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26 results for “costly signalling”
Data from: Pleiotropy alleviates the fitness costs associated with resource allocation trade-offs in immune signaling networks
<p>Many genes and signaling pathways within plant and animal taxa drive the expression of multiple organismal traits. This form of genetic pleiotropy instigates trade-offs among life-history traits if a mutation in the pleiotropic gene improves the fitness contribution of one trait at the expense of another. Whether or not pleiotropy gives rise to conflict among traits, however, likely depends on the resource costs and timing of trait deployment during organismal development. To investigate factors that could influence the evolutionary maintenance of pleiotropy in gene networks, we developed an agent-based model of co-evolution between parasites and hosts. Hosts comprise signaling networks that must faithfully complete a developmental program while also defending against parasites, and trait signaling networks could be independent or share a pleiotropic component as they evolved to improve host fitness. We found that hosts with independent developmental and immune networks were significantly more fit than hosts with pleiotropic networks when traits were deployed asynchronously during development. When host genotypes directly competed against each other, however, pleiotropic hosts were victorious regardless of trait synchrony because the pleiotropic networks were more robust to parasite manipulation, potentially explaining the abundance of pleiotropy in immune systems despite its contribution to life history trade-offs.</p>
Digitized Raw Output Signals of a Low-cost Aerosol PM Sensor Sharp GP2Y
<p>The data contains the digitized traces of low-cost PM sensor Sharp GP2Y1010AU0F pulse outputs during calibration and environmental measurements. The work was done within the Aeromet EMPIR project 19ENV08.</p> <p>Further details are given in the article:</p> <p>Bučar, K.; Malet, J.; Stabile, L.; Pražnikar, J.; Seeger, S.; Žitnik, M. Statistics of a Sharp GP2Y Low-Cost Aerosol PM Sensor Output Signals. Sensors 2020, 20, 6707. <a href="https://doi.org/10.3390/s20236707">https://doi.org/10.3390/s20236707</a></p> <p>Also see the included README.pdf file.</p> <p> </p>
Data from: Pleiotropy alleviates the fitness costs associated with resource allocation trade-offs in immune signaling networks
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Conspicuous animal signals avoid the cost of predation by being intermittent or novel: confirmation in the wild using hundreds of robotic prey
<p>Social animals are expected to face a trade-off between producing a signal that is detectible by mates and rivals, but not obvious to predators. This trade-off is fundamental for understanding the design of many animal sig- nals, and is often the lens through which the evolution of alternative communication strategies is viewed. We have a reasonable working knowl- edge of how conspecifics detect signals under different conditions, but how predators exploit conspicuous communication of prey is complex and hard to predict. We quantified predation on 1566 robotic lizard prey that per- formed a conspicuous visual display, possessed a conspicuous ornament or remained cryptic. Attacks by free-ranging predators were consistent across two contrasting ecosystems and showed robotic prey that performed a conspicuous display were equally likely to be attacked as those that remained cryptic. Furthermore, predators avoided attacking robotic prey with a fixed, highly visible ornament that was novel at both locations. These data show that it is prey familiarity—not conspicuousness—that determine predation risk. These findings replicated across different preda- tor–prey communities not only reveal how conspicuous signals might evolve in high predation environments, but could help resolve the paradox of aposematism and why some exotic species avoid predation when invad- ing new areas.</p>
Dataset: The role of social costs as a mechanism enforcing the honesty of ultraviolet-reflecting signals in a lizard
<p>Here are the data associated with the study entitled "The role of social costs as a mechanism enforcing the honesty of ultraviolet-reflecting signals in a lizard<strong>"</strong> authored by Anna Kawamoto, Jean-François Le Galliard, and Arnaud Badiane and published in <em>Biological Journal of the Linnean Society</em>.</p> <p>Four different data sets are provided and the Notes.xlsx file explains the content of these data sets.</p> <p>We also added three short videos showing typical lizards' behaviours scored in this study.</p> <p> </p>
Data from: Male rock lizards may compensate reproductive costs of an immune challenge affecting sexual signals
<p><span><span><span><span><span><span><span><span><span><span><span><span><span>Sexual signals can be evolutionarily stable if they are condition dependent or costly to the signaler. One of these costs may be the trade-off between maintaining the immune system and the elaboration of ornaments. Experimental immune challenges in captivity show a reduction in the expression of sexual signals, but it is not clear whether these detrimental effects are important in nature and, more importantly, whether they have reproductive consequences. We designed a field experiment to challenge the immune system of wild male Carpetan rock lizards, Iberolacerta cyreni, with a bacterial antigen (LPS). The immune challenge decreased relative reflectance of UV structural and melanin-dependent sexual coloration in the throat and the lateral ocelli, whereas the carotenoid-dependent dorsal green coloration was not affected. Immune activation also decreased proportions of ergosterol and cholesta-5,7-dien-3-ol in femoral secretions. These results support a trade-off between the immune system and both visual and chemical sexual ornaments. Moreover, reproductive success of males, estimated with DNA microsatellites, depended on the expression of some color and chemical traits. However, the immune challenge did not cause overall differences in reproductive success, although it increased with body size/age in control but not in challenged males. This suggests the use of alternative reproductive strategies (e.g. forced matings) in challenged males, particularly in smaller ones. These males might consider that their survival probabilities are low and increase reproductive effort as a form of terminal investment in spite of their "low-quality" sexual signals and potential survival costs.</span></span></span></span></span></span></span></span></span></span></span></span></span></p>
Data from: Male rock lizards may compensate reproductive costs of an immune challenge affecting sexual signals
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Conspicuous animal signals avoid the cost of predation by being intermittent or novel: confirmation in the wild using hundreds of robotic prey
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Data from: Predation cost of a sexual signal in the threespine stickleback
Much evidence exists for sexually selected traits reflecting various components of mate quality, but the factors that limit signal expression and ensure honest signaling are less well known. Predation risk has been proposed to be one factor that could constrain the elaboration of visually conspicuous signals and ensure honesty, but little evidence exists because of limitations of earlier used methods. We investigated using a combination of field observations and experimental work if a conspicuous sexual signal of the threespine stickleback Gasterosteus aculeatus, the red nuptial coloration of the male, increases predation risk. We compared the proportion of colorful males in the gut of a predator in the wild, the perch Perca fluviatilis, to that in the population, and found proportionally more red-colored stickleback in the gut. This indicates that the predator selectively preys on colorful males under natural conditions. To differentiate between the effects of color and behavior on susceptibility to predation, we experimentally investigated the attack behavior of the predator towards breeding stickleback males differing in coloration. We found the predator to preferentially attack more colorful males, independent of their behavior. These results indicate that predation risk is a cost of the sexual signal that could limit expression and influence the honesty of the signal as an indicator of mate quality.
Data from: The metabolic costs of sexual signalling in the chirping katydid Plangia graminea (Serville) (Orthoptera: Tettigoniidae) are context dependent: cumulative costs add up fast
Katydids produce acoustic signals via stridulation which they use to attract conspecific females for mating. However, direct estimates of the metabolic costs of calling to date have produced diverse cost estimates and are limited to only a handful of insect species. In this study, we therefore investigated the metabolic cost of calling in a unstudied sub-Saharan katydid, Plangia graminea. Using wild-caught animals, we measured katydid metabolic rate using standard flow-through respirometry while simultaneously recording the number of calls produced. Overall, the metabolic rate during calling in P. graminea males was 59% higher than the resting metabolic rate (0.443±0.056 vs. 0.279±0.028 CO2 ml g−1 h−1) although highly variable among individuals. While individual call costs were relatively inexpensive (ranging from 0.02–5.4% increase in metabolic rate per call) the individuals with cheaper calls called more often and for longer than those with expensive calls resulting in the former group having significantly greater cumulative costs over a standard amount of time (9.5 h). The metabolic costs of calling are however context dependent since the amount of time spent calling greatly influenced these costs in our trials. A power law function described this relationship between cumulative cost and percentage increase per call (y=130.21x−1.068, R2=0.858); where y=cumulative cost, and x=percentage increase per call. The choice of metric employed for estimating energy costs (i.e. how costs are expressed) also affects the outcome and any interpretation of costs of sexual signalling. For example, the absolute, relative and cumulative metabolic costs of calling yield strongly divergent estimates and any fitness implications depend on the organism's energy budget and the potential trade-offs in allocation of resources that are made as a direct consequence of increased calling effort.
Data from: Costs and constraints conspire to produce honest signalling: insights from an ant queen pheromone
Signal costs and evolutionary constraints have both been proposed as ultimate explanations for the ubiquity of honest signalling, but the interface between these two factors is unclear. Here, I propose a pluralistic interpretation, and use game theory to demonstrate that evolutionary constraints determine whether signals evolve to be costly or cheap. Specifically, when the costs or benefits of signalling are strongly influenced by the sender's quality, low-cost signals evolve. The model reaffirms that cheap and costly signals can both be honest, and predicts that expensive signals should have more positive allometric slopes than cheap ones. The new framework is applied to an experimental study of an ant queen pheromone that honestly signals fecundity. Juvenile hormone was found to have opposing, dose-dependent effects on pheromone production and fecundity and was fatal at high doses, indicating that endocrine-mediated trade-offs preclude dishonesty. Several lines of evidence suggest that the realised cost of pheromone production may be non-trivial, and the antagonistic effects of juvenile hormone indicate the presence of significant evolutionary constraints. I conclude that the honesty of queen pheromones and other signals is likely enforced by both the cost of dishonesty and a suite of evolutionary constraints.
Data from: Corticosterone: a costly mediator of signal honesty in sand lizards
The mechanisms underlying honest signal expression remain elusive and may involve the integration of social and physiological costs. Corticosterone is a socially modulated metabolic hormone that mediates energy investment and behavior and may therefore function to deter dishonest signal expression. We examined the relationship between corticosterone and green badge coloration in male sand lizards (Lacerta agilis), hypothesizing that physiological and behavioral costs resulting from elevated baseline glucocorticoids function in maintenance of honest signal expression. We found that large-badged males had higher corticosterone titer, with this relationship apparent at the end of the season and absent early in the season. Large-badged males also suffered higher ectoparasite load (number of tick nymphs), despite being in better condition than small-badged males. Ectoparasite load was positively related to corticosterone titer early in the season at the time of badge formation. High-condition individuals had lower corticosterone and lower numbers of ectoparasites than low-condition individuals, suggestive of conditional variation in ability to withstand costs of corticosterone. We found an opposing negative relationship between corticosterone titer and endoparasite load. Corticosterone titer was also negatively associated with male mobility, a fitness-determining behavior in this species. Because badge size is involved in mediating agonistic social interactions in this species, our results suggest that badge-dependent variation in corticosterone is likely reflective of variation in social conditions experienced over the course of the season. Our results implicate corticosterone in maintenance of signal honesty, both early in the season through enforcement of physiological costs (ectoparasite load) and during the season through behavioral costs (male mobility). We propose that socially modulated variation in corticosterone critically functions in mediation of signal honesty without requiring a direct role for corticosterone in trait expression.
Data from: Do aggressive signals evolve toward higher reliability or lower costs of assessment?
It has been suggested that the evolution of signals must be a wasteful process for the signaller, aimed at the maximization of signal honesty. However, the reliability of communication depends not only on the costs paid by signallers but also on the costs paid by receivers during assessment, and less attention has been given to the interaction between these two types of costs during the evolution of signalling systems. A signaller and receiver may accept some level of signal dishonesty by choosing signals that are cheaper in terms of assessment but that are stabilized with less reliable mechanisms. I studied the potential trade-off between signal reliability and the costs of signal assessment in the corncrake (Crex crex). I found that the birds prefer signals that are less costly regarding assessment rather than more reliable. Despite the fact that the fundamental frequency of calls was a strong predictor of male size, it was ignored by receivers unless they could directly compare signal variants. My data revealed a response advantage of costly signals when comparison between calls differing with fundamental frequencies is fast and straightforward, whereas cheap signalling is preferred in natural conditions. These data might improve our understanding of the influence of receivers on signal design because they support the hypothesis that fully honest signalling systems may be prone to dishonesty based on the effects of receiver costs and be replaced by signals that are cheaper in production and reception but more susceptible to cheating.
Divergent sexual signals reflect costs of local parasites
<p>Many closely related populations are distinguished by variation in sexual signals and this variation is hypothesized to play an important role in reproductive isolation and speciation. Within populations, there is considerable evidence that sexual signals provide information about the incidence and severity of parasite infections, but it remains unclear if variation in parasite communities across space could play a role in initiating or maintaining sexual trait divergence. To test for variation in parasite-associated selection, we compared three barn swallow subspecies with divergent sexual signals. We found that parasite community structure and host tolerance to ecologically similar parasites varied between subspecies. Across subspecies we also found that different parasites were costly in terms of male survival and reproductive success. For each subspecies, the preferred sexual signal(s) were associated with the most costly local parasite(s), indicating that divergent signals are providing relevant information to females about local parasite communities. Across subspecies, the same traits were often associated with different parasites, indicating that parasite-sexual signal links are quite flexible and may evolve relatively quickly. This study provides evidence for 1) variation in parasite communities and 2) different parasite-sexual signal links among three closely related subspecies with divergent sexual signal traits, suggesting that parasites may play an important role in initiating and/or maintaining the divergence of sexual signals among these closely related, yet geographically isolated populations.</p>
Data from: Predation cost of a sexual signal in the threespine stickleback
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Data from: Costs and constraints conspire to produce honest signalling: insights from an ant queen pheromone
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Data from: The metabolic costs of sexual signalling in the chirping katydid Plangia graminea (Serville) (Orthoptera: Tettigoniidae) are context dependent: cumulative costs add up fast
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Data from: Corticosterone: a costly mediator of signal honesty in sand lizards
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Data from: Costs of injury for scent signalling in a strepsirrhine primate
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Divergent sexual signals reflect costs of local parasites
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