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Teleogryllus

Teleogryllus is a genus of field crickets in the subfamily Gryllinae, family Gryllidae, and order Orthoptera, encompassing approximately 55 species distributed primarily across tropical and temperate regions of Africa, Asia, Australia, and the Pacific islands.^[1]^[2] These crickets are characterized by their robust bodies, long antennae, and the ability of males to produce species-specific calling songs through stridulation of their forewings, which serve for mate attraction and territorial defense.^[2] Species in this genus are often nocturnal, omnivorous feeders that consume plant material, fungi, and occasionally other insects, contributing to decomposition while sometimes acting as pests to crops and pastures.^[3]^[2] Taxonomically, Teleogryllus was established within the Gryllidae family, with species distinguished by morphological traits such as the shape of the male genitalia, tegmen venation, and auditory structures like the complex tracheal system that amplifies sound production.^[2] Notable species include T. commodus, the black field cricket endemic to Australia, known for its jet-black coloration, 2–4 cm body length, and habitat in grasslands where it hides in soil cracks during the day; T. oceanicus, the Pacific field cricket found in coastal Australia, Oceania, and introduced to Hawaii; and T. emma, widespread in Southeast Asia.^[3]^[2] Other species, such as T. infernalis, occur in East Asia, and the genus's diversity is particularly high in India with 14 recognized species.^[1]^[4] Biologically, Teleogryllus crickets exhibit a hemimetabolous life cycle, with nymphs resembling adults and undergoing several molts before reaching maturity in a few months; females can lay up to 2,000 eggs in soil.^[3] They possess cellulase enzymes (family 9) in their digestive systems to break down plant cell walls, reflecting their herbivorous tendencies.^[2] Calling songs are neurologically controlled by central pattern generators in the abdominal ganglia, making these crickets valuable models for studying acoustic communication, auditory processing, and ecdysis behaviors, which involve distinct phases like preparatory detachment and wing expansion post-molt.^[2] Genome sizes for species like T. oceanicus range from 1.6–2 Gb, with 12,000–19,000 protein-coding genes, supporting genomic research in neuroethology and insect physiology.^[2] Ecologically and economically, Teleogryllus species play dual roles: as decomposers aiding nutrient cycling by feeding on decaying organic matter, and as pests damaging pastures and crops in warmer regions, particularly in Australia and Asia.^[3]^[2] In research, they serve as key model organisms for behavioral ecology, including studies on sexual selection via song variation and responses to predators or parasites like nudiviruses that cause high mortality in lab-reared populations.^[2] Their adaptability to diverse habitats underscores their evolutionary success in orthopteran biodiversity.^[1]

Taxonomy

Etymology and history

The genus name Teleogryllus derives from the Ancient Greek téleios (complete or perfect) combined with Gryllus, the Latin term for a cricket genus.^[5]^[6] The genus Teleogryllus was established by Lucien Chopard in 1961 through a revision of the genus Gryllus (Gryllidae), primarily based on differences in the male copulatory apparatus that distinguished it from related genera such as Gryllus.^[7]^[6] Chopard designated Gryllus posticus as the type species by original designation, placing several previously described species into the new genus to reflect their distinct genital morphology.^[6] Early taxonomic history includes descriptions of key species now assigned to Teleogryllus, such as Gryllus mitratus by Hermann Burmeister in 1838 from India and Gryllus occipitalis by Jules Pierre Serville in 1838 from Africa, both later transferred to the genus following Chopard's revision.^[8]^[9]^[10] These species were initially classified under Gryllus but recognized for their unique traits in subsequent studies.^[8] Developments include the 2021 description of T. rohinae Jaiswara & Jain from Kerala, India, as part of a taxonomic revision that updated distributions and identifications for Indian Teleogryllus species, incorporating morphological and genetic data; a 2025 study further extended the known distribution of T. derelictus to India, increasing the reported species count there to 14.^[8]^[1] This addition highlights ongoing refinements to the genus, now comprising 55 species worldwide within Gryllidae as of 2025.^[6]

Classification

Teleogryllus belongs to the kingdom Animalia, phylum Arthropoda, class Insecta, order Orthoptera, family Gryllidae, subfamily Gryllinae, tribe Gryllini, and genus Teleogryllus.^[6] The genus was established by Chopard in 1961.^[6] The genus is divided into five recognized subgenera: Afroteleogryllus (Gorochov, 1988), Brachyteleogryllus (Gorochov, 1988), Cryncoides (Gorochov, 1986), Macroteleogryllus (Saussure, 1877), and Teleogryllus sensu stricto (Chopard, 1961).^[6] These subgenera are distinguished primarily by morphological and acoustic characteristics, with recent taxonomic revisions supporting their validity based on genetic analyses.^[11] As of 2025, the genus comprises 55 valid species, distributed across Africa, Asia, Australia, and the Pacific islands.^[6] Phylogenetic studies have confirmed the monophyly of Teleogryllus, with support from molecular data such as the COI gene, alongside acoustic and morphological traits that define clade boundaries.^[11] Evolutionary analyses indicate that egg diapause has evolved independently multiple times within the genus, likely as an adaptation to varying environmental conditions across its range.^[11]

Description

Morphology

Teleogryllus crickets are medium to large orthopterans, with adult body lengths typically ranging from 20 to 35 mm, though females often exceed males in size due to the presence of an ovipositor.^[12]^[8] Their coloration is predominantly black to dark brown, frequently accented by longitudinal stripes along the posterior head, which aids in species identification within the genus.^[12]^[8] The body structure is robust and cylindrical, featuring a transverse pronotum that is wider than long and equipped with distinct lateral edges for structural support.^[8] The abdomen is elongated and cylindrical, covered dorsally by folded forewings known as tegmina, which extend over the rear segments and provide protection while facilitating other functions. Hind legs are prominently robust, with enlarged femora and spined tibiae adapted for powerful jumping. Chewing mouthparts, typical of gryllids, consist of robust mandibles suited for processing plant material.^[8] Sensory structures include long, filiform antennae that extend well beyond the body length, enabling detection of chemical and mechanical stimuli in the environment. At the abdominal terminus, paired cerci serve as mechanoreceptors for monitoring vibrations and air currents. A specialized complex acoustic tracheal system, including an acoustic vesicle and connecting septum, runs through the body to amplify and propagate sounds efficiently. Females possess a long, curved ovipositor, approximately 10-15 mm in length, for depositing eggs into substrates.^[13]^[8]

Sexual dimorphism

Sexual dimorphism in the genus Teleogryllus is characterized by distinct morphological adaptations that reflect sex-specific reproductive functions, with males exhibiting traits suited for acoustic signaling and competition, while females possess structures optimized for egg-laying.^[14] Females typically display larger body sizes than males, as seen in T. oceanicus where females measure 33–42 mm in length due to the ovipositor, compared to males at 28–35 mm. Male forewings, or tegmina, are modified with a stridulatory file on one wing and a scraper on the other, enabling sound production for mate attraction. Males also have broader heads and stronger mandibles, which may aid in agonistic interactions during mating rivalries.^[12]^[15] In contrast, females feature a prominent long ovipositor, reaching up to 15 mm in length, used to deposit eggs into soil substrates. Although overall body size is larger, females have a more robust abdomen to accommodate egg production and development.^[16] These morphological differences support a division of reproductive roles, with males prioritizing signaling and territorial defense, and females focusing on efficient oviposition and offspring provisioning.^[17]

Distribution and habitat

Geographic range

The genus Teleogryllus is primarily distributed across the Old World tropics and subtropics, with species recorded in Africa, Asia, Australia, and the Pacific islands, encompassing a total of 55 described species.^[1] This range reflects adaptation to warmer climates, with limited presence in temperate zones.^[18] In Africa, Teleogryllus species are concentrated in sub-Saharan regions, particularly eastern and southern areas such as Kenya, Tanzania, and South Africa, including several endemics.^[19] Asian populations dominate in diversity, with at least 14 species reported in India, extending to East Asia (e.g., China north and south of the Yangtze River, Japan, Korea) and Southeast Asia (e.g., Vietnam, Thailand, Malaysia, Philippines, Indochina).^[20]^[18] Recent records indicate expansions, such as in southern Guangxi, China, and Assam, India.^[1] Australian species, such as T. commodus, occur widely across the continent, often in coastal and eastern regions.^[3] In the Pacific, T. oceanicus spans Oceania, including numerous islands and atolls, with introduced populations established in Hawaii.^[21]^[22] The genus's spread likely involves natural dispersal across island chains, supplemented by human-mediated introductions in agricultural zones.^[20]

Habitat preferences

Teleogryllus crickets exhibit a strong preference for soils that allow burrowing and provide shelter, such as cracking or fissured ground in dry or semi-arid conditions. Species like Teleogryllus commodus commonly hide in soil cracks, fissures, or self-constructed burrows during the day, using these as protected refuges and calling sites for males.^[3]^[23]^[24] In resource-rich patches, such as pastures with loose or sandy soils, population densities increase due to the availability of suitable burrow sites that offer protection from environmental stressors.^[25] These crickets are associated with vegetated landscapes that provide cover and foraging opportunities, including grasslands, forests, heathlands, and edges of urban or agricultural areas. For instance, T. commodus thrives in heath and forest habitats with dense low vegetation, while T. emma shows higher abundance in forest remnants and grassy fields compared to open areas, indicating a dependency on vegetation structure for shelter.^[3]^[26] They favor moist, vegetated microhabitats near human-modified lands like crop fields, where ground cover supports their lifecycle.^[23] Teleogryllus species are adapted to warm, humid climates typical of tropical and subtropical regions, with some tolerance for seasonal dryness but aversion to extreme cold. Nymphs of T. emma, for example, fail to survive below 18°C under laboratory conditions, though wild populations endure wider fluctuations through diapause in temperate zones.^[27] Higher temperatures accelerate development but reduce longevity, aligning with their native ranges in areas experiencing average temperatures around 23–28°C.^[28]^[29] Behavioral adaptations enhance survival in these preferred habitats, including strictly nocturnal activity to avoid daytime heat and predators, with individuals emerging from burrows at night for foraging and calling.^[3]^[23] Burrowing provides thermal regulation and moisture retention during dry periods, while gregarious clustering in vegetated patches boosts resource access without compromising shelter.^[24]^[25]

Behavior and ecology

Communication and sound production

In the genus Teleogryllus, males produce acoustic signals primarily through stridulation, a process in which the file—a row of fine teeth on the underside of one forewing—is rubbed against the scraper, a hardened ridge on the opposing forewing, during rhythmic opening and closing movements of the wings.^[30] This mechanism generates short sound pulses, or syllables, with each closing stroke producing a pulse via frictional vibration, and the overall song amplified by resonance in specialized wing structures such as the harp and mirror, as well as through air-filled tracheae connected to the spiracles that enhance sound radiation.^[30]^[31] The primary song types include the calling song, used for long-range attraction of females, which consists of chirps typically lasting 3–5 seconds and featuring carrier frequencies around 4–5 kHz in many species; this is followed by a courtship song, often comprising trills that are produced in close proximity to stimulate female receptivity.^[32]^[33] Songs exhibit species-specific differences in temporal patterns, such as syllable structure and duration; for example, T. emma calling songs feature long chirps composed of up to 12 single pulses followed by variable short chirps, whereas T. mitratus produces short chirps with approximately 6 syllables and longer chirps averaging 19–20 syllables, contributing to distinct acoustic signatures.^[34]^[35] Beyond airborne acoustics, Teleogryllus species employ alternative signals including substrate-borne vibrations generated during stridulation, which propagate through surfaces and temporally align with calling and courtship songs to convey information at short ranges.^[36] In T. oceanicus, some males produce percussive "purring" sounds via rapid wing taps against the substrate, representing a novel signal that evolved alongside traditional stridulation and may facilitate private communication by evading eavesdropping predators.^[37]^[38] A striking example of signal evolution is the recent emergence of "flatwing" mutants in T. oceanicus populations on Kauai, Hawaii, where a single X-linked genetic mutation alters wing morphology to prevent stridulation, rendering males silent and spreading rapidly since the early 2000s due to selection pressure from parasitoid flies. This morph swept to >95% prevalence on Kauai in fewer than 20 generations and has arisen independently on other islands like Oahu, as of 2024.^[39]^[40]^[41] These acoustic signals primarily function in premating isolation, with species-specific song traits enabling females to discriminate conspecific males and reduce interspecific mating; regional variations in song parameters, such as increased divergence in sympatric zones, further promote speciation by reinforcing reproductive barriers.^[42]^[43]^[44]

Mating and reproduction

Mating in Teleogryllus species typically begins with males producing calling songs to attract females from a distance, followed by a courtship phase upon the female's approach. During courtship, the pair engages in mutual antennal fencing, where mechano- and chemosensory cues are exchanged, assessing compatibility before the male mounts the female and transfers a spermatophore.^[45] This sequence ensures selective mate choice, with females often rejecting unsuitable males through kicking or fleeing behaviors. Multiple matings are common, particularly in females, which can copulate with several males to gain direct benefits such as enhanced egg production and nutrient provisioning from spermatophores.^[46] Following mating, females of Teleogryllus species deposit eggs into moist soil using a specialized ovipositor, which penetrates the substrate during a series of searching, positioning, and thrusting movements to create deposition sites.^[47] Oviposition peaks after high rainfall in field conditions, with females capable of laying hundreds to thousands of eggs over their adult lifespan. In temperate populations, such as those of T. commodus and T. emma, many eggs enter diapause shortly after oviposition, remaining dormant through winter to synchronize hatching with favorable spring conditions.^[48]^[49] The life cycle of Teleogryllus exhibits incomplete metamorphosis, progressing from egg to nymph through 7-10 instars before reaching adulthood, with the exact number varying by species and environmental factors. Nymphal development typically spans 40-60 days in warm conditions (around 25-30°C), resulting in a generation time of 1-2 months without diapause, though cooler temperatures or photoperiod cues can extend this period significantly.^[50]^[51] Behavioral syndromes influence mate choice in Teleogryllus, particularly in species like T. emma, where bolder, more active males exhibit higher aggression toward rivals and greater mating success, while females show no such activity-aggression correlation. These sex-specific traits link exploratory behavior to reproductive outcomes, with aggressive males securing more copulations despite potential costs like injury risk.^[52]

Diet and foraging

Teleogryllus species exhibit an omnivorous diet, predominantly herbivorous in nature, consisting mainly of leaves, grasses, seeds, stems, pods, and decaying plant material. They opportunistically consume smaller insects, dead organic matter, or other animal remains when available, reflecting the varied natural food sources in their habitats. This flexible feeding strategy allows adaptation to fluctuating resource availability in the wild.^[53]^[3]^[54] Foraging behavior is primarily nocturnal and ground-based, with individuals emerging from burrows, soil cracks, or vegetation cover after dark to search for food. In areas of high population density, crickets form gregarious clusters, potentially enhancing foraging efficiency through collective detection of resources. Juveniles and adults share similar feeding patterns, though nymphs often target softer plant parts such as tender leaves and seedlings. Activity peaks after rainfall, which stimulates emergence and movement.^[3]^[25]^[24] As agricultural pests, particularly in Australia, Teleogryllus crickets inflict significant damage to crops including pulses, pastures, emerging cereals, sunflowers, and soybeans by chewing leaves, stems, pods, and seedlings, sometimes necessitating replanting. Outbreaks are more pronounced in dry years, where reduced vegetation leads to intensified feeding pressure and depletion of available forage.^[25]^[55] Digestive adaptations in Teleogryllus support their plant-heavy diet, including an efficient gut system for breaking down cellulose-rich materials, aided by symbiotic microbes such as Firmicutes and Bacteroidetes that enhance polysaccharide fermentation and nutrient extraction. These microbial communities respond dynamically to dietary shifts, broadening the range of utilizable carbohydrates from plant sources.^[53]^[56]

Predators and threats

Teleogryllus crickets face predation from a diverse array of natural enemies across their life stages. Adult males are particularly vulnerable to acoustically orienting predators such as Australian long-eared bats (Nyctophilus major and N. geoffroyi), which use passive listening to locate calling individuals, with crickets singing from burrows showing reduced predation risk compared to those in open areas.^[57] Nymphs are often targeted by invertebrate predators including spiders and ants, which exploit their ground-dwelling habits during foraging.^[58] Additionally, birds, reptiles like lizards, and small mammals such as rodents prey on various life stages, contributing to overall mortality in natural populations.^[59] Phonotactic parasitoid flies (Ormia spp.), rather than wasps, pose a significant threat by laying eggs on adults and nymphs attracted to calling songs, with larvae developing internally and often killing the host.^[60] To counter these threats, Teleogryllus species employ several defensive behaviors. Burrowing into soil serves as a primary escape mechanism, allowing individuals to evade ground-based predators like ants and lizards by retreating to protected refuges.^[59] Stridulation patterns can function as a warning signal in aggressive encounters or to deter close-range threats, though calling also inadvertently attracts acoustically hunting predators.^[61] Some species produce chemical secretions from metathoracic glands, which may repel certain invertebrate predators, though this defense is less prominent in the genus compared to other Orthoptera.^[62] Their nocturnal foraging further heightens vulnerability to bat predation, as activity peaks align with predator hunting times.^[57] Anthropogenic factors exacerbate natural threats to Teleogryllus populations. Pesticide applications, particularly insecticide baits containing maldison, pirimiphos-methyl, or fenitrothion, are commonly used in agricultural settings to control pest species like T. commodus, leading to direct mortality and reduced population sizes.^[63] Habitat loss due to urbanization fragments grasslands and reduces suitable burrowing sites, limiting distribution and increasing exposure to urban stressors.^[64] Climate change disrupts diapause in eggs, with warmer temperatures altering intensity and threshold responses—southern populations of T. emma exhibit stronger diapause at higher latitudes, potentially shifting ranges and phenology under rising global temperatures.^[65] High predation pressure from bats, parasitoids, and other enemies helps regulate Teleogryllus populations, preventing large-scale outbreaks by culling calling males and vulnerable nymphs.^[58] This resilience is bolstered by rapid reproductive rates, with females producing multiple large egg clutches per season, enabling quick population recovery despite intense selective pressures.^[27]

Species

Subgenera

The genus Teleogryllus is divided into five subgenera, reflecting morphological, genitalic, and geographic distinctions among its approximately 55 species. These subgenera were primarily established by A. V. Gorochov in the late 1980s, building on earlier work by L. Chopard, with subsequent adjustments such as the subordination of the former genus Cryncoides under Teleogryllus. The species are distributed unevenly across the subgenera, with Brachyteleogryllus being the most speciose.^[6]^[66] The subgenus Afroteleogryllus Gorochov, 1988, encompasses African species adapted to arid conditions, featuring shorter wings that likely aid in thermoregulation and reduced flight in dry habitats. Its type species is T. clarus Gorochov, 1988, with additional species added by Gorochov in 1990.^[66]^[67] Brachyteleogryllus Gorochov, 1988, includes about 20 species primarily from Asia and Australia, distinguished by robust body builds and convex median lobes in male genitalia. Representative species include T. commodus Walker, 1869, known for its sturdy form suited to temperate grasslands. This subgenus dominates in species diversity, reflecting adaptive radiation in continental environments.^[11] The subgenus Cryncoides Gorochov, 1988 (formerly a separate genus), comprises endemics to Pacific islands, with morphological specializations such as modified wing structures for insular dispersal limitations and resource scarcity. It was downgraded to subgeneric status by D. Otte in 1994.^[11]^[66] Macroteleogryllus Gorochov, 1985, features larger-bodied species from Southeast Asia, characterized by extended antennae that enhance sensory detection in humid forest understories. The type species is T. mitratus (Burmeister, 1838), exemplifying the subgenus's emphasis on size-related traits for competitive interactions.^[11]^[68] The nominotypical subgenus Teleogryllus (s.s.) Chopard, 1961, forms the core group with the type species T. posticus (Walker, 1869), widespread across Asia and Australia. It is diagnosed by distinct pronotal patterns, including darker lateral margins, aiding in camouflage and species recognition. This subgenus includes many of the remaining species not fitting other categories.^[69]^[11]

Notable species

Teleogryllus oceanicus, commonly known as the Pacific field cricket, is native to coastal regions of Australia and has spread across Oceania, including introductions to islands like Hawaii. This species serves as a key model organism for studying rapid evolutionary changes in sexual signaling, particularly through the "flatwing" mutation that silences male calling songs by altering wing structure to prevent sound production. In Hawaiian populations, the flatwing morph has rapidly increased to over 90% prevalence in less than 20 generations on Kauai, driven by natural selection from parasitoid flies that target singing males, providing insights into adaptive signal loss and parallel evolution across islands.^[21]^[70]^[71] Teleogryllus commodus, the Australian black field cricket, is endemic to Australia and recognized as a significant agricultural pest, particularly damaging pastures in regions like New Zealand through feeding on foliage and roots. It produces complex calling songs characterized by chirps and trills, facilitated by an intricate acoustic tracheal system that amplifies and directs sound for mate attraction and rival deterrence. This species is extensively used in neurobiology research to investigate auditory processing, with studies on ascending interneurons revealing how the cricket's brain decodes species-specific song patterns for behavioral responses.^[72]^[13]^[73] Teleogryllus emma is a field cricket widely distributed across East Asia, including Korea, Japan, and China, where it exhibits univoltine life cycles in northern populations but shows potential for bivoltinism influenced by photoperiod and latitude. Males of this species demonstrate a strong positive behavioral syndrome linking activity levels to aggression, with more active individuals also displaying heightened aggressive responses in territorial contests, though this pattern is absent in females. These behavioral traits highlight T. emma's role in studies of individual variation and plasticity in social interactions.^[74]^[75]^[76] Teleogryllus mitratus occurs in India and parts of Southeast Asia, noted for its medium body size and contributions to taxonomic revisions within the genus. Recent analyses using molecular markers like COI have clarified its phylogenetic placement, distinguishing it from close relatives and updating species boundaries in the region. This species is occasionally implicated in minor crop damage due to its herbivorous habits, though it is less economically impactful than other congeners.^[11]^[77] Among other notable members, Teleogryllus occipitalis is a widespread pest across tropical and temperate Asia, extending to Australia and New Zealand, where it inflicts serious damage to pastures and grasslands as a foliage feeder. Additionally, Teleogryllus rohinae, newly described in 2021 from Kerala, India, represents an emerging species in the genus, identified through detailed morphological and molecular examination that also refined the taxonomy of related Indian Teleogryllus.^[66]^[2]^[77]

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genetic control of the mutation 'flatwing' that renders male ... - PubMed
Rapid evolutionary change in a sexual signal: genetic control of the mutation 'flatwing' that renders male field crickets (Teleogryllus oceanicus) mute.
[42]
Difference in calling song of three field crickets of the genus ...
My results show similarities and differences in the calling songs of three Teleogryllus species that are distributed across the Japanese Archipelago.
[43]
Divergent mechanisms of acoustic mate recognition between closely ...
We tested how females of field cricket sister species evaluate male song. The species used a mix of shared and different signal recognition mechanisms.
[44]
Difference in calling song of three field crickets of the genus ...
Aug 8, 2025 · The character of egg diapause may or may not be responsible for eliminating precocious adults. The size trend might have been molded by the ...
[45]
The Mating Behavior of Teleogryllus commodus (Walker) and its ...
Aug 6, 2025 · The mating stage initiates with a calling or courtship song and ends with spermatophore extrusion, while the RS begins with spermatophore ...Missing: papers | Show results with:papers
[46]
Large Numbers of Matings Give Female Field Crickets a Direct ...
Oct 20, 2009 · Female crickets can potentially gain both direct and indirect benefits from mating multiple times with different males.
[47]
Oviposition behaviour of the cricket Teleogryllus commodus
The sequential steps of oviposition behaviour in Teleogryllus commodus are: searching, positioning, penetration of ovipositor, short lift of ovipositor, ...
[48]
Black field cricket (Teleogryllus commodus) oviposition and egg ...
The main oviposition period began in March with peaks occurring in March and April following high rainfall and culminating in a maximum density in April or May.Missing: laying | Show results with:laying
[49]
Free amino acid changes associated with diapause in the egg of the ...
Abstract. The free amino acids in the diapausing egg of Teleogryllus commodus were determined during the course of its development from oviposition to eyespot ...Missing: laying | Show results with:laying
[50]
Identification of the juvenile hormone from the cricket, Teleogryllus ...
In the cricket, Teleogryllus commodus, eggs, haemolymph of 7th and 8th (last)-larval instars, and haemolymph of adults of both sexes contain only juvenile ...
[51]
Artificial Diet for Mass Rearing the Emma Field Cricket, Teleogryllus ...
Nymph of the emma field cricket, Teleogryllus emma, were reared on several types of artificial diets. The development period of nymphs were 55.4 days when ...<|control11|><|separator|>
[52]
Activity‐aggression behavioural syndromes exist in males but not in ...
Oct 18, 2023 · In this study, we conducted repeated measurements of activity and aggression in male and female field crickets Teleogryllus emma, providing ...
[53]
The influence of diet and environment on the gut microbial ... - NIH
We found that both environment and diet greatly altered the structure of the gut bacterial community. Wild crickets had greater gut microbial diversity.
[54]
How dietary protein and carbohydrate influence field cricket ...
Our findings revealed that male crickets developed significantly faster and grew larger when they were reared on a protein-rich diet.
[55]
Pasture production losses from black field cricket (Teleogryllus ...
Jan 20, 2012 · In the dry 1979, 1982, and 1983 years, cricket populations were moderate (8–22/m2) and significantly affected pasture production. Responses ...
[56]
The contribution of hindgut bacteria to dietary carbohydrate ...
Gut bacteria in crickets aid the insect's ability to utilize a wider range of dietary carbohydrates by responding to changes in dietary sources.
[57]
Risks of calling by the field cricket Teleogryllus oceanicus; potential ...
Feb 28, 2006 · Anti-predator defences and ecology of Neotropical forest katydids, especially the Pseudophyllinae. In The Tettigoniidae: biology ...
[58]
Risks of calling by the field cricket Teleogryllus oceanicus
Apr 1, 1998 · Sensory ecology of predator–prey interactions: responses of the AN2 interneuron in the field cricket, Teleogryllus oceanicus to the ...
[59]
Teleogryllus oceanicus - an overview | ScienceDirect Topics
Teleogryllus oceanicus is defined as a species of cricket characterized by male individuals that produce song through a mechanism involving a toothed file ...Missing: coloration | Show results with:coloration
[60]
Acoustically‐orienting parasitoids in calling and silent males of the ...
Acoustically-orienting parasitoids in calling and silent males of the field cricket Teleogryllus oceanicus ... Department of Biology, University of California, ...
[61]
Species-Recognition in the Field Cricket, Teleogryllus oceanicus
Predators are recognized largely on the basis of spectral frequencies that are contained in their acoustic signals. Puffs of air and very low frequencies ...
[62]
Stridulation - an overview | ScienceDirect Topics
Stridulation produces sound by frictional mechanisms, involving the movement of two specialised body parts against each other in a systematically coupled way ( ...
[63]
Insecticide baits for control of the black field cricket (Teleogryllus ...
Jan 17, 2012 · Maldison treated sawdust bait was effective at high cricket densities. Pirimiphos-methyl, fenitrothion, and decamethrin gave kills comparable to ...Missing: affecting | Show results with:affecting
[64]
Artificial light at night and temperature as combined stressors on the ...
The Pacific field cricket is an ectothermic, largely nocturnal species, which is distributed across urban and rural areas of the western and northern coasts of ...<|separator|>
[65]
(PDF) Geographical Variation in Diapause Intensity and Threshold ...
Aug 5, 2025 · The results showed that the diapause intensity for eggs of T. emma was stronger for the Changsha population at lower latitude than for the ...
[66]
Teleogryllus (Brachyteleogryllus) occipitalis (Serville, 1838)
Teleogryllus is commonly known as black field cricket. Species of this genus are reported as a serious pasture pest in Australia and the warmer northern regions ...
[67]
A review of Gryllidae (Grylloidea) with the description of one new ...
Teleogryllus is commonly known as black field cricket. Species of this genus are reported as a serious pasture pest in Australia and the warmer northern regions ...
[68]
Teleogryllus (Macroteleogryllus) Gorochov, 1985
The Orthoptera Species File (OSF) is a taxonomic database of the world's Orthoptera (grasshoppers, katydids, crickets, and related insects) both living and ...Missing: characteristics | Show results with:characteristics
[69]
http://orthoptera.speciesfile.org/Common/basic/Taxa.aspx?TaxonNameID=1122674
[70]
Silent night: adaptive disappearance of a sexual signal in a ... - NIH
We have collected T. oceanicus on Oahu, Kauai and the Big Island of Hawaii regularly since 1991. We localize calling males by sound and thoroughly scan ...
[71]
Rapid parallel adaptation despite gene flow in silent crickets - Nature
Jan 4, 2021 · ... habitat. In contrast, introgressive hybridisation between different ... (Teleogryllus oceanicus). Evolution 70, 82–97 (2016). Article ...
[72]
Ultrastructural changes to the midgut of the black field cricket ...
The black field cricket, Teleogryllus commodus, provides a typical example. This insect, which is a significant insect pest of pasture in New Zealand and ...
[73]
Ascending auditory interneurons in the cricket Teleogryllus ...
Ascending auditory interneurons of the cricket, Teleogryllus commodus (Walker), were investigated using simultaneous intracellular and extracellular recording ...
[74]
Activity‐aggression behavioural syndromes exist in males but not in ...
Oct 18, 2023 · In this study, we conducted repeated measurements of activity and aggression in male and female field crickets Teleogryllus emma, providing ...
[75]
Activity‐aggression behavioural syndromes exist in males but ... - NIH
Oct 18, 2023 · Sexually antagonistic selection, sexual dimorphism, and the resolution of intralocus sexual conflict. ... genus Teleogryllus: The role in ...
[76]
Seasonal and geographical adaption of two field crickets in China ...
Oct 24, 2017 · Teleogryllus emma (Ohmachi and Matsumura) and T. occipitalis (Serville) are widely distributed in east Asia, but their distribution and life ...
[77]
Jain sp. nov. and a key for Teleogryllus species from India ... - PubMed
In addition, we revise the description of the two widespread Teleogryllus species, i.e., T. mitratus (Burmeister, 1838) and T. occipitalis (Serville, 1838) and ...