Search bioRxivSearch

bioRxiv · 10.1101/2020.08.26.268185

The hidden links between animal weapons, fighting style and their expression on contest resolution

Abstract

In many species that fight over resources, individuals use specialized structures to gain mechanical advantage over their rivals during contests (i.e., weapons). Although weapons are widespread across animals, how they affect the probability of winning contests is still debated. According to theory, understanding the weapons function in contests depends on identifying differences in how weapons are measured (e.g., weapon length versus shape), and in how weapons are used during fights. Here, we developed a meta-analysis spanning 1,138 studies, from which were drawn 52 species and 107 effect sizes to identify: (1) what aspects of animal weapons are measured in the literature, and how these measures bias our knowledge; (2) how animals use their weapons during fights - i.e., weapon function; and (3) if weapon function correlates to the magnitude of how weapons influence contest resolution. First, we found that most of the literature focuses on linear measures of weapons, such as length. The few reports on weapon performance (e.g., biting force) were found only for Crustacea and Squamata. This bias highlights that measuring performance of weapons such as horns and spines might increase the breadth of our knowledge on weapons. Furthermore, we also found that linear measures showed stronger effects on contest success than performance measures. Second, we divided weapon function into displays and fighting style (i.e., how the weapon is used during fights). Regarding displays, most species displayed their weapons before contests (59.61%), rather than the body (34.61%). A minority (three species, 5.76%) engaged in fights without any type of display. Thus, species that bear weapons almost always perform displays before engaging in physical contact, a common hypothesis in contest theory that was never tested across taxa until now. Regarding fighting style, we found that most weapons were used for more than one behaviour during fights (e.g., squeezing and pushing). Further, pushing seems to be the most common behaviour among species, but it is usually accompanied by another behaviour, such as lifting or squeezing. Thus, oversimplifying fighting style can bias results because some styles might impose contrasting biomechanical pressures (e.g., pushing vs squeezing). Third, we found that display type did not influence the importance of weapon size on contests. Fighting style, on the other hand, influenced the effect of weapon size on contest outcome significantly. Species that used their weapons to impact, pierce or squeeze showed smaller differences between winners and losers when compared to pushing or lifting (and multifunctional weapons). Thus, pushing and lifting seem important for selecting larger weapons - even though some of them might also be used for squeezing, piercing or impacting. Overall, our results show that we have a biased understanding of animal weapons, built mostly on weapon size alone. Further, our analyses show that the importance of weapon size differs depending on the fighting style. If we lessen those biases, we will have a better and broader understanding of how weapons evolve and diversify.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Palaoro, A. V., Peixoto, P. E. C.. 2020-08-27. The hidden links between animal weapons, fighting style and their expression on contest resolution. https://doi.org/10.1101/2020.08.26.268185

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

Geometry of antigenic evolution improves influenza vaccine selection

Anticipating antigenic evolution is essential for selecting effective seasonal influenza A/H3N2 vaccine strains. To this end, we integrated hemagglutination-inhibition and neutralization titers spanning 2002 to 2025 into a unified Bayesian antigenic map. The map resolves twelve antigenic clusters advancing in discrete steps, with several clusters co-circulating in most seasons. In 15 of 21 seasons, the WHO-recommended vaccine belonged to an earlier cluster than the dominant circulating cluster. The direction of each vaccine update relative to recent viral drift predicted vaccine effectiveness one season ahead in out-of-sample forecasts. Antigenic distance, the conventional measure of vaccine-virus match, was weakly associated with effectiveness until update direction was accounted for. Retrospectively ranking candidate strains by predicted effectiveness would have selected a strain predicted to outperform the WHO recommendation in every season, raising mean predicted effectiveness by 10 percentage points.

evolutionary biology

Evolutionary replay of duplicate-gene retention across independent whole-genome duplications

Whole-genome duplications repeatedly expose ancestral gene lineages to the same broad evolutionary outcome-retention or loss of duplicated copies-but it remains unclear whether this history replays similarly across evolutionary scales. We placed duplicate retention in shared hierarchical orthologous-group coordinates and compared percentile ranks defined within each event-wide mapped universe. Three independent angiosperm whole-genome duplications showed reproducible replay (global rank effect T-replay = 0.210, bootstrap 95% confidence interval 0.172-0.248; permutation P = 1/100,001). A plant reference-panel score specified before target outcomes were examined predicted retention after the Apple/Pear duplication ({rho} = 0.169, n = 373). Deep transfer was heterogeneous: the teleost-genome-duplication estimate was positive but unresolved ({rho} = 0.107, n = 151, 95% confidence interval -0.050 to 0.260), whereas transfer to the ancient budding-yeast whole-genome duplication (yeast WGD) was supported ({rho} = 0.280, n = 186). Independently reconstructed animal outcomes also replayed between teleost and Stylommatophora duplications (r = 0.226, n = 146, P = 0.00326), although the effect remained below a prespecified strong-effect threshold. A strict plant-animal comparison was limited to 25 deeply one-to-one lineages and was unresolved (r = 0.033, 95% confidence interval -0.303 to 0.340). Thus, ancestral gene-lineage identity contributes reproducibly to duplicate retention after independent whole-genome duplications, but replay is structured by evolutionary lineage and modified by event-specific history rather than governed by one universal gene-fate ranking.

evolutionary biology

A Hymenoptera-restricted gene mediating ant castes co-opts deeply conserved machinery to control organ size

Lineage-specific genes are widespread and have been implicated as phenotypic innovation inducers, but how they acquire complex developmental functions remains poorly understood. Ant queens and workers develop dramatically different organ sizes from identical genomes under juvenile hormone (JH) control, yet the molecular effectors translating JH signalling into caste-specific organ growth remain unknown. Here we identify torch, a Hymenoptera-restricted gene, as the most consistently gyne-biased and JH-responsive gene across 68 ant species. Knockdown of torch in virgin queens of Monomorium pharaonis produces a worker-like, multi-organ growth-restricted phenotype. Mechanistically, torch harbours an E-box-like motif activated by the JH receptor Gce-Tai and acts as a GA-repeat-binding transcription factor that regulates Hippo signalling, the deeply conserved organ-size control pathway in animals. Expressing torch heterologously in mice and a growth-restricted Drosophila background shows that the gene retained its general growth-promoting activity across more than 700 million years of animal evolution in lineages that lack the gene, establishing that its function is mediated through conserved rather than ant-specific machinery. A lineage-specific gene can therefore acquire complex morphogenetic function by co-opting ancient organ-size circuitry, providing a general route by which novel genes can drive phenotypic innovation.

evolutionary biology