http://confocal-microscopy-list.275.s1.nabble.com/Nyquist-sampling-advice-for-a-short-talk-tp7591495p7591505.html
and include the link in your posting.
I really like the way Jeff Lichtman addresses sampling in his lecture of Resolution of a microscope on iBiology.
> On 11 Nov 2020, at 09:30, Straatman, Kees (Dr.) <
[hidden email]> wrote:
>
> *****
> To join, leave or search the confocal microscopy listserv, go to:
>
http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy> Post images on
http://www.imgur.com and include the link in your posting.
> *****
>
> But does this not assume that your objects is in de squares. What if the objects are in between two squares? Dividing by 2 would just result in 4 squares with more or less the same intensity. So, I normally advice to divide by 3.
>
> Best wishes
>
> Kees
>
>
> Dr Ir K.R. Straatman
> Advanced Imaging Facility
>
> University of Leicester
> www.le.ac.uk/advanced-imaging-facility<
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>
>
> ________________________________
> From: Confocal Microscopy List <
[hidden email]> on behalf of Benjamin Smith <
[hidden email]>
> Sent: 10 November 2020 16:42
> To:
[hidden email] <
[hidden email]>
> Subject: Re: Nyquist sampling advice for a short talk
>
> *****
> To join, leave or search the confocal microscopy listserv, go to:
>
https://eur03.safelinks.protection.outlook.com/?url=http%3A%2F%2Flists.umn.edu%2Fcgi-bin%2Fwa%3FA0%3Dconfocalmicroscopy&data=04%7C01%7Ckrs5%40LEICESTER.AC.UK%7C3baa416276914588fa9d08d885987487%7Caebecd6a31d44b0195ce8274afe853d9%7C0%7C0%7C637406237134631398%7CUnknown%7CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0%3D%7C1000&sdata=hrSoXR%2BYeiT5u2UZ2pqe08DSR58%2FsEWcCFhW9u%2B0xFY%3D&reserved=0> Post images on
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> *****
>
> GIven that most microscopy has the luxury of being a simpler specific case
> of the Nyquist sampling theorem, I like to simplify it to a discrete model
> using a checkerboard. I first show a grid of squares and ask, "What is the
> smallest feature we can resolve on this grid?" I then show a checkerboard
> pattern next to a grid with all white squares. I point out that in order
> to resolve two objects means to be able to distinguish between two point
> sources and one bigger solid source. Therefore, you need to sample not
> only the peak intensities (your resolution) but also a local minimum
> between them to distinguish a pair of points from a solid object.
> Therefore, you need to sample at 2x your resolution.
>
> The hope here is to give people an intuitive sense of where Nyquist
> sampling theory comes from without delving into more complex issues like
> aliasing.
>
> On Tue, Nov 10, 2020 at 8:26 AM Sara Parker <
[hidden email]>
> wrote:
>
>> *****
>> To join, leave or search the confocal microscopy listserv, go to:
>>
https://eur03.safelinks.protection.outlook.com/?url=http%3A%2F%2Flists.umn.edu%2Fcgi-bin%2Fwa%3FA0%3Dconfocalmicroscopy&data=04%7C01%7Ckrs5%40LEICESTER.AC.UK%7C3baa416276914588fa9d08d885987487%7Caebecd6a31d44b0195ce8274afe853d9%7C0%7C0%7C637406237134631398%7CUnknown%7CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0%3D%7C1000&sdata=hrSoXR%2BYeiT5u2UZ2pqe08DSR58%2FsEWcCFhW9u%2B0xFY%3D&reserved=0>> Post images on
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>> *****
>>
>> Dale,
>>
>> I really like the following applets for demonstrating resolution and
>> sampling in practice, and connecting theory to experimental design.
>>
>>
https://eur03.safelinks.protection.outlook.com/?url=http%3A%2F%2Fwww.iscopecalc.com%2F&data=04%7C01%7Ckrs5%40LEICESTER.AC.UK%7C3baa416276914588fa9d08d885987487%7Caebecd6a31d44b0195ce8274afe853d9%7C0%7C0%7C637406237134631398%7CUnknown%7CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0%3D%7C1000&sdata=ure5inAP00fuI4A6vWsRdgvpskjbhqQWrTnNPOGTrhg%3D&reserved=0>>
>>
https://eur03.safelinks.protection.outlook.com/?url=https%3A%2F%2Fwww.olympus-lifescience.com%2Fen%2Fmicroscope-resource%2Fprimer%2Fjava%2Fimageformation%2Frayleighdisks%2F&data=04%7C01%7Ckrs5%40LEICESTER.AC.UK%7C3baa416276914588fa9d08d885987487%7Caebecd6a31d44b0195ce8274afe853d9%7C0%7C0%7C637406237134641396%7CUnknown%7CTWFpbGZsb3d8eyJWIjoiMC4wLjAwMDAiLCJQIjoiV2luMzIiLCJBTiI6Ik1haWwiLCJXVCI6Mn0%3D%7C1000&sdata=E90C0TWKjpw2mx5UNXRlI5VtvxmNcq8n1yftIDmU%2BO0%3D&reserved=0>>
>> Sara Parker
>> Postdoctoral Fellow, Mouneimne Lab
>> (520) 626-3860
>>
[hidden email]
>> Department of Cellular & Molecular Medicine
>> University of Arizona
>>
>
>
> --
> Benjamin E. Smith, Ph. D.
> Imaging Specialist, Vision Science
> University of California, Berkeley
> 195 Life Sciences Addition
> Berkeley, CA 94720-3200
> Tel (510) 642-9712
> Fax (510) 643-6791
> e-mail:
[hidden email]
>
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