Abstract: The process of domestication involves adaptation, usually to a captive environment. Domestication is attained by some combination of genetic changes occurring over generations and developmental mechanisms (e.g., physical maturation, learning) triggered by recurring environmental events or management practices in captivity that influence specific biological traits. The transition from free-living to captive status is often accompanied by changes in availability and/or accessibility of shelter, space, food and water, and by changes in predation and the social environment. These changes set the stage for the development of the domestic phenotype. Behavioral development in animals undergoing domestication is characterized by changes in the quantitative rather than qualitative nature of responses. The hypothesized loss of certain behavior patterns under domestication can usually be explained by the heightening of response thresholds. Increases in response frequency accompanying domestication can often be explained by atypical rates of exposure to certain forms of perceptual and locomotor stimulation. Genetic changes influencing the development of the domestic phenotype result from inbreeding, genetic drift, artificial selection, natural selection in captivity, and relaxed selection. Experiential contributions to the domestic phenotype include the presence or absence of key stimuli, changes in intraspecific aggressive interactions and interactions with humans. Man's role as a buffer between the animal and its environment is also believed to have an important effect on the development of the domestic phenotype. The domestication process has frequently reduced the sensitivity of animals to changes in their environment, perhaps the single-most important change accompanying domestication. It has also resulted in modified rates of behavioral and physical development. Interest in breeding animals in captivity for release in nature has flourished in recent decades. The capacity of domestic animals to survive and reproduce in nature may depend on the extent to which the gene pool of the population has been altered during the domestication process and flexibility in behavioral development. “Natural” gene pools should be protected when breeding wild animals in captivity for the purpose of reestablishing free-living natural populations. In some cases, captive-reared animals must be conditioned to live in nature prior to their release.

Abstract: Humans' relationships with animals, increasingly the subject of controversy, have long been of interest to those whose primary aim has been the better understanding of humans' relationships with other humans. Since this topic was last reviewed here, human-animal relationships have undergone considerable reexamination, reflecting key trends in the history of social analysis, including concerns with connections between anthropology and colonialism and with the construction of race, class, and gender identities. There have been many attempts to integrate structuralist or symbolic approaches with those focused on environmental, political, and economic dimensions. Human-animal relationships are now much more likely to be considered in dynamic terms, and consequently, there has been much interdisciplinary exchange between anthropologists and historians. Some research directly engages moral and political concerns about animals, but it is likely that sociocultural research on human-animal relationships will continue to be as much, if not more, about humans.

Abstract: There is a considerable amount of evidence that mammals and birds can use different spatial learning strategies based on multiple learning and memory systems. Unfortunately, only a few studies have investigated spatial learning and memory mechanisms in other vertebrates. This study aimed to identify the strategies used by goldfish to solve two different spatial tasks in a series of three experiments. In experiment 1, two groups of goldfish (Carassius auratus) were trained either in a spatial constancy task (SC), in which visual cues signalled the goal indirectly, or in a directly cued task (DC) in which similar cues signalled the goal directly. Transfer tests were conducted to study the effects of discrete cue deletion on the performance in both tasks. In these transfer tests the performance of the animals trained in the DC task dropped to chance level when the cue that signalled the goal directly was removed. In contrast, the removal of any single cue did not disrupt SC performance. In experiment 2, fish trained in the SC or the DC task were trained with the goal reversed. Goldfish in the SC group needed fewer sessions to master the reversal task than DC animals. Finally, experiment 3 investigated the effects of a substantial modification of the geometrical features of the apparatus on the performance of animals trained in the SC or in the DC condition. The performance of DC goldfish was not affected, whereas the same change disrupted performance in the SC animals despite the presence of the visual cues. These results suggest that there are separate spatial learning and memory systems in fish. Whereas the DC animals used a typical guidance strategy, relying only on the cue that signalled the goal directly, SC fish relied on a strategy with the properties of an actual spatial mapping system. Thus, the comparative approach points to the generality of these learning strategies among vertebrates.

Abstract: Humans have the ability to chunk together information from nonadjacent serial positions in sequential patterns. For example, human subjects can extrapolate the pattern, A-M-B-N-C-O-D-P-E-..., to find the missing element, Q, by sorting pattern elements into two component interleaved subpatterns: A-B-C-D-E and M-N-O-P-... Two experiments investigated the ability of rats to reorganize pattern elements from nonadjacent serial positions into chunks not presented by the experimenter. Rats learned either a structured or unstructured sequence interleaved with elements of a repeating sequence (experiment 1) or an alternation sequence (experiment 2). In both experiments, rats learned the interleaved subpatterns at different rates. Acquisition rate was correlated with the structural properties of component subpatterns and the nature of the rules required to describe the interleaved subpatterns. The results indicate that rats are sensitive to the organization of nonadjacent elements in serial patterns and that they can detect and sort structural relationships in interleaved patterns.

Abstract: A typical feature of vertical orb-webs is the 'top/bottom' asymmetry, where the lower web region is larger than the upper web region. This asymmetry may improve prey capture success, because, sitting in the hub of the web, a spider can reach prey entangled below the hub faster than prey entangled in the area above the hub. While web asymmetry is known to vary intraspecifically, we tested if this variation also exists at the individual level and whether it is the result of experience, using two orb-web spider species, Argiope keyserlingi and Larinioides sclopetarius. The results reveal that experienced web-building spiders constructed more asymmetric webs than conspecifics deprived of any prior building experience over a period of several months. Experienced individuals invested more silk material into the web region below the hub, which covered a larger area. Moreover, web asymmetry was also influenced by previous prey capture experiences, as spiders increased the lower region of the web if it intercepted the most prey over a period of 6 days. Consequently, spiders may be able to use long-term web-building experience as well as short-term prey capture experience to build better traps. In contrast to previous views of spiders, experience can contribute to intraspecific as well as to individual variations in web design.