An image processing method includes: generating two images by performing two image enhancement processes for a microscopic image; and generating a corrected image obtained by compositing the two images, wherein the generating the two images includes generating a high-frequency enhanced image in which high-frequency components of the microscopic image are enhanced relative to low-frequency components of the microscopic image that have a lower frequency than the high-frequency components, and generating a microstructure enhanced image in which a microstructure in an observation sample included in the microscopic image is enhanced.

A microscopy system includes a microscope, a stand configured to mount the microscope and including a drive device configured to move the microscope, a detection device configured to detect a spatial position of a target fastened to a body part or to an instrument, wherein the position detection device includes the target with at least one marker element and an image capture device configured to optically capture the target. The microscopy system further includes at least one control device configured to operate the microscopy system according to the detected position of the target, wherein the position detection device is configured to determine the position of the target by evaluating a two-dimensional image of the image capture device. In addition, a method for operating the microscopy system is provided.

A sample shape measuring method includes a step of preparing illumination light passing through a predetermined illumination region, a step of applying the illumination light to a sample, and a predetermined processing step. The predetermined illumination region is set so as not to include the optical axis at a pupil position of the illumination optical system and is set such that the illumination light is applied to part of the inside of the pupil and the outside of the pupil at a pupil position of the observation optical system. The predetermined processing step includes a step of receiving light, a step of obtaining the quantity of light, a step of calculating the difference or the ratio between the quantity of light and a reference quantity of light, and a step of calculating the amount of tilt in the surface of the sample from the difference or the ratio.

A standing wave interferometric microscope is disclosed herein. An example microscope may include an illuminator, for illuminating a specimen with a standing wave of input radiation at an analysis location to cause the specimen to fluoresce, the specimen arranged in the analysis location, a pair of projection systems, arranged at opposite sides of the analysis location, coupled to collect at least a portion of the fluorescence and direct a corresponding pair of fluorescence light beams into a respective pair of inputs of an optical combining element, a wavefront modifier for producing astigmatism in at least one of the fluorescence light beams entering the optical combining element, and a detector for examining output light from said combining element.

An apparatus, method and storage medium for controlling a pathologic microscope are provided. The method includes obtaining a pathological digital image from an incident optical path of the pathologic microscope; performing artificial intelligence (AI) analysis on the pathological digital image to generate AI analysis information; and controlling an augmented reality (AR) projection component to project the AI analysis information on a microscopic field of the pathologic microscope on an outgoing optical path.

A phase difference observation apparatus includes a light source; an illumination guide to guide illumination light from the light source to an observation target object in a cell culture vessel; an optical imager to form an optical image of the observation target object on an image sensor; and a controller. The illumination guide includes a spatial modulator to change an intensity distribution of the illumination light; the controller contains intensity distribution correction information associating a position of the imaging guide with respect to the cell culture vessel with an intensity distribution of illumination light at the position of the optical imager; the controller acquires imaging system position information, which is the position of the optical imager; and the controller changes an intensity distribution of illumination light in the spatial modulator on the basis of the imaging system position information and the intensity distribution correction information.

A viewing apparatus for producing a stereoscopic image for an observer, the viewing apparatus comprising: first and second video projectors for projecting respective ones of first and second video images of an object, the first and second images being different images which are one or both of spatially and angularly shifted in relation to the object so as to convey parallax between the images; a mirror arrangement comprising a concave mirror which receives light from the first and second video projectors, the mirror arrangement being located in relation to the first and second video projectors such that focussed images of the object are produced at the mirror arrangement; and a viewing lens for relaying exit pupils corresponding to each of the focussed images as reflected by the mirror arrangement to a viewing plane so as to be viewable at the respective eyes of the observer as a stereoscopic image without use of adapted eyewear; wherein the video projectors comprise first and second video displays which are driven by first and second video signals to display respective ones of the first and second video images, and first and second optical arrangements for focussing light from the respective images as displayed by the first and second displays to the mirror arrangement.

A method for producing a preview image with an inclined-plane microscope with a tilted illumination plane include illuminating, at successive points in time, different illumination planes, which are tilted relatively to an optical axis of an optical viewing element and spaced apart from one another. The illumination planes are imaged onto a sensor with photosensitive elements arranged line-by-line. The preview image is produced by successively reading out strip-type read-out areas of the sensor, a longitudinal extension of the read-out areas being oriented parallel to the lines of the photosensitive elements, such that the preview image reproduces a viewing plane perpendicular to the optical axis of the optical viewing element.

An augmented reality microscope (ARM) includes an objective lens, an eyepiece, an N-ocular observation tube, where N is a positive integer greater than 2, an image obtaining assembly physically connected to the N-ocular observation tube by a physical interface on the N-ocular observation tube, and an image projection assembly including, an image projection apparatus, a lens apparatus, and a light splitting apparatus. Light generated by an observed object during observation that enters an optical path through the objective lens and light generated by the image projection apparatus that enters the optical path through the lens apparatus converges at the light splitting apparatus in the image projection assembly, the converged light passes through the N-ocular observation tube.

Exemplary embodiments of the present invention relate generally to the fields for indicating a location on an image in a multi-viewer display. In particular embodiments, the multi-viewer display may be a multi-viewer microscope.