Mionectes oleagineus (Aves, Tyrannidae) is a small, sexually monomorphic, lek breeding bird. The behaviour and mating system of this species were studied on Costa Rica's Osa Peninsula over two years. In this thesis I ask three questions: 1) What kind of social organization does M. oleagineus exhibit? 2) Does habitat influence male display dispersion? and 3) What is the function of song in attracting mates and in male-male interactions? In Chapter 2, I describe M. oleagineus' social organization. There were three categories of males: territory owners, satellites and floaters. The latter 2 categories were non-territorial and represented half of the male population. I describe interactions between displaying males and visitors to their territories, including courtship display and aggressive interactions between males. Male display dispersion was highly variable in the study area, including classical leks, in which territories shared contiguous boundaries, an exploded lek, where the territories did not share boundaries, and solitary display territories. In Chapter 3, I test the hypothesis that the number of males that can settle in an area, and their subsequent display dispersion, is determined by the availability and dispersion of suitable habitat. Discriminant function analysis of measures of vegetation structure from both territories and non-territory sample plots showed that territory habitat could be distinguished from non-territory habitat. Eleven percent of the sample plots were described as suitable habitat in the analysis. Given that half the male population is non-territorial, the existence of unoccupied, suitable habitat makes it unlikely that habitat availability determines the number of males settling, or their display dispersion. The major occupation of males on their display territories is singing. In Chapter 4, I investigate the function of song for M. oleagineus using behavioural observation and an experiment involving temporary muting. Males which sang at higher rates received more visitors of both sexes. The territories of most muted territorial males were rapidly usurped by other males. Two of the muted males regained their territories upon regaining the ability to sing. This study is the first to directly demonstrate a key role for song in male-male interactions on leks. It also provides evidence that females use song in mate assessment. / Science, Faculty of / Zoology, Department of / Graduate

The mating behaviour and reproductive ecology of the big-handed crab Heterozius rotundifrons was studied at Kaikoura between November 1997 and December 1998. H. rotundifrons was found at mean densities of 7.6 per m² (± 1.4) within the middle and low shore levels and varied little between seasons. The variance! mean ratio indicated that males and females aggregated within these shore levels. The sex ratio was significantly female biased during the majority of the year. Allometric growth rates indicated that males and females reached sexual maturity at 11 mm carapace width (CW). In males, spermatozoa production occurred between 9-9.99 mm CW. Ovigerous females were present every month except February. The first broods of the year were produced in March which coincides with a decrease in the female gonado-somatic index (GSI). These broods were incubated for approximately nine months whereas broods produced in August were incubated for only five months. Female brood production appeared to be cyclical, alternating between a winter incubation period and a summer incubation period. The completed cycle takes approximately three years with two broods produced during the cycle. Fecundity increased with female size but egg mortality was quite high (19%). Instantaneous mortality rate increased with increasing brood development. Females mate when recently moulted (soft-shelled). Although females moulted through out the year, in small numbers, there was a peak in female moulting during October and November. The operational sex ratio (OSR) was male biased during all months of the year. Females released an attractant prior to moulting which initiated pre-copulatory mate guarding by the male. Once the female moulted, copulation occurred approximately 6 h later. Copulation lasted for approximately 3 h and was followed by a period of post-copulatory mate guarding. Males increased the duration of post-copulatory mate guarding if another male was present. Large males out competed small males for receptive females. Males used their large cheliped to subdue competitors and to provide protection for the soft female. Mate guarding was shown to reduce cannibalism from other females. Spermatozoa are packaged in spermatophores within the vas deferens of males but are quickly dehisced within the spermathecae (ventral-type) of newly mated females. Last male to copulate probably achieves the highest level of paternity. Postcopulatory mate guarding by the male was found and ejaculates were found in discrete packets within the spermatheca. Sperm competition appeared to be important because large males displaced small males during copulation, males left when a female was still receptive and the females could retain sperm between moults. It is concluded that H. rotundifrons probably has a polygynous mating system in which males compete for soft females (female centered competition)

The mating behaviour and reproductive ecology of the big-handed crab Heterozius rotundifrons was studied at Kaikoura between November 1997 and December 1998. H. rotundifrons was found at mean densities of 7.6 per m² (± 1.4) within the middle and low shore levels and varied little between seasons. The variance! mean ratio indicated that males and females aggregated within these shore levels. The sex ratio was significantly female biased during the majority of the year. Allometric growth rates indicated that males and females reached sexual maturity at 11 mm carapace width (CW). In males, spermatozoa production occurred between 9-9.99 mm CW. Ovigerous females were present every month except February. The first broods of the year were produced in March which coincides with a decrease in the female gonado-somatic index (GSI). These broods were incubated for approximately nine months whereas broods produced in August were incubated for only five months. Female brood production appeared to be cyclical, alternating between a winter incubation period and a summer incubation period. The completed cycle takes approximately three years with two broods produced during the cycle. Fecundity increased with female size but egg mortality was quite high (19%). Instantaneous mortality rate increased with increasing brood development. Females mate when recently moulted (soft-shelled). Although females moulted through out the year, in small numbers, there was a peak in female moulting during October and November. The operational sex ratio (OSR) was male biased during all months of the year. Females released an attractant prior to moulting which initiated pre-copulatory mate guarding by the male. Once the female moulted, copulation occurred approximately 6 h later. Copulation lasted for approximately 3 h and was followed by a period of post-copulatory mate guarding. Males increased the duration of post-copulatory mate guarding if another male was present. Large males out competed small males for receptive females. Males used their large cheliped to subdue competitors and to provide protection for the soft female. Mate guarding was shown to reduce cannibalism from other females. Spermatozoa are packaged in spermatophores within the vas deferens of males but are quickly dehisced within the spermathecae (ventral-type) of newly mated females. Last male to copulate probably achieves the highest level of paternity. Postcopulatory mate guarding by the male was found and ejaculates were found in discrete packets within the spermatheca. Sperm competition appeared to be important because large males displaced small males during copulation, males left when a female was still receptive and the females could retain sperm between moults. It is concluded that H. rotundifrons probably has a polygynous mating system in which males compete for soft females (female centered competition)

Magister Legum - LLM

La vie en groupe représente de nombreux défis pour les animaux et l’un d’entre eux est le maintien de la cohésion groupe. Comment les animaux décident collectivement vers où et quand se déplacer,se nourrir, se reposer alors qu’ils n’ont pas les mêmes motivations ou besoins ? Dans ce travail de thèse je me suis intéressée aux mécanismes qui sous-tendent les décisions collectives lors des déplacements chez le cheval domestique et notamment le poids des différences interindividuelles et des relations sociales sur ces mécanismes. Pour cela, j’ai étudié quatre groupes de chevaux contenant uniquement des juments ou des groupes familiaux contenant un étalon et des juments.J’ai pu mettre en évidence 1) l’absence de leader et l’existence de décision partagée par l’ensemble du groupe, 2) l’importance de la personnalité et des relations sociales sur les décisions, 3) l’impact de la période précédant le départ sur la rapidité du consensus et 4) la coexistence de mécanismes auto-organisés et individualisés. Enfin en étudiant plus précisément les étalons, j’ai pu montrer quecontrairement à l’idée populaire, ils ne sont pas les leaders de leur groupe. Leur rôle s’apparente plus à celui d’un surveillant et ils sont parfois un des catalyseurs du phénomène. Ces résultats suggèrent que les chevaux vivent au sein d’un système hybride ou décisions partagée et non partagée coexistent. / Living in groups is challenging on many levels for animals and one of this challenge is the maintenance of group cohesion. How animals that do not share the same motives or needs, decide collectively where and when to go, to rest or to eat? In this work, I studied the mechanisms underlying collective decision during group movements in domestic horses, and notably the weight of interindividual differences and social relationships on those mechanisms. In order to achieve thatgoal, I studied four groups of domestic horses containing only females or one male and several females (i.e. natural group organisation). I was able to show that in horses 1) there is no leader and the decision is shared among group members, 2) personality and social relationships play a key role on the individual decisions, 3) the period before departure is crucial in determining the speed of the consensus, 4) both individualized and self-organised mechanisms underlie collective decisions. Finally by studying thoroughly the behaviour of stallions, I was able to debunk the myth that stallionsare the leader of their group. Their role is closer to that of a supervisor and sometimes of a catalyseras they can push females forward. Overall these results suggest that horses live in a hybrid system where shared and unshared decision coexist.