Abstract:
A ballast water monitoring device and a method for detecting live phytoplankton are disclosed. The device comprises a chamber for receiving a sample, at least one light source to emit light towards the sample, a light detector to receive light from the sample and generate a light signal, and a controller. The controller is configured to control the at least one light source to emit a single pulse of light, calculate the variable fluorescence [Fv] of the sample in response to the pulse of light, at time intervals less than the duration of the pulse of light, compare the calculated variable fluorescence to a predetermined reference limit, and perform an action if the calculated variable fluorescence is greater than the predetermined reference limit.
Abstract:
A biological information detector includes a wristband, a housing, an opening, a light-emitting part, a reflecting part, a light-receiving part, and a protecting part. The opening is defined in a surface of the housing adapted to face a surface of the wrist of the user. The light-emitting part is disposed inside the housing and configured to emit green light. The reflecting part is disposed in periphery of the light emitting part, and configured to reflect the light emitted by the light-emitting part, wherein the reflecting part is disposed inside the housing. The light-receiving part is disposed inside the housing, and configured to receive reflected light reflected at a detection site of the wrist of the user. The protecting part is configured to protect the light-emitting part and the reflecting part, and is disposed at the opening of the housing to contact with the detection site.
Abstract:
An objective optical system includes a convex secondary mirror configured to reflect a measurement light irradiated from an infrared microscope, a concave primary mirror configured to reflect the measurement light reflected by the secondary mirror, a prism to which the measurement light reflected by the primary mirror is irradiated, and a light shielding means provided on an optical path of the measurement light between the primary mirror and the prism to shield a part of the light beam of the measurement light.
Abstract:
This detection device has a holder and a heating unit. The holder holds a detection chip that has the following: a prism that has an incidence surface and a film-formation surface; a metal film formed on said film-formation surface; trapping bodies laid out on the surface of said metal film; and a substrate that is laid out on the surface of the metal film, and together with the metal film, forms a liquid collection section in which a liquid is collected. The heating unit heats at least one of the substrate, the prism, and the metal film either while in contact therewith or without contacting same. Also, the heating unit is positioned so as to avoid the path that excitation light takes from an excitation-light emission unit to the abovementioned incidence surface.
Abstract:
A plankton examination apparatus comprises: a sub-pipe in which a transparent pipe unit; a light source unit which radiates only blue-series light; a detection unit which receives light radiated in the direction on the other side outside the transparent pipe unit through the transparent pipe unit from the light source unit and generates an image of the plankton; and a dichroic mirror installed between the transparent pipe unit and the detection unit in such a way as to transmit only red-series light which belongs to the light radiated by the light source unit and passed through the transparent pipe unit and has a wavelength of 620 nm to 780 nm and to deliver the red-series light to the detection unit.
Abstract:
A live biological specimen is imaged by generating a plurality of light sheets; directing the plurality of light sheets along an illumination axis through the biological specimen such that the light sheets spatially and temporally overlap within the biological specimen along an image plane, and optically interact with the biological specimen within the image plane; and recording, at each of a plurality of views, images of the fluorescence emitted along a detection axis from the biological specimen due to the optical interaction between the light sheets and the biological specimen. The temporal overlap is within a time shift that is less than a resolution time that corresponds to a spatial resolution limit of the microscope.
Abstract:
A biological body inspection apparatus includes a measurement module that acquires an amount of light having a wavelength under measurement contained in light incident on the measurement module and an enclosure that accommodates the measurement module and has a window that transmits light traveling toward the measurement module. An adhesive member is provided on a surface of the enclosure at least in an area thereof that surrounds the window. The adhesive member has a light blocking section that is located in an area outside the window and surrounds the window in a plan view in the direction along the optical axis of the light traveling toward the measurement module and blocks light that belongs to a measurement wavelength region within which at least the wavelength under measurement is present.
Abstract:
A biological fluid sample analysis chamber and a method for analyzing a biological fluid sample is provided. The chamber includes a first chamber panel, a second chamber panel, and a plurality of beads disposed between the first chamber panel and the second chamber panel, which beads are configured to not reflect light incident to the beads in an amount that appreciably interferes with a photometric analysis of the biologic fluid.
Abstract:
A fluorescent biological sample operating and monitoring system for restricting the range of movement of a biological sample to facilitate observation. The system includes: a base formed with a predetermined observation position; a shield formed with an operation opening and cooperating with the base to define a light shielding cavity; an infrared illuminating device for illuminating the predetermined observation position; a low-angle excitation light source device including an excitation light source that emits light in a direction oriented toward the predetermined observation position and of a wavelength smaller than that of light emitted by the infrared illuminating device; and an observation display device including an image capturing device having a lens disposed within the shield for capturing an infrared image and oriented toward the predetermined observation position, and an image display.
Abstract:
This invention discloses a super-resolution microscopy method and device, of which the method comprises the following steps: converting laser beam into linearly polarized light after collimation; linearly polarized light is deflected and phase modulated by a spatial light modulator; the deflected beam is focused, collimated and then converted into circularly polarized light for projection on the sample to collect signal light from various scanning points on the sample, and obtaining the first signal light intensity; switching over modulation function to project linearly polarized light modulated by the second phase modulation on the sample to collect signal light from various scanning points on the sample, and obtaining the second signal light intensity; calculating valid signal light intensity to obtain the super-resolution image. This device features in a simple structure and easy operation, which can obtain a super-resolution beyond diffraction limit at a lower luminous power; it is quick in image formation with the frame frequency over 15 frames when the number of scanning points in each image is 512×512 .