Emerging issues in the evolution of animal nuptial gifts

Uniquely positioned at the intersection of sexual selection, nutritional ecology and life-history theory, nuptial gifts are widespread and diverse. Despite extensive empirical study, we still have only a rudimentary understanding of gift evolution because we lack a unified conceptual framework for considering these traits. In this opinion piece, we tackle several issues that we believe have substantively hindered progress in this area. Here, we: (i) present a comprehensive definition and classification scheme for nuptial gifts (including those transferred by simultaneous hermaphrodites), (ii) outline evolutionary predictions for different gift types, and (iii) highlight some research directions to help facilitate progress in this field.     

Mating stimulates female feeding: testing the implications for the evolution of nuptial gifts

Nutritional benefits from nuptial gifts have been difficult to detect in some species, raising the question: what maintains nuptial feeding when gifts do not benefit females? The sensory trap hypothesis proposes that nuptial feeding may be explained by pre‐existing sensory responses that predispose females to ingest gifts. Recent studies have shown that male seminal proteins can induce a nonspecific increase in female feeding after mating, which may represent a sensory trap for nuptial feeding if it results in increased intake of post‐mating gifts. I tested these ideas using female beetles that ingest a spermatophore after mating. I show that males stimulate strongly increased female feeding post‐mating. However, there was little evidence for dose dependence in the feeding response that could allow males to stimulate feeding beyond the female optimum. Moreover, the post‐mating feeding response could not explain nuptial feeding: despite feeding more in general, newly mated females were less likely than nonmated females to ingest spermatophore gifts.     

Unpredictable environments,nuptial gifts and the evolution of sexual size dimorphism in insects: an experiment

Many insects have a mating system where males transfer nutrients to females at mating, which are often referred to as ''nuptial gifts''. Among butterflies, some of the characteristic features of these species are polyandry (females mate multiple times), and relatively large male ejaculates. When males produce part of the resources used for offspring, the value of body size might then increase for males and decrease for females. The male/female size ratio is also observed to increase when the degree of polyandry and gift size increase. Butterfly species where gift-giving occurs are generally more variable in body size, suggesting that food quality/quantity fluctuates during juvenile stages. This will cause some males to have much to provide and some females to be in great need, and could be conducive to the evolution of a gift-giving mating system. In such a system, growing male and female juveniles should react differently to food shortage. Females should react by maturing at a smaller size since their own lack of reproductive resources can partly be compensated for by male contributions. Males have to pay the full cost of decreased reproduction if they mature at a small size, making it more important for males to keep on growing, even when growth is costly. An earlier experiment with the polyandrous and gift-giving butterfly, Pieris napi, supported this prediction. The pattern is expected to be absent or reversed for species with small nuptial gifts, where females do not benefit from mating repeatedly, and will thus be dependent on acquiring resources for reproduction on their own. To test this prediction, we report here on an experiment with the speckled wood butterfly, Pararge aegeria. We find that growth response correlates with mating system in the two above species, and we conclude that differences in environmental conditions between species may act as an important factor in the evolution of the mating system and sexual size dimorphism.     

The energetics of trading nuptial gifts for copulations in katydids

During copulation, male Isophya kraussi transfer a large nuptial gift to females. In this study, we hypothesized that the energy content of spermatophores should meet the energy requirements of both body maintenance and egg production of females. We measured the field metabolic rate of male and female I. kraussi using the doubly labeled water method and the energy content of spermatophores and male bodies with microbomb calorimetry. The energy content of male nuptial gifts averaged 0.66+/-0.09 kJ, approximately 20% of the total body energy content of male I. kraussi (3.24+/-0.26 kJ). Field metabolic rates averaged 0.41+/-0.17 kJ d(-1) (n = 8) for males and 0.30+/-0.15 kJ d(-1) (n = 5) for female I. kraussi. Thus, the energy content of spermatophores exceeded the daily energy requirements of existence in male I. kraussi. A single nuptial gift provides for all energy requirements of females for 1 or 2 d, depending on their activity, egg production, and ambient temperature. Because the shortest known remating interval of female katydids varies between 1 and 3 d, female I. kraussi could theoretically exist exclusively on spermatophores to meet their nutritional requirements.     

Diet‐dependent female evolution influences male lifespan in a nuptial feeding insect

Theory predicts that lifespan will depend on the dietary intake of an individual, the allocation of resources towards reproduction and the costs imposed by the opposite sex. Although females typically bear the majority of the cost of offspring production, nuptial feeding invertebrates provide an ideal opportunity to examine the extent to which reproductive interactions through gift provisioning impose a cost on males. Here we use experimental evolution in an Australian ground cricket to assess how diet influences male lifespan and how the costs of mating evolve for males. Our findings show that males had significantly shorter lifespans in populations that adapted to a low‐quality diet and that this divergence is driven by evolutionary change in how females interact with males over reproduction. This suggests that the extent of sexual conflict over nuptial feeding may be under‐realized by focusing solely on the consequences of reproductive interactions from the female’s perspective.     

Paternity of offspring in multiply-mated,female crickets: the effect of nuptial food gifts and the advantage of mating first

The spermatophore transferred by male decorated crickets (Gryllodes sigillatus) includes a large gelatinous mass, the spermatophylax, that is consumed by the female after mating. This nuptial gift preoccupies the female while sperm are discharged from the remaining portion of the spermatophore, the sperm ampulla, into her reproductive tract. There is considerable variation in the mass of the spermatophylax, and about half of all males produce spermatophylaxes that are too small to ensure complete sperm transfer. We tested two hypotheses concerning the maintenance of this variation: (i) males trade-off investment in spermatophylaxes against copulation frequency; and (ii) males synthesize the largest spermatophylaxes of which they are physiologically capable. Males synthesizing large and small food gifts were permitted multiple mating opportunities with the same females, and allozyme markers were used to establish the paternity of offspring. There was a significant advantage to those males that mated first irrespective of gift size. This advantage probably arose, in part, because the sperm of first males would have had exclusive access to females'' eggs during the first 24 hours of oviposition, and underscores the benefits of matings with virgin females. The paternity of ''small-gift'' males increased with gift mass, but there was no such increase in ''large-gift'' males. This difference probably stems from the relationship between gift mass and sperm transfer: most of the gifts of the large-gift males would have been above the threshold needed to achieve complete inseminations, whereas those of small-gift males would have been below the threshold. Within mating-order positions, there was no significant difference in the paternity of large-gift and small-gift males, a result seemingly consistent with the ''trade-off'' hypothesis. However, there was no correlation between spermatophylax mass and male mating frequency, so that the mechanism by which small-gift males offset their fertilization disadvantage remains unknown.     

Conflict, cheats and the persistence of symbioses

Many symbioses are widespread, abundant, and evolutionarily persistent. This is despite unambiguous evidence for conflict between the partners and the existence of cheats that use benefits derived from their partners while providing reduced or no services in return. Evidence from a diversity of associations suggests that symbioses are robust to cheating in several ways. Some symbioses persist despite conflict and cheating because of the selective advantage of cost-free interactions (also known as byproduct mutualistic interactions), which incur no conflict. There is also evidence for the suppression of cheating by sanctions imposed by partners in some symbioses, and vertical transmission has been shown experimentally to promote traits that enhance partner performance. It is argued that these processes contribute to the apparent rarity of evolutionary transitions from symbiosis to parasitism. There is strong phylogenetic evidence for the evolutionary reversion of various symbiotic organisms to free-living lifestyles, but at least some of these transitions can be attributed to selection pressures other than within-symbiosis conflict. The principal conclusion is that, although conflict is common in symbioses, it is generally managed and contained.     

Weighing costs and benefits of mating in bushcrickets (Insecta: Orthoptera: Tettigoniidae), with an emphasis on nuptial gifts,protandry and mate density

ABSTRACT: Sexual selection is a major force driving evolution and is intertwined with ecological factors. Differential allocation of limited resources has a central role in the cost of reproduction. In this paper, I review the costs and benefits of mating in tettigoniids, focussing on nuptial gifts, their trade-off with male calling songs, protandry and how mate density influences mate choice. Tettigoniids have been widely used as model systems for studies of mating costs and benefits; they can provide useful general insights. The production and exchange of large nuptial gifts by males for mating is an important reproductive strategy in tettigoniids. As predicted by sexual selection theory spermatophylax size is condition dependent and is constrained by the need to invest in calling to attract mates also. Under some circumstances, females benefit directly from the nuptial gifts by an increase in reproductive output. However, compounds in the nuptial gift can also benefit the male by prolonging the period before the female remates. There is also a trade-off between adult male maturation and mating success. Where males mature before females (protandry) the level of protandry varies in the direction predicted by sperm competition theory; namely, early male maturation is correlated with a high level of first inseminations being reproductively successful. Lastly, mate density in bushcrickets is an important environmental factor influencing the behavioural decisions of individuals. Where mates are abundant, individuals are more choosey of mates; when they are scarce, individuals are less choosey. This review reinforces the view that tettigoniids provide excellent models to test and understand the economics of matings in both sexes.     

Accelerating invasion rates result from the evolution of density-dependent dispersal

Evolutionary processes play an important role in shaping the dynamics of range expansions, and selection on dispersal propensity has been demonstrated to accelerate rates of advance. Previous theory has considered only the evolution of unconditional dispersal rates, but dispersal is often more complex. For example, many species emigrate in response to crowding. Here, we use an individual-based model to investigate the evolution of density dependent dispersal into empty habitat, such as during an invasion. The landscape is represented as a lattice and dispersal between populations follows a stepping-stone pattern. Individuals carry three ‘genes’ that determine their dispersal strategy when experiencing different population densities. For a stationary range we obtain results consistent with previous theoretical studies: few individuals emigrate from patches that are below equilibrium density. However, during the range expansion of a previously stationary population, we observe evolution towards dispersal strategies where considerable emigration occurs well below equilibrium density. This is true even for moderate costs to dispersal, and always results in accelerating rates of range expansion. Importantly, the evolution we observe at an expanding front depends upon fitness integrated over several generations and cannot be predicted by a consideration of lifetime reproductive success alone. We argue that a better understanding of the role of density dependent dispersal, and its evolution, in driving population dynamics is required especially within the context of range expansions.     

Out of the blue: adaptive visual pigment evolution accompanies Amazon invasion

Incursions of marine water into South America during the Miocene prompted colonization of freshwater habitats by ancestrally marine species and present a unique opportunity to study the molecular evolution of adaptations to varying environments. Freshwater and marine environments are distinct in both spectra and average intensities of available light. Here, we investigate the molecular evolution of rhodopsin, the photosensitive pigment in the eye that activates in response to light, in a clade of South American freshwater anchovies derived from a marine ancestral lineage. Using likelihood-based comparative sequence analyses, we found evidence for positive selection in the rhodopsin of freshwater anchovy lineages at sites known to be important for aspects of rhodopsin function such as spectral tuning. No evidence was found for positive selection in marine lineages, nor in three other genes not involved in vision. Our results suggest that an increased rate of rhodopsin evolution was driven by diversification into freshwater habitats, thereby constituting a rare example of molecular evolution mirroring large-scale palaeogeographic events.     

A phylogenetic analysis of the frog genera Vibrissaphora and Leptobrachium, and the correlated evolution of nuptial spine and reversed sexual size dimorphism

A phylogeny of the frog genus Vibrissaphora and seven Leptobrachium species was reconstructed based on 3808 base pairs of mitochondrial and nuclear DNA sequence data. Maximum parsimony, Bayesian, and statistical parsimony approaches were employed to reveal the historical relationships among the recovered haplotypes. The species of the genera Vibrissaphora and Leptobrachium failed to form their respective monophyletic groups. Therefore, Vibrissaphora should be part of the genus Leptobrachium. Our analysis also further delineated several species boundaries; Leptobrachium chapense is not a single species, rather, a species complex. On the other hand, although L. liui demonstrated substantial morphological variation, all populations belong to one species. The RAG-1 data revealed a case of species-level non-monophyly; when studying slowly evolving genes, population coalescence may not have been reached within species. The phylogenetic comparative analysis revealed a positive correlation between evolution of male nuptial spines and reversed sexual size dimorphism in this group. Resource defense polygyny and male parental care are possible explanations for the presence of large male size.     

Investigating the evolution of floras: problems and progress — An introduction

The Cape flora of southern Africa is a remarkable hotspot for plant species diversity and endemism. At a meeting in Zurich in 2004 progress in understanding the evolution of this diversity was reviewed. In this symposium, four papers presenting several of the methods used in this investigation were reported. These papers deal with molecular dating methods, the reconstruction of ancestral habitats, with possible speciation scenarios for the Cape flora, and the importance of the correct sampling strategies.     

The geometric theory of adaptive evolution: trade-off and invasion plots

The purpose of this paper is to take an entirely geometrical path to determine the evolutionary properties of ecological systems subject to trade-offs. In particular we classify evolutionary singularities in a geometrical fashion. To achieve this, we study trade-off and invasion plots (TIPs) which show graphically the outcome of evolution from the relationship between three curves. The first invasion boundary (curve) has one strain as resident and the other strain as putative invader and the second has the roles of the strains reversed. The parameter values for one strain are used as the origin with those of the second strain varying. The third curve represents the trade-off. All three curves pass through the origin or tip of the TIP. We show that at this point the invasion boundaries are tangential. At a singular TIP, in which the origin is an evolutionary singularity, the invasion boundaries and trade-off curve are all tangential. The curvature of the trade-off curve determines the region in which it enters the singular TIP. Each of these regions has particular evolutionary properties (EUS, CS, SPR and MI). Thus we determine by direct geometric argument conditions for each of these properties in terms of the relative curvatures of the trade-off curve and invasion boundaries. We show that these conditions are equivalent to the standard partial derivative conditions of adaptive dynamics. The significance of our results is that we can determine whether the singular strategy is an attractor, branching point, repellor, etc. simply by observing in which region the trade-off curve enters the singular TIP. In particular we find that, if and only if the TIP has a region of mutual invadability, is it possible for the singular strategy to be a branching point. We illustrate the theory with an example and point the way forward.     

The developmental cytology of the nuptial pad in the red-spotted newt.

The ultrastructure of developing, mature and regressing nuptial pads has been examined and interpreted in the red-spotted newt. The development of the pad begins with a thickening of the dermis. Mitotic activity then increases the cell layers of the epidermis from about four to approximately eight. Simultaneously, keratinocytic synthetic activity shifts to produce more tonofilaments and fewer mucous granules. In the upper cell layers, the shift is followed by an increase in cytoplasmic volume with bundles of tonofilaments accumulating on the anterior side of each cell, displacing the nucleus posteriorly. After this rearrangement, the enlarged cells become grouped into ascending columns that tilt posteriorly from the basal epidermal layer at an angle of about 45°. Also the flattened cells of the monolayered stratum corneum become superficially roughened and with successive molts are replaced by orderly rows of cornified conical structures possessing cusps that are directed posteriorly. Each cone then lies at the top of one of the germinative columns. In rudimentary pads induced on female newts, the epidermis attains a height of only five or six layers and columns are not evident, but other developmental features of the male are present. During regression, mitosis is slowed and the developmental sequence is reversed.