis on herbivorous feeding. Species such as and consume a variety of plant materials, including roots, stems, leaves, flowers, fruits, seeds, and grasses, which form the bulk of their intake. They also opportunistically engage in carnivory, feeding on dead or dying insects, small invertebrates, and occasionally conspecifics, particularly in resource-limited environments. Arboreal species within the subfamily Oecanthinae, such as tree crickets, supplement their diet with and other small insects found on vegetation. Foraging behavior in most Gryllidae is predominantly nocturnal and ground-based, with individuals emerging from burrows or hiding spots at dusk to search for food. Ground-dwelling species like those in the genus actively explore soil surfaces and low vegetation, often defending territories that include foraging areas. This nocturnal activity minimizes predation while allowing access to dew-moistened matter and nocturnal prey. In contrast, some arboreal forms forage higher in , targeting during evening hours. Nutritionally, Gryllidae require a balanced intake of proteins and carbohydrates, with elevated protein demands supporting and growth; studies on species like show that higher protein ratios enhance adult mass and survival. In settings, diets combining oats for carbohydrates and food or other protein sources mimic natural needs and promote optimal development. is prevalent under crowded conditions, where nymphs readily consume eggs or moribund conspecifics to meet protein requirements, as observed in and related species. In subsocial species like Anurogryllus muticus, females provision nymphs with trophic eggs, providing a controlled protein source that reduces opportunistic among offspring.

Ecological role and interactions

Predators and defenses

Gryllidae species face predation from diverse taxa, including birds such as great crested flycatchers (Myiarchus crinitus) that consume crickets alongside other insects like beetles and grasshoppers, American crows (Corvus brachyrhynchos) that exploit high cricket abundances, reptiles including that attack foraging individuals, and small mammals like (Sorex spp.) which incorporate crickets into their diet of . These predators often target active, calling males, whose acoustic signals increase detectability in open habitats. Parasitic threats include nematodes such as Mehdinema alii in the decorated cricket (Gryllodes sigillatus), which inhabit the hindgut and are transmitted venereally during mating, and tachinid flies like Ormia ochracea whose larvae develop internally in field crickets (Gryllus spp.), using the host's calling song for location and causing host debilitation. Some nematodes, including hairworms (Paragordius varius), manipulate host behavior by inducing water-seeking in infected crickets, elevating drowning risk and facilitating transmission to aquatic predators like fish. In response to such invasions, crickets mount cellular immune defenses involving hemocytes that encapsulate and melanize parasites, limiting larval development in species like Gryllus bimaculatus. To counter predation, Gryllidae employ behavioral and morphological adaptations; cryptic coloration blends individuals with and , reducing visibility to sight-hunting predators like and , while many species, such as field crickets ( spp.), burrow rapidly into for concealment upon disturbance. Thanatosis, or feigning death through rigid immobility, occurs in when leg movements are restrained, deterring further attack from predators. Aggressive displays, including antennal fencing and flaring, can escalate to physical combat in males, serving as a against potential threats beyond conspecific rivals. Predation and parasitism collectively regulate Gryllidae population densities in grasslands, where higher predator activity in open areas constrains abundances and prevents outbreaks, as observed in tropical systems where cricket numbers decline with intensified vertebrate foraging.

Role in ecosystems

Gryllidae, commonly known as true crickets, play a significant role as decomposers in various ecosystems by consuming and breaking down detritus, such as leaf litter and wood, which facilitates recycling in soils. Through their feeding activities, crickets contribute to the of , releasing essential minerals back into the soil and promoting , particularly in and environments. For instance, in ecosystems, crickets help return nutrients to the soil, supporting overall by aiding in the breakdown of dead material. This process is vital for maintaining , as crickets act as secondary decomposers alongside and fungi, enhancing turnover in nutrient-limited habitats. As a key component of food webs, Gryllidae serve as an important prey base for numerous insectivores, including birds, reptiles, amphibians, and small mammals, thereby supporting higher trophic levels and . Their abundance and phytophagous diet position them as in many terrestrial , where they provide a reliable source that sustains predator populations. Additionally, crickets function as bioindicators of habitat health, with their acoustic signaling and community structure reflecting ; declines in cricket populations can signal disruptions in balance. In tropical forests, crickets also aid via frugivory, consuming fruits and transporting seeds, often at night. In neotropical forests, crickets disperse an equivalent number of seeds as but carry larger seeds farther, potentially reducing seed aggregation and altering spatial distribution patterns for plants like those in the Marantaceae family. Crickets within Gryllidae act as indicators of , with their abundance and varying predictably across disturbance gradients, helping to monitor habitat recovery. In tropical systems, such as those in , cricket populations are lowest in early-successional shrublands (e.g., 16.5 individuals per site) and increase markedly in mature forests (up to 57.13 individuals per site), with rising from 7 to 20 species along the gradient. Unique dominate disturbed areas, while specialized taxa prevail in mature habitats, mirroring patterns observed in post-fire recovery and forest regeneration elsewhere, such as in Brazilian systems. This sensitivity makes Gryllidae valuable for assessing restoration success in disturbed ecosystems.

Relationship with humans

Economic and agricultural impacts

Species within the Gryllidae family, such as field crickets (Gryllus spp.), occasionally emerge as agricultural pests by consuming seedlings and foliage, leading to reduced crop yields in affected fields. These crickets primarily target young in crops including , , strawberries, , and cereals, where they clip stems and create irregular feeding holes that can destroy entire rows during stand establishment. For instance, the common black field cricket () has been documented damaging seedlings of strawberries, red cedar, and other vegetation, exacerbating losses in vulnerable areas. House crickets (Acheta domesticus), while less destructive to crops, frequently invade homes and structures, where they chew on fabrics, , , and stored food, resulting in nuisance complaints and minor property damage. Management of Gryllidae pests in agricultural settings relies on integrated approaches to minimize environmental impact. Cultural methods, such as early weed removal, to disrupt egg-laying sites, and habitat reduction around fields, help prevent population buildup before migrate to crops. Chemical controls involve targeted applications of insecticides like pyrethroids or bait formulations containing sodium fluosilicate, applied during when damaging densities are observed. Biological options include entomopathogenic nematodes (Steinernema spp.), which parasitize and kill crickets in , offering a sustainable alternative for soil-dwelling stages. Economically, Gryllidae contribute to localized crop losses, though they represent a smaller fraction compared to other orthopterans like grasshoppers and locusts, which collectively cause billions in global agricultural damage annually through widespread outbreaks. In regions with high cricket densities, such as parts of North America and South Asia, infestations can lead to significant reductions in seedling survival, prompting increased control costs for farmers. Conversely, certain Gryllidae species provide economic benefits in human-managed systems; house crickets are commercially reared and sold as fish bait and pet food, supporting a growing feeder insect industry valued at around USD 400 million as of 2024. Additionally, crickets serve as host insects in biocontrol laboratories, aiding the propagation of parasitic nematodes and other agents used against broader pest populations. Their role in pollination remains minimal, with incidental flower visitation offering negligible agricultural value.

Cultural and culinary uses

In various cultures, crickets of the family Gryllidae hold symbolic importance, often representing the continuity of life and natural rhythms. In , ' 1816 sonnet "On the Grasshopper and Cricket" portrays the cricket as a of enduring and vitality during winter, contrasting with the grasshopper's summer to emphasize the ceaseless "poetry of earth." This depiction underscores crickets' association with seasonal persistence in Western folklore, where their chirping evokes themes of resilience and harmony with nature. In Asian traditions, particularly in , crickets have been revered for over 3,000 years, initially kept as singing pets in ornate gourds during winter to ward off silence and bring good fortune. Historical records from the (618–907 CE) describe elite rearing practices, with crickets housed in golden cages near silk quilts for their auspicious songs. By the 13th century, texts like Jia Sidao's Tsu chi king (Book of Crickets) detailed breeding and fighting techniques, elevating the practice to an imperial pastime symbolizing virility and status. , using species such as , remains a cultural spectacle in and , where males compete in bouts for wagering, rooted in a 1,500-year-old tradition once favored by emperors. Culinary uses of Gryllidae span global traditions, with crickets valued as a nutrient-dense protein source. The (Acheta domesticus) is widely farmed for consumption due to its high protein content, typically 60–70% of dry weight, providing all essential and surpassing many conventional meats in efficiency. In , where insectivory is longstanding, approximately 31 cricket species worldwide have been documented as edible, with a significant portion—over 20 documented in alone—consumed fried, ground into flour, or incorporated into dishes for their 50–70% protein and rich profile. These practices highlight crickets' role in addressing protein , as their farming requires far less land and water than . As of 2024, the global crickets market is valued at approximately USD 418 million, with projections to USD 1.2 billion by 2033. In 2023, the approved Acheta domesticus for consumption, boosting commercial farming. Beyond culture and cuisine, Gryllidae serve practical modern applications. Crickets like Acheta domesticus are staples in for reptiles, amphibians, and , offering balanced with high protein and low fat. They also function as effective , attracting and due to their natural movement and scent, a tradition sustained by commercial suppliers. In scientific research, Gryllus bimaculatus is a key in neurobiology, used to study learning, memory, and neural circuits for and , owing to its well-mapped and genetic tractability.

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