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  1. The initial brain concept: A work in progress.Karl Zilles & Gerd Rehkämper - 1988 - Behavioral and Brain Sciences 11 (1):105-106.
  • Brain evolution: Some problems of interpretation.Jan Wind - 1988 - Behavioral and Brain Sciences 11 (1):104-105.
  • Evolutionary events and the “modification/multiplication” relationship.Walter Wilczynski - 1988 - Behavioral and Brain Sciences 11 (1):103-104.
  • Competition for the sake of diversity.F. Valverde - 1988 - Behavioral and Brain Sciences 11 (1):102-103.
  • Elegant hypotheses are intellectually rewarding; even more so if more hard data were available.János Szentágothai - 1988 - Behavioral and Brain Sciences 11 (1):102-102.
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  • Climbing the evolutionary ladder of success: The scala naturae in models of brain evolution.Horst D. Steklis - 1988 - Behavioral and Brain Sciences 11 (1):101-102.
  • Concepts of brain evolution.Barry E. Stein - 1988 - Behavioral and Brain Sciences 11 (1):100-101.
  • Elephants have a large neocortex too.Jeheskel Shoshani - 1988 - Behavioral and Brain Sciences 11 (1):100-100.
  • Inside / Outside.Stanley N. Salthe - 2009 - Biosemiotics 2 (2):247-253.
  • Hierarchical structures.Stanley N. Salthe - 2012 - Axiomathes 22 (3):355 - 383.
    This paper compares the two known logical forms of hierarchy, both of which have been used in models of natural phenomena, including the biological. I contrast their general properties, internal formal relations, modes of growth (emergence) in applications to the natural world, criteria for applying them, the complexities that they embody, their dynamical relations in applied models, and their informational relations and semiotic aspects.
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  • A hierarchical framework for levels of reality: Understanding through representation. [REVIEW]Stanley N. Salthe - 2009 - Axiomathes 19 (1):87-99.
    Levels of reality reflect one kind of complexity, which can be modeled using a specification hierarchy. Levels emerged during the Big Bang, as physical degrees of freedom became increasingly fixed as the expanding universe developed, and new degrees of freedom associated with higher levels opened up locally, requiring new descriptive semantics. History became embodied in higher level entities, which are increasingly individuated, aggregate patterns of lower level entities. Development is an epigenetic trajectory from vaguer to more definite and individuated embodiment, (...)
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  • Cetacean brain evolution.S. H. Ridgway & F. G. Wood - 1988 - Behavioral and Brain Sciences 11 (1):99-100.
  • What about Sirenia?Bernhard Rensch - 1988 - Behavioral and Brain Sciences 11 (1):99-99.
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  • The “initial brain”: Initial considerations.Roger L. Reep - 1988 - Behavioral and Brain Sciences 11 (1):98-99.
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  • Putting all cetacean brains in one category is a big order.Sue T. Parker - 1988 - Behavioral and Brain Sciences 11 (1):97-98.
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  • The concept of association cortex should be abandoned.E. J. Neafsey - 1988 - Behavioral and Brain Sciences 11 (1):97-97.
  • Objekt und Methode in der Biologie.F. E. Lehmann - 1947 - Synthese 6 (1-2):44-56.
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  • Determining species differences in numbers of cortical areas and modules: The architectonic method needs supplementation.Jon H. Kaas - 1988 - Behavioral and Brain Sciences 11 (1):96-97.
  • Whose brain is initial-like?John Irwin Johnson - 1988 - Behavioral and Brain Sciences 11 (1):96-96.
  • Morphogenetic versus morphofunctional theory.F. J. Irsigler - 1988 - Behavioral and Brain Sciences 11 (1):95-96.
  • Developmental axes and evolutionary trees.G. M. Innocenti - 1988 - Behavioral and Brain Sciences 11 (1):94-95.
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  • The “initial” brain concept: Its uses and misuses.Ilya I. Glezer, Myron S. Jacobs & Peter J. Morgane - 1988 - Behavioral and Brain Sciences 11 (1):106-116.
    We review the evidence for the concept of the “initial” or prototype brain. We outline four possible modes of brain evolution suggested by our new findings on the evolutionary status of the dolphin brain. The four modes involve various forms of deviation from and conformity to the hypothesized initial brain type. These include examples of conservative evolution, progressive evolution, and combinations of the two in which features of one or the other become dominant. The four types of neocortical organization in (...)
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  • Implications of the “initial brain” concept for brain evolution in Cetacea.Ilya I. Glezer, Myron S. Jacobs & Peter J. Morgane - 1988 - Behavioral and Brain Sciences 11 (1):75-89.
    We review the evidence for the concept of the “initial” or prototype brain. We outline four possible modes of brain evolution suggested by our new findings on the evolutionary status of the dolphin brain. The four modes involve various forms of deviation from and conformity to the hypothesized initial brain type. These include examples of conservative evolution, progressive evolution, and combinations of the two in which features of one or the other become dominant. The four types of neocortical organization in (...)
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  • Fish, sea snakes, dolphins, teeth and brains – some evolutionary paradoxes.Kathleen R. Gibson - 1988 - Behavioral and Brain Sciences 11 (1):93-94.
  • Allometry cannot be ignored in brain evolution studies.Dean Falk - 1988 - Behavioral and Brain Sciences 11 (1):92-93.
  • Cetacean brains have a structure similar to the brains of primitive mammals; does this imply limits in function?John F. Eisenberg - 1988 - Behavioral and Brain Sciences 11 (1):92-92.
  • The re-emergence of emergence, and the causal role of synergy in emergent evolution.Peter A. Corning - 2012 - Synthese 185 (2):295-317.
    Despite its current popularity, “emergence” is a concept with a venerable history and an elusive, ambiguous standing in contemporary evolutionary theory. This paper briefly recounts the history of the term and details some of its current usages. Not only are there radically varying interpretations about how to define emergence but “reductionist” and “holistic” theorists hold very different views about the issue of causation. However, these two seemingly polar positions are not irreconcilable. Reductionism, or detailed analysis of the parts and their (...)
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  • The re‐emergence of “emergence”: A venerable concept in search of a theory.Peter A. Corning - 2002 - Complexity 7 (6):18-30.
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  • Evolution of the brain in Cetacea – is bigger better?Mary Carlson - 1988 - Behavioral and Brain Sciences 11 (1):91-92.
  • Primitive survivors and neocortical evolution.C. B. G. Campbell - 1988 - Behavioral and Brain Sciences 11 (1):90-91.
  • Conservative aspects of the dolphin cortex match its behavioral level.Lester R. Aronson & Ethel Tobach - 1988 - Behavioral and Brain Sciences 11 (1):89-90.
  • Levels of Organization in Biology.Markus Eronen & Daniel Stephen Brooks - unknown - Stanford Encyclopedia of Philosophy.
    Levels of organization are structures in nature, usually defined by part-whole relationships, with things at higher levels being composed of things at the next lower level. Typical levels of organization that one finds in the literature include the atomic, molecular, cellular, tissue, organ, organismal, group, population, community, ecosystem, landscape, and biosphere levels. References to levels of organization and related hierarchical depictions of nature are prominent in the life sciences and their philosophical study, and appear not only in introductory textbooks and (...)
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  • Organismo y organización en la biología teórica¿ Vuelta al organicismo.Arantza Etxeberria & Jon Umerez - 2006 - Ludus Vitalis 14 (26):3-38.
    ABSTRACT. This paper contemplates Organicism and its relation with molecular and evolutionary biology. We explore whether twentieth-first century biology is returning to positions held at the beginning of the twentieth century and then abandoned. The guiding line is a history of theoretical biology in which we distinguish three periods: 1. The 20s-30s, and the Theoretical Biology Club (Needham, Woodger, and Waddington, among others); 2. An intermediate period in the 60s-70s, in which, in spite of the eclosion of the molecular and (...)
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