• bobn2panorama_fish_eye
    2 years ago

    That's correct on my observations also. I think that the problem here is those weasel words 'all else equal'. To use that condition, you need to know what is included in 'all else', which isn't that simple, because changing the pixel pitch only has many knock-on consequences which unavoidably change performance parameters, not necessarily in the same direction. I've always thought that if one wants an artificial scenario to assess somehow 'inherent' effect of pixel pitch 2-D scaling is more sensible than 'all else equal', and under 2-D scaling reducing pixel size does not affect light collection and improves DR (per unit area in both cases).

    The second issue is that sensors simply aren't designed that way. The pixel circuitry and optics will to a large extent be designed for the pixel pitch, and production economics tends to mean that they are processed on lines suitable for the pixel pitch and no finer.

  • bobn2panorama_fish_eye
    2 years ago

    Fc(lens) is not subject to Nyquist - it's not sampled.

  • JACShelp_outline
    878 posts
    2 years ago

    It is the cut-off, by definition, sampled or not. Also, if this a reply to me, I did not say "Nyquist."

    Before we go to another rabbit hole, I can see that Q is not Jim's definition. I am still curious where that factor came from.

  • bobn2panorama_fish_eye
    2 years ago

    Not my rabbit hole.
    Jim's formula is Q = 2 * (lambda * N) / (2 * pitch) = lamda * N / pitch
    derived from
    Q = 2 * Fcsensor / Fclens
    Where
    Fcsensor = 1 / (2 * pitch), which is simply the cut-off frequency of the sensor due to the Nyquist limit, and
    Fclens = 1 / lambda * N, which is the standard formula for the cut-off frequency due to sampling.
    In short there are two cut-off frequencies, one is determined by diffraction, one is determined by sampling frequency.
    Or possibly you were thinking of the other '2', in which case this is a miscommunication caused by different interpretations of the word 'factor' which some take to mean specifically 'divisor', and others to mean any term in a multiplication or division.

  • JACShelp_outline
    878 posts
    2 years ago

    It is about the factor 2 here:

    Q = 2 * Fcsensor / Fclens

  • bobn2panorama_fish_eye
    2 years ago

    So the misunderstanding is different use of 'factor'.
    Anyhow, the source that Jim quotes gives the Q formula as Q=λ fn/PixelPitch directly. Looks to me like it's an arbitrary scale factor to allow λ fn/PixelPitch to be used as the metric. The only thing that it affects is which values you consider to mean what. They give Q=1.00 for panchromatic imaging, Q=0.25 for multispectral imaging and Q=2.00 for be critically sampled, or 2 samples per resolution element - which is the Nyquist condition. All that changes is the number for each condition. Jim was explaining it in terms of Nyquist and diffraction, but to do that you need the '2' to arrive at the Q formula. I suspect that the Q formula is as it is because the scale of the value doesn't matter, and making it Q=λ fn/PixelPitch just makes it simpler.

  • DonaldBpanorama_fish_eye
    2366 posts
    2 years ago

    not when you are shooting microscopic detail . didnt you read any of the 3 links posted !

  • DonaldBpanorama_fish_eye
    2366 posts
    2 years ago

    post some of your images to prove what you are proposing.

  • IliahBorgpanorama_fish_eye
    976 posts
    2 years ago

    At some point Zeiss were showing that with a microscope "Q" up to 3 were showing visible improvements, but above 3 (they went to 5 for the critics to be sure) no visible improvement happened. That was with a monochrome sensor.

  • IliahBorgpanorama_fish_eye
    976 posts
    2 years ago

    Have you tried asking a random Sony Eng. to post an image to prove they know how to make sensors?

  • DonaldBpanorama_fish_eye
    2366 posts
    2 years ago

    thats right from what ive read. my objetives are f 4 X magnifacation 4 x and now we are hitting f16. do the same with another objective 10x and thats = f40. i hope in on the right path.

  • DonaldBpanorama_fish_eye
    2366 posts
    2 years ago

    exactlly. and when your stacking images noise is stacked its not magically disapearing. its been proven also by hi res images form a m43 camera compared to 42meg FF single image. the single image wins hands down every time.

  • JimKassonpanorama_fish_eye
    1738 posts
    2 years ago

    That's why I'm trying to get a Zeiss S Planar 50/1.6 working on my GFX 100S. At 10:1 (the ratio it's designed for), that'll be f/16. Monochromatic, though.

  • bobn2panorama_fish_eye
    2 years ago

    Stacking purely for noise reduction is a thing. It's equivalent to giving a larger exposure. It also works with focus stacking, if the focus stacking software is clever enough.

  • DonaldBpanorama_fish_eye
    2366 posts
    2 years ago

    but we are looking at images made from microscope objectives with extremely fine detail. read the olympus imaging link a poster had provided. you want the best image quality use a larger sensor. but under most curcomstances good enough is good enough.

  • JimKassonpanorama_fish_eye
    1738 posts
    2 years ago

    I've been writing some of my own stacking software, so I can control that.

  • DonaldBpanorama_fish_eye
    2366 posts
    2 years ago

    only under common circumstances. thats why i chose the a74 over the a7r4 or a7r5 .as i shoot low light concerts and bigger pixels produce cleaner images.

  • IliahBorgpanorama_fish_eye
    976 posts
    2 years ago

    Magic.