[MORPHMET] Replicating the scores and Mahalanobis distance

2019-06-07 Thread 'Angelo Emmanuel Ho' via MORPHMET
To those who sent me messages for helping me in my paper, thank you very 
much. Hopefully I could still ask for more help from you with my following 
concerns:

1. I have the five canonical variates (CV) score and per row are the CV 
loadings of each shape configurations. There are, let's say 15 scores 
belonging to group 1, 20 to group 2, 18 to group 3, and 24 to group 4. How 
will I replicate (through an R code) these scores such that it will 
replicate into 1000 per group, so that per CV score, there are 4000 
loadings, 1000 each? 

2. In relation to 1, how will I get the Mahalanobis distance of each group? 
I will use the Mahalanobis distance for the minimum spanning tree and 
dendogram to compare the minimum spanning tree and dendogram of the 
original sample size?

Thank you very much. 

  

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[MORPHMET] An R code for full Procrustes mean shape by GPA

2019-06-05 Thread 'Angelo Emmanuel Ho' via MORPHMET
Hello! I would like to ask for help as I use the book of Dryden and Mardia, 
"Statistical Shape Analysis with Application in R"? I cannot find where in 
the book (or maybe I just overlooked), how did he plot the mean shapes in 
Figure 8.4. Thank you very much. 

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[MORPHMET] Integrated Morphometrics Package Installer

2019-06-04 Thread 'Angelo Emmanuel Ho' via MORPHMET
Hello! As I do morphometrics study, I am looking for the Integrated 
Morphometrics Package software. However, I searched the very website but it 
is not working anymore and I do not know where to find. Hopefully I may 
request for anybody for a copy of this software. Your help is very much 
appreciated. Thank you very much. 

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[MORPHMET] morphmet - 1000 subscribers!

2019-05-19 Thread MORPHMET
I note that we recently have achieved 1000 subscribers to morphmet!

Caveat 1: Over the years, some have removed themselves from the list or 
asked me to remove them. So, there have actually been more than 1000 people 
subscribing, but we have never had 1000 subscribers on the list at the same 
time.

Caveat 2: We have about 50 addresses that are either bouncing or disabled 
indicating members who have probably moved on from their subscribed 
addresses. In the future, I will remove those with persistent bouncing 
dropping the list (temporarily, no doubt) below 1000.

-the moderator

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Re: [MORPHMET] morphmet - list problems

2019-05-19 Thread morphmet
Yeah! This msg came through. Let's see/hope if/that the list continues 
to function.

-the moderator

On 5/19/19 3:56 AM, morphmet_moderator wrote:
There seem to be some problems with the mailing list that have come to 
my attention over the past several days, e.g., it thinks every post is 
spam, but doesn't give me the chance to moderate such posts. Even I, the 
moderator, am only able to post via the website intermittently.


There is a notice that the server-side software will be changed this 
month, so I suspect this is part of the problem, but I don't know. I am 
in contact with support to try to see what is going on. For now, I have 
no idea if your individual posts to the list (including this one - 
fourth attempt) will appear.


In the meantime, please be patient.

-the moderator

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[MORPHMET] Re: PREPRINT: between-group principal components analysis (bgPCA)

2019-05-18 Thread MORPHMET
[Final, summary post.]

I thought I should post some notes about the responses to Andrea’s recent 
postings. Several people seem to have extrapolated beyond what Andrea said.

After a few months of the Cardini, O’Higgins, Rohlf, and Bookstein 
collaboration (Polly was CC:ed on the very early emails but I do not 
remember him engaging), I suggested to Andrea that there should be two 
publications not one. I could see that while writing about the same flaws 
in the same method the approaches Fred and I were taking would be difficult 
to combine in the same paper. Andrea and Paul agreed and Andrea then 
suggested to Fred that he write a paper separate from ours.  Thus, Fred did 
not unilaterally jump ahead and just write his own paper as some seem to 
have assumed. The understanding was that we expected the two papers to be 
published together as “companion papers” in some journal yet to be 
determined.

I know that Fred was concerned about the ethics of waiting a long time to 
warn people that they were using a severely flawed (I would say strongly 
biased) method.  The usage of BG-PCA seems to have increased lately and it 
did not seem fair to let people continue to write papers and dissertations 
based on this method once we knew how bad it was. His biorxiv upload and 
his announcement of it on morphmet were not a surprise to us. There were 
emails exchanged about the need to warn users. At the time, Fred told me 
that he needed to go ahead with the biorxiv upload as it was unclear how 
long it would take our ms. to be completed due to other demands on our time.

Reading Fred’s papers can take time but if one just looks at his Fig. 1 
(Google "biorxiv 627448" if you lost the link that Fred posted) you will 
see the magnitude of the problem. It is not subtle! Incidentally, the 
Cardini et al. draft also has a more extensive Figure illustrating the same 
problem as a function of n but the rest of the paper is very different. In 
fact, I found it interesting how two papers about the same defect in the 
same method and reaching the same conclusion could have so little overlap. 
Thus, Fred’s paper does not infringe on the content of the Cardini et al. 
manuscript or interfere with its publication – in fact I think it makes it 
more important as it will show the problem does not require an 
understanding of an abstract theorem. I believe the Cardini et al. paper 
will show that the defects in the method are very easy to understand and 
obvious once you think about it in the right way.


F. James Rohlf, Distinguished Professor, Emeritus. Ecology & Evolution
Research Professor, Anthropology
Stony Brook University


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[MORPHMET] Re: PREPRINT: between-group principal components analysis (bgPCA)

2019-05-16 Thread MORPHMET
Dear MorphMetters,

Yesterday David Polly reminded us of the existence of a 3.5-page draft 
fragment emailed by Andrea Cardini on September 5, 2018 and headed as by 
"Cardini, O'Higgins, Polly, Rohlf, Bookstein." So, yes, David Polly was 
indeed present at the creation. It begins with paragraphs of an 
introduction acknowledged to be "largely borrowed" from me and continues 
with a summary of some of Cardini's simulation results, which are 
consistent with mine but reported using mostly different simulations and 
quantifications, together with a sketch of a discussion quite different 
from mine.  This fragment, particularly its style of simulating and 
reporting, may have served later as the basis of the second of the two 
papers as I referred to it both in my Monday morphmet posting and in my 
biorxiv preprint. (I say "may have" because I have not seen any more recent 
state of that second manuscript.) So my Monday note to morphmet pointing to 
my biorxiv preprint should have mentioned the September document as part of 
the history of our project before it split into two. I apologize to David 
for not realizing the role he played in this early history, and apologize 
to Andrea for overlooking this early draft of the less algebraic half of 
our joint project.  I hope the authors of this second paper will post it to 
biorxiv as urgently as mine was posted once theirs, too, is in final draft.

FB


On Tuesday, May 14, 2019 at 1:32:24 PM UTC-4, MORPHMET wrote:
>
> Dear MorphMetters,
>
> Some of you may have been in the auditorium in the Department of Botany, 
> University of Vienna, back in March when Philipp Mitteroecker and I were 
> the two scheduled discussants for the conference "GMAustria19" on 
> applications of geometric morphometrics.  Several of the papers delivered 
> there used between-group principal components analysis (bgPCA), and after 
> each of those papers I mentioned in the course of my commentary that bgPCA 
> was fatally flawed in applications to most GMM data sets and should NEVER 
> be used here. In my keynote address, which closed the meeting, I had one 
> cryptic slide about this assertion, with an example that flashed on the 
> screen but was immediately replaced by the next slide.
>   
> The typical response to both my own talk and my criticism of the talks of 
> others, as far as bgPCA was concerned, was along the lines of "Hunh?" or 
> sometimes "What are you blathering about this time? Isn't bgPCA in the 
> standard toolkit?" I answered that the Bookstein paper they should read was 
> just then being written, as one of a pair jointly arising from 
> conversations with Andrea Cardini, Jim Rohlf, and Paul O'Higgins following 
> an original hunch of Cardini's, and that my argument would be pretty 
> convincing once it was actually written down.  The claim isn't that people 
> are using bgPCA incorrectly. They're using it according to the published 
> formulas, yes, but the method itself yields biological nonsense much too 
> often.
>  
> That was March.  In April, two different articles in Nature (one by 
> Detroit et al., one by Chen et al.) buttressed claims about sister species 
> of Homo sapiens using the bgPCA method, and so suddenly it became clear 
> that we authors had to do something quickly lest this become an epidemic of 
> bad biometrics. So we accelerated our writing. My paper was the first to be 
> finished, probably because it is a single-authored item by an emeritus with 
> no other obligations, and it seemed like a good idea to upload the final 
> draft to https://www.biorxiv.org even before submitting the paper, so 
> that any letter to the editors of Nature could include a link to  the 
> argument as to exactly WHY bgPCA is nearly always unsound and its 
> inferences invalid for applications in contemporary GMM. 
>  
> That is the draft that has just appeared as 
>
> https://www.biorxiv.org/content/10.1101/627448v1
>
> For those of you who were at the March meeting, this is the argument 
> (complete with formulas) defending my stern condemnation there. I won't try 
> to summarize it in this morphmet note -- if you're interested, just read 
> the abstract on page 1 of the link.  For those of you who have already 
> published bgPCA analyses, you know who you are -- my paper argues strongly 
> that you need to go back and revisit the inferences of those papers in a 
> mood of much more intense multivariate skepticism.  For the rest of you, 
> please consider this draft manuscript to be a wake-up call. A technique 
> that has appeared in dozens of papers and that was, alas, specifically 
> praised by Mitteroecker and Bookstein personally (back in 2011) could 
> nevertheless, when examined closely (for the first time!), turn out to be 
>

[MORPHMET] PREPRINT: between-group principal components analysis (bgPCA)

2019-05-14 Thread MORPHMET
Dear MorphMetters,

Some of you may have been in the auditorium in the Department of Botany, 
University of Vienna, back in March when Philipp Mitteroecker and I were 
the two scheduled discussants for the conference "GMAustria19" on 
applications of geometric morphometrics.  Several of the papers delivered 
there used between-group principal components analysis (bgPCA), and after 
each of those papers I mentioned in the course of my commentary that bgPCA 
was fatally flawed in applications to most GMM data sets and should NEVER 
be used here. In my keynote address, which closed the meeting, I had one 
cryptic slide about this assertion, with an example that flashed on the 
screen but was immediately replaced by the next slide.
  
The typical response to both my own talk and my criticism of the talks of 
others, as far as bgPCA was concerned, was along the lines of "Hunh?" or 
sometimes "What are you blathering about this time? Isn't bgPCA in the 
standard toolkit?" I answered that the Bookstein paper they should read was 
just then being written, as one of a pair jointly arising from 
conversations with Andrea Cardini, Jim Rohlf, and Paul O'Higgins following 
an original hunch of Cardini's, and that my argument would be pretty 
convincing once it was actually written down.  The claim isn't that people 
are using bgPCA incorrectly. They're using it according to the published 
formulas, yes, but the method itself yields biological nonsense much too 
often.
 
That was March.  In April, two different articles in Nature (one by Detroit 
et al., one by Chen et al.) buttressed claims about sister species of Homo 
sapiens using the bgPCA method, and so suddenly it became clear that we 
authors had to do something quickly lest this become an epidemic of bad 
biometrics. So we accelerated our writing. My paper was the first to be 
finished, probably because it is a single-authored item by an emeritus with 
no other obligations, and it seemed like a good idea to upload the final 
draft to https://www.biorxiv.org even before submitting the paper, so that 
any letter to the editors of Nature could include a link to  the argument 
as to exactly WHY bgPCA is nearly always unsound and its inferences invalid 
for applications in contemporary GMM. 
 
That is the draft that has just appeared as 

https://www.biorxiv.org/content/10.1101/627448v1

For those of you who were at the March meeting, this is the argument 
(complete with formulas) defending my stern condemnation there. I won't try 
to summarize it in this morphmet note -- if you're interested, just read 
the abstract on page 1 of the link.  For those of you who have already 
published bgPCA analyses, you know who you are -- my paper argues strongly 
that you need to go back and revisit the inferences of those papers in a 
mood of much more intense multivariate skepticism.  For the rest of you, 
please consider this draft manuscript to be a wake-up call. A technique 
that has appeared in dozens of papers and that was, alas, specifically 
praised by Mitteroecker and Bookstein personally (back in 2011) could 
nevertheless, when examined closely (for the first time!), turn out to be 
algebraic garbage when applied to data sets where there are far more shape 
coordinates than specimens. But isn't that the usual situation in GMM these 
days?  
 
As always, I welcome all responses, both positive and negative. The biorxiv 
posting is permanent, but there is plenty of time for me to make changes 
before the paper is published (at present it has not yet even been 
submitted anywhere), so feel free to try to find the flaws in my argument.  
But I hope you will want to try some of these simulations on your own 
before you argue against mine. You will also want to study the companion 
piece by Cardini, O'Higgins, and Rohlf that should likewise be available 
for download before too long.    
 
Fred Bookstein

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Re: [MORPHMET] How to fix erroneous 3D coordinates took by microscribe

2019-05-07 Thread morphmet
 474.6507
85.1190 135.9783473.3503
79.3694 122.8234477.4590
78.4327 115.8613477.4715
84.2949 108.1328485.4598
97.2760 93.4345 481.8105
89.2901 111.8870483.4924
90.0784 117.8522490.4405
91.4313 106.3994494.9362
79.4173 144.0817472.9395
88.3825 141.0176474.3985
90.9274 140.2106477.6371
85.2512 140.7932478.2403

I would apreciate if somebody could help me.
Please don't hesitate to ask me for more details.

King regards
Azadeh




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[MORPHMET] Re: New Article: Reflections on a Biometrics of Organismal Form

2019-04-30 Thread MORPHMET
For some reason, the link to the article I rec'd was excessively long. 
After some research, I figured out how to edit the original post, but 
elected not to since many receive messages as email. I am not sure they 
would get/see the edit. Hence, I provide a shorter link here:

https://link-springer-com.proxy.lib.fsu.edu/journal/13752

-ds [the MORPHMET moderator]

On Tuesday, April 30, 2019 at 11:01:15 AM UTC-4, MORPHMET wrote:
>
> [Posted on behalf of Dr. Bookstein] 
>
> Dear MorphMetters, 
>
> I'm happy to announce that my paper "Reflections on a Biometrics of 
> Organismal Form" has just been posted for open access by the Springer 
> journal Biological Theory. You can get a free copy by pointing your browser 
> at 
>
>
> https://urldefense.proofpoint.com/v2/url?u=https-3A__link.springer.com_journal_13752=DwIBAg=HPMtquzZjKY31rtkyGRFnQ=T8Sxf-U51iRHIXQayyjGAA=xOGtb5kpXyYsx7O1ZPeSGHSsh8sLGcIwYOsLoNWTC3I=wQclw8xhArX7488PAUkyik6iPqlhj-vA5-el7VYzF-E=
>  
>
> and clicking on what is, for now, the top entry in the Latest Articles 
> table on the home page. 
>
> This article is a sequel to my 2015 article in Benedikt Hallgrimsson's 
> journal Evolutionary Biology that introduced the BE-PwV plot as the best 
> tool for studying integration in GMM data sets. I trace the basic idea here 
> back nearly a hundred years, not to D'Arcy Thompson but to a 
> hitherto-untranslated critique of his ideas by the Vivarium group under 
> Hans Przibram in Vienna arguing that the only valid way that a biologist 
> should study organismal form is by direct experimental observation of 
> transformation grids: "Thompson's holistic deformations can be made 
> comprehensible if we can visualize a space lattice upon the living form, so 
> as to assess how each little piece changes its shape under conditions that 
> vary by species. Here lies open a rich, nearly undeveloped field that 
> invites a mathematization, one whose erection we hope will begin very 
> soon." But the timing seems to have slipped a bit, namely, by 97 years. The 
> new paper argues that BE-PwV is exactly the "mathematization" they were 
> envisioning, which could not be made empirical until the development of 
> geometric morphometrics, and further that it is the only morphometric 
> method consistent with the most fundamental fact in all of biology, "the 
> repetitive production of organized heterogeneity" (Hotchkiss 1958) or, as 
> Walter Elsasser put it in 1987, "the transfer of information over finite 
> intervals of time without an intermediate message." For instance, the new 
> article demonstrates how to recognize a growth-gradient explicitly even in 
> the presence of unstructured residual variability. I close with a plea that 
> others help me build the bridge that we need so urgently between the 
> arithmetic of today's burgeoning image-based data resources and the 
> rhetoric of biological explanations of organismal form both over evolution 
> and over development. 
>
> As always I welcome all comments on these ideas, enthusiastic or 
> otherwise. 
>
>    Fred Bookstein 
>

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[MORPHMET] New Article: Reflections on a Biometrics of Organismal Form

2019-04-30 Thread MORPHMET
[Posted on behalf of Dr. Bookstein] 

Dear MorphMetters, 

I'm happy to announce that my paper "Reflections on a Biometrics of 
Organismal Form" has just been posted for open access by the Springer 
journal Biological Theory. You can get a free copy by pointing your browser 
at 

https://urldefense.proofpoint.com/v2/url?u=https-3A__link.springer.com_journal_13752=DwIBAg=HPMtquzZjKY31rtkyGRFnQ=T8Sxf-U51iRHIXQayyjGAA=xOGtb5kpXyYsx7O1ZPeSGHSsh8sLGcIwYOsLoNWTC3I=wQclw8xhArX7488PAUkyik6iPqlhj-vA5-el7VYzF-E=
 

and clicking on what is, for now, the top entry in the Latest Articles 
table on the home page. 

This article is a sequel to my 2015 article in Benedikt Hallgrimsson's 
journal Evolutionary Biology that introduced the BE-PwV plot as the best 
tool for studying integration in GMM data sets. I trace the basic idea here 
back nearly a hundred years, not to D'Arcy Thompson but to a 
hitherto-untranslated critique of his ideas by the Vivarium group under 
Hans Przibram in Vienna arguing that the only valid way that a biologist 
should study organismal form is by direct experimental observation of 
transformation grids: "Thompson's holistic deformations can be made 
comprehensible if we can visualize a space lattice upon the living form, so 
as to assess how each little piece changes its shape under conditions that 
vary by species. Here lies open a rich, nearly undeveloped field that 
invites a mathematization, one whose erection we hope will begin very 
soon." But the timing seems to have slipped a bit, namely, by 97 years. The 
new paper argues that BE-PwV is exactly the "mathematization" they were 
envisioning, which could not be made empirical until the development of 
geometric morphometrics, and further that it is the only morphometric 
method consistent with the most fundamental fact in all of biology, "the 
repetitive production of organized heterogeneity" (Hotchkiss 1958) or, as 
Walter Elsasser put it in 1987, "the transfer of information over finite 
intervals of time without an intermediate message." For instance, the new 
article demonstrates how to recognize a growth-gradient explicitly even in 
the presence of unstructured residual variability. I close with a plea that 
others help me build the bridge that we need so urgently between the 
arithmetic of today's burgeoning image-based data resources and the 
rhetoric of biological explanations of organismal form both over evolution 
and over development. 

As always I welcome all comments on these ideas, enthusiastic or otherwise. 

   Fred Bookstein 

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[MORPHMET] 2019 CALL FOR NOMINATIONS: The Rohlf Medal for Excellence in Morphometrics

2019-02-18 Thread morphmet

2019 CALL FOR NOMINATIONS

The Rohlf Medal for Excellence in Morphometrics
(http://life.bio.sunysb.edu/ee/rohlf_medal/)

The Rohlf Medal was established in 2006 by the family and friends of F. 
James Rohlf to mark his 70th birthday. He has been a longtime Stony 
Brook University faculty member and is currently Emeritus Distinguished 
Professor in the Department of Ecology and Evolution, and Research 
Professor in the Department of Anthropology.


Recipients of the Rohlf Medal will be recognized for excellence in their 
body of work on the development of new morphometric methods or for their 
applications in the biomedical or biological sciences, including 
evolutionary biology, population biology, physical anthropology, 
developmental biology, neurobiology, computer sciences, and medicine. 
The term "morphometrics" is intended to include high-dimensional pattern 
analyses of biological shape, especially those that analyze shape in a 
comprehensive way, or of covariation of shape with other variables. The 
award can recognize advances in the mathematical or statistical theory 
underlying morphometric methods, new software that implements or 
visualizes new methods, or specific new biological findings that rely 
crucially on contemporary morphometric methods and represent major 
advances.


Candidates for the Rohlf Medal may be self-nominated or nominated by 
others. They must possess a Ph.D. degree or the equivalent.


The winning candidate must agree to attend the award ceremony in 
person in order to accept the Rohlf Medal and then deliver the award 
lecture.



Nomination packages should include,
(1) a description of the body of work (not to exceed two pages) on which 
the candidacy is based,
(2) reprints of no more than three relevant papers and/or software 
products,

(3) a curriculum vitae, and
(4) three letters of support.

Nominating packages should be uploaded to the Rohlf Medal website 
(http://life.bio.sunysb.edu/ee/rohlf_medal/apply.html) and received by 5 
pm, EST, 15 July 2019 to be assured of full consideration.


The successful candidate will receive the Rohlf Medal and a cash prize 
at Stony Brook University, planned for Thursday October 24th, 2019.  She 
or he will deliver a lecture that is appropriate for a broad audience, 
ranging from the exact sciences to the humanities, concerning the 
morphometric methodology, software, or findings for which the Rohlf 
Medal was awarded.


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Re: [MORPHMET] MorphoJ: problem with reading the tps files

2019-01-02 Thread morphmet
Your system is set up to us commas (',') to mark the decimal instead of 
the period ('.'). I think there is an option as to which to use within 
the tps programs. Some morphometrics programs assume the use of the 
period. -ds


On 12/31/18 2:55 PM, Ewa Krzeminska wrote:

When trying to create a dataset from a tps file I got a response: Invalid 
number format in the file. The file was created in TpsDig, and the text in a 
notepad is:
LM=18
943,0 1455,0
902,0 1097,0
947,0 981,0
954,0 866,0
945,0 632,0
954,0 397,0
817,0 1313,0
664,0 1335,0
797,0 1429,0
559,0 1477,0
679,0 1503,0
391,0 1217,0
485,0 1093,0
533,0 914,0
880,0 809,0
849,0 715,0
707,0 802,0
496,0 632,0
IMAGE=3572.jpg
ID=0

The option "tps" was chosen. What can be wrong?



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[MORPHMET] Geometric morphometrics of nested symmetries unravels hierarchical inter- and...[published version]

2018-12-22 Thread 'Yoland SAVRIAMA' via MORPHMET
Dear colleagues,

Here is the published version of the manuscript previously deposited at 
BioRxiv, now entitled "Geometric morphometrics of nested symmetries 
unravels hierarchical inter- and intra-individual variation in biological 
shapes".

Y. Savriama & S. Gerber. 2018. “Geometric morphometrics of nested 
symmetries unravels hierarchical inter- and intra-individual variation in 
biological shapes,” Sci. Rep., 8, no. 18055.
DOI:10.1038/s41598-018-36147-z
https://rdcu.be/bd7BP

Best wishes,
Yoland Savriama, PhD
Institute of Biotechnology
P.O. Box 56 (Viikinkaari 5)
FIN-00014 FINLAND

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[MORPHMET] Bracketing phenogenotypic limits of mammalian hybridization [Published Version]

2018-11-28 Thread 'Yoland SAVRIAMA' via MORPHMET
Dear colleagues,

Here is the published version of the manuscript previously deposited at 
BioRxiv, now entitled "Bracketing phenogenotypic limits of mammalian 
hybridization".

This is the first study combining seals' genome data, 3D geometric 
morphometrics of crania, and computational modeling of teeth to examine 
the potential for mammalian hybridization between phenotypically disparate 
taxa.

Savriama, Y., Valtonen, M., Kammonen, J. I., Rastas, P., Smolander, O.-P., 
Lyyski, A., Häkkinen,T.J.,Corfe, I.J., Gerber, S.,Salazar-Ciudad, I.,Paulin, 
L.,Holm, L., Löytynoja, A.,Auvinen, P., Jernvall, J. (2018). Bracketing 
phenogenotypic limits of mammalian hybridization. *Royal Society Open 
Science*,*5*(11). http://rsos.royalsocietypublishing.org/content/5/11/180903


Best wishes,

Yoland Savriama, PhD
Institute of Biotechnology
P.O. Box 56 (Viikinkaari 5)
FIN-00014 FINLAND




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[MORPHMET] Human Skull Evolution Video?

2018-11-19 Thread 'abbygracedrake' via MORPHMET
Hello!

Has anyone ever used 3D data to make a video showing the shape changes in 
human skull evolution? For example warping from a chimpanzee to modern 
human? I think it would be great to have a movie like this to use when 
teaching human evolution.

Thanks!
Abby

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[MORPHMET] Re: Morphometrics in Solanaceas

2018-10-25 Thread 'Yoland SAVRIAMA' via MORPHMET
Hi Christian,

I just released a step-by-step guide for geometric morphometrics of 
flowers. This could be of interest. 

SAVRIAMA, Y. (2018). A Step-by-Step Guide For Geometric Morphometrics Of 
Floral Symmetry. *Frontiers in Plant Science*, *9*, 1433.

https://doi.org/10.3389/fpls.2018.01433

Best wishes,

Yoland


On Thursday, October 25, 2018 at 6:21:09 PM UTC+3, Christian Borja Tacuri 
wrote:
>
> Hi everyone.
>
> I'm here looking for some help. I've been assigned to create a small 
> project where I have to compare morphometric characteristics among the 
> flowers of 10 species of Solanaceas in my country, Ecuador. So, I'd like 
> some help because I need to locate the landmarks and semilandmarks and I'm 
> not sure in which parts of the flower I should put the marks for the 
> comparison. Also, I need to look for differences between the flowers, based 
> on the abiotic factors of the places the plants live in. 
>
> I'll be so thankful for any guide that you can provide me. 
>

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[MORPHMET] New Book Announcement: A Course in Morphometrics for Biologists (Cambridge, University Press, 2018)

2018-10-10 Thread morphmet

Posted on behalf of Dr. Bookstein...

Dear Morphmetters,

   I'm delighted to announce the publication of my latest
 book, A Course in Morphometrics for Biologists (Cambridge
 University Press, 2018).  There are very nice comments
 on the back cover from several of our colleagues, including
 Morphmet's own Dennis Slice.  Here's the blurb, from
 the first inside page:

 "This book builds a much-needed bridge between biostatistics
  and organismal biology by linking the arithmetic of statistical
  studies of organismal form to the biological inferences
  that may follow from it. It incorporates a cascade of
  new explanations of regression, correlation, covariance
  analysis, and principal components analysis, before
  applying these techniques to an increasingly common
  data resource: the description of organismal forms
  by sets of landmark point configurations. For each data set,
  multiple analyses are interpreted and compared for
  insight into the relation between the arithmetic of
  the measurements and the rhetoric of the subsequent
  biological explanations. The text includes examples
  that range broadly over growth, evolution, and disease.
  For graduate students and researchers alike, this book
  offers a unique consideration of the scientific context
  surrounding the analysis of form in today's biosciences."

  For those of you who have been intrigued by any of my recent
 papers -- on integration and the BE-PwV plot, on the serious
 problems with Procrustes analysis, on the many pathologies of
 principal components in GMM, or on the possible resolution of
 these problems via a new version of factor analysis --
 all of these topics are touched on here, and many, many others as well.

  Fred Bookstein

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[MORPHMET] A Step-by-Step Guide For Geometric Morphometrics Of Floral Symmetry

2018-10-10 Thread 'Yoland SAVRIAMA' via MORPHMET


Dear colleagues,


I would like to attract your attention on this newly published paper.


SAVRIAMA, Y. (2018). A Step-by-Step Guide For Geometric Morphometrics Of 
Floral Symmetry. *Frontiers in Plant Science*, *9*, 1433.

https://doi.org/10.3389/fpls.2018.01433


A detailed guide for shape analysis of flowers with any type of symmetry 
using tpsdig2 (or equivalent) for data acquisition, R for data formatting 
and MorphoJ for visualisations. 

This is a practical translation of the theoretical and mathematical 
framework contained in Savriama & Klingenberg (2011).


Savriama, Y., & Klingenberg, C. P. (2011). Beyond bilateral symmetry: 
geometric morphometric methods for any type of symmetry. *BMC evolutionary 
biology*, *11*(1), 280.


Best wishes!

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[MORPHMET] Bracketing phenotypic limits of mammalian hybridization

2018-05-05 Thread 'Yoland SAVRIAMA' via MORPHMET
Dear colleagues,

I would like to attract your attention on another manuscript we deposited 
to bioRxiv. Our study combines 3D geometric morphometrics, computational 
modeling with genomics to investigate the phenotypic limits of mammalian 
hybridization.

Yoland Savriama, Mia Valtonen, Juhana Kammonen, Pasi Rastas, Olli-Pekka 
Smolander, Annina Lyyski, Teemu J Hakkinen, Ian J Corfe, Sylvain Gerber, 
Isaac Salazar-Ciudad, Lars Paulin, Liisa Holm, Ari Loytynoja, Petri 
Auvinen, Jukka Jernvall 2018. Bracketing phenotypic limits of mammalian 
hybridization. bioRxiv 310789; doi: https://doi.org/10.1101/310789

Best wishes,
Yoland Savriama

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[MORPHMET] Geometric Morphometrics of Nested Symmetries

2018-04-26 Thread 'Yoland SAVRIAMA' via MORPHMET
 

Dear colleagues,

 

I would like to attract your attention on this manuscript we just deposited 
to bioRxiv.

 

Savriama, Y. & Gerber, S. 2018. Geometric morphometrics of nested 
symmetries: Hierarchical inter- and intra-individual variation in 
biological shapes. *bioRxiv*. 

bioRxiv 306712; doi: https://doi.org/10.1101/306712

 

Best wishes,

Yoland Savriama

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[MORPHMET] digitizing very variable leaves

2018-03-19 Thread 'Tina Klenovšek' via MORPHMET
Thank you all for sharing experiences and ideas.

For the moment we decided to stick to methods based on landmarks but analyze 
simple leaves and leaves with exactly three lobes separately.
In addition, leaves from simple oval to heavily lobed will be analyzed jointly 
with outline methods as most of you suggested.
Hopefully all works out well.
Kind regards from Slovenia,
Tina


[cid:image002.jpg@01D3BF71.6B169C90]

doc. dr. Tina Klenovšek, koordinatorica doktorskega
študijskega programa Ekološke znanosti
Univerza v Mariboru | University of Maribor
Fakulteta za naravoslovje in matematiko
Faculty of Natural Sciences and Mathematics
Koroška cesta 160, 2000 Maribor, Slovenija
T: +386 41 808 366
E: tina.klenov...@um.si<mailto:ime.prii...@um.si>, 
www.fnm.um.si<http://www.fnm.uni-mb.si>



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RE: [MORPHMET] digitizing very variable leaves

2018-03-15 Thread 'Tina Klenovšek' via MORPHMET
Thanks to all, Javier, Vincent, William, Joanna and Dr. Rohlf,

my dilemma occurred because some botanists (I work with mammal skulls) have 
asked me to help them evaluate leaf variability of two tree species from 
different localities. So, variability within and among individual trees and 
species.

In which user friendly program (like MorphoJ ☺) can I analyse outline data and 
visualize variability?

Thank you again,
Tina

From: Joanna Lenarczyk [mailto:j.kowal...@botany.pl]
Sent: Thursday, March 15, 2018 10:21 AM
To: Tina Klenovšek
Subject: Re: [MORPHMET] digitizing very variable leaves

Hello Tina,
You can try a program which does not need landmarks:

http://www.eletel.p.lodz.pl/pms/SoftwareQmazda.html

I hope it will help you :) I have not tried it yet by myself, but it can be 
useful when you cannot or do not want use landmarks :)
Best,
Joanna

2018-03-15 8:40 GMT+01:00 
<f.james.ro...@stonybrook.edu<mailto:f.james.ro...@stonybrook.edu>>:
One could do that computationally but I would worry about the homology it might 
imply for such variable leaf shapes. You might try it and then check to see if, 
for example, a lobe on one leaf might be 20% of the linear distance around the 
outline but in another it might be 30% of the way around. In such a case the 
lobe on one leaf would effectively be treated as homologous to a location 
between lobes on another leaf. If so, does that make biological sense for your 
study? If simple leaves were also included the implied homology of a point 
along its outline to that of one of the lobed leaves might be pretty arbitrary. 
Would be better if one knew something about the development of these leaves 
(which I do not!) and used that knowledge.

An alternative would be to use outline methods to group shapes for the purpose 
of say identification with little implication that groups need be biologically 
meaningful. Sorry to be rather negative but I find highly variable leaf shapes 
difficult to put in a simple standard framework. Perhaps others will have 
better suggestions.


F. James Rohlf, Distinguished Professor, Emeritus. Ecology & Evolution
Research Professor, Anthropology
Stony Brook University

From: Tina Klenovšek <tina.klenov...@um.si<mailto:tina.klenov...@um.si>>
Sent: Wednesday, March 14, 2018 12:28 AM
To: f.james.rohlf 
<f.james.ro...@stonybrook.edu<mailto:f.james.ro...@stonybrook.edu>>
Cc: morphmet@morphometrics.org<mailto:morphmet@morphometrics.org>
Subject: RE: [MORPHMET] digitizing very variable leaves

Thanks to everyone who answered.

Dear Dr. Rohlf,
I assumed great variability would be a problem.
I was thinking the best way of digitizing would be to draw a curve on the 
outline of each leaf (simple and lobed leaves). Resample curves by length with 
approx. 40 landmarks. Then append curves to landmarks. Two landmarks, the leaf 
tip and base, would be fixed others could be defined as semi-landmarks. Is this 
sensible?
Alternatively, we could analyse simple and lobed leaves separately.
Thank you a lot for your help.

Tina


From: f.james.rohlf [mailto:f.james.ro...@stonybrook.edu]
Sent: Wednesday, March 14, 2018 3:59 AM
To: Tina Klenovšek
Subject: Re: [MORPHMET] digitizing very variable leaves

An assumption of the usual GMM methods is that shape variation is "small". I 
think these leaves exceed this quite a bit! Another problem is landmarks. How 
to match leaves with and without lobes?

__
F. James Rohlf, Distinguished Prof. Emeritus
Dept. Anthropology and Ecology & Evolution
Stonybrook University

---- Original message 
From: 'Tina Klenovšek' via MORPHMET 
<morphmet@morphometrics.org<mailto:morphmet@morphometrics.org>>
Date: 3/12/18 10:56 AM (GMT-10:00)
To: morphmet@morphometrics.org<mailto:morphmet@morphometrics.org>
Subject: [MORPHMET] digitizing very variable leaves

Hello everyone,

we would like to digitize tree leaves that are very variable (from simple oval 
to strongly lobed on one tree).

1.)I am wondering if TpsDig can do some kind of automatic digitizing like 
the LeafAnalyser software: 
http://www.plant-image-analysis.org/software/leaf-gp, which evenly distributes 
a defined number of landmarks on the leaf outline...

LeafAnalyser does not seem flexible or precise enough. Or I can’t use it 
properly. Any experience?


2.)Is it possible/sensible to put objects that are so differently shaped 
(photos attached) into the same group or is it better to analyse simple and 
lobed leaves separately?


I apologize if similar questions have been already answered...

Kind regards,
Tina







Napaka! Ime datoteke ni navedeno.

doc. dr. Tina Klenovšek, koordinatorica doktorskega
študijskega programa Ekološke znanosti
Univerza v Mariboru | University of Maribor
Fakulteta za naravoslovje in matematiko
Faculty of Natural Sciences and Mathematics
Koroška cesta 
160<https://maps.google.com/

RE: [MORPHMET] digitizing very variable leaves

2018-03-14 Thread 'Tina Klenovšek' via MORPHMET
Thanks to everyone who answered.

Dear Dr. Rohlf,
I assumed great variability would be a problem.
I was thinking the best way of digitizing would be to draw a curve on the 
outline of each leaf (simple and lobed leaves). Resample curves by length with 
approx. 40 landmarks. Then append curves to landmarks. Two landmarks, the leaf 
tip and base, would be fixed others could be defined as semi-landmarks. Is this 
sensible?
Alternatively, we could analyse simple and lobed leaves separately.
Thank you a lot for your help.

Tina


From: f.james.rohlf [mailto:f.james.ro...@stonybrook.edu]
Sent: Wednesday, March 14, 2018 3:59 AM
To: Tina Klenovšek
Subject: Re: [MORPHMET] digitizing very variable leaves

An assumption of the usual GMM methods is that shape variation is "small". I 
think these leaves exceed this quite a bit! Another problem is landmarks. How 
to match leaves with and without lobes?

__
F. James Rohlf, Distinguished Prof. Emeritus
Dept. Anthropology and Ecology & Evolution
Stonybrook University

 Original message 
From: 'Tina Klenovšek' via MORPHMET <morphmet@morphometrics.org>
Date: 3/12/18 10:56 AM (GMT-10:00)
To: morphmet@morphometrics.org
Subject: [MORPHMET] digitizing very variable leaves

Hello everyone,

we would like to digitize tree leaves that are very variable (from simple oval 
to strongly lobed on one tree).

1.)I am wondering if TpsDig can do some kind of automatic digitizing like 
the LeafAnalyser software: 
http://www.plant-image-analysis.org/software/leaf-gp, which evenly distributes 
a defined number of landmarks on the leaf outline...

LeafAnalyser does not seem flexible or precise enough. Or I can’t use it 
properly. Any experience?


2.)Is it possible/sensible to put objects that are so differently shaped 
(photos attached) into the same group or is it better to analyse simple and 
lobed leaves separately?


I apologize if similar questions have been already answered...

Kind regards,
Tina







[cid:image002.jpg@01D3BA4C.D9433EA0]

doc. dr. Tina Klenovšek, koordinatorica doktorskega
študijskega programa Ekološke znanosti
Univerza v Mariboru | University of Maribor
Fakulteta za naravoslovje in matematiko
Faculty of Natural Sciences and Mathematics
Koroška cesta 160, 2000 Maribor, Slovenija
T: +386 41 808 366
E: tina.klenov...@um.si<mailto:ime.prii...@um.si>, 
www.fnm.um.si<http://www.fnm.uni-mb.si>



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[MORPHMET] The ecological origins of snakes as revealed by skull evolution [New Publication]

2018-02-03 Thread 'Yoland SAVRIAMA' via MORPHMET
Dear colleagues,

I would like to attract your attention on this newly published paper.

Da Silva, F. O., A.-C. Fabre, Y. Savriama, J. Ollonen, K. Mahlow, A.
Herrel, J. Müller, and N. Di-Poï. 2018. The ecological origins of snakes as
revealed by skull evolution. Nature communications 9:376.
doi:10.1038/s41467-017-02788-3

Best wishes,
Yoland Savriama

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[MORPHMET] Re: Dino-lite/digital microscope

2017-12-01 Thread 'Heather Edgar' via MORPHMET
I love my dino-lite, but I use it to take pictures of human teeth, not rodents! 
I generally work at 100x and have used my microscope in a variety of different 
situations. I find it easy to use and love the portability. I just would wonder 
if the levels of magnification it works best at, under 150x, would work for you.

Best of luck!

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[MORPHMET] New Publication on Geometric Morphometrics and Genetics of Floral Symmetry

2017-11-20 Thread 'Yoland SAVRIAMA' via MORPHMET
Dear colleagues,

I would like to attract your attention on this newly published paper.

Berger, BA, Ricigliano, VA, Savriama, Y., Lim, A., Thompson, V. & Howarth 
DG. 2017. Geometric morphometrics reveals shifts in flower shape symmetry 
and size following gene knockdown of *CYCLOIDEA* and *ANTHOCYANIDIN 
SYNTHASE*.* BMC Plant Biology*. 17:205.
https://doi.org/10.1186/s12870-017-1152-x

The very first study coupling geometric morphometrics and Virus Induced 
Gene Silencing (VIGS) to quantify the phenotypic effects of knocking down a 
single CYC2 paralog, FgCYC2A, as well as the reporter gene, FgANS in 
symmetry of flowers. 

Best wishes!
Yoland Savriama

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[MORPHMET] Post-doc in morphometric analysis in phenotypic evolution and embryonic development:

2017-08-15 Thread 'Isaac Salazar' via MORPHMET
 conclusions and its underlying motivation. 

-Application should be sent to Isaac Salazar-Ciudad by email: 

isaac.sala...@helsinki.fi 

No official documents are required for the application first stage but these 
may be required latter on. 

6. Deadline:

There is no specific deadline, the position will be filled as soon as a 
suitable candidate is found.

7. Examples of recent publications by Isaac Salazar-Ciudad group.


-Salazar-Ciudad I, Marín-Riera M. Adaptive dynamics under development-based 
genotype-phenotype maps. Nature. 2013 May 16;497(7449):361-4. 

-Salazar-Ciudad I, Jernvall J. A computational model of teeth and the 
developmental origins of morphological variation. Nature. 2010 Mar 
25;464(7288):583-6. 


8. Interested candidates should check our group webpage: 

http://www.biocenter.helsinki.fi/salazar/index.html 

The center of Excellence webpage:

http://www.biocenter.helsinki.fi/bi/evodevo/ECDev.html

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[MORPHMET] New Bookstein GMM papers: PCA and Factor Analysis...

2017-08-07 Thread morphmet
 roster of variables.  
But contemporary applications of PCA in organismal systems biology, 
particularly in geometric morphometrics (GMM), generally involve much 
greater counts of variables. The way one might expect pure noise to 
degrade the biometric signal in this more contemporary context is 
described by a different mathematical literature concerned with the 
situation where the count of variables itself increases while remaining 
proportional to the count of specimens. The founders of this literature 
established a result of startling simplicity.


Consider steadily larger and larger data sets consisting of completely 
uncorrelated standardized Gaussians (mean zero, variance 1) such that 
the ratio of variables to cases (the so-called p/n ratio) is fixed at a 
value y.  Then the largest eigenvalue of their covariance matrix tends 
to (1+\sqrt{y})^2, the smallest tends to (1-\sqrt{y})^2, and their ratio 
tends to the limiting value ((1+\sqrt{y})/(1-\sqrt{y}))^2, whereas in 
the uncorrelated model both of these eigenvalues and also their ratio 
should be just 1.0.  For y=1/4, not an atypical value for GMM data sets, 
this ratio is 9; for y=1/2, which is still not atypical, it is 34.  
These extrema and ratios, easily confirmed in simulations of realistic 
size and consistent with real GMM findings in typical applied settings, 
bear severe negative implications for any technique that involves 
inverting a covariance structure on shape coordinates, including 
multiple regression on shape, discriminant analysis by shape, canonical 
variates analysis of shape, covariance distance analysis from shape, and 
maximum-likelihood estimation of shape distributions that are not 
constrained by strong prior models. The theorem also suggests that we 
should use extreme caution whenever considering a biological 
interpretation of any Partial Least Squares analysis involving large 
numbers of landmarks or semilandmarks.  I illuminate these concerns with 
the aid of one simulation, two explicit reanalyses of previously 
published data, and several little sermons.


For the second one:
Currently the most common reporting style for a geometric morphometric 
(GMM) analysis of anthropological data begins with the principal 
components of the shape coordinates to which the original landmark data 
have been converted.  But this focus often frustrates the organismal 
biologist, mainly because principal component analysis (PCA) is not 
aimed at scientific interpretability of the loading patterns actually 
uncovered.  The difficulty of making biological sense of a PCA is 
heightened by aspects of the shape coordinate setting that further 
diverge from our intuitive expectations of how morphometric measurements 
ought to combine.  More than fifty years ago one of our sister 
disciplines, psychometrics, managed to build an algorithmic route from 
principal component analysis to scientific understanding via the toolkit 
generally known as factor analysis.  This article introduces a 
modification of one standard factor-analysis approach, Henry Kaiser's 
varimax rotation of 1958, that accommodates two of the major differences 
between the GMM context and the psychometric context for these 
approaches: the coexistence of "general" and "special" factors of form 
as adumbrated by Sewall Wright, and the typical loglinearity of partial 
warp variance as a function of bending energy.  I briefly explain the 
history of principal components in biometrics and the contrast with 
factor analysis, introduce the modified varimax algorithm I am 
recommending, and work three examples that are reanalyses of previously 
published cranial data sets. A closing discussion emphasizes the 
desirability of superseding PCA by algorithms aimed at anthropological 
understanding rather than classification or ordination.


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Re: [MORPHMET] geiger rescale error

2016-12-06 Thread marko.djurakic via MORPHMET

Hi Andrea,
The code you provided works for me and I am using R 3.2.2, geiger 2.0.6 
and ape_4.0.


However, ensure that the gegier is loaded in the R environment or ensure 
that other packages with the same function name do not possibly 
interfere with geiger (see this post: 
http://stackoverflow.com/questions/5564564/r-2-functions-with-the-same-name-in-2-different-packages). 
What might happen here is that when you called rescale function, R used 
rescale function from some other (loaded) packages (from different 
namespaces...). Try to run the new R session and load just geiger (with 
dependencies) using library (geiger) command, check the rescale function 
by getAnywhere("rescale") command and if rescale is called from the 
geiger () you will likely get an expected 
output (without error).
There is a shorter way as well. Load geiger and just type 
geiger::rescale().


Marko

On 2016-12-06 10:19, andrea cardini wrote:

Dear All,

I've just tried the rescale function in geiger on my data and got an
error message. As I have no experience with it, I tried the first
example for this function in the help: same error message (see below).

Has anyone had similar issues? Probably I made some silly mistake.

Thanks in advance for your feedback.

Cheers


Andrea


geo <- get(data(geospiza))
ltrns <- rescale(geo$phy, "lambda")
plot(ltrns(0))
title("lambda: 0.0")

Error message:

Error in rescale(as.numeric(x, range = range, domain = domain, ...)) :
  (list) object cannot be coerced to type 'double'


--

Dr. Andrea Cardini
Researcher, Dipartimento di Scienze Chimiche e Geologiche, Università
di Modena e Reggio Emilia, Via Campi, 103 - 41125 Modena - Italy
tel. 0039 059 2058472

Adjunct Associate Professor, School of Anatomy, Physiology and Human
Biology, The University of Western Australia, 35 Stirling Highway,
Crawley WA 6009, Australia

E-mail address: alcard...@gmail.com, andrea.card...@unimore.it
WEBPAGE: https://sites.google.com/site/alcardini/home/main

FREE Yellow BOOK on Geometric Morphometrics:
http://www.italian-journal-of-mammalogy.it/public/journals/3/issue_241_complete_100.pdf

ESTIMATE YOUR GLOBAL FOOTPRINT:
http://www.footprintnetwork.org/en/index.php/GFN/page/calculators/


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Re: [MORPHMET] problems opening ply files

2016-10-28 Thread morphmet

Two possibilities...

1) Make sure you are using the latest version and running the program 
via a .bat, .sh, or .app. There could be memory problems if you try to 
run the .java file directly. The scripts provide for more memory.


but more likely...

2) Some programs create .ply files that are somehow indigestible by 
Morpheus. Open the file in Meshlab and (re)save it (binary or ascii 
doesn't matter). That might clear up any problems.


-ds

On 10/28/16 1:37 PM, Gabriel Wrobel wrote:

Hi all.  I am new to this sort of analysis, so apologize in advance for
the rudimentary nature of my question. I am attempting to open ply files
of 3D cranial models built with Agisoft Photoscan on Morpheus and am not
having any luck at all. Morpheus reads the file, but does not open it.
 It seems to be fine with ply files created from laser scans.  Is this
an issue anyone is familiar with? Thanks!

gabe wrobel

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Re: [MORPHMET] Trying to trace a quote

2016-10-19 Thread 'Abby Drake' via MORPHMET
According to wikiquote it was John von Neumann:
https://en.wikiquote.org/wiki/John_von_Neumann
except they have it as: "With four parameters I can fit an elephant, and
with five I can make him wiggle his trunk."
Abby







*Abby Grace Drake, PhDDepartment of Ecology and Evolutionary BiologyCornell
UniversityPhone: 508.981.2783Skype: abby.drake*

On Wed, Oct 19, 2016 at 1:10 PM, Bill Sellers <w...@mac.com> wrote:

> Dear All,
>
> I wonder if anyone can help me. I'm trying to trace a quotation that a now
> long retired colleague of mine used to use. He doesn't remember where he
> got it from but it is very apt, and since it relates to animal shape I'm
> hoping someone on this mailing list will recognise it (particularly since
> I'm probably not remembering it quite properly and google is being
> unhelpful). The quote as best I remember it is:
>
> "Give me 4 parameters and I can build you an elephant. Give me 5 and I can
> make it wag its tail."
>
> I've always imagined it was something that a 1930s developmental biologist
> or mathematician would have said when discussing the utility of
> developmental models at the time.
>
> Can anyone help?
>
> Cheers
> Bill
> --
> Bill Sellers, Tel: 01612751719, Mobile: 07857655786,
> http://www.animalsimulation.org
> University of Manchester, D1239 Michael Smith Building, Manchester, M13
> 9PT.
>
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[MORPHMET] New publication on patterns of skull modularity and integration over postnatal ontogeny

2016-09-29 Thread 'Tina Klenovšek' via MORPHMET
Dear Morphometricians,



we wish to inform you about a publication on skull modularity and integration 
across ontogenetic stages in a long-lived vole with well-defined age stages 
conducted on wild and laboratory bred specimens from two phylogenetic groups:





Modularity and cranial integration across ontogenetic stages in Martino's vole, 
Dinaromys bogdanovi

Link: http://www.ctoz.nl/vol85/nr03/a02



Abstract: We explored modularity and morphological integration of the ventral 
cranium during postnatal ontogeny in Martino's vole (Dinaromys bogdanovi). Two 
closely related phylogenetic groups, originating from the Central and 
Southeastern part of the species range in the western Balkans, were considered. 
As expected, both phylogroups had similar patterns of ontogenetic changes in 
cranial size and shape variation, modularity and integration. At the level of 
within individual variation, the hypothesis that the viscerocranial and 
neurocranial regions are separate modules was rejected, indicating that the 
hypothesized modules are not developmental, but rather functional. At the level 
of among individual variation, the viscerocranium and the neurocranium could 
not be recognized as separate modules at the juvenile stage. The strength of 
association between the hypothesized modules becomes lower with age which 
finally results in a clear 2-module organization of the ventral cranium at the 
adult stage. On the other hand, patterns of morphological integration for the 
cranium as a whole, the viscerocranium and the neurocranium stay consistent 
across ontogenetic stages. The developmental mechanism producing integration of 
the cranium as a whole, as well as integration of the neurocranium, varies 
throughout postnatal ontogeny. In contrast, we detected the ontogenetic 
stability of the mechanism responsible for covariation of viscerocranial traits 
which could provide ongoing flexibility of the viscerocranial covariance 
structure for high functional demands during lifetime. Findings from our study 
most likely support the idea of the 'palimpsest-like' model of covariance 
structure. Moreover, similarity or dissimilarity in the patterns of within and 
among individual variation in different sets of analyzed traits and comparisons 
across ontogenetic stages demonstrate how studies on small mammals other than 
mice can give new insights into postnatal cranial development.



Kind regards,



Tina Klenovšek and Vida Jojić






[cid:image002.jpg@01CDF575.0D631B30]

doc. dr. Tina Klenovšek
Univerza v Mariboru | University of Maribor
Fakulteta za naravoslovje in matematiko
Faculty of Natural Sciences and Mathematics
Koroška cesta 160, 2000 Maribor, Slovenija
T: (00 386) 041 808 366
E: tina.klenov...@um.si<mailto:tina.klenov...@um.si>,
www.fnm.um.si<http://www.fnm.uni-mb.si/>









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[MORPHMET] 2-year post-doc in artefact morphometrics

2016-08-27 Thread 'Felix Riede' via MORPHMET
Dear all,

I am advertising a 2-year post-doctorial fellowship focused on artefact 
morphometrics (lithics). Those interested, please have a look here 
http://www.au.dk/om/stillinger/videnskabelige-stillinger/stillinger/Vacancy/show/852090/5285/;
 
feel free to share.

Yours,

Felix


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[MORPHMET] Please send links to online morphometrics resources...

2016-08-27 Thread MORPHMET
I would like to freshen up the online resource links on the 
www.morphometrics.org page. If you have any relevant active links, please 
post them so I can add them to the website (if I can remember how). 

Thanks, the MORPHMET Management

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[MORPHMET] Append tps Curve to Landmarks

2016-08-24 Thread 'MrMupped223' via MORPHMET
Hi,
I have a similar problem like a girl who wrote asked a question on this site  
in 2012. 
I coppied her Email because my written english isn't the best. 
 
"I just started to use the tps suite and I'm having problems with
sliding 2D semilandmarks. I have digitised curves in tpsDig with the curve tool 
and then resampled them to get an equal number of points for each individual."
 
I then removed the control lines 'Ponints=' and 'Curves='.
 
"As I understand it, I then need to turn the points into landmarks (appending) 
and then create a slider file to slide them in tpsUtil. The bit I'm stuck with 
is'appending tps curve to landmarks' in tpsUtil. I enter the file name in 
'input' and chose a file name for 'output', but when I press 'create', I just 
get the error
message:"
 
This is my error massege: 
 
'435.0' is not a valid floating point value Bad decimal character in 
coordinates?.'
 
I get the same error for tps files with and without removed control lines. 
 
I hope someone has an idea why this Problem shows up and can help me.
 
Thanks 
Jan 

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[MORPHMET] New paper by Bookstein: The inappropriate symmetries of multivariate statistical analysis in GM

2016-05-03 Thread MORPHMET


Dear MorphMetters,

  As I did last year, I'd like to grab your attention for a moment
 to advertise a long essay of mine,
 "The inappropriate symmetries of multivariate statistical analysis
 in geometric morphometrics," just posted by the Springer
 journal Evolutionary Biology. The article is free for download via
 http://link.springer.com/article/10.1007/s11692-016-9382-7/fulltext.html
 or from the journal's own website.

  The paper runs to 37 double-column pages, but a summary
 can be brief. I am claiming
 that the ways we use GMM in most of today's organismal
 biological applications, whether of growth, evolution,
 or disease, don't actually make much biological sense.
 I go on to offer a small assortment of better alternatives,
 including but not limited to the idea of deflated Procrustes analysis
 that I published in the same journal last year.  The article incorporates
 two appendices that might merit your closer attention.  Appendix 1
 is a principled criticism of the RV coefficient some people are recommending
 nowadays for use in connection with PLS analyses; my conclusion is
 that it serves no valid scientific purpose and should never
 be used.  Appendix 2 shows
 what covariances of Procrustes shape coordinates actually look like
 and why it follows that principal components of these
 covariance matrices are usually less useful than we hoped they were.

   Feel free to go get your own copy of this publication and
 either learn from it or send me your objections.  Yours from Vienna
 with best wishes, Fred Bookstein

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Re: [MORPHMET] Information on 3d portable scanner

2015-12-15 Thread morphmet

Replying to the list...

Hi, Anna! No, I am not familiar with that. For the grant that secured 
the HDI, we also included the purchase of the similar Artec hand scanner 
(http://landing.artec3d.com/?keyword=artec%20scanner=CNHLk8TL3skCFUQ2gQod2YQMTQ) 
for archaeological field work, but did not get enough money for both. 
For our lab, the table-top seemed the best choice. I have used (well, 
minions, you know...) the Artec hand scanner some years ago and it was a 
bit flaky, but worked. I understand now that folks are using it quite 
successfully. I wish we had one. I might can refer you to someone if no 
one on the list has info.


-ds

On 12/15/15 2:12 PM, Anna Loy wrote:

Thank you Dennis!

Do you have any info regarding the portables CREAFORM?

Best

Anna

Anna Loy
Dip. Bioscienze e Territorio
Università del Molise
Contrada Fonte Lappone
I-86090 Pesche (IS), Italy
Tel. 0874 404100
Cell. 3316265137
mail: a@unimol.it <mailto:a@unimol.it>




Il giorno 15/dic/2015, alle ore 19:31, Dennis E. Slice
<dsl...@morphometrics.org <mailto:dsl...@morphometrics.org>> ha scritto:


We have the HDI 109 scanner with automatic turntable. My minions tell
me it is quite easy to use with ridiculous resolution (I no longer get
to play with the toys. This is probably for the best.). Part of the
proposal for this was to digitize mouse skulls, so we opted for higher
resolution without color.

We were recently asked to scan a human skull at full resolution. The
resulting file was 10s of gigabytes. I believe bear skulls would be a
challenge because of both physical and digital size. I suspect
resolution is controllable. One student is currently looking at
morphometrics-appropriate decimation algorithms.

Attached are pics of a macaque we scanned rendering only the vertices.
The skull is about 100cm.

Morpheus can't handle the full-res scan. Rendering done in Meshlab.
full resolution: 3.4 million vertices
(only vertices shown)6.8 million faces

Morpheus
Pic 1) 500k vertices, 1000k faces
Pic 2) 50k vertices, 100k faces

-ds

On 12/13/15 2:54 PM, ANNA LOY wrote:

Hello everyone

Do any of you have experience with portable 3d scanner (no structured
light) like

*CREAFORM HANDY SCAN700 AMETEK
*http://www.creaform3d.com/en/metrology-solutions/portable-3d-scanner-handyscan-3d

*GOSCAN 3D CREAFORM*video demo
https://www.youtube.com/watch?v=4IY1IN8swEc 2pounds no structured light
(no laser) molto veloce, res fino a 0.1 mm.


They seems very fast and easy to use

Also which are differences with portable structured light 3d scanners
like
*HDI 120 Blue-Light Scanner
<http://www.3d-microscribe.com/HDI%20Blitz%20Scanner%20Page.htm>*?

I should scan mammal skulls, from otters to bears, in various museum
collections

Any advice or suggestions would be appreciated

Thanks

Anna
___

Anna Loy
Dip. Bioscienze e Territorio
Università del Molise
Contrada Fonte Lappone
86090 Pesche (IS), Italy
e-mail istituzionale: a@unimol.it <mailto:a@unimol.it>
<mailto:a@unimol.it>
e-mail: anna.lo...@gmail.com <mailto:anna.lo...@gmail.com>
<mailto:anna.lo...@gmail.com>
Tel: +39 0874404140
Fax: +39 087440123
skype:anna.loy56
http://scholar.google.com/citations?hl=it=_dVgP6YJ
Project 'It is never too Darwin':
Project therio.it <http://therio.it> : https://dibt.unimol.it/therio/
Assistan Editor Italian Journal of Zoology
http://www.tandfonline.com/toc/tizo20/current#.Uuv5YfjANf9

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<500k_vertices_1000k_faces.png><50k_vertices_100k_faces.png><3400k_vertices_6800k_faces.png>




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Re: [MORPHMET] Information on 3d portable scanner

2015-12-15 Thread morphmet
Sorry, that should have been 10cm for the skull length, and that is just 
a guess - it's less than fist size, IIRC. -ds


On 12/15/15 1:31 PM, Dennis E. Slice wrote:

We have the HDI 109 scanner with automatic turntable. My minions tell me
it is quite easy to use with ridiculous resolution (I no longer get to
play with the toys. This is probably for the best.). Part of the
proposal for this was to digitize mouse skulls, so we opted for higher
resolution without color.

We were recently asked to scan a human skull at full resolution. The
resulting file was 10s of gigabytes. I believe bear skulls would be a
challenge because of both physical and digital size. I suspect
resolution is controllable. One student is currently looking at
morphometrics-appropriate decimation algorithms.

Attached are pics of a macaque we scanned rendering only the vertices.
The skull is about 100cm.

Morpheus can't handle the full-res scan. Rendering done in Meshlab.
full resolution: 3.4 million vertices
(only vertices shown)6.8 million faces

Morpheus
Pic 1) 500k vertices, 1000k faces
Pic 2) 50k vertices, 100k faces

-ds

On 12/13/15 2:54 PM, ANNA LOY wrote:

Hello everyone

Do any of you have experience with portable 3d scanner (no structured
light) like

*CREAFORM HANDY SCAN700 AMETEK
*http://www.creaform3d.com/en/metrology-solutions/portable-3d-scanner-handyscan-3d


*GOSCAN 3D CREAFORM*video demo
https://www.youtube.com/watch?v=4IY1IN8swEc 2pounds no structured light
(no laser) molto veloce, res fino a 0.1 mm.


They seems very fast and easy to use

Also which are differences with portable structured light 3d scanners
like
*HDI 120 Blue-Light Scanner
<http://www.3d-microscribe.com/HDI%20Blitz%20Scanner%20Page.htm>*?

I should scan mammal skulls, from otters to bears, in various museum
collections

Any advice or suggestions would be appreciated

Thanks

Anna
___

Anna Loy
Dip. Bioscienze e Territorio
Università del Molise
Contrada Fonte Lappone
86090 Pesche (IS), Italy
e-mail istituzionale: a@unimol.it <mailto:a@unimol.it>
e-mail: anna.lo...@gmail.com <mailto:anna.lo...@gmail.com>
Tel: +39 0874404140
Fax: +39 087440123
skype:anna.loy56
http://scholar.google.com/citations?hl=it=_dVgP6YJ
Project 'It is never too Darwin':
Project therio.it <http://therio.it> : https://dibt.unimol.it/therio/
Assistan Editor Italian Journal of Zoology
http://www.tandfonline.com/toc/tizo20/current#.Uuv5YfjANf9

--
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[MORPHMET] 750 subscribers to morphmet...

2015-10-27 Thread MORPHMET
Sitting in the Atlanta airport on my way back from the third Rohlf Medal 
award ceremony, and I just approved the 750th subscriber to the list. 
Congratulations to HS in Alaska who wins a free subscription to MORPHMET. 
:) 

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Re: [MORPHMET] Post-hoc calculation of PC and CV scores

2015-08-20 Thread morphmet

I have a vague recollection from some years ago of lda() having a small
bug/feature. Something like division by n instead of (n-1) or 
vice-versa. As  always, best to check code and results against other, 
independent programs and resolve the reason for any differences. -ds


On 8/19/15 7:08 PM, Fábio Machado wrote:

I would consider using the lda() function from MASS package. The
function allows for the use of a training dataset (the extant data, in
your case) and the associated predict function gives you the score of
all specimens (extant and fossil). In my experience, the ordination of
specimens on the discriminant functions of lda and on the canonical
variate axis of cva from Morpho are identical, except for arbitrary
inversion of the sign of some axis, usually the first. Additionally,
predict.lda already give you group membership probabilities.

As for PCA, I think that princomp and prcomp functions have a predict
option that would produce scores for specimens not included in the
original analysis.

Best,

Fabio Andrade Machado
Laboratório de Evolução de Mamíferos
Departamento de Genética e Biologia Evolutiva- USP
f.mach...@usp.br mailto:f.mach...@usp.br ; macfa...@gmail.com
mailto:macfa...@gmail.com
+55 11 982631029
skype: fabio_a_machado

Lattes: http://lattes.cnpq.br/3673327633303737
Google Scholar: http://scholar.google.com/citations?hl=enuser=2l6-VrQJ


Em 19/08/2015, à(s) 18:40, Blake Dickson bdick...@g.harvard.edu
mailto:bdick...@g.harvard.edu escreveu:

Hey Morphmetricians,

So I have a question regarding calculating PC scores and CV scores
post-hoc:

I have a GMM dataset of extant and fossil species which I want to plot
using PCA and CVA. I want to calculate the extant species first, then
use the eigenvectors from this the plot the scores for the fossil taxa.

I have done this successfully for the PCA in R by centering the whole
dataset, then calculating the covariance matrix and eigenvectors for
the extant species only. I then calculate the PC scores for the fossil
taxa using these eigenvalues.

I am not certain whether the same tactic for the CVA is valid. I have
tried it: performing the CVA (using the Morpho package) on the extant
dataset with associated groupings, then correcting the fossil
coordinates by the mean of this CVA and calculating the CV scores for
the fossil taxa using the canonical variates (CV) matrix. This gives
me a result, with plot-able CV scores for the fossil taxa, but I want
to be certain the method is valid.

In addition, assuming that what I have done with the CVA is correct;
how would I best go about testing the likelihood of group membership
for these fossil taxa?

Cheers all,

Blake Dickson

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[MORPHMET] Re: The Rohlf Medal: 2015 Call for Nominations

2015-07-07 Thread MORPHMET
The deadline approaches: July 15, 2015! Time to get your applications in.

On Monday, March 9, 2015 at 8:24:10 AM UTC-4, MORPHMET wrote:

 *2015 CALL FOR NOMINATIONS*

 *The Rohlf Medal*

 The Rohlf Medal was established in 2006 by the family and friends of F. 
 James Rohlf to mark his 70th birthday. He has been a longtime Stony Brook 
 University faculty member and is currently Emeritus Distinguished Professor 
 in the Department of Ecology and Evolution, and Research Professor in the 
 Department of Anthropology. 

  

 Recipients of the Rohlf Medal will be recognized for excellence in their 
 body of work on the development of new morphometric methods or for their 
 applications in the biomedical sciences, including evolutionary biology, 
 population biology, physical anthropology, and medicine. The term 
 ‘morphometrics’ is intended to include high-dimensional pattern analyses of 
 biological shape, especially those that analyze shape in a comprehensive 
 way, or of covariation of shape with other variables. The award can 
 recognize advances in the mathematical or statistical theory underlying 
 morphometric methods, new software that implements or visualizes new 
 methods, or specific new biological findings that rely crucially on 
 contemporary morphometric methods and represent major advances.

  

 Candidates for the Rohlf Medal may be self-nominated or nominated by 
 others. They must possess a Ph.D. degree or the equivalent.

  

 The winning candidate must agree to attend the award ceremony in person in 
 order to accept the Rohlf Medal and then deliver the award lecture.

  

  

 Nomination packages should include, 

 (1) a description of the body of work (not to exceed two pages) on which 
 the candidacy is based, 

 (2) reprints of no more than three relevant papers and/or software 
 products, 

 (3) a curriculum vitae, and 

 (4) the names and addresses of three referees. 

  

 Nominating packages should be uploaded to the Rohlf Medal website (
 http://life.bio.sunysb.edu/ee/rohlf_medal/apply.html) and received by 5 
 pm, EST, 15 July 2015 to be assured of full consideration.

  

 The successful candidate will receive the Rohlf Medal and a cash prize at 
 Stony Brook University, planned for October 26th, 2015.  She or he will 
 deliver a lecture that is appropriate for a broad audience, ranging from 
 the exact sciences to the humanities, concerning the morphometric 
 methodology, software, or findings for which the Rohlf Medal was awarded

  


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Re: [MORPHMET] image names tps series

2015-06-10 Thread 'Elis Marina Damasceno Silva' via MORPHMET
Dear Patrick,
If you convert the tps into a NTS file (you can do that using tpsutil), and 
then open the nts file in MorphoJ, you should get the names of the images.
Best,
Elis Damasceno
PhD CandidateMichael Smith BuildingFaculty of Life SciencesUniversity of 
Manchester 


 Em Quarta-feira, 10 de Junho de 2015 10:25, Patrick Arnold 
patrick.arn...@uni-jena.de escreveu:
   

 Dear all,

I am having a tiny problem when combining tps series and MorphoJ. I  
created tps file with tpsutil, digitized landmarks with tpsdig2 and  
import the dataset into MorphoJ. Unfortunately, image names are not  
included in MorphoJ and thus I am not able to extract classifiers from  
ID. I thought image names are automatically included when creating tps  
file and I cannot find to option to do this manually.
How to solve this? Thanks in advance.

Patrick


-- 
Patrick Arnold, M.Sc.

Institut für Spezielle Zoologie und Evolutionsbiologie
mit Phyletischem Museum
Friedrich-Schiller-Universität Jena
Germany


This message was sent through https://webmail.uni-jena.de

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[MORPHMET] Re: The Rohlf Medal: 2015 Call for Nominations

2015-05-31 Thread MORPHMET
A friendly reminder to start getting your nominations packages together.

On Monday, March 9, 2015 at 1:24:10 PM UTC+1, MORPHMET wrote:

 *2015 CALL FOR NOMINATIONS*

 *The Rohlf Medal*

 The Rohlf Medal was established in 2006 by the family and friends of F. 
 James Rohlf to mark his 70th birthday. He has been a longtime Stony Brook 
 University faculty member and is currently Emeritus Distinguished Professor 
 in the Department of Ecology and Evolution, and Research Professor in the 
 Department of Anthropology. 

  

 Recipients of the Rohlf Medal will be recognized for excellence in their 
 body of work on the development of new morphometric methods or for their 
 applications in the biomedical sciences, including evolutionary biology, 
 population biology, physical anthropology, and medicine. The term 
 ‘morphometrics’ is intended to include high-dimensional pattern analyses of 
 biological shape, especially those that analyze shape in a comprehensive 
 way, or of covariation of shape with other variables. The award can 
 recognize advances in the mathematical or statistical theory underlying 
 morphometric methods, new software that implements or visualizes new 
 methods, or specific new biological findings that rely crucially on 
 contemporary morphometric methods and represent major advances.

  

 Candidates for the Rohlf Medal may be self-nominated or nominated by 
 others. They must possess a Ph.D. degree or the equivalent.

  

 The winning candidate must agree to attend the award ceremony in person in 
 order to accept the Rohlf Medal and then deliver the award lecture.

  

  

 Nomination packages should include, 

 (1) a description of the body of work (not to exceed two pages) on which 
 the candidacy is based, 

 (2) reprints of no more than three relevant papers and/or software 
 products, 

 (3) a curriculum vitae, and 

 (4) the names and addresses of three referees. 

  

 Nominating packages should be uploaded to the Rohlf Medal website (
 http://life.bio.sunysb.edu/ee/rohlf_medal/apply.html) and received by 5 
 pm, EST, 15 July 2015 to be assured of full consideration.

  

 The successful candidate will receive the Rohlf Medal and a cash prize at 
 Stony Brook University, planned for October 26th, 2015.  She or he will 
 deliver a lecture that is appropriate for a broad audience, ranging from 
 the exact sciences to the humanities, concerning the morphometric 
 methodology, software, or findings for which the Rohlf Medal was awarded

  


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Re: [MORPHMET] Why exported raw coordinates differ from the imported in MorphoJ?

2015-05-25 Thread 'Marko Djurakic' via MORPHMET

On 25.5.2015 5:52, lv xiao wrote:

Dear all,

I am using morphoJ to do geometric morphometric analysis.

I imported the TPS file with three specimens into MorphoJ.*Without 
doing any further analysis, I exported the raw coordinates from 
MorphoJ.* To my surprise, I found that *the exported coordinates 
differ from the imported one, except for the first specimen.*

*
*
May I know why does this happen? Will this affect subsequent analyses?

Your kind reply is highly appreciated!

Best regards,
Patrick
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Hi Patric,
MorphoJ provided you with appropriate output.
Note that you have set a SCALE argument in the tps file for last two 
specimens (line 85 and 128), but not for the first one. Therefore, 
coordinates for the last two specimens were rescaled. That is each 
coordinate were multiplied by respective value of SCALE argument (e.g. 
raw x1 for second specimen is 1144.0; x1 from MorphoJ will be 
1144.0*0.146663 = 167.782472).
Maybe you forgot to set the SCALE value for the first specimen during 
digitization procedure.


Hope this helps,
Marko

--
Marko Djurakic,

Teaching assistant,
Faculty of Sciences
Department of Biology and Ecology
University of Novi Sad
Trg Dositeja Obradovića 2
21 000 Novi Sad
Serbia

PhD student at Faculty of Biology,
University of Belgrade
Studentski trg 16
11000 Belgrade
Serbia

e-mail: marko.djura...@dbe.uns.ac.rs

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[MORPHMET] New paper by Bookstein: Integration, Disintegration, and Self-Similarity

2015-05-09 Thread MORPHMET
   Vienna, April 22, 2015

Dear MorphMetters,

As some of you may know already, for years I've been working on a 
methodology that replaces the Procrustes method with an alternative where, 
intuively speaking, the closer together two landmarks lie, the more their 
shifts of position with respect to the rest are correlated (which of course 
is the actual situation in just about every organismal data set we ever 
encounter).

If you happened to be in St. Louis last month for the AAPA national 
conference you might have seen my poster on the new method, but a topic 
this mathematical isn't really suited to a poster format. Today, at last, 
my first fundamental article on this stuff has been published online by the 
Springer journal Evolutionary Biology.  This is an open-access article, 
which means you can just go grab your own copy of the 32 double-column 
pages and 22 diagrams without having to involve your university library.  
Just point your browser to link.springer.com/journal/11692 and click on the 
button reading View Open Access Articles. As of this morning, anyway, my 
piece Integration, Disintegration, and Self-Similarity is the first item 
that comes up on offer.  

The title is what it is because there is an immediate application to 
integration studies in GMM whereby the Procrustes model must be replaced by 
something different as the null model for such studies. 

With best wishes, Fred Bookstein

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Re: [MORPHMET] Analysis of semilandmark data

2015-05-06 Thread morphmet
On a technical point, one does not transform landmarks into 
semilandmarks. They either are landmarks or semilandmarks. The fact that 
they are semilandmarks is sometimes ignored, and they are treated as 
landmarks if the ambiguity in positioning on one direction is deemed 
sufficiently small or they can be allowed to slide to take out 
variability in that direction. So, semilandmarks are semilandmarks, but 
they can be transformed into sliding landmarks.


-ds

On 5/6/15 7:29 AM, Nico Posnien wrote:

Dear all,

I have a question concerning the analysis of landmark and semilandmark
data in fly heads. So far I placed landmarks on 2D images. Some of these
actually represent semilandmarks. I used tps Util (Make Sliders File;
see attched picture) to generate a sliders file. In the attached
picture, 1 and 8 are landmarks and 2-7 in between them are supposed to
be semilandmarks.

My first question is: Is this the right way to transform landmarks into
semilandmarks?

My second question is: What is the best (most accepted,
straight-forward) way to further analyze this data? I am mainly
interested in shape differences between different groups (2 species +
hybrids, males and females). Which programs should be used? I saw that
geomorph can handle this kind of data. Any UI software? Are there any
suggestions for good tutorials?

Thanks a lot for any recommendation and help!

Cheers,

Nico

--

Nico Posnien

Georg-August-University Göttingen

Johann-Friedrich-Blumenbach Institute for Zoology and Anthropology

Department of Developmental Biology

Ernst-Caspari-Haus (GZMB)

Justus-von-Liebig-Weg 11

37077 Göttingen

Germany

Phone: +49 (0) 55139 20817

E-mail: npos...@gwdg.de

web: http://www.evolution.uni-goettingen.de/posnienlab/index.html

web: http://www.uni-goettingen.de/en/44993.html

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[MORPHMET] The Rohlf Medal: 2015 Call for Nominations

2015-03-09 Thread MORPHMET


*2015 CALL FOR NOMINATIONS*

*The Rohlf Medal*

The Rohlf Medal was established in 2006 by the family and friends of F. 
James Rohlf to mark his 70th birthday. He has been a longtime Stony Brook 
University faculty member and is currently Emeritus Distinguished Professor 
in the Department of Ecology and Evolution, and Research Professor in the 
Department of Anthropology. 

 

Recipients of the Rohlf Medal will be recognized for excellence in their 
body of work on the development of new morphometric methods or for their 
applications in the biomedical sciences, including evolutionary biology, 
population biology, physical anthropology, and medicine. The term 
‘morphometrics’ is intended to include high-dimensional pattern analyses of 
biological shape, especially those that analyze shape in a comprehensive 
way, or of covariation of shape with other variables. The award can 
recognize advances in the mathematical or statistical theory underlying 
morphometric methods, new software that implements or visualizes new 
methods, or specific new biological findings that rely crucially on 
contemporary morphometric methods and represent major advances.

 

Candidates for the Rohlf Medal may be self-nominated or nominated by 
others. They must possess a Ph.D. degree or the equivalent.

 

The winning candidate must agree to attend the award ceremony in person in 
order to accept the Rohlf Medal and then deliver the award lecture.

 

 

Nomination packages should include, 

(1) a description of the body of work (not to exceed two pages) on which 
the candidacy is based, 

(2) reprints of no more than three relevant papers and/or software 
products, 

(3) a curriculum vitae, and 

(4) the names and addresses of three referees. 

 

Nominating packages should be uploaded to the Rohlf Medal website (
http://life.bio.sunysb.edu/ee/rohlf_medal/apply.html) and received by 5 pm, 
EST, 15 July 2015 to be assured of full consideration.

 

The successful candidate will receive the Rohlf Medal and a cash prize at 
Stony Brook University, planned for October 26th, 2015.  She or he will 
deliver a lecture that is appropriate for a broad audience, ranging from 
the exact sciences to the humanities, concerning the morphometric 
methodology, software, or findings for which the Rohlf Medal was awarded

 

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Re: [MORPHMET] Testing Group Mean Differences, Nonparametric Framework

2015-02-07 Thread 'Marko Djurakic' via MORPHMET

On 6.2.2015 22:54, Eugenia Leone Gold wrote:

Hi everyone,
I am trying to run a non-parametric test for group mean differences using PC 
scores and I can’t seem to find a function to do that. I am using PC scores 
instead of Procrustes Coordinates so as to have fewer variables than specimens. 
Does anyone know of a function that can do this? I came across the function 
adonis in Vegan, but that seems to use distances so I don’t think it’s 
applicable to this situation. Thanks for any help!

Best,
Eugenia


Hi Eugenia,

If you want (just) to make a statistical inference regarding difference 
between two shape means, you can use permutation test. You can do it in 
MorphoJ, geomorph, PAST...All of them are distance based.


If you want to perform hypothesis testing that describe patterns of 
shape variation and covariation in regard to some factor(s), solution is 
to perform appropriate linear model. However, regardless whether 
dependent variables are original procrustes residuals or PC scores of 
them, small sample size may be a problem in traditional (parametric) 
approaches. There is recent paper by Collyer and Adams published in 
Heredity 
(http://www.nature.com/hdy/journal/vaop/ncurrent/abs/hdy201475a.html) 
which demonstrated efficacy of non-parametric approach that is not 
constrained by low sample size compared to number of variables. That 
approach can evaluate effect size of factors in the model even if sample 
size is small relative to number of variables. Procedure is described 
and justified in the paper and you can perform it in the geomorph 
package (procD.lm function).


Regarding non-parametric tests, as far as I know, most of them use 
distance based methods. E.g. see here: 
http://www.entsoc.org/PDF/MUVE/6_NewMethod_MANOVA1_2.pdf


Hope this help.
All the best.

--
Marko Djurakic,

Teaching assistant,
Faculty of Sciences
Department of Biology and Ecology
University of Novi Sad
Trg Dositeja Obradovića 2
21 000 Novi Sad
Serbia

PhD student at Faculty of Biology,
University of Belgrade
Studentski trg 16
11000 Belgrade
Serbia

e-mail: marko.djura...@dbe.uns.ac.rs

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[MORPHMET] Re: Migration update

2014-10-03 Thread MORPHMET
I have just sent out the final re-re-...invitations to addresses on the old 
MORPHMET mailing list. When these expire, they addresses will be deleted, 
and anyone wanting to join will have to do so using the standard procedure. 
At this writing, we have 640 subscribers, which is pretty impressive in my 
estimation.

-The Management

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[MORPHMET] POSTDOCTORAL POSITION: Max Planck CIAA, IEA, Leipzig, Germany

2014-09-29 Thread MORPHMET
POSTDOCTORAL POSITION - DOMESTICATION EFFECTS ON BITING PERFORMANCE IN RATS
Max Planck Weizmann Center for Integrative Archaeology and Anthropology, 
Leipzig, Germany

The Max Planck Weizmann Center for Integrative Archaeology and 
Anthropology at the Max Planck Institute for Evolutionary Anthropology, 
Leipzig (Germany) invites applications for a post-doctoral position to 
work on a collaborative project to study the effect of domestication on 
bite force performance and skull and muscle anatomy in rats.

We are seeking a highly qualified and motivated candidate with 
experience in in vivo bite force measurements, anatomical dissection, 
muscle physiology, microscopy, histology, immunohistochemistry, CT 
imaging and/or geometric morphometrics.

This position is set to begin as soon as 1 November 2014, and 
applications will be considered until the position is filled. The 
initial length of the appointment will be one year, with an option for 
extension. The selected candidate should have a Ph.D. (or be close to 
completion) in a relevant area and a significant track record of 
research. The Max Planck Society is committed to employing more 
physically impaired individuals and to increasing the share of women in 
areas where they are underrepresented, and therefore expressly 
encourages applications from such qualified individuals.

Applications including cover letter, curriculum vitae, reprints of 
selected publications, a short statement of research interests and the 
names of at least two referees should be sent as a single PDF document 
to Dr Kornelius Kupczik (kupczik (AT) eva (DOT) mpg (DOT) de). For further 
information 
about the Max Planck Weizmann Center see http://www.eva.mpg.de/mpwc.

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Re: [MORPHMET] 3D stuff

2014-09-19 Thread morphmet
Chapter 6: More Complex Examples in the User's Guide for the latest 
version of Morpheus et al. (http://morphlab.sc.fsu.edu/index.html) shows 
how to do this via batch processing.


More common landmarks are much better, but this worked for croc skulls 
with only three. Actually, this surprised me since when I tried this 
years ago with three landmarks, the computations collapsed the data into 
the three-landmark plane.


-ds

On 9/18/14 6:08 AM, Gaëtan Bourgeois wrote:

Hello everybody,

I did acquisition of 3D landmarks (about skulls) with a Microscribe in 2
views (superior and inferior) and I have to put together these series now.
I know I need to do multiregression but I don't know how exactly I have
to proceed.
Is anyone can help me to do this?
Other question: what is the best freeware for 3D landmarks treatment in
your opinion?

Thank you, have a nice day!

--
Gaëtan Bourgeois
--
PhD Student
Université de Perpignan Via Domitia, ED 544, UR MEDI-TERRA
Centre Européen de Recherche Préhistorique de Tautavel, UMR CNRS 7194
--
EPCC - CERPT
Avenue Léon-Jean Grégory
66720
Tautavel

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[MORPHMET] Recent site outage

2014-09-11 Thread MORPHMET
Yesterday, the website and MORPHMET went down. The reason was that I asked 
to cancel account with the original (more expensive) service provider. When 
they did this, it wiped out something called the Zone File. I spent a 
significant part of today getting that restored. I think it works, now, but 
I cannot be certain about access to non-owners - I am, of course, the owner 
and it works perfectly for me. I think, but am not certain, that it should 
now be accessible to all as before: http://www.morphometrics.org.

-The Management

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[MORPHMET] Re: Migration update

2014-09-09 Thread MORPHMET
Delight has been achieved!

I am delighted to report that membership in the new MORPHMET has surpassed 
the 600 subscriber mark - 603 as of this writing. Also, 
www.morphometrics.org has rec'd nearly 400 unique (by IP) visits from 
computers in 45 countries (see embedded map on the website).

We began with  subscribed email addresses to the old MORPHMET mailing 
list. These had accumulated over a decade, and my personal goal was that 
we achieve near or above a 50% response to the new list.

I still have about 500 pending invitations that expire approximately 
weekly. I will continue to reissue these (a tedious process) periodically 
through September, then purge the list.

Thank you for your continued interest and support, The Management

On Saturday, August 16, 2014 10:34:42 AM UTC-4, MORPHMET wrote:

 Hi, Folks. This is just an update on the ongoing migration to the new 
 system. 

 First, I am pleased to note that we currently have 456 subscribed members. 
 These are real, interested parties who have either initiated their own 
 subscription or responded to my invitations. The old subscriber list 
 included over 1100 addresses. If we get 500+ active subscribers I will be 
 satisfied. 600+ and I will be delighted. After more than a decade of 
 subscription accumulation, getting 50% response will be pretty good, I 
 think. And, I know many are currently on vacation.

 Second, I have over the past two days reissued subscription invitations to 
 over 600 addresses. The subscriptions expire after a week, and I must 
 reissue them...ten at a time, typing in those illegible security codes. I 
 plan to continue to reissue unanswered subscriptions periodically through 
 September. I appreciate your patience in this should you get multiple 
 subscription invitations you don't want. Please ignore them, but if they 
 are too annoying, write me and I will manually remove you from the 
 invitation list. I can also make manual adjustments to the subscribed 
 address. But note,...

 To use the web interface, you must be logged in via a Google account. If 
 you do not have one (and are subscribed), you may post to the list by 
 sending an email to morphmet@morphometrics.org or replying (to the list) 
 to postings appearing in your email account. Users are initially set up to 
 receive real-time email of individual list posts, but you can change that 
 to no email, or a digest format including multiple postings. I am not sure 
 how one responds to the latter, but I suspect some sort of obvious reply 
 would work.

 Also, you can adjust your own email subscription by either subscribing to 
 the list by sending an email message from your desired subscription address 
 to

 morphmet+subscr...@morphometrics.org
 
 and you can unsubscribe by sending an email from the address to be 
 unsubscribed to:

 morphmet+unsubscr...@morphometrics.org
 
 As always, earlier posts to the list (new or old) can be found at 
 mail-archive.com

 Best, ds


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[MORPHMET] Re: Migration update

2014-08-21 Thread MORPHMET
Satisfaction obtained - currently at exactly 500 subscribers.

Now, anticipating delight...600

The Management

On Saturday, August 16, 2014 10:34:42 AM UTC-4, MORPHMET wrote:

 Hi, Folks. This is just an update on the ongoing migration to the new 
 system. 

 First, I am pleased to note that we currently have 456 subscribed members. 
 These are real, interested parties who have either initiated their own 
 subscription or responded to my invitations. The old subscriber list 
 included over 1100 addresses. If we get 500+ active subscribers I will be 
 satisfied. 600+ and I will be delighted. After more than a decade of 
 subscription accumulation, getting 50% response will be pretty good, I 
 think. And, I know many are currently on vacation.

 Second, I have over the past two days reissued subscription invitations to 
 over 600 addresses. The subscriptions expire after a week, and I must 
 reissue them...ten at a time, typing in those illegible security codes. I 
 plan to continue to reissue unanswered subscriptions periodically through 
 September. I appreciate your patience in this should you get multiple 
 subscription invitations you don't want. Please ignore them, but if they 
 are too annoying, write me and I will manually remove you from the 
 invitation list. I can also make manual adjustments to the subscribed 
 address. But note,...

 To use the web interface, you must be logged in via a Google account. If 
 you do not have one (and are subscribed), you may post to the list by 
 sending an email to morphmet@morphometrics.org or replying (to the list) 
 to postings appearing in your email account. Users are initially set up to 
 receive real-time email of individual list posts, but you can change that 
 to no email, or a digest format including multiple postings. I am not sure 
 how one responds to the latter, but I suspect some sort of obvious reply 
 would work.

 Also, you can adjust your own email subscription by either subscribing to 
 the list by sending an email message from your desired subscription address 
 to

 morphmet+subscr...@morphometrics.org
 
 and you can unsubscribe by sending an email from the address to be 
 unsubscribed to:

 morphmet+unsubscr...@morphometrics.org
 
 As always, earlier posts to the list (new or old) can be found at 
 mail-archive.com

 Best, ds


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[MORPHMET] Joining - you don't need a gmail account.

2014-08-19 Thread MORPHMET
Please be aware that you DO NOT have to have a gmail account to subscribe 
to the list. That is only necessary if you want to use the web interface. 
You can request to join the list from any email address (as far as I know) 
by sending a message to:

morphmet+subscr...@morphometrics.org

The google account (with requisite gmail address) is only required for 
using the web interface.

Note, you can join from whatever address you want AND create a google 
account to use the web interface. Your preferred email address will receive 
and be able to send messages as always. Only posts made via the web 
interface (I am guessing a bit, here) will appear to come from your gmail 
account. In such a configuration, you might want to turn off email 
notifications of postings for your google account to prevent them from 
going, unseen, to your gmail account.

The Management

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[MORPHMET] Migration update

2014-08-16 Thread MORPHMET
Hi, Folks. This is just an update on the ongoing migration to the new 
system. 

First, I am pleased to note that we currently have 456 subscribed members. 
These are real, interested parties who have either initiated their own 
subscription or responded to my invitations. The old subscriber list 
included over 1100 addresses. If we get 500+ active subscribers I will be 
satisfied. 600+ and I will be delighted. After more than a decade of 
subscription accumulation, getting 50% response will be pretty good, I 
think. And, I know many are currently on vacation.

Second, I have over the past two days reissued subscription invitations to 
over 600 addresses. The subscriptions expire after a week, and I must 
reissue them...ten at a time, typing in those illegible security codes. I 
plan to continue to reissue unanswered subscriptions periodically through 
September. I appreciate your patience in this should you get multiple 
subscription invitations you don't want. Please ignore them, but if they 
are too annoying, write me and I will manually remove you from the 
invitation list. I can also make manual adjustments to the subscribed 
address. But note,...

To use the web interface, you must be logged in via a Google account. If 
you do not have one (and are subscribed), you may post to the list by 
sending an email to morphmet@morphometrics.org or replying (to the list) to 
postings appearing in your email account. Users are initially set up to 
receive real-time email of individual list posts, but you can change that 
to no email, or a digest format including multiple postings. I am not sure 
how one responds to the latter, but I suspect some sort of obvious reply 
would work.

Also, you can adjust your own email subscription by either subscribing to 
the list by sending an email message from your desired subscription address 
to

morphmet+subscr...@morphometrics.org

and you can unsubscribe by sending an email from the address to be 
unsubscribed to:

morphmet+unsubscr...@morphometrics.org

As always, earlier posts to the list (new or old) can be found at 
mail-archive.com

Best, ds

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[MORPHMET] The new MORPHMET is now open for business.

2014-08-08 Thread MORPHMET
I am pleased to announce that the new MORPHMET is open for business. Usage 
notes follow.

1) Anyone can view the list's content, but only subscribers can post.

2) moderation - Initial posts from all users will be moderated. When your 
first post is approved, moderation will be turned off. All subsequent posts 
from your address will go directly to the entire list. Posts can be 
deleted, but not recalled. Be careful with the Send button if you are 
prone to rash commentary. 

3) archive - Posts will continue to be archived at www.mail-archive.com. 
With the new system, however, all posts will remain available at the list 
website.

4) email - If you prefer, you may continue to use MORPHMET as before. To 
post, simply send your content via email to morphmet@morphometrics.org or 
use the Reply to list option for replying the posts of others.

To subscribe or unsubscribe from the list, send an email to either 
morphmet+subscr...@morphometrics.org or 
morphmet+unsubscr...@morphometrics.org, as appropriate.

5) web - In addition to the classic email interface, you can view and post 
messages through the MORPHMET webpage at http://www.morphometrics.org site 
or access it directly at http://www.morphometrics.org/home/morphmet . 
Anyone can view the posts, but to add or reply to a post or request to 
subscribe via the web, you must be logged in to a Google account. You must 
be logged in to a subscribed account to post. There is a sign-in item at 
the bottom of the page. 

A basic account that will allow you to post or request a subscription is 
free and can be created at http://accounts.google.com (because I have 
multiple accounts, I cannot see what a user without an account would see 
here, but you can directly go to the site to create an account at 
https://accounts.google.com/signup?service=mail ).

Enjoy!

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MORPHMET may be accessed via its webpage at http://www.morphometrics.org

To unsubscribe from this group and stop receiving emails from it, send an email 
to morphmet+unsubscr...@morphometrics.org.


MORPHMET - progress, but not there, yet.

2014-07-31 Thread morphmet
I have been making progress preparing the migration to the new system, 
but not quite there, yet. I hope to have this done by or over the weekend.


I am writing this to let you know that when MORPHMET does come back up, 
you will receive an invitation to join the new list (actually just the 
old list in a new environment). You need to reply to this message when 
you receive it to continue to be a subscriber to the new (=old) MORPHMET.


-dslice



Re: Slicer question

2014-07-30 Thread morphmet




 Original Message 
Subject:Re: Slicer question
Date:   Mon, 28 Jul 2014 21:16:07 -0400
From:   m...@uw.edu
To: morphmet@morphometrics.org morphmet@morphometrics.org



Hi Donna,
We use it daily, what would you like to know?

*From:* morphmet_modera...@morphometrics.org
mailto:morphmet_modera...@morphometrics.org
*Sent:* ‎Monday‎, ‎July‎ ‎28‎, ‎2014 ‎4‎:‎33‎ ‎PM
*To:* morphmet@morphometrics.org mailto:morphmet@morphometrics.org


- Forwarded message from Jones, Donna donna.jon...@cchmc.org -

Date: Sat, 26 Jul 2014 12:01:24 -0400
From: Jones, Donna donna.jon...@cchmc.org
Reply-To: Jones, Donna donna.jon...@cchmc.org
Subject: Slicer question
To: morphmet@morphometrics.org morphmet@morphometrics.org

Dear Morphmet,



Does anyone have experience working with 3D Slicer and dicom slices from
microCT? If yes, I’d be interested in asking you some direct questions
about functionality.



Cheers,


Donna



*
Donna C. Jones, Ph.D.
Research Assistant Professor
Division of Plastic Surgery


Division of Biostatistics and Epidemiology
Cincinnati Children's Hospital Medical Center
 Burnett Ave. ML 2020
Cincinnati, OH 45229
phone: 513-803-0383


donna.jon...@cchmc.org





- End forwarded message -







MORPHMET - going down for upgrades

2014-07-30 Thread morphmet
It is my intention to take morphmet down shortly (today?). I believe I 
have cleared all pending postings and subscription requests.


If all goes well, it should be down for a few hours or a couple of days. 
Most likely the latter to give me a chance to test the new system.


If all goes well, when it comes back online, users may see no difference 
whatsoever (other than improved performance) if they do not wish to, 
i.e., same mailing list as before. Others will be able to avail 
themselves of new features.


Any messages posted during the downtime may be lost.

On the other hand, if all does not go well, I suppose you may never hear 
from me again. =8O


-dslice



Fwd: Re: Image rotation data loss

2014-06-29 Thread morphmet




 Original Message 
Subject: Re: Image rotation data loss
Date: Sun, 29 Jun 2014 03:38:32 -0400
From: Dennis E. Slice dsl...@morphometrics.org
To: morphmet@morphometrics.org

First guess would be your landmarks are out of order on one or more
specimens. You can check this by creating a set of links in tpsUtil and
plotting the data showing the links. And/or, in tps, plot the data
showing points and vectors. -ds

On 6/29/14, 12:27 AM, morphmet_modera...@morphometrics.org wrote:


Hello all,

I'm trying to digitize photos in tpsDig for a geometric morphometrics
study on Notropis fishes. In order to test for digitization error I've
copied the first fish photo I took 10 times and digitized each one onto
the same TPS file (made in tpsUtil). I then performed a relative warps
analysis in tpsRelw and performed a Procruste's superimposition in R
(package geomorph) to glance and see if any landmarks varied
significantly. My results show very drastic variation in landmark
placement, with dots all over the place in the GPA plot. I know my
landmark placement isn't that bad, so I think it might have something to
do with data loss. When I photographed the specimen the fish was
flipped, so I had to rotate and flip it to turn it rightside up before
digitization. Is it possible that rotating the photo resulted in data
loss and therefore digitization error? The TPS file had the landmark
coordinates for each specimen pretty close together (about normal
landmark placement error), but the GPA and relative warps plots showed
drastic variance. I've attached the GPA plot to show what I mean. The
landmarks are supposed to go around the entire fish. Also let me know if
you have any other ideas for why there might be crazy variance.

Best,


Connor
connorfre...@utexas.edu mailto:connorfre...@utexas.edu



- End forwarded message -





- End forwarded message -





- End forwarded message -










ANNOUNCEMENT: morphometrics.org to go down for upgrades

2014-04-03 Thread morphmet

Sorry for jumping the queue, but...

Over time, we have had a number of problems with message distribution on 
MORPHMET. The fundamental issue is that when multiple messages are 
distributed the host sometimes shuts down the list thinking it is spam. 
We believe the problem ultimately arises from the list exceeding the 
1000-subscriber limit of the host system. Anyway, we have taken to 
approving a limit of five messages per day to try to avoid this. This is 
unacceptable. So,...


In the very near future, the morphometrics.org domain will go down for 
major changes. If successful and despite the magnitude of the changes, 
subscribers may be insulated from noticing any difference at all besides 
the downtime if they so desire. Otherwise, we hope to have some major 
enhancements to MORPHMET for those who wish to avail themselves of them.


Of immediate relevance to me is that this will also mean that my mail 
address at morphometrics.org will be inoperable for a while. This might 
be a couple of hours, a couple of days, or you might never hear from me 
again. Hopefully it will be something closer to the former than the 
latter. During this period, if you really need to contact me, please do 
so through my university (fsu.edu) address.


I have come very close to pushing the button for this at least twice 
in the past, but hesitated about bringing the whole domain down. This 
time, I promise to push that button. I am currently (re)familiarizing 
myself with the necessary steps and software. I wanted to do it today, 
but we have events at the university that demand my attention Friday and 
early next week. So, I am thinking it will happen around the 
middle-to-end of next week. I would like an entire free day to deal with 
the transition and any associated problems. I will advise the membership 
immediately before the domain goes down.


Thank you, Dennis E. Slice



RE: bilat.symmetry output in geomorph

2013-07-17 Thread morphmet




 Original Message 
Subject:RE: bilat.symmetry output in geomorph
Date:   Sun, 14 Jul 2013 18:30:13 -0400
From:   Adams, Dean [EEOBS] dcad...@iastate.edu
To: morphmet@morphometrics.org morphmet@morphometrics.org
CC: Dean Adams (dcad...@iastate.edu) dcad...@iastate.edu



Milos,

At present, bilat.symmetry() does not return the symmetric components
for each specimen. That is something we could add in the next version.
  As for FA, one can assess this for a population using bilat.symmetry()
(see the help file for instructions).

--

Dr. Dean C. Adams

Professor

Department of Ecology, Evolution, and Organismal Biology Department of
Statistics Iowa State University Ames, Iowa

50011

www.public.iastate.edu/~dcadams/ http://www.public.iastate.edu/~dcadams/

phone: 515-294-3834

*From:*morphmet_modera...@morphometrics.org
[mailto:morphmet_modera...@morphometrics.org]
*Sent:* Saturday, July 13, 2013 10:16 PM
*To:* morphmet@morphometrics.org
*Subject:* bilat.symmetry output in geomorph


- Forwarded message from Milos Blagojevic spearsata...@hotmail.com
mailto:spearsata...@hotmail.com -

Date: Sat, 13 Jul 2013 08:29:45 -0400
From: Milos Blagojevic spearsata...@hotmail.com
mailto:spearsata...@hotmail.com
Reply-To: Milos Blagojevic spearsata...@hotmail.com
mailto:spearsata...@hotmail.com
Subject: bilat.symmetry output in geomorph
To: morphmet@morphometrics.org mailto:morphmet@morphometrics.org
morphmet@morphometrics.org mailto:morphmet@morphometrics.org

Hi to all morphometricians,


I was wondering how to use bilat.symmetry function from geomorph package
in order to extract symmetric and asymmetric components of shape
variation in the case of object symmetry.


By looking at the function code it can be observed that DA.mns and
FA.mns arrays are used for plotting shape changes associated with
directional and fluctuating asymmetry, but they only represent extreme
configurations. Is it possible to return landmark coordinate arrays for
every individual so that they can be used as the gpagen$coords output,
but separately for symmetric and asymmetric component of shape variation
(individual scores on symmetric and asymmetric component and their
coordinates)?


Also I am wondering is there a way to quantify FA per populations (or
any groups) using this package?


Best regards,
Milos Blagojevic, PhD student
University of Kragujevac,
Serbia



- End forwarded message -





possible duplicate posts

2013-07-17 Thread morphmet
Dear Morphmeters, I may sent out some duplicate messages from the past 
few days - some seemed familiar, though not in my personal archive. If 
so, I apologize. -the morphmet mod (dslice)




Re: Morpheus: java versions

2013-07-03 Thread morphmet

Thought I would post an update.

On one system running Apple OS X 10.8.4, I uninstalled Apple Java 1.6(1) 
and installed Oracle Java 1.7(2).


Morpheus runs just fine in this environment, and there is no need to run 
the mac_os_x_prepare script.


jEdit(3) is still partially broken, but looking into that.

-ds


(1) Deleted Java directory from /System/Library, requires admin-level 
access, e.g., sudo rm -rf ./Java


(2) Requires installation of Java Development Kit (jdk) from here: 
http://www.oracle.com/technetwork/java/javase/downloads/jdk7-downloads-1880260.html


The Java Runtime Environment (jre) only installs web-related files. You 
need the jdk to run local, standalone applications like Morpheus et al.


(3) jEdit is an excellent text editor that easily handles huge files 
and, especially, supports block/column-mode operations - great for 
moving around, editing, etc. columns of data in a text file. See. 
http://www.jedit.org/


-ds

On 6/28/13 12:32 PM, Dennis E. Slice wrote:

Some background and current status of Morpheus et al., Java Edition.

The software was developed and tested on Mac OS X with the Apple-default
Java version 1.6. The resulting distribution was tested on various
Windows and Linux platforms available to me (mostly installations
running on virtual machines). In those cases, the general structure
worked, but Morpheus would not run because the default environments (in
the VMs) did not have sufficient openGL capabilities. On an old
MacBookPro, I installed Windows 7 and Linux. I upgraded the Windows 7
drivers and it worked fine. I was not successful upgrading the Ubuntu
drivers for the MacBookPro given the limited time I spent trying. My
students have reported it to run on various proper Windows and Linux
systems, though some problems are reported on older, less contemporary
systems probably due to openGL drivers.

This is relevant because java 1.6 was provided and maintained by Apple,
but Apple has suspended this effort as of 1.6 and has turned future
development over to the general java development community. Apple's 1.6,
in fact, is the source of the outdated (java3D) files require the
execution of the mac_os_x_prepare script - they must be hidden from
view. However, 1.6 is still, for now, the default installation when java
programs are detected.

A few days ago, I had to install Java 1.7 to run some lab code that
requires that version. This broke two of my favorite programs, jEdit and
Morpheus. Installing 1.6 alongside 1.7 allowed jEdit to run, but
Morpheus still did not.

There are two issues at play - the shift from Apple 1.6 to
community-provided 1.7 and the difference between Oracle and the openJDK
products. We are currently looking into this, and I have some leads that
should address one or more of these issues. Also, I have information
that some of these problems will be addressed in a new release of java
due out this summer.

I would generally prefer to avoid commenting on future developments, but
I will a bit since it provides context for the current situation. The
current 3D graphics in Morpheus use java3d running on top of jogl 2.0.
We are currently developing a new graphics engine that will be built
directly on top of jogl 2.0 and using OpenGL shader language. This is a
significant and fundamental change, but better in the long term. This is
also the reason I am reluctant to develop new graphics windows and
options until we see what adjustments are necessary to the existing
graphics objects to work with our new graphics engine.

I will keep you posted.

-ds






RE: tps format problem reading in R

2013-07-03 Thread morphmet




 Original Message 
Subject: RE: tps format problem reading in R
Date: Wed, 3 Jul 2013 11:32:55 -0400
From: Adams, Dean [EEOBS] dcad...@iastate.edu
To: morphmet@morphometrics.org morphmet@morphometrics.org

Hi John,

There were two issues here, and both of which have easy fixes. First, 
there is only 1 specimen in your tps file, and the current version of 
readland.tps() was written for datasets with more than one specimen (we 
didn't envision folks reading in a single specimen for a morphometric 
analysis).  This is easily fixed by changing the 3rd to last line of the 
function as below. Next, your file had a non-numeric ID for the 
specimen. To catch this, change the 4th to last line of the function as 
below.  These two lines should now read:


ID -sub(ID=, , tpsfile[grep(ID, tpsfile)])   #delete the 'as.numeric'
dimnames(coords)[[3]] - as.list(imageID)   # add 'as.list'


The updated function code is attached, and will be in the next update of 
geomorph.


Thanks for catching these; this makes the function more general.

Best,

Dean

--
Dr. Dean C. Adams
Professor
Department of Ecology, Evolution, and Organismal Biology Department of 
Statistics Iowa State University Ames, Iowa

50011
www.public.iastate.edu/~dcadams/
phone: 515-294-3834


-Original Message-
From: morphmet_modera...@morphometrics.org 
[mailto:morphmet_modera...@morphometrics.org]

Sent: Wednesday, July 03, 2013 1:31 AM
To: morphmet@morphometrics.org
Subject: tps format problem reading in R


- Forwarded message from John Denton jden...@amnh.org -

 Date: Tue, 2 Jul 2013 23:04:22 -0400
  From: John Denton jden...@amnh.org
  Reply-To: John Denton jden...@amnh.org
  Subject: tps format problem reading in R
  To: morphmet@morphometrics.org morphmet@morphometrics.org

Hi folks,

I'm trying to read a tps file in the geomorph v1.1-1 R package using

readland.tps(file),

but every time I try the above, I get the error

Error in dimnames(coords)[[3]] - imageID : 'dimnames' must be a list In 
addition: Warning message:

In readland.tps(Lter_mean.TPS) : NAs introduced by coercion

I do not get the error when I read in some of my other tps files (all of 
which were produced using append files in tpsUtil). The file I'm trying 
to read in is the side-averaged Procrustes coordinates, generated in 
MorphoJ.


I've checked the hidden formatting, the line breaks, the number of 
decimal places, and the file extension, but I can't seem to figure it out.


The file is attached.

~John

John S. S. Denton
Ph.D. Candidate
Department of Ichthyology and Richard Gilder Graduate School American 
Museum of Natural History www.johnssdenton.com


- End forwarded message -





readland.tps
Description: Binary data


Remembrances of Robert Sokal

2012-10-19 Thread morphmet
[Added to the Announcements page at www.morphometrics.org -the morphmet 
moderator (dslice)]


Remembrances of Robert Sokal

Save the date: Sunday November 18, 2-4 P.M., Wang Center Chapel at Stony 
Brook University


Robert Sokal passed away last April and his funeral and memorial service 
were completed quickly in accordance with his faith. Because of his 
great impact as a beloved friend, mentor, scholar, and university 
citizen we would like to give Bob’s family, friends, and colleagues an 
opportunity to remember him at a public memorial, open to all who wish 
to remember fondly his many contributions to our lives.


We ask that you register at the link given below as soon as possible so 
we can get an idea of how many will attend. We ask especially that you 
indicate whether you would like to speak, send text for a brief 
remembrance, or even a brief video (less than one minute, please).


We look forward to your response,
Warmly,
Jim Rohlf and Jeff Levinton

http://life.bio.sunysb.edu/ee/memsokal/memorial.html



RE: multi-class ANOVA analogue for geometric morphometrics

2012-06-07 Thread morphmet



 Original Message 
Subject: RE: multi-class ANOVA analogue for geometric morphometrics
Date: Mon, 4 Jun 2012 14:59:23 -0400
From: F. James Rohlf ro...@life.bio.sunysb.edu
Reply-To: ro...@life.bio.sunysb.edu
Organization: Stony Brook University
To: morphmet@morphometrics.org

Once you have projected your shapes into the tangent space (e.g., 
partial warp scores) then you have what can be treated as ordinary 
multivariate data. You can use any multivariate method that is 
appropriate for the questions you wish to ask.


Note that you should not normally use Goodall's test as it makes many 
unrealistic assumptions and thus in practice has much higher Type I 
error rates than you would expect.


--
F. James Rohlf, John S. Toll Professor, Stony Brook University
The much revised 4th editions of Biometry and Statistical Tables are now 
available:

http://www.whfreeman.com/Catalog/product/biometry-fourthedition-sokal
http://www.whfreeman.com/Catalog/product/statisticaltables-fourthedition-rohlf
 Please consider the environment before printing this email




-Original Message-
From: morphmet_modera...@morphometrics.org
[mailto:morphmet_modera...@morphometrics.org]
Sent: Monday, June 04, 2012 2:05 AM
To: morphmet@morphometrics.org
Subject: multi-class ANOVA analogue for geometric morphometrics


- Forwarded message from Robert Richardson  -

 Date: Fri, 1 Jun 2012 17:42:44 -0400
  From: Robert Richardson
  Reply-To: Robert Richardson
  Subject: multi-class ANOVA analogue for geometric morphometrics
  To: morphmet-requ...@morphometrics.org

Fellow morphers,

I'm familiar with the need to account for the lower degrees of freedom, when
testing for differences between groups, hence the use of Goodall's-F test.
However, as with basic (M)ANOVA, that just tells you if there's at least one
group that's statistically different but doesn't identify which one(s) when you
have more than two categories.
Are there multi-class (M)ANOVAs (e.g. Ryan-Einot-Gabrial-Welsch Q-test or
Tukey's test) that are out there that will directly identify which categories 
are
different when dealing with many categories (e.g.
samples from seven geographical locations)?  Maybe there's a way to load the
data into an R-script and manually adjust the degrees of freedom for a regular
multi-category (M)ANOVA?

Thanks for the input!

Robert-

--
=== === === ===
Robert Richardson, PhD candidate
Department of Biology
Portland State University
1719 SW 10th Ave; SB 2, #246
Portland, OR 97201
503.725.8004; r...@pdx.edu
=== === === ===

- End forwarded message -







RE: CV shape variation

2012-06-07 Thread morphmet



 Original Message 
Subject:RE: CV shape variation
Date:   Mon, 4 Jun 2012 15:05:53 -0400
From:   F. James Rohlf ro...@life.bio.sunysb.edu
Reply-To:   ro...@life.bio.sunysb.edu
Organization:   Stony Brook University
To: morphmet@morphometrics.org



I am not sure of the question being asked. Perhaps what was meant was
how to visualize the shape deformation implied by changes along each
axis? I think the CVAGen6 software has an option for that. Basically,
one regresses shape on the CVA scores. This can be done in the tpsRegr
software.

--

F. James Rohlf, John S. Toll Professor, Stony Brook University

The much revised 4^th editions of Biometry and Statistical Tables are
now available:

http://www.whfreeman.com/Catalog/product/biometry-fourthedition-sokal

http://www.whfreeman.com/Catalog/product/statisticaltables-fourthedition-rohlf

PPlease consider the environment before printing this email

*From:*morphmet_modera...@morphometrics.org
[mailto:morphmet_modera...@morphometrics.org]
*Sent:* Monday, June 04, 2012 2:03 AM
*To:* morphmet@morphometrics.org
*Subject:* Re: CV shape variation


- Forwarded message from Philipp Mitteröcker -

Date: Fri, 1 Jun 2012 05:52:44 -0400
From: Philipp Mitteröcker
Reply-To: Philipp Mitteröcker
Subject: Re: CV shape variation
To: morphmet@morphometrics.org mailto:morphmet@morphometrics.org

For a single canonical variate, you can compute the variance along this
CV and divide it by the total variance (computed, e.g., as the sum of
the variances of all variables). But in contrast to PCA, you cannot add
up the variances for two or more CVs, because the CV axes are not
orthogonal. You could compute the variance within the plane spanned by
two CVs when orthogonalizing the two CV axes.

However, explained variance among the individuals is not often reported
for CVA, as it is not the quantity that is maximized.

Best,

Philipp

Am 01.06.2012 um 06:27 schrieb morphmet_modera...@morphometrics.org
http://mailto:morphmet_modera...@morphometrics.org:




- Forwarded message from beatriz gamarra-

Date: Wed, 30 May 2012 13:29:58 -0400
From: beatriz gamarra
Reply-To: beatriz gamarra
Subject: CV shape variation
To:morphmet-requ...@morphometrics.org
http://mailto:morphmet-requ...@morphometrics.org

Hi,

I amanalyzinga dataset with 12 landmarks and 12 groups. I have run CVA
by using CVAGen6 from IMP and I want to obtain the shape variation
associated with first CVs. How could I achieve?

Thanks in advance.

Beatriz Gamarra



- End forwarded message -

___

Dr. Philipp Mitteroecker

Department of Theoretical Biology
University of Vienna
Althanstrasse 14
A-1090 Vienna, Austria

Tel: +43 1 4277 56705
Fax: +43 1 4277 9544
email: philipp.mitteroec...@univie.ac.at
http://mailto:philipp.mitteroec...@univie.ac.at
homepage: http://theoretical.univie.ac.at/people/mitteroecker



- End forwarded message -



PhD in morphological evolution

2012-05-25 Thread morphmet



 Original Message 
Subject: PhD in morphological evolution
Date: Wed, 23 May 2012 05:35:58 -0400
From: coue...@mnhn.fr
To: morphmet@morphometrics.org

Hello,
You'll find below a PhD subject proposed to the Ecole Pratique des
Hautes Etudes (France)

The subject (and ONE applicant) will be proposed to the EPHE, examined
and the applicant will be interviewed in order to get the fellowship.
Interviws are planned on July  4th and 5th in Paris. For further
informations, please go to the EPHE website:
http://www.ephe.sorbonne.fr/recherche/contrat-doctoral-2012.html)


Applicants must contact Pr.Sophie Montuire
(sophie.montu...@u-bourgogne.fr) before june 20th  2012.
-
Ecole Pratique des Hautes Etudes PhD

Section of Life and Earth sciences



Title: Evolutionary novelties and emergence of dental phenotypes in Mammals.



Host laboratory: EPHE Paléobiodiversité et évolution – UMR 6282 
Biogéosciences




Laboratory address:

UMR 6282 uB/CNRS – Biogéosciences
Phone / Fax

6 bd Gabriel, 2100 Dijon, FRANCE +333 80 39 63 47
/ +333 80 39 63 87



PhD supervisors:

Names: Montuire Sophie, Couette Sébastien, Navarro Nicolas

Address: UMR 6282 uB/CNRS Biogéosciences, 6 bd Gabriel, 2100 Dijon,
FRANCE   Téléphone /Fax

+333 80 39 63 47 / +333 80 39 63 87

Emails : sophie.montu...@u-bourgogne.fr,
sebastien.coue...@u-bourgogne.fr, nicolas.nava...@u-bourgogne.fr





Descriptions and objectives



Background –

Mammals display a high dental diversity in terms of number and
complexity of teeth. This diversity attests of the influence of
several parameters including diet and suggests a mammalian morphospace
on which shape changes are possible in every direction. However,
morphological changes within lineages seem to be constrained.
Developmental processes producing the phenotypic expression of genetic
variation are under natural selection. Favouring or limiting some
directions of change in the morphospace, these processes will modify
the evolutionary capacity on the short and long time scales. These
constraints can influence the diversity of a clade (at a
macroevolutionay level), forcing the accumulation of new species in
one peculiar direction of the morphospace. In the dental raw the
eruption of teeth follows an iterative developmental model in which
interactions between teeth are controlled and lead to a final dental
phenotype. Within teeth themselves, interactions occur between cusps
following the same iterations and defining tooth morphology (number,
position and shape of cusps). Some recent works showed that small
modifications of cusp interactions can imply large modifications at
the tooth scale, and for instance the development of new cusps.





Objectives – This subject will focus on two different mammal groups
(rodents and primates) at different scales (population, lineages,
clades). Complementary approaches will be addressed by both groups.
Rodents display a reduced variation of the dental formula but a high
diversity of molar form. In primates, the major part of variation
occurs on the number of teeth and number of cusps on each tooth rather
than on their shape. The main goal of this project is to understand
the cusp interactions and their consequences on dental formula and
teeth complexity (gains or losses of cusps and teeth). These
variations of complexity will be analysed in the historic and
evolutionary frameworks of the groups, and of the biotic (size, diet…)
and abiotic parameters.



National and international context– The « EPHE -Paléobiodiversité et
évolution » and « UMR uB/CNRS 6282 Biogéosciences » laboratories have
national and international recognition for their knowledge and skills
in form analysis. The evolution of dental morphology in rodents and
especially Arvicolinae is an historic and major topic of the EPHE
laboratory since it establishment. These last years, people from the
laboratory developed international collaborations on Evo-Devo themes
on teeth.

--
Sébastien Couette
Maitre de Conférences
Laboratoire EPHE d'Evolution des Primates
Muséum national d'Histoire naturelle
Département Histoire de la Terre
Centre de Recherche sur la Paléobiodiversité et les Paléoenvironnements 
(CR2P)

UMR 7207 du CNRS/MNHN/UPMC
8, rue Buffon CP 38
F-75231 Paris cedex 05
Tel.: (+33) 1 40793061



PhD proposal.doc
Description: MS-Word document


tpsUtil update

2012-05-25 Thread morphmet



 Original Message 
Subject:tpsUtil update
Date:   Wed, 23 May 2012 21:46:50 -0400
From:   F. James Rohlf ro...@life.bio.sunysb.edu
Reply-To:   ro...@life.bio.sunysb.edu
Organization:   Stony Brook University
To: morphmet@morphometrics.org



I have just uploaded version 1.49 to the Stony Brook University server at

http://life.bio.sunysb.edu/morph

It improved on some error messages when invalid files were loaded.

--

F. James Rohlf, John S. Toll Professor, Stony Brook University

The much revised 4^th editions of Biometry and Statistical Tables are
now available:

http://www.whfreeman.com/Catalog/product/biometry-fourthedition-sokal

http://www.whfreeman.com/Catalog/product/statisticaltables-fourthedition-rohlf

PPlease consider the environment before printing this email



Geometric Morphometrics courses

2012-05-25 Thread morphmet



 Original Message 
Subject: Geometric Morphometrics courses
Date: Fri, 25 May 2012 05:06:01 -0400
From: Soledad Esteban soledad.este...@icp.cat
To: morphmet@morphometrics.org

Dear colleagues:

This e-mail is to inform you of some courses on Geometric Morphometrics, 
which may would be of your interest. I would appreciate if you could 
distribute this information between your colleagues:


Introduction to Geometric Morphometrics. June 12-15, 2012. 
Instructors: Dr. Chris Klingenberg (University of Manchester, UK) and 
Dr. Jesús Marugán-Lobón (Universidad Autónoma de Madrid). Just 5 places 
left. More information at: 
http://www.transmittingscience.org/introduction_to_gm.htm


“3D Geometric Morphometrics”. July 17-20, 2012. Instructor: Dra Melissa 
Tallman (CUNY/AMNH, New York). Early registration until May 31. More 
information at: http://www.transmittingscience.org/3d_gm.htm


“Geometric Morphometrics and Phylogeny”. September 4-7, 2012. 
Instructor: Dr. Chris Klingenberg (University of Manchester, UK). More 
information at: http://www.transmittingscience.org/gm_and_phylogeny.htm


For any questions: cour...@transmittingscience.org.
These courses will be held in the premises of Sabadell of the Institut 
Català de Paleontologia Miquel Crusafont (Barcelona, Spain). They are 
co-organized by Transmitting Science and el Institut Catalá de 
Paleontologia Miquel Crusafont.


Best regards

Soledad De Esteban Trivigno
Area de Paleobiología
Institut Català de Paleontologia
Edifici ICP, Campus de la UAB
08193 Cerdanyola del Vallès
Barcelona. Spain
00-34-935868334
www.icp.cat









Re: EVAN Toolbox lighting problem

2012-05-19 Thread morphmet



 Original Message 
Subject:Re: EVAN Toolbox lighting problem
Date:   Thu, 17 May 2012 06:58:11 -0400
From:   Helgi Pétur Gunnarsson helgipe...@gmail.com
To: morphmet@morphometrics.org



Hello Stephanie,
The lighting sometimes can get messed up if you do a GPA on the surface
(pass it through the GPA node).
There is no easy solution but there may be a workaround, but it requires
you to change the network a little.

You could try to export the procrustes fitted surface, import again, and
use it without sending it through the GPA node.

This is what you have to do:
Export the surface
- connect the surface output of the GPA node to an Export node.
- run the network again
- export the surface from the Export node

Then Import the surface again.
- select the newly exported surface file from the Import node

Use the surface in your network without sending it through the GPA node.
- delete the links that lead to and from the surface ports of the GPA node
- connect the surface directly from the Import Node to the Warper node.
- run the network again


If that does not work,
you could also try to save the surface in another format (for example
*.ply).

Hope this helps,
Helgi Petur Gunnarsson
Evan Society


On 16 May 2012 23:10, morphmet morphmet_modera...@morphometrics.org
mailto:morphmet_modera...@morphometrics.org wrote:



 Original Message 
Subject:EVAN Toolbox lighting problem
Date:   Wed, 16 May 2012 16:21:40 -0400
From:   Stephanie Kozakowski stephanie.kozakowski@__utoronto.ca
mailto:stephanie.kozakow...@utoronto.ca
To: morphmet@morphometrics.org mailto:morphmet@morphometrics.org



Hi all,

I am using the EVAN Toolbox v.1.52 and am having trouble getting the
light to shine on the appropriate area of the object during surface
warping in the 3D viewer.
For example, the light will be shining on the inferior and posterior
portions of the skull I am warping. However I would prefer to show the
warpings in sagittal view but am unable to since the surface is
completely black.
Can the lighting be controlled within the Toolbox? If not, is there a
way I can change where the light shines in the .stl surface file before
loading it into the Toolbox?

Sincerely,
Stephanie Kozakowski


Ph.D Candidate
Evolutionary Anthropology
University of Toronto
stephanie.kozakowsk@utoronto.__ca
mailto:stephanie.kozako...@utoronto.ca
mailto:stephanie.kozakowsk@__utoronto.ca
mailto:stephanie.kozako...@utoronto.ca




RE: Soft tissue analyse

2012-05-16 Thread morphmet



 Original Message 
Subject: RE: Soft tissue analyse
Date: Tue, 15 May 2012 01:03:26 -0400
From: Ivan Huber i...@randomtech.com
To: morphmet@morphometrics.org morphmet@morphometrics.org

Interesting problem,.  What about either freezing the organ in a 
standard way or preserving it in an appropriate solution, possibly 
formaldehyde or Bouin's.  Please let us know-- What organ and what 
animal?  Best wishes, Ivan Huber


-Original Message-
From: morphmet [mailto:morphmet_modera...@morphometrics.org]
Sent: Monday, May 14, 2012 12:33 AM
To: morphmet
Subject: Re: Soft tissue analyse



 Original Message 
Subject: Re: Soft tissue analyse
Date: Sun, 13 May 2012 13:04:45 -0400
From: Carmelo Fruciano c.fruci...@unict.it
To: morphmet@morphometrics.org



Dear all,

I would like to quantify the shape of an soft tissue organ. However I
am not sure what would be the best method to use.
Working with soft tissue organs, I am having two problems: one is the
absent of landmarks, and the other is that sometimes the preparation of
the specimens may cause some deformations on the shape.   Is there any
way to get around this situation?



Dear Julia,
I think that your question is a bit tricky as not everyone likes 
semilandmarks and the like.
My idea is that if the organ you're interested in is so soft and 
flexible that you cannot realy imagine a standard situation, then it's 
a bit too tricky and studying shape variation might even be not 
particularly meaningful in itself.
On the other hand, if there is some sort of normal status that you can 
imagine your organ in (and you can get your organ in this status), then 
you can use sliding semilandmark or other outline methods.
About the deformation, apart the obvious of avoiding it, if it's 
somewhat predictable then maybe it can be modeled and removed from your 
data.

Sorry if I sound too vague but your question is quite general...
I hope that the answer is of some help, though...
Best,
Carmelo



--
Carmelo Fruciano
Post-doc - University of Konstanz - Konstanz, Germany Honorary Fellow - 
University of Catania - Catania, Italy e-mail c.fruci...@unict.it 
http://www.fruciano.it/research/



Universita' di Catania - A.P.Se.Ma.
Servizio di Posta Elettronica







correcting for body size

2012-05-16 Thread morphmet



 Original Message 
Subject: correcting for body size
Date: Tue, 15 May 2012 11:03:28 -0400
From: Saad Arif arifs...@gmail.com
To: morphmet@morphometrics.org

Hello all,

I have linear measurements for eye area and body size in Drosophila. I 
want to get residuals for eye area by regressing it on body size. Both 
variables appear to have a straight-line relationship. my question is: 
do i need to square my body size measurement before i regress it to eye 
area even if they are both seemingly linearly related?


Any response would be appreciated!

Thanks in advance.

Saad




Re: Soft tissue analyse

2012-05-16 Thread morphmet



 Original Message 
Subject: Re: Soft tissue analyse
Date: Wed, 16 May 2012 08:26:16 -0400
From: Kim van der Linde k...@kimvdlinde.com
To: morphmet@morphometrics.org
CC: morphmet morphmet_modera...@morphometrics.org

I would suggest looking into techniques that go beyond the techniques
using landmarks. One article for which I have a reference handy is Parr,
WCH, Ruto, A, Soligo, C and Chatterjee, HJ (2011) Allometric shape
vector projection: A new method for the identification of allometric
shape characters and trajectories applied to the human astragalus
(talus), Journal of Theoretical Biology, 272, 64–71.

Good luck...

Kim

On 5/13/2012 12:15 PM, morphmet wrote:



 Original Message 
Subject: Soft tissue analyse
Date: Wed, 9 May 2012 12:55:57 -0400
From: Julia Klaczko jklac...@gmail.com
To: morphmet@morphometrics.org



Dear all,

I would like to quantify the shape of an soft tissue organ. However I am
not sure what would be the best method to use.
Working with soft tissue organs, I am having two problems: one is the
absent of landmarks, and the other is that sometimes the preparation of
the specimens may cause some deformations on the shape. Is there any
way to get around this situation?
Thank you very much for your help,
Julia



--
http://www.kimvdlinde.com




Re: correcting for body size

2012-05-16 Thread morphmet



 Original Message 
Subject: Re: correcting for body size
Date: Wed, 16 May 2012 08:30:33 -0400
From: Kim van der Linde k...@kimvdlinde.com
To: morphmet@morphometrics.org
CC: morphmet morphmet_modera...@morphometrics.org

You effectively ask for an allometric regression.

1. take the square root of the eye area
2. log transform the measurements
3. use a type 2 regression (major axis, reduced major axis)
4. calculate the distance between the point and the regression line

This should do it.

Kim


On 5/16/2012 2:59 AM, morphmet wrote:



 Original Message 
Subject: correcting for body size
Date: Tue, 15 May 2012 11:03:28 -0400
From: Saad Arif arifs...@gmail.com
To: morphmet@morphometrics.org

Hello all,

I have linear measurements for eye area and body size in Drosophila. I
want to get residuals for eye area by regressing it on body size. Both
variables appear to have a straight-line relationship. my question is:
do i need to square my body size measurement before i regress it to eye
area even if they are both seemingly linearly related?

Any response would be appreciated!

Thanks in advance.

Saad




--
http://www.kimvdlinde.com




EVAN Toolbox lighting problem

2012-05-16 Thread morphmet



 Original Message 
Subject:EVAN Toolbox lighting problem
Date:   Wed, 16 May 2012 16:21:40 -0400
From:   Stephanie Kozakowski stephanie.kozakow...@utoronto.ca
To: morphmet@morphometrics.org



Hi all,

I am using the EVAN Toolbox v.1.52 and am having trouble getting the
light to shine on the appropriate area of the object during surface
warping in the 3D viewer.
For example, the light will be shining on the inferior and posterior
portions of the skull I am warping. However I would prefer to show the
warpings in sagittal view but am unable to since the surface is
completely black.
Can the lighting be controlled within the Toolbox? If not, is there a
way I can change where the light shines in the .stl surface file before
loading it into the Toolbox?

Sincerely,
Stephanie Kozakowski


Ph.D Candidate
Evolutionary Anthropology
University of Toronto
stephanie.kozako...@utoronto.ca mailto:stephanie.kozako...@utoronto.ca



Re: Soft tissue analyse

2012-05-14 Thread morphmet



 Original Message 
Subject: Re: Soft tissue analyse
Date: Sun, 13 May 2012 13:04:45 -0400
From: Carmelo Fruciano c.fruci...@unict.it
To: morphmet@morphometrics.org



Dear all,

I would like to quantify the shape of an soft tissue organ. However I am
not sure what would be the best method to use.
Working with soft tissue organs, I am having two problems: one is the
absent of landmarks, and the other is that sometimes the preparation of
the specimens may cause some deformations on the shape.   Is there any
way to get around this situation?



Dear Julia,
I think that your question is a bit tricky as not everyone likes
semilandmarks and the like.
My idea is that if the organ you're interested in is so soft and
flexible that you cannot realy imagine a standard situation, then
it's a bit too tricky and studying shape variation might even be not
particularly meaningful in itself.
On the other hand, if there is some sort of normal status that you
can imagine your organ in (and you can get your organ in this status),
then you can use sliding semilandmark or other outline methods.
About the deformation, apart the obvious of avoiding it, if it's
somewhat predictable then maybe it can be modeled and removed from
your data.
Sorry if I sound too vague but your question is quite general...
I hope that the answer is of some help, though...
Best,
Carmelo



--
Carmelo Fruciano
Post-doc - University of Konstanz - Konstanz, Germany
Honorary Fellow - University of Catania - Catania, Italy
e-mail c.fruci...@unict.it
http://www.fruciano.it/research/


Universita' di Catania - A.P.Se.Ma.
Servizio di Posta Elettronica





Re: Head Shape Question

2012-05-14 Thread morphmet



 Original Message 
Subject:Re: Head Shape Question
Date:   Sun, 13 May 2012 14:15:46 -0400
From:   kalpana das kkalpanaa1...@gmail.com
To: morphmet@morphometrics.org



Dear Dustin,
I had somewhat similar kind of question.I used sliding semilandmark
method to capture the snout shape in frog.
You can try selecting the landmark along a curve in TpsDIG and then
change those landmarks into sliding semilandamrks in TPSutil.
I think this way you can be able to capture the outline.
Correct me if i am wrong.

Regards,
Kalpana

On Sun, May 13, 2012 at 9:43 PM, morphmet
morphmet_modera...@morphometrics.org
mailto:morphmet_modera...@morphometrics.org wrote:



 Original Message 
Subject: Head Shape Question
Date: Mon, 7 May 2012 15:07:29 -0400
From: Owen, Dustin A dao...@bsu.edu mailto:dao...@bsu.edu
To: morphmet@morphometrics.org mailto:morphmet@morphometrics.org
morphmet@morphometrics.org mailto:morphmet@morphometrics.org

I am an undergraduate researcher looking to describe differences in
head shape among male and female salamanders.  I have been using
tpsDig, but have had no success with the outline function.  I would
ideally like to outline the entire head and have a set number of
landmarks digitally placed along the curve.



Dustin Owen
dao...@bsu.edu mailto:dao...@bsu.edu





--
*Kalpana*
MSc.Biodiversity and Conservation(2009-11)
University School of Environment Management
Guru Gobind Sigh Indraprastha University
Dwarka,Delhi-110075
Email- kkalpanaa1...@gmail.com mailto:email-kkalpanaa1...@gmail.com
Mobile no-9620313751/8010255368

/Not everything that counts can be counted, and not everything that can
be counted counts.

/



Soft tissue analyse

2012-05-13 Thread morphmet



 Original Message 
Subject:Soft tissue analyse
Date:   Wed, 9 May 2012 12:55:57 -0400
From:   Julia Klaczko jklac...@gmail.com
To: morphmet@morphometrics.org



Dear all,

I would like to quantify the shape of an soft tissue organ. However I am
not sure what would be the best method to use.
Working with soft tissue organs, I am having two problems: one is the
absent of landmarks, and the other is that sometimes the preparation of
the specimens may cause some deformations on the shape.   Is there any
way to get around this situation?
Thank you very much for your help,
Julia

--
Julia Klaczko
Museum of Comparative Zoology and
Department of Organismic and Evolutionary Biology
Harvard University
26 Oxford St.
Cambridge, MA 02138
phone: 617-384-8437 tel:617-384-8437



RE: permutations in TPSRegr and asymmetry in pictures

2012-05-02 Thread morphmet



 Original Message 
Subject: RE: permutations in TPSRegr and asymmetry in pictures
Date: Thu, 26 Apr 2012 22:07:27 -0400
From: F. James Rohlf ro...@life.bio.sunysb.edu
Reply-To: ro...@life.bio.sunysb.edu
Organization: Stony Brook University
To: morphmet@morphometrics.org

What the tpsRegr  program does is pretty simple. For the 'all option' it 
just scrambles the order of the independent variable relative to the 
dependent variable across all individual specimens.


For within blocks it simply scrambles the order within each block (it 
assume blocks correspond to adjacent specimens in the input files). An 
example could be where the blocks corresponded to individuals and a pair 
of observations within each block could correspond to its shape before 
and after some treatment that could change its shape.


For the among blocks option it scrambles the order of the blocks but 
keeps each block intact. This would give a user an idea of how important 
the blocks were.


I will have to add more text to the help file! I should add some more 
options to make the program more flexible.


Jim

--
F. James Rohlf, John S. Toll Professor, Stony Brook University
The much revised 4th editions of Biometry and Statistical Tables are now 
available:

http://www.whfreeman.com/Catalog/product/biometry-fourthedition-sokal
http://www.whfreeman.com/Catalog/product/statisticaltables-fourthedition-rohlf
 Please consider the environment before printing this email



-Original Message-
From: morphmet [mailto:morphmet_modera...@morphometrics.org]
Sent: Wednesday, April 25, 2012 5:00 PM
To: morphmet
Subject: permutations in TPSRegr and asymmetry in pictures



 Original Message 
Subject: permutations in TPSRegr and asymmetry in pictures
Date: Mon, 23 Apr 2012 07:16:58 -0400
From: andrea cardini alcard...@gmail.com
To: morphmet@morphometrics.org

Dear Morphometricians,
please, has anyone got any experience with the different options for
permutation tests in TPSRegr?
I did not manage to find an example in the help file but I may have missed it 
and
would really like to find something like the detailed protocol Jim describes for
the test of common slopes etc.

A second unrelated question. I was wondering how studies of asymmetries
might be affected by using pictures of 3D objects (e.g., human faces).
I can easily imagine biases that could spuriously introduce DA in the data and
may not be obvious to detect. Even without any systematic error, I wonder
whether the 2D approximation of a 3D object may affect FA.

Thanks for your help.
Cheers

Andrea



Dr. Andrea Cardini
Dipartimento di Biologia, Universitá di Modena e Reggio Emilia, via Campi 213,
41100, Modena, Italy
tel: 0039 059 2055017 ; fax: 0039 059 2055548

Centre for Anatomical and Human Sciences University of Hull, Cottingham Road,
Hull, HU6 7RX, UK University of York, Heslington, York YO10 5DD, UK

Centre for Forensic Science , The University of Western Australia
35 Stirling Highway, Crawley WA 6009, Australia

E-mail address: alcard...@gmail.com, andrea.card...@unimore.it
Webpage: http://sites.google.com/site/hymsfme/drandreacardini

Editorial board for:
Zoomorphology:
http://www.springer.com/life+sciences/animal+sciences/journal/435
Journal of Zoological Systematics and Evolutionary Research:
http://www.wiley.com/bw/journal.asp?ref=0947-5745site=1
Hystrix, the Italian Journal of Mammalogy:
http://www.italian-journal-of-mammalogy.it/








Re: Alternatives to Geomagic (UNCLASSIFIED)

2012-05-02 Thread morphmet

Correction as per Dr. Corner:

archit...@headus.com.au
should be
archi...@headus.com.au.

-the mod [dslice]

On 5/1/12 11:38 PM, morphmet_modera...@morphometrics.org wrote:


- Forwarded message from Corner, Brian D CIV (US) -

Date: Tue, 1 May 2012 12:49:27 +
From: Corner, Brian D CIV (US)
Reply-To: Corner, Brian D CIV (US)
Subject: Alternatives to Geomagic (UNCLASSIFIED)
To: morphmet_modera...@morphometrics.org

Classification: UNCLASSIFIED
Caveats: NONE

RapidForm is more expensive than GeoMagic, at least it was until GM
raised its price. I’ve pretty much given up working with MeshLab, after
spending a very frustrating afternoon trying to merge a couple very high
density meshes. Too many crashes and quirks. In the 3d Lab here at the
US Army Natick Soldier RDEC, we used CySlice and related software from
Headus (http://www.headus.com.au/home). Headus is run by Phil Dench 
Jill Smith (Perth, Australia) who started supporting Cyberware scan
merging  editing way back when (1995-ish). Phil’s software is very
useful and more-or-less user friendly (we call it Phil-friendly). He
uses his own flavor of PLY which cannot be read by MeshLab, kind of a
pain but we wrote a little converter we can share. His on-line  email
support is superb. Price is reasonable and within the range of most
grants. He has provided 30-day trials in the past. You may contact
Headus through the above link or Phil directly at
archit...@headus.com.au http://mailto:archit...@headus.com.au.

For full disclosure, I have an on-going contract with Headus to support
the software we purchased.

Cheers,

-bc

*

Brian D. Corner, PhD

Research Anthropologist

WarSTAR

US Army Natick Soldier RDEC

Comm: 508-233-5317

DSN: 256-5317

**

* Note new email address as of 25 April 2012 *

*brian.d.corner@mail.mil*


Classification: UNCLASSIFIED
Caveats: NONE



- End forwarded message -





--
/* Replies will be sent to the (moderated) list. */
For more information visit http://www.morphometrics.org



Re: Regression of Shape with size

2012-05-02 Thread morphmet



 Original Message 
Subject:Re: Regression of Shape with size
Date:   Wed, 2 May 2012 10:09:13 -0400
From:   Antigoni Kaliontzopoulou ant...@gmail.com
To: morphmet@morphometrics.org



Hello Kaplana,

if your images were not made from the same distance and you don't have a
size reference within them that you can use to calibrate and calculate a
scale factor, you are actually lacking information about size in your
coordinates. This means that centroid size is not a correct measure of
size in your case (it is OK for the Procrustes superimposition but it
doesn't represent the relative size of your specimens, because it is not
standardised).

You could use SVL as the size measure, but that would give you a result
that is difficult to interpret, as it would tell you about the allometry
of the shape of the structure you are studying on total body size (but
not of shape on size of the structure, which can be tricky because you
can have different allometry components in your system).

The best solution would be if you have some size measure you can use to
calibrate your photographs. This does not need to be necessarily
millimetric paper or a ruler: if you have in your pictures a structure
that you have measured (a linear biometric variable you can see well and
without distortion in the photos), you can use that (you would need to
set the reference lengths for each specimen in tpsDig, say by indicating
the distance between the eyes of each animal and inputting the
equivalent measure).

Hope this helps
Antigoni

On Wed, May 2, 2012 at 8:38 AM, morphmet_modera...@morphometrics.org
mailto:morphmet_modera...@morphometrics.org wrote:


- Forwarded message from kalpana das __ -

Date: Wed, 2 May 2012 06:13:10 -0400
From: kalpana das __
Reply-To: kalpana das __
Subject: Regression of Shape with size
To: morphmet@morphometrics.org mailto:morphmet@morphometrics.org

Dear all,
I want to regress the size on shape and want to see how shape is
changing with respect to size.
But i have images without scale factor.
So ,I was just wondering if it is appropriate to use SVL (snout to
vent length in frogs which is equivalent to total body length)
as size instead of centroid size in Tpsregr Programm.
Or is there any other way i can put the scale in images .?
Any kind of suggestion is welcome.

Thank you

Regards,
Kalpana

--
*Kalpana*
MSc.Biodiversity and Conservation(2009-11)
University School of Environment Management
Guru Gobind Sigh Indraprastha University
Dwarka,Delhi-110075
Email- kkalpanaa1...@gmail.com
http://mailto:email-kkalpanaa1...@gmail.com
Mobile no-9620313751/8010255368

/Not everything that counts can be counted, and not everything that
can be counted counts.

/



- End forwarded message -



__




--


Antigoni Kaliontzopoulou

CIBIO, Centro de Investigação em Biodiversidade e Recursos Genéticos
Campus Agrário de Vairão, 4485-661 Vairão
PORTUGAL
Department of Ecology, Evolution, and Organismal Biology
Iowa State University, Ames,
Iowa 50011, USA

tel: +351 91 3086188
mail to: ant...@gmail.com mailto:ant...@gmail.com
antig...@mail.icav.up.pt mailto:antig...@mail.icav.up.pt



Re: Regression of Shape with size

2012-05-02 Thread morphmet



 Original Message 
Subject: Re: Regression of Shape with size
Date: Wed, 2 May 2012 17:01:05 -0400
From: F. James Rohlf ro...@life.bio.sunysb.edu
Reply-To: ro...@life.bio.sunysb.edu
To: Morphmet morphmet@morphometrics.org

If you have the SVL for each specimen then you can use that to set the 
scale for each specimen in tpsDig - assuming that you can see the entire 
distance in each image. You then can use centroid size.

---
Sent remotely by F. James Rohlf,
John S. Toll Professor, Stony Brook University

-Original Message-
From: morphmet morphmet_modera...@morphometrics.org
Date: Wed, 02 May 2012 16:51:27
To: morphmetmorphmet@morphometrics.org
Reply-To: morphmet@morphometrics.org
Subject: Re: Regression of Shape with size



 Original Message 
Subject:Re: Regression of Shape with size
Date:   Wed, 2 May 2012 10:09:13 -0400
From:   Antigoni Kaliontzopoulou ant...@gmail.com
To: morphmet@morphometrics.org



Hello Kaplana,

if your images were not made from the same distance and you don't have a
size reference within them that you can use to calibrate and calculate a
scale factor, you are actually lacking information about size in your
coordinates. This means that centroid size is not a correct measure of
size in your case (it is OK for the Procrustes superimposition but it
doesn't represent the relative size of your specimens, because it is not
standardised).

You could use SVL as the size measure, but that would give you a result
that is difficult to interpret, as it would tell you about the allometry
of the shape of the structure you are studying on total body size (but
not of shape on size of the structure, which can be tricky because you
can have different allometry components in your system).

The best solution would be if you have some size measure you can use to
calibrate your photographs. This does not need to be necessarily
millimetric paper or a ruler: if you have in your pictures a structure
that you have measured (a linear biometric variable you can see well and
without distortion in the photos), you can use that (you would need to
set the reference lengths for each specimen in tpsDig, say by indicating
the distance between the eyes of each animal and inputting the
equivalent measure).

Hope this helps
Antigoni

On Wed, May 2, 2012 at 8:38 AM, morphmet_modera...@morphometrics.org
mailto:morphmet_modera...@morphometrics.org wrote:


 - Forwarded message from kalpana das __ -

 Date: Wed, 2 May 2012 06:13:10 -0400
 From: kalpana das __
 Reply-To: kalpana das __
 Subject: Regression of Shape with size
 To: morphmet@morphometrics.org mailto:morphmet@morphometrics.org

 Dear all,
 I want to regress the size on shape and want to see how shape is
 changing with respect to size.
 But i have images without scale factor.
 So ,I was just wondering if it is appropriate to use SVL (snout to
 vent length in frogs which is equivalent to total body length)
 as size instead of centroid size in Tpsregr Programm.
 Or is there any other way i can put the scale in images .?
 Any kind of suggestion is welcome.

 Thank you

 Regards,
 Kalpana

 --
 *Kalpana*
 MSc.Biodiversity and Conservation(2009-11)
 University School of Environment Management
 Guru Gobind Sigh Indraprastha University
 Dwarka,Delhi-110075
 Email- kkalpanaa1...@gmail.com
 http://mailto:email-kkalpanaa1...@gmail.com
 Mobile no-9620313751/8010255368

 /Not everything that counts can be counted, and not everything that
 can be counted counts.

 /



 - End forwarded message -



 __




--


Antigoni Kaliontzopoulou

CIBIO, Centro de Investigação em Biodiversidade e Recursos Genéticos
Campus Agrário de Vairão, 4485-661 Vairão
PORTUGAL
Department of Ecology, Evolution, and Organismal Biology
Iowa State University, Ames,
Iowa 50011, USA

tel: +351 91 3086188
mail to: ant...@gmail.com mailto:ant...@gmail.com
antig...@mail.icav.up.pt mailto:antig...@mail.icav.up.pt




CT Scan + MorphoJ

2012-04-25 Thread morphmet



 Original Message 
Subject: CT Scan + MorphoJ
Date: Wed, 18 Apr 2012 23:14:11 -0400
From: Gabrielle Openshaw gabrielle.opens...@gmail.com
To: morphmet@morphometrics.org

Hi all,
Has anybody tried using CT scan data in MorphoJ? I want to analyse
skull shape disparity and really need to avoid damaging specimens so
am using a CT scanner to acquire shape data. However, I am only really
familiar with 2D analysis in MorphoJ, and most 3D studies that use
MorphoJ seem to use a surface scanner (digitizer).

Can MorphoJ handle large CT files, or do I need to change them in some
way? If anybody has any suggestions for landmark digitization or an
alternative program for analysis of CT data, please let me know!

Thanks in advance!!
Gabi Openshaw
(gabrielle.opens...@gmail.com)




permutations in TPSRegr and asymmetry in pictures

2012-04-25 Thread morphmet



 Original Message 
Subject: permutations in TPSRegr and asymmetry in pictures
Date: Mon, 23 Apr 2012 07:16:58 -0400
From: andrea cardini alcard...@gmail.com
To: morphmet@morphometrics.org

Dear Morphometricians,
please, has anyone got any experience with the different options for
permutation tests in TPSRegr?
I did not manage to find an example in the help file but I may have missed
it and would really like to find something like the detailed protocol Jim
describes for the test of common slopes etc.

A second unrelated question. I was wondering how studies of asymmetries
might be affected by using pictures of 3D objects (e.g., human faces).
I can easily imagine biases that could spuriously introduce DA in the data
and may not be obvious to detect. Even without any systematic error, I
wonder whether the 2D approximation of a 3D object may affect FA.

Thanks for your help.
Cheers

Andrea



Dr. Andrea Cardini
Dipartimento di Biologia, Universitá di Modena e Reggio Emilia, via Campi
213, 41100, Modena, Italy
tel: 0039 059 2055017 ; fax: 0039 059 2055548

Centre for Anatomical and Human Sciences
University of Hull, Cottingham Road, Hull, HU6 7RX, UK
University of York, Heslington, York YO10 5DD, UK

Centre for Forensic Science , The University of Western Australia
35 Stirling Highway, Crawley WA 6009, Australia

E-mail address: alcard...@gmail.com, andrea.card...@unimore.it
Webpage: http://sites.google.com/site/hymsfme/drandreacardini

Editorial board for:
Zoomorphology:
http://www.springer.com/life+sciences/animal+sciences/journal/435
Journal of Zoological Systematics and Evolutionary Research:
http://www.wiley.com/bw/journal.asp?ref=0947-5745site=1
Hystrix, the Italian Journal of Mammalogy:
http://www.italian-journal-of-mammalogy.it/





No Subject: one of the most remarkable, scientific artifacts of our time -the mod

2012-04-25 Thread morphmet



 Original Message 
Date: Sun, 22 Apr 2012 07:59:15 -0700
From: Fred Bookstein f...@brainmap.stat.washington.edu
To: morphmet_modera...@morphometrics.org


April 22, 2012
 Dear colleagues,

  Anybody who finds themselves anywhere near Vienna during the
 next eight weeks should make a side trip to the Ring
 to see one of the most remarkable
 scientific artifacts of our time: a four-meter-tall (lifesize) cast of
 the surface of a living 2000-year-old olive tree.
 This remarkable object is not in the Naturhistorische Museum
 where it ought to be, but instead finds itself in
 the Theseustempel, the little building inside the Volksgarten that
 originally housed the statue Theseus and the Centaur
 before it was moved to the landing of the grand staircase in
 the then-new Kunsthistorische Museum in 1891.
 Here in the Tempel the cast of the tree is displayed as an art object,
 entitled wisdom?  peace? blank? all of this?,
 by the contemporary Swiss conceptual artist
 Ugo Rondinone, of whom I had never previously heard.
 I found some good views of it on Google Image, particularly this one,
 which shows the scale (and the ceiling of the Tempel):
http://derstandard.at/1334795666279/Wiener-Volksgarten-Der-Wind-als-Bildhauer
 [the German phrase there means The wind as sculptor].

  Whether a representation of a particular
 superannuated organism or instead a work of art,
 this object forces us to keep in mind the
 immense complexity of organismal form (a trope first treated
 in biomathematical terms by Walter Elsasser around 1975) and the likewise
 immense difficulty of saying, in any abstract language, what the
 form of an organism actually is.  In this role the Rondinone piece 
supplies an

 endlessly paradoxical series of challenges to the foundations of
 any competent morphometrics, whether zoological or botanical.
 I recommend the images to anybody on this
 mailing list and the object itself to anyone within a couple
 of hundred miles of Vienna anytime from now through June 24, when
 the exhibit closes and the object is removed. The exhibit is
 free, by the way.

   If you like olive trees as symbols of human transience, here's
 another photo: http://www.dhm.de/ausstellungen/mueller/k_0.htm.
 The human is the dying ex-chancellor of Austria, Bruno Kreisky. The
 tree is 1000 years old, not 2000, but the idea is the same, this
 time photographed by Konrad Mueller.

 Fred Bookstein




MorphoJ and CVA

2012-04-25 Thread morphmet



 Original Message 
Subject: MorphoJ and CVA
Date: Wed, 25 Apr 2012 13:46:30 -0400
From: Robert Ward r.w...@bangor.ac.uk
To: morphmet@morphometrics.org

Please forgive me if I'm making an obvious error. I'm trying to 
reconcile different outputs relating to CVA results in MorphoJ.


The analysis is looking for sex differences in a 6-landmark shape and 
the output from MorphoJ is shown below (I left out the Procrustes tests 
and canonical coefficients). The MorphoJ output seems to suggest that 
CVA was not able to find a set of shape features to make a highly 
reliable discrimination, p=.06, not terrible but not great.


On the other hand, if I export the CV1 scores from that analysis, and 
compare the male and female scores, then I get highly significant 
differences with either a two-sample t-test, t(85)=3.8, p=.0002, or a 
two-sample permutation test, Z=3.55, p=.0004.


So I reckon I am misunderstanding something somewhere. If CVA is finding 
a vector through shape space that best discriminates the two groups, and 
the CV1 score reflects position on this vector, then shouldn't it be 
fine to test for a sex difference by a two-sample test of some kind? If 
so, then I wonder why the big discrepancy between the MorphoJ results, 
and tests using the CV1 scores?


Thanks for your help,
Rob

Canonical Variate Analysis: CVA x6 ... Sex
Dataset: mouthx6
Classification criterion: Sex
Groups   Observations
1.  F   40
2.  M   48

Variation among groups, scaled by the inverse of the within-group variation
Eigenvalues % Variance   Cumulative %
 1.  0.16891938   100.000 100.000

Mahalanobis distances among groups:
F
M  0.8160

P-values from permutation tests (1 permutation rounds) for 
Mahalanobis distances among groups:

F
M   0.0621




categorical variables in pls

2012-04-25 Thread morphmet



 Original Message 
Subject: categorical variables in pls
Date: Wed, 25 Apr 2012 16:46:51 -0400
From: Rodrigo Lima rodrigo.l...@mail.mcgill.ca
To: morphmet@morphometrics.org morphmet@morphometrics.org

Dear morphometricians,

Does it make sense to use categorical variables in a PLS analysis?

I have landmark configurations of animals collected in 3 ecozones, and 
these ecozones succeed each other in a (more or less) latitudinal 
gradient. I think it doesn't make sense to give them values 1, 2, and 3, 
but would it make sense to code them as dummy variables and use these in 
PLS together with other environment variables?


Thank you,
Rodrigo




Announcement of Robert R. Sokal's Death from Mike Bell

2012-04-16 Thread morphmet



 Original Message 
Subject: Announcement of Robert R. Sokal's Death from Mike Bell
Date: Sun, 15 Apr 2012 23:01:28 -0400
From: Michael A. Bell mab...@life.bio.sunysb.edu
Reply-To: mab...@life.bio.sunysb.edu
To: morphmet@morphometrics.org
CC: mab...@life.bio.sunysb.edu

We are sad to report that Distinguished Professor Emeritus Robert R. Sokal
passed away in Stony Brook on Monday, April 9, 2012 at the age of 86.
Prof. Sokal was a founding member of the Department of Ecology and
Evolution at Stony Brook University, co-founder of the methodological
school of Numerical Taxonomy, and the principle investigator for major
research programs in the spatial variation of insects and humans and the
evolutionary response to selection in insects. He supervised the training
of numerous Ph.D. students and taught biometry to a much larger number. He
was a member of the National Academy of Sciences of the USA and received
many other honors during his remarkable career. We in the Department of
Ecology and Evolution at Stony Brook will miss his insights, support, and
friendship.

Prof. Sokal was born into a middle class Jewish family on January 13, 1926
in Vienna, Austria, the only child of Klara and Siegfried Sokal. He fled
the looming Nazi menace with his family in 1938 to Shanghai, China, which
became the refuge for tens of thousands of European Jews during World War
II. Robert attended secondary school and college in Shanghai, earning his
B.S. degree in Biology from St. John’s University in 1947. There he also
met a young Chinese student, Julie Chenchu Yang, who became his wife and
lifelong love. A book entitled Letzte Zuflucht Schanghai (Final Refuge
Shanghai) by Stefan Schomann (2008) in German and translated into Chinese
chronicled Robert’s flight from Vienna, his family’s refuge in Shanghai,
and the start of his life with Julie, before he came to the United States
for his graduate education.

Prof. Sokal received his graduate training at the University of Chicago,
where he earned his Ph.D. in Zoology in 1952 under the direction of
entomologist Alfred E. Emerson and was strongly influenced by Sewall
Wright. He joined the Entomology Department at the University of Kansas in
1951 as an instructor, and rose rapidly through the academic ranks to
Professor of Statistical Biology in 1961. He was recruited by Lawrence B.
Slobodkin to the fledgling Department of Ecology and Evolution at the
State University of New York at Stony Brook in 1968, where he spent the
remainder of his career.

Prof. Sokal’s scientific publications span a broad range of subjects and
seven decades. He published major papers in ecology, evolution,
anthropology, geography, statistics, and of course systematics. His papers
appeared in Science, Nature, PNAS USA, and many of the best specialty
journals in ecology, evolution, systematics, anthropology, and statistics.
He is probably best known to evolutionary biologists and ecologists for
his Biometry textbook with F. James Rohlf, the fourth edition of which he
completed less than a year before his death. A recent search of Google
Scholar indicated that the third edition of Biometry had been cited 19,851
times. Prof. Sokal is also well known as the co-founder of Numerical
Taxonomy with Peter H. A. Sneath in 1963. This work promoted statistical
methods for classification and was controversial both because it advocated
abandonment of traditional evolutionary systematics and led to the debate
between the advocates of phenetic and cladistic methods. Regardless, it is
undeniable that Prof. Sokal pioneered the use of rigorous, objective
statistical methods and the employment of computers in systematics. Prof.
Sokal started his career with dissertation research on patterns of
geographical variation in Pemphigus aphids. Later, he initiated research
on the evolutionary response to selection in laboratory populations of
Tribolium beetles and house flies. His last major empirical project, which
he pursued for more than two decades, focused on analysis of patterns of
spatial variation in human populations for a variety of traits and the
development of new methods for these analyses. Prof. Sokal published 12
books (5 translated) and 206 articles, and his publications have been
cited tens of thousands of times.

Prof. Sokal came to Stony Brook University as a Professor in 1968. He was
named Leading Professor in 1972 and Distinguished Professor in 1991. He
retired in 1995 and became a very active Distinguished Professor Emeritus.
He served as the Chair and Graduate Program Director of the Department of
Ecology and Evolution at Stony Brook University from 1980 to 1983 and as
Vice Provost for Research and Graduate Studies from 1981 to 82. He
remained very active in scientific research, the Department of Ecology and
Evolution, university affairs, and the National Academy of Sciences, even
attending departmental colloquia until the last year of his life, when his
declining health precluded it.

Prof. Sokal

MorphoJ

2012-04-13 Thread morphmet



 Original Message 
Subject: MorphoJ
Date: Fri, 13 Apr 2012 09:31:57 -0400
From: John  Elizabeth Cook jpc...@ptialaska.net
To: morphmet@morphometrics.org

Are there any online tutorials for MorphoJ?




Re: Strange tpsDig2 problem

2012-04-13 Thread morphmet



 Original Message 
Subject:Re: Strange tpsDig2 problem
Date:   Tue, 10 Apr 2012 02:08:25 -0400
From:   Saber Sadeghi sabersade...@yahoo.com
To: morphmet@morphometrics.org




Dear Karl
at first you have to make a file for your samples' pictures with
separate names using tpsUtil before digitizing, then you can see your
pictures and back and forth your digitized pictures using tpsDig toolbar.
hope it can help
saber
--- On *Mon, 4/9/12, morphmet /morphmet_modera...@morphometrics.org/*
wrote:


From: morphmet morphmet_modera...@morphometrics.org
Subject: Strange tpsDig2 problem
To: morphmet morphmet@morphometrics.org
Date: Monday, April 9, 2012, 9:50 PM



 Original Message 
Subject: Strange tpsDig2 problem
Date: Tue, 3 Apr 2012 14:13:39 -0400
From: Karl Fetter karl.fet...@gmail.com
http://us.mc1133.mail.yahoo.com/mc/compose?to=karl.fet...@gmail.com
To: morphmet@morphometrics.org

http://us.mc1133.mail.yahoo.com/mc/compose?to=morphmet@morphometrics.org



Hi Morphometricians,

I have a strange problem in tpsDig2 I want to bring up and see if 
anyone

has experienced the same problem. I have a file that contains images
I've scanned and images I've photographed with an overhead camera set
up. The images are all named with unique names and are contained in one
file. When I make the tps file, and view the images in tpsDig2, it will
skip come images if I'm scrolling though the images with the red Get
next image button, and then skip through different images if I'm using
the red Get previous images button (these buttons are the one at the
top left that you use to scroll through images in your tps file).
tpsDig2 seems to have a preference to skip my scanned images, but not
all of them. It behaves like this on my mac (running VirtualBox) and on
my office computer that runs windows.

So, there are a few images that are in the folder and written to 
the tps

file that I cannot view or digitize landmarks. Has anyone experienced
this? I downloaded tpsDig2 again, but the problem remains.

Any ideas?

Thanks

Karl Fetter



update to tpsUtil

2012-04-09 Thread morphmet



 Original Message 
Subject:update to tpsUtil
Date:   Wed, 4 Apr 2012 22:28:00 -0400
From:   F. James Rohlf ro...@life.bio.sunysb.edu
Reply-To:   ro...@life.bio.sunysb.edu
Organization:   Stony Brook University
To: morphmet@morphometrics.org



I have just uploaded version 1.48 of tpsUtil to the
life.bio.sunysb.edu/morph server. It fixes a problem in the ‘compute
area’ function (thanks to Etienne Low-Décarie) for finding the problem.
It also now includes the ability to transform landmark coordinates in an
.NTS file into a .TPS file (a feature requested by Kevin Parsons).

--

F. James Rohlf, John S. Toll Professor, Stony Brook University

The much revised 4^th editions of Biometry and Statistical Tables are
now available:

http://www.whfreeman.com/Catalog/product/biometry-fourthedition-sokal

http://www.whfreeman.com/Catalog/product/statisticaltables-fourthedition-rohlf

PPlease consider the environment before printing this email



Next Engine scanner protocol

2012-04-09 Thread morphmet



 Original Message 
Subject:Next Engine scanner protocol
Date:   Mon, 9 Apr 2012 18:01:31 +0200
From:   Javier Santos javiersant...@hotmail.com
To: Morphomet New Mailing List morphmet_modera...@morphometrics.org



Hello morphometricians,

I am working with snow vole skulls and have been provided a Next Engine
surface scanner to obtain my shape data. I have done various tests with
the scanner, but I still don't achieve the resolution I was expecting in
the quality of the scans after alignment. I was hoping that somebody who
has used or is using this scanner could give me some tips on how they
program the scanner to obtain their images, such as number of divisions,
starting angle, starting tilt, etc. As well, any tip on what to use to
position and maintain the skull still during scanning (especially as I
use the optional robotic arm for the Next Engine scanner). I would also
appreciate any other useful information you might know on how to obtain
fine morphological data from micromammal skulls using other techniques,
software, etc. Thank you a lot in advance!


All the best,
Javier Santos

Museo Nacional de Ciencias Naturales (MNCN-CSIC)
Biodiversity and Evolutionary Biology Department



Question about integration indices compared at a common level of sampled population variance

2012-04-09 Thread morphmet



 Original Message 
Subject:Question about integration indices compared at a common level
of sampled population variance
Date:   Mon, 9 Apr 2012 14:41:49 -0400
From:   Makedonska, Jana jmakedon...@albany.edu
To: morphmet@morphometrics.org morphmet@morphometrics.org



Dear Morphometricians,

I would like to inquire if some of you are familiar with a method for
comparing magnitudes of morphological integration between species at a
common level of sampled population variance.
This method was first presented in Young et al. (2010) Development and
the evolvability of the human limbs (PNAS 107) and subsequently applied
to cranial integration in papers such as this by Shirai and Marroig (2010).
If you are familiar with this method, I would like to ask how to
interpret the following results:
Two species have integration indices (ICVs in my case calculated as the
standard deviation in eigenvalues divided by the mean eigenvalue) whose
bootstrap distributions extensively overlap, yet their bootstrap
distributions for the average trait coefficients of variation differ
significantly from each other.
As expected, both species show a positive association between the
integration indices and average trait CVs (although the slope is quite
steep).
Would this result mean that the species characterized by a lower average
trait CV has a more integrated structure, because its significantly less
variable traits co-vary more consistently to produce a similar
integration magnitude?

Thanks very much in advance for your input!

Best regards,
Jana



Re: Strange tpsDig2 problem

2012-04-09 Thread morphmet



 Original Message 
Subject: Re: Strange tpsDig2 problem
Date: Mon, 9 Apr 2012 14:58:15 -0400
From: Liu Idárraga liuidarr...@gmail.com
To: morphmet@morphometrics.org

Hi Karl,

I also have files .tps with a mixture of images: obtained with scanner
and also with camera. I haven't had any problems; however, what I did
was to make two files: one for scanner images, and the other for the
camera images. I did the digitalization and then joined them with the
TPSutil. And if I open the new file, showing me all the images with
their landmarks, without problem.
I suggest that you try to do the same with your images.

Regards,

Liu




On 9/04/12 14:20, morphmet wrote:



 Original Message 
Subject: Strange tpsDig2 problem
Date: Tue, 3 Apr 2012 14:13:39 -0400
From: Karl Fetter karl.fet...@gmail.com
To: morphmet@morphometrics.org



Hi Morphometricians,

I have a strange problem in tpsDig2 I want to bring up and see if anyone
has experienced the same problem. I have a file that contains images
I've scanned and images I've photographed with an overhead camera set
up. The images are all named with unique names and are contained in one
file. When I make the tps file, and view the images in tpsDig2, it will
skip come images if I'm scrolling though the images with the red Get
next image button, and then skip through different images if I'm using
the red Get previous images button (these buttons are the one at the
top left that you use to scroll through images in your tps file).
tpsDig2 seems to have a preference to skip my scanned images, but not
all of them.  It behaves like this on my mac (running VirtualBox) and on
my office computer that runs windows.

So, there are a few images that are in the folder and written to the tps
file that I cannot view or digitize landmarks. Has anyone experienced
this? I downloaded tpsDig2 again, but the problem remains.

Any ideas?

Thanks

Karl Fetter






Re: Re: Next Engine scanner protocol

2012-04-09 Thread morphmet



 Original Message 
Subject:Re: Re: Next Engine scanner protocol
Date:   Mon, 9 Apr 2012 16:22:25 -0400
From:   Caley Orr caley@gmail.com
To: morphmet@morphometrics.org



I concur with Heather that the HD Pro software is absolutely essential
and also that doing the final alignment in Geomagic or another software
program usually works better.  Be sure to download the updates to the HD
software as they are released, because NextEngine has made a lot of
improvements over the last few years.  However, with your small samples,
you'll probably want to use one of the standard or high definition
settings (so slower speed) depending on how small your specimens are,
but not necessarily the maximum.  Try the highest SD or first or second
notch in the HD zone.  You can offset the long scan time by doing fewer
divisions.  Nine divisions seems to work out pretty well in most cases
and 16 on the HD setting will probably oversample the surface and make
the files too large to work with.  The HD settings have gotten much
better and there seems to be less noise than there used to be.  Use the
Macro setting and pay attention to the suggested distance from the
scanner (ends up being ~16cm, I believe).

I would try the Align function for putting together the divisions using
the colored 'pins' to match homologous points, use the Volume Merge as
Heather suggests, and then output the merged divisions as a PLY file.
If you are attempting to get the whole skull scanned, then reorient the
specimen, repeat the scan steps and output that second merged scan as a
separate PLY file.  Then do the merge the two PLYs in Geomagic or similar.

I don't bother with the tilt or anything (doing mostly hand bones), so
have no advice there.

Unless these skulls are really tiny (and depending on what anatomy you
need to see), the NextEngine can do a decent job, but can take some
fiddling.  Good luck!

-Caley

--
Caley M. Orr, PhD
Research Instructor
Department of Anatomical Sciences
Health Sciences Center T-8 040
Stony Brook University
Stony Brook, NY  11794-8081

http://www.wix.com/caleyorr/phd



On Mon, Apr 9, 2012 at 3:41 PM, morphmet
morphmet_modera...@morphometrics.org
mailto:morphmet_modera...@morphometrics.org wrote:



 Original Message 
Subject:Re: Next Engine scanner protocol
Date:   Mon, 9 Apr 2012 14:09:32 -0400
From:   Heather Garvin heama...@aol.com mailto:heama...@aol.com
To: morphmet@morphometrics.org mailto:morphmet@morphometrics.org



I haven't scanned anything that small(I was scanning human 
skulls),but I
can tell you that paying the extra money for the HD Pro software 
makes a

world of a difference. Not only does it give you higher quality scans,
but it cuts your scanning time pretty much in half.

Besides that, I was given advice by Matt Tocheri to use the maximum
number of divisions under the highest speed. This may sound
counter-intuitive, but the rationale is that you get better accuracy
when you have more regions of overlap (from different angles). With a
high degree of overlap you can obtain just as many surface points than
going more slowly over less divisions. Also in the slower speeds 
(higher
dpi), it was suggested to me because the laser is going over each 
region

more slowly, there's more of a chance it will pick up noise or reflect
back oddly, creating more inaccuracies. So I followed this advice with
human skulls (using the HD program, highest number of divisions, 
fastest

speed). I'm not sure how it would work out on the smaller skulls.

Finally, the NextEngine software does okay aligning the divisions 
from a

single scan (given that the object doesn't move). I use the Volume
Merge instead of any of the fusion options, to get a uniform mesh.
But I found that it really sucked at aligning more than one 360 degree
scan together (for example, if you took one 360 scan, changed position
and took another). So after each scan I would save the .ply and open it
in another program, such as GeoMagic or Rapidworks, and do the rest of
the aligning and merging in there. The problem is, these programs are
expensive, but if you have an associated engineering program they may
already have an institutional copy.

Hope this helps a little. Goodluck!
--Heather

*




~~__
Heather Garvin*
PhD Candidate
Center for Functional Anatomy  Evolution
Johns Hopkins School of Medicine
http://www.hopkinsmedicine.__org/fae/HMG.htm
http://www.hopkinsmedicine.org/fae/HMG.htm
hmgar...@gmail.com mailto:hmgar...@gmail.com





-Original Message-
From: morphmet morphmet_moderator@__morphometrics.org
mailto:morphmet_modera...@morphometrics.org
To: morphmet morphmet@morphometrics.org
mailto:morphmet@morphometrics.org
Sent: Mon, Apr 9, 2012 1:56 pm
Subject

Re: Strange tpsDig2 problem

2012-04-09 Thread morphmet



 Original Message 
Subject: Re: Strange tpsDig2 problem
Date: Mon, 9 Apr 2012 16:25:09 -0400
From: F. James Rohlf ro...@life.bio.sunysb.edu
Reply-To: ro...@life.bio.sunysb.edu
To: Morphmet morphmet@morphometrics.org

Send me a copy of the tps file (not the actual images) and perhaps I can 
find the problem.

---
Sent remotely by F. James Rohlf,
John S. Toll Professor, Stony Brook University

-Original Message-
From: morphmet morphmet_modera...@morphometrics.org
Date: Mon, 09 Apr 2012 13:20:12
To: morphmetmorphmet@morphometrics.org
Reply-To: morphmet@morphometrics.org
Subject: Strange tpsDig2 problem



 Original Message 
Subject:Strange tpsDig2 problem
Date:   Tue, 3 Apr 2012 14:13:39 -0400
From:   Karl Fetter karl.fet...@gmail.com
To: morphmet@morphometrics.org



Hi Morphometricians,

I have a strange problem in tpsDig2 I want to bring up and see if anyone
has experienced the same problem. I have a file that contains images
I've scanned and images I've photographed with an overhead camera set
up. The images are all named with unique names and are contained in one
file. When I make the tps file, and view the images in tpsDig2, it will
skip come images if I'm scrolling though the images with the red Get
next image button, and then skip through different images if I'm using
the red Get previous images button (these buttons are the one at the
top left that you use to scroll through images in your tps file).
tpsDig2 seems to have a preference to skip my scanned images, but not
all of them.  It behaves like this on my mac (running VirtualBox) and on
my office computer that runs windows.

So, there are a few images that are in the folder and written to the tps
file that I cannot view or digitize landmarks. Has anyone experienced
this? I downloaded tpsDig2 again, but the problem remains.

Any ideas?

Thanks

Karl Fetter




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