Abstract: Provided are an apparatus and a method that can acquire a shaded three-dimensional image having a high contrast for a thick cell culture specimen. Provided are an apparatus and a method that observe a biological sample accommodated in a container by a modulation contrast method using a near-infrared wavelength, at least the bottom surface of the container being formed of a plastic raw material.

Abstract: Provided are an apparatus and a method that can acquire a shaded three-dimensional image having a high contrast for a thick cell culture specimen. Provided are an apparatus and a method that observe a biological sample accommodated in a container by a modulation contrast method using a near-infrared wavelength, at least the bottom surface of the container being formed of a plastic raw material.

Abstract: An immersion liquid retainer is an immersion liquid retainer used for an observation made with a microscope including an immersion objective. The immersion liquid retainer includes a fixing part in which a first penetration hole for viewing an observed portion of a specimen is formed and which is fixed to the specimen, and an immersion liquid retaining part where a concave part that has a bottom surface configured with a transparent flat plate and is intended to retain an immersion liquid is formed. The immersion liquid retaining part is joined to the fixing part or formed integrally with the fixing part so that the transparent flat plate covers the first penetration hole.

Abstract: An image forming method for a biological sample includes calculating a component corresponding to a phase distribution of the sample and a component corresponding to a matter other than the phase distribution according to a plurality of pieces of images with different image contrasts, to form a normalized phase component; separating the phase component image into a plurality of frequency components according to spatial frequencies of the image; merging the phase distribution of the refraction component and the phase distribution of the structure component calculated by applying a deconvolution process to each of the frequency components using an optical response characteristic corresponding to each, to calculate the phase distribution, and forming a phase distribution image from the calculated phase distribution; and merging the phase distribution image with an image of the sample in which a biochemical phenomenon and/or a physical phenomenon in the sample are visualized.

Abstract: Time lapse observation method includes: before a process to obtain a first time lapse image, capturing an image of a reference area on a sample being a partial area of a target area or an area in a vicinity of the target area being a smaller area than the target area to obtain a reference image; storing a position of a capturing area in capturing the reference image as a reference position; before a process to obtain the time lapse image performed, setting a position of the capturing area sequentially at different positions in the optical axis direction of an objective including the reference position and capturing an image at each of the positions to obtain comparison target images; and matching the capturing area with the target area, based on a comparison result of the reference image and the comparison target images.

Abstract: An immersion liquid retainer is an immersion liquid retainer used for an observation made with a microscope including an immersion objective. The immersion liquid retainer includes a fixing part in which a first penetration hole for viewing an observed portion of a specimen is formed and which is fixed to the specimen, and an immersion liquid retaining part where a concave part that has a bottom surface configured with a transparent flat plate and is intended to retain an immersion liquid is formed. The immersion liquid retaining part is joined to the fixing part or formed integrally with the fixing part so that the transparent flat plate covers the first penetration hole.

Abstract: A light intensity measuring unit for measuring an intensity of light emitted from a microscope includes an aperture stop, a field stop, at least one measurement lens arranged between the aperture stop and the field stop, and an interface for attachment to a microscope. The aperture stop is positioned on or close to a back focal plane of the at least one measurement lens. The field stop is positioned on or close to a front focal plane of the at least one measurement lens.

Abstract: Time lapse observation method includes: before a process to obtain a first time lapse image, capturing an image of a reference area on a sample being a partial area of a target area or an area in a vicinity of the target area being a smaller area than the target area to obtain a reference image; storing a position of a capturing area in capturing the reference image as a reference position; before a process to obtain the time lapse image performed, setting a position of the capturing area sequentially at different positions in the optical axis direction of an objective including the reference position and capturing an image at each of the positions to obtain comparison target images; and matching the capturing area with the target area, based on a comparison result of the reference image and the comparison target images.

Abstract: A light intensity measuring unit for measuring an intensity of light emitted from a microscope includes an aperture stop, a field stop, at least one measurement lens arranged between the aperture stop and the field stop, and an interface for attachment to a microscope. The aperture stop is positioned on or close to a back focal plane of the at least one measurement lens. The field stop is positioned on or close to a front focal plane of the at least one measurement lens.

Abstract: It in an object to acquire a high-precision polarization image.