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Troubles with Imaging - Troubleshooting » History » Version 2

Amber Herold, 04/27/2010 02:15 PM

1 1 Amber Herold
h1. Troubles with Imaging - Troubleshooting
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* <link linkend="imageno">Empty Image</link>
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* <link linkend="imageartifact">Image or FFT contains artifacts</link>
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* <link linkend="cor_not_read">Reference image from other users not readable</link>
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* <link linkend="beamshifttime">Beam shifts away from the imaging area over
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time</link>
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* <link linkend="beamshifttime">Beam shifts away from the imaging area after a large
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defocus correction</link>
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* <link linkend="beamshiftimage">Beam shifts away from the imaging area upon image shift
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targeting</link>
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* <link linkend="beamshiftstage">Beam shifts away from the imaging area upon stage shift
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targeting in LM mode</link>
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* <link linkend="apertureoff">Objective aperture is off-centered in LM when it is centered
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in HM</link>
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* <link linkend="specimenoverdose_gatan">The specimen appears over-dosed in the high
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magnification images (while using a Gatan CCD)</link>
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* <link linkend="specimenoverdose_gatan">Bright/Dark correction has no effect on the image
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(while using a Gatan CCD)</link>
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* <link linkend="badinput">Acquired image configuration is not what was
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inputted</link>
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* <link linkend="melt_beam_imprint">Exposure image has a circular focus
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imprint</link>
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* <link linkend="melt_beam_imprint">Image acquired at the wrong stage
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position</link>
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h2. Image is acquired but contains no real information
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Commonly Why:
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* Main screen at the scope is down
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* Camera is not inserted (Gatan camera)
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* Digital Micrograph program is not running (Gatan camera)
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* Shutter switch box is set to CM, i.e., to collect film data only (Tietz
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camera)
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h2. Image is acquired but contains artifacts either in image or
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in Fourier Transform
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Commonly Why:
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* Beam is partially covering the CCD.
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* Scope viewing window is not covered and room light is on
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* Dark/Bright images are not available or need to be reaquire.
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* Bias level and quadrant correction may need to be reset (Digital Micrograph and
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Gatan camera)
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h2. Can not read reference images that were acquired by other
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users
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Commonly Why: You don't have permission to read their image files
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Solution:
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*  Have the person change the group or even world permission for reading the data
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directory and the image files in it.
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The person is not around when this happens:
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Acquire your own reference images at the camera setting that needs the dark and bright
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images. However, Leginon always look for the most recent calibration in the database by
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anyone. Every user will have to do this everytime if the permission problem is not
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solved.
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h2. Beam shifts away from imaging area over time
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Commonly Why:
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* Residual lens hysteresis if you haven't allowed the scope to warm up for HM mode
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after acquiring LM atlas.
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* Focus correction has taken the absolute focus point far away from U-centric
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focus.
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<title>Solutions:</title>
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* Wait until the optics is stabilized
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* Activate "Publish and wait for the reference target" in Exposure Node. This will
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enable "Fix Beam" node to search for the beam in the desired range and shift the beam
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to the best result. A reference target, normally an empty square, need to be selected
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on the grid to use this function. See description in the node description chapter for
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usage.
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* Pause MSI and correct for residual beam shift
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*  Pause before next hole or square by clicking Hole/Toolbar>Pause button
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(Pause icon) or Square/Toolbar>Pause button (Pause icon), respectively. Which
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one to pause depends on what is the next target.
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*  Leginon/Presets Manager> When the acquisition sequence is stopped, send
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the preset that has beam shift problem "To Scope" (ToScope icon).
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*  Leginon/Navigation/Toolbar> Choose move type to be "Beam Shift" and make
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sure "Use Camera Configuration" is unchecked in settings.
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*  Leginon/Navigation> "Navigate"*(navigate icon) to center the beam. If
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"Navigate" does not bring the beam in, manually shift the beam at the
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microscope. Do not forget to lift the screen and cover the viewing area after
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done.
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*  Leginon/Presets Manager> save the new beam shift by retrieving it "From
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Scope" (From Scope icon).
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*  "Continue" data collection on next hole or square target by clicking
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Hole/Toolbar> "Continue" button or Square/Toolbar> "Continue" button,
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respectively.
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*"Navigate" means selecting the navigate tool on the top right of image
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display and then single-left-clicking the location of the new center that is
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translated by the given TEM Parameter.
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* Reset the defocus=0 point back to U-centric focus.
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* Leginon reset defocus after each defocus correction. Therefore, the point where
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the user defines as defocus=0 may drift away from U-centric focus over time or after a
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very large correction before it is reset to U-centric focus by z focus
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correction.
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*  Pause before next hole or square by clicking Hole/Toolbar>Pause button
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(Pause icon) or Square/Toolbar>Pause button (Pause icon), respectively. Which
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one to pause depends on what is the next target.
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*  Leginon/Presets Manager> Send "hl" preset "To Scope" (ToScope
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icon).
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*  Leginon/Z Focus/Toolbar> Send stored U-centric focus to scope.
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*  Leginon/Z Focus/Toolbar> Reset defocus to 0
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*  Scope> U-center the stage if it is very out of focus.
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*  Leginon/Presets Manager> Send the preset that showed bad beam shift "To
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Scope"
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*  Scope and Leginon/Presets Manager> Check the beam shift, make
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correction, and then retrieve the correct value "From Scope"
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*  Leginon/Drift Manager> Declare Drift (declare drift icon) to force
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correction at next possible point in the process.
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*  "Continue" data collection on next hole or square target by clicking
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Hole/Toolbar> "Continue" button or Square/Toolbar> "Continue" button,
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respectively.
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h2. Beam shifts away from imaging area only when targeting
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move type is image shift
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Commonly Why:
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* Image/Beam Shift calibration on the microscope is not optimal
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* Defocus is very far from eucentric focus
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<title>Solutions:</title>
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* Bad Image/Beam calibration
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Follow instruction for performing the calibration for FEI Tecnai machines under
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Alignments/Image HM-TEM(or LM)/Image-Beam calibration
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*  Pause before next hole or square by clicking Hole/Toolbar>Pause button
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(Pause icon) or Square/Toolbar>Pause button (Pause icon), respectively. Which
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one to pause depends on what is the next target. If in queuing mode, pause at the
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node that process the queue.
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*  Scope> move to an unimportant area or pull the holder out enough to allow
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the beam to go through.
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*  Scope> reset defocus to eucentric height.
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*  Scope> Follow instruction for performing the calibration for FEI Tecnai
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machines under Alignments/Image HM-TEM(or LM)/Image-Beam calibration.
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*  Leginon/Presets Manager> Cycle the presets a few times. The calibration
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takes the scope to conditions outside the presets, and can cause strong hysteresis
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if this step is not done.
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*  Leginon> Follow the procedures for confirming and saving good image shift
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at various presets.
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*  "Continue" data collection on next hole or square target by clicking
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Hole/Toolbar> "Continue" button or squares/Target Toolbar> "Continue"
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button, respectively.
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*"Navigate" means selecting the navigate tool on the top right of image
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display and then single-left-clicking the location of the new center that is
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translated by the given TEM Parameter.
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* Defocus far from eucentric focus
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Image/Beam shift coupling worsens when the defocus is away from where it was
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calibrated. If, after the above calibration, the problem remains during MSI
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acquisition, additional focusing sequence should be added at lower magnification that
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move the stage to close to eucentric height so that the image shift target is selected
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on an image of a close-to-eucentric location.
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*  Leginon/Z Focus/Focus Sequence> activate both Stage_Wobble and
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Z_to_Encentric steps.
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*  Leginon/Hole (or Subsquare) Targeting> selection a focus target if not
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already done so when a newly acquired sq image comes in.
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If the accuracy of moving stage to eucentric height by the focus sequences in "Z
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Focus" is still not sufficient. Add another focus step performing the same task as
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Z_to_Encentric step. Repeating beam-tilt based autofocusing often improve the accuracy
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unless the calibration is off.
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Still not working: You have chosen a target that requires too much image shift for an
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independent image shift from beam shift. This is necessary when the lower mag targetting is
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not good either because the preset image shifts are not aligned or the stage position
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movement is not properly modeled.
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Solution: For image shift problem see solution for "Target is consistently off in the
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same direction and distance". For stage model problem, see "Modeled stage calibration" in
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setup notes.
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h2. Beam shifts away from imaging area when targeting move
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type is stage movement
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Commonly Why:
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* U-center defocus not set to 0 in LM mode.
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* LM alignment such as rotation center is way off.
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Solution: Check and correct microscopic alignment error. Preset parameters checking and
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reset may be necessary after the correction.
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Comments: If the problem persist, the original stage matrix calibration may have been
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performed with a bad alignment. The calibration should be redone with a well-aligned scope
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in LM mode.
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h2. Objective aperture appears off in "sq" preset when it is
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centered in HM mode
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Commonly Why:
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* U-center defocus not set to 0 in LM mode.
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* LM alignment such as image shift is way off.
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Solution: Check and correct microscopic alignment error. Preset parameters checking and
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reset may be necessary after the correction.
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h2. The specimen appears over-dosed in the high
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magnification images or the dark correction image has a high value (while using a Gatan
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CCD)
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This issue may occur when the shutter is incorrectly configured through Digital
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Micrograph (the imaging software for the Gatan CCD that resides on the TEM computer) or
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simply a bad dose calibration or too long an exposure time. To issue these
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corrections:
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*  Set the "shutter" to "Auto" on the external control box attached to the
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TEM.
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*  Open Digital Micrograph on the Microscope computer and go to the Camera Set-up
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page.
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*  Go to Configuration
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*  Set the Primary Shutter to Pre-specimen
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*  Set the Alternate Shutter to Post-specimen
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*  Set the Default Primary Shutter to the Normally Closed position.
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h2. The exposure image has a circular imprint of the beam
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at the size of the preset used for melting the ice
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This issue may occur when the main screen is left up during very long (such as over 30
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sec) ice melting and at high HT. Leginon has a mechanism that put the screen down during ice
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melting. It is caused by over-saturating the Phosphur layer on the CCD. If you see this
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effect, the screen may have failed to lower. Please test it by observing the screen movement
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with simulating target in any focuser node that has ice melt time set not to zero. Report
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the problem back to the leginon team if you are sure it is not your scope's problem.
488 2 Amber Herold
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[[Hardware Troubles|< Hardware Troubles]] | [[Troubles with Targeting|Troubles with Targeting >]]
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