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1 arning), or learn from other adults (oblique social learning).
2 les of alliances, behavioral innovation, and social learning.
3 tion of the population will always engage in social learning.
4 only from personal experience but also from social learning.
5 h as darcin can be highly potent stimuli for social learning.
6 of traits inherited epigenetically, through social learning.
7 in systems for perception and action support social learning.
8 reated traditions can be transmitted through social learning.
9 more usually associated with vertebrates and social learning.
10 ed only very weak and transitory evidence of social learning.
11 ons that are potentially conducive to infant social learning.
12 hich may aid in information transmission via social learning.
13 of choreographed movements are dependent on social learning.
14 e initial state engenders and supports rapid social learning.
15 a rich repertoire of mathematical models of social learning.
16 from "innovators" to others in the group via social learning.
17 essed why primates vary in how much they use social learning.
18 ed through social networks via high-fidelity social learning.
19 plays a role in both appetitive and aversive social learning.
20 rm, the olfactory sensory cortex, to mediate social learning.
21 o switch strategies from vertical to oblique social learning.
22 ns in the piriform cortex during odor-driven social learning.
23 nce (relative to subordinate individuals) on social learning.
24 y by relatively well-informed individual and social learning.
25 iors in animals spread through individual or social learning.
26 s should be widespread in species capable of social learning.
27 vide basic insights into the neural basis of social learning.
29 s can sometimes learn from conspecifics, and social learning abilities often correlate with individua
30 underlying mechanisms not only improves this social learning ability but also the asocial (individual
31 has shown the importance for this species of social learning about novel prey using auditory, rather
32 ure may result from this interaction between social learning accuracy and number of demonstrators.
36 significant for evolutionary biology because social learning affords faster adaptation than genetic c
41 gmoidal acquisition curves are not unique to social learning and are often mistaken for other acceler
42 education and support group, parents in the social learning and cognitive behavioral therapy group r
43 education and support group, children in the social learning and cognitive behavioral therapy group r
47 any other human behaviors, is underpinned by social learning and cultural transmission alongside biol
48 et of commonalities between the phenomena of social learning and culture in the lives of chimpanzees
49 les (unbiased social learning, payoff-biased social learning and frequency-dependent biased social le
50 d the relaxation of selective constraints on social learning and increased experimentation with point
51 s submitted strategies specifying how to use social learning and its asocial alternative (for example
52 Our tool-rich culture may be more reliant on social learning and more limited by domain-general const
53 earning: curiosity and intrinsic motivation, social learning and natural interaction with peers, and
55 Model 2) indicates that both the accuracy of social learning and the number of cultural demonstrators
56 n between the abundance of opportunities for social learning and the size of the local cultural reper
57 iscountmachine) relied nearly exclusively on social learning and weighted information according to th
58 t the behavioral patterns are the product of social learning and, therefore, can be considered cultur
59 rs, it has been argued that they result from social learning and, therefore, can be regarded as cultu
61 and suggests that the evolution of tool use, social learning, and cumulative culture may have involve
63 climate change adaptation in public health, social learning, and management of socioeconomic systems
65 s in frequency of PPC apparently result from social learning, are stable across generations, and last
66 alify their scheme by arguing that different social learning biases should be treated distinctly, and
68 evolution, the empirical validity of assumed social learning biases, the relative role of transformat
70 n to suggest a role for conformity in animal social learning, but evidence from the wild remains circ
71 light escort, we found evidence of long-term social learning, but no effect of genetic relatedness on
72 eal is known about the adaptive functions of social learning, but very little about the cognitive mec
73 ses seek to recognise diffusions mediated by social learning by detecting a correspondence between pa
75 mains an open question whether a reliance on social learning can also lead to mismatched or maladapti
79 challenges these assumptions by showing that social learning covaries with asocial learning; occurs i
82 in humans might contribute to enhancement of social learning during development and transmission of c
83 -social learning, though participants in the social learning experiment appeared to additionally bene
87 age than in vertebrates, the study of insect social learning has a rich history with spectacular exam
89 network analyses and experimental studies of social learning have each become important domains of an
92 plastic behavioural response, perpetuated by social learning imposing an altered natural selection re
96 underlie traditions, yet evidence indicating social learning in capuchin monkeys (Cebus apella), whic
97 hat Richerson et al. adjust their account of social learning in cultural group selection (CGS) by tak
98 er presents the first study of dominance and social learning in humans and challenges the lay stereot
100 applicable by researchers wishing to detect social learning in natural and captive populations of an
101 n artificial fruit (AF) was used to test for social learning in pig-tailed macaques (Macaca nemestrin
104 work can encompass complex, context-specific social learning in the insect world and beyond, and base
106 le prey by placing bats in three groups: (a) social learning, in which a bat inexperienced with the n
107 cial learning and frequency-dependent biased social learning, including conformism and anti-conformis
110 e contribution of genetic and environmental (social learning) influences on the development of IBS by
113 become established in the long run, through social learning, irrespective of the initial number of c
115 nonhuman social learning are continuous, and social learning is adaptively specialized--it becomes di
121 lled by genetic factors and that the role of social learning is likely in facilitating the extinction
122 iguing, but it presents a paradox insofar as social learning is often suggested to instead reduce rel
125 ld capacities for stakeholder collaboration, social learning, knowledge governance, and researcher tr
126 ying others: they can copy peers (horizontal social learning), learn from their parents (vertical soc
132 ots, to investigate how reasoning abilities, social learning mechanisms and population structure affe
134 is still no direct experimental evidence for social learning, nor has there been any direct observati
137 del of fear conditioning can help to explain social learning of fear through observation and instruct
141 mission of abusive parenting are mediated by social learning or experience-induced physiological alte
142 earning), learn from their parents (vertical social learning), or learn from other adults (oblique so
143 of a small selection of such rules (unbiased social learning, payoff-biased social learning and frequ
145 e discovery of the roles that individual and social learning play in creating recurring phenotypes on
147 tion in orangutans and show that a number of social learning processes are likely to be involved in t
148 ngs thus help to specify adolescent-specific social learning processes.SIGNIFICANCE STATEMENT Adolesc
149 w that, across primate species, a measure of social learning proclivity increases with absolute and r
150 self-administered (IVSA) nicotine, and that social learning promoted nicotine IVSA with flavor cues.
152 t ecological or genetic factors, rather than social learning, provide a more parsimonious explanation
157 specificity/generality of core processes in social learning, reward, and attention, and we highlight
158 ural selection has favoured the evolution of social learning rules that make selective use of social
159 he repeated successful invasion of different social learning rules, should continuously favour a redu
160 learning, and propose that, among competing social learning rules, the dominant rule will be the one
161 of others, and avoid endangering themselves, social learning should be used around novel and unpredic
162 Whales and dolphins (Cetacea) have excellent social learning skills as well as a long and strong moth
164 ations of biases and experiential effects on social learning, social information use, and mirror syst
165 aggression include cognitive neoassociation, social learning, social interaction, script, and excitat
167 results show that individual differences in social learning strategies are crucial for understanding
170 mance requires taking into consideration the social learning strategies of individual team members.
171 nces of different mixtures of individual and social learning strategies on the frequencies of differe
172 Even in the case of imitation, a type of social learning studied in both comparative psychology a
173 g developmental stress, we further show that social learning targets are phenotypically plastic.
176 function representation, executive control, social learning, teaching, social intelligence, and lang
178 port an egocentric influence on this type of social learning that is reflected in both performance an
180 to explain why humans evolved capacities for social learning that resulted in cumulative culture.
183 ronmental factors and merges constructs from social learning theory with American Indian customs and
184 ss evaluation was based on diffusion theory, social learning theory, and the desire for triangulation
185 sessment process, using an approach based on social learning theory, for the development of a school-
186 ifferences: evolutionary theories, cognitive social learning theory, sociocultural theory, and expect
188 t shows that these effects generalize to non-social learning, though participants in the social learn
189 that combines local agent interactions with social learning, thus enables both strategic behavior as
190 mplex forms of memory, including spatial and social learning, thus indicating that CREB may be a univ
192 al learning rules that make selective use of social learning to acquire relevant information in a cha
195 Prior to any subsequent coevolution with social learning, we suggest that aspects of general inte
196 , however, strategies that relied heavily on social learning were found to be remarkably successful,
197 edity contributes to development of IBS, but social learning (what an individual learns from those in
199 rowess may lie in the interplay of strategic social learning with other cognitive traits including th
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