Performing CVA on the first PC axes seems a good approach. However,
using it, I have run into a problem as to how many PC axes to use and
how to justify including the first 5, or 6, or 7? One way is to use no
more PC than the number of specimens in a group, given that enough
variation (90-95%) is included. Does that seem to make sense? Or should
there be a more stringent criterion?


> I have a version of CVAGen that will first perform a PCA on the partial
> warp scrores and uniform components, and then perform a CVA on a limited
> number of the PCA scores.  So if you have 20 variables in the data and
> only 20 specimens, you might find that the first 5 or 6 PCA axes have
> 90% or more of the variance, so that a CVA using only 5 or 6 PCA axes
> might might produce reasonable results.  This approach may be
> particularly useful if you are using a lot of semi-landmarks.

regards,
Asta


***
Asta Audzijonyte
Finnish Museum of Natural History
POB 26 (Teollisuuskatu 23)
FI-00014 University of Helsinki
www.fmnh.helsinki.fi/english/zoology/invertebrates/research/molecular/asta.htm

vision without action is a daydream
action without vision is a nightmare



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