Merker’s definition of consciousness excludes self-reflective thought, making his proposal for decorticate consciousness not particularly groundbreaking. He suggests that brainstem sites are neglected in current theories of consciousness. This is so because broader definitions of consciousness are used. Split-brain data show that the cortex is important for full-blown consciousness; also, behaviors exhibited by hydranencephaly patients and decorticated rats do not seem to require reflective consciousness.

A discussion that has gained relevance in recent years in the research on anthropological difference - if the human being possess specific and unique features in nature - is whether the rest of the animals have episodic memory. The present work analyzes the possibility of its attribution in one of the species that have shown greater competence successfully to solve different memory tests: the scrub jay. To this end, the different approaches to episodic memory and empirical tests that were developed (...) to corroborate its attribution in non-human animals are described and analyzed: the behavioral criterion of remembering the information “what, where and when” of Clayton and Dickinson, the conception of mental time travel of Suddendorf and Corballis and the new approaches that understand episodic memory through the distinctive feature of self-reflexivity or temporal reasoning. The behavioral evidence obtained so far is susceptible to being explained by other capabilities that do not involve episodic memories. Consequently, it is of current interest to analyze the theoretical scope of the new lines of research and to design experiments to design experiments to test this capacity in these birds. (shrink)

A persisting question in the philosophy of animal minds is which nonhuman animals share our capacity for episodic memory. Many authors address this question by primarily defining EM, trying to capture its seemingly unconstrained flexibility and independence from environmental and bodily constraints. EM is therefore often opposed to clearly context-bound capacities like tracking environmental regularities and forming associations. The problem is that conceptualizing EM in humans first, and then reconstructing how humans evolved this capacity, provides little constraints for understanding the (...) evolution of memory abilities in other species: it defines “genuine” EM as independent from animals’ evolved sensorimotor setup and learning abilities. In this paper, I define memory in terms of perceptual learning: remembering means “knowing what to do in later situations because of past experience in similar earlier situations”. After that, I explain how episodic memory can likewise be explained in terms of perceptual learning. For this, we should consider that the information in animals’ ecological niches is much richer than has hitherto been presumed. Accordingly, instead of asking “given that environmental stimuli provide insufficient information about the cache, what kind of representation does the jay need?” we ask “given that the animal performs in this way, what kind of information is available in the environment?” My aim is not to give a complete alternative explanation of EM; rather, it is to provide conceptual and methodological tools for more zoocentric comparative EM-research. (shrink)

Euan Macphail’s work and ideas captured a pivotal time in the late 20th century when behavioral laws were considered to apply equally across vertebrates, implying equal intelligence, but it was also a time when behaviorism was challenged by the view that language was unique to humans, and bestowed a superior mental status. Subsequent work suggests greater continuity between humans and their forebears, challenging the Chomskyan assumption that language evolved in a single step (“the great leap forward”) in humans. Language is (...) now understood to be based on an amalgam of cognitive functions, including mental time travel, theory of mind, and what may be more broadly defined as imagination. These functions probably evolved gradually in hominin evolution and are present in varying degrees in non-human species. The blending of language into cognition provides for both interspecies differences in mental function, and continuity between humans and other species. What does seem to be special to humans is the ability to communicate the contents of imagination, although even this is not absolute, and is perhaps less adaptive than we like to think. (shrink)

Ape species-specific communication is grounded on the present, possesses some referential qualities and is mostly used to request objects or actions from others. Artificial systems of communication borrowed from humans transform apes' communicative exchanges by freeing them from the present (i.e. displaced reference) although requests still predominate as the main reason for communicating with others. Symbol use appears to enhance apes' relational abilities and their inhibitory control. Despite these substantial changes, it is concluded that even though artificial communication enhances thought (...) and enables its expression more openly, it does not create it or modify the motivation behind communicative exchanges. (shrink)