john hawks weblog

paleoanthropology, genetics and evolution

language

  • Putting two calls together

    Fri, 2006-05-19 20:53 -- John Hawks

    A very brief paper by Arnold and Zuberbüler in Nature presents a case of a complex call in guenons:

    Putty-nosed monkeys rely on two basic calling sounds to construct a message of utmost urgency.

    Syntax sets human language apart from other natural communication systems, although its evolutionary origins are obscure. Here we show that free-ranging putty-nosed monkeys combine two vocalizations into different call sequences that are linked to specific external events, such as the presence of a predator and the imminent movement of the group. Our findings indicate that non-human primates can combine calls into higher-order sequences that have a particular meaning.

    The two calls (called "pyow" and "hack") generally are used to signify two different predators, leopards and crowned eagles, respectively. The different calls help the monkeys use different escape routes -- they "sometimes" move through the canopy to escape from leopards, but avoid such a route in response to eagles; the paper indicates that the group does not move in response to the "hack" warning call alone.

    Sometimes, males vocalize a sequence involving several of both calls (a "pyow-hack", or P-H sequence). The research found that these sequences are indicators of group movement, in response to either kind of predator:

    Using a global positioning satellite unit (see methods in supplementary information), we found that the groups whose males had produced P-H sequences in response to growls had travelled significantly farther than other groups [significance test]....

    The monkeys' response to P-H sequences was not confined to the predator context, but was generally related to whether the group moved. We recorded a total of 72 natural call sequences (that is, not experimentally induced) over two months from the single male of a group habituated to human observers and monitored the group's travelling patterns. A large proportion of the calls contained P-H sequences (40.3%) and elicited movement of the group over significantly greater distances than after P-H-free call series [significance test]....

    Most animals have a restricted repertoire of calls, with innate and structurally fixed vocalizations. Combining existing calls into meaningful sequences increases the variety of messages that can be generated. The simple system used by putty-nosed monkeys encodes the presence of different types of danger and triggers group movement with just two basic call types.

    It seems especially likely that an animal might exploit already-existing calls in such a way. These are sounds that are both statistically improbable and already recognized, so if there is a way to alter their interpretation by context, they provide ready channels for communication. In this case, the alternative "meaning" is about movement, it is piggybacked upon the simpler calls themselves.

    You might call it monkey multiplexing.

    References:

    Arnold K, Zuberbüler K. 2006. Language evolution: Semantic combinations in primate calls. Nature 441:303. DOI link

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  • More on the starling syntax study

    Mon, 2006-05-01 22:36 -- John Hawks

    Chris at Mixing Memory has a post from last week reflecting on the meaning of the finding that starlings can learn certain patterns of syntactic recursion.

    He also links to two message-board posts by linguists on the topic. This one, by Mark Liberman explains why recursion is important and what a Dyck language is:

    If you're like every other human I've tested, you find this task pretty hard. If you're quick and you care enough, you can count on your mental fingers, so to speak, adding one for each higher pitch and subtracting one for each lower pitch, and "parse" the sequence that way. But the difference between the Dyck and non-Dyck patterns is not, in the general case, cognitively salient to humans without intellectual scrutiny. In contrast, we don't need to count on our mental fingers to understand the structures of real spoken language. And I'd be astounded if the difference between Dyck and non-Dyck strings is cognitively salient to starlings or to any other animals either.

    This post by David Beaver has a practical illustration, and reflects on the study:

    Faced with the facts about starlings innate ability to learn Dyck languages, and the facts about center embeddings for you and me, a contrarian might well conclude that yes, at last, we have firm and amazing evidence for a biologically unique language module. The trouble is, starlings have it, and we don't.

    And this post at Tenser, said the Tensor is another explanation:

    However, this does not imply that the birds are recognizing context-free languages when they're processing the songs. It's true that CFGs are the next step up the Chomsky hierarchy from regular languages, but that's a fact about the hierarchy, not about the universe -- there are other kinds of languages that are supersets of the regular languages while still being subsets of context-free languages. The researchers propose a few of these and show why they're not sufficient to account for the birds' success, but I suspect the birds may be processing one they didn't consider. In particular, the starlings may just be using memory.

    It's heavy stuff, but important to the evolution of language, since it reflects on the logical prerequisites for generating and processing linguistic messages.

    Meanwhile, before I posted, I found that Carl Zimmer has written about the study for the NY Times. Nice exchange between Gentner, Chomsky and Hauser at the end:

    Dr. Chomsky also rejects Dr. Gentner's conclusions. He suggests the starlings are merely counting rattles, storing the number in their memory, then counting warbles. "It has nothing remotely to do with language -- probably just with short-term memory," he said via e-mail. Dr. Gentner argues that even if the starlings are counting, they are still using a strategy more sophisticated than has been seen before in animals.

    "Chomsky may find this trivial, but that is a bit like saying apes use tools, but only the trivial kind that lack the sophistication of a tri-square or a laser level," he said.

    Tags: 
  • Starling syntax

    Sat, 2006-04-29 08:41 -- John Hawks

    Generative grammar -- the theory of language structure originated by Noam Chomsky -- is lost on most people. It has a unique place in biology, because it is a self-consistent system that entails specialized brain systems to learn and use it, but Chomsky himself has shown great skepticism about the power of natural selection to create it.

    The theory has several elements, which it predicts are shared by all human languages. A question has been whether these elements may in fact be prerequisites of any equivalently complex form of serial communication. If so, one or more of them might spontaneously appear in species with complex vocalizations.

    This week, Nature has a paper by Timothy Gentner and colleagues that shows that a humanlike syntactic structure can be learned by starlings. From the abstract:

    Recent hypotheses make the central claim that the capacity for syntactic recursion forms the computational core of a uniquely human language faculty. Here we show that European starlings (Sturnus vulgaris) accurately recognize acoustic patterns defined by a recursive, self-embedding, context-free grammar. They are also able to classify new patterns defined by the grammar and reliably exclude agrammatical patterns. Thus, the capacity to classify sequences from recursive, centre-embedded grammars is not uniquely human. This finding opens a new range of complex syntactic processing mechanisms to physiological investigation.

    The "self-embedding" part here is the crucial descriptor. A LiveScience article by Sara Goudarzi explains it fairly well:

    A common characteristic of human grammar is inserting words and clauses within a sentence, without limit. For example, "Oedipus ruled Thebes" can become "Oedipus, who killed his father, ruled Thebes" or "Oedipus, who killed his father, whom he met on the road from Delphi, ruled Thebes," ad infinitum.

    More simply stated, you can insert as many brackets as you want within a sentence as long as there are as many brackets on the right as there are on the left.

    Chomskian linguists believe that this characteristic, known as "recursive center embedding," is a universal feature of human language, and the ability to process it forms the core of human language ability.

    There is also an accompanying "News and Views" feature by Gary Marcus.

    Gentner and colleagues rewarded European starlings for pressing a bar in response to AnBn strings of starling-generated sounds, such as rattle rattle warble warble, and withheld the reward for responses to the (AB)n grammar (and vice versa for another group of starlings). Although learning was not instantaneous, nine of eleven birds eventually (after 10,000-50,000 trials) learned to discriminate reliably between the two grammars, succeeding where the monkeys had failed. An extensive series of control comparisons strongly suggests that the ultimately acquired grammar is robust. Notwithstanding some minor worries, this is strong evidence that humans are not alone in their capacity to recognize recursion.

    This is not a challenge to the uniqueness of human language as a communication system, but like several other observations, it does suggest that some of the interesting characteristics of human communication may be generally necessary of any complex form of serial communication. If you are going to have any kind of complex vocalization -- that is, one that includes more than around three signs -- then you will need some way to arrange those signs to denote meanings among them. If it is possible to have descriptors of one or more signs, there must be some syntactic (i.e., sign-order-related) conventions to relate them. Recursion may be a logical necessity for such communication, and from that aspect, there is every reason to think that species with relatively long vocalizations might be able to use it. I would expect cetaceans might have such a structure also, which is speculated by Marcus:

    Can other varieties of birds that don't (in contrast to starlings) naturally acquire new songs also acquire self-embedded structures? Are humans alone among primates in their capacity to do so? Might the capacity for recursion be general across great apes, even if it were absent in monkeys? An intriguing possibility is that the capacity to recognize recursion might be found only in species that can acquire new patterns of vocalization, for example songbirds, humans and perhaps some cetaceans.

    According to the LiveScience article, Chomsky isn't buying it:

    "The article is based on an elementary mathematical error," said Chomsky, professor of linguistics at Massachusetts Institute of Technology. "They are overlooking the fact that there are many intermediate systems that are ignored in mathematical linguistics because their properties are empirically irrelevant."

    Based on other work done 50 years ago by George Miller, Chomsky thinks further research would show that the birds are not grasping linguistics in the way the new study concludes.

    "It has nothing remotely to do with language; probably just with short-term memory," Chomsky told LiveScience.

    Yes, that would be where these kind of syntactic abilities should begin, I would think. In humans, there are undoubtedly specialized adaptations to build out syntactic structures quickly and over long utterances with many recursions. For most other species, one or two recursions depending on generalized short-term memory might be all there is. But the chance of continuity between the two is very interesting.

    References:

    Marcus GF. 2006. Language: Startling starlings. Nature 440:1117-1118. DOI link

    Gentner TQ, Fenn KM, Margoliash D, Nusbaum HC. 2006. Recusive syntactic pattern learning by songbirds. Nature 440:1204-1207. DOI link

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  • Chimpanzee language antics

    Mon, 2005-10-31 23:39 -- John Hawks

    Carl Zimmer has an article in Forbes covering recent experiments in chimpanzee vocal communication.

    But don't write off those grunts and hoots just yet, at least according to a new study that appears in the Oct. 15 issue of the journal Current Biology. Katie Slocombe and Kaus Zuberbuhler, two primatologists at the University of St. Andrews in Scotland, investigated a particular noise chimpanzees make when they find food, called a "rough grunt." At the Edinburgh Zoo, the scientists fed the chimpanzees two different foods--apples and bread--and recorded the sounds they made. Chimpanzees prefer bread to apples, and Slocombe and Zuberbuhler discovered a corresponding difference in the rough grunts they made for each food. They hit a distinctively high note when they came across the bread, and but made lower and noisier grunts for apples.

    It's a short article, supplemented by an entry on the Loom.

    This online issue of Forbes

    There are a number of short interview excerpts in the issue. One has Noam Chomsky discussing spontaneous language innovation in deaf communities. Another from Jane Goodall on the perils of e-mail communication:

    I remember when I worked for Lewis [sic] Leakey, first as his secretary. He was very impulsive. He'd get a letter in the mail, and he would open it, and it would be perhaps something from a scientist he thought was quite ridiculous. You could hear him muttering "Bosh! Rubbish!" The poor bit of paper would be scored with his marks, and he'd turn to me and say "Get so and so on the phone!" I got very wise to his moods, so I would pretend the number was engaged, or the man wasn't there, and then an hour or two later, he was rational again.

    And other interviews and articles, with Arthur C. Clarke, Wil Wheaton, Desmond Morris, Steven Pinker and many others. Many thanks to the reader who pointed me to the site.

  • Barbara King reviews The Singing Neanderthal

    Thu, 2005-10-06 16:31 -- John Hawks

    At the online book review section of Bookslut, the new Steven Mithen book, The Singing Neanderthal: The Origins of Music, Language, Mind, and Body is reviewed by primatologist Barbara J. King. It's a good review to get the main themes of the book, and generally positive. Here's an excerpt:

    On page five, Mithen commands attention by announcing a dual intention to take on academic superstar Steve Pinker's (The Blank Slate, How the Mind Works, The Language Instinct) views on the evolution of music and to atone for his own "embarrassing" past neglect of music (The Prehistory of the Mind). I was hooked; Pinker-worthy, non-ego-driven scientists don't grow on trees. Happily, this initial promise of provocation is fulfilled, for Mithen offers a fascinating argument about the evolutionary relationship between music and language. To be precise, it is provocative, fascinating and, I think, quite wrong on multiple points. But how much fun is it, really, to curl up with a book that lulls you into placid agreement?

    Somewhat convoluted, Mithen's argument depends on three key moves. First, he starkly splits apart language and music: language tells us about the world, music manipulates our emotions. Second, he proposes a single evolutionary precursor to both language and music. This is the communication system he calls "Hmmmm" for holistic, multi-modal, manipulative, and musical: "Its essence would have been a large number of holistic utterances, each functioning as a complete message in itself rather than as words that could be combined to generate new meanings." Though elements of Hmmmm are present in the communication of modern day apes (and thus, probably, our apelike ancestors), this system really took off once bipedalism evolved in the human lineage. Walking on two legs changed much in our ancestors' anatomy and behavior, and promoted the use of Hmmmm in specific ways.

    I may review it myself when I can get my hands on a copy.

    I often discuss Mithen's previous book The Prehistory of the Mind in classes. In this earlier book also, Mithen argues that the evolution of human minds involved breaking apart old cognitive systems and stitching them back together in different ways after a period of independent development. It's a sort of mosaic theory of cognitive evolution, coupled with a terminal period of intertentaclation of different mental services into a single conscious experience.

    What's "intertentaclation"? I figure it's the octopus equivalent of interdigitation. I guess you could say it makes me go "Hmmmm".

  • Probing the correlates of SLI

    Tue, 2005-09-27 22:33 -- John Hawks

    This week's (9/27/95) PNAS has an article by Johannes Ziegler and colleagues (Université de Provence) titled, "Deficits in speech perception predict language learning impairment". The paper concerns specific language impairment, or SLI.

    Readers may remember that a rare monogenic form of SLI is the disorder that led to the identification of the FOXP2 gene (OMIM). Later work showed that most SLI is not directly caused by FOXP2 variants, but apparently the adjacent cystic fibrosis gene (CFTR) does show a strong association with SLI. Interesting.

    The current study investigated the behavioral correlates of SLI to see what might cause the language learning deficits. The abstract:

    Specific language impairment (SLI) is one of the most common childhood disorders, affecting 7% of children. These children experience difficulties in understanding and producing spoken language despite normal intelligence, normal hearing, and normal opportunities to learn language. The causes of SLI are still hotly debated, ranging from nonlinguistic deficits in auditory perception to high-level deficits in grammar. Here, we show that children with SLI have poorer-than-normal consonant identification when measured in ecologically valid conditions of stationary or fluctuating masking noise. The deficits persisted even in comparison with a younger group of normally developing children who were matched for language skills. This finding points to a fundamental deficit. Information transmission of all phonetic features (voicing, place, and manner) was impaired, although the deficits were strongest for voicing (e.g., difference between/b/and/p/). Children with SLI experienced perfectly normal "release from masking" (better identification in fluctuating than in stationary noise), which indicates a central deficit in feature extraction rather than deficits in low-level, temporal, and spectral auditory capacities. We further showed that speech identification in noise predicted language impairment to a great extent within the group of children with SLI and across all participants. Previous research might have underestimated this important link, possibly because speech perception has typically been investigated in optimal listening conditions using non-speech material. The present study suggests that children with SLI learn language deviantly because they inefficiently extract and manipulate speech features, in particular, voicing. This result offers new directions for the fast diagnosis and remediation of SLI.

    From an evolutionary perspective, a disorder that affects 7 percent of people is not a disorder; it is a normal variant. The 7 percent value comes from a study by Tomblin et al. (1997), who screened a sample of over 7000 monolingual English speaking kindergarteners, finding only small differences between boys and girls in the incidence of SLI. Such a high frequency raises a question: Why has this apparent problem persisted in human populations, when it would seem that language ability is very important to survival and successful integration into society?

    Of course, more basic statistical answers must come before we worry too much about the evolutionary history of SLI. For one thing, is this actually a unique phenotypic variant, or is it merely the end of a continuous distribution of language-learning skill in children? And are all cases of SLI actually part of a single package of correlated symptoms, or is there a broader spectrum of different deficits in language learning that belong to the disorder?

    The current paper by Ziegler et al. (2005) starts by looking at the actual behavioral correlates of SLI. The introduction to the paper gives some background on the issues:

    The causes of SLI are still hotly debated. Current theories of SLI fall into two categories: those that attribute SLI to a specifically linguistic deficit and those that attribute SLI to general processing limitations (for a review, see ref. 5). Linguistic deficit theories typically assume that children with SLI have difficulty acquiring linguistic mechanisms, such as past tense rules or the grammatical principle of inflection (6, 7). Children with SLI are thought to be "stuck" at an early stage of grammatical development. Such a delay could actually reflect a general maturational delay of language and other cognitive systems (8, 9).

    In contrast, general processing deficit theories assume that it is not the specific nature of the material that is important but rather how it is processed in the brain. Nonlinguistic deficits in either perception or memory are thought to be responsible for language disorder (10Ð12). The most prominent theory of this kind, also called the fast temporal-processing deficit hypothesis, maintains that SLI is a consequence of a deficit in processing brief and/or rapidly changing auditory information and/or in remembering the temporal order of auditory information (13Ð16). For example, Tallal and Piercy (13) found that some children with SLI have difficulty reporting the order of pairs of high- and low-frequency sounds when these sounds are brief in duration and presented rapidly. Such a deficit may underlie difficulties in perceiving grammatical forms (e.g., the or is), which are generally brief and unstressed (17).

    The paper additionally presents possible criticisms of these views. The main idea of the research presented here is to test the hypothesis of auditory processing deficits by looking not at kids in sterile laboratory settings, but in normal listening conditions with background noise. The logic is that they might have trouble distinguishing speech sounds within complex aural environments.

    The discussion fairly succinctly states the results:

    The main findings of the present study can be summarized as follows. Under optimal listening conditions (silence), children with SLI showed only subtle speech perception deficits. However, under conditions of stationary noise and fluctuating noise, children with SLI showed substantial speech perception deficits. Note that conditions of fluctuating noise are not artificial; they are actually very representative of the kind of listening conditions that children will encounter in their daily life (in schools, for example). Thus, the present results raise the possibility that children with language learning disabilities have very serious problems with noise exclusion, which will certainly have tremendous consequences for normal phonological development. A similar proposal has recently been made with regard to visual (magnocellular) deficits that seem frequently associated with dyslexia (45). The authors showed that dyslexic children do not have visual (magnocellular) processing problems per se but rather problems of noise exclusion that become apparent in visual tasks using noisy displays. Noise exclusion could therefore be a very general problem responsible for poor phonological development of children with language learning problems and dyslexia.

    To me, this is illuminating about the frequency of the disorder. If the problem is distinguishing sounds quickly and accurately in a complex aural environment, then it may be a problem that manifested much less, or possibly not at all, before people began living in crowds. The comparison with dyslexia may be quite relevant, since, of course, people didn't have to read through most of human existence either. This does leave the question of why the variation exists as it presently does. Are there other behaviors that weigh in a different direction from language learning? Is ADHD a pertinent analogy? Are there alternate strategies for learning langauge?

    Probably the most important thing would be to get a better idea of the cross-cultural incidence of these traits. If SLI is really significantly associated with CFTR, there might well be significant variation among populations today. Just a glimpse into what child psychology can tell us about the evolution of culture.

    References:

    Tomblin JB, Records NL, Buckwalter P, Zhang X, Smith E, O'Brien M. 1997. Prevalance of specific language impairment in kindergarten children. J Speech Lang Hear Res 40:1245-1260. PubMed

    Ziegler JC, Pech-Georgel C, George F, Alario F-X, Lorenzi C. 2005. Deficits in speech perception predict language learning impairment. Proc Nat Acad Sci USA 102:14110-14115. Full text online

  • Macaques have neural homologue of Broca's area

    Fri, 2005-07-01 00:08 -- John Hawks

    A paper by Michael Petrides (McGill University) and colleagues reports that a brain region on the left side of the macaque brain, in the same general area as Broca's area in the human brain, is associated with functions of the mouth and face. The authors consider some uncertainty about the full extent of Broca's area, particularly as related to speech function, and consider it equivalent to area 44. They then express the problem as applied to monkeys, particularly in relation to the famous "mirror neurons":

    Although it is not disputed that, in the macaque monkey as in the human, the most ventral part of the precentral gyrus (areas 4 and 6) is involved with the motor control of the orofacial musculature, there is considerable confusion and debate as to whether, just rostral to the premotor area 6, there might be a cortical region corresponding to area 44 of the human brain. This debate has become of particular concern in recent years with the discovery of a class of neurons known as 'mirror neurons' in part of the ventral premotor cortical area 6 (also known as area F5c) of the macaque monkey. These neurons become active both when the monkey performs a particular action and when the monkey observes a similar action being performed by another individual. Because there has been considerable theoretical interest in the possibility that the mirror-neuron system might be important for the evolution of language, it has been suggested that the homologue of Broca's area in the monkey might be the ventral premotor cortical area F5 (part of area 6) within which the mirror neurons were discovered. However, this area is agranular, whereas area 44 (Broca's area) in the human brain is a dysgranular architectonic entity that lies rostral to the ventral agranular premotor cortex. The key question is therefore: Is there a cortical area immediately in front of premotor cortical area 6 of the macaque monkey brain that is comparable to area 44 of the human brain? Such an area should have the following three properties: first, it should exhibit the key architectonic characteristics of area 44 of the human brain; second, it should be bounded topographically by the same architectonic areas as in the human brain; and third, it should be involved, at least, with the orofacial musculature. (Petrides et al. 2005:1236, citations omitted).

    They went looking for the area, recording neuron activity with electrodes and stimulating brain regions to observe whether an effect was observed on the mouth or face musculature.

    In short, they find it:

    The present study has established that a cortical area comparable in architecture to human area 44 exists in the macaque monkey immediately in front of premotor cortical area 6V and that it is involved with the orofacial musculature. The lack of an outgroup comparison limits our ability to provide further inferential evidence that area 44 in the human and the macaque monkey brain reflect shared common ancestry. Area 44 in the monkey lies rostral to the convexity of the premotor cortex where the mirror neurons were recorded (area F5c). Thus, the involvement (if any) of area 44 in the mirror neuron system remains to be established. Furthermore, it has recently been argued that mirror neurons cannot provide a basis for an essential structural relation in human language, namely the bi-directional arbitrary mapping between sound and meanings. In the human brain, area 44 is involved with the motor aspects of speech production. Studies of the effects of lesions that are more or less restricted to area 44 have yielded an apraxia of speech (that is, a problem with the motor aspects of speech production), and not the classic full-blown aphasic syndrome including a major disruption of syntax, which was previously thought to be the result of damage to Broca's area (Petrides et al. 2005:1237, citations omitted).

    If you don't know about mirror neurons, they're pretty cool. They are neurons in monkey brains (and in human brains as well) that are active both when an individual does an action, and also when an individual watches someone else doing the same action. They have been suggested to be the basis of imitative learning, in that merely watching another individual do an action might prime the brain -- by strengthening neural connections -- to take the same actions itself in the same contexts.

    The study does not comment on topics of comparative interest, such as the relative size of this presumed area 44 in the monkey brains compared to humans, or the previous literature on the comparative neuroanatomy of Broca's area in humans and chimpanzees. But this is interesting in its own right: it is a demonstration of a deep homology in language-related brain anatomy between humans and other anthropoids. Clearly there is no functional analogue in macaques for the full array of processes influenced by Broca's area in humans, but the fact that similar functional systems exist in both species gives a clear indication that human language has developed by the elaboration of many previously evolved neural systems.

    It remains to be seen whether other aspects of neural architecture related to language may have arisen only within the hominid lineage; indeed, most of the neural functions related to language as yet have no precisely defined neuroanatomical correlates. This may be suggestive in itself, particularly if it indicates (as some think) that the neural basis of language is significantly self-constructed in the brains of different individuals.

    References:

    Petrides M, Cadoret G, Mackey S. 2005. Orofacial somatomotor responses in the macaque monkey homologue of Broca's area. Nature 435:1235-1238. Full text online

  • Language evolution update

    Thu, 2005-06-30 22:36 -- John Hawks

    Carl Zimmer has put together this week's news about language evolution. In one paper, mice with knockout versions of the FoxP2 gene were found to have trouble with their squeaks! In other words, the gene may be involved in vocal communication in most mammals. The second paper demonstrates the existence of a neural area homologous with Broca's area in macaques. This would show that one cortical region underlying language function in humans is broadly shared among anthropoid primates, although not elaborated to the extent found in living and fossil Homo.

    Both of these are stories about homology. Humans aren't unique in the presence of either FoxP2 or Broca's area. Instead, these emerged long ago. Both of them may have been involved in vocal communication for a long time in our lineage, in other primates, and potentially in many other mammals.

    So human evolution didn't have to originate new language-related functions for these elements out of whole cloth. There was already a simple structure there to work with. Human evolution elaborated on this ancient foundation.

    The details, of course, remain to be worked out. FoxP2 is far from the only gene related to language, and Broca's area is far from the only cortical region. Different areas may have yet other origins, may have been put together in new ways during human evolution, and may have been expanded upon (or in some cases possibly even reduced) to result in our unique configuration.

    Anyway, read Zimmer, and I may write more on the Broca's discovery later.

  • The Singing Neandertal

    Fri, 2005-03-18 11:04 -- John Hawks

    Is it just me, or does this remind anyone of "The Dancing Cavalier" from Singin' in the Rain?

    ABC News has an item (March 15, 2005) called
    "Neanderthals sang like sopranos". The report is referencing a research presentation at University College London by Stephen Mithen, and it says he is making the argument the centerpiece of a book expected later this year, titled The Singing Neanderthal: The Origin of Language, Music, Body and Mind.

    Here are some central quotes:

    Neanderthals had strong, yet high-pitched, voices that the stocky hominins used for both singing and speaking, says a UK researcher.

    Mithen compared related skeletal Neanderthal data with that of monkeys and other members of the ape family, including modern humans. In a recent University College London seminar, Mithen explained that Neanderthal anatomy suggests the early hominins had the physical ability to communicate with pitch and melody. He believes they probably used these abilities in a form of communication that was half spoken and half sung.

    At first glace, this seems remarkably similar to work I heard presented at the AAPA meetings last year by Margaret Clegg
    (University College London). Here is a quote from the abstract (Clegg 2004:76):

    Evidence is presented in this paper to suggest that the reversal proposed in the Neanderthals may be a consequence of the sex used to model the vocal tract. There has been a concentration on male vocal anatomy in the research so far undertaken. However, human males have a large secondary growth in both laryngeal size and position. This secondary growth appears to have little to do with the ability to produce speech sounds. Furthermore, we have no way of knowing when this secondary growth spurt evolved. It is plausible that this growth spurt was not found in Neanderthal males. The use of the human male as the standard model for human vocal tracts may therefore be responsible for the apparent reversal in laryngeal position found in Neanderthals.

    She made the argument in her talk that Neandertals would have likely had high, feminine-sounding voices because of their high laryngeal position. To me, this sounds like exactly the same thing Mithen is basing his argument on.

    In an entirely unrelated point of interest, later in the article Jeffrey Laitman gives his idea of what killed the Neandertals:

    Laitman believes Neanderthals were a separate species that modern humans actually helped to kill off.

    "Their ear, nose, and throat anatomy would have made them very susceptible to respiratory infections and to middle ear infections," he says.

    "We know they traded and were in contact with modern humans, so Neanderthals would have been in harm's way for germs.

    "In the days before cures like penicillin, illness could have flown through their populations very quickly and contributed to their demise."

    References:

    Clegg M. 2004. A new model for the Neanderthal vocal tract. Am J Phys Anthropol 123(Supp 38):76.

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Neandertals

For years, I've worked on their bones. Now I'm working on their genes. Read more about the science studying these ancient people.

Denisova

From a finger bone of an ancient human came the record of a completely unexpected population. My lab is working on the science of the Denisova genome.

Acceleration

The advent of agriculture caused natural selection to speed up greatly in humans. We're uncovering some of the ways that populations have rapidly changed during the last 10,000 years.

Malapa

Just outside Johannesburg, the Malapa site is producing some of the most exciting finds in human evolution. This site is the headquarters of the Malapa Soft Tissue Project.