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Doctor of Philosophy / Department of Biology / Brett K. Sandercock / Sexual selection via female choice and male-male aggression leads to elaboration of male traits. If male traits correlated with reproductive success are honest signals of male quality, survival costs may be associated with the expression of those traits. Testosterone (hereafter ‘T’) may enhance male breeding success, but T can also reduce immunocompetence and survival. Socially monogamous male birds with higher circulating T experience reproductive advantages, but the role of T in lek mating systems is largely unknown. To address these issues, I individually marked and conducted focal behavioral observations of greater prairie-chickens (Tympanuchus cupido) at five lek sites over a 5-year period. Females were fitted with radio-telemetry to monitor nesting success and survival. I examined the relationship between male traits and mating success using multinomial discrete choice models, a statistical method not previously applied to studies of sexual selection. Male mating success was highly skewed at greater prairie-chicken leks with 18.5% of males obtaining 87.2% of all successful copulations (n = 108 males; 85 copulations). Mating success was influenced most by male behavior, followed by several morphological attributes. The role of T was quantified using blood samples and by experimentally implanting a subset of males with T. T did not consistently affect mating success. Non-territorial males had lower T levels than territorial males. Among territory holders, T was unexpectedly negatively correlated with mating success. However, the odds of receiving a copulation were 4.3 times (0.42 to 45.3) greater for T-implanted males than males with sham implants. Future work should explore the interactions among the immune system, parasite load, and mating success of prairie-chickens. Annual survival of male prairie-chickens was not related to mating success, behavior, age or T level, suggesting there is no cost of increased male mating success. Like males, reproductive success of females was also highly skewed because < 10% of nests successfully hatched young. Comparisons of seasonal and annual survival rates indicate that females experience increased mortality during the breeding season relative to the nonbreeding season. Synthesis of field estimates of demographic parameters indicates prairie-chicken populations will decline without changes in rangeland management to reduce predator numbers or provide more nesting cover.

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This theses focuses on olfactory and visual components of mate choice in grey partridge. The aim is to evaluate the importance of melanin-based ornametnation and olfaction in mate choice and to explain the role of sexual selection in the evolution of secondary ornamentation in this socially monogamous galliform bird. To do that several experiments were conducted to (1) assess the ability of individuals to recognize conspecific odour and (2) to estimate the significance of melanin based feather ornamentation in male-male and male-female interactions. In some experiments I manipulated the expression (size) of feather maleanin- based ornamentation while in others I used birds forced to pair randomly to find out how the size of ornament and similarity in ornament expression between males and females (assortative pairing) affects reproductive success and investments (egg hatchability and number of eggs laid).

<p>Harmony and cooperation was for long believed to dominate sexual interactions. This view slowly started to change 25 years ago and is today replaced with a view where males and females act based on what is best from a costs-benefits perspective. When sex specific costs and benefits differ, concerning reproductive decision influenced by both sexes, sexual conflict will occur. The basis for discordant reproductive interests between the sexes is that males produce many small gametes, while females’ produce few and large gametes. One result of this difference is that the optimal mating rate differs between the sexes. Males, with their many small sperm, maximize their reproductive output by mating with many females, while females often do best by not mating more frequently than to fertilize their eggs, since mating often entails a cost. Sexual conflict over mating is thus an important factor shaping the interactions between the sexes. In this thesis I study this and related conflicts between the sexes, using mathematical models, fruit flies and comparative methods. Mathematical modelling was used to explore how males and females may coevolve under sexual conflict over mating. This model shows that sexual conflict over mating results in the evolution of costly female mate choice, in terms high resistance to matings, and costly exaggerated male sexual traits, aimed to manipulate females into mating. A key assumption in this model is that males which females find attractive also are more harmful to females. This assumption was tested by housing fruit fly females with either attractive or unattractive males. Females kept with attractive males were courted and mated more, and suffered a 16 percent reduction in lifetime offspring production. In another study I measured genetic variation in two antagonistic male traits used to compete over females; offence - a male’s ability to acquire new mates and supplant stored sperm, and defence - a male’s ability to induce fidelity in his mates and prevent sperm displacement when remating occurs. Independent additive genetic variation and positive selection gradients were found for both these traits, indicating an ongoing arms race between these male antagonistic traits. This arms race also had a negative impact on females, since high values of offence compromised female fitness. Genetic variation in female ability to withstand male harm was also tested for and found, indicating that females evolve counter adaptations to reduce the effect of harmful male traits. Finally, the proposed link between sexual conflict and speciation was tested. Theory suggests that perpetual sexual arms races will cause allopatric populations to evolve along different evolutionary trajectories, resulting in speciation. This theory was tested using comparative methods by contrasting the number of extant species in taxa with high and low opportunity for sexual conflict. The study showed that taxa with high opportunity for sexual conflict, on average, has four times as many species as those with low opportunity, supporting that sexual conflict is a key process in speciation.</p>

Harmony and cooperation was for long believed to dominate sexual interactions. This view slowly started to change 25 years ago and is today replaced with a view where males and females act based on what is best from a costs-benefits perspective. When sex specific costs and benefits differ, concerning reproductive decision influenced by both sexes, sexual conflict will occur. The basis for discordant reproductive interests between the sexes is that males produce many small gametes, while females’ produce few and large gametes. One result of this difference is that the optimal mating rate differs between the sexes. Males, with their many small sperm, maximize their reproductive output by mating with many females, while females often do best by not mating more frequently than to fertilize their eggs, since mating often entails a cost. Sexual conflict over mating is thus an important factor shaping the interactions between the sexes. In this thesis I study this and related conflicts between the sexes, using mathematical models, fruit flies and comparative methods. Mathematical modelling was used to explore how males and females may coevolve under sexual conflict over mating. This model shows that sexual conflict over mating results in the evolution of costly female mate choice, in terms high resistance to matings, and costly exaggerated male sexual traits, aimed to manipulate females into mating. A key assumption in this model is that males which females find attractive also are more harmful to females. This assumption was tested by housing fruit fly females with either attractive or unattractive males. Females kept with attractive males were courted and mated more, and suffered a 16 percent reduction in lifetime offspring production. In another study I measured genetic variation in two antagonistic male traits used to compete over females; offence - a male’s ability to acquire new mates and supplant stored sperm, and defence - a male’s ability to induce fidelity in his mates and prevent sperm displacement when remating occurs. Independent additive genetic variation and positive selection gradients were found for both these traits, indicating an ongoing arms race between these male antagonistic traits. This arms race also had a negative impact on females, since high values of offence compromised female fitness. Genetic variation in female ability to withstand male harm was also tested for and found, indicating that females evolve counter adaptations to reduce the effect of harmful male traits. Finally, the proposed link between sexual conflict and speciation was tested. Theory suggests that perpetual sexual arms races will cause allopatric populations to evolve along different evolutionary trajectories, resulting in speciation. This theory was tested using comparative methods by contrasting the number of extant species in taxa with high and low opportunity for sexual conflict. The study showed that taxa with high opportunity for sexual conflict, on average, has four times as many species as those with low opportunity, supporting that sexual conflict is a key process in speciation.

Among the different sensory modalities that play a role in sexual selection, acoustic communication plays an important one. Acoustic communication has been known to be used for male-male competition (territory maintenance, male aggression during mating),for advertisement to the opposite sex (mating status, body condition, genetic quality, nutritional status) and used by females to sample and choose conspecific preferred males. The use of acoustic communication for sexual display and information exchange has been extensively studied in multiple taxa, including insects, anurans, birds and mammals. Among insects, crickets have proven to be good model systems to study sexual selection based on acoustic communication as most species have an elaborate acoustic communication system, male advertisements, diverse types of mating incentives for females (such as glandular feeding) and a female dominated mating system. Generally, in crickets males produce species-specific calls which are used by females to localize conspecific males. Besides, calls show high levels of intraspecific variation and are energetically costly to produce. Moreover, as in crickets predominantly the females show phonotaxis towards male calls, calls also can play a role in mate sampling and choice by acting as indicators of preferred male quality. Despite being studied for many decades there are certain gaps in the studies examining mate choice in crickets. Some of them are, lack of understanding of the variation of male calling traits in nature and its role in signal evolution, lack of understanding regarding the ecological context of mate sampling and the evolution of alternative mating strategies. Hence, the tree cricket Oecanthus henryi was chosen as a study system to address these gaps in the understanding of female choice based on acoustic signals. In the tree cricket Oecanthus henryi, males call and females use calls to localize conspecific males and hence potentially females can choose males based on acoustic cues. To understand the evolution of female preference for male acoustic cues it is important to understand the variation in the calling songs in the field and identify repeatable call features that are reliable indicators of preferred male traits (morphological, developmental or genetic). I measured repeatability of male call traits in the field to understand their variation, reliability and consistency. Carrier frequency was the only call trait that was highly repeatable and hence was reliable and consistent. Following this I examined whether any of these call traits were indicators of male morphological traits (such as male size and fluctuating asymmetry) which are known to be preferred by females. It was found that carrier frequency was negatively correlated with body size; hence carrier frequency was both reliable and indicated male size. I also found that females preferred larger males during mating, as revealed by the longer mating durations and longer spermatophore retention time. Interestingly, though this study indicated that females could in principle use lower call carrier frequency to localize preferred larger males, simultaneous choice experiments done in the laboratory revealed that the females do not use this cue. These contrasting results may be because females are incapable of discriminating small differences in frequency or because they use non-acoustic cues for mate choice. However, whichever cues the females use to discriminate between males in the laboratory conditions, often these preferences are not realized in the field. The main reason behind this is that searching for preferred mates in the field can be costly and this might force females to choose sub-optimal males. Theoretical models predict that male movement and spacing in the field should influence female sampling tactics and in turn, females should drive the evolution of male movement and spacing to sample them optimally. Moreover, simultaneous sampling of males using the best-of-n or comparative Bayes strategy should yield maximum mating benefits to females. Many of the theoretical mate sampling strategies involves recall of the quality and location of individual males, which in turn requires male positions to be stable within a night. Calling males of O. henryi showed high site fidelity within a night, potentially enabling female sampling strategies that require recall. To examine the possibility of simultaneous acoustic sampling of males, I estimated male acoustic active spaces using information on male spacing, call transmission and female phonotactic threshold. Males were found to be spaced far apart and active space overlap was rare. I then examined female sampling scenarios by studying female spacing relative to male acoustic active spaces. Only 15% of sampled females could hear multiple males, suggesting that simultaneous mate sampling is rare in the field. Moreover, the relatively large distances between calling males suggest high search costs, which may favor threshold strategies that do not require memory. Using the insights gathered from these two studies I examined a unique calling behaviour from leaf holes, baffling, observed in this species. Baffling behaviour has been found in multiple species of the genus Oecanthus where the males call from selfmade holes in leaves rather than calling from leaf edges (their natural calling surface) thus increasing their loudness many fold. I started by examining the natural history of baffling and found that baffling is an extremely rare behaviour in the field. However field observations and laboratory experiments revealed that many males can baffle and hence it is not an obligatory behaviour shown only by a few males. It was hypothesized that one reason for the rarity of baffling could be resource limitation. It was found that baffling males prefer larger leaves possibly due to higher SPL gains achieved by baffling on the larger leaves, which is a limited resource in the field. However this alone was insufficient to explain extreme rarity of bafflers in the field. Hence I examined which males were using this behaviour in the field. Using field observations and laboratory experiments it was found that less preferred males (smaller and quieter) baffled more which provided them with higher calling SPL and greater sound-field volume and thus a higher number of potential mates. Moreover, baffling also increased the mating duration for the less preferred males thus providing more time to these males for sperm transfer. The females could not differentiate between an inherently loud caller and a caller whose SPL was increased artificially (as if it was baffling). Hence I concluded that baffling is probably a cheater strategy used by the less preferred males to fool the females into approaching them and mating for longer durations. To my knowledge, this is the first study that has estimated male call variation in the field to understand its role in female choice in tree crickets. Moreover this is also the first study to examine the ecological context of mate choice in tree crickets. This is also the first study to examine the advantages of baffling behaviour and its potential evolutionary implications. the different sensory modalities that play a role in sexual selection, acoustic communication plays an important one. Acoustic communication has been known to be used for male-male competition (territory maintenance, male aggression during mating),for advertisement to the opposite sex (mating status, body condition, genetic quality, nutritional status) and used by females to sample and choose conspecific preferred males. The use of acoustic communication for sexual display and information exchange has been extensively studied in multiple taxa, including insects, anurans, birds and mammals. Among insects, crickets have proven to be good model systems to study sexual selection based on acoustic communication as most species have an elaborate acoustic communication system, male advertisements, diverse types of mating incentives for females (such as glandular feeding) and a female dominated mating system. Generally, in crickets males produce species-specific calls which are used by females to localize conspecific males. Besides, calls show high levels of intraspecific variation and are energetically costly to produce. Moreover, as in crickets predominantly the females show phonotaxis towards male calls, calls also can play a role in mate sampling and choice by acting as indicators of preferred male quality. Despite being studied for many decades there are certain gaps in the studies examining mate choice in crickets. Some of them are, lack of understanding of the variation of male calling traits in nature and its role in signal evolution, lack of understanding regarding the ecological context of mate sampling and the evolution of alternative mating strategies. Hence, the tree cricket Oecanthus henryi was chosen as a study system to address these gaps in the understanding of female choice based on acoustic signals. In the tree cricket Oecanthus henryi, males call and females use calls to localize conspecific males and hence potentially females can choose males based on acoustic cues. To understand the evolution of female preference for male acoustic cues it is important to understand the variation in the calling songs in the field and identify repeatable call features that are reliable indicators of preferred male traits (morphological, developmental or genetic). I measured repeatability of male call traits in the field to understand their variation, reliability and consistency. Carrier frequency was the only call trait that was highly repeatable and hence was reliable and consistent. Following this I examined whether any of these call traits were indicators of male morphological traits (such as male size and fluctuating asymmetry) which are known to be preferred by females. It was found that carrier frequency was negatively correlated with body size; hence carrier frequency was both reliable and indicated male size. I also found that females preferred larger males during mating, as revealed by the longer mating durations and longer spermatophore retention time. Interestingly, though this study indicated that females could in principle use lower call carrier frequency to localize preferred larger males, simultaneous choice experiments done in the laboratory revealed that the females do not use this cue. These contrasting results may be because females are incapable of discriminating small differences in frequency or because they use non-acoustic cues for mate choice. However, whichever cues the females use to discriminate between males in the laboratory conditions, often these preferences are not realized in the field. The main reason behind this is that searching for preferred mates in the field can be costly and this might force females to choose sub-optimal males. Theoretical models predict that male movement and spacing in the field should influence female sampling tactics and in turn, females should drive the evolution of male movement and spacing to sample them optimally. Moreover, simultaneous sampling of males using the best-of-n or comparative Bayes strategy should yield maximum mating benefits to females. Many of the theoretical mate sampling strategies involves recall of the quality and location of individual males, which in turn requires male positions to be stable within a night. Calling males of O. henryi showed high site fidelity within a night, potentially enabling female sampling strategies that require recall. To examine the possibility of simultaneous acoustic sampling of males, I estimated male acoustic active spaces using information on male spacing, call transmission and female phonotactic threshold. Males were found to be spaced far apart and active space overlap was rare. I then examined female sampling scenarios by studying female spacing relative to male acoustic active spaces. Only 15% of sampled females could hear multiple males, suggesting that simultaneous mate sampling is rare in the field. Moreover, the relatively large distances between calling males suggest high search costs, which may favor threshold strategies that do not require memory. Using the insights gathered from these two studies I examined a unique calling behaviour from leaf holes, baffling, observed in this species. Baffling behaviour has been found in multiple species of the genus Oecanthus where the males call from self- made holes in leaves rather than calling from leaf edges (their natural calling surface) thus increasing their loudness many fold. I started by examining the natural history of baffling and found that baffling is an extremely rare behaviour in the field. However field observations and laboratory experiments revealed that many males can baffle and hence it is not an obligatory behaviour shown only by a few males. It was hypothesized that one reason for the rarity of baffling could be resource limitation. It was found that baffling males prefer larger leaves possibly due to higher SPL gains achieved by baffling on the larger leaves, which is a limited resource in the field. However this alone was insufficient to explain extreme rarity of bafflers in the field. Hence I examined which males were using this behaviour in the field. Using field observations and laboratory experiments it was found that less preferred males (smaller and quieter) baffled more which provided them with higher calling SPL and greater sound-field volume and thus a higher number of potential mates. Moreover, baffling also increased the mating duration for the less preferred males thus providing more time to these males for sperm transfer. The females could not differentiate between an inherently loud caller and a caller whose SPL was increased artificially (as if it was baffling). Hence I concluded that baffling is probably a cheater strategy used by the less preferred males to fool the females into approaching them and mating for longer durations. To my knowledge, this is the first study that has estimated male call variation in the field to understand its role in female choice in tree crickets. Moreover this is also the first study to examine the ecological context of mate choice in tree crickets. This is also the first study to examine the advantages of baffling behaviour and its potential evolutionary implications.

The aim of this study was to obtain an understanding of the basis to female mating decisions in the Chinese rose bitterling (Rhodeus ocellatus). Bitterling have a resource-based mating system that involves the female laying her eggs inside the gills of a freshwater mussel. Male bitterling perform elaborate courtship behaviour and are territorial and aggressively guard mussels in their territory from other territory holders and non-territorial males. Using a series of laboratory experiments it was shown in this study that females were choosy over the males they mated with, but females were not congruent in their preferences. Female mate preferences correlated positively with offspring growth rates and survival during early development. Female mate choice did not correspond with male dominance, and there may be an intersexual conflict between female mate preferences and male dominance as a result. Females tended to prefer males with functionally dissimilar MHC alleles. MHC alleles may influence male odour cues, and females showed a preference for mussels in which the sperm of multiple males had been released, possibly indicating that females use odour cues associated with sperm release in mating decisions. Bitterling show an innate preference for the colour red in a foraging context and there may be a receiver bias for red nuptial colouration in female mating preferences. Despite a significant role for mate preferences, direct (oviposition) mating preferences were shown to be more important in the mating system. Choice of oviposition sites has both immediate (survival) consequences for offspring, as well as longer-term fitness effects.