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Question for counting particles from Nanoscope analysis

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Top 150 Contributor
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iwei posted on Thu, Apr 14 2011 2:29 PM

Dear All,

I would like to count particles in the seleted areas by Nanoscope analysis -> particle analysis.  After scanning a image in 1 um, the image shows alot of and condense particles.  I try to find a quatitative number by software.  I move threshold height from low to high and feature direction: above, but I cannot understand the number from total count.  For example: threshold height: 10 nm -->total count: 4, threshold height: 40 nm --> total count: 20, threshold height: 100 nm-->total count: 1.  I understand higher threshold height may has less particles, but why is in lower threshold height only 4? Dose any one know how to get right counting by Nanoscope analysis software?

Thanks a lot~

Iwei

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Top 10 Contributor
288 Posts
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Bruker Employee
Suggested by Bede Pittenger

Iwei,

The help section for Particle Analysis is very good (go to Help -> Help, and search Particle Analysis), and I think should answer your questions. I have also copied it below. If not, can you post your file and settings?

Thanks,

Steve

You are here: Analysis Functions > Particle Analysis

Particle Analysis

The Particle Analysis command defines features of interest based on the height of pixel data. This command was designed for analyzing well isolated particles or features of interest. Particles may be analyzed singly or in quantities. Particles in this context, are conjoined pixels above or below a given threshold height.

The analysis includes a histogram of particle size, which can be used to identify specific particles by size. Measurements on this analysis include: the mean area and standard deviation of the particle sizes, the total number of particles, a correlation histogram, and a depth histogram.

The figure below illustrates how particles can be isolated by height. This type of analysis works well on materials in which particle size or type is linked to height.

Figure: Particles Isolated by Height

Dilate & Erode 

As applied to the Particle Analysis command on NanoScope Analysis images, Dilate is used to clump grains together and Erode is used to separate grains. Pixels comprising an image are evaluated in square matrices (i.e., neighborhoods), sized according to the Neighborhood Size and Number Pixels Off parameters. Executing Dilate will increase the size of particles. Conversely, executing Erode will decrease the size of particles.

Dilate—The effect of digital dilation is to conjoin otherwise separate grains, and to mend broken grains. If the Number Pixels Off for Dilate parameter is set to 1, the dilation process is triggered if even one pixel is off, making dilation more sensitive at a setting of 1. Furthermore, if the Dilate Neighborhood Size is large, dilation is applied to larger areas of the image. Therefore, maximum dilation is attained with a large Dilate Neighborhood Size setting and a small Number Pixels Off for Dilate setting. Minimum dilation is attained with a small Dilate Neighborhood Size setting and a large Number Pixels Off for Dilate setting.

Erode—The effect of digital erosion is to separate grains which otherwise touch or conjoin one another. If the Number Pixels Off for Erode parameter is set to 1, the erosion process is triggered if even one pixel is off, making erosion more sensitive at a setting of 1. Furthermore, if the Erode Neighborhood Size is large, erosion is applied to larger areas of the image. Therefore, maximum erosion is obtained with a large Erode Neighborhood Size setting and a small Number Pixels Off for Erode setting. Minimum erosion is attained with a small Erode Neighborhood Size setting and a large Number Pixels Off for Erode setting. 

Particle Analysis Procedure

The Particle Analysis command is designed to detect and measure the lateral and vertical dimensions of isolated particles on the sample surfaces. The procedure for using Particle Analysis is as follows:

  1. Open an image in NanoScope Analysis.
  2. Select Analysis > Particle Analysis from the Menu bar or click on the Particle Analysis icon from the Icon toolbar. The file opens in the Particle Analysis window with the Detect tab showing.

Figure: Particle Analysis Menu & Window

  1. Choose Above or Below from the Feature Direction parameter in the Detect tab. If the interested features are above the surface, choose Above. If they are below the surface, for example pits, choose Below.
  2. Adjust the threshold by moving the red vertical cursor in the Depth Histogram to the preferred location (usually between the two most defined peaks). The particles (features of interest) will turn to sky blue in the Particle Analysis window. Data for the selected particles is captured at the bottom of the window in the Detect tab Data Box.
  3. When satisfied with the particles selected in the Particle Analysis window, click the Next button at the bottom of the Detect tab. NanoScope Analysis opens the Modify tab.

Figure: Modify Tab

  1. Adjust the Erode and Dilate parameters as preferred. For details on the Erode and Dilate parameters, please click on the following link: Dilate & Erode. Once completed, click on the Next button. NanoScope Analysis opens the Select tab.

Figure: Select Tab

  1. Modify the Select tab parameters to get the desired results. For details on the Select tab parameters, click on the following link Select Tab Parameters. The Select tab also contains 3 histograms: Diameter, Height, and Area. Each histogram provides a different way to analyze particles. Slide the cursor laterally along the bottom of each histogram to highlight each particle plotted. The corresponding data for each particle is displayed in the Data Box at the bottom of the window.

Particle Analysis Interface

Table: Detect Tab Parameters

Parameter Description
Threshold:  
Threshold Height Sets threshold height (distance between the green “substrate” and red “threshold” slider cursors) used to differentiate particle boundaries, exactly as the Red Slider cursor does on the Correlation histogram. Unlike the slider cursor, this parameter allows for precise pinpointing of threshold values.
Feature Direction Select Above or Below, depending if particles are in high or low-lying (e.g. pits) areas of the image.
Depth Histogram:  
X Axis Choose Relative or Absolute
Number of Histogram Bins The number of data points which result from the filtering calculation. Note: Having more histogram bins than pixels is unnecessary.
Histogram Filter Cutoff Lowpass filter which smoothes out the wavelengths that lie below the cutoff in the depth correlation histogram. Used to reduce noise in the Correlation histogram.
Min Peak to Peak Sets the minimum distance between the maximum peak and the second peak marked by a cursor. The second peak is the next largest peak to meet this distance criteria.
Left Peak Cutoff The left (smaller in depth value) of the two peaks chosen by the cursors. Value used to define how much of the left peak is included when calculating the centroid. Note: At 0%, only the maximum point on the curve is included. At 25%, only the maximum 25% of the peak is included in the calculation of the centroid.
Right Peak Cutoff The right (larger in depth value) of the two peaks marked by the cursors. Value used to define how much of the right peak is included when calculating the centroid. Note: At 0%, only the maximum point on the curve is included. At 25%, only the maximum 25% of the peak is included in the calculation of the centroid.

Table: Detect Tab Data Box

Parameter Mean Minimum Maximum Sigma
Total Count Average count of particles in data set Minimum count of particles in data set Maximum count of particles in data set Standard deviation of total count of particles in data set
Density Average density of all particles in data set Minimum density of all particles in data set Maximum density of all particles in data set Standard deviation of density of all particles in data set
Height Average height of all particles in data set Minimum height of all particles in data set Maximum height of all particles in data set Standard deviation of height of all particles in data set
Area Average area of all particles in data set Minimum area of all particles in data set Maximum area of all particles in data set Standard deviation of area of all particles in data set
Diameter Average diameter of all particles in data set Minimum diameter of all particles in data set Maximum diameter of all particles in data set Standard deviation of diameter of all particles in data set

Table: Modify Tab - Dilate & Erode Parameters

Parameter Description
Dilate Erode:  
Neighborhood Size N x N square pixel matrix used to Dilate/Erode an image where N equals the Neighborhood Size. For example, a Dilate/Erode Neighborhood Size of 3 uses a 3 x 3 matrix to evaluate local erosion in the image.
Number Pixels Off Number of “Off” pixels required in a square matrix of Dilate/Erode Neighborhood Size to apply to Dilation/Erosion.

Table: Select Tab Parameters

Parameter Description
Particle Selection:  
Image Cursor Mode Choose Particle Select, Particle Remove or Particle Accumulate.
Boundary Particles When selected, includes particles along the boundary of the cursor box. When deselected, includes only those grains which fall entirely within the boundary of the cursor box.
Non-Representative Particles  
Output:  
Height Reference Choose Relative to Threshold or Relative to Max Peak.
Histograms:  
Number of Histograms The number of data points which result from the filtering calculation. Note: Having more histogram bins than pixels is unnecessary.

 

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Top 500 Contributor
2 Posts
Points 22

Hi Stephen,

I am trying to understand the histogram i get from the particle analysis. In the height histogram, what is the y axis (height)? is it the mean height of the area pixels selected in each particle? or is it the absolute height of this particle?

thank you!

--DING

 

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