A display device including a display to generate a real image, and an optical system. The optical system includes a plurality of lenslets, each having one cluster of object pixels, where the assignation of object pixels to clusters may change periodically in time intervals. Each lenslet produces a ray pencil from each object pixel of its cluster which has waists laying close to a waist surface. The ray pencils are projected towards an eye position. The ray pencils are configured to generate a partial virtual image from the real image of its corresponding cluster. At least two of the lenslets cannot be made to coincide by a simple translation rigid motion. Foveal rays are a subset of rays emanating from the lenslets.

Methods and systems are provided for improving resolution, acquisition speed, and/or illumination dose for microscopy systems. In some embodiments, a microscopy system having multiple objective setups may include illumination generators to provide selectively-blanked illumination line scans, objective lenses to introduce the selectively-blanked illumination line scans to a sample and to collect fluorescence emissions from the sample, and detectors to receive the fluorescence emissions from the objective lenses. The microscopy system may also include one or more processors in operative communication with the detectors, which may combine the fluorescence emissions to generate a composite image.

The present invention relates to a method of reading out information from a data carrier and to a data carrier utilizing the concept of structured-illumination microscopy or saturated structured-illumination microscopy.

A method includes receiving collimated light from an optical imaging system and dividing the received light into multiple bands of wavelength. Each band is refocused onto a corresponding diffraction grating having an amplitude function matched to a point spread function (PSF) of the optical imaging system. The light that is not filtered out by the diffraction grating is transmitted onto a corresponding pixel array. An image is reconstructed from data provided by the pixel arrays for each band. The intensity of light scattered by each diffraction grating may be detected, with the image being reconstructed as a function of an average value of detected intensity of scattered light used to scale the known zero-order mode profile, which is added to the image on the pixel array.

A method includes receiving collimated light from an optical imaging system and dividing the received light into multiple bands of wavelength. Each band is refocused onto a corresponding diffraction grating having an amplitude function matched to a point spread function (PSF) of the optical imaging system. The light that is not filtered out by the diffraction grating is transmitted onto a corresponding pixel array. An image is reconstructed from data provided by the pixel arrays for each band. The intensity of light scattered by each diffraction grating may be detected, with the image being reconstructed as a function of an average value of detected intensity of scattered light used to scale the known zero-order mode profile, which is added to the image on the pixel array.

A system includes a light source, a deflection unit configured to deflect a light beam having a wavelength λ emitted from the light source, and a lens unit including a plurality of lenses that focuses deflected light on a surface to be scanned, at least one lens among the plurality of lenses has a micro concavo-convex structure in an optical surface, and the optical surface having the micro concavo-convex structure has a transmittance distribution for the light beam having the wavelength λ according to a light quantity distribution of the deflected light and entering the lens unit.

A confocal microscope device for scanning a two-dimensional array of illumination beams over a target surface and scanning a corresponding two-dimensional array of emission beams stimulated by the array of illumination beams on to a sensor of an imaging device. The device comprises first scanning optics operable to scan the array of illumination beams over the target surface along a first axis and scan the array of emission beams over the sensor along the first axis. The device further comprises second scanning optics operable to deflect, on a second axis, the array of illumination beams as they are scanned over the target surface along the first axis, such that uneven stimulation of the target surface by the array of illumination beams due to interference of the illumination beams is reduced, and deflect, on the second axis, the array of emission beams as they are scanned over the sensor of the imaging device along the first axis such that uneven stimulation of the sensor by the array of emission beams due to interference of the emission beams is reduced.

A confocal microscope device for scanning a two-dimensional array of illumination beams over a target surface and scanning a corresponding two-dimensional array of emission beams stimulated by the array of illumination beams on to a sensor of an imaging device. The device comprises first scanning optics operable to scan the array of illumination beams over the target surface along a first axis and scan the array of emission beams over the sensor along the first axis. The device further comprises second scanning optics operable to deflect, on a second axis, the array of illumination beams as they are scanned over the target surface along the first axis, such that uneven stimulation of the target surface by the array of illumination beams due to interference of the illumination beams is reduced, and deflect, on the second axis, the array of emission beams as they are scanned over the sensor of the imaging device along the first axis such that uneven stimulation of the sensor by the array of emission beams due to interference of the emission beams is reduced.

It comprises optical assemblies that focus light onto individual first optical fibers which are combined together in a final single optical fiber, collecting a considerable amount of light from a target, to feed an instrument such as a spectrograph. The first optical fibers are kept centred on the target through image devices that also provide images, and these images can be combined to give rise to a high-quality image of the field surrounding the target. The final effective aperture of the device is scalable, using different numbers of optical assemblies and depending on their diameters.

The present invention relates to a photodetector array for capturing image data, comprising: photodetector cells arranged on a substrate, each including a single-photon avalanche diode, wherein the active areas of the photodetector cells are neighbored along a hexagonal grid; microlenses, having a hexagonal or circular shape, each arranged on one photodetector cell to focus light onto the photodiode.