In order to formulate hypotheses about the evolutionary underpinnings that preceded the first glimmerings of language, mother-infant gestural and vocal interactions are compared in chimpanzees and humans and used to model those of early hominins. These data, along with paleoanthropological evidence, suggest that prelinguistic vocal substrates for protolanguage that had prosodic features similar to contemporary motherese evolved as the trend for enlarging brains in late australopithecines/early Homo progressively increased the difficulty of parturition, thus causing a selective shift toward females that gave birth to relatively undeveloped neonates. It is hypothesized that hominin mothers adopted new foraging strategies that entailed maternal silencing, reassuring, and controlling of the behaviors of physically removed infants (i.e., that shared human babies' inability to cling to their mothers' bodies). As mothers increasingly used prosodic and gestural markings to encourage juveniles to behave and to follow, the meanings of certain utterances (words) became conventionalized. This hypothesis is based on the premises that hominin mothers that attended vigilantly to infants were strongly selected for, and that such mothers had genetically based potentials for consciously modifying vocalizations and gestures to control infants, both of which receive support from the literature.

The brain of Homo floresiensis was assessed by comparing a virtual endocast from the type specimen (LB1) with endocasts from great apes, Homo erectus, Homo sapiens, a human pygmy, a human microcephalic, specimen number Sts 5 (Australopithecus africanus), and specimen number WT 17000 (Paranthropus aethiopicus). Morphometric, allometric, and shape data indicate that LB1 is not a microcephalic or pygmy. LB1's brain/body size ratio scales like that of an australopithecine, but its endocast shape resembles that of Homo erectus. LB1 has derived frontal and temporal lobes and a lunate sulcus in a derived position, which are consistent with capabilities for higher cognitive processing.

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The “radiator” theory of brain evolution is proposed to account for “mosaic evolution” whereby brain size began to increase rapidly in the genus Homo well over a million years after bipedalism had been selected for in early hominids. Because hydrostatic pressures differ across columns of fluid depending on orientation (posture), vascular systems of early bipeds became reoriented so that cranial blood flowed preferentially to the vertebral plexus instead of the internal jugular vein in response to gravity. The Hadar early hominids and robust australopithecines partly achieved this reorientation with a dramatically enlarged occipital/marginal sinus system. On the other hand, hominids in the gracile australopithecine through Homo lineage delivered blood to the vertebral plexus via a widespread network of veins that became more elaborate through time. Mastoid and parietal emissary veins are representatives of this network, and increases in their frequencies during hominid evolution are indicative of its development. Brain size increased with increased frequencies of mastoid and parietal emissary veins in the lineage leading to and including Homo, but remained conservative in the robust australopithecine lineage that lacked the network of veins. The brain is an extremely heatsensitive organ and emissary veins in humans have been shown to cool the brain under conditions of hyperthermia. Thus, the network of veins in the lineage leading to Homo acted as a radiator that released a thermal constraint on brain size. The radiator theory is in keeping with the belief that basal gracile and basal robust australopithecines occupied distinct niches, with the former living in savanna mosaic habitats that were subject to hot temperatures and intense solar radiation during the day.

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