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Abstract We explore the complexity of the signal repertoire and sequences of behavioural interactions involved in pair formation inEnchenopa binotatatreehoppers, which communicate via plant-borne vibrational signals, and whose pair formation involves prolonged male-female duetting interactions. We recorded these interactions using laser vibrometry and video assays. In males, we report two phases of signalling: a searching phase in which males use a basic repertoire to solicit engagement from females; and a more complex phase incorporating additional signal types and elements males used once engaged by females. In females, we report a novel three-stage process of selective cooperation with males, as well as a novel signal type that was necessary but not sufficient for copulation to occur. These three stages include active duetting with a male that was necessary for him to locate and mount females; the novel signal that females produce after continued mounted duetting that prompts the male to attempt genital coupling; and the female actively allowing coupling. We discuss implications of our observations for these insects’ cognitive abilities in terms of the memory and selective attention required to sustain signalling interactions and proceed along the decision-making stages of mate choice. Using attention to detail as an aid to discovery, we aim to promote research on how such animals express such capabilities. 

Much is known about how the maternal environment can shape offspring traits via intergenerational effects. It is less clear, however, whether such effects may reach adult offspring sexual traits, with potential consequences for sexual selection and speciation. Here, we report effects of adult female aggregation density on the mating signals and mate preferences of their offspring in an insect that communicates via plant-borne vibrational signals. We experimentally manipulated the density of aggregations experienced by egg-laying mothers, reared the offspring in standard densities, and tested for corresponding differences in their signals and preferences. We detected a strong effect in male signals, with sons of mothers that experienced low aggregation density signalling more. We also detected a weak effect on female mate preferences, with daughters of mothers that experienced low aggregation density being less selective. These adjustments may help males and females find mates and secure matings in low densities, if the conditions they encounter correspond to those their mothers experienced. Our results thus extend theory regarding adjustments to the social environment to the scale of intergenerational effects, with maternal social environments influencing the expression of the sexual traits of adult offspring. 

Socially induced plasticity in mating signals and mate preferences is widespread in animals. The timing of plasticity induction is key for mating and evolutionary consequences: plasticity induced before and after dispersal often results in different patterns of mate choices. Here we discuss two additional factors that may be of importance: the nature of social interactions that are involved at different stages, and the direction and strength of the effects. We review a case study with the Enchenopa binotata species complex of treehoppers. In spite of a wide scope for social plasticity in E. binotata across life stages, effects of the juvenile social environment were stronger and more common, especially those influencing the signalepreference relationship. These results emphasize the importance of studying variation in plasticity induced along various life stages and of considering all the mating traits that may be socially plastic. We suggest that systematic investigation of these patterns across taxa will help better understand the origin of diversity in animal communication systems. 

The social environment is often the most dynamicandfitness-relevant environment animals experience. Here we testedwhether plasticity arising from variation in social environments canpromote signal-preference divergence—a key prediction of recentspeciation theory but one that has proven difficult to test in natural sys-tems. Interactions in mixed social aggregations could reduce, create,or enhance signal-preference differences. In the latter case, social plas-ticity could establish or increase assortative mating. We tested this byrearing two recently diverged species ofEnchenopatreehoppers—sap-feeding insects that communicate with plant-borne vibrationalsignals—in treatments consisting of mixed-species versus own-speciesaggregations. Social experience with heterospecifics (in the mixed-species treatment) resulted in enhanced signal-preference species dif-ferences. For one of the two species, we tested but found no differencesin the plastic response between sympatric and allopatric sites, sug-gesting the absence of reinforcement in the signals and preferencesand their plastic response. Our results support the hypothesis that so-cial plasticity can create or enhance signal-preference differences andthat this might occur in the absence of long-term selection against hy-bridization on plastic responses themselves. Such social plasticity mayfacilitate rapid bursts of diversification. 

Sexual competition hinges on the ability to impress other conspecifics, to drive them away or attract them. In such cases, the selective environment may be hedonic or affective in nature, as it consists of the evaluations of the individuals making the decisions. This may contribute to the power of sexual selection because evaluations may range from positive to negative rather than simply from positive to neutral. Selection due to mate choice may therefore be stronger than currently appreciated. Further, change in preferred mate types can occur simply by changes (flips) in the evaluation of similar display features, adding to the dynamism of sexual selection as well as its strength. We tested the hypothesis of positive-to-negative behavioural responses in mate choice with a playback experiment using two treefrog species with ‘mirror image’ structures in their advertisement and aggressive calls. Female treefrog responses ranged from approach to evasion, and the presence of an aversive stimulus tainted evaluation of an attractive stimulus. Further, females in the two species showed flips in approach/evasion of stimuli with comparable signal structure. These results suggest that hedonic evaluation may have an important role in mate choice and showcase how mechanistic analysis can help understand evolutionary processes. 

Abstract The chemical reduction of π‐conjugated bilayer nanographene1(C₁₃₈H₁₂₀) with K and Rb in the presence of 18‐crown‐6 affords [K⁺(18‐crown‐6)(THF)₂][{K⁺(18‐crown‐6)}₂(THF)_0.5][C₁₃₈H₁₂₂³⁻] (2) and [Rb⁺(18‐crown‐6)₂][{Rb⁺(18‐crown‐6)}₂(C₁₃₈H₁₂₂³⁻)] (3). Whereas K⁺cations are fully solvent‐separated from the trianionic core thus affording a “naked”1^.3−anion, Rb⁺cations are coordinated to the negatively charged layers of1^.3−. According to DFT calculations, the localization of the first two electrons in the helicene moiety leads to an unprecedented site‐specific hydrogenation process at the carbon atoms located on the edge of the helicene backbone. This uncommon reduction‐induced site‐specific hydrogenation provokes dramatic changes in the (electronic) structure of1as the helicene backbone becomes more compressed and twisted upon chemical reduction, which results in a clear slippage of the bilayers.