Evolution Of Sexual Signals Research Articles

Rapid sexual signal diversification is facilitated by permissive females

The initial process by which novel sexual signals evolve remains unclear, because rare new variants are susceptible to loss by drift or counterselection imposed by prevailing female preferences.1,2,3,4 We describe the diversification of an acoustic male courtship signal in Hawaiian populations of the field cricket Teleogryllus oceanicus, which was brought about by the evolution of a brachypterous wing morph ("small-wing") only 6 years ago.5 Small-wing has a genetic basis and causes silence or reduced-amplitude signaling by miniaturizing male forewings, conferring protection against an eavesdropping parasitoid, Ormia ochracea.5 We found that wing reduction notably increases the fundamental frequency of courtship song from an average of 5.1 kHz to 6.4 kHz. It also de-canalizes male song, broadening the range of peak signal frequencies well outside normal song character space. As courtship song prompts female mounting and is sexually selected,6,7,8,9 we evaluated two scenarios to test the fate of these new signal values. Females might show reduced acceptance of small-wing males, imposing counterselection via prevailing preferences. Alternatively, females might accept small-wing males as readily as long-wing males if their window of preference is sufficiently wide. Our results support the latter. Females preferred males who produced some signal over none, but they mounted sound-producing small-wing males as often as sound-producing long-wing males. Indiscriminate mating can facilitate the persistence of rare, novel signal values. If female permissiveness is a general characteristic of the earliest stages of sexual signal evolution, then taxa with low female mate acceptance thresholds should be more prone to diversification via sexual selection.

Sexual signal evolution and patterns of assortative mating across an intraspecific contact zone.

Contact zones provide important insights into the evolutionary processes that underlie lineage divergence and speciation. Here, we use a contact zone to ascertain speciation potential in the red-eyed treefrog (Agalychnis callidryas), a brightly coloured and polymorphic frog that exhibits unusually high levels of intraspecific variation. Populations of A. callidryas differ in a number of traits, several of which are known sexual signals that mediate premating reproductive isolation in allopatric populations. Along the Caribbean coast of Costa Rica, a ~100 km contact zone, situated between two phenotypically and genetically divergent parent populations, contains multiple colour pattern phenotypes and late-generation hybrids. This contact zone provides the opportunity to examine processes that are important in the earliest stages of lineage divergence. We performed analyses of colour pattern variation in five contact zone sites and six parental sites and found complex, continuous colour variation along the contact zone. We found discordance between the geographic distribution of colour pattern and previously described genomic population structure. We then used a parental site and contact zone site to measure assortative mating and directional selection from naturally-occurring amplectant mating pairs. We found assortative mating in a parental population, but no assortative mating in the contact zone. Furthermore, we uncovered evidence of directional preference towards the adjacent parental phenotype in the contact zone population, but no directional preference in the parent population. Combined, these data provide insights into potential dynamics at the contact zone borders and indicate that incipient speciation between parent populations will be slowed.

Peacock spiders prefer image statistics of average natural scenes over those of male ornamentation

Abstract The origins of preferences that drive the evolution of arbitrary sexual signals have been hotly debated for more than 150 years. An emerging but little-tested theory, efficient coding theory, proposes that male visual courtship displays are adapted to pre-existing processing biases shaped by the statistical properties of the natural environment. Natural scenes show strong spatial correlations with average amplitudes of spatial frequencies falling with an average spectral slope of –1 and humans have been shown to prefer random amplitude spectrum images that possess similar slopes. It has been proposed that other animals may also prefer the statistics of their natural environment and that this preference drives the evolution of sexual signaling displays. Here, we measure the spectral slope of the male display pattern of the Australian peacock jumping spider Maratus spicatus and test for a general preference toward that slope. We present spiders (male, female and juvenile) with random images of the male slope of –1.7 compared with: (a) a shallower slope of –1.0 and (b) a steeper slope of –2.3. Spiders spent more time oriented toward the shallower slope than toward the male slope and spent the same amount of time oriented toward the male slope and the steeper slope. Our results indicate that spiders, like humans, prefer the average natural slope of –1, suggesting that this is likely the slope typically found in their natural habitat. Rather than exploiting a potential processing bias it seems that males have evolved slopes that contrast with the visual background to enhance conspicuousness.

Decoupling of sexual signals and their underlying morphology facilitates rapid phenotypic diversification.

How novel phenotypes evolve is challenging to imagine because traits are often underlain by numerous integrated phenotypic components, and changes to any one form can disrupt the function of the entire module. Yet novel phenotypes do emerge, and research on adaptive phenotypic evolution suggests that complex traits can diverge while either maintaining existing form-function relationships or through innovations that alter form-function relationships. How these alternate routes contribute to sexual signal evolution is poorly understood, despite the role of sexual signals in generating biodiversity. In Hawaiian populations of the Pacific field cricket, male song attracts both female crickets and a deadly acoustically orienting parasitoid fly. In response to this conflict between natural and sexual selection, male crickets have evolved altered wing morphologies multiple times, resulting in loss and dramatic alteration of sexual signals. More recently, we and others have observed a radical increase in sexual signal variation and the underlying morphological structures that produce song. We conducted the first combined analysis of form (wing morphology), function (emergent signal), and receiver responses to characterize novel variation, test alternative hypotheses about form-function relationships (Form-Function Continuity vs. Form-Function Decoupling), and investigate underlying mechanistic changes and fitness consequences of novel signals. We identified three sound-producing male morphs (one previously undescribed, named "rattling") and found that relationships between morphology and signals have been rewired (Form-Function Decoupling), rapidly and repeatedly, through the gain, loss, and alteration of morphological structures, facilitating the production of signals that exist in novel phenotypic space. By integrating across a hierarchy of phenotypes, we uncovered divergent morphs with unique solutions to the challenge of attracting mates while evading fatal parasitism.

Multi‐night territorial behavior, chorus attendance, and mating success in red‐eyed treefrogs

AbstractFor many frog species that aggregate around ponds or streams, chorus attendance, the percentage of time or nights a given male is present and actively calling at an aggregation, is the strongest documented predictor of inter‐male variation in reproductive success in the wild. Males are, thus, thought to compete via endurance rivalry, where available energetic reserves and individual physiology interact to determine chorus tenure. Frogs often exhibit territorial behavior within these aggregations, and territorial status is likely to influence a male's rate of energy expenditure. While males of several anuran species have been shown to hold territories across nights, it is not well understood whether such calling site fidelity is correlated with chorus attendance or mating success. Using subdermal RFID (PIT) tags to minimize disturbance to chorus structure, we quantified site fidelity, chorus attendance, and mating success for all male red‐eyed treefrogs (Agalychnis callidryas) within a breeding aggregation in Panama across 50 consecutive nights. We found that nearly half of these males held territories across nights, that this cross‐night territorial behavior was highly correlated with chorus attendance, and that chorus attendance was, in turn, the strongest predictor of male mating success. Males were most faithful to calling sites containing vegetation contiguous with adjacent sites and were more likely to remain at a site if they were successful in acquiring a mate there on the previous night. To our knowledge, this is the first study linking male site fidelity to chorus attendance and mating success in anurans. While female mate choice is an established driver of lineage diversification and the evolution of sexual signals, agonistic interactions between males at breeding aggregations are well‐documented from a wide range of anuran taxa. The relationship between male–male interactions and mating success deserves broader research attention among anuran species.

How urbanization affects sexual communication.

Urbanization is rapidly altering landscapes worldwide, changing environmental conditions, and creating novel selection pressures for many organisms. Local environmental conditions affect the expression and evolution of sexual signals and mating behaviors; changes in such traits have important evolutionary consequences because of their effect on reproduction. In this review, we synthesize research investigating how sexual communication is affected by the environmental changes associated with urbanization—including pollution from noise, light, and heavy metals, habitat fragmentation, impervious surfaces, urban heat islands, and changes in resources and predation. Urbanization often has negative effects on sexual communication through signal masking, altering condition‐dependent signal expression, and weakening female preferences. Though there are documented instances of seemingly adaptive shifts in trait expression, the ultimate impact on fitness is rarely tested. The field of urban evolution is still relatively young, and most work has tested whether differences occur in response to various aspects of urbanization. There is limited information available about whether these responses represent phenotypic plasticity or genetic changes, and the extent to which observed shifts in sexual communication affect reproductive fitness. Our understanding of how sexual selection operates in novel, urbanized environments would be bolstered by more studies that perform common garden studies and reciprocal transplants, and that simultaneously evaluate multiple environmental factors to tease out causal drivers of observed phenotypic shifts. Urbanization provides a unique testing ground for evolutionary biologists to study the interplay between ecology and sexual selection, and we suggest that more researchers take advantage of these natural experiments. Furthermore, understanding how sexual communication and mating systems differ between cities and rural areas can offer insights on how to mitigate negative, and accentuate positive, consequences of urban expansion on the biota, and provide new opportunities to underscore the relevance of evolutionary biology in the Anthropocene.

Experimental evidence for female mate choice in a noctuid moth

Sexual signal evolution is shaped by whether only one or both sexes execute mate choice. When mate choice by both sexes is considered, the same signalling modality is generally inferred for males and females. In the noctuid moth Chloridea ( Heliothis ) virescens (Lepidoptera: Noctuidae), both sexes may be signallers and responders, as both emit a sex-specific pheromone. Male mate choice is based on the female sex pheromone, perceived via the antennae, and has been well documented. However, whether females choose partners and whether their choice is based on the male pheromone are unknown. Since female mate choice is expected when males vary in quality, we reared males on two different larval diets that affected their size, which correlated positively with their fitness. When given a choice, more females mated with larger than with smaller males, and these females produced more eggs and larvae. Female choice was not affected by the absolute amount or composition of the male pheromone. Moreover, we found that antennaless females mated as readily as intact females, indicating that antennal sensory input is not required for females to mate. To determine whether females make an active choice, we studied courtship behaviour in detail and observed that females determined the outcome of courtship by moving away from the male (avoidance) or by facilitating copulation with an abdominal bend (acceptance). Additionally, we discovered that tactile sensory stimuli may be involved during courtship. Because tactile interactions may mediate contact-based (chemical) communication, we also investigated putative pheromone components on moth legs, but found no differences between the sexes. Together, our study is the first comprehensive investigation of female mate choice in a heliothine moth. • In the noctuid moth Chloridea virescens , females mated more with larger males. • Larger males were higher quality mating partners than smaller males. • The quality and quantity of male hairpencil pheromone did not explain female choice. • Females showed avoidance and acceptance behaviour, and thus chose partners actively. • Male traits other than the hairpencil pheromone likely affect female choice.

What doesn't kill you makes you stronger: Detoxification ability as a mechanism of honesty in a sexually selected signal

Abstract Sexual selection leads to the expression and maintenance of colourful signals. The metabolic pathways to produce such signals often involve toxic byproducts that can reduce survival. However, rather than discarding these otherwise harmful byproducts, animals may use them by integrating them into sexually selected traits. We tested this using the damselfly Hetaerina americana, where males bear a red wing spot (RWS) that has evolved by intrasexual competition. By using confocal microscopy and several biochemical techniques, we determined that the RWS are generated by ommochrome pigments derived from tryptophan metabolism. Second, we injected a group of males with the toxic precursor of these ommochromes, 3‐hydroxy‐kynurenine (3‐Hk), confirming the toxicity of this compound in adult males. Finally, we showed that adult males injected with a median lethal concentration of 3‐Hk had more ommochromes in their RWS than controls but similar survival, suggesting that the deposition of ommochrome pigment in the wing counteracts the 3‐HK toxicity. Thus, we report that sexually selected pigmented signals may involve the co‐option of excreted compounds that could otherwise have lethal effects, a hypothesis we call ‘detoxifying ability signalling’. Our results provide new insights about the evolution of sexual signals, elucidating a mechanism for the evolution of honest indicators of quality that could have arisen due to natural selection.

Different underlying mechanisms drive associations between multiple parasites and the same sexual signal

Associations between parasite loads and sexual signal expression have long been the focus of research. However, our understanding of how sexual selection operates in the context of multiple parasite infections within the same host is still quite limited. We examined the expression of plumage coloration, which is sexually selected in North American barn swallows, Hirundo rustica erythrogaster , and tail streamer length, which is sexually selected in other barn swallow subspecies, in the context of eight different parasite infections. We found that two parasites, nest mites and Plasmodium , were associated with colour expression, but in opposite directions. Attractive males were less likely to have mites in their nests, but more likely to be infected with Plasmodium . We found that different underlying mechanisms were generating the links between these different parasites and the same colour signal. Males that invested more in colour expression were less likely to survive when infected with Plasmodium , suggesting a physiological mechanism linking colour to Plasmodium infections. However, we found no clear cost to males when examining nest mites, which primarily infect offspring. Instead, using experimental mite manipulations, we provide evidence for a behavioural mechanism, where territorial behaviour and male–male competition likely drive the association between colour expression and nest mite infections. We did not find associations between parasites and streamer length in this subspecies, suggesting that the links between divergent sexual signals and parasites may be quite flexible. These results suggest that the evolution of a single sexual signal can be shaped by several, even opposing, links with different parasite infections. • We examined associations between plumage colour and parasite loads in barn swallows. • Darker males had fewer nest mites but greater likelihood of Plasmodium infection. • Colour investment decreased survival when males were infected with Plasmodium. • Territorial behaviour likely drives colour expression–nest mite association. • Sexual signal evolution can be shaped by different links with multiple parasites.

When night never falls: female sexual signalling in a nocturnal insect along a latitudinal gradient

The environment can play an important role in animal communication by affecting signal transmission and detection. Variation in the signalling environment is expected to be especially pronounced in widely distributed species, potentially affecting how their signals are detected. Such environmental variability is presumably relevant for sedentary females of a nocturnal capital breeder, the European common glow-worm (Lampyris noctiluca), which produce green light during the night to attract flying males to mate. Being widely distributed in Europe, glow-worm populations are exposed to both rapidly descending, darker summer nights in the south, and slowly dimming, brighter summer nights further north, with the latter potentially posing challenges to the visibility of the female glow. To test how female signalling is affected by latitude, we sampled glowing females during summer nights along a latitudinal gradient in Finland, Northern Europe, and used a novel apparatus to measure the intensity and peak wavelength (hue/colour) of their glow. Surprisingly, females at higher latitudes, similar to those at lower latitudes, were commonly glowing during the brightest (and hence the shortest) nights of the year. Females also glowed brighter in more northern areas, partly due to their larger body size, whereas the colour of their glow was not associated with latitude. Since females glow even during midsummer, independent of latitude, the increase in glow intensity at higher latitudes presumably serves to maintain signal visibility in brighter signalling conditions. Overall, these findings highlight the influence of environmental conditions on the evolution of sexual signals, especially in the context of species distribution range.Significance statementWhen environmental conditions impact signal transmission and perception, local conditions can have a crucial role in shaping animal communication and signal evolution. To analyse how dark-dependant common glow-worm females cope with variable nocturnal light environments, we used a novel apparatus, presumably not applied to living animals before, to measure female glow intensity at various latitudes along a latitudinal gradient. Interestingly, females did not avoid signalling during the brightest summer nights, but instead, their glow intensity and body size both increased with latitude. These findings suggest that females can ensure visibility to mate-searching males over a range of local conditions. Our study therefore shows how females can adapt to environmental constraints on signal visibility, and how the expression of sexual signals is shaped not only by social interactions but also by the signalling environment.

The size of signal detection and emission organs in a synchronous firefly: sexual dimorphism, allometry and assortative mating.

The size of the organs responsible for emitting and detecting sexual communication signals is a likely target for selection. Communication via bioluminescent signals in synchronous fireflies is a promising model to test hypotheses regarding differences between males and females in the effect of the size of signal emission and detection organs on fitness components. Synchronous firefly species congregate in large numbers during the mating season, displaying bioluminescent signals aimed at potential mates during relatively short nightly periods. Operational sex ratios are male-biased and, thus, the so-called typical sex roles (indiscriminate males and choosy females) are expected to evolve. We studied the synchronous firefly Photinus palaciosi, a species that during the mating season congregates in forests of central Mexico offering a magnificent natural show that attracts numerous tourists. P. palaciosi females have reduced wings (brachyptery) and cannot fly. Our field study tested the hypothesis that the male-biased operational sex ratio and the short daily mating period result in strong male-male competition that selects for males with larger lanterns and larger eyes, and against male mate choice, whereas female-female mate competition is absent and, thus, no selection on lantern or eye size is expected. Even though lantern, eye or body size do not predict the probability of being found in copula for either sex, sexual dimorphism in these features, along with allometric slopes of lantern size and assortative mating in terms of relative lantern size, support not only the hypothesis of intense sexual selection among males, but the possibility of subtle mechanisms of sexual selection among females. Trade-offs between investment in signaling (lanterns) versus detection (eyes) structures, or with pressures different from sexual selection such as those imposed by predators, are also likely to be important in shaping the evolution of sexual signaling in these fireflies.

The evolution of sexual signaling is linked to odorant receptor tuning in perfume-collecting orchid bees

Sexual signaling is an important reproductive barrier known to evolve early during the formation of new species, but the genetic mechanisms that facilitate the divergence of sexual signals remain elusive. Here we isolate a gene linked to the rapid evolution of a signaling trait in a pair of nascent neotropical orchid bee lineages, Euglossa dilemma and E. viridissima. Male orchid bees acquire chemical compounds from their environment to concoct species-specific perfumes to later expose during courtship. We find that the two lineages acquire chemically distinct perfumes and are reproductively isolated despite low levels of genome-wide differentiation. Remarkably, variation in perfume chemistry coincides with rapid divergence in few odorant receptor (OR) genes. Using functional assays, we demonstrate that the derived variant of Or41 in E. dilemma is specific towards its species-specific major perfume compound, whereas the ancestral variant in E. viridissima is broadly tuned to multiple odorants. Our results show that OR evolution likely played a role in the divergence of sexual communication in natural populations.

Attractive male sticklebacks carry more oxidative DNA damage in the soma and germline.

Trade-offs between the expression of sexual signals and the maintenance of somatic and germline tissues are expected when these depend upon the same resources. Despite the importance of sperm DNA integrity, its trade-off with sexual signalling has rarely been explored. We experimentally tested the trade-off between carotenoid-based sexual coloration and oxidative DNA damage in skeletal muscle, testis and sperm by manipulating reproductive schedule (early vs. late onset of breeding) in male three-spined sticklebacks. Oxidative DNA damage was measured as the amount of 8-hydroxy-2-deoxyguanosine in genomic DNA. Irrespective of the experimentally manipulated reproductive schedule, individuals investing more in red coloration showed higher levels of oxidative DNA damage in muscle, testis and sperm during the peak breeding season. Our results show that the expression of red coloration traded off against the level of oxidative DNA damage possibly due to the competing functions of carotenoids as colorants and antioxidants. Thus, female sticklebacks may risk fertility and viability of offspring by choosing redder, more deteriorated partners with decreased sperm DNA integrity. The evolution of sexual signal may be constrained by oxidative DNA damage in the soma and germline.

Direct and indirect effects of sexual signal loss on female reproduction in the Pacific field cricket (Teleogryllus oceanicus).

Sexual signal evolution may present fitness consequences for the non-signaling sex due to shared genes and altered social conditions, but this is rarely studied in natural populations. On the Hawaiian Island of Kauai, most male Teleogryllus oceanicus (Pacific field crickets) lack the ability to sing because of a novel wing mutation (flatwing) that arose and spread in <20 generations. Obligately silent flatwing males have been highly successful because they avoid detection by a deadly, acoustically-orienting parasitoid fly. Little is known about how the flatwing mutation and resulting song-less acoustic environment affects female fitness. We found that Kauai females carrying the flatwing allele invested less in reproductive tissues and experienced more instances of mating failure than normal-wing-carrying females, though total offspring production did not differ between female genotypes. Females from Oahu (HI, where the parasitoid and flatwing also occur) and Mangaia (an island in the Cook Islands which harbors neither the parasitoid nor flatwing) invested less in reproductive tissues when reared in a song-less acoustic environment. Kauai females did not exhibit this plasticity, perhaps because they have experienced nearly song-less conditions for the past ~15years following the establishment of flatwing. We show that female T.oceanicus experience a mix of costly and beneficial effects of sexual signal loss, which should help maintain the wing polymorphism in the wild. Our results demonstrate that the non-signaling sex can experience a nuanced set of phenotypic consequences resulting from signal evolution, which can further shape dynamics of sexual signal evolution.

Purring Crickets: The Evolution of a Novel Sexual Signal.

Opportunities to observe contemporary signal change are incredibly rare but critical for understanding how diversity is created and maintained. We discovered a population of the Pacific field cricket (Teleogryllus oceanicus) with a newly evolved song (purring), different from any known cricket. Male crickets use song to attract females from afar and to court females once near. Teleogryllus oceanicus is well known for sexual signal evolution, as exemplified by a recent signal loss. In this study, we characterized the new purring sound and investigated the role of the purr in long-distance and short-distance communication. The purring sound differed from typical ancestral calls in peak frequency, amplitude, and bandwidth. Further, the long-distance purring song facilitated mate location, though the role of courtship purring song is less clear. Our discovery of purring male crickets is an unprecedented opportunity to watch the emergence of a newly evolved sexual signal unfold in real time and has potential to illuminate the mechanisms by which evolutionary novelties arise and coevolve between the sexes.

Limited flexibility in female Pacific field cricket (Teleogryllus oceanicus) exploratory behaviors in response to perceived social environment

AbstractHow populations adapt, or not, to rapid evolution of sexual signals has important implications for population viability, but is difficult to assess due to the paucity of examples of sexual signals evolving in real time. In Hawaiian populations of the Pacific field cricket (Teleogryllus oceanicus), selection from a deadly parasitoid fly has driven the rapid loss of a male acoustic signal, calling song, that females use to locate and evaluate potential mates. In this newly quiet environment where many males are obligately silent, how do phonotactic females find mates? Previous work has shown that the acoustic rearing environment (presence or absence of male calling song) during late juvenile stages and early adulthood exposes adaptive flexibility in locomotor behaviors of males, as well as mating behaviors in both sexes that helps facilitate the spread of silent (flatwing) males. Here, we tested whether females also show acoustically induced plasticity in walking behaviors using laboratory‐reared populations of T. oceanicus from Kauai (HI; &gt;90% flatwings), Oahu (HI; ~50% flatwings), and Mangaia (Cook Islands; no flatwings or parasitoid fly). Though we predicted that females reared without song exposure would increase walking behaviors to facilitate mate localization when song is rare, we discovered that, unlike males, female T. oceanicus showed relatively little plasticity in exploratory behaviors in response to an acoustic rearing environment. Across all three populations, exposure to male calling song during development did not affect latency to begin walking, distance walked, or general activity of female crickets. However, females reared in the absence of song walked slower and showed a marginally non‐significant tendency to walk for longer durations of time in a novel environment than those reared in the presence of song. Overall, plasticity in female walking behaviors appears unlikely to have facilitated sexual signal loss in this species.

Color and behavior differently predict competitive outcomes for divergent stickleback color morphs.

Our knowledge of how male competition contributes to speciation is dominated by investigations of competition between within-species morphs or closely related species that differ in conspicuous traits expressed during the breeding season (e.g. color, song). In such studies, it is important to consider the manner in which putatively sexually selected traits influence the outcome of competitive interactions within and between types because these traits can communicate information about competitor quality and may not be utilized by homotypic and heterotypic receivers in the same way. We studied the roles of breeding color and aggressive behaviors in competition within and between two divergent threespine stickleback Gasterosteus aculeatus color types. Our previous work in this system showed that the switch from red to black breeding coloration is associated with changes in male competition biases. Here, we find that red and black males also use different currencies in competition. Winners of both color types performed more aggressive behaviors than losers, regardless of whether the competitor was of the same or opposite color type. But breeding color differently predicted competitive outcomes for red and black males. Males who were redder at the start of competition were more likely to win when paired with homotypic competitors and less likely to win when paired with heterotypic competitors. In contrast, black color, though expressed in the breeding season and condition dependent, was unrelated to competitive outcomes. Placing questions about the role of male competition in speciation in a sexual signal evolution framework may provide insight into the “why and how” of aggression biases and asymmetries in competitive ability between closely related morphs and species.

Male mate choice, male quality, and the potential for sexual selection on female traits under polygyny.

Observations of male mate choice are increasingly common, even in species with traditional sex roles. In addition, female traits that bear the hallmarks of secondary sexual characters are increasingly reported. These concurrent empirical trends have led to the repeated inference that, even under polygyny, male mate choice is a mechanism of sexual selection on female traits. It is often either assumed or argued that in these cases females are competing for males of superior "quality"; females might experience sexual selection under polygyny if they compete for mates that provide either direct or indirect benefits. However, the theoretical foundation of this testable hypothesis remains largely uninvestigated. We develop a population genetic model to probe the logic of this hypothesis and demonstrate that, contrary to common inferences, male mate choice, variation in male quality (in the form of a direct fecundity benefit to females), and female ornamentation can coexist in a population without any sexual selection on female ornamentation taking place at all. Furthermore, even in a "best case scenario" where high quality males with a preference for ornamented females are able to mate disproportionately more often with them, the evolution of female traits by sexual selection may be relatively weak. We discuss the implication of these findings for ongoing empirical and theoretical research on the evolution of sexual-signaling in females.

Mixed messages: wild female bonobos show high variability in the timing of ovulation in relation to sexual swelling patterns.

BackgroundThe evolution of primate sexual swellings and their influence on mating strategies have captivated the interest of biologists for over a century. Across the primate order, variability in the timing of ovulation with respect to females’ sexual swelling patterns differs greatly. Since sexual swellings typically function as signals of female fecundity, the temporal relation between ovulation and sexual swellings can impact the ability of males to pinpoint ovulation and thereby affect male mating strategies. Here, we used endocrine parameters to detect ovulation and examined the temporal relation between the maximum swelling phase (MSP) and ovulation in wild female bonobos (Pan paniscus). Data were collected at the Luikotale field site, Democratic Republic of Congo, spanning 36 months. Observational data from 13 females were used to characterise female swelling cycles (N = 70). Furthermore, we measured urinary oestrone and pregnanediol using liquid chromatography–tandem mass spectrometry, and used pregnanediol to determine the timing of ovulation in 34 cycles (N = 9 females).ResultsWe found that the duration of females’ MSP was highly variable, ranging from 1 to 31 days. Timing of ovulation varied considerably in relation to the onset of the MSP, resulting in a very low day-specific probability of ovulation and fecundity across female cycles. Ovulation occurred during the MSP in only 52.9 % of the analysed swelling cycles, and females showed regular sexual swelling patterns in N = 8 swelling cycles where ovulation did not occur. These findings reveal that sexual swellings of bonobos are less reliable indicators of ovulation compared to other species of primates.ConclusionsFemale bonobos show unusual variability in the duration of the MSP and in the timing of ovulation relative to the sexual swelling signal. These data are important for understanding the evolution of sexual signals, how they influence male and female mating strategies, and how decoupling visual signals of fecundity from the periovulatory period may affect intersexual conflict. By prolonging the period during which males would need to mate guard females to ascertain paternity, the temporal variability of this signal may constrain mate-guarding efforts by male bonobos.Electronic supplementary materialThe online version of this article (doi:10.1186/s12862-016-0691-3) contains supplementary material, which is available to authorized users.

Carotenoid‐based plumage colouration is predicted by age and parasites in the male European serin

A fundamental assumption of theories on the evolution of sexual signals is that they should be costly to produce in order to honestly signal the quality of the sender. The expression of carotenoid‐based plumage signals is considered to be condition‐dependent, due to the role of carotenoids functioning as pigments and as health modulators. We assessed carotenoid‐based plumage colouration in relation to male condition in a free living population of male European serins Serinus serinus during the breeding season. Male serins were trapped for morphometric and colouration measurements, during a four‐year field study, in order to evaluate the signalling value of colouration in relation to body condition and parasites level. We compared two different forms of colour quantification based on spectral data – the most commonly used tristimulus colour variables and physiological models of avian colour vision – and found that they were highly correlated for this species. We investigated the signalling value of male plumage colouration and it was found to be related to age and ectoparasite load. Plumage double cone and patch size were negatively related to parasites level, whereas SWS ratio was positively related to parasites and age. Colouration was also related with the time since moult. Our results indicate that the colour expression of serin's plumage is age dependent and is related, in complex ways, with the ability to cope with parasitic infection.