A broader perspective sees grammar as just one of many hierarchically organised behaviours being processed in similar, prefrontal neurological regions (Greenfield, 1991; Givon, 1998). As Broca’s area is found to be functionally salient in grammatical processing, it is logical to assume that this is the place to search for activity in analogous hierarchical sequences. Such is the basis for studies into music (Maess et al., 2001), action planning (Koechlin and Jubault, 2006) and tool-production (Stout et al., 2008).
Ever since its discovery in 1861, Broca’s area (named after its discoverer, Paul Broca) has been inextricably linked with language (Grodzinsky and Santi, 2008). Found in the left hemisphere of the Pre-Frontal Cortex (PFC), Broca’s region traditionally comprises of Broadmann’s areas (BA) 44 and 45 (Hagoort, 2005). Despite being relegated in its status as the centre of language, this region is still believed to play a vital role in certain linguistic aspects.
Of particular emphasis is syntax. However, syntactic processing is not unequivocally confined to Broca’s area, with a vast body of evidence from “Studies investigating lesion deficit correlations point to a more distributed representation of syntactic processes in the left perisylvian region.” (Fiebach, 2005, pg. 80). A more constrained approach places Broca’s area as processing an important functional component of grammar (Grodzinsky and Santi, 2007). One of these suggestions points specifically to how humans are able to organise phrases in hierarchical structures.
In natural languages, “[…] the noun phrases and the verb phrase within a clause typically receive their grammatical role (e.g., subject or object) by means of hierarchical relations rather than through the bare linear order of the words in a string. [my emphasis]” (Musso et al., 2003, pg. 774). Furthermore, these phrases can be broken down into smaller segments, with noun phrases, for example, consisting of a determiner preceding a noun (Chomsky, 1957). According to Chomsky (1957) these rules exist without the need for interaction in other linguistic domains. Take for example his now famous phrase of “Colourless green ideas sleep furiously.” (ibid, pg. 15). Despite being syntactically correct, it is argued the sentence as a whole is semantically meaningless.
The relevant point to take away is a sentence is considered hierarchical if phrases are embedded within other phrases. Yet, examples of hierarchical organisation are found in many domains besides syntax. This includes other language phenomena, such as prosody. Also, non-linguistic behaviours – such as music (Givon, 1998), action sequences (Koechlin and Jubault, 2006), tool-use (cf. Scott-Frey, 2004) and tool-production (Stout et al., 2008) – are all cognitively demanding tasks, comparable with that of language. We can even see instances of non-human hierarchical representations: from the songs of humpback whales (Suzuki, Buck and Tyack, 2006) to various accounts of great apes (McGrew, 1992; Nakamichi, 2003) and crows (Hunt, 2000) using and manufacturing their own tools.
With this in mind, we can ask ourselves two questions corresponding to Broca’s area and hierarchical organisation: Does Broca’s area process hierarchically organised sequences in language? And if so, is this processing language-specific? The logic behind this two-part approach is to help focus in on the problem. For instance, it may be found hierarchical structures in sentences are processed by Broca’s area. But this belies the notion of other hierarchically organised behaviours also utilising the same cognitive abilities.
A prominent idea in linguistics is that humans have an array of specialised organs geared towards the production, reception and comprehension of language. For some features, particularly the physical capacity to produce and receive multiple vocalizations, there is ample evidence for specialisation: a descended larynx (Lieberman, 2003), thoracic breathing (MacLarnon & Hewitt, 1999), and several distinct hearing organs (Hawks, in press). Given that these features are firmly in the domain of biology, it makes intuitive sense to apply the theory of natural selection to solve the problem: humans are specially adapted to the production and reception of multiple vocalizations.
Here’s some stuff I’ve been reading over the last month or so:
- Babel’s Dawn discusses Michael Arbib’s paper, Invention and Community in the Emergence of Language: Insights from New Sign Languages.
- Over at Neurophilosophy there is an overview of a fascinating paper on the Universal Grammar of birdsong (also check out my comment, it’s the first one under JW).
- John Hawks talks about some of my favourite topics: learning, population size, and modern human behaviour.
- The recent resurgence of the Sapir-Whorf hypothesis and Lera Boroditsky are the topics of discussion over at Mind Hacks.
- Deric Bownds’ MindBlog mentions the “origins of altruism toward one’s own social group and the emergence of cultural complexity“.
- Evolution can occur in less than 10 years… In guppy fish.
- Researchers at Brown find: “A front portion of the brain that handles tasks like decision-making also helps decipher different phonetic sounds“.
- And lastly, Dienekes’ anthropology blog discusses a paper that investigates the role of drift and selection in the shaping of human skulls, concluding “that neutral processes have been much more important than climate in shaping the human cranium”.
Okay, so that brings you up to date with my reading from May through to July. Next round up will cover August. How fascinating :-/
In the year of Darwin, I’m not too surprised at the number of articles being published on the interactions between cultural change and biological evolution — this synthesis, if achieved, will certainly be a crucial step in explaining how humans evolved. Still, it’s unlikely we’re going to see the Darwin of culture in 2009, given we’re still disputing some of the fundamentals surrounding these two modes of evolution. One of these key arguments is whether or not culture inhibits biological evolution. That we’re seeing accelerated changes in the human genome seems to suggest (for some) that culture is one of these evolutionary selection pressures, as John Hawks explains:
Continue reading “How do biology and culture interact?”
As part of my assessment this term I’m to write four mock peer-reviewed items for a module called Current Issues in Language Evolution. It’s a great module run by Simon Kirby, examining some of the best food for thought in the field. Alone this is an interesting endeavour, after all we’re right in the middle of a language evolution renaissance, however, even cooler are the lectures, where students get to do their own presentations on a particular paper. I already did my presentation at the start of this term, on Dediu and Ladd’s paper, which went rather well, even if one of my slip ups did not go unnoticed (hint: always label the graphs). So, over the next few weeks, in amongst additional posts covering some of the presentations in class, I’ll hopefully be writing articles on these four five papers:
Disclaimer: I know this post is on a paper released over a year ago; however, I’m still going to write about it for three reasons: 1) I did a presentation about it earlier this week (20/01/08); 2) I think it relates to a recent buzz around gene-culture co-evolution; and, 3) It’s a bloody awesome paper.
So, what is the paper called? Okay, once you read this title, do not yawn, go to another website or… Linguistic tone is related to the population frequency of the adaptive haplogroups of the two brain size genes, ASPM and Mircocephalin. See, now we’ve got the hard part out of the way, I can begin to discuss exactly what the authors, Dan Dediu and Robert ‘Bob’ Ladd, found and why it’s important to our understanding of linguistics, genetics and evolution. It’s really interesting, honestly.
Continue reading “ASPM, Microcephalin and Tone”