-------- Original Message --------
Subject: Re: predicting selection response
Date: Wed, 23 Mar 2011 09:13:29 -0400
From: Chris Klingenberg <[email protected]>
Reply-To: [email protected]
Organization: University of Manchester
To: [email protected]

Dear Milos

I think there is no simpler way to do what you are asking to do. To
predict the response to selection is a rather ambitious thing to do, and
so you just have to live with the complexity that goes with it.

The mechanics of this sort of analyses is helped by the fact that they
are implemented in MorphoJ. See:
http://www.flywings.org.uk/MorphoJ_guide/frameset.htm?genetics/resp_selection.htm

There is also a more recent paper that uses the same method with some
slight modifications:
Klingenberg, C. P., V. Debat, and D. A. Roff. 2010. Quantitative
genetics of shape in cricket wings: developmental integration in a
functional structure. Evolution 64:2935–2951.
http://www.flywings.org.uk/PDF%20files/Evol2010.pdf

The critical point is that you do need the G matrix. So you do need
either breeding experiments or pedigree information from a natural
population to estimate the G matrix. There is no way around having
genetic information.
Some people have used a scalar multiple P matrix as a substitute for the
G matrix (G matrix = heritability * G matrix). That is assuming that the
genetic and phenotypic covariances are proportional. If this were true,
it would make everybody's life a lot easier. The problem is that
analyses that have checked this assumption with easonably powerful tests
have tended to reject the hypothesis of proportionality.

If you cannot get genetic data, my advice would be to stick to the sort
of things you can do with phenotypic data. I think there are a lot of
interesting things about integration that can be done with phenotypic
data, without pretending to do quantitative genetics.

I hope this helps clarifying this issue.

Best wishes,
Chris




On 3/23/2011 11:50 AM, morphmet wrote:


-------- Original Message --------
Subject: predicting selection response
Date: Tue, 22 Mar 2011 12:07:37 +0100
From: Milos Blagojevic <[email protected]>
To: <[email protected]>



Hello to all Morphmet users,

Again, only a question to clarify things up a bit... If, for example, my
study aim was to model hypothesized shape change along some selection
gradient, what approach should I use? The procedure outlined in
Klingenberg and Leamy`s paper "Quantitative genetics of geometric shape
in the mouse mandible" is helpful with respect to information about the
way that GM landmark analysis can be linked to multivariate Qgenetic
analyses, but it is too complex for me. For starters I would like an
easier way to incorporate landmark data in multivariate breeder`s
equation and G matrix. I am aware that shape alone must be reduced, e.g.
by PCA but can PCA scores be used as direct measurements sensu Lande and
Arnold`s classic paper "The measurement of selection on correlated
characters"?

Finally the simulated selection differentials should depict shape change
of certain regions of the skull and then these model shapes used for
testing how and if the overall skull morphological integration has
changed. Of course, all data is strictly from natural populations and no
breeding experiment can be designed, just simulation.

Best regards,

Milos Blagojevic
Faculty of Science
Institute for biology and ecology
Kragujevac, Serbia


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Christian Peter Klingenberg
Faculty of Life Sciences
The University of Manchester
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Fax: +44 161 275 5082
E-mail: [email protected]
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