An apparatus to provide a label-free or native particle analysis comprises a light generating system producing first light pulses at a first wavelength and second light pulses at a second wavelength; and a flow cell coupled to the light generating system to convey particles for analysis. The light generating system is configured to chirp at least one of the first light pulses and the second light pulses to analyze the particles.

A method and an apparatus for inspecting security of an object to be detected. The method includes: guiding an exciting light to the object, collecting a first optical signal from the object and generating .a first spectrum from the first optical signal; guiding the exciting light to the object again after a certain time interval, collecting a second optical signal from the object and generating a second spectrum from the second optical signal; and comparing the first spectrum with the second spectrum to determine whether or not the object is damaged.

An optical filter including filter regions arrayed two-dimensionally, in which the filter regions include a first region and a second region; a wavelength distribution of an optical transmittance of the first region has a first local maximum in a first wavelength band and a second local maximum in a second wavelength band that differs from the first wavelength band, and a wavelength distribution of an optical transmittance of the second region has a third local maximum in a third wavelength band that differs from each of the first wavelength band and the second wavelength band and a fourth local maximum in a fourth wavelength band that differs from the third wavelength band.

An ultrashort light pulse oscillated from an ultrashort pulse oscillator enters a waveguide (2) via a polarization control element (3). After conversion into a supercontinuum by a nonlinear optical effect, it is compressed by a prism pair compressor (71) as pulse compressor (7), and then emitted. The waveguide (2), which is a nonlinear fiber with normal dispersion in the wavelength range from 850 to 1550, generates the supercontinuum having a spectrum continuous in a wavelength band width of at least 200 nm included in the wavelength range from 850 to 1550 nm. The supercontinuum, which has a peak power within 1 to 100 kW, can be used as excitation light in a multiphoton excitation fluorescence microscope for fluorescence observation of biological samples.

An ultrashort light pulse oscillated from an ultrashort pulse oscillator enters a waveguide 2 via a polarization control element 3. After conversion into a supercontinuum by a nonlinear optical effect, it is compressed by a prism pair compressor 71 as pulse compressor 7, and then emitted. The waveguide 2, which is a nonlinear fiber with normal dispersion in the wavelength range from 850 to 1550, generates the supercontinuum having a spectrum continuous in a wavelength band width of at least 200 nm included in the wavelength range from 850 to 1550 nm. The supercontinuum, which has a peak power within 1 to 100 kW, can be used as excitation light in a multiphoton excitation fluorescence microscope for fluorescence observation of biological samples.

The described method and system allow the simultaneous detection of multicolored samples, e.g. in live cells or tissues, in a simple experimental geometry. It relies on combining ultrashort ultra- broadband laser sources (10) with a fluorescence microscope setup able to collect fluorescence intensities and/or photon arrival times per excitation volume, as well as nonlinear signals, such as second/third-harmonic and sum-frequency generation. In the description, the presented method is referred to as “SyncRGB method”.

Provided is a carbon isotope analysis device including a carbon dioxide isotope generator provided with a combustion unit that generates gas containing carbon dioxide isotope from carbon isotope, and a carbon dioxide isotope purifying unit; a spectrometer including optical resonators having a pair of mirrors, and a photodetector that determines intensity of light transmitted from the optical resonators; and a light generator including a single light source, a first optical fiber that transmits first light from the light source, a second optical fiber that generates second light of a longer wavelength than the first light, the second optical fiber splitting from the first optical fiber and coupling therewith downstream, a first amplifier on the first optical fiber, a second amplifier on the second optical fiber, different in band from the first amplifier, and a nonlinear optical crystal.

The present invention enables an analysis device that utilizes light absorption to measure concentrations of target components by means of a simple calculation, and without any complex spectrum calculation processing being required, and analyzes target components that are contained in a sample, and is provided with a light source that emits modulated light whose wavelength is modulated relative to a central wavelength using a predetermined modulation frequency, a photodetector that detects an intensity of sample light obtained when the modulated light is transmitted through the sample, a correlation value calculation unit that calculates correlation values between intensity-related signals that are related to the intensity of the sample light, and predetermined feature signals, and a concentration calculation unit that calculates concentrations of the target components using the correlation values obtained by the correlation value calculation unit.

The invention encompasses analyzers and analyzer systems that include a single molecule analyzer, methods of using the analyzer and analyzer systems to analyze samples, either for single molecules or for molecular complexes. The single molecule uses electromagnetic radiation that is translated through the sample to detect the presence or absence of a single molecule. The single molecule analyzer provided herein is useful for diagnostics because the analyzer detects single molecules with zero carryover between samples.

A method for detecting the presence of or quantification of carbon black and/or black carbon in a sample or carrier medium. The method includes providing the sample or carrier medium without labelling or pre-treatment of the carbon black and/or black carbon particles; illuminating the sample or carrier medium at a temperature below 90° C. by a pulsed light with a pulse duration below 500 femtoseconds, a repetition rate above 1 MHz with an average power below 20 mW, and a wavelength of a femtosecond laser pulse ranging from 700 to 1200 nm, to generate non-incandescence related light emission from the carbon black and/or black carbon particles; and analysis of the light emission.