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Rogers, L. J., & Andrew, R. (Eds.). (2002). Comparative Vertebrate Lateralization. New York: Cambridge University Press.
Abstract: No longer viewed as a characteristic unique to humans, brain lateralization is considered a key property of most, if not all, vertebrates. This field of study provides a firm basis from which to examine a number of important issues in the study of brain and behaviour. This book takes a comparative and integrative approach to lateralization in a wide range of vertebrate species, including humans. It highlights model systems that have proved invaluable in elucidating the function, causes, development, and evolution of lateralization. The book is arranged in four parts, beginning with the evolution of lateralization, moving to its development, to its cognitive dimensions, and finally to its role in memory. Experts in lateralization in lower vertebrates, birds, non-primate mammals, and primates have contributed chapters in which they discuss their own research and consider its implications to humans. The book is suitable for researchers, graduates and advanced undergraduates in psychology, neuroscience and the behavioral sciences.
- Unique in its truly comparative approach, covering fish, amphibians, birds, and mammals (including primates and humans) – World-class editors and contributors – Very broad coverage of both theoretical and technical aspects of laterality, including evolution, development, behaviour, and memory
Contents
Preface; Introduction; Part I. Evolution of Lateralization: 1. How ancient is lateralization? G. Vallortigara and A. Bisazza; 2. The earliest origins and subsequent evolution of lateralization R. J. Andrew; 3. The nature of lateralization in tetrapods R. J. Andrew and L. J. Rogers; 4. Advantages and disadvantages of lateralization L. J. Rogers; Part II. Development of Lateralization: 5. Behavioral development and lateralization R. J. Andrew; 6. Factors affecting the development of lateralization in chicks C. Deng and L. J. Rogers; 7. Ontogony of visual lateralization in pigeons O. Güntürkün; 8. Development of laterality and the role of the corpus callosum in rodents and humans P. E. Cowell and V. H. Denenberg; 9. Posture and laterality in human and nonhuman primates: asymmetries in maternal handling and the infant"s early motor asymmetries E. Damerose and J. Vauclair; Part III. Cognition and Lateralization: 10. Evidence of cerebral lateralization from senses other than vision R. J. Andrew and J. A. S. Watkins; 11. Facing an obstacle: lateralization of object and spatial cognition G. Vallortigara and L. Regolin; 12. Laterality of communicative behaviors in nonhuman primates: a critical analysis W. D. Hopkins and S. F. Carriba; 13. Specialized processing of primate facial and vocal expressions: evidence for cerebral asymmetries D. J. Weiss, A. A. Ghazanfar, C. T. Miller and M. D. Hauser; Part IV. Lateralization and Memory: 14. Memory and lateralized recall A. N. B. Johnston and S. P. R. Rose; 15. Memory formation and brain lateralization R. J. Andrew; Epilogue; Appendix; Index.
Reviews
'Andrew & Roger perform an enormous service in bringing data from animal behaviour, neuroanatomy and electrophysiology into contact with traditional zoological concerns such as genetics, embryology and population biology.' Journal of Animal Behaviour
'Whatever the outcome of the war, this book will be a key starting point for those trying to understand it (or perhaps to fight in it).' Annals of Human Biology
Contributors
Richard J. Andrew, Angelo Bisazza, Samuel F. Carriba, Patricia E. Cowell, Eric Damerose, Victor H. Denenberg, Chao Deng, Asif A. Ghazanfar, Onur Güntürkün, Mark D. Hauser, William D. Hopkins, Amy N. B. Johnston, Cory T. Miller, Lucia Regolin, Lesley L. Rogers, Steven Rose, Giorgio Vallortigara, J. Vauclair, J. A. S. Watkins, Daniel J. Weiss
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Rogers, L. J. (2002). Advantages and disadvantages of lateralization. In L. J. Rogers, & R. Andrew (Eds.), (pp. 126–153). New York: Cambridge University Press.
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R. J. Andrew, & J. A. S. Watkins (Eds.). (2002). Evidence of cerebral lateralization from senses other than vision. New York: Cambridge University Press.
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Barton, R. (2002). The evolutionary ecolgy of the primate brain. In P. C. Lee (Ed.), Comparative Primate Socioecology (pp. 167–204). Cambridge: Cambridge University Press.
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McDonough, P., Kindig, C. A., Ramsel, C., Poole, D. C., & Erickson, H. H. (2002). The effect of treadmill incline on maximal oxygen uptake, gas exchange and the metabolic response to exercise in the horse. Experimental Physiology, 87(04), 499–506 M3– null.
Abstract: In healthy man, conditions that change muscle O2 delivery affect the achievable maximum rate of O2 uptake (V[dot above]O2,max) as well as the metabolic (e.g. lactate threshold, LT) and gas exchange (e.g. gas exchange threshold, Tge) responses to incremental exercise. Inclined (I) compared to level (L) running increases locomotory muscle EMG at a given speed in the horse, indicative of elevated metabolic demand. To our knowledge, the effect of treadmill incline on V[dot above]O2,max, LT and Tge has not been addressed in the exercising quadruped. We used blood sampling and breath-by-breath expired gas analysis to test the hypothesis that I (10 % gradient) would increase V[dot above]O2,max and the rate of O2 uptake (V[dot above]O2) at LT and Tge in six Thoroughbred horses during incremental running to volitional fatigue. V[dot above]O2,max was significantly higher for I (I, 77.8 ± 4.1; L, 65.5 ± 5.3 l min-1; P < 0.05), but peak plasma lactate concentration was not (I, 28.0 ± 3.7; L, 25.9 ± 3.0 mM). Arterial PCO2 increased to 62.1 ± 3.3 and 57.9 ± 2.7 Torr (I vs. L; P < 0.05), yet despite this relative hypoventilation, a distinct Tge was present. This Tge occurred at a significantly different absolute (I, 49.6 ± 3.2; L, 42.4 ± 3.2 l min-1; P < 0.05), but nearly identical relative V[dot above]O2 (I, 63.6 ± 1.2; L, 63.9 ± 1.6 % V[dot above]O2,max) in I and L. Similarly, LT occurred at a significantly greater absolute V[dot above]O2 (I, 37.3 ± 2.8; L, 26.9 ± 2.1 l min-1), but a relative V[dot above]O2 that was not different (I, 47.9 ± 2.1; L, 43.9 ± 4.5 % V[dot above]O2,max). In addition, Tge occurred at a significantly higher (P [less-than-or-equal] 0.05) absolute and relative V[dot above]O2 than LT for both I and L tests. In conclusion, V[dot above]O2,max is higher during inclined than level running and both LT and Tge in the horse occur at a similar percentage of V[dot above]O2,max irrespective of the absolute level of V[dot above]O2,max. In contrast to humans, LT is a poor analogue of Tge in the horse.
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Mettke-Hofmann, C., Winkler, H., & Leisler, B. (2002). The Significance of Ecological Factors for Exploration and Neophobia in Parrots. Ethology, 108(3), 249–272.
Abstract: Exploratory behaviour plays an important role in most animals for gathering information about their environment. If it constitutes an adaptation to different environmental conditions exploratory behaviour should differ between species. This has been tested with several hypotheses. Sixty-one parrot species (Psittacidae) from eight tribes with different diets and habitat preferences were investigated in aviaries. Two tests were carried out. First, a novel object (wooden ring) in the familiar aviary was presented on two test days in the exploration test. Latencies until first contact with the object and the duration of exploration were recorded. Secondly, in the neophobia test, novel objects were placed beside the feeding dish and latencies until first food intake were recorded. The exploration and neophobia data were related to 12 (13) ecological variables using multiple regression analyses. Phylogenetic relationships were considered. Species that inhabit complex habitats, such as forest edges, or that feed on buds or species from islands showed the shortest latencies in the exploration test. In contrast, long latencies were related to a diet including a great amount of seeds and/or flowers. The longest duration of exploration occurred in species eating nuts or originating from islands, whereas short durations were related to feeding on seeds. Neophobia was positively related to a diet consisting of insects, and negatively to a diet of leaves. There was no relationship between measures of exploration and neophobia. Exploration and neophobia seem to be tightly related to the ecology of a species.
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Hemelrijk, C. K. (2002). Understanding Social Behaviour with the Help of Complexity Science (Invited Article). Ethology, 108(8), 655–671.
Abstract: Abstract In the study of complexity, a new kind of explanation has been developed for social behaviour. It shows how patterns of social behaviour can arise as a side-effect of the interaction of individuals with their social or physical environment (e.g. by self-organization). This development may influence our ideas about the direct causation and evolution of social behaviour. Furthermore, it may influence our theories about the integration of different traits. This new method has been made possible by the increase in computing power. It is now applied in many areas of science, such as physics, chemistry, sociology and economics. However, in zoology and anthropology it is still rare. The major aim of this paper is to make this method more generally accepted among behavioural scientists.
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Borgatti, S. P., Everett, M.G., Freeman, L.C. (2002). Ucinet for Windows: Software for Social Network Analysis.
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Morgan, K., Funkquist, P., & Nyman, G. (2002). The effect of coat clipping on thermoregulation during intense exercise in trotters. Equine Veterinary Journal, 34(S34), 564–567.
Abstract: Summary The aim of this study was to study the physiological, especially thermoregulatory, responses during intense exercise in the clipped horse compared to the horse with winter coat. Six Standardbred trotters were studied before and after clipping. They performed an inclined incremental high intensity treadmill exercise test and were monitored during recovery. The clipped horse differed significantly (ANOVA) during exercise as compare to coated: less increase in central venous blood temperature, higher skin surface temperature, greater difference skin to ambient temperature and higher rate of nonevaporative heat loss. The clipped horse had significantly lower total cutaneous evaporative heat loss from walk to end of peak exercise and a shorter time for recovery for the respiratory rate using a paired t test. The clipped horse showed a tendency (P = 0.059) to decreased oxygen uptake during the stepwise increase in workload. We concluded that the clipped horse experienced less strain on the thermoregulatory system due to an enhanced heat loss. Some clipped horses in the study showed a more efficient power output; future studies with emphasis on respiration and oxygen demand are needed to explain this.
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Byrne, R. W. (2002). Imitation of novel complex actions: What does the evidence from animals mean? In C. T. Snowdon, T. J. Roper, & J. S. Rosenblatt (Eds.), Advances in the Study of Behavior (Vol. 31, pp. 77–105). San Diego: Academic Press.
Abstract: Summary Underlying the various behaviors that are classified as imitation, there may be several distinct mechanisms, differing in adaptive function, cognitive basis, and computational power. Experiments reporting “true motor imitation” in animals do not as yet give evidence of production learning by imitation; instead, contextual imitation can explain their data, and this can be explained by a simple mechanism (response facilitation) which matches known neural findings. When imitation serves a function in social mimicry, which applies to a wide range of phenomena from neonatal imitation in humans and great apes to pair-bonding in some bird species, the fidelity of the behavioral match is crucial. Learning of novel behavior can potentially be achieved by matching the outcome of a model's action, and it is argued that vocal imitation by birds is a clear example of this method (which is sometimes called emulation). Alternatively, the behavior itself may be perceived in terms of actions that the observer can perform, and thus it may be copied. If the imitation is linear and stringlike (action level), following the surface form rather than the underlying plan, then its utility for learning new instrumental methods is limited. However, the underlying plan of hierarchically organized behavior is visible in output behavior, in subtle but detectable ways, and imitation could instead be based on this organization (program level), extracted automatically by string parsing. Currently, the most likely candidates for such capacities are all great apes. It is argued that this ability to perceive the underlying plan of action, in addition to allowing highly flexible imitation of novel instrumental methods, may have resulted in the competence to understand the intentions (theory of mind) of others.
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