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Submit your abstract for the Symposium organised by Ivana Rešetnik and me at the XX International Botanical Congress in Madrid (21-27 July 2024)!
The deadline for abstract submission is November, 30 for oral presentations and February 1, 2024, for posters.
The general link to the congress: https://ibcmadrid2024.com/
Our symposium is the n. 13
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Thank you
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Hello, I am a dentist doing my research to graduate. I am measuring a bone structure of the skull in adolescents through morphometric analysis. This is my first time using this kind of software. I am been reading some information in internet and I was looking for MorhoJ sotware but it is no available on internret anymore. Could you recommendme another one. Thanks
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From my view IdavLandmark is the better option
All the best for your work
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I have a drainage network polyline feature the course of which is structurally controlled. To determine the dominant direction trends of the streams I need to plot a rose diagram. However, I am unable to derive directions of these polylines. There are 3500+ streams present in my AOI.
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In ArcGIS, you can determine the direction of a polyline feature by using the "Calculate Geometry Attributes" tool.
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I wish to conduct a study involving the geometric morphometric analysis of entorhinal cortex and hippocampal shape variations. As I hope to acquire MRI scans from online databases, I would just like to ask if there are any recommended MRI parameters that accurately capture the overall shape of these two structures. For example: would it be more ideal to gather T1-weighted or T2-weighted images, and what imaging plane (e.g. axial, sagittal, coronal) would be optimal for viewing these structures?
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You may consider using the following software when you're ready to collect landmark point data to support your geometric morphometric analysis:
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Dear all:
Greetings,
I'm asking this question to look for experts' advice for our thesis. We are looking to study x-ray images of human hands with and without osteoarthritis, and use geometric morphometrics as a tool in trying to find something new out of it (i.e. possibly quantify the differences between the severity levels of osteoarthritis based on the alterations in the bone/joint structure). In line with this, we would want to hear your thoughts regarding what specific bones/joints are best to focus on in carrying out the study. Your answer/idea regarding this matter would be much appreciated.
Thank you and God bless!
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Which ever joint you decide to analyze, you may want to try using the joint primitive within the Checkpoint software below:
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there are many papers using channel classification as single phase and two phase but i am not able to find the definition of the both type of channels. Most of such studies used reference as Brice classification, but i am not able to find the that paper.
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I am not familiar with this classification to comment, but the meaning of phase is not obvious to me from the diagram. Phase is not a term I remember being used in describing channels.
I think the classification developed by David Rosgen would be more helpful and descriptive. His classification has been reviewed and recommended by Luna Leopold and many field hydrologists have used the Rosgen classification as a descriptive and analysis tool.
Of course, there may be other river, stream and channel classifications, descriptions and possibly terms that have been developed, and applied. If it is a common term used in your region, then hopefully you can find applicable answers to its meaning.
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I need to do a morphometric analysis of a watershed using ARC GIS software. However I am unable to find the morphometric toolbox to perform the analysis. Please advice where can I get the tool box from??
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Thankyou @Mainak choudhuri
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Leaf morphometric analysis
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You can use leaf area meter of LiCor for leaf blade width.. not sure if it would help with leaf base angle
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I am trying to determine how the facial deformity progresses in juvenile cisco over time in various treatment groups using geometric morphometrics. Our first sample (taken 1 week after being put into their treatments for acclimation), had significant differences in shape. We want to correct for these significant differences by compiling all our samples (weeks 1-8) into one PC analysis and determining the PC score for our first-week treatment groups. Could we then use these week 1 PC scores as a covariate for a Procrustes analysis on a week-by-week basis? We are already tried to correct for differences using length, but that didn't work. Could the PC score realistically work as a covariate? If not, are there any other ways to correct for differences in that first week?
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You should be able to complete the analysis using RRPP (which can handle mixed models). The pairwise function in RRPP is more flexible than trajectory analysis because you use it after running the model to set up the pairwise comparisons that you want to do. You run the model, see if you have interesting interactions, and design the pairwise analyses to show you whether those are because of different magnitudes of directions of the response. I thought of the trajectory analysis because of the "shape" parameter which compares the shapes of the curves (of the response, over time), but there are many possibilities for designing analyses. You know that there are differences at the outset, but you can compare population means over the course of the treatment to find out if they increase/decrease of if the differences, over time, are in the same direction. So even if your design isn't optimal, there is a lot that you can do.
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Using ArcMap, Archydro or any other application package
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ArcHydro does all you need. But simply, Upstream Flowlength + Downstream Flowlength = Basin Length
You can distinguish the ridgelines by analyzing the flow direction and/or aspect map of the watershed.
Topographic Index ; I am sorry I know several indexes maybe you write the exact equation that you need.
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In first order watersheds, can the shape index (Ff=A/Lb²) and the elongation ratio (Er=(2/Lb)*(A/Pi^0.5) return values >= 1?
Working with large watersheds, these values tend to be < or = unity. However, working on small hydrographic basins (1st order) I find some volers above the unit.
Is there any convention that the values of Ff and Er cannot exceed unity?
Thanks.
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It is necessary to define the parameters which are in your formula Ff=A/Lb² because in this form Ff is not dimensionless.
Usually, the following parameters are defined for the watershed:
1. Form factor: Watershed Area/(Watershed length)2 = A/L2, Value < 1
2. Shape factor Bs : (Watershed length)2/Watershed Area = L/A2, Value > 1
3. Elongation ratio: Diameter of the circle of watershed area / Watershed length = 1.128A0.5 /L, Value < or equal to 1.
4. Circulatory ratio: Watershed area/Area of the circle of watershed area = 12.57A/P2, where P is the watershed perimeter, Value < or equal to 1
5. Compactness Coefficient: Watershed perimeter/perimeter of the circle of watershed area = 0.2821P/A0.5, Value > or equal to 1.
Regards
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Query on research tool
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Dear collegue .
Arc hydro in Arc GIS will be morehelpfull tool for your task.
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It has been noted in many researches that gully headcuts are main drivers of gully erosion and upstream migration. Most commonly used definitions describe gully headcut as near-vertical step at which most intense erosion occurs, e.g.:
Rengers and Tucker, 2014. - Headcuts are near‐vertical steps that erode the valley network by migrating upstream over time (Bull and Kirkby , 2002) and add mobile sediment to gully channels downstream (Tucker et al. , 2006).
Vanmaercke et al., 2016. - A gully headcut is a natural, nearly vertical drop in gully channel-bed elevation (Poesen et al., 2003).
Since these are predominately descriptive definitions, I would like to know is it possible to delineate quantifiable definition of a gully headut ?
Such definition would be based on measurements that could be extracted from high-resolution DEM (e.g. required slope angle; headcut horizontal length; headcut height…), rather than on the descriptive, non-quantifiable information.
I understand that such definition would vary depending on local terrain characteristics and characteristics of local gully erosion predisposing factors. But even general quantifiable definition would be very helpful for detection of gully headcuts.
In the attachment is large gully headcut from my research study area, located at Pag Island, Croatia. Within Pag Island large number of small headcuts can be found, that are less distinguishable then the one in this picture.
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That is a good question.
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I am working with dem images for morphometric analysis. I am using topotoolbox for Ksn calculation. In my study area there is several dams in a single river and when I am using topotoolbox, it is taking the stream reach between two dams as the longest river stretch resulting in an erroneous result. I wan to effect of the dam from the dem for further analysis.
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Depends on the software and whether you have mapped all of the dams or not. I've done something similar with culverts in order to "hydro condition" the DEM. If you have GIS software like ArcGIS or QGIS you can digitize small polygons on top of where the dam is. Then attribute those polygons with the elevation of the river below the dam. Convert the polygon to a raster with the same cell size as your original DEM. In ArcMap you can run the mosaic tool, add both the new rasters and the original DEM, and then set the preference for FIRST but making sure that the new rasters are on top in terms of the order that you enter them into the mosaic tool. The general approach can also be automated if you have a shapefile of dams and the locations are accurate.
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To compare morphometric data of two or more bees.
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Specifically what kind of analysis you have in mind? You can use any kind of general morphometry software like MorphoJ (https://morphometrics.uk/MorphoJ_page.html) or R package like geomorph (https://cran.r-project.org/web/packages/geomorph/geomorph.pdf).
The measurements themselves can be done in a variety of ways (micrometric eyepiece, software like Digimizer, etc), and the analyses can be performed with any kind of statistical software.
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Using TPS Series of Prof. James Rohlf for resolving problems related to morphology is a common technique in academia. I already used this series in previous successful works, however I do not remember how we can produce NTS files for Thin Plate Spline analysis. I appreciate any help from experts.
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Is there a certain point in the procedure where you are getting stuck? Or maybe an error message ?
I know you may have already tried these, but they were helpful to me when I got stuck with a similar problem -
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Hi,
I am creating stream orders for morphometric analysis.
At what threshold will we write to the "Con" tool when creating a stream? (Example "Value > 100").
As known, this affects all accounts as it affects the number of Strahler stream orders.
How can I determine the threshold that I am going to write in the "Con" tool and that is suitable for my basin?
Best wishes, Ahmet.
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First need to determine in which stream order network delineation then based on the river order determine the threshold value.
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1.Mean Bifurcation Ratio (Rb)
2.Drainage Density
3.Stream Frequency
4. Form Factor
5.Stream length Ratio (RL)
I am able to find values for the above using certain formulae. But, how do I know if it is less or more and what does it signify?
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I see that there is another scientific shortcut looming, purporting the well-known “philosopher´s stone” of geomorphology and basin analysis. It is similar to the approach taken in geochemistry where a plethora of indices and ratios pretend to avoid experience and knowledge in geology and mineralogy prior to the use of endless numerical datasets.
In the current issue there will be no by-pass of geoscientific anamnesis and visual examination (mapping, sampling leading to 2- and 3-D visualization as well as follow-up laboratory analysis.
Numerical analysis encompassing hydrography such as sinuosity of channel systems, slope angle must be supported by hydrodynamic investigations (GMS tool = granulometry, morphology, situmetry) all of which is grouped under the header “geoscientific measurements, analysis, and computations”. It needs to be corroborated by measurements in structural geology and by in-door analysis of the mineralogy, petrography and chemistry as well geochronology using methods appropriate for the Quaternary and Neogene , in particular. Any stand-alone synthetic geomorphometric analysis will yield synthetic results.
To substantiate my arguments I refer to the following papers dealing with this holistic approach in basin analysis and geomorphology.
DILL, H.G., BUZATU A., BALABAN S.-I. , UFER K., GÓMEZ TAPIAS J., BÎRGĂOANU D. and CRAMER T. (2020) The “badland trilogy” of the Desierto de la Tatacoa, Upper Magdalena Valley, Colombia, a result of geodynamics and climate: With a review of badland landscapes.- Catena 194: 1-20.
DILL, H.G., BUZATU A., BALABAN S.-I. , UFER K., TECHMER A. SCHEDLINSKY, W., and FÜSSL M., (2020) The transition of very coarse-grained meandering to straight fluvial drainage systems in a tectonized foreland-basement landscape during the Holocene (SE Germany) – A joint geomorphological-geological study.- Geomorphology (in print)
Available and ready for download on the RG server.
H.G.Dill
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I'm using MorphoJ, and the software gives me the eigen values but it doesn't give you the eigen vector. For each landmark it gives you a x and y value for each PC but I'm looking for a value that showesme which ones vary more. Is there any command on the software to see this?
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Dear Alejandra,
The eigenvectors are available in MorphoJ in tabular form in the text ouput. They are called 'PC coefficients'.
Best,
Dimitri
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I have cell images from Confocal Microscopy and want to do Nuclear Morphometric Analysis. Can anybody share a detailed protocol to do so?
Thanks in advance.
Swarnali
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If you are good in Python/R there are couple of scripts available. If not, try ImageJ- depends on what depth of morphometry analysis you want to do. You can also use NucleusJ plugin in Image J. Check these paper-
Good Luck !!!
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SL gradient index = (change in elevation/change in length of river)*L(river length), how can we calculate the L values?
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The length of river (L) can be defined in two ways; 1) straight line from river head to mid of two point of measurement or 2) the slope of the length of river from head river to mod of two point of measurement.
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After flow accumulation analysis, what will be the criteria to define the threshold to extract the stream network from DEM? As stream threshold value will influence the extracted drainage networks and stream order level and thus the basin morphometric analysis.
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I think it depends on your requirements. Each software comes with default parameters, but they can be adjusted to increase or decrease the number of streams. The topography is an important factor, flat areas do not require a dense drainage extraction.
You could try with GRASS GIS, see the documentation of r.stream.extract module.
Lizardo
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I'm testing different methods of calculating missing landmarks for geomorphic morphometric analysis of rodent footprints. After an initial literature review, I came across Bayesian PCA (BPCA) and a least squares regression (LSQR). After calculating these, in R using the PCA wrapper functions in pcaMethods package for BPCA and the best.reg() for LSQR, I am left with a 2D matrix (I believe nxm), but require a 3D array (pxkxn) for all Procrustes analysis. Unfortunately I am struggling to do this step, any advice?
Note: I've tried arrayspecs() in geomorph and vecx() in Morpho. vecX() produced a matrix, but then Procrustes analysis failed to work due to an error with pcAlign.
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Your welcome
regards
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I have exactly the same question as the person who is asking in this link:
All I know is that the number of rows and columns in this matrix are double the number of landmarks because one of them (either rows or columns) represents the variables, that is, the x- and y- coordinates of the landmarks within the tps format. The main issue with interpreting this matrix would be figuring out how does R arrange the variables. I'm guessing this would be 1x, 1y, 2x, 2y, 3x, 3y,...
Also this does not explain why columns and rows are BOTH double the number of landmarks. I'm (again) guessing that columns are (maybe) representing variables, and rows are (maybe) representing a number of principal components arranged by variation percentage explained, set by default to be the same as variables.
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I would not try to interpret the pattern of loadings by reading the numbers. Instead, I would plot the results. The function returns the shapes at the extreme values for each PC, so you can use the plotRefToTarget function to show the difference between the two extremes (or you could show the change from the mean to an extreme. In this example, the shape data are coordinates of landmarks, in a 3D array, in a file called "niger.shape". This returns a plot of the scores and the changes along the first two PCs, from the shape with the minimum to the maximum score along each.
niger.gm<-gm.prcomp(niger.shape)
plot(niger.gm,pch=21,cex=1.5,bg="black")
plotRefToTarget(niger.gm$shapes$shapes.PC1$min,
niger.gm$shapes$shapes.PC1$max,method="vector")
title("PC1")
plotRefToTarget(niger.gm$shapes$shapes.PC2$min,
niger.gm$shapes$shapes.PC2$max,method="vector")
title("PC2")
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I am working on fish geometric morphometrics using truss network. I have fishes of one species from two sites. I have applied Principal component analysis PCA on the data to extract components. What other statistical tests can be applied on data for comparison of fish morphometrics of two sites. Moreover If I apply other tests, should I apply these tests only on principal components extracted by PCA or on all data. Thank you in anticipation!
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Trust network measurement in fish involves anaesthetizing with benzocaine (ethyl-p-amino-benzoate) [26] before being weighed and measured Figure 1. The first step is to take and record the standard length (LS), post-orbital length (LPO) and maximum body width of the fish. Standard length will be taken from the tip of the upper jaw to the base of the caudal peduncle. Then a truss network is constructed between landmark points, homologous throughout the population, chosen because they describe the major features of the fish (Figure 1). The landmarks were linked closely to the skeletal structure of fish and were easily observed by eye.
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Truss is a geometric protocol for character selection which largely overcomes the disadvantages of conventional data sets and it leads to certain style of analysis. In truss system, homologous landmarks on the boundary of the form are divided into two tiers and paired. The distance measures connect these landmarks into an over determinate truss network which is a series of quadrilaterals each having internal diagonals. Each quadrilateral shares one side with each succeeding and preceding quadrilaterals. Please following the link below:
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I'm looking for any studies that have used or developed landmarks on the whole body of any species of rhino. I have lateral and posterior view photographs from 6 rhinos (both sexes) over 18 months and would like to assess how their body shape has changed during this time.
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Thanks Bader, your paper is particularly useful.
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Dear All,
I performed an immunohistochemistry in mouse brain tissue looking for astrocytes (stained for GFAP). Now, I would like to evaluate any morphologic change between the different groups I am comparing.
I do know it would be possible with Fiji/ImageJ through Sholl analysis and I did read several papers suggesting so, but I do not understand what I am actually measuring.
Do you have any idea, protocol, suggestion on how to do the image analysis using either ImageJ or another software (I'd prefer an open-source software).
Thank you,
Salvo.
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I used ImageJ, ZEN 2.5, and Imaris® for morphometric analysis of GFAP positive astrocytes.
Take a look:
If you are going to perform a large-scale analysis of 3D astrocyte morphology, I would strongly recommend Imaris. With this piece of software, you can reconstruct individual cells and analyze the number of astrocytic protoplasmic processes. The analysis of the stain intensity and cell volume can be done very easily in ZEN 2.5, which is much more powerful compared to ImageJ.
Good luck!
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I tried to use Morphologika to format my data, but even the sample data set won't work (a message pops up "error in data") and the new software, EVAN toolbox, costs money to use. I want to be able to look at vectors to examine sex differences in shape to determine the severity and directionality of the sex variation at each landmark. But whenever I attempt to do the compare vector analyses, it says that there isn't enough appropriate data to analyze. Does anyone have this problem? Maybe there's a better software that I can use to study vectors/angles? Any suggestions?
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The angle between the vectors is a measure of the difference in the directions of shape change. If the two vectors point in the same direction, the angle between them is zero. So (in geomorph) the statistical test determines whether that angle exceeds what would be expected by chance. There are two functions that perform the analysis in geomorph, depending on whether the vectors are trajectories between means or regression coefficients (slopes). The functions that did the analyses up until this most recent version of geomorph (3.10) are two of the major changes The function for comparing trajectories between means is trajectory.analysis, which is now in the RRPP package (but geomorph depends on RRPP so this is a minor change except in the manual and in the arguments for the function). The function that compares slopes is now procDlm used in conjunction with anova.lm.rrpp, and pairwise (in the previous version, you'd use trajectory.analysis and advanced.procD.lm) You can see examples of these analyses in the vignette for the newest version of geomorph.
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A little nerdy game:
The attached document shows a selection of suture lines arranged by their values on the 1st three axes of a geometric morphometric analysis on the external suture line of Changhsingian (Late Permian) to Smithian (Early Triassic) ammonoids. This analysis follows strictly the method of Allen (2007), using Windowed, Short-Time Fourier Transform. Since this method uses a mean value between different windows, it cannot be reversed like classical fourier analysis where a shape corresponding to fixed values can be calculate in order to know what do the axes correspond to in term of morphological variation. So I made this diagram to try to decipher it. I of course already have some ideas, but would be curious what others would say about it!
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Kenneth De Baets and it seems you miss my point too. These "classical measurements" cannot be implemented here. Even counting lobes, which seems trivial, cannot be objectively done as soon as the suture line is a bit complex. For example, tell me how many lobes do the 2 sutures with highest PC1 have? Where do you place the boundary between an indentation a bit stronger than the others on one lobe, and a subdivision of a lobe into 2 separate lobe? When does an indentation becomes a proper individualised lobe? My point (and in total disagreement with Dieter) is that these classical measurements or counting are not applicable here. They are easy to make with goniatitic and similar suture lines, but not in this case. These measurements will reflect more the observer's point of view than an actual morphological signal. one of the interests of geometric morphometry is exactly that, to provide an objective description of shape, independent from the observer.
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Please Let me clarify my doubt how to calculate Basin length and Perimeter through ArcGIS software for Morphometric Analysis of River Basin.
Thank you in Advance.
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Hi
for perimeter calculation you just right click on basin shapfile and then select attribute table and then create a field with a specific name. Then right click on this column and select calculate geometry tool. when you select this tool a window will appear that say which geometry you want to calculate. you should choose Perimeter and press Ok button. After this you can find the calculated perimeter..
For basin length calculation you need longest flow path and basin area. By dividing basin area per longest flow path, basin length can be obtained. For calculating longest flow path a suggest you GeoHMS or ArcHydro extensions. If you need more help, don't hesitate to contact me.
the best
Azizian
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In the attached file you can find picture with 13 LM as my suggestion. Many thanks in advance for all comments!
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Thanks Aleks!
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I am exporting a phylogenetic tree with bootstrap from MEGA and I need the following NEXUS format to integrate the phylo data into a geometric morphometric analysis in MorphoJ software.
The following data is an example that can be imported into MorphoJ:
#NEXUS
BEGIN TREES;
Title Imported_trees;
LINK Taxa = Taxa;
TRANSLATE
1 fruticosa,
2 parvifolia,
3 palustris,
4 neumaniana,
5 crantzii,
6 pensylvani,
7 atro_Yellow,
8 atro_Gibson,
9 thurberi,
10 flabellifo,
11 aurea,
12 pimpinello,
13 argentea,
14 saundersia,
15 hirta,
16 heptaphyll,
17 thuringiac,
18 goldbachii,
19 recta,
20 dickinsii,
21 Rosa;
TREE 'Imported tree 0+' = ((((1,2),3),(((4,5),(((6,(7,8)),(9,10)),(((11,12),(((13,14),15),16)),((17,18),19)))),20)),21);
TREE 'Imported tree 1+' = (((((14,6),((16,(15,(((5,(13,4)),((7,8),(9,10))),((17,18),19)))),(11,12))),20),(3,(1,2))),21);
TREE 'Imported tree 2+' = ((((1,2),3),(20,(13,(((14,(7,8)),(10,9)),(((4,5),((17,18),19)),(((11,12),6),(15,16))))))),21);
TREE 'Imported tree 3+' = (((3,(1,2)),(20,(((14,6),(((13,(12,11)),((16,((7,8),((4,(17,18)),19))),15)),(5,10))),9))),21);
TREE 'Imported tree 4+' = ((((1,2),3),((9,(((10,5),((19,((((4,13),16),15),(17,18))),(12,((7,8),11)))),(14,6))),20)),21);
TREE 'Imported tree 5+' = (((3,(1,2)),(((12,11),((((((13,((5,4),((17,18),(15,16)))),19),(14,(7,8))),10),9),6)),20)),21);
TREE 'Imported tree 6+' = (((20,(((10,((14,(7,8)),6)),9),(((11,12),(15,(16,13))),(19,(4,(5,(17,18))))))),(3,(1,2))),21);
[etc.]
END;
Would I have to use a different software (e.g. Mesquite) to create such a format?
Many thanks,
Juniper
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Hi Juniper,
From Mega, you can save your tree in newick format, which can then be read in programs such as FigTree that can export the tree(s) as a nexus file and including the tree annotations.
Best - Thierry
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I ´ve recently submitted a paper dealing with Geometric Morphometrics in plants. I used PCA in order to show variation as a previous step to proceed with statistical tests (Procrustes ANOVA, DAs, etc). One reviewer asked us:
"Are there any reasons why PCA analysis limitations (use of variance, linear projection) should not considered important in this analysis ? This kind of question should be addressed, because they are at the heart of any interesting question anyone would ask in performing such analysis : the relations between morphogenesis and variance. It seems unclear to me, after having read the article, why kernel PCA should not be privileged versus PCA"
As I have never read about kernel PCA in GM papers, I want to know if it should be mandatory to compare it with regular PCA in these kind of papers. If not, what do you think the best response should be?
Thanks you all!
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The justification for PCA is that, being just a rotation of the data, it preserves the Procrustes distances between points in the tangent space. Your plot thus shows the (main dimensions of) variation around the mean in units of Procrustes distance and your Procrustes Anova uses those distances when computing sums of squares. So you are depicting the variation in the same units that you use to quantify deviations from the mean in the statistical analysis. As far as I know, kernel PCA is used when the units are meaningless (or incommensurate across variables). 
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I am working on Insects (Micro-hymenopterans) and trying to differentiate the two species of the same genus using morphometric as a tool. I found that Geometric Morphometric could be used for the objective proposed. So where can I learn this tool.
Please help in this regard.
Thanks in Advance.
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In addition to MorphoJ, you could also use PAST for analysis. It has several tools for morphometrics analysis and it is easy to use, just like MorphoJ. The other thing is you could just enroll for one of Klingenberg's GMM courses. He wrote the MorphoJ software plus he is an excellent teacher!
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I have done morphometric analysis of watershed ,which gives bifurcation ratio as 4.57, elongation ratio is 0.57,shows that this watershed is elongated and peak flow is extended .(it will come early?)
means,if normal watershed what ever peak flow occur ,in elongated watershed ,the peak flow is some what in later stage
is it so!
is anyone has books related to river morphometry(specially for drainage of river is concern),I have refered but few things came across!
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I agree with the answers of both Dr. William and Dr. Kevin. Considering all the other parameters being the same, it is quite a general rule that the occurrence of  flash floods is more in circular watersheds and there is extended time for the peak discharge in the elongated watersheds. There are class books written by the greats like Horton, Strahler and Schumm.
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Concerning methods of rodents measurements: weight, sex-ratio morphologies and craniometrics.
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Have you link of this books ?
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regarding prioritization of watershed and land use pattern
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It is not clear for which river basin. However, what you are asking is a processed information, which will not be available in public domain unless it is published by the analyzer. 
Prioritization of watershed for what purpose ? First of all you have to spell out what type of problem you want to solve, based on that one can guide what parameters you have to study; what approach you have to adopt and what should be your fixation of criteria for prioritization of any given watershed. 
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I want to apply a PCA analysis with missing values for a morphological analysis using bones. Any  method with missing at random (MAR) values? 
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Hi again
I'm dealing with some morphometric data, and I have the doubt if variation in indexes can be due to clinal variation or to separated species.
Could you recommend any paper on the subject?
Thanks a lot!
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Thanks a lot Thomas
I'm running some clustering analysis with R. Quite difficult with so few material available, most of the times just one ant per sample.
Some patterns are emerging, though
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Geometric morphometrics, semilandmarks
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I do not know if it includes reflection, I think you have to do this manually. But better check before doing all the work...
Best, Thomas
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Taking photomicrographs of wings for further geometric morphometric analysis. 
Wings are mounted on microscopic slides with BERLESE mounting medium
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Have you tried using polarized light  filters?  
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method of taking photos in geometric morphometric studies 
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Dear Rahim,
I'm not sure how much this would influence the final results, but lens distortion from the camera itself might influence your landmark positioning as well if you took your photos with different zooms and angles. As long as you don't do image-stacking, your pictures will always have some slight distortion expecially towards the corners of the photo, which will obviously result in different distortions of the object you photograph with variable zoom and angle.
Does anybody know of a study assessing this possible technical error? Would be interesting to see how much that actually influences the landmarks...
Cheers,
Emanuel
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I'm not really sure whether this diatoms are from genus Coscinodiscus or Actinocyclus. Can anyone help me with this identification? Thank you.
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Dear Aysha:
Your first picture belong to the genus Thalassiosira which processes has not external tubes, with a central fultoportula, a rimoportula on the valve surface at ca 11 hs and a marginal ring of fultoportulae. You need internal view of the valve and details of the morphometric data. Your material could belong to the group of T. oestrupii probably.
The other pictures correspond to the genus Actinocyclus, they show submarginal pseudonodula. You need internal views of the valves of the species.
See Tomas (1997) for seeing most important features of genera.
Kind regards.
Eugenia
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We are working with some fossil cones and would like to identify the species, and its closest extant relative, if possible.  Is there a method to determine conifer species on the basis of cone morphology and histology?
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Danilo:
This link may prove to be of some help:
Best
Syed
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I've found a number of tutorials on line but none of them describe step by step how to go about doing this. Any help would be appreciated. I'm including two of the images that I'm trying to process.
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Dear Travis,
Maybe you will find this step-by-step ImageJ morphometrics tutorial useful:
All the best,
Eszter
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Handling out of vocabulary words in morph analysis
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Dear Colleague,
I suggest that you contact Dr. Paula Mabee (in RG).  She has worked intensively on this subject, especially on ontologies. See her list of publications.
Best wishes,
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Dear all,
I am working on morphometry of a beetle community (cca. 30 species) belonging to three distinct families, but some of them clearly showing same way of life. We would like to detect which of 25+ morphological characters (mostly lenghts of different body parts, including legs) can be attributed to convergent evolution (i.e. in species belonging to different families but showing same way of life), and divergences (i.e. in species belonging to the same family but evolved differently, accordingly to their different ways of life).
Is there any explicit test for showing that? Is this possible to test without molecular data? (we know there are three distinct molecular groups, but we do not have our own molecular data)
I would be very happy to receive suggestions of any kind.
All the best,
Jure
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I just found a study of leporid lagomorphs that tackles a similar problem and uses 3D landmarks for morphometrics and phylo-morphospace plots:
Kraatz B, Sherratt E. 2016. Evolutionary morphology of the rabbit skull. PeerJ 4:e2453 https://doi.org/10.7717/peerj.2453
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when I use the "Residuals/Predicted Values From Other Regression" function in MorphoJ, I can't found the independent variables "data matric" and "variables"in the drop-down menus. Is there something wrong during my opretion? Thanks
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Dear Dominique Ponton,
I have sent my project to your email. 
Thanks
Rongrong Li
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I am using 2 curves with 15 evenly-spaced semilandmarks to capture the lateral morphology of a very disparate sample of bird beaks. The 2 curves are constraining by 3 regular lndmks forming a triangle, the tip-of-the-beak one constrains both curves. When I slide the smlndmks in tpsRelw with min-dsquare slide method most of the smlndmks collapse in a very narrow section of both 2 curves in the Procrustes superimposition. Minimum bending energy slide method does not affect the superimposition in this way, but I need to use min-dsquare.  Any idea what is going on here? Is it a bug of the program or is a proper statistical effect?
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You could subdivide the data set, use a subset of the landmarks or use statistical methods to analyze the data in shape space without projecting them onto the tangent space.
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It is possible that these molars have malformations? Or they were just growing in a wrong way ?
I identify them as Mammuthus primigenius? and the black spots represents burning traces. Probably found near a paleolithic site.
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I am an MSc student and for my final thesis project I had set out to perform a comparative morphometric analysis between three avian families. My own dataset of one family returned results, however the dataset I was sent to perform the comparison with is unusable (none of us can work out why or how to fix this). Sadly, I do not have time to repeat any procedure and am having to settle with extremely restricted, unoriginal results. I have PCA results for all datasets, but as I am unable to run the datasets together, I cannot directly compare them.
I am struggling to write my report as no direct comparison between the groups was possible and as such I have no overall results. Is there a 'way' I can still write a decent report?
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Dear Roseanne,
If I am understanding you correctly the data that you have collected yourself plus the others from other workers are the subject of your Master thesis. For some reasons you were asked to do the comparison of three data sets: your own plus other two of other people. You write that the other two data set are not useful at all. Thus, I would suggest that you check the goals of your thesis, that are the foundation of what you are doing, and revise why you were asked for this work. It is not just to say that the other two data sets are not useful, because it is your duty to explain your reasons for saying this. It could be the case that they are not useful, but in sciences it is not just to say that others are wrong; you have to demonstrate that the data from others are wrong! You say that you do not have time now to run new analyses of those two data sets, but this is your problem not a problem of the comparative study that you were asked to perform.  My best suggestion is that you talk to your main advisor as soon as possible, and if it is needed, organize a meeting with your graduate committee about the problem that you have in hands. I strongly suggest to do this, other way you put your thesis in a risky situation.
With my best wishes,
Gloria Arratia
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I  just started working with Geometric Morphometrics. I am using the landmark method to test shape variation in gastropod shells. But with very few homologous landmarks, I also decided to use semi landmarks to capture shell shape. Do I have to digitize semi landmarks as curves? The outlines of my specimens are quite irregular and damaged
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Hi Epa, you can use the draw background curve tool in tps.Dig (yellow pencil) to draw the curves and re-sampled the curve with a number of point which can append to landmarks using tps.util. 
Kind regards
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from srtm data i am getting stream network. in which number of stream are not correct when manually counting. how can i solve this problem?  
1 st image showing wrong and 2nd image denotes correct.  i am getting problem in 1 st image.
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Thank you sir, i will do with the help of advanced editing tools in Arc GIS as your mentioned above. 
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Does anyone know of any (published) 2D geometric morphometric analyses that have used coordinate data that is scaled and transformed, but not rotated?
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In principle, it is possible to scale and translate landmark configurations (to remove variation in size and position), without rotating them. Of course, this requires an interpretable orientation of the studied objects and a common reference system.
Best,
Philipp
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program to do geometric morphometric .
Thanks in advance.
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THank you dear Michael
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Hi, I've wrote a program that calculates the normalized elliptic Fourier coefficients of a closed polyline. I used it for a set of polylines and found that some of the polylines differ in orientation (one part oriented CW, other CCW).
I found NEFD of all polylines and kept them. After that I want to make all polylines oriented CCW, and calculate new set of NEFD. Will the values of NEFD of the polylines, that are previously oriented CW, changed or not?
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I've made a test and found that the orientation of the source outline influences on the signs of NEFD coefficients.
On the attached images there is the same outline with two different orientation. Yellow segments indicate orientation. Bellow are NEFD corresponded to each case (starting from the 2nd harmonic). It is apparent that bn and dn change their sign.
Does obtained results mean that all compared outlines should be equally oriented?
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I have digitized outlines of some exemplars and want to prove that they are belong to two or more different species or constitute one species.
I could not place landmarks on outlines therefore decide to use Elliptic Fourier transform. I found harmonics of EFT but don't exactly know what to do next.
Which method do I need to use to distinguish similar groups through my outlines using EFT harmonics?
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Dear Anton:
I suggest you that you look at my Book Fourier Descriptors and their applications in Biology, Cambridge University Press (1997) for background and some case studies using elliptical Fourier analysis (EFA). Also, if you do an internet search you will find a large number of studies that have now used EFA. I hope this is useful for you. If you have any questions you can reach me at plestrel@earthlink.net.
Pete E. Lestrel, PhD
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I am interested in determining sex in Cape Hare from a collection of mandible.
I have not succeeded in finding anything in the literature. I do however know that sex can be determined via mandibular diastema length in some species of rabbits. 
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check this paper may be u will find it helpe you : C. Mengoni , N. Mucci, E. Randi, 2015 - Sex identification in four leporid species (Lepus corsicanus, Lepus europaeus, Lepus timidus and Lepus capensis mediterraneus)
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I am starting a plant morphometric study and have got a lot of inspiration from Julien Claude's (2008) book. It uses the "Rmorph" package quite much, but I failed to find its copy on CRAN pages. I would be grateful if someone could send me a copy of this package or give a link where to find it.
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I'm not familiar with RMorphand a cursory online search only brings up references to that book.
I've had success with the R Package Geomorph which may be of help to you; it's designed to handle general landmark geometric morphometrics in 2 and 3 dimensions.
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Hello everyone, I'm trying to make a morphometric analysis on Dakhla basin in Egypt using Arc-map 10.2, well I started to delineate the basin of Dakhla in this order: 1- Filling stage, 2- Flow Direction stage, 3- Flow Accumulation stage, after the 3rd stage is done this drainage pattern appeared with the shape presented in the attached file, I couldn't interpret what is the wrong with those straight dashed lines presented in the center of the basin. Is it an error with the DEM data, or is it an error with handling the data? I don't know, so please if anybody could help me with this, I'll be appreciated. Thanks in advance.
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Likely, and I have seem this many times, the DEM developed flat surfaces such as flood plains and terraces, and the flow accumulation tool does not know what to do, so you get straight lines in the direction of the flat slope (grade).  If you obtain LIDAR, you can generally get the stream connections right in modeling or by hand.  If you can see ground surfaces, you may not need LIDAR for this detail.  In wide heavily vegetated valleys, there is no way to predict fairly precise stream connection detail without LiDAR or ground surface surveys.  But as you see, the straight lines are just a remnant caused by how they predict water will flow across a relatively flat surface.  Some flow accumulation modelers have gone to raster with infinite flow directions instead of the normal 8 directions.  But sometimes the DEMs have these flat gradient areas, perhaps from filling sinks or ???  You may have manually go in and correct when streams flow through these flat areas.
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Dear scholars,
I am looking for a paper in which the morphometric analysis or measurements of male and female genitalic attributes have been measured/compared by considering principal component analysis for scatter plot analysis.
I am dealing with populations of certain taxa which are occurring in closely related mountain landscapes.
Critiques and suggestions are welcome.  
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Taking a typical claw for example, the tip of the claw is easy to determined while there is hard to find other landmarks. And there must enough (and not too many ) landmarks for geometric morphometrics analysis.
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This is a problem that people have tried to solve when applying land marks to snail shells, which are almost just a continuous curve, so there are few places on can add fixed landmarks. One solution that I saw was to add a rectangle in a drawing package that touches the extreme edges of the stricture. The four points where the box contacts the structure become homologous locations where fixed landmarks can be added. The slider can be strategically placed between them.
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How should we do a morphometric analysis of a drainage system?
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Googleearth, DEM for morphometric analysis and GIS.
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Has anyone used stationary 3D cameras to reconstruct mesh images of moving objects, and derived morphometrics from them?
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I have found this article about these topic, because I'am interested in farm animal 3D techniques, that's about filming, modelling. And when you have the modell 3D geomorph is close, as I think...
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I'm trying to derive the Nuclear Area Factor index as defined by Mark A DeCoster in 2007 (paper attached).
I've been thinking that morphometric analysis of the nucleus is going to be problematic if nuclear area is merely going to be a function of how deep we cut into the cell. Thus we'd have nuclei of varying sizes but they wouldn't reflect the actual size of the nucleus at its maximum girth but rather just the planar depth of cutting.
My impression is that in monolayer cultures visualised by confocal microscopy in conjunction with nuclear-specific dyes, you *do* get an impression of the full nucleus, whereas images resulting from microtomy have this issue of the planar depth variable. Incidentally some papers I have encountered have ignored this issue and gone ahead with morphometric analysis on nuclei in histological sections.
Do you have any suggestions on how to deal with this?  I cannot do another experiment.  I can only make use of the ultramicrotomy sections I have, in which cells are cut at a variable depth of plane through fixed liver.
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You are entirely correct in your analysis, in that cells grown over slides will tend to be flat and you will have the entire nucleus visualized, whereas tissue sections will have nuclei sections taken at random nuclear sites and orientation. Therefore tissue sections are not the appropriate sample to accurately measure things like cell or nuclear size. However if you are looking for large variations, ie. nuclei that are markedly increased or decreased in size compared to controls, then it might still work; if you measure enough nuclei, you can get beyond the noise inherent in size variation due to sectioning. But if what you are looking for is a subtle, minor difference, you may be out of luck.
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I'm analyzing certain structures in annelids through scanning electron microscopy, and I would like to obtain morphometric data for comparisons.
Could you recommend me free software to do it?
Some features I would appreciate are easy scaling of different images and an intuitive interface.
Thanks.
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Hola Daniel,
Look at this page: SB Morphometrics http://life.bio.sunysb.edu/morph/
by Prof. F. James Rohlf.
Excellent catalogue of software, bibliography, manuals....
Have fun!
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Let's say, I have landmark data for three different structures (A,B,C; e.g. three different teeth along the tooth row or fingers on one hand) for one sample of specimens and I would like to know whether structure A is stronger integrated with structure B than structure B with structure C. Is it possible to compare RV-coefficients calculated for the A-B and B-C interaction and would the resulting difference be valid to make inferences on relative integration strengths?
I have already asked some colleagues about the problem but got somewhat contradicting answers. So I am curious about your opinons. Maybe comparing the values would be possible under the condition of the same landmark number on all structures?!
Best regards,
Stefan
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Well, a problem is that the RV coefficient makes little sense for biological structures because it ignores spatial scale and the distribution of landmarks across a structure. 
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Drainage Texture ratio is Morphometric analysis parameter used to estimate erodibility.
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You may wish to contact Dr. Richard Heck at U of Guelph in Canada.  He does a lot on soil texture, tomography, and such.
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I'm doing morphometric analysis of splenocytes and from the data that I have processed up to now I see quite strange numbers for Feret diameter and I wanna know how big are splenocytes?
Some publications indicate size that range from 8-12 um (peripheral blood Ly) while altered cells (enlarged) above 12 um. How ever other textbook data are that the size of Ly - normal - is fro 8-25 um! This "subtle" differences are the point of my work/analysis can you help me with some suggestions/references?
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Consult any textbook of hematology or clinical chemistry and ask somebody who can guide you personally through the anatomy of granulocytes,lymphocytes and monocytes. You can not feel SAVE without personal feedback from an experienced person.
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Mormophetric analysis.
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thanks
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I have a plan to conduct a study about the different cultivar of cassava found in Romblon. And, to determine the phylogenetic tree of cultivar, what kind of morphometric analysis should I use?
Thank you.  :)
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I am planning to use a Traditional Morphometric Analysis to determine the quantitative measurement of morphological parts. If I already get a morphometric data, is it applicable to undergo a phylogenetic analysis to determine the evolutionary relationship of a different cultivars of Cassava?
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Except resolution of 30 meters, How far is the ASTER DEM accurate for the mapping, for morphometric analysis or any other purpose of study, over SRTM DEM?
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SRTM DEM is better for  Morphometric Analysis compare to ASTER 
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I want to measure aorta diameter but the shape is not find round.
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maybe this reference also can help you:
Importance of Measurement of the Diameter of the Aorta during Peroperative Blood Flow Monitoring; 14th Annual International Conference of the IEEE Engineering in Medicine and Biology Society; p.2402 - 2403; DOI: 10.1109/IEMBS.1992.5761425.