The hippocampus is a brain region that can undergo tremendous plasticity in adulthood. The hippocampus is related to the formation of spatial memories in birds and mammals. In birds, plasticity in the hippocampus occurs when formation of such memories is directly relevant to survival or reproduction, such as for breeding or food caching. In reptiles, the homologues to the hippocampus are the dorsal and medial cortices (DC and MC). In several lizard, snake and turtle species, these structures have been related to spatial memory. Experimental investigations indicate that differences in DC volume are related to space use associated with differing foraging ecologies. Differences in MC volume have been associated with territory size-based mate acquisition strategies. Furthermore, territory size has previously been correlated with plasma testosterone (T) levels. Therefore, I hypothesized that neuroplasticity within the MC/DC is controlled by demands on spatial navigation and seasonal differences and that these changes may involve the action of T. During two experimental trials, male Western Fence Lizards (Sceloporus occidentalis) were placed into either large or small semi-natural enclosures and allowed to interact with a female and intruder males over the span of seven weeks. One trial was performed during the spring breeding season and the other during the summer non breeding season, to examine seasonal differences in plasticity. Blood samples were collected at initial time of capture and before sacrifice to measure plasma T. Immunostaining for doublecortin was used to determine the density of immature neurons in each region, and cresyl violet staining allowed for volume measurements of specific regions. MC cell layer neurogenesis was higher in lizards placed in large enclosures than those in small enclosures and higher in the summer than in the spring. DC volume was smaller in lizards held in large enclosures than those in small enclosures. The decreased DC volume seen lizards held in large enclosures may indicate a cost to the increased neurogenesis in the MC of lizards in the same enclosures. These results indicate a possible trade-off between DC volume and MC neurogenesis that allows for switching between the ability to solve novel spatial tasks using the DC while storing a cognitive map in the MC. During the spring, T had no relationship with MC volume, while during the summer this was negative, so effects of T on the MC may be seasonal.

In social primates, the acquisition and maintenance of social dominance may augment reproductive success while incurring immunological costs. This trade-off is hypothetically facilitated by hormones that modulate both status-enhancing behavior and immune function. In the three studies comprising this dissertation, I investigated hormonal mechanisms by which social dominance may reflect immune health, testing relationships between behavioral correlates of dominance rank, steroid hormone secretion, and immune activity in wild adult male chimpanzees (Pan troglodytes schweinfurthii). Between January 2016 and July 2017, I collected behavioral observations and urine samples from adult males at Ngogo in Kibale National Park, Uganda, home to the largest community of habituated wild chimpanzees yet described. In the first study, I assessed behavioral and anatomical mechanisms that may link dominance rank to the secretion of testosterone, the primary male sex hormone. Testosterone was positively correlated with dominance rank and creatinine, a product of muscle catabolism and noninvasive proxy for lean muscle mass. Contrary to expectations, testosterone was negatively correlated with overall rates of aggression, indicating that aggressiveness does not itself account for positive linear correlations between dominance and testosterone in this species. In the second study, I analyzed reproductively salient correlates of cortisol, a glucocorticoid hormone secreted in response to psychosocial and metabolic demands. Urinary measures of reproductive effort and immune challenge were positively correlated with cortisol, indicating adaptive energy allocation. Furthermore, dominance rank was positively correlated with urinary cortisol when c-peptide of insulin, as a measure of energy intake, was low. This indicates that high ranking males deprioritize energy intake in certain social contexts, including competition for sexually receptive mates. In the third study, I found that although urinary testosterone seemingly diminished immune function, high ranking males were less likely to die from severe acute immune challenge than low ranking conspecifics. My results provide evidence that mating effort increases immune challenge both by increasing testosterone secretion and reallocating energy away from immune function. However, despite the increased mating effort exhibited by high ranking males, social dominance does not incur notable immunological costs. On the contrary, social dominance likely reflects immunocompetence and male quality in nonhuman primates. / 2021-12-06T00:00:00Z

Twenty untrained men (18-25 y) were assigned to consume either a milk supplement (MILK) or a carbohydrate-electrolyte supplement (CHO) immediately following each resistance workout during a 10 wk resistance training program. Subjects trained 3 d/wk beginning with an intensity of 55% 1-RM and progressing to 97% 1-RM by wk 10. Muscle strength (1-RM), body composition (DEXA) and resting, fasted serum concentrations of total and free testosterone and IGF-1 were measured pre- and post-training. CHO tended to reduce, while MILK increased body weight (P = 0.10). All subjects significantly reduced percent body fat (1.1%) and significantly increased lean body mass (1.21 kg) as a result of the resistance training with no significant differences between treatments. However, MILK tended to increase lean body mass (P = 0.1) more than CHO (1.6 and 0.8 kg, respectively). About 39% of lean mass gain for all subjects was in the leg region, while the arms accounted for about 28% of lean gain. Resistance training also caused a similar significant 44% increase in muscle strength for the seven exercises combined for both groups. Resting total and free testosterone concentrations significantly decreased from baseline values in both groups of subjects (16.7% and 11%, respectively), while resting insulin concentrations significantly increased in all subjects (P<0.01). There were no significant changes in resting, fasted IGF-1 concentrations. In summary, dietary supplementation with a MILK or CHO beverage immediately following resistance exercise resulted in similar changes in muscle strength and hormone concentrations following a 10 wk periodized resistance training program. MILK tended to increase body weight and lean body mass more so than CHO. / Master of Science

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Life-history strategies are adaptations in behavior, physiology, and anatomy that influence survival and reproductive success. Variation in life-history strategies is often determined by adaptations to environmental conditions and trade-offs with sexually-selected signals. One of the aspects controlling life-history trade-offs is the endocrine system. Testosterone is a hormone that mediates several key aspects of male reproduction, yet little is known about the causes and consequences of variation in testosterone. Using rufous-collared sparrows (Zonotrichia capensis), a Neotropical songbird with a wide distribution, I explored geographical patterns of variation in testosterone levels and infection by haemosporidians, a type of blood parasite. I found that testosterone did not vary with elevation, nor predict haemosporidian infection, but males in breeding condition were more likely to be infected (Chapter I). High levels of testosterone have been associated with an increased number of sexual contacts and can suppress the immune response, thus it may increase the risk of sexually transmitted infections. By studying the communities of bacteria that reside in the cloaca of birds, I found that they were different depending on testosterone levels, and that high-testosterone males had higher relative abundance of Chlamydiae, a class of intracellular pathogens (Chapter II). During the breeding season there is an increase in physical contacts among individuals, testosterone levels increase in males, and there are additional energetic demands, all of which can increase exposure to bacteria or facilitate infection. I compared the cloacal microbiome of the same individuals between breeding and non-breeding seasons, and found that in males, but not in females, bacterial richness and phylogenetic diversity increased when birds were in reproductive condition. This suggested that the cloacal microbiome in birds is dynamic and responsive to breeding condition and sex of the host (Chapter III). Lastly, I synthesized the most relevant findings and suggested directions for future work (Chapter IV). I conclude that variation in testosterone is not always associated with immune suppression, and that the links among reproductive physiology, behavior, and the microbiome can provide insight into the evolution of life-history strategies. / Ph. D.

Au cours des 150 dernières années, l'évolution de la coopération n'a cessé d'intriguer les biologistes de l'évolution. Les comportements coopératifs, qui procurent un avantage direct au bénéficiaire, ne peuvent être sélectionnés que si, pour le coopérateur, les bénéfices directs et/ou indirects dépassent le coût. De nombreuses observations chez l'Homme et chez d'autres espèces animales suggèrent que les comportements coopératifs pourraient être maintenus par la sélection sexuelle. Pourtant, ce champ de recherche est quasiment inexploré, que ce soit chez l'Homme ou chez les autres espèces sociales. Afin d'examiner le rôle potentiel de la sélection sexuelle sur les comportements coopératifs, deux modèles biologiques ont été utilisés : l'Homme et la Souris glaneuse (Mus spicilegus). Chez l'Homme, la propension à coopérer a été quantifiée dans deux populations humaines (française et sénégalaise) principalement par des méthodes empruntées à l'économie expérimentale (jeu du bien public). Chez la souris glaneuse, l'investissement individuel dans la construction collective d'un tumulus pour l'hivernage a été mesuré en captivité. Les résultats soutiennent partiellement nos prédictions, à savoir : (i) que les individus coopèrent davantage en présence de partenaires sexuels potentiels, (ii) que les coopérateurs sont préférés comme partenaires sexuels, et que (iii) ces préférences conduisent à un appariement selon la coopérativité. De plus, ils suggèrent que des traits physiques (visuels, olfactifs, ou acoustiques) puissent être utilisés pour détecter la coopérativité d'un individu. Chez l'Homme, en particulier, des traits statiques du visage, dont au moins certains sont lisibles inter-culturellement, semblent impliqués. Enfin, une éventuelle association entre les comportements coopératifs et une hormone sexuelle, la testostérone, a été examinée. Pris dans leur ensemble, nos résultats suggèrent que la sélection sexuelle pourrait être impliquée dans l'évolution et le maintien de la coopération et ouvrent donc la voie à de nouvelles recherches, examinant son influence dans diverses populations humaines, ainsi que dans de nombreuses autres espèces sociales. Mots clés : Coopération, Altruisme, Générosité, Investissement parental, Attractivité, Jeu du bien public, Choix de partenaire, Homogamie, signal de coopérativité et détection, Régulation hormonale, Testostérone. / Over the past 150 years, the evolution of cooperation has challenged evolutionary biologists. Cooperative behaviour provide a benefit to the recipient and can only be selected for if it also provides direct and/or indirect benefits to the actor that accepted the costs of the cooperative action. Many observations in humans and other animal species suggest that cooperative behaviour could be maintained by sexual selection. However, the hypothesis that sexual selection could be involved in the evolution of cooperation has not received much attention in the recent literature. In order to examine the potential role of sexual selection in cooperative behaviour, two biological models were used: humans and the Mound-building mouse (Mus spicilegus). In two human populations (French and Senegalese populations), cooperativeness was quantitatively measured, mainly by an economic game (the public good game). The spontaneous cooperativeness exhibited during collective mound-building for overwintering was assessed in captivity for Mus spicilegus. The results partly support our predictions: (i) individuals cooperativeness increase in the presence of potential sexual partners, (ii) cooperators are preferred as sexual partners, (iii) these preferences lead to assortative mating based on cooperativeness. Moreover, they suggest that physical traits (visual, olfactory, or acoustic) could be used to detect individual cooperativeness. In humans, static facial traits seem to be involved, and some of them appear to be inter-culturally readable. Finally, a potential association between cooperative behaviour and testosterone levels, a sex hormone, was examined. Together, these results suggest that sexual selection could be involved in the evolution and the maintenance of cooperation. Furthers studies are needed, in different human populations and in different social species, to further investigate the role of sexual selection in cooperative behaviour. Keywords: Cooperation, Altruism, Generosity, Parental investment, Attractiveness, Public Good Game, Mate choice, Homogamy, Detection, Signaling, Hormonal regulation, Testosterone.

Androgens are critical for the development and maintenance of adult male characteristics such as muscle mass and sexual function. Consequently, the established decline with age of serum testosterone (T) in males has major health implications. While the androgen receptor (AR) is the major mediator of genomic androgen action and is required for the development of the male phenotype, reproductive organs and the maintenance of male secondary sexual characteristics, it is the entrance of androgens into the cell that mediates the activation of the AR and the subsequent modulation of expression of androgen regulated genes. Testosterone, biologically the most important androgen in male serum, circulates either free, loosely bound to albumin or tightly bound to sex hormone binding globulin (SHBG). Each of these forms of serum T have different abilities to enter cells, and which proportion of serum T is capable of entering cells and initiating the androgen signalling cascade, thereby leading to the activation of the AR has not been precisely defined. The AR amino terminal domain (NTD) is responsible for the majority of the ability of the AR to activate genes but the relative roles of the two activation functions in the AR NTD (activation functions 1 and 5; AF1 and 5) have not been precisely defined while the role of the AF2 surface which forms in the ligand binding domain upon agonist binding is responsible for interactions with key coregulators and also with the NTD in the amino-carboxyl (N/C) interaction. Our laboratory has recently identified a region within AF5 between amino acids 500-535 to which somatic mutations in castrate resistant prostate tumour samples collocate. Due to the lack of functional information on the AF5 region and the NTD in general, the function of this region and the functional consequences of the mutations remain to be defined. The objectives of this thesis were to develop a specific mammalian cell based bioassay capable of reliable measuring T in serum and to determine the ability of this bioassay to measure a physiologically relevant fraction of T in serum. Additionally, this thesis aimed to determine the relative contributions and roles of the activation functions of the AR to overall AR transcriptional activity along with the functional consequences for AR signalling of prostate cancer mutations which have previously been identified in the AF5 region of the AR NTD. The mammalian-cell based bioassay developed in this thesis is capable of sensitively and reliably measuring serum T. However, evaluation of this bioassay utilising approximately 1000 serum samples from the Florey Adelaide Male Aging Study reveals that this bioassay measures a fraction of T in serum that most closely relates to serum T. Furthermore, this measure does not correlate more strongly with grip strength, sexual function or waist circumference than the existing immunoassay-based measures of serum T, highlighting the limitations of utilising a static mammalian cell-based androgen bioassay to measure physiological levels of serum T in males. The investigation of the roles of the activation functions in the AR in this thesis have revealed that while the AF1 domain is responsible for the majority of the transactivation activity of the AR, AF5 and AF2 govern the sensitivity and cellular response of the AR to androgens by providing protein and interdomain interaction interfaces. Furthermore, the evidence in this thesis demonstrates that the AR requires interdomain communication for sensitive AR signalling. Finally, the findings in this thesis demonstrate that the AF5 surface is required for the N/C interaction and coregulator interactions while advanced prostate cancer mutations identified within this region confer increased transactivation activity of the AR in the presence of high cellular levels of coregulators. Collectively, the findings in this thesis provide several novel insights into the mechanism of action of serum androgens and challenges several long held assumptions of androgenic action in males. These findings also delineate a mechanism of treatment failure in advanced prostate cancer, provide a novel model for the events leading to sensitive AR transactivation and contribute to the understanding of physiologically relevant levels of serum T. / Thesis (Ph.D.) -- University of Adelaide, School of Medicine, 2008