Described and represented is a method for determining the content of at least one plant substance of at least one part of a plant. In order for the content of plant substances, in particular secondary plant substances, of at least one part of a plant to be determined and optimized more expediently, it is provided that the at least one part of the plant is irradiated successively with light of different wavelengths and/or wavelength ranges and that, in response to the irradiation of the at least one part of the plant with light of each wavelength and/or at each wavelength range, the chlorophyll fluorescence at least substantially the same wavelength and/or at least substantially the same wavelength range is measured in each case.

The present technology relates to an imaging apparatus, an imaging method, and a program that perform appropriate exposure control, to thereby enable a desired object to be appropriately imaged. The present technology includes: an imaging unit including a plurality of pixels having different spectral characteristics; and an exposure control unit setting information associated with exposure control on the plurality of pixels depending on specification information for specifying a kind of a measurement target. Alternatively, the present technology includes: an imaging unit including a plurality of pixels having different spectral characteristics; and an exposure control unit setting information associated with exposure control on the plurality of pixels on the basis of a predicted output value of each of the plurality of pixels based on a spectral characteristic related to a measurement target. The present technology is applicable to an imaging apparatus which senses vegetation, for example.

Methods of deep ultraviolet fluorescence (DUVF) and multi spectral imaging (MSI) detection are disclosed herein for the detection and identification of pathogens on plants. DUV light and visible or near-infrared light are used to illuminate plants or plant leaves such that the light intensity reflected or emitted by the plant or plant leaves can be used to identify the type of pathogen and measure the amount of pathogen on the plant or plant leaves and, additionally, be used to measure the plant's stress response to such pathogen. Also provided herein is a biophotonic analyzer device that uses both DUVF and MSI detection for the monitoring and surveillance of plant health and for the identification and enumeration of pathogens on plants or plant leaves.

An approach to remotely and noninvasively detect and evaluate the response of a plant or plant population to a man-made or natural treatment regime (e.g., herbicide, fungicide or fertilizer treatment) via spectral imaging methods and systems comprising the capture of a plurality of spectral images for a common plant scene, each associated with a selected wavelength region of the electromagnetic spectrum, the formulation of an index function from the spectral information indicative of the plant response over time, and the assessment of mathematical parameters quantifying the time-varying plant response to the treatment regime. The plant response to a treatment regime may be quantified in illustrative embodiments in a fraction of the time previously required by many conventional approaches. Applying varying herbicide dosages to segments of the same plant population enables easy determination of a dose-response curve.

Cell counting device A cell counting device and a method of using a cell counting device are disclosed. The cell counting device comprises a chamber for receiving a sample, at least one light source to emit light towards a section of the chamber. The section of the chamber comprises a sub-sample of the sample. The cell counting device also comprises a light detector to receive a light emitted from the section of the chamber and to generate an electronic signal associated with the received light, and a controller. The controller is configured to estimate the number of photoactive cells in the sample by calculating the distribution of variable fluorescence [F.sub.v] values of a predetermined number of sub-samples about the mean F.sub.v value.

A method of detecting cannabis pigments in a cannabis extract includes providing a sample of the cannabis extract, illuminating the sample with an excitation wavelength of ultraviolet light, detecting a fluorescence from the sample with a fluorescence detector, identifying carotenoid pigments by a fluorescence of 300 nm to 600 nm in the fluorescence spectrum, and identifying chlorophyll pigments by a fluorescence of 650 nm to 750 nm in the fluorescence spectrum.

An apparatus for remote detection of plant growth dynamics is described. The apparatus includes an excitation LED (light emitting diode) module, a detection module and a controller module coupled to the excitation LED module and the detection module. The excitation LED module includes at least one LED. Each LED is configured to emit an excitation light in response to an excitation control signal. The excitation light has an emitted light spectrum.

The detection module includes a photodetector configured to detect an initial chlorophyll a fluorescence (“ChlF”) light and an excited ChlF light from a plant species. The photodetector is further configured to convert the detected initial ChlF light into an initial detection electrical signal and the detected excited ChlF light into an excited detection electrical signal. The excited ChlF light is emitted from the plant species in response to receiving the excitation light.

The controller module is configured to provide the excitation control signal to the excitation module, to capture the initial and excited detection electrical signals from the detection module and to determine chlorophyll fluorescence data based, at least in part, on the initial and excited detection electrical signals. The excitation LED module and the detection module are configured to be positioned remotely from the plant species. The chlorophyll fluorescence data represents a growth characteristic of the plant species.

A solution for illuminating plants is provided. An illustrative system can include: a set of visible light sources configured to emit visible radiation directed at the plant; a set of ultraviolet radiation sources configured to emit ultraviolet radiation directed at the plant; and a set of sensors, wherein at least one sensor is configured to detect a fluorescence emitted from the plant due to the ultraviolet radiation and a fluorescence emitted from the plant due to the visible radiation.

A quality determination apparatus includes a state detector and a main processing unit. The state detector detects a state index. The state index is an index indicating a state of a target article contained in a storage space where an internal environment is controlled. The main processing unit performs a determination operation. The determination operation is an operation of determining whether a sign condition indicating a sign of degradation of the target article is met based on the state index detected by the state detector.

The present invention provides a device (1) for detecting contamination with a photosynthesis inhibitor, the device including a collection device (10) configured to collect a test liquid, a light-blocking pretreatment tank (21) configured to store the test liquid (2) collected by the collection device in a state of containing phytoplankton, a stirring device configured to maintain a floating state of the phytoplankton in the test liquid stored in the pretreatment tank, an irradiation light source configured to irradiate the phytoplankton in the test liquid stored in the pretreatment tank with weak light having an underwater photon flux density that does not cause photoinhibition, a drainage conduit (40) configured to allow the test liquid discharged from the pretreatment tank to flow thereinto, and a fluorescence quantum efficiency measuring machine (50) provided for the drainage conduit and configured to measure a fluorescence quantum efficiency of the phytoplankton in the test liquid discharged from the pretreatment tank, and a method for detecting contamination with a photosynthesis inhibitor, the method including a liquid supply step, a storing and weak-light irradiation step, and a fluorescence quantum efficiency measurement step.