| Preface |
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v | |
| Panel of Reviewers |
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vii | |
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Evolutionary parallels between language and tool use |
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3 | (8) |
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Cortico-cortical and cortico-cerebellar computations in language change |
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11 | (8) |
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Towards language acquisition by cognitive developmental robotics |
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19 | (7) |
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Protolanguage, discrete infinity and interfaces: Investigating the evolution of the language and music faculty within the minimalist program |
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26 | (8) |
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Language and friendships: A co-evolution model of social and linguistic conventions |
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34 | (8) |
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Campbell's monkeys alarm calls are not morpheme-based |
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42 | (8) |
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On the inference `Neanderthals had FOXP2 = they had complex language' |
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50 | (8) |
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The impact of L2 speakers on the evolution of case marking |
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58 | (6) |
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Introducing pressure for expressivity into language evolution experiments |
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64 | (8) |
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The evolution of the Greenbergian word order correlations |
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72 | (8) |
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Semiotic investigations into early forms of symbolism and language |
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80 | (8) |
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Sea crossings are an unreliable indicator of language ability in hominids |
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88 | (8) |
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Overgeneralization of verbs --- The change of the German verb system |
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96 | (8) |
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Was the introduction of writing an evolutionary transition? |
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104 | (6) |
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Medium and long-run properties of linguistic community evolution |
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110 | (8) |
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Scales, salience and referential safety: The benefit of communicating the extreme |
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118 | (8) |
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Non-human primates cannot decontextualize and objectify the actions of their conspecifics |
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126 | (8) |
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How did predication evolve? |
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134 | (8) |
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Individual and social effects on linguistic diffusion |
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142 | (8) |
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Ontogeny of two communicative tools: Distance encoding & multimodality in deictic pointing |
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150 | (8) |
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Speech development in previously aphonic children after airway reconstruction recapitulates evolution of spoken language |
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158 | (7) |
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165 | (8) |
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The case for Neanderthal language -- How strong is it? |
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173 | (8) |
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Meanings of touching object parts in pointing |
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181 | (8) |
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The evolution of morphology and the diversity of grammatical systems |
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189 | (7) |
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What's the scope of the Naming Game? Constraints on semantic categorization |
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196 | (8) |
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The origins of linguistic predicate/argument structure |
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204 | (8) |
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The voice of things: The revolution of human language and its origin from sound imitation |
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212 | (7) |
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Empirical approaches to recursion |
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219 | (8) |
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Outgroup: The study of chimpanzees to know the human mind |
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227 | (7) |
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A modulation-demodulation model for speech communication and its emergence |
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234 | (8) |
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Signaling conventions: Who learns what where and when in a social network? |
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242 | (8) |
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Hominin cooperation and language evolution |
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250 | (8) |
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Morphing social communication networks from chimpanzee to human type |
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258 | (8) |
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Gesture and the origins of language |
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266 | (8) |
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Ambiguity resolution and evolution of word order |
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274 | (8) |
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When recursion collapses: Evidence from discourse interaction |
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282 | (6) |
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Cognitive construal, mental spaces and the evolution of language and cognition |
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288 | (8) |
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Spatial dynamics of language |
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296 | (8) |
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Are web search queries an evolving protolanguage? |
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304 | (8) |
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Language change in socially structured populations |
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312 | (8) |
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Language lateralization, categorical perception and language evolution |
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320 | (8) |
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Potential stages in the cultural evolution of spatial language |
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328 | (8) |
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Visual artificial grammar learning: Comparative research on humans and birds |
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336 | (8) |
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Syntax of mind -- Semantics of mind: Two Frameworks for comparative approaches to the evolution of language and music |
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344 | (8) |
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Displacement in communication |
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352 | (8) |
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The emergence of morphosyntactic case systems |
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360 | (8) |
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Holistic or synthetic protolanguage: Evidence from iterated learning of whistled signals |
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368 | (8) |
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The information rate of modern speech and its implications for language evolution |
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376 | (8) |
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Robustness as a design feature of speech communication |
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384 | (8) |
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The cooperative nature of conversation: Evidence from conversational exchanges |
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392 | (11) |
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Postnatal acquirement of the ability to discriminate culturaly shared song syntax in songbirds |
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403 | (2) |
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A simple integrated framework for investigating genetic and cultural evolution of language |
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405 | (2) |
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An adaptationist approach to the audience design hypothesis |
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407 | (2) |
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The the exponent of Zipf's law in language ontogeny |
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409 | (2) |
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Reconciling the diversity of languages with the biological uniformity of their speakers |
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411 | (2) |
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413 | (3) |
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The effects of modified variables on an iterated learning model of linguistic evolution by cultural transmission |
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416 | (2) |
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Is pantomime a likely stage in language evolution? Evidence from human and primate gesture |
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418 | (2) |
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Is And a fossil?: Coordination and the origin of compositionality |
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420 | (2) |
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The first word was not a noun |
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422 | (2) |
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Iconicity in structured form and meaning spaces |
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424 | (2) |
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Neither nature nor nurture: Coevolution, devolution, and universality of language |
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426 | (2) |
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Comparative histological data between the vocal folds of humans and bonobo |
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428 | (2) |
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On some parallels between the vocal apparatus and musical instruments, and their consequences for the evolution of language and music |
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430 | (2) |
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Jose Roberto do Carmo Jr. |
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Topographic learning and the arbitrary, categorial lexicon |
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432 | (2) |
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Social interaction is critical to the evolution of human communication systems (and why) |
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434 | (2) |
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Searching for substance in the Baldwin Effect: When learning causally affects genetic adaptation |
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436 | (2) |
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Molecular windows into speech and language |
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438 | (2) |
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Me to we: Cooperation, conflict, and the evolution of language |
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440 | (2) |
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A search for metacognition in avians |
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442 | (2) |
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Simulating the coevolution of language and joint attention |
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444 | (2) |
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Neutral models for language evolution |
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446 | (2) |
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Paleogenomics and the vocal auditory channel in archaic humans |
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448 | (2) |
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Infants' own-cry perception for language acquisition |
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450 | (2) |
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Evolution of symbolic communication in the perceptual crossing experiment |
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452 | (2) |
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Recent archaeological evidence suggests much earlier emergence of human UG |
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454 | (2) |
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Sound symbolism helps infants' word learning |
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456 | (2) |
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Male gibbons change the note order according to the behavioral situations |
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458 | (2) |
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Triadic niche construction: A scenario of human brain evolution realizing tool-use and language |
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460 | (2) |
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Phase theory and the role of cognitive constraints in the maximal expansion of syntactic trees |
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462 | (2) |
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Modelling the evolution of Creoles |
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464 | (2) |
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Innate template difference could induce signal complexity: A comparison of song features under auditory isolation between wild and domesticated finches |
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466 | (2) |
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The role of STS in mimetic-word processing: Sound symbolism or biological motion? |
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468 | (2) |
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A parsimonious representation with hidden states for birdsong syntax: An implication to human syntax evolution |
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470 | (2) |
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Expression analysis of language-related genes in the common marmoset brain |
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472 | (2) |
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Song memory including sequential information in male Bengalese finches auditory area |
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474 | (2) |
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Pitch intervals in relation to the origin of language |
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476 | (2) |
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Minimization of Universal Grammar, reliance on third factor principles, and feasibility of inquiry into evolutionary origins |
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478 | (2) |
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Why language has structure: New evidence from studying cultural evolution in the lab and what it means for biological evolution |
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480 | (2) |
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How is pragmatic grounding formed in symbolic communication systems? |
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482 | (2) |
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The evolution of morphological agreement |
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484 | (2) |
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Re-dating the loss of laryngeal air sacs in Homo sapiens |
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486 | (2) |
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On the origin of the hierarchy of color names |
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488 | (2) |
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The meaning of nonsense words |
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490 | (2) |
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Nonhuman primates do declare! Declaratives as evidence for mental time-travel in apes |
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492 | (2) |
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Building a language-competent species: Contributions of brain and environment to cognition and communication in apes and monkeys |
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494 | (2) |
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Dynamic expression of cadherins controls vocal learning |
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496 | (2) |
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Simulating the effects of cultural coadaptation on rates of endogenous and exogenous language change |
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498 | (2) |
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The Drosophila FoxP gene is required for operant self-learning: Implications for the evolution of language |
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500 | (2) |
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The evolution of miscommunication |
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502 | (2) |
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The Gricean intentional structure of ape gestural communication |
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504 | (2) |
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Cerebral laterality for prosody processing in human neonates: Evidence from multichannel near-infrared spectroscopy |
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506 | (2) |
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The irreducible semantic communicative drive: Imagination and culture beyond the hands |
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508 | (2) |
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Structural reanalysis of responses to musical tonality: Commonality with the neural processing of emotion in language |
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510 | (2) |
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Failure of operant discrimination learning of simple algebraic concept in a songbird |
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512 | (2) |
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Rodent ultrasonic vocalization as a model of human speech: A molecular and cellular view |
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514 | (2) |
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Parrots as models for language evolution |
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516 | (2) |
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A model of the evolution of frequent social communication |
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518 | (2) |
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Recursivity is a by-product of associative learning and working memory constraints: Evidence from baboons (Papio papio) |
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520 | (3) |
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A bottom-up approach to language evolution |
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523 | (2) |
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The nature of coordination: Evidence from Russian |
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525 | (2) |
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No words without syntax no syntax without words |
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527 | (2) |
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Out of the brains of babes: Domain-general learning mechanisms and domain-specific systems |
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529 | (4) |
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Evolution of `small-world' birdsong syntax: An implication for language evolution |
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533 | (2) |
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How do communication systems emerge, and what does this tell us about language? |
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535 | (2) |
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The origin of the learning system of sequential vocalizations: Neural activity of basal-ganglia in singing behavior and a cognitive task in songbirds |
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537 | (2) |
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Simulating language convergence |
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539 | (2) |
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Linguistic replicators: A wild goose chase? |
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541 | (2) |
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Iterated learning in populations: Learning and evolving expectations about linguistic homogeneity |
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543 | (2) |
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Regularization of linguistic variation in populations |
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545 | (2) |
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Abductive inference and insight in the evolution of symbolic communication |
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547 | (2) |
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Grammaticalization, light verbs, and the origins of complex language |
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549 | (2) |
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Divergence and convergence in vocal cultures |
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551 | (2) |
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Replication and emergence processes in language evolution |
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553 | (2) |
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The effects of generation turnover and interlocutor negotiation on linguistic structure |
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555 | (2) |
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Cultural evolution renders linguistic nativism implausible |
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557 | (2) |
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Naming a structured world: A cultural route to duality of patterning |
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559 | (2) |
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Neural correlates of song perception during Zebra finch song learning as shown by bold fMRI |
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561 | (2) |
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Human non-lexical vocal events and prosody in the perspective of language evolution |
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563 | (2) |
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Biased copying in the evolution of human communication systems |
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565 | (2) |
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Emotion, approach-avoidance motivation, and blending in the evolution of language |
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567 | (2) |
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Barbara Lewandowska-Tomaszczyk |
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The myth surrounding the ban by Societe de Linguistique de Paris |
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569 | (2) |
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Why language evolved only once |
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571 | (3) |
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Intersubjectivity as the key precondition for language: Its Evolution (and possible devolution) |
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574 | (3) |
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| Author Index |
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577 | |
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