Stalk-eyed Flies Research Articles

Stalk-eyed flies carrying a driving X chromosome compensate by increasing fight intensity

Exaggerated ornaments provide opportunities to understand how selection can operate at different levels to shape the evolution of a trait. While these features aid their bearer in attracting mates or fending off competitors, they can also be costly and influenced by the environment and genetic variation. The eyestalks of the stalk-eyed fly, Teleopsis dalmanni, are of interest because eyestalk length is the target of both intra- and intersexual selection and is also reduced by loci on a highly-divergent sex ratio X chromosome (XSR), a meiotic driver accounting for up to 30% of wild X chromosomes. Male stalk-eyed flies fight to control access to females and over food using a combination of low-intensity displays and high-intensity physical fights. We staged, filmed, and scored contests between pairs of eyespan-matched males to evaluate whether X chromosome type impacts the behavior and outcome of aggressive interactions. While our results broadly match expectations from previous studies, we found that XSR males used more high-intensity behaviors than males carrying a non-driving, standard X chromosome (XST), particularly when their eyestalks were of similar size or smaller than their opponents. Additionally, we found that when XSR males use high-intensity behaviors, they win more bouts than when they use low-intensity behaviors. Taken together, these results suggest that XSR impacts male aggressive behavior to compensate for the shorter eyestalks of XSR males and may help to explain how this selfish chromosome is maintained.

Yield Loss Quantification Due to Stalk-Eyed Fly (Diopsidae) Infestations on Rice Crops (Oryza Sativa) in Fogera Plain

Stalk-Eyed Flies (Diopsidae) pose a significant threat to rice crops (Oryza sativa), causing yield loss and affecting crop development. This study aims to quantify yield loss due to Stalk-Eyed Fly infestations and identify susceptible growth stages of rice crops to this insect. Field experiments were conducted to assess the yield loss of rice due to stalk eyed fly at Fogera, in 2021 and 2022. With the treatments Both Thiamethoxam seed treatment and Chlorpyrifos systemic foliar insecticide were applied to combat the infestation, with untreated varieties serving as controls. And the pot experiment was conducted to assess susceptibility of rice growth stage to the stalk eye fly artistically analyses, were employed to evaluate treatment impacts. With the treatments of different crop stages, Seedling Stage, Tillering Stage, Stem Elongation Stage, Panicle Initiation Stage, Booting, Heading, Flowering. The effect of rice growth stage on stalk eyed fly infestation showed that there is statistically significant difference among the different growth stage, tillering stage appears to be the most susceptible to Stalk-Eyed Fly infestations in terms of the impact on tiller growth in rice crops. During this stage, the mean percentage change of tillers is the highest at 59.3%, indicating a substantial impact of infestations on tiller growth. This suggests that rice crops are particularly vulnerable to stalked fly infestations during the tillering stage, highlighting the importance of effective pest management strategies during this critical growth phase to mitigate potential yield losses. In the field experiment, significant variations in yield loss were observed across treatments. The presence of dead hearts, indicative of infestation, varied notably between treated and untreated rice. Rice varieties incorporating pesticide applications demonstrated lower dead heart percentages, suggesting there is rice yield loss if the stalk-eyed fly is not controlled. Notably, treatments influenced grain yield, with insect protection measures resulting in higher yields and lower yield loss compared to controls. In conclusion, stalk-eyed fly infestation impacts rice crop productivity, particularly during vulnerable growth stages. Pesticide applications show promise in reducing infestation severity and mitigating yield loss. We recommend implementing targeted treatment strategies, focusing on susceptible growth stages, to effectively manage infestations and optimize rice crop yields.

Digest: A sex chromosome driver without a sperm deficit.

Meiotic drivers that act during spermatogenesis derive a transmission advantage by disabling sperm that do not carry the driver, often leading to substantially reduced overall sperm number and function. A new study by Bates et al. shows no sperm deficit for a driver in a stalk-eyed fly, in contrast to a related species. This observed sperm compensation is possibly due to secondary testes-expanding mutations linked to the driving genomic locus.

Close to complete conservation of the brachyceran opsin repertoire in the stalk-eyed fly Teleopsis dalmanni.

Due to the unique morphology of their adult visual system, stalk-eyed flies represent an important model of exaggerated trait evolution through sexual selection. Early physiological measurements indicated wavelength sensitivity peaks in the ultraviolet (360 nm), blue (450), blue-green (490 nm), and red (>550 nm) ranges in the compound eye retina of the stalk-eyed fly Teleopsis dalmanni, consistent with the trichromatic color and broad range motion detection vision system of brachyceran Diptera. A previous study of dipteran opsin gene diversification, however, detected only homologs of members of the long wavelength range sensitive opsin subfamilies Rh2 and Rh6 in T. dalmanni. Here, I report findings from analyzing the most recent T. dalmanni genome assembly, which revealed the conservation of most brachyceran opsin homologs except for the UV wavelength range-sensitive homolog Rh4. These results and other examples highlight the caution that needs to be applied to gene loss conclusions.

Compensation for a costly ornament depends on the development of flight performance in stalk-eyed flies

Several species of stalk-eyed flies exhibit exaggerated sexual dimorphism where females favor males with longer eyespans. Longer eyespan increases a fly’s moment of inertia, and may, therefore, impact flight behavior and fitness, specifically maneuverability and predator evasion. However, these putative costs may be ameliorated by co-selection for compensatory traits, as flies with longer eyespans tend to have larger thoraces and wings, which allows them to perform turns similar to flies with shorter eyespans. Furthermore, the capacity to compensate for a potentially costly ornament may not be fixed across the life-history of the adult stage, as stalk-eyed flies achieve sexual maturity at 3-4 weeks of age, accompanied by significant growth of reproductive tissues and organs. Thus, growth of the abdomen and body mass over time may impose constraints on flight performance that may affect whether an adult reaches the age of reproductive viability. The purpose of this study was to investigate the flight performance of stalk-eyed flies and its relationship to body morphology and development. The flight performance of 1-to-30 day oldTeleopsis dalmanni(n=124) andDiasemopsis meigenii(n=83) were assessed by presenting normoxic, variable-density mixtures of heliox (O2, N2and He) in 10% increments ranging from air to pure heliox; the least-dense gas allowing flight represented maximal performance. Flight kinematics were analyzed using high-speed (5930fps) videography. Immediately following flight assessment, flies were euthanized, photographed, dissected and weighed. In both species, total body mass, thorax and abdominal mass increased across age. Wing kinematics and maximal flight capacity were associated with thorax mass, and increased with age as flies became heavier. Although flies with longer eyespans were indeed heavier, they had larger wings and thoraces; however, maximal flight capacity and kinematics were generally independent of eyespan. Thus, bearing long eye-stalks did not impair flight performance, nor did the increase in mass attributable to reproductive maturation. Instead, variation in flight performance appears associated with the development of the flight motor, and improved ratio of thorax-to-total mass, across age.

Meiotic drive does not impede success in sperm competition in the stalk-eyed fly, Teleopsis dalmanni.

Male X-linked meiotic drive systems, which cause the degeneration of Y-bearing sperm, are common in the Diptera. Sperm killing is typically associated with fitness costs that arise from the destruction of wildtype sperm and collateral damage to maturing drive sperm, resulting in poor success under sperm competition. We investigate X-linked meiotic drive fertility in the stalk-eyed fly, Teleopsis dalmanni. Drive male paternity was measured in double mating trials under sperm competition against a wildtype male. Drive males sired the same number of offspring as wildtype males, both when mated first or second. This is the first evidence that drive males can compete equally with non-drive males in double matings, challenging the assumption that drive males inevitably suffer reduced fertility. The finding is in accord with previous work showing that the number of sperm per ejaculate transferred to females during non-competitive single matings does not differ between drive and wildtype males, which is likely due to the adaptive evolution of enlarged testes in drive males. Future experiments will determine whether the competitive ability of drive males is maintained under higher rates of female remating likely to be experienced in nature.

X chromosome drive is constrained by sexual selection and influences ornament evolution.

Experimental evolution provides an integrative method for revealing complex interactions among evolutionary processes. One such interaction involves sex-linked selfish genetic elements and sexual selection. X-linked segregation distorters, a type of selfish genetic element, influence sperm transmission to increase in frequency and consequently alter the population sex ratio and the opportunity for sexual selection, while sexual selection may impact the spread of X-linked distorters. Here we manipulated sexual selection by controlling female mating opportunities and the presence of a distorting X chromosome in experimental lines of the stalk-eyed fly, Teleopsis dalmanni, over 11 generations. We find that removal of sexual selection leads to an increase in the frequency of the X-linked distorter and sex ratio across generations and that post-copulatory sexual selection alone is sufficient to limit the frequency of distorters. In addition, we find that male eyestalk length, a trait under pre-copulatory sexual selection, evolves in response to changes in the strength of sexual selection with the magnitude of the response dependent on X chromosome type and the frequency of distorting X chromosomes. These results reveal how a selfish X can interact with sexual selection to influence the evolution of sexually selected traits in multiple ways.

Impacts of Sex Ratio Meiotic Drive on Genome Structure and Function in a Stalk-Eyed Fly.

Stalk-eyed flies in the genus Teleopsis carry selfish genetic elements that induce sex ratio (SR) meiotic drive and impact the fitness of male and female carriers. Here, we assemble and describe a chromosome-level genome assembly of the stalk-eyed fly, Teleopsis dalmanni, to elucidate patterns of divergence associated with SR. The genome contains tens of thousands of transposable element (TE) insertions and hundreds of transcriptionally and insertionally active TE families. By resequencing pools of SR and ST males using short and long reads, we find widespread differentiation and divergence between XSR and XST associated with multiple nested inversions involving most of the SR haplotype. Examination of genomic coverage and gene expression data revealed seven X-linked genes with elevated expression and coverage in SR males. The most extreme and likely drive candidate involves an XSR-specific expansion of an array of partial copies of JASPer, a gene necessary for maintenance of euchromatin and associated with regulation of TE expression. In addition, we find evidence for rapid protein evolution between XSR and XST for testis expressed and novel genes, that is, either recent duplicates or lacking a Dipteran ortholog, including an X-linked duplicate of maelstrom, which is also involved in TE silencing. Overall, the evidence suggests that this ancient XSR polymorphism has had a variety of impacts on repetitive DNA and its regulation in this species.

Meiotic drive adaptive testes enlargement during early development in the stalk-eyed fly.

The sex ratio (SR) X-linked meiotic drive system in stalk-eyed flies destroys Y-bearing sperm. Unlike other SR systems, drive males do not suffer fertility loss. They have greatly enlarged testes which compensate for gamete killing. We predicted that enlarged testes arise from extended development with resources re-allocated from the accessory glands, as these tend to be smaller in drive males. To test this, we tracked the growth of the testes and accessory glands of wild-type and drive males over 5-6 weeks post-eclosion before males attained sexual maturity. Neither of the original predictions is supported by these data. Instead, we found that the drive male testes were enlarged at eclosion, reflecting a greater allocation of resources to the testes during pupation. Testes grow at a higher rate during early adult development in drive males, but there was no evidence that this retards the growth of the accessory glands. Further experiments are proposed to investigate whether smaller accessory glands only arise in drive males post-copulation or when flies are subjected to nutritional stress. Our experimental findings support the idea that enlarged testes in drive males arise as an adaptive allocation of resources to traits that enhance male reproductive success.

The First Biological Portrait of Stalk-Eyed Fruit Flies: Life History, Reproductive Biology and Host Use Patterns in Pelmatops spp. (Diptera: Tephritidae)

Abstract The stalk-eyed fruit flies, with their eyes borne at the ends of long stalks, are distinctly different from all other members of the family Tephritidae (Diptera). They resemble stalk-eyed flies (Diptera, Diopsidae) but they are much larger and their antennae are located in the middle of the head instead of on the eye stalks. The stalk-eyed fruit flies are represented by two genera (Pelmatops Enderlein and Pseudopelmatops Shiraki) mainly found in the Oriental tropics and subtropics, but their basic biology remains poorly documented. Here, we describe the life history, reproductive biology, and host use patterns of Pelmatops spp. (mainly P. ichneumoneus (Westwood)). These flies used two local brambles, Rubus setchuenensis and R. multibracteatus (Rosales, Rosaceae), as hosts, with females laying eggs below the epidermal tissue. The larvae bore into the stem, where they feed, eventually dropping to the ground to pupate in the soil. We describe the pupal morphology and eclosion, including the elongation of their eye stalks, feeding, mating, and agonistic behavior in adults. We observed mating between female P. ichneumoneus and male P. tangliangi and tentatively suggest that the two species could be conspecific. Our work presents the first detailed report on the biology of stalk-eyed fruit flies and it lays a significant foundation for future studies on the ecology and evolution of this group.

Differences in energy source storage in eye stalks between two species of stalk-eyed flies, Sphyracephala detrahens and Cyrtodiopsis dalmanni

Some diopsid flies have sexually dimorphic eye stalks that are assumed to require considerable nutrition for growth but are advantageous in competition and courtship. According to the handicap theory, the eye span in some dimorphic species serves as a reliable signal of individual quality to an opponent. However, it is not well understood how well eye span represents energy source storage. In this study, we focused on two species: Sphyracephala detrahens, which has weak dimorphism, and Cyrtodiopsis dalmanni, which has moderate dimorphism. We found that the eye stalks of the former species contained more fat bodies than those of the latter species. When the flies were starved, the fat body cells in the eye stalks underwent autophagy. A strong positive correlation was consistently found between eye span and starvation tolerance for S. detrahens, while a weak correlation was found for C. dalmanni. Furthermore, starvation decreased the contest winning rate between S. detrahens pairs with similar eye spans. These findings suggest that the presentation of resource holding potential may be larger than the actual storage ability and that the fidelity of nutritional storage signaling varies; the signal presented by S. detrahens is more reliable than that presented by C. dalmanni.

Lack of discrimination of sex and maturity of conspecifics in the copulation attempts of the male stalk-eyed fly, Sphyracephala detrahens (Diptera: Diopsidae)

Among insects, males have evolved the ability to discriminate potential mates to avoid vain mating attempts. In Diptera, courtship and mating behaviors of species that do not discriminate potential mates have rarely been studied. In this study, we investigated copulation attempts of the stalk-eyed fly, Sphyracephala detrahens males, which do not engage in any observable pre-copulatory courtship behavior. We found that sexually mature males attempted to copulate with mature males and immature adults of both sexes, as frequently as with mature females. Successful copulation only occurred with mature females. Immature females rejected mounting males by vibrating their bodies and immature and mature males by incurving their abdomen downward. Comparison of the cuticular hydrocarbon components of individuals of different sexes and maturity levels indicated that the cuticular hydrocarbon profiles were similar regardless of the sex and sexual maturity. Therefore, we suggest that visual or chemical information are of little use for males S. detrahens in discriminating receptive conspecific mates. Since elaborate mate discrimination behaviors lead to additional time and energy costs when discrimination is difficult, S. detrahens may increase reproductive success simply by increasing the number of copulation attempts. Digital video images related to this article are available at http://www.momo-p.com/showdetail-e.php?movieid=momo211123sd01a, http://www.momo-p.com/showdetail-e.php?movieid=momo211123sd02a, http://www.momo-p.com/showdetail-e.php?movieid=momo211123sd03a, and http://www.momo-p.com/showdetail-e.php?movieid=momo211123sd04a.

A review of Madagopsina Feijen, Feijen & Feijen (Diptera, Diopsidae) with description of a new species, key to the species, and discussion of intrageneric relationships.

For the recently established genus Madagopsina (Diopsidae, stalk-eyed flies), Madagopsinamakayensis Feijen, Feijen & Feijen, sp. nov. is described from Madagascar. A concise catalogue is given for the genus and an identification key is presented for its six species. The differential character states are listed for the two species groups of the genus: the Madagopsinaapollo species group and the Madagopsinaapographica species group. The intrageneric relations are discussed based on morphology, geometric morphometrics analysis of wing shape, and allometric data for eye span against body length. Each of these three procedures places the new species in the M.apollo species group with Madagopsinaparvapollina as its closest relative. New records are presented for M.apographica and M.parvapollina.

Meiotic drive does not cause condition-dependent reduction of the sexual ornament in stalk-eyed flies.

Meiotic drive systems are associated with low-frequency chromosomal inversions. These are expected to accumulate deleterious mutations due to reduced recombination and low effective population size. We test this prediction using the 'sex-ratio' (SR) meiotic drive system of the Malaysian stalk-eyed fly Teleopsis dalmanni. SR is associated with a large inversion (or inversions) on the X chromosome. In particular, we study eyespan in males carrying the SR chromosome, as this trait is a highly exaggerated, sexually dimorphic trait, known to have heightened condition-dependent expression. Larvae were raised in low and high larval food stress environments. SR males showed reduced eyespan under the low and high stress treatments, but there was no evidence of a condition-dependent decrease in eyespan under high stress. Similar but more complex patterns were observed for female eyespan, with evidence of additivity under low stress and heterosis under high stress. These results do not support the hypothesis that reduced sexual ornament size in meiotic drive males is due to a condition-dependent response to the putative increase in mutation load. Instead, reduced eyespan likely reflects compensatory resource allocation to different traits in response to drive-mediated destruction of sperm.

Feats of Strength

Feats of Strength is well worth reading for any interested student of biology: a pleasurable read and fascinating analysis of amazing examples of biological adaptation. The theme is the central concept of biology itself: the driving force of evolutionary fitness (successful transfer of genes to the next generation). The author, a scientist who obviously loves biology, provides the reader with clear and fascinating examples of evolutionary fitness, along with interesting descriptions of the research behind our understanding of these traits. Further, Lailvaux is clearly interested in asking the question “Why?” – why has this trait evolved – and in developing research methods to find the answer.Each chapter examines a theme of biological fitness (survival and successful reproduction): “Running, Jumping, and Biting,” “Eating and Not Being Eaten,” “Lovers and Fighters,” and so on. Final chapters address the complex question of “nature versus nurture” in evolution and phenotypic expression, as well as applications in understanding human evolution. Examples lead to frequent mental exclamations of “No way!” or a need for the reader to find a family member to read a choice tidbit out loud. The author’s love of biology is evident throughout, as he presents stalk-eyed flies, migrating swifts, mating spiders (a highly risky business for the males), and racing lizards in his overarching discussion of animal adaptation for survival and reproduction. The overarching imperative of reproductive fitness is evident in examples such as the wolverine frog, which fights to the death for reproductive rights by creating claws by “breaking the tips of its own fingers such that sharp broken bones pierce the flesh”; the mantis shrimp, which can break aquarium glass with a snap of its claw; and the cellular structure of snakes’ muscle, which gives them extra strength. Key concepts about evolution are highlighted, including that adaptation is a functional tradeoff (excellence in one trait often comes at a cost to other traits), that organisms must balance their “energy budgets” (every physical or behavioral adaptation has both a benefit and a cost), and that “evolution is a tinkerer.”Lailvaux’s easy, conversational writing style makes his delight in his material obvious. Particularly evident is his interest in observing a phenomenon, asking why, and figuring out how to research the question. His descriptions of research highlight both elegant solutions to research problems (including lizards in mink coats!) and the difficulties of obtaining research results in a true field setting, or in applying results from controlled experiments to conditions outside the laboratory. There are some flaws in this generally excellent presentation. Lailvaux’s descriptions are occasionally marred by analogies to movies or sports that are not necessarily helpfully familiar to the reader. In several instances, the author alludes to videos that clearly demonstrate the phenomenon under discussion, but without specifically naming the video or including the link, leaving an interested reader to hunt through YouTube to find the material. His final chapter on “Mice and Men” is less clearly organized and presented, perhaps as a reflection of the more theoretical and fluid nature of the research involved. Despite these issues, Feats of Strength is an excellent recommendation for any interested student or teacher of biology and the evolutionary process.

Handicap theory is applied to females but not males in relation to mate choice in the stalk-eyed fly Sphyracephala detrahens

Handicap theory explains that exaggeratedly developed sexual traits become handicaps but serve as honest signals of quality. Because very weak signals are less likely to provide benefits than to simply incur costs, it is interesting to elucidate how sexual traits are generated and developed during evolution. Many stalk-eyed fly species belonging to tribe Diopsini exhibit marked sexual dimorphism in their eye spans, and males with larger eye spans have larger bodies and reproductive capacities, which are more advantageous in terms of contests between males and acceptance for mating by females. In this study, we investigated the role of eye span in a more primitive species, Sphyracephala detrahens, in tribe Sphyracephalini with less pronounced sexual dimorphism. Male-male, female-female, and male–female pairs showed similar contests influenced by eye span, which was correlated with nutrition and reproductive ability in both sexes. During mating, males did not distinguish between sexes and chose individuals with larger eye spans, whereas females did not choose males. However, males with larger eye spans copulated repeatedly. These results indicate that, in this species, eye span with a small sexual difference does not function in sex recognition but affects contest and reproductive outcomes, suggesting the primitive state of sexual dimorphism.

The evolutionary history of mariner elements in stalk-eyed flies reveals the horizontal transfer of transposons from insects into the genome of the cnidarian Hydra vulgaris.

The stalk-eyed flies (Diopsidae, Diptera) are a family of approximately 100 species of calypterate dipterans, characterised by extended head capsules. Species within the family have previously been shown to possess six subfamilies of mariner transposons, with nucleotide substitution patterns suggesting that at least two subfamilies are currently active. The vertumnana subfamily has been shown to have been involved in a horizontal transfer event involving Diopsidae and a second dipteran family in the Tephritidae. Presented here are cloned and sequenced mariner elements from three further diopsid species, in addition to a bioinformatic analysis of mariner elements identified in transcriptomic and genomic data from the genus Teleopsis. The newly identified mariner elements predominantly fall into previously recognised subfamilies, however the publicly available Teleopsis data also revealed a novel subfamily. Three of the seven identified subfamilies are shown to have undergone horizontal transfer, two of which appear to involve diopsid donor species. One recipient group of a diopsid mariner is the Bactrocera genus of tephritid flies, the transfer of which was previously proposed in an earlier study of diopsid mariner elements. The second horizontal transfer, of the mauritiana subfamily, can be traced from the Teleopsis genus to the cnidarian Hydra vulgaris. The mauritiana elements are shown to be active in the recipient H. vulgaris and transposase expression is observed in all body tissues examined in both species. The increased diversity of diopsid mariner elements points to a minimum of four subfamilies being present in the ancestral genome. Both vertical inheritance and stochastic loss of TEs have subsequently occurred within the diopsid radiation. The TE complement of H. vulgaris contains at least two mariner subfamilies of insect origin. Despite the phylogenetic distance between donor and recipient species, both subfamilies are shown to be active and proliferating within H. vulgaris.

A revision of the genus Teleopsis Rondani (Diptera, Diopsidae) in Sri Lanka with descriptions of two new species and a review of the other stalk-eyed flies from the island.

The literature on Sri Lankan Diopsidae is reviewed. Eight Diopsidae are now known to occur in Sri Lanka, five species in the genus Teleopsis and one species each in the genera Sphyracephala, Diopsis, and Cyrtodiopsis. The presence of Cyrtodiopsis requires confirmation to exclude the possibility of mislabelling. All five Teleopsis species are endemic, as are the Diopsis species and probably the Cyrtodiopsis species. Only Sphyracephala bipunctipennis Senior-White has a larger distribution as it also occurs in India. A key is presented for the Diopsidae of Sri Lanka. Three Teleopsis species were already known to occur in Sri Lanka: T. ferruginea Röder, T. krombeini Feijen and T. maculata Feijen. These species form the T. ferruginea species group. Two new species are now described for this group: Teleopsis neglectasp. nov. and Teleopsis sororasp. nov.Teleopsis ferruginea is redescribed, as an earlier redescription turned out to be based on a series of specimens of its sister species T. sororasp. nov. The other three Diopsidae of Sri Lanka are listed and illustrated. Allometric aspects of the five Teleopsis species are discussed. Three Teleopsis species are sexually dimorphic with regard to eye span, while two species are monomorphic. It is assumed that sexual dimorphism developed independently in the T. ferruginea species group. This brings the number of known cases of independent development of sexual dimorphism in the Diopsidae to ten.

Maintenance of Fertility in the Face of Meiotic Drive.

Selfish genetic elements that gain a transmission advantage through the destruction of sperm have grave implications for drive male fertility. In the X-linked meiotic drive system (SR) of a stalk-eyed fly, we found that SR males have greatly enlarged testes and maintain high fertility despite the destruction of half of their sperm, even when challenged with fertilizing large numbers of females. Conversely, we observed reduced allocation of resources to the accessory glands that probably explains the lower mating frequency of SR males. Body size and eye span were also reduced, which are likely to impair viability and precopulatory success. We discuss the potential evolutionary causes of these differences between drive and standard males.

The stalk-eyed fly as a model for aggression - is there a conserved role for 5-HT between vertebrates and invertebrates?

Serotonin (5-HT) has largely been accepted to be inhibitory to vertebrate aggression, whereas an opposing stimulatory role has been proposed for invertebrates. Herein, we argue that critical gaps in our understanding of the nuanced role of 5-HT in invertebrate systems drove this conclusion prematurely, and that emerging data suggest a previously unrecognized level of phylogenetic conservation with respect to neurochemical mechanisms regulating the expression of aggressive behaviors. This is especially apparent when considering the interplay among factors governing 5-HT activity, many of which share functional homology across taxa. We discuss recent findings using insect models, with an emphasis on the stalk-eyed fly, to demonstrate how particular 5-HT receptor subtypes mediate the intensity of aggression with respect to discrete stages of the interaction (initiation, escalation and termination), which mirrors the complex behavioral regulation currently recognized in vertebrates. Further similarities emerge when considering the contribution of neuropeptides, which interact with 5-HT to ultimately determine contest progression and outcome. Relative to knowledge in vertebrates, much less is known about the function of 5-HT receptors and neuropeptides in invertebrate aggression, particularly with respect to sex, species and context, prompting the need for further studies. Our Commentary highlights the need to consider multiple factors when determining potential taxonomic differences, and raises the possibility of more similarities than differences between vertebrates and invertebrates with regard to the modulatory effect of 5-HT on aggression.