Re: interference fringes in SP5 scans at 10x

Posted by manoj mathew on
URL: http://confocal-microscopy-list.275.s1.nabble.com/interference-fringes-in-SP5-scans-at-10x-tp7586028p7586035.html

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Dear Aryeh,

As mentioned already  fringes are almost always due to coherent excitation light from the laser/s entering the detectors. Fluorescence is non-choherent and cannot possibly give off fringes.

On SP5, essentially you have three barriers preventing the excitation light from entering the detectors:

1. AOBS

2. Notch filters 

3. Spectral Sliders 

This might be problem with the AOBS settings. The 405nm on Leica SP5 is not routed through the AOBS but through a separate primary dichroic mirror. This might explain why you don't see fringes with the 405nm.

Check the following AOBS settings:

1. Check if it is in reflection or fluorescence mode. You need to select the fluorescence mode

2. Check if appropriate notch filter (to cut of excitation light) is inserted. 

Also check your emission spectral slider settings:

If they are not properly set (sufficiently away from the excitation wavelengths) it could allow excitation light into the detectors. 

However even if the spectral sliders are set properly there could be issues if the spectral calibration of the system is off. Spectral calibration is done through the service software and needs to be done periodically along with pinhole alignment etc. by the service engineer. 

Best Regards,

Manoj

On Sun, Nov 20, 2016 at 8:38 PM, MODEL, MICHAEL <[hidden email]> wrote:

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Fluorescent light cannot produce interference. So this has to be reflection. It could be due to something with filters or from reflection from something inside. Have you try to remove the sample? Defocus the sample? Try single line scanning?

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From: Aryeh Weiss <[hidden email]> on behalf of Aryeh Weiss <[hidden email]>
Sent: Sunday, November 20, 2016 9:49 AM
To: MODEL, MICHAEL; [hidden email]
Subject: Re: interference fringes in SP5 scans at 10x

 

Thank you for your reply. This is fluorescence, not reflectance, imaging. The passbands are set to reject the excitation wavelengths.

--aryeh

On 20/11/2016 16:18, MODEL, MICHAEL wrote:

Hello Aryeh,

You are doing fluorescence or reflection? If reflection then the fringes are almost unavoidable. For example, light reflecting from the front and from the back of the coverslip should interfere because of the long coherence length of the laser

Mike

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From: Confocal Microscopy List [hidden email] on behalf of Aryeh Weiss [hidden email]
Sent: Sunday, November 20, 2016 7:25 AM
To: [hidden email]
Subject: interference fringes in SP5 scans at 10x

 

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We are observing what appear to be interference fringes form reflected light in  our Leica SP5, with our 10x objective.

Example images can be seen using this link:
https://drive.google.com/drive/folders/0Bytu294eIohjVHQ1elVTSElscjg?usp=sharing

There is a README file that says which excitation lines were used.

Basically, when the 405nm excitation is used alone, we do not see the fringes. When the other lines (ie the "visible" lines, as opposed to what Leica calls UV, which is really V) are used, there are fringes even in the channel which is set to pass wavelengths shorter than the shortest excitation in use (in our case 488nm).

So, in brief, the "visible" laser lines all produce interference fringes in all channels. The fringe spacing changes with excitation wavelength (as expected), but not with scan speed. They are not apparent when working with 40x oil. However, I note that with the oil objective, there is much less reflection from the coverslip . We do not have other air objectives with which to test the system.

The fringes appear with various samples.

It is quite possible that this has always been there, but no one noticed because confocal at 10x is not done very often.

If anyone on the list can tell us more about these fringes, we would appreciate it.

Thanks in advance.
--aryeh