Abstract:
A hyperspectral imaging system and a method are described herein for providing a hyperspectral image of an area of a remote object (e.g., scene of interest). In one aspect, the hyperspectral imaging system includes at least one optic, a rotatable disk (which has at least one spiral slit formed therein), a spectrometer, a two-dimensional image sensor, and a controller. In another aspect, the hyperspectral imaging system includes at least one optic, a rotatable disk (which has multiple straight slits formed therein), a spectrometer, a two-dimensional image sensor, and a controller. In yet another aspect, the hyperspectral imaging system includes at least one optic, a rotatable drum (which has a plurality of slits formed on the outer surface thereof and a fold mirror located therein), a spectrometer, a two-dimensional image sensor, and a controller.
Abstract:
A hyperspectral imaging system and a method are described herein for providing a hyperspectral image of an area of a remote object (e.g., scene of interest). In one aspect, the hyperspectral imaging system includes at least one optic, a rotatable disk (which has at least one spiral slit formed therein), a spectrometer, a two-dimensional image sensor, and a controller. In another aspect, the hyperspectral imaging system includes at least one optic, a rotatable disk (which has multiple straight slits formed therein), a spectrometer, a two-dimensional image sensor, and a controller. In yet another aspect, the hyperspectral imaging system includes at least one optic, a rotatable drum (which has a plurality of slits formed on the outer surface thereof and a fold mirror located therein), a spectrometer, a two-dimensional image sensor, and a controller.
Abstract:
An image analysis method includes acquiring an image of an observation region including a plurality of pixels respectively having a plurality of time serially acquired data, setting an analysis region on the image of the observation region, setting a sub analysis region smaller than the analysis region, intermittently moving the sub analysis region in increments of a pixel interval over the entire analysis region, executing correlation analysis using data of pixels in the sub analysis region every time the sub analysis region is moved, so as to estimate at least a molecular number or a diffusion constant of the sub analysis region, and forming a molecular number or diffusion constant image by mapping the molecular numbers or the diffusion constants.
Abstract:
Microscope, particularly laser scanning microscope, for optical detection of light radiation excited in a specimen, having a detection beam path for detecting spectral components of the light radiation in a plurality of detection channels, wherein the light radiation arrives at a variable longpass filter or shortpass filter from which reflected and/or transmitted components are reflected back with a parallel offset, and the latter arrive at a detector after at least one back-reflection of this kind.
Abstract:
A layered waveguide stack radiant energy converter array having a plurality of superposed waveguides, each waveguide having a core layer having a radiant energy converter disposed therein, and two cladding layers disposed on opposing sides of the core. In some embodiments the conductive layers are electrically coupled to the converter and act as charge carriers for it, and in other wires are provided for individual converters. Each waveguide has at least one inlet for passage of radiant energy therethrough, the inlet extending between the cladding layers, such that radiant energy entering the waveguide impinges on at least two layers of the waveguide, the inlet further defining a minimum cutoff frequency for the energy to propagate in the waveguide. In some embodiments such as solar panels, energy is harvested. In other embodiments energy is detected such as for example is done in a camera focal plane sensor. In some embodiments the stack is used to emit light.
Abstract:
Disclosed is an arrangement for detecting first light (L1) and second light (L2), with the first light (L1) and second light (L2) having no wavelength in common. The arrangement includes a first effective detector area (D1) and a second effective detector area (D2). The first effective detector area (D1) is exposed to the first light (L1) and/or second light (L2) different from the first light (L1) and/or second light (L2) to which the second effective detector area (D2) is exposed when the arrangement is exposed to spatially uniformly distributed first light (L1) and second light (L2). The difference between the first light (L1) and/or second light (L2) to which said first detector area (D1) and second detector area (D2) are exposed to can be a difference in intensity and/or difference in an angle of incidence relative to the arrangement.
Abstract:
A system for performing high-speed, high-resolution imaging cytometry utilizes a line-scan sensor. A cell to be characterized is transported past a scan region. An optical system focuses an image of a portion of the scan region onto at least one linear light sensor, and repeated readings of light falling on the sensor are taken while a cell is transported though the scan region. The system may image cells directly, or may excite fluorescence in the cells and image the resulting light emitted from the cell by fluorescence. The system may provide a narrow band of illumination at the scan region. The system may include various filters and imaging optics that enable simultaneous multicolor fluorescence imaging cytometry. Multiple linear sensors may be provided, and images gathered by the individual sensors may be combined to construct an image having improved signal-to-noise characteristics.
Abstract:
A single aperture three channel optical system is disclosed. In one embodiment, the optical system includes a front optical group and a back optical group that is disposed in substantially close proximity to the front optical group. Further, the optical system includes a first sensor, a second sensor, and a third sensor. The front optical group and the second optical group receives an object beam and splits into a reflected beam having first wavelengths and a transmitted beam of second wavelengths. Furthermore, the front optical group and the second optical group splits the reflected beam having first wavelengths into a transmitted beam having third wavelengths and a reflected beam having fourth wavelengths. The first sensor, the second sensor and the third sensor receive the transmitted beam of second wavelengths, transmitted beam of third wavelengths, and reflected beam of fourth wavelengths, respectively and produce the coaxial three channel images.
Abstract:
Various embodiments for facilitating optical communications utilizing a apparatus are disclosed. One embodiment, among others, is an apparatus that comprises a dispersion element configured to transmit a beam through a plurality of optical paths in a spectral dispersion element to generate a spectrally dispersed beam. The apparatus further comprises a second-harmonic generation (SHG) element integrated into the dispersion element, the SHG element configured to generate second-harmonic light beam from the dispersed beam by splitting the dispersed beam into a plurality of beams, wherein the plurality of beams traverse a common axis. The apparatus further comprises a collimator configured to collimate the second-harmonic light beam over a predetermined path length and a phase decoder configured to receive the collimated beam and measure characteristics associated with the collimated beam.
Abstract:
A photometric device (18) for quantifying a nucleic acid in a sample (518) in a tube (58), comprises a light emission unit (28), a sample obtaining unit (38) for holding the tube (58) with the nucleic acid sample (518) and a detection unit (48) wherein the sample obtaining unit (38) is arranged in between the light emission unit (28) and the detection unit (48) in particular, the light emission unit (28) and the detection unit (48) are arranged to provide light through the sample obtaining unit (38) such that light of a first wavelength of about 230 nanometers and light of a second wavelength of about 260 nanometers are simultaneously detectable within the detection unit (48). The photometric device (18) allows for efficiently analysing the nucleic acid sample by only considering invisible light. In particular, content of nucleic acid such as particularly a RNA or a DNA and a nucleic acid/salt ratio can simultaneously be determined such that efficiency of quantification of the nucleic acid sample (518) can be increased. Furthermore, since in addition thereto the sample obtaining unit (38) is arranged to hold the tube (58) or cuvette and the light directly passes the sample (518) being arranged in the tube (58) or cuvette, loss of sample, contamination of sample, need of additional sample treatment equipment such as pipettes or additional tubes as well as frequent cleaning of optics of the photometric device can be printed or reduced.