Re: ***SPAM*** [MORPHMET] Re: Digitizing landmarks on live larvae

2018-03-14 Thread Avi Koplovich
Hi,
Thank you both!
I asked this question since I guess that deciding on how many 
semi-landmarks I can digitize isn't only a matter of how complex the 
specimen is, or my willing to estimate missing data (Gunz & Mitteroecker, 
2013), but also the number of specimens I posses. So just to clarify Jim's 
answer: 2p-4 means that having for instance 300 specimens I can use a total 
of 154 landmarks in 2D?
Thanks,
Avi

On Wednesday, March 14, 2018 at 5:06:03 AM UTC+2, f.james.rohlf wrote:
>
> Actually the rule is that the number of specimens should be larger than 
> the number of variables 2p-4 not p landmarks in the case of 2D data.
>
>
>
> __
> F. James Rohlf, Distinguished Prof. Emeritus 
> Dept. Anthropology and Ecology & Evolution 
> Stonybrook University
>
>  Original message 
> From: Carmelo Fruciano > 
> Date: 3/12/18 9:51 PM (GMT-10:00) 
> To: MORPHMET > 
> Subject: Re: ***SPAM*** [MORPHMET] Re: Digitizing landmarks on live larvae 
>
> Dear Avi,
>
> I guess it's hard to formulate any rule of thumb.
>
> Some analyses might not be defined if the number of variables exceed the 
> number of observations. Some other analyses might be defined (there is many 
> distance-based analyses nowadays which circumvent that problem).
>
> However, whether a given analysis is defined doesn't mean that the 
> inference is necessarily accurate. I guess it depends on what you plan to 
> test/measure and the effect size you expect.
>
>
> Andrea Cardini has some papers that can give you some hint on this, such 
> as:
>
> Cardini & Elton 2007 - Zoomorphology
>
> Cardini et al. 2015 - Zoomorphology
>
> Cardini & Elton 2017 - Hystrix
>
> They should be downloadable from his website 
> https://sites.google.com/site/alcardini/home/pubs
>
>
> Obviously, having an idea of variation on your own data would be better.
> I hope this helps.
> Carmelo
>
>
>
>
> On 3/12/2018 8:27 PM, Avi Koplovich wrote:
>
> Hi Carmelo,
> Thank you for those answers.
> One more question please:
> I know that the number of specimens should exceed the number of the total 
> landmarks (fixed-landmarks + semi-landmarks). Is there a rule of thumb of 
> by how much or what ratio between specimens to semi-landmarks one should 
> keep? 
>
> Thank you,
>
> Avi
>
> On Sunday, March 11, 2018 at 5:15:24 PM UTC+2, Carmelo Fruciano wrote: 
>>
>>
>>
>> Il 6/03/2018 4:44 PM, Avi Koplovich ha scritto: 
>> > Hi Carmelo, 
>> > Thank you for your answer. 
>> > My project tests for the influence of kairomones of a predator fish on 
>> > the morphology of Salamander larvae during its development. To do this, 
>> > I take pictures every other week of larvae spawned from six different 
>> > females and assigned to 3 treatments: No fish, 3 caged fish, 6 caged 
>> fish. 
>>
>> Hi Avi, 
>> it sounds like an interesting experiment. I will try to answer to your 
>> questions but keeping in mind that I'm not very knowledgeable on 
>> salamander development. 
>>
>> >  1. I intend to use landmark 1 (dorsal connection of the tail fin) as a 
>> > fixed factor. But I thought I may be able to use the tail tip 
>> > (landmark 20) and head tip (landmark 48) as fixed landmarks as 
>> well. 
>> > Do you think it's ok in an ontogeny experiment? 
>>
>> I guess it will depend on how long into ontogeny you will track the 
>> larvae and whether or not that point will "disappear" over ontogeny 
>> and/or slide unreasonably (depends also on your question). You, being 
>> knowledgeable on their biology, are the best judge on that. 
>>
>> > If not, do you think 
>> > it's ok to slide all semi-landmarks of the tail on landmark 1, and 
>> > all head semi-landmarks on an eye landmark? Since the eye isn't 
>> part 
>> > of the head contour, is it ok if I slide one semi-landmark to the 
>> > eye and all rest semi-landmarks of the head one to each other as a 
>> > closed shape? 
>>
>> The point(s) slid relative to the eye won't be sliding along the 
>> direction tangent to the curve you want to approximate (i.e., the 
>> curvature of the head). A good starting point on the method could be 
>> Gunz & Mitteroecker 2013 - Hystrix 
>>
>> >  2. Is it ok if landmarks 1 and 39 slid relative to each other as well 
>> > as 41 and 55, since both describe a closed shape? 
>>
>> It's not particularly desirable (see answer above). 
>>
>> >  3. A

Re: ***SPAM*** [MORPHMET] Re: Digitizing landmarks on live larvae

2018-03-13 Thread f.james.rohlf
Actually the rule is that the number of specimens should be larger than the 
number of variables 2p-4 not p landmarks in the case of 2D data.


__F. James Rohlf, Distinguished Prof. Emeritus Dept. 
Anthropology and Ecology & Evolution Stonybrook University
 Original message From: Carmelo Fruciano  
Date: 3/12/18  9:51 PM  (GMT-10:00) To: MORPHMET  
Subject: Re: ***SPAM*** [MORPHMET] Re: Digitizing landmarks on live larvae 

Dear Avi,
I guess it's hard to formulate any rule of thumb.
Some analyses might not be defined if the number of variables
  exceed the number of observations. Some other analyses might be
  defined (there is many distance-based analyses nowadays which
  circumvent that problem).
However, whether a given analysis is defined doesn't mean that
  the inference is necessarily accurate. I guess it depends on what
  you plan to test/measure and the effect size you expect.



Andrea Cardini has some papers that can give you some hint on
  this, such as:
Cardini & Elton 2007 - Zoomorphology


Cardini et al. 2015 - Zoomorphology
Cardini & Elton 2017 - Hystrix


They should be downloadable from his website
  https://sites.google.com/site/alcardini/home/pubs






Obviously, having an idea of variation on your own data would be
better.

I hope this helps.

Carmelo









On 3/12/2018 8:27 PM, Avi Koplovich
  wrote:



  Hi Carmelo,

Thank you for those answers.

One more question please:

I know that the number of specimens should exceed the number of
the total landmarks (fixed-landmarks + semi-landmarks). Is there
a rule of thumb of by how much or what ratio between specimens
to semi-landmarks one should keep?
Thank you,
Avi




On Sunday, March 11, 2018 at 5:15:24 PM UTC+2, Carmelo Fruciano
wrote:

  

  

  Il 6/03/2018 4:44 PM, Avi Koplovich ha scritto:
  

  > Hi Carmelo,
  

  > Thank you for your answer.
  

  > My project tests for the influence of kairomones of a
  predator fish on 

  > the morphology of Salamander larvae during its
  development. To do this, 

  > I take pictures every other week of larvae spawned from
  six different 

  > females and assigned to 3 treatments: No fish, 3 caged
  fish, 6 caged fish.
  

  

  Hi Avi,
  

  it sounds like an interesting experiment. I will try to answer
  to your 

  questions but keeping in mind that I'm not very knowledgeable
  on 

  salamander development.
  

  

  >  1. I intend to use landmark 1 (dorsal connection of the
  tail fin) as a
  

  >     fixed factor. But I thought I may be able to use the
  tail tip
  

  >     (landmark 20) and head tip (landmark 48) as fixed
  landmarks as well.
  

  >     Do you think it's ok in an ontogeny experiment?
  

  

  I guess it will depend on how long into ontogeny you will
  track the 

  larvae and whether or not that point will "disappear" over
  ontogeny 

  and/or slide unreasonably (depends also on your question).
  You, being 

  knowledgeable on their biology, are the best judge on that.
  

  

  > If not, do you think
  

  >     it's ok to slide all semi-landmarks of the tail on
  landmark 1, and
  

  >     all head semi-landmarks on an eye landmark? Since the
  eye isn't part
  

  >     of the head contour, is it ok if I slide one
  semi-landmark to the
  

  >     eye and all rest semi-landmarks of the head one to
  each other as a
  

  >     closed shape?
  

  

  The point(s) slid relative to the eye won't be sliding along
  the 

  direction tangent to the curve you want to approximate (i.e.,
  the 

  curvature of the head). A good starting point on the method
  could be
  

  Gunz & Mitteroecker 2013 - Hystrix
  

  

  >  2. Is it ok if landmarks 1 and 39 slid relative to each
  other as well
  

  >     as 41 and 55, since both describe a closed shape?
  

  

  It's not particularly desirable (see answer above).
  

  

  >  3. Another worry I have is that landmark 40 which I used
   

Re: ***SPAM*** [MORPHMET] Re: Digitizing landmarks on live larvae

2018-03-13 Thread Carmelo Fruciano

Dear Avi,

I guess it's hard to formulate any rule of thumb.

Some analyses might not be defined if the number of variables exceed the 
number of observations. Some other analyses might be defined (there is 
many distance-based analyses nowadays which circumvent that problem).


However, whether a given analysis is defined doesn't mean that the 
inference is necessarily accurate. I guess it depends on what you plan 
to test/measure and the effect size you expect.



Andrea Cardini has some papers that can give you some hint on this, such as:

Cardini & Elton 2007 - Zoomorphology

Cardini et al. 2015 - Zoomorphology

Cardini & Elton 2017 - Hystrix

They should be downloadable from his website 
https://sites.google.com/site/alcardini/home/pubs




Obviously, having an idea of variation on your own data would be better.
I hope this helps.
Carmelo




On 3/12/2018 8:27 PM, Avi Koplovich wrote:

Hi Carmelo,
Thank you for those answers.
One more question please:
I know that the number of specimens should exceed the number of the 
total landmarks (fixed-landmarks + semi-landmarks). Is there a rule of 
thumb of by how much or what ratio between specimens to semi-landmarks 
one should keep?


Thank you,

Avi


On Sunday, March 11, 2018 at 5:15:24 PM UTC+2, Carmelo Fruciano wrote:



Il 6/03/2018 4:44 PM, Avi Koplovich ha scritto:
> Hi Carmelo,
> Thank you for your answer.
> My project tests for the influence of kairomones of a predator
fish on
> the morphology of Salamander larvae during its development. To
do this,
> I take pictures every other week of larvae spawned from six
different
> females and assigned to 3 treatments: No fish, 3 caged fish, 6
caged fish.

Hi Avi,
it sounds like an interesting experiment. I will try to answer to
your
questions but keeping in mind that I'm not very knowledgeable on
salamander development.

>  1. I intend to use landmark 1 (dorsal connection of the tail
fin) as a
>     fixed factor. But I thought I may be able to use the tail tip
>     (landmark 20) and head tip (landmark 48) as fixed landmarks
as well.
>     Do you think it's ok in an ontogeny experiment?

I guess it will depend on how long into ontogeny you will track the
larvae and whether or not that point will "disappear" over ontogeny
and/or slide unreasonably (depends also on your question). You, being
knowledgeable on their biology, are the best judge on that.

> If not, do you think
>     it's ok to slide all semi-landmarks of the tail on landmark
1, and
>     all head semi-landmarks on an eye landmark? Since the eye
isn't part
>     of the head contour, is it ok if I slide one semi-landmark
to the
>     eye and all rest semi-landmarks of the head one to each
other as a
>     closed shape?

The point(s) slid relative to the eye won't be sliding along the
direction tangent to the curve you want to approximate (i.e., the
curvature of the head). A good starting point on the method could be
Gunz & Mitteroecker 2013 - Hystrix

>  2. Is it ok if landmarks 1 and 39 slid relative to each other
as well
>     as 41 and 55, since both describe a closed shape?

It's not particularly desirable (see answer above).

>  3. Another worry I have is that landmark 40 which I used to
create the
>     comb fan for both the tail and the head is too far from both
of them
>     so it doesn't bypass the bending.
>  4. I'm affraid I don't fully understand why landmark 40 can not be
>     treated as a fixed landmark. In the book of Zelditch 2004,
she says
>     that one of the basic differences between fixed-landmark and
>     semi-landmark is the degree of freedom, while fixed has two
because
>     it is docked on both X and Y axes while semi only on one of
them
>     (depending on the nature of the specific fan). Please
correct me if
>     I'm wrong, but what if I use the side line of the larvae
(which is
>     an anatomical/homologous feature) as my X axis and use the Y
>     component of landmark 1 (dorsal connection of the tail fin)
to dock
>     landmark 40 on the Y axis? Is it wrong because of the
dependency of
>     landmark 40 on landmark 1 regarding the Y coordinate?

I think Don has covered these two very well.

>  5. Emma Sherratt told me she straightened the bent tail-body
using TPS
>     software in her paper Sherratt et al. 2017 - Nature ecology &
>     evolution. In the supplementary material of her paper she
wrote:
>     "To correct for dorso-ventral bending in the landmark
configurations
>     (caused by the joint of the tail with the head/body), we
used the
>     ‘unbend specimens’ function of tpsUtil v.1.86 (Rohlf 2015). The
>     landmark configurations for each specimen were transformed
using the
>     qu

Re: ***SPAM*** [MORPHMET] Re: Digitizing landmarks on live larvae

2018-03-12 Thread Avi Koplovich
Hi Carmelo,
Thank you for those answers.
One more question please:
I know that the number of specimens should exceed the number of the total 
landmarks (fixed-landmarks + semi-landmarks). Is there a rule of thumb of 
by how much or what ratio between specimens to semi-landmarks one should 
keep?

Thank you,

Avi

On Sunday, March 11, 2018 at 5:15:24 PM UTC+2, Carmelo Fruciano wrote:
>
>
>
> Il 6/03/2018 4:44 PM, Avi Koplovich ha scritto: 
> > Hi Carmelo, 
> > Thank you for your answer. 
> > My project tests for the influence of kairomones of a predator fish on 
> > the morphology of Salamander larvae during its development. To do this, 
> > I take pictures every other week of larvae spawned from six different 
> > females and assigned to 3 treatments: No fish, 3 caged fish, 6 caged 
> fish. 
>
> Hi Avi, 
> it sounds like an interesting experiment. I will try to answer to your 
> questions but keeping in mind that I'm not very knowledgeable on 
> salamander development. 
>
> >  1. I intend to use landmark 1 (dorsal connection of the tail fin) as a 
> > fixed factor. But I thought I may be able to use the tail tip 
> > (landmark 20) and head tip (landmark 48) as fixed landmarks as well. 
> > Do you think it's ok in an ontogeny experiment? 
>
> I guess it will depend on how long into ontogeny you will track the 
> larvae and whether or not that point will "disappear" over ontogeny 
> and/or slide unreasonably (depends also on your question). You, being 
> knowledgeable on their biology, are the best judge on that. 
>
> > If not, do you think 
> > it's ok to slide all semi-landmarks of the tail on landmark 1, and 
> > all head semi-landmarks on an eye landmark? Since the eye isn't part 
> > of the head contour, is it ok if I slide one semi-landmark to the 
> > eye and all rest semi-landmarks of the head one to each other as a 
> > closed shape? 
>
> The point(s) slid relative to the eye won't be sliding along the 
> direction tangent to the curve you want to approximate (i.e., the 
> curvature of the head). A good starting point on the method could be 
> Gunz & Mitteroecker 2013 - Hystrix 
>
> >  2. Is it ok if landmarks 1 and 39 slid relative to each other as well 
> > as 41 and 55, since both describe a closed shape? 
>
> It's not particularly desirable (see answer above). 
>
> >  3. Another worry I have is that landmark 40 which I used to create the 
> > comb fan for both the tail and the head is too far from both of them 
> > so it doesn't bypass the bending. 
> >  4. I'm affraid I don't fully understand why landmark 40 can not be 
> > treated as a fixed landmark. In the book of Zelditch 2004, she says 
> > that one of the basic differences between fixed-landmark and 
> > semi-landmark is the degree of freedom, while fixed has two because 
> > it is docked on both X and Y axes while semi only on one of them 
> > (depending on the nature of the specific fan). Please correct me if 
> > I'm wrong, but what if I use the side line of the larvae (which is 
> > an anatomical/homologous feature) as my X axis and use the Y 
> > component of landmark 1 (dorsal connection of the tail fin) to dock 
> > landmark 40 on the Y axis? Is it wrong because of the dependency of 
> > landmark 40 on landmark 1 regarding the Y coordinate? 
>
> I think Don has covered these two very well. 
>
> >  5. Emma Sherratt told me she straightened the bent tail-body using TPS 
> > software in her paper Sherratt et al. 2017 - Nature ecology & 
> > evolution. In the supplementary material of her paper she wrote: 
> > "To correct for dorso-ventral bending in the landmark configurations 
> > (caused by the joint of the tail with the head/body), we used the 
> > ‘unbend specimens’ function of tpsUtil v.1.86 (Rohlf 2015). The 
> > landmark configurations for each specimen were transformed using the 
> > quadratic approach, straightening from the eye (1) along the 
> > notochord landmarks (46 to 55) to the tip of the tail (8)." 
> > Jim mentioned this unbending function here before. I read the help 
> > about unbending specimens and thought I can use landmarks 20 (tail 
> > tip), 48 (head tip) and several semi-landmarks I can digitize using 
> > the comb fan (equally spaced) along the side line of the larvae, in 
> > order to create the quadratic curve (while the side line "helper" 
> > semi-landmarks can be later omitted from the dataset - I saw 
> > Fruciano et al. 2016). Does this sound good? 
> > I bet that this can basically solve the problems I mentioned in 3 & 
> > 4, since then I can digitized the whole body contour. 
>
> That function is great but, as everything, relies on a set of 
> assumptions (see also Fruciano 2016 - Development Genes and Evolution 
> for a brief discussion). In your case: 
> - that you can consistently identify those points along an hypothetical 
> line (which you wo

Re: ***SPAM*** [MORPHMET] Re: Digitizing landmarks on live larvae

2018-03-11 Thread Carmelo Fruciano



Il 6/03/2018 4:44 PM, Avi Koplovich ha scritto:

Hi Carmelo,
Thank you for your answer.
My project tests for the influence of kairomones of a predator fish on 
the morphology of Salamander larvae during its development. To do this, 
I take pictures every other week of larvae spawned from six different 
females and assigned to 3 treatments: No fish, 3 caged fish, 6 caged fish.


Hi Avi,
it sounds like an interesting experiment. I will try to answer to your 
questions but keeping in mind that I'm not very knowledgeable on 
salamander development.



 1. I intend to use landmark 1 (dorsal connection of the tail fin) as a
fixed factor. But I thought I may be able to use the tail tip
(landmark 20) and head tip (landmark 48) as fixed landmarks as well.
Do you think it's ok in an ontogeny experiment?


I guess it will depend on how long into ontogeny you will track the 
larvae and whether or not that point will "disappear" over ontogeny 
and/or slide unreasonably (depends also on your question). You, being 
knowledgeable on their biology, are the best judge on that.



If not, do you think
it's ok to slide all semi-landmarks of the tail on landmark 1, and
all head semi-landmarks on an eye landmark? Since the eye isn't part
of the head contour, is it ok if I slide one semi-landmark to the
eye and all rest semi-landmarks of the head one to each other as a
closed shape?


The point(s) slid relative to the eye won't be sliding along the 
direction tangent to the curve you want to approximate (i.e., the 
curvature of the head). A good starting point on the method could be

Gunz & Mitteroecker 2013 - Hystrix


 2. Is it ok if landmarks 1 and 39 slid relative to each other as well
as 41 and 55, since both describe a closed shape?


It's not particularly desirable (see answer above).


 3. Another worry I have is that landmark 40 which I used to create the
comb fan for both the tail and the head is too far from both of them
so it doesn't bypass the bending.
 4. I'm affraid I don't fully understand why landmark 40 can not be
treated as a fixed landmark. In the book of Zelditch 2004, she says
that one of the basic differences between fixed-landmark and
semi-landmark is the degree of freedom, while fixed has two because
it is docked on both X and Y axes while semi only on one of them
(depending on the nature of the specific fan). Please correct me if
I'm wrong, but what if I use the side line of the larvae (which is
an anatomical/homologous feature) as my X axis and use the Y
component of landmark 1 (dorsal connection of the tail fin) to dock
landmark 40 on the Y axis? Is it wrong because of the dependency of
landmark 40 on landmark 1 regarding the Y coordinate?


I think Don has covered these two very well.


 5. Emma Sherratt told me she straightened the bent tail-body using TPS
software in her paper Sherratt et al. 2017 - Nature ecology &
evolution. In the supplementary material of her paper she wrote:
"To correct for dorso-ventral bending in the landmark configurations
(caused by the joint of the tail with the head/body), we used the
‘unbend specimens’ function of tpsUtil v.1.86 (Rohlf 2015). The
landmark configurations for each specimen were transformed using the
quadratic approach, straightening from the eye (1) along the
notochord landmarks (46 to 55) to the tip of the tail (8)."
Jim mentioned this unbending function here before. I read the help
about unbending specimens and thought I can use landmarks 20 (tail
tip), 48 (head tip) and several semi-landmarks I can digitize using
the comb fan (equally spaced) along the side line of the larvae, in
order to create the quadratic curve (while the side line "helper"
semi-landmarks can be later omitted from the dataset - I saw
Fruciano et al. 2016). Does this sound good?
I bet that this can basically solve the problems I mentioned in 3 &
4, since then I can digitized the whole body contour.


That function is great but, as everything, relies on a set of 
assumptions (see also Fruciano 2016 - Development Genes and Evolution 
for a brief discussion). In your case:
- that you can consistently identify those points along an hypothetical 
line (which you would remove after the unbending)

- that your arching is well represented by the chosen function

You are the best judge on whether these assumptions are satisfied in 
your case or not.
I suggested the Valentin et al. (2008 - Journal of Fish Biology) 
approach because it's more flexible (less stringent assumptions, which 
obviously doesn't mean assumption-free) and therefore more generally 
applicable. But, of course, the approach in tpsUtil can be a great 
solution if it's appropriate to your data.


Best,
Carmelo

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