DOI – Replicated Typo

Cultural Evolution and the Impending Singularity: The Movie

Here’s a video of a talk I gave at the Santa Fe Institute‘s Complex Systems Summer School (written with roboticist Andrew Tinka-check out him talking about his fleet of floating robots). The talk was a response to the “Evolution Challenge”:

Has Biological Evolution come to an end?
Is belief an emergent property?
Will advanced computers use H. Sapiens as batteries?

I also blogged about a part of this talk here (why a mad scientist’s attempt at creating A.I. to make new scientific discoveries was doomed).

The talk was given a prise for best talk by the judging panel which included David Krakauer, Tom Carter and best-selling author Cormac McCarthy. At several points in the talk, I completely forget what I was supposed to say because the people filming the event asked me to set my screen up in a way so I couldn’t see my notes.

Sperl, M., Chang, A., Weber, N., & Hübler, A. (1999). Hebbian learning in the agglomeration of conducting particles Physical Review E, 59 (3), 3165-3168 DOI: 10.1103/PhysRevE.59.3165

Chater N, & Christiansen MH (2010). Language acquisition meets language evolution. Cognitive science, 34 (7), 1131-57 PMID: 21564247

Ay N, Flack J, & Krakauer DC (2007). Robustness and complexity co-constructed in multimodal signalling networks. Philosophical transactions of the Royal Society of London. Series B, Biological sciences, 362 (1479), 441-7 PMID: 17255020

Ackley, D.H., and Cannon, D.C.. “Pursue Robust Indefinite Scalability”. In Proceedings of the Thirteenth Workshop on Hot Topics in Operating Systems (HOTOS-XIII) (2011, May). Abstract, PDF.

Guttal V, & Couzin ID (2010). Social interactions, information use, and the evolution of collective migration. Proceedings of the National Academy of Sciences of the United States of America, 107 (37), 16172-7 PMID: 20713700

Sonority and Sex: Why smaller communities are louder

Through this post on Sprogmuseet about Atkinson’s analysis of the out of Africa hypothesis, I found an article by Ember & Ember (2007) (who also quantified the link between colour lexicon size and distance from the equator, see my post here) on Sonority and climate. The article extends work by Fought et al. (2004) which finds that a language’s sonority is related to climate. Sonority is a measure of amplitude (loudness) as is greater for vowels than for consonants (for example, see here). Basically, the warmer the climate, the greater the sonority of the phoneme inventory of the population. The theory is that “people in warmer climates generally spend more time outdoors and communicate at a distance more often than people in colder climates”.

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Creative cultural transmission as chaotic sampling

Last week I attended a lecture by Liz Bradley on chaos. Chaos has been used to create variations on musical and dance sequences (Dabby, 2008; Bradley & Stuart, 1998). I was interested to see whether this technique could be iterated and applied to birdsong or other culturally transmitted systems. I present a model of creative cultural transmission based on this.

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Cultural Evolution and the Impending Singularity

Prof. Alfred Hubler is an actual mad professor who is a danger to life as we know it. In a talk this evening he went from ball bearings in castor oil to hyper-advanced machine intelligence and from some bits of string to the boundary conditions of the universe. Hubler suggests that he is building a hyper-intelligent computer. However, will hyper-intelligent machines actually give us a better scientific understanding of the universe, or will they just spend their time playing Tetris?

Let him take you on a journey…

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Bayesian phylogenetic analysis of Japonic languages

Lee & Hasegawa (2011) use phylogenetic methods to trace the origins of Japonic languages and dialects. Two hypotheses are considered: First, the farming/language dispersal hypothesis posits that the main factor for the divergence of genetic and linguistic diversity was agricultural expansion. Second, the diffusion/transformation hypothesis posits that cultural innovations such as farming can diffuse between societies, and so genetic and linguistic diversity should not be linked. The estimate of the common linguistic ancestor was in accordance with the farming/language dispersal hypothesis, again suggesting that that linguistic diversity followed genetic diversity.

The study is notable in considering dialects as well as languages and using etymology dictionaries to reconstruct forms from Middle and Old Japanese. The analysis is also done with their own reconstructions and another, unrelated set. The technique is similar to that used by Russel Gray et al. (2009) to study Pacific settlement patterns.

Lee S, & Hasegawa T (2011). Bayesian phylogenetic analysis supports an agricultural origin of Japonic languages. Proceedings. Biological sciences / The Royal Society PMID: 21543358

Gray, R., Drummond, A., & Greenhill, S. (2009). Language Phylogenies Reveal Expansion Pulses and Pauses in Pacific Settlement Science, 323 (5913), 479-483 DOI: 10.1126/science.1166858

Phonemic Diversity Supports a Serial Founder Effect Model of Language Expansion from Africa

Just read about an article on phoneme diversity via GNXP and Babel’s Dawn. Hopefully I’ll share some of my thoughts on the paper this weekend as it clearly ties in with work I’m currently doing (see here and here). Below is the abstract:

Human genetic and phenotypic diversity declines with distance from Africa, as predicted by a serial founder effect in which successive population bottlenecks during range expansion progressively reduce diversity, underpinning support for an African origin of modern humans. Recent work suggests that a similar founder effect may operate on human culture and language. here I show that the number of phonemes used in a global sample of 504 languages is also clinal and fits a serial founder-effect model of expansion from an inferred origin in Africa. This result, which is no explained by more recent demographic history, local language diversity, or statistical non-independence within language families, points to parallel mechanisms shaping genetic and linguistic diversity and supports an African origin of modern human languages.

Reference: Atkinson, Q.D (2011). Phonemic Diversity Supports a Serial Founder Effect Model of Language Expansion from Africa. Science 332, 346. DOI: 10.1126/science.1199295.

Update: I’ve given a lengthier response here.

How old am I?

It’s my birthday! But how old am I? Well, that’s not such a straightforward question. Even a seemingly well-defined concept such as age can be affected by cultural factors

First, my age in years is a bit of an estimate of the actual amount of time I’ve been alive, due to leap-years etc. Second, a year is a culturally determined (although not all that arbitrary) amount of time. But these are petty squabbles.

There are bigger differences. For instance, there are cultural differences when it comes to the recall of birth dates. And I’m not talking about saying you’re 24 when you’re 68. Matched comparisons of age reporting in death certificates and census data found minimal differences for white Americans (Hill et al., 2000) but nearly half were inconsistent for African-Americans (Hill et al., 1997). These may be due to economic differences.

Furthermore, the definition of age can vary cross-culturally. Knodel & Chyovan (1991) surveyed women between the ages of 15 and 49 in Thailand. As well as finding that up to 20% reported an age that was more than one year different to their actual age, they surmised that most calculated their age as difference between the present year and the year of their birth, disregarding whether their birthday had passed.

So in some parts of the world I’ve been 26 for four months now, or was it 25?

Hill, M., Preston, S., Elo, I., & Rosenwaike, I. (1997). Age-Linked Institutions and Age Reporting among Older African Americans Social Forces, 75 (3) DOI: 10.2307/2580528

Hill, M., Preston, S., & Rosenwaike, I. (2000). Age Reporting among White Americans Aged 85+: Results of a Record Linkage Study Demography, 37 (2) DOI: 10.2307/2648119

Knodel J, & Chayovan N (1991). Age and birth date reporting in Thailand. Asian and Pacific population forum / East-West Population Institute, East-West Center, 5 (2-3) PMID: 12343437

Prairie Dog Communication

istockphoto.com A recent NPR radio show covered the research of the biosemiotician Con Slobodchikoff of the Univeristy of Arizone on prairie dog calls. The piece is very public-orientated, but still might be worth listening to.

We’ve all (I hope) heard of the vervet monkeys, which have different alarm calls for different predators, such as for leopard (Panthera pardus), martial eagle (Polemaetus bellicosus), and python (Python sebae). (Seyfarth et al. 1980) For each of these predators, an inherent and unlearned call is uttered by the first spectator, after which the vervet monkeys respond in a suitable manner – climb a tree, seek shelter, etc. It appears, however, that prairie dogs have a similar system, and that it is a bit more complicated.

Slobodchikoff conducted a study where three girls (probably underpaid, underprivaleged, and underappreciated (under)graduate students) walked through a prairie dog colony wearing shirts of the colors green, yellow, and blue. The call of the first prairie dog to notice them was recorded, after which the prairie dogs all fled into their burrows. The intern then walked through the entire colony, took a break for ten minutes, changed shirts, and did it again.

What is interesting is that the prairie dogs have significantly different calls (important, as they are pretty much exactly the same to human ears) for blue and yellow, but not for yellow and green. This is due to the dichromatic nature of praire dog eyesight (for a full study of the eyesight of retinal photoreceptors of subterranean rodents, consult Schleich et al. 2010). The distinction between blue and yellow is important, however, as there isn’t necessarily any reason that blue people are any more dangerous to praire dogs than yellow ones. “This in turn suggests that the prairie dogs are labeling the predators according to some cognitive category, rather than merely providing instructions on how to escape from a particular predator or responding to the urgency of a predator attack.” (Slobodchikoff 2009, pp. 438)

Another study was then done where two towers were built and a line was strung between them. When cut out shapes were slung down the line, the prairie dogs were able to distinguish a triangle from a circle, but not a circle from a square. So, the prairie dogs are not entirely perfect at encoding information. The conclusion still stands however that more information is encoded in the calls than is entirely relevant to a suitable reaction (unless one were to argue that evolutionary pressure existed on prairie dogs to distinguish blue predators from yellow ones.)

NPR labels this ‘prairiedogese’, which makes me shiver and reminds me of Punxatawney Pennsylvania, where Bill Murray was stuck on a vicious cycle in the movie Groundhog Day, forced every day to watch the mayor recite the translated proclamation of the Groundhog, which of course spoke in ‘groundhogese’. Luckily, however, there won’t be courses in this ‘language’.

References:

Schleich, C., Vielma, A., Glösmann, M., Palacios, A., & Peichl, L. (2010). Retinal photoreceptors of two subterranean tuco-tuco species (Rodentia, Ctenomys): Morphology, topography, and spectral sensitivity The Journal of Comparative Neurology, 518 (19), 4001-4015 DOI: 10.1002/cne.22440

Seyfarth, R., Cheney, D., & Marler, P. (1980). Monkey responses to three different alarm calls: evidence of predator classification and semantic communication Science, 210 (4471), 801-803 DOI: 10.1126/science.7433999

Slobodchikoff CN, Paseka A, & Verdolin JL (2009). Prairie dog alarm calls encode labels about predator colors. Animal cognition, 12 (3), 435-9 PMID: 19116730

On Phylogenic Analogues

A recent post by Miko on Kirschner and Gerhart’s work on developmental constraints and the implications for evolutionary biology caught my eye due to the possible analogues which could be drawn with language in mind. It starts by saying that developmental constraints are the most intuitive out of all of the known constraints on phenotypic variation. Essentially, whatever evolves must evolve from the starting point, and it cannot ignore the features of the original. Thus, a winged horse would not occur, as six limbs would violate the basic bauplan of tetrapods. In the same way, a daughter language cannot evolve without taking into account the language it derives from and language universals. But instead of viewing this as a constraint which limits the massive variation we see biologically or linguistically between different phenotypes, developmental constraints can be seen as a catalyst for regular variation.

A pretty and random tree showing variation among IE languages.

Looking back over my courses, I’m surprised by how little I’ve noticed (different from how much was actually said) about reasons for linguistic variation. The modes of change are often noted: <th> is fronted in Fife, for instance, leading to the ‘Firsty Ferret’ instead of the ‘Thirsty Ferret’ as a brew, for instance. However, why the <th> is fronted at all isn’t explained beyond cursory hypothesis. But that’s a bit besides the point: what is the point is that phenotypic variation is not necessarily random, as there are constraints – due to the “buffering and canalizing of development” – which limit variation to a defined range of possibilities. There clearly aren’t any homologues between biological embryonic processes and linguistic constraints, but there are developmental analogues: the input bottleneck (paucity of data) given to children, learnability constraints, the necessity for communication, certain biological constraints to do with production and perception, etc. These all act on language to make variation occur only within certain channels, many of which would be predictable.

Another interesting point raised by the article is the robustness of living systems to mutation. The buffering effect of embryonic development results in the accumulation of ‘silent’ variation. This has been termed evolutionary capacitance. Silent variation can lay quiet, accumulating, not changing the phenotype noticeably until environmental or genetic conditions unmask them. I’ve seen little research (not that I don’t expect there to be plenty) on the theoretical implications of the influence of evolutionary capacitance on language change – in other words, how likely a language is to make small variations which don’t affect language understanding before a new language emerges (not that the term language isn’t arbitrary based on the speaking community, anyway). Are some languages more robust than others? Is robustness a quality which makes a language more likely to be used in multilingual settings – for instance, in New Guinea, if seven languages are mutually indistinguishable, is it likely the that local lingua franca is forced by its environment to be more robust in order to maximise comprehension?

The article goes on about the cost of robustness: stasis. This can be seen clearly in Late Latin, which was more robust than the daughter languages as it was needed to communicate in different environments where the language had branched off into the Romance languages, and an older form was necessary in order for communication to ensue. Thus, Latin retained usage well after the rest of it had evolved into other languages. Another example would be Homeric Greek, which retained many features lost in Attic, Doric, Koine, and other dialects, as it was used in only a certain environment and was therefore resistant to change. This has all been studied before better than I can sum it up here. But the point I am making is that analogues can be clearly drawn here, and some interesting theories regarding language become apparent only when seen in this light.

A good example, also covered, would be exploratory processes, as Kirschner and Gerhart call them. These are processes which allow for variation to occur in environments where other variables are forced to change. The example given is the growth of bone length, which requires corresponding muscular, circulatory, and other dependant systems to also change. The exploratory processes allow for future change to occur in the other systems. That is, they expedite plasticity. So, for instance, an ad hoc linguistic example would be the loss of a fixed word order, which would require that morphology step in to fill the gap. In such a case, particles or affixes or the like would have to have already paved the way for case markers to evolve, and would have had to have been present to some extent in the original word order system. (This may not be the best example, but I hope my point comes across.)

Naturally, much of this will have seemed intuitive. But, as Miko stated, these are useful concepts for thinking about evolution; and, in my own case especially, the basics ought to be brought back into scrutiny fairly frequently. Which is justification enough for this post. As always, comments appreciated and accepted. And a possible future post: clade selection as a nonsensical way to approach phylogenic variation.

References:

Caldwell, M. (2002). From fins to limbs to fins: Limb evolution in fossil marine reptiles American Journal of Medical Genetics, 112 (3), 236-249 DOI: 10.1002/ajmg.10773

Gerhart, J., & Kirschner, M. (2007). Colloquium Papers: The theory of facilitated variation Proceedings of the National Academy of Sciences, 104 (suppl_1), 8582-8589 DOI: 10.1073/pnas.0701035104

Domain-General Regions and Domain-Specific Networks

The notion of a domain-specific, language acquisition device is something that still divides linguists. Yet, in an ongoing debate spanning at least several decades, there is still no evidence, at least to my knowledge, for the existence of a Universal Grammar. Although, you’d be forgiven for thinking that the problem was solved many years ago, especially if you were to believe the now sixteen-year old words of Massimo Piattelli-Palmarini (1994):

The extreme specificity of the language system, indeed, is a fact, not just a working hypothesis, even less a heuristically convenient postulation. Doubting that there are language-specific, innate computational capacities today is a bit like being still dubious about the very existence of molecules, in spite of the awesome progress of molecular biology.

Suffice to say, the analogy between applying scepticism of molecules and scepticism of Universal Grammar is a dud, even if it does turn out that the latter does exist. Why? Well, as stated above: we still don’t know if humans have, or for that matter, even require, an innate ability to process certain grammatical principles. The rationale for thinking that we have some innate capacity for acquiring language can be delineated into a twofold argument: first, children seem adept at rapidly learning a language, even though they aren’t exposed to all of the data; and second, cognitive science told us that our brains are massively modular, or at the very least, should entail some aspect that is domain specific to language (see FLB/FLN distinction in Hauser, Chomsky & Fitch, 2002). I think the first point has been done to death on this blog: cultural evolution can provide an alternative explanation as to how children successfully learn language (see here and here and Smith & Kirby, 2008). What I haven’t really spoken about is the mechanism behind our ability to process language, or to put it differently: how are our brains organised to process language?

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