September 4, 2021

 Dear Morphmetters,

        I'm writing to draw your attention to a paper of mine
 published last week in Benedikt Hallgrimsson's journal
 Evolutionary Biology.  You can get a copy by clicking
 "Explore online first articles" on the journal home page
 https://www.springer.com/journal/11692.
 The paper has the rather recondite title
 "A new method for landmark-based studies of the
 dynamic stability of growth, with
 implications for evolutionary analyses," and
 it indulges my customary prolixity, running 30 double-column
 pages including 18 figures, most of them multipanel.  
        The paper was stimulated by a paper
 Philipp Mitteroecker and Ekaterina Stansfield published
 earlier this year ("A model of developmental
 canalization, applied to human cranial form," 
 PLoS Computational Biology, 17(2), e1008381) suggesting
 that longitudinal landmark data deserve a better protocol
 for analysis than our usual approaches, which are based
 on the covariance matrix of transformed landmark coordinates
 pooled over ages.  Both papers argue
 that the matrix being analyzed should not
 be that pooled version, but instead the series of
 covariance matrices for each time-specific set of
 those coordinates against their changes to the next age
 of observation.  M. and S. suggested a Partial Least
 Squares analysis of the Procrustes shape coordinates of
 such growth data sets.   My paper instead recommends and demonstrates
 a version relying on what I've been calling Boas coordinates
 (Procrustes without the size-standardization
 step) and, instead of PLS, a true eigenanalysis, meaning,
 one using the same R call "eigen" that we
 use for PCA.  The difference is that instead of 
 eigen(t(X)%*%X) we ask for, diagram, scatter, and
 interpret eigen(t(X)%*%Y) where X is the form data matrix
 at time i and Y is the changes of form from  there to time i+1
 after both have been mean-centered by columns.
        What makes this small code change unexpectedly challenging is
 that the eigenanalysis of those growth-by-form covariance matrices
 can result in complex eigenvalues and eigenvectors (quantities
 that involve terms in the square root of minus 1).  
 The paper takes a lot of space to explain an intuitive
 version of that complex arithmetic that, in effect, replaces
 a complex-valued thin plate spline by a pair of real-valued
 ones.  The engineers have already named these _canonical
 vectors,_ a label I'm suggesting here as well, even though
 these vectors are different from the vectors you get from
 canonical correlations, from multivariate discriminant analysis,
 and so on. (The other multivariate statisticians
 have no copyright on the word "canonical.")
        The reviewers thought my argument was logical but the
 requirement of complex numbers would situate the technique
 out of reach for most organismal biologists.  I argued back
 basically that (i) many biologists already do indeed master
 complex arithmetic, especially in bioengineering applications,
 and (ii) the resulting findings are worth the cognitive
 stretch.  Also, I've included a sort of tutorial, not on
 the square root of minus 1, exactly, but on the meaning of
 those complex eigenvalues and their eigenvectors as expressed
 in our usual scatterplots of scores and deformation grids.
       This, in turn, suggests an experiment of the sort most of you
 already had to navigate back when you were taught that the struggle
 to learn enough about matrix algebra, matrix inverses, and
 principal component analysis was worth the effort.  I've argued
 for years that the benefits of matching more advanced mathematics
 than that to appropriate biological questions
 are worth the cost of mastering that
 advanced math.  So I'm hoping (as are the reviewers of the
 second version, and also, I presume, the journal editor)
 that some of you out there, particularly the more
 mathematically adventuresome, might suspend your disbelief
 in the square root of minus 1 long enough to enjoy dipping into
 the arguments of my paper and its extended 8-landmark, 8-age,
 18-animal example.  The paper is free at 
 https://doi.org/10.1007/s11692-021-09548-8
 or, as I mentioned already, you can get to it from
 the journal home page.

             Thanks for considering this challenge, Fred Bookstein 
 

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