Shared Ancestor to Humans, Present-day Non-human Primates
May Be Linchpin in the Evolution of Language
When contemplating the coos and screams of a fellow member of its species,
the rhesus monkey, or macaque, makes use of brain regions that correspond to
the two principal language centers in the human brain, according to research
conducted by scientists at the National Institute on Deafness and Other Communication
Disorders (NIDCD) and the National Institute of Mental Health (NIMH), two of
the National Institutes of Health. The finding, published July 23 in the advance
online issue of Nature Neuroscience, bolsters the hypothesis that a shared ancestor
to humans and present-day non-human primates may have possessed the key neural
mechanisms upon which language was built. Principal collaborators on the study
are Allen Braun, M.D., chief of NIDCD’s Language Section, Alex Martin, Ph.D.,
chief of NIMH’s Cognitive Neuropsychology Section, and Ricardo Gil-da-Costa,
Gulbenkian Science Institute, Oeiras, Portugal, who conducted the study during
a three-year joint appointment at the NIDCD and NIMH.
“This intriguing finding brings us closer to understanding the point at which
the building blocks of language appeared on the evolutionary timeline,” says
James F. Battey, Jr., M.D., Ph.D., director of the NIDCD. “While the fossil record
cannot answer this question for us, we can turn to the here and now — through
brain imaging of living non-human primates — for a glimpse into how language,
or at least the neural circuitry required for language, came to be.”
While non-human primates do not possess language, they are able to communicate
about such things as food, identity, or danger to members of their species by
way of vocalizations that are interpreted and acted upon. In humans, the two
main regions of the brain that are involved in encoding this type of information
in language are known as Broca’s area and Wernicke’s area, named for the physician-researchers
who discovered them. Both areas are located along the Sylvian fissure (and are
therefore referred to as perisylvian areas) with Broca’s area located in the
frontal lobe and Wernicke’s area located behind it in the temporal and parietal
lobes. Scientists once believed that Broca’s area was chiefly involved in language
production while Wernicke’s area dealt more with comprehension, however current
thinking suggests that the two areas work in tandem with one another. Although
monkeys are not able to perform the mental activities required for language,
their brains possess regions that are structurally similar to the perisylvian
areas in humans in both hemispheres. The functional significance of such similarities,
however, has been unclear up to this point.
To measure brain activity, the researchers injected water labeled with oxygen-15,
a biologically safe, fast-degrading radioisotope, into the bloodstream of three
adult macaques. As neural activity increases in a given region of the brain,
blood — and the radioactive water it carries — rushes into that region. Using
the brain imaging technology known as positron emission tomography (PET), researchers
capture an image of the radioactive areas, thus highlighting the regions of heightened
activity. In this way, brain scans were taken of the monkeys as they listened
to three types of sounds: the recorded coos and screams of other rhesus monkeys,
and assorted non-biological sounds, such as musical instruments and computer-synthesized
sounds, which matched the vocalizations in frequency, rate, scale, and duration.
For each monkey, 16 scans were recorded for each sound type and compared.
Although the coo of a monkey is acoustically very different from a high-pitched
scream, the researchers found that both of these meaningful species-specific
sounds elicited significantly more activity than the non-biological control stimuli
in the same three regions of the macaque’s brain. Moreover, these regions correspond
to the key language centers in humans, with the ventral premotor cortex (PMv)
corresponding to Broca’s area, and the temporoparietal area (Tpt) and posterior
parietal cortex (PPC) corresponding to Wernicke’s area. In contrast, the non-biological
sounds — which were acoustically similar to the coos and screams but had no meaning
for the animals — elicited significantly less activity in these regions; rather,
they were associated with greater activation of the brain’s primary auditory
areas. (The reason for this, the researchers suggest, is that these sounds were
new to the monkeys and the primary auditory areas may be especially attuned to
novel stimuli.)
Based on these findings, the researchers suggest that the communication centers
in the brain of the last common ancestor to macaques and humans — particularly
those centers used for interpreting species-specific vocalizations — may have
been recruited during the evolution of language in humans. In the macaque, these
areas may currently play a parallel, prelinguistic function, in which monkeys
are able to assign meaning to species-specific sounds. In addition, in light
of an earlier study published by the same group, in which species-specific vocalizations
of macaques activated brain regions that process higher-order visual and emotional
information, the researchers suggest that the language areas of the brain may
have evolved from a much larger system used to extract meaning from socially
relevant situations — a system in which humans and non-human primates may share
similar neural pathways.
Further studies to be conducted include investigating which regions of the non-human
primate brain are activated when animals listen to meaningful auditory stimuli
other than species-specific vocalizations, such as a predators’ calls, sounds
made by humans, or other relevant environmental stimuli. In addition, they are
interested in studying the pattern of brain activation elicited by non-auditory
stimuli that convey the same meaning, such as visual images of monkeys producing
vocalizations.
Other institutions represented on the study include Harvard University, Cambridge,
MA; University College London/Institute of Child Health, London; and the University
of Maryland, College Park. The work was supported by NIDCD, NIMH, and Fundação
para a Ciência e Tecnologia, Portugal.
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| Photo credit: Marc Hauser, Ph.D., Harvard University |
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NIDCD supports and conducts research and research training on the normal
and disordered processes of hearing, balance, smell, taste, voice, speech and
language and provides health information, based upon scientific discovery,
to the public. For more information about NIDCD programs, see the Web site
at www.nidcd.nih.gov.
The National Institute of Mental Health (NIMH) mission is to reduce the
burden of mental and behavioral disorders through research on mind, brain,
and behavior. More information is available at the NIMH website, http://www.nimh.nih.gov.
The National Institutes of Health (NIH) — The Nation's Medical Research
Agency — includes 27 Institutes and Centers and is a component of
the U.S. Department of Health and Human Services. It is the primary federal
agency for conducting and supporting basic, clinical and translational medical
research, and it investigates the causes, treatments, and cures for both common
and rare diseases. For more information about NIH and its programs, visit www.nih.gov. |