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  1. Origin and Evolution of the Brain.Marcello Barbieri - 2011 - Biosemiotics 4 (3):369-399.
    Modern biology has not yet come to terms with the presence of many organic codes in Nature, despite the fact that we can prove their existence. As a result, it has not yet accepted the idea that the great events of macroevolution were associated with the origin of new organic codes, despite the fact that this is the most parsimonious and logical explanation of those events. This is probably due to the fact that the existence of organic codes in all (...)
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  • Introduction: Mentis Naturalis. [REVIEW]Liz Stillwaggon Swan & Louis J. Goldberg - 2013 - Biosemiotics 6 (3):297-300.
  • How Is Meaning Grounded in the Organism?Liz Stillwaggon Swan & Louis J. Goldberg - 2010 - Biosemiotics 3 (2):131-146.
    In this paper we address the interrelated questions of why and how certain features of an organism’s environment become meaningful to it. We make the case that knowing the biology is essential to understanding the foundation of meaning-making in organisms. We employ Miguel Nicolelis et al’s seminal research on the mammalian somatosensory system to enrich our own concept of brain-objects as the neurobiological intermediary between the environment and the consequent organismic behavior. In the final section, we explain how brain-objects advance (...)
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  • On the Genetic and Epigenetic Bases of Primate Signal Processing.Louis J. Goldberg & Leonard A. Rosenblum - 2013 - Biosemiotics 6 (2):161-176.
    Four sequential, sub-processes are identified as the fundamental steps in the processing of signals by big-brained animals. These are, Detection of the signal, its Representation in correlated sensory brain structure, the Interpretation of the signal in another part of the brain and the Expression of the receiver’s response. We label this four-step spatiotemporal process DRIE. We support the view that when the context within which such signals are produced and received is relatively constant, the DRIE process can be ultimately assimilated (...)
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  • Face Recognition and the Social Individual.Louis J. Goldberg - 2013 - Biosemiotics 6 (3):573-583.
    Face recognition depends upon the uniqueness of each human face. This is accomplished by the patterns formed by the unique relationship among face features. Unique face-patterns are produced by the intrusion of random factors into the process of biological growth and development. Processes are described which enable a unique face-pattern to be represented as a percept in the visual sensory system. The components of the face recognition system are analyzed as is the manner in which the precept is connected through (...)
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  • A biosemiotic analysis of Braille.Louis J. Goldberg & Liz Stillwaggon Swan - 2011 - Biosemiotics 4 (1):25-38.
    Abstract A unique aspect of human communication is the utilization of sets of well- delineated entities, the morphology of which is used to encode the letters of the alphabet. In this paper, we focus on Braille as an exemplar of this phenomenon. We take a Braille cell to be a physical artifact of the human environment, into the structure of which is encoded a representation of a letter of the alphabet. The specific issue we address in this paper concerns an (...)
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  • Neural systems behind word and concept retrieval.H. Damasio, D. Tranel, T. Grabowski, R. Adolphs & A. Damasio - 2003 - Cognition 92 (1-2):179-229.
  • The evolution of distributed association networks in the human brain.Randy L. Buckner & Fenna M. Krienen - 2013 - Trends in Cognitive Sciences 17 (12):648-665.
  • Hierarchical Categorical Perception in Sensing and Cognitive Processes.Luis Emilio Bruni - 2008 - Biosemiotics 1 (1):113-130.
    This article considers categorical perception (CP) as a crucial process involved in all sort of communication throughout the biological hierarchy, i.e. in all of biosemiosis. Until now, there has been consideration of CP exclusively within the functional cycle of perception–cognition–action and it has not been considered the possibility to extend this kind of phenomena to the mere physiological level. To generalise the notion of CP in this sense, I have proposed to distinguish between categorical perception (CP) and categorical sensing (CS) (...)
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  • What Does it Take to Produce Interpretation? Informational, Peircean and Code-Semiotic Views on Biosemiotics.Søren Brier & Cliff Joslyn - 2013 - Biosemiotics 6 (1):143-159.
    This paper presents a critical analysis of code-semiotics, which we see as the latest attempt to create paradigmatic foundation for solving the question of the emergence of life and consciousness. We view code semiotics as a an attempt to revise the empirical scientific Darwinian paradigm, and to go beyond the complex systems, emergence, self-organization, and informational paradigms, and also the selfish gene theory of Dawkins and the Peircean pragmaticist semiotic theory built on the simultaneous types of evolution. As such it (...)
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  • The Paradigms of Biology.Marcello Barbieri - 2013 - Biosemiotics 6 (1):33-59.
    Today there are two major theoretical frameworks in biology. One is the ‘chemical paradigm’, the idea that life is an extremely complex form of chemistry. The other is the ‘information paradigm’, the view that life is not just ‘chemistry’ but ‘chemistry-plus-information’. This implies the existence of a fundamental difference between information and chemistry, a conclusion that is strongly supported by the fact that information and information-based-processes like heredity and natural selection simply do not exist in the world of chemistry. Against (...)
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  • Code-duality and the semiotics of nature.Claus Emmeche - manuscript
    The final version of the paper is published pp. 117-166 in: Myrdene Anderson and Floyd Merrell (eds.): On Semiotic Modeling . Mouton de Gruyter, Berlin and New York, 1991.
     
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