The evolution and socioecology of dominance in primate groups: A theoretical formulation,classification and assessment

Dominance hierarchies are presumed to evolve by individual selection from an evolutionary compromise between intraspecific competition for resources and for mates. The hypothesis is put forward that when competition in “stable” habitats leads to “niche breadth,” a species is preadapted to life in heterogeneous environments and the consequent selection for fecundity. Status patterns are viewed as systems of signals communicating differential tendencies among individuals to attack or retreat, and a simple graphical model is presented which relates the costs or benefits to fitness of aggressive or appeasement behavior and interindividual distance. Primate societies are classified on the basis of their dominance hierarchies, and the ecological correlates of these patterns are discussed. Based on hypotheses presented in the paper, topics for future research are suggested.     

Pirouettes: the rotational play of wild chimpanzees

A pirouette is a locomotor-rotational movement in which a young chimpanzee spins around in a (mostly) quadruped posture while advancing forward in a straight line. We addressed whether this behavior evolved as a practice of general athletic ability or of sexual selection. The former hypothesis would predict no sex differences in skill or the developmental process, while the latter would predict the opposite. Chimpanzees most likely master the pirouette around the time of weaning. We found no conspicuous sex differences in the developmental process or the number of rotations per bout of pirouettes, so the pirouette’s main function may be to facilitate general athletic ability. Infants pirouetted regardless of the context of rest or travel, whereas juveniles and adolescents pirouetted primarily during travel. This is consistent with the survival strategy hypothesis, because juveniles and adolescents would be expected to display pirouettes to many watchers if this practice were sexually selected. However, the fact that males tend to pirouette faster than females and to pirouette even during adolescence suggests that sexual selection has some influence in shaping the evolution of the practice. Despite this, no conspicuous tendency was found for juveniles or adolescent chimpanzees to display pirouettes to opposite-sex individuals. More data on adolescent individuals are needed to definitively determine the role of sex differences in pirouetting behavior.     

Stability of behavioral syndromes but plasticity in individual behavior: consequences for rockfish stock enhancement

This study investigated behavioral syndromes, which are defined as correlations between behaviors. Behavioral syndromes can lead to the unintentional alteration of a wide range of behavioral traits of hatchery fish if unintentional selection on one behavior leads to selection on a correlated behavior. Specifically, this study used brown rockfish, Sebastes auriculatus, to test the hypothesis that a fish that feeds at high rates in the absence of a predator also takes more risks when a predator is present, and that through such a correlation, unintentional hatchery selection for high feeding rates may also lead to changes in risk taking behavior (here defined as behavior that increases predation risk). Behavioral syndromes were found—feeding behavior in the absence of a predator tended to correlate positively with both feeding behavior in the presence of a predator model and time near the model. These syndromes were stable through time—that is, the same correlations appeared 10 days later when the behavioral assays were repeated. However individual behavior was inconsistent (plastic). A fish could both feed and take risks at high rates on Day 1, but then both feed and take risks at low rates on Day 10. Thus, while behavioral syndromes were stable (i.e. present in both rounds 1 and 2), individuals were plastic in their behavior (i.e. inconsistent between rounds 1 and 2). After 16 weeks of hatchery rearing, neither growth nor survival were predicted by behavior. It is suggested that the behavioral plasticity within individuals through time makes consistent selection for strong feeders less likely, and that species with more plastic behavior may be less susceptible to unintentional selection on behavioral syndromes than species with behavior that is more fixed.     

Brain evolution by brain pathway duplication

Understanding the mechanisms of evolution of brain pathways for complex behaviours is still in its infancy. Making further advances requires a deeper understanding of brain homologies, novelties and analogies. It also requires an understanding of how adaptive genetic modifications lead to restructuring of the brain. Recent advances in genomic and molecular biology techniques applied to brain research have provided exciting insights into how complex behaviours are shaped by selection of novel brain pathways and functions of the nervous system. Here, we review and further develop some insights to a new hypothesis on one mechanism that may contribute to nervous system evolution, in particular by brain pathway duplication. Like gene duplication, we propose that whole brain pathways can duplicate and the duplicated pathway diverge to take on new functions. We suggest that one mechanism of brain pathway duplication could be through gene duplication, although other mechanisms are possible. We focus on brain pathways for vocal learning and spoken language in song-learning birds and humans as example systems. This view presents a new framework for future research in our understanding of brain evolution and novel behavioural traits.     

Molecular mapping of movement-associated areas in the avian brain: a motor theory for vocal learning origin

Vocal learning is a critical behavioral substrate for spoken human language. It is a rare trait found in three distantly related groups of birds-songbirds, hummingbirds, and parrots. These avian groups have remarkably similar systems of cerebral vocal nuclei for the control of learned vocalizations that are not found in their more closely related vocal non-learning relatives. These findings led to the hypothesis that brain pathways for vocal learning in different groups evolved independently from a common ancestor but under pre-existing constraints. Here, we suggest one constraint, a pre-existing system for movement control. Using behavioral molecular mapping, we discovered that in songbirds, parrots, and hummingbirds, all cerebral vocal learning nuclei are adjacent to discrete brain areas active during limb and body movements. Similar to the relationships between vocal nuclei activation and singing, activation in the adjacent areas correlated with the amount of movement performed and was independent of auditory and visual input. These same movement-associated brain areas were also present in female songbirds that do not learn vocalizations and have atrophied cerebral vocal nuclei, and in ring doves that are vocal non-learners and do not have cerebral vocal nuclei. A compilation of previous neural tracing experiments in songbirds suggests that the movement-associated areas are connected in a network that is in parallel with the adjacent vocal learning system. This study is the first global mapping that we are aware for movement-associated areas of the avian cerebrum and it indicates that brain systems that control vocal learning in distantly related birds are directly adjacent to brain systems involved in movement control. Based upon these findings, we propose a motor theory for the origin of vocal learning, this being that the brain areas specialized for vocal learning in vocal learners evolved as a specialization of a pre-existing motor pathway that controls movement.     

Evolutionary pathways in shorebird breeding systems: sexual conflict, parental care, and chick development

Sexual selection, mating opportunities, and parental behavior are interrelated, although the specific nature of these relationships is controversial. Two major hypotheses have been suggested. The parental investment hypothesis states that the relative parental investment of the sexes drives the operation of sexual selection. Thus, the sex that invests less in offspring care competes more intensely and monopolizes access to mates. The sexual conflict hypothesis proposes that sexual selection (the competition among both males and females for mates), mating opportunities, and parental behavior are interrelated and predicts a feedback loop between mating systems and parental care. Here we test both hypotheses using a comprehensive dataset of shorebirds, a maximum-likelihood statistical technique, and a recent supertree of extant shorebirds and allies. Shorebirds are an excellent group for these analyses because they display unique variation in parental care and social mating system. First, we show that chick development constrains the evolution of both parental care and mate competition, because transitions toward more precocial offspring preceded transitions toward reduced parental care and social polygamy. Second, changes in care and mating systems respond to one another, most likely because both influenced and are influenced by mating opportunities. Taken together, our results are more consistent with the sexual conflict hypothesis than the parental investment hypothesis.     

Circuits,hormones, and learning: Vocal behavior in songbirds

Species-typical vocal patterns subserve species identification and communication for individual organisms. Only a few groups of organisms learn the sounds used for vocal communication, including songbirds, humans, and cetaceans. Vocal learning in songbirds has come to serve as a model system for the study of brain-behavior relationships and neural mechanisms of learning and memory. Songbirds learn specific vocal patterns during a sensitive period of development via a complex assortment of neurobehavioral mechanisms. In many species of songbirds, the production of vocal behavior by adult males is used to defend territories and attract females, and both males and females must perceive vocal patterns and respond to them. In both juveniles and adults, specific types of auditory experience are necessary for initial song learning as well as the maintenance of stable song patterns. External sources of experience such as acoustic cues must be integrated with internal regulatory factors such as hormones, neurotransmitters, and cytokines for vocal patterns to be learned and produced. Thus, vocal behavior in songbirds is a culturally acquired trait that is regulated by multiple intrinsic as well as extrinsic factors. Here, we focus on functional relationships between circuitry and behavior in male songbirds. In that context, we consider in particular the influence of sex hormones on vocal behavior and its underlying circuitry, as well as the regulatory and functional mechanisms suggested by morphologic changes in the neural substrate for song control. We describe new data on the architecture of the song system that suggests strong similarities between the songbird vocal control system and neural circuits for memory, cognition, and use-dependent plasticity in the mammalian brain. © 1997 John Wiley & Sons, Inc. J Neurobiol 33: 602–618, 1997     

大鲵的水下发声与相关行为

无尾类两栖动物的复杂的声行为对其繁殖与物种的识别具有重要的作用,而有尾类除了少数种类可以发出 微弱的“吱吱”声或吠声外,在过去一直被认为是基本不发声的。但是,最近的基于解剖学的证据的研究显示隐腮 鲵科(Cryptobranchidae)可能是一个例外。为了检验这一假说,作者对实验室严格控制的条件下的4只中国大鲵(An- drias davidianus)进行了观察。观察结果不仅表明动物在水下发声,同时也观察到了与之相关联的行为。作者对进 一步在野生条件下开展研究提出了建议。     

Specialized Motor-Driven dusp1 Expression in the Song Systems of Multiple Lineages of Vocal Learning Birds

Mechanisms for the evolution of convergent behavioral traits are largely unknown. Vocal learning is one such trait that evolved multiple times and is necessary in humans for the acquisition of spoken language. Among birds, vocal learning is evolved in songbirds, parrots, and hummingbirds. Each time similar forebrain song nuclei specialized for vocal learning and production have evolved. This finding led to the hypothesis that the behavioral and neuroanatomical convergences for vocal learning could be associated with molecular convergence. We previously found that the neural activity-induced gene dual specificity phosphatase 1 (dusp1) was up-regulated in non-vocal circuits, specifically in sensory-input neurons of the thalamus and telencephalon; however, dusp1 was not up-regulated in higher order sensory neurons or motor circuits. Here we show that song motor nuclei are an exception to this pattern. The song nuclei of species from all known vocal learning avian lineages showed motor-driven up-regulation of dusp1 expression induced by singing. There was no detectable motor-driven dusp1 expression throughout the rest of the forebrain after non-vocal motor performance. This pattern contrasts with expression of the commonly studied activity-induced gene egr1, which shows motor-driven expression in song nuclei induced by singing, but also motor-driven expression in adjacent brain regions after non-vocal motor behaviors. In the vocal non-learning avian species, we found no detectable vocalizing-driven dusp1 expression in the forebrain. These findings suggest that independent evolutions of neural systems for vocal learning were accompanied by selection for specialized motor-driven expression of the dusp1 gene in those circuits. This specialized expression of dusp1 could potentially lead to differential regulation of dusp1-modulated molecular cascades in vocal learning circuits.     

Comprehensive,Population-Based Sensitivity Analysis of a Two-Mass Vocal Fold Model

Previous vocal fold modeling studies have generally focused on generating detailed data regarding a narrow subset of possible model configurations. These studies can be interpreted to be the investigation of a single subject under one or more vocal conditions. In this study, a broad population-based sensitivity analysis is employed to examine the behavior of a virtual population of subjects and to identify trends between virtual individuals as opposed to investigating a single subject or model instance. Four different sensitivity analysis techniques were used in accomplishing this task. Influential relationships between model input parameters and model outputs were identified, and an exploration of the model’s parameter space was conducted. Results indicate that the behavior of the selected two-mass model is largely dominated by complex interactions, and that few input-output pairs have a consistent effect on the model. Results from the analysis can be used to increase the efficiency of optimization routines of reduced-order models used to investigate voice abnormalities. Results also demonstrate the types of challenges and difficulties to be expected when applying sensitivity analyses to more complex vocal fold models. Such challenges are discussed and recommendations are made for future studies.     

Parasites affect song complexity and neural development in a songbird

There is now considerable evidence that female choice drives the evolution of song complexity in many songbird species. However, the underlying basis for such choice remains controversial. The developmental stress hypothesis suggests that early developmental conditions can mediate adult song complexity by perturbing investment in the underlying brain nuclei during their initial growth. Here, we show that adult male canaries (Serinus canaria), infected with malaria (Plasmodium relictum) as juveniles, develop simpler songs as adults compared to uninfected individuals, and exhibit reduced development of the high vocal centre (HVC) song nucleus in the brain. Our results show how developmental stress not only affects the expression of a sexually selected male trait, but also the structure of the underlying song control pathway in the brain, providing a direct link between brain and behaviour. This novel experimental evidence tests both proximate and ultimate reasons for the evolution of complex songs and supports the Hamilton-Zuk hypothesis of parasite-mediated sexual selection. Together, these results propose how developmental costs may help to explain the evolution of honest advertising in the complex songs of birds.     

Sexual selection,genital morphology,and copulatory behavior in male Galagos

Variations in penile morphology among galago species are pronounced and complex. Comparative studies of galagos and other primate species show that elongation of the baculum (os penis)is associated with copulatory patterns involving a prolonged period of intromission. The enlarged penile “spines” of male galagos may be important in maintaining a genital “lock” during copulation. In primate species where females mate with a number of partners, sexual selection may have favored the rapid evolution of such features of penile morphology and masculine copulatory behavior. It is suggested that evolution of complex penile morphologies in galagos has been influenced by sexual selection and that such morphological variations are extremely useful in taxonomic studies.     

Wild Chimpanzees Produce Group‐Specific Calls: a Case for Vocal Learning?

Vocal learning, where animals can modify the structure of their vocalizations as a result of experience, has been found in a range of birds and mammals. Although vocal learning is a fundamental aspect of developing spoken language, there is as yet little evidence that vocal learning occurs in primates. Here we examine whether vocal learning may occur in chimpanzees. We analysed whether wild male chimpanzees, Pan troglodytes verus, of four communities living in a similar habitat in the Taï Forest, Côte d'Ivoire, developed community specific pant hoots. If so, we expected males of three contiguous communities to have distinct pant hoots, while pant hoots of males from a fourth, distant community, located 70 km away, should only differ from those of the contiguous communities by chance. Our analysis confirmed these expectations. In addition, the acoustic distances between the pant hoots of pairs of individuals did not correlate with the genetic relatedness of those pairs, where genetic relatedness was determined using nuclear DNA analysis. Thus, neither habitat nor genetic differences accounted for the observation that there were acoustic differences in the pant hoot structure of males living in neighbouring communities, but not in those of males from a distant community. This suggests that chimpanzees may actively modify pant hoots to be different from their neighbours, providing support for the vocal learning hypothesis.     

Chance, time allocation, and the evolution of adaptively flexible sex role behavior

An alternative to classic sexual selection hypotheses for sex differentiated pre-mating behavior is that time available for mating-as individuals experience it-along with fitness differences among alternative potential mates, induces choosy versus indiscriminate mating behavior. This alternative hypothesis says that selection has acted so that all individuals flexibly express fitness-enhancing choosy, indiscriminate, and competitive mating behavior, induced by time-varying life histories, environmental and social cues. Key predictions of DYNAMATE, the formal model of adaptively flexible sex role behavior of individuals of both sexes within dynamically changing populations, include: (1) All individuals regardless of sex assess likely fitness outcomes from mating with alternative potential mates before expressing choosy or indiscriminate behavior. (2) Males and females express adaptively flexible, choosy and indiscriminate behavior so that individuals may change their behavior-from moment to moment-to fit dynamically changing circumstances. (3) Indiscriminate behavior of males and (4) choosy behavior of females would often be maladaptive even in species with greater female than male parental investment, when females have longer latencies to receptivity to re-mating than males, and when the relative reproductive rate of males is greater than in females. (5) Whether or not females show choosy behavior will not affect whether or not males exhibit choosy or indiscriminate behavior, and vice versa. (6) When other model parameters are equal, the proportion of individuals of a given sex expressing choosy or indiscriminate mating behavior is a function of the distribution of fitness ratios (a distribution of all fitness differences that would be conferred on an individual by mating with any two sequentially or simultaneously encountered alternative potential mates). (7) Whether same-sex individuals behaviorally compete is a function of the fitness that would be conferred if the strategist won access to a potential mate, but not a function of relative reproductive rate or its proxy, the operational sex ratio. We call for re-evaluation of sex differences in choosy, indiscriminate, and competitive behavior under strong experimental controls that level the ecological playing fields of males and females, i.e., under experimental conditions informing the mechanisms of phenotypic expression. We end with comments on the classic question of questions: why are the sexes as they are?     

鸣禽鸣叫学习的神经生物学机制

鸣禽鸣叫具有复杂的神经生理和生化基础,表现为一种复杂的学习过程。鸣啭控制系统是研究神经系统与学习、行为和发育关系的重要模型。而鸣禽鸣叫学习行为与鸣啭控制系统内长时程增强效应、神经元超微结构的改变和神经核团内的电活动、激素水平高低及其周期性变化、神经元再生或改变、即早基因的表达等方面密切相关。对鸣禽鸣叫的神经生物学机制进行了综述。     

Differential effects of prenatal testosterone timing and duration on phenotypic and behavioral masculinization and defeminization of female sheep

The process of sexual differentiation leaves genetically female individuals at risk of being masculinized by exogenous androgens. Previous research with sheep indicates that exposure to excess testosterone from Gestational Day (GD) 30 to GD 90 of the 147-day gestation masculinizes and defeminizes behavior as well as genitalia. Lower doses and shorter durations produce animals with varying degrees of genital virilization and alterations of the hypothalamic-pituitary-gonadal axis, but to our knowledge, the effects on complex behavior and its prediction by the amount of external virilization have not been explored. Previous research in rodents has suggested that sexual differentiation of the central nervous system and the external genitalia can be dissociated. Therefore, we hypothesized that the extent of virilization of external genitalia would not be predictive of the lack of female-typical, or the presence of male-typical, mating behavior. To test this hypothesis, we compared control females, females exposed to exogenous testosterone from GD 30 to GD 90 (T60 females) that have virilized genitalia, and females exposed to testosterone from GD 60 to GD 90 (T30 females) that have female-typical genitalia. Both natural behavioral estrus in the flock and hormonally controlled behavioral tests were used to explore reproductive behavior. The T60 and T30 females exhibited more masculinized reproductive behavior than the controls; however, the T30 females also exhibited feminine behavior. Neither testosterone-treated group was receptive or was mounted at rates comparable to those of controls. These data illustrate that variation in the timing or duration of exposure to prenatal testosterone during a critical period for masculinization can have variable effects on defeminization and that the effects of testosterone on genitalia are not entirely predictive of behavior.     

The Evolution of Human Homosexual Behavior

Homosexuality presents a paradox for evolutionists who explore the adaptedness of human behavior. If adaptedness is measured by reproductive success and if homosexual behavior is nonreproductive, how has it come about? Three adaptationist hypotheses are reviewed here and compared with the anthropological literature. There is little evidence that lineages gain reproductive advantage through offspring care provided by homosexual members. Therefore, there is little support for the hypothesis that homosexuality evolved by kin selection. Parents at times control children's reproductive decisions and at times encourage children in homosexual behavior. There is therefore more support for the hypothesis of parental manipulation. Support is strongest, however, for the hypothesis that homosexual behavior comes from individual selection for reciprocal altruism. Same-sex alliances have reproductive advantages, and sexual behavior at times maintains these alliances. Nonhuman primates, including the apes, use homosexual behavior in same-sex alliances, and such alliances appear to have been key in the expanded distribution of human ancestors during the Pleistocene. Homosexual emotion and behavior are, in part, emergent qualities of the human propensity for same-sex affiliation. Adaptationist explanations do not fully explain sexual behavior in humans, however; social and historical factors also play strong roles.     

The Evolution of Human Homosexual Behavior

Homosexuality presents a paradox for evolutionists who explore the adaptedness of human behavior. If adaptedness is measured by reproductive success and if homosexual behavior is nonreproductive, how has it come about? Three adaptationist hypotheses are reviewed here and compared with the anthropological literature. There is little evidence that lineages gain reproductive advantage through offspring care provided by homosexual members. Therefore, there is little support for the hypothesis that homosexuality evolved by kin selection. Parents at times control children's reproductive decisions and at times encourage children in homosexual behavior. There is therefore more support for the hypothesis of parental manipulation. Support is strongest, however, for the hypothesis that homosexual behavior comes from individual selection for reciprocal altruism. Same-sex alliances have reproductive advantages, and sexual behavior at times maintains these alliances. Nonhuman primates, including the apes, use homosexual behavior in same-sex alliances, and such alliances appear to have been key in the expanded distribution of human ancestors during the Pleistocene. Homosexual emotion and behavior are, in part, emergent qualities of the human propensity for same-sex affiliation. Adaptationist explanations do not fully explain sexual behavior in humans, however; social and historical factors also play strong roles.     

The Evolution of Human Homosexual Behavior

Homosexuality presents a paradox for evolutionists who explore the adaptedness of human behavior. If adaptedness is measured by reproductive success and if homosexual behavior is nonreproductive, how has it come about? Three adaptationist hypotheses are reviewed here and compared with the anthropological literature. There is little evidence that lineages gain reproductive advantage through offspring care provided by homosexual members. Therefore, there is little support for the hypothesis that homosexuality evolved by kin selection. Parents at times control children's reproductive decisions and at times encourage children in homosexual behavior. There is therefore more support for the hypothesis of parental manipulation. Support is strongest, however, for the hypothesis that homosexual behavior comes from individual selection for reciprocal altruism. Same-sex alliances have reproductive advantages, and sexual behavior at times maintains these alliances. Nonhuman primates, including the apes, use homosexual behavior in same-sex alliances, and such alliances appear to have been key in the expanded distribution of human ancestors during the Pleistocene. Homosexual emotion and behavior are, in part, emergent qualities of the human propensity for same-sex affiliation. Adaptationist explanations do not fully explain sexual behavior in humans, however; social and historical factors also play strong roles.     

Sensory-motor interactions modulate a primate vocal behavior: antiphonal calling in common marmosets

A fundamental issue in neuroscience pertains to how different cortical systems interact to generate behavior. One of the most direct ways to address this issue is to investigate how sensory information is encoded and used to produce a motor response. Antiphonal calling is a natural vocal behavior that involves individuals producing their species-specific long distance vocalization in response to hearing the same call and engages both the auditory and motor systems, as well as the cognitive neural systems involved in decision making and categorization. Here we present results from a series of behavioral experiments investigating the auditory–vocal interactions during antiphonal calling in the common marmoset (Callithrix jacchus). We manipulated sensory input by placing subjects in different social contexts and found that the auditory input had a significant effect on call timing and propensity to call. Playback experiments tested the significance of the timing of vocal production in antiphonal calling and showed that a short latency between antiphonal calls was necessary to maintain reciprocal vocal interactions. Overall, this study shows that sensory-motor interactions can be experimentally induced and manipulated in a natural primate vocal behavior. Antiphonal calling represents a promising model system to examine these issues in non-human primates at both the behavioral and neural levels.