EP2167941A1 - Appareil d'analyse de vegetaux sur le terrain, procede de suivi de l'etat ou de l'evolution d'une culture et procede de gestion d'un traitement de vegetaux - Google Patents

Appareil d'analyse de vegetaux sur le terrain, procede de suivi de l'etat ou de l'evolution d'une culture et procede de gestion d'un traitement de vegetaux

Info

Publication number
EP2167941A1
EP2167941A1 EP08805884A EP08805884A EP2167941A1 EP 2167941 A1 EP2167941 A1 EP 2167941A1 EP 08805884 A EP08805884 A EP 08805884A EP 08805884 A EP08805884 A EP 08805884A EP 2167941 A1 EP2167941 A1 EP 2167941A1
Authority
EP
European Patent Office
Prior art keywords
fluorescence
measurement
excitation
detection means
light
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP08805884A
Other languages
German (de)
English (en)
French (fr)
Inventor
Nicolae Moise
Gwendal Latouche
Zoran Cerovic
Yves Goulas
Jean-Luc Ayral
Camelia Tinei-Moise
Andrei Nicolae Moise
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
FORCE-A
Centre National de la Recherche Scientifique CNRS
Universite Paris Saclay
Original Assignee
Force-A
Centre National de la Recherche Scientifique CNRS
Universite Paris Sud Paris 11
FORCE A
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Force-A, Centre National de la Recherche Scientifique CNRS, Universite Paris Sud Paris 11, FORCE A filed Critical Force-A
Publication of EP2167941A1 publication Critical patent/EP2167941A1/fr
Withdrawn legal-status Critical Current

Links

Classifications

    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N21/00Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
    • G01N21/62Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light
    • G01N21/63Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light optically excited
    • G01N21/64Fluorescence; Phosphorescence
    • G01N21/645Specially adapted constructive features of fluorimeters
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N21/00Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
    • G01N21/17Systems in which incident light is modified in accordance with the properties of the material investigated
    • G01N2021/1734Sequential different kinds of measurements; Combining two or more methods
    • G01N2021/1736Sequential different kinds of measurements; Combining two or more methods with two or more light sources
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N21/00Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
    • G01N21/62Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light
    • G01N21/63Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light optically excited
    • G01N21/64Fluorescence; Phosphorescence
    • G01N2021/6417Spectrofluorimetric devices
    • G01N2021/6419Excitation at two or more wavelengths
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N21/00Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
    • G01N21/62Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light
    • G01N21/63Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light optically excited
    • G01N21/64Fluorescence; Phosphorescence
    • G01N2021/6417Spectrofluorimetric devices
    • G01N2021/6421Measuring at two or more wavelengths
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N21/00Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
    • G01N21/62Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light
    • G01N21/63Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light optically excited
    • G01N21/64Fluorescence; Phosphorescence
    • G01N2021/6491Measuring fluorescence and transmission; Correcting inner filter effect
    • G01N2021/6493Measuring fluorescence and transmission; Correcting inner filter effect by alternating fluorescence/transmission or fluorescence/reflection
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N21/00Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
    • G01N21/84Systems specially adapted for particular applications
    • G01N2021/8466Investigation of vegetal material, e.g. leaves, plants, fruits
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N2201/00Features of devices classified in G01N21/00
    • G01N2201/02Mechanical
    • G01N2201/022Casings
    • G01N2201/0221Portable; cableless; compact; hand-held
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N2201/00Features of devices classified in G01N21/00
    • G01N2201/06Illumination; Optics
    • G01N2201/062LED's
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N2201/00Features of devices classified in G01N21/00
    • G01N2201/06Illumination; Optics
    • G01N2201/062LED's
    • G01N2201/0627Use of several LED's for spectral resolution
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N2201/00Features of devices classified in G01N21/00
    • G01N2201/06Illumination; Optics
    • G01N2201/069Supply of sources
    • G01N2201/0696Pulsed

Definitions

  • the present invention relates to an apparatus for plant analysis, by light excitation and fluorescence measurement, usable in the field without plant preparation.
  • the invention further relates to an apparatus for evaluating the content of a compound in the skin or epidermis of a plant. From the use of such an apparatus, the invention also relates to a method for evaluating and monitoring the evolution and maturation of a crop, as well as a process for controlling and controlling the treatment. of plants.
  • the invention applies to the field of the analysis and evaluation of biological tissues, for example plants and more particularly crops in the context of so-called precision farming.
  • This term is used when one seeks to manage more precisely the state and the evolution of a culture, for example over time or according to its local specificities within a geographical extent. It may be for example to optimize the quality of the products obtained, or limit the inputs in treatment or nutrients to what is necessary or useful.
  • the document US2005 / 0098713 proposes to evaluate certain states of a culture through the pigments of a sheet, in particular chlorophyll or carotene, by measuring the reflectance with modulation and phase detection.
  • This apparatus uses a network of emission diodes and an array of detectors, arranged side by side, each emitting or receiving a beam gathered and collimated by a collimation optics.
  • This reflectance measurement technique has certain disadvantages, for example a high sensitivity to the state or cleanliness of the surfaces to be measured.
  • Each emission wavelength uses a single source materialized by a single beam collimated by a lens.
  • the detectors also use collimating optics to receive the generated fluorescence.
  • the measurement of a single fluorescence in a given wavelength is not sufficient to provide certain important information, such as the content of certain compounds characteristic of the evolution of the culture.
  • the use of only two fluorescence excitation lengths limits the use of such a device, while occupying a significant volume in a device whose characteristics make it necessary to mount it on a vehicle.
  • An object of the invention is to overcome the drawbacks of the prior art, and in particular to improve the following points: allow a non-destructive and rapid measurement in the field,
  • Another object of the invention is to improve or optimize the possibilities of monitoring plants over time or within a heterogeneous geographical area, and in particular:
  • the invention proposes a device for the non-destructive analysis of plants by fluorescence measurement, comprising:
  • excitation means emitting excitation light in a wavelength band determined to generate a fluorescence in the tissues of a target zone
  • the excitation means and the detection means are arranged according to a geometry determined so that the direction of the rays of the excitation light illuminating said target zone on the one hand and the direction of the fluorescence light rays detected by the detection means on the other hand are not collinear with each other.
  • the detection means receive the fluorescence light generated by the target area without crossing optical convergence means.
  • the measurement distance can be reduced to around 5cm or 7cm, and commonly around 10cm or 15cm. While a natural tendency would be to seek to increase the sensing distance to save on mechanical travel, this short measurement distance can also have benefits. Thus, it allows greater accuracy in measurements, requires fewer means or targeting methods (such as image analysis), and decreases the influences of ambient light.
  • the excitation means include a set of transmitters comprising at least two light emitters located on either side of the detection means, illuminating the target area in non-collinear directions with each other and in the same length band. wave. This multiplicity of transmitters allied to their position relative to the detector allows in particular a more uniform illumination of the target, from different angles. For an object with a heterogeneous relief, the area viewed and processed by the detector is thus illuminated more consistently regardless of its orientation in space.
  • the device according to the invention comprises:
  • excitation means according to a plurality of bands of different wavelengths determined so as to make it possible to carry out a plurality of fluorescence measurements, and / or detection means able to detect a fluorescence light in a plurality of bands of wavelengths determined to allow a plurality of fluorescence measurements.
  • RF G Red Fluorescence - with Green excitation
  • the device further comprises means for selecting a fluorescence measurement from among a plurality of possible measurements, said selection realizing a selection of the excitation and detection means and the mode of treatment to be implemented. corresponding to the selected fluorescence measurement.
  • the management and processing means may then be arranged to select and automatically perform, successively or alternatively, a plurality of different fluorescence measurements. It is then possible to program the acquisition of several different measurements in a single action of the user or during a single movement.
  • the device according to the invention comprises a self-powered portable box having a first face carrying user interface means and a second so-called measuring face directed towards a measurement direction.
  • This measuring face comprises: on the one hand on its periphery a surface carrying the excitation means, and on the other hand at its center a part extending in the measuring direction.
  • This extension constitutes a detection module which encloses at least a part of the detection electronics and carries the detection means on its face on the side of the measurement direction, preferably at the same level as the end of the excitation transmitters. .
  • the excitation and detection means being collected on a single face of the device, the measurement can be performed on one side of the plant to be analyzed, so without sampling or manipulation. It is therefore possible to carry out these measurements in a non-destructive manner, and fast enough to be carried out on the fly during a course in front of a multitude of plants, such as a plantation or a field or a lawn.
  • a preferred embodiment of the invention comprises such a device whose management and processing means are arranged and programmed to provide at least two fluorescence measurements. different, determined to be combined and correlated with each other by the processing means so as to calculate a measurement of the content of a component present in the target.
  • the management and processing means are arranged and programmed to provide a measurement of the content of a chromophoric and non-fluorescent compound, by screen effect on a light excitation generating a fluorescence of another compound located above beyond the compound to be measured.
  • An interesting application example is that of measuring the content of compounds of the family Anthocyanins or Flavonoids, in the skin of grapes, the fluorescent compound located above is chlorophyll.
  • this screen effect measurement comprises two different fluorescence measurements, generated in a fluorescent compound, for example chlorophyll.
  • These two fluorescence measurements are chosen by using, in general for excitation, wavelengths which are absorbed differently by the targeted chromophore compound. That of these measurements whose excitation is absorbed by the targeted compound is called the "affected" measure, and the other is called the reference measure.
  • the reference measure By treatments combining and correlating these two fluorescence measurements, we deduce the amount of target compound screened to the excitation light, keeping a good independence with respect to the measurement distance.
  • the device characterized here is particularly well suited to carry out this measurement of content, since this requires two different measurements of fluorescence.
  • the invention also proposes a biological or agricultural management system including such an analysis device.
  • a biological or agricultural management system including such an analysis device.
  • Such a system may in particular comprise means for communicating with digital means of geolocation, or control of measurements, or control of a treatment, or computer communication, or a combination of several of these means.
  • the invention further provides a method for evaluating the state of a biological entity, and more particularly a plant, implementing such a device.
  • This method makes it possible in particular to monitor the evolution of a culture over time, by comparing a plurality of measurements taken over time for a specific compound in the same plant or plot.
  • It also allows monitoring of the state of a crop within a geographical area comprising a plurality of plots, by comparing a plurality of measurements made in said plots for a particular compound.
  • the versatility and flexibility of the device or system according to the invention also make it possible to determine one or more indices, which may be partly empirical, corresponding to a state of the plant analyzed and / or to its evolution.
  • indices which may be partly empirical, corresponding to a state of the plant analyzed and / or to its evolution.
  • FFF Far Red Fluorescence
  • FFF far red fluorescence
  • Different embodiments of the invention make it possible, by endowing such a device with the wavelengths of the corresponding emitters and detectors, to measure in particular the following compounds or indices: FRF B / FRF G : anthocyanins and certain carotenoids.
  • FRF A / FRF G anthocyanins and some carotenoids.
  • FRF R / FRF G anthocyanins and some carotenoids.
  • BGFuv / FRFuv composite index that can represent fairly closely the anthocyanin content, and also has good stability when the measurement distance varies. This index is sensitive to the presence of certain types of pathogens. By correlation with another measurement on anthocyanins, it makes it possible to check the presence or the absence of pathogens, for example during a harvest or for the adjustment of a treatment.
  • this index is sensitive to the presence of dicotyledone weeds (eg, lamb's-quarters) in a monocotyledon-type crop (eg corn).
  • YGF B / FRF B composite index that can represent the presence of lignin, cutin and other phenolic polymers, it has the advantage of not requiring excitation in Ultra Violet, whose emitters are often more bulky and smaller in scope than commonly available RGB diode arrays.
  • FRFR / FRFUV flavonoids.
  • FRF R / FRF B composite index mainly based on flavonoids, but also sensitive to carotenoids, which it can detect in correlation with another measurement of flavonoids.
  • FRFB / RFB chlorophyll.
  • UV 300-400nm (ultraviolet), more particularly 360-390nm B: 400-470nm (blue)
  • BGF 400-500nm (blue-green fluorescence)
  • G 510-540nm (green)
  • YGF 520-570nm (yellow-green fluorescence)
  • R 620-650nm (red)
  • FRF 705-800nm (far red fluorescence) Improved measurement ranges
  • the versatility of the device according to the invention also makes it possible to improve and optimize the ranges of possible measurements, and the continuity of measurements in these ranges.
  • the absorption of the excitation may be too great for the generated fluorescence to be separable from the noise specific to the measurement conditions.
  • the evolution of the fluorescence measurement affected by the targeted compound is then no longer significant.
  • the device comprises the possibility of processing the reference measurement as an affected measure using the small variations of this measurement when it is slightly affected by the targeted compound.
  • the apparatus then comprises locating or guiding means for maintaining a constant measurement distance, for example a skirt surrounding the measuring face.
  • These guide means advantageously comprise an extension projecting from the measuring face, and of sufficient rigidity to allow the user to fold the measured plants by lightly pressing on them with these guide means.
  • the plants to be measured are thus quickly and without effort brought to a good distance from the measuring face.
  • This extension can be perforated and surround the measurement face in whole or in part.
  • the skirt mentioned above can be made by a simple rigid or elastic mesh, for example elastic wire or molded plastic lattice.
  • the user can measure many plants in succession quickly or continuously, just passing in front of these plants while slightly pressing the guide means on the ends of these plants or on the surface of the cover they are. He can thus traverse the surface of a wheat field by slightly setting the ears to quickly measure the ends of a large number of feet. It is also possible to quickly browse the foliage of a hedge, or the grass sprigs of a grass or meadow.
  • the mathematical result of the usual formula, called “canonical” then follows a descending curve while the content of compound increases.
  • the processing means then perform a mathematical correction of inverting the ratio between the affected fluorescence and the reference fluorescence. This inversion makes it possible to provide values that continue to increase, which is more meaningful for the user and makes it possible to construct a more ergonomic calibration to provide the compound content.
  • the apparatus may use another fluorescence measurement to determine whether the main measurement is saturated or not, for example the BGF UV / FRF UV measurement in the case of Anthocyanins.
  • the apparatus may also use the YGF A / FRF A measurement. The power of the sources in amber light then allows a measurement at a greater distance than with the UV sources described, for example up to about Im.
  • Another possibility is to exceed the saturation threshold of the initial measurement of a compound, using a new excitation wavelength, different from the absorption peak of this target compound.
  • the versatility of the apparatus thus makes it possible to combine a third measurement of fluorescence, for example for anthocyanins by the measurement FRF A / FRF G when the measure FRF R / FRF G is saturated.
  • variations of chemical compositions outside the measured content can affect the performance of this measurement of content, for example by a change in pH during evolution and according to the season.
  • the apparatus comprises the choice of using one or more different fluorescence measurements, according to these measurement conditions. These possibilities are programmed in the means of treatment of the device, and allow better measurement continuity over a larger range of measurement of compound, without requiring new fluorescence measurements, and therefore with the same means of emission and detection. This choice can be recommended or automated, depending on the season or the results of a first measurement of content or fluorescence, or based on information provided by another device.
  • the invention has applications in many agricultural fields, or management of natural areas.
  • Flavonoids and anthocyanins can often be associated with the nutritional value of a fruit, such as the apple.
  • Anthocyanins can often be associated with the maturity of a fruit, and more specifically with phenolic ripening.
  • Another interesting use is the precise evaluation of the state of a plant space having a certain heterogeneity, for example in cartographic form. These may be wilderness areas such as nature parks, cultivated areas or maintained areas such as golf courses or stadiums.
  • Other compounds such as carotenoids, may be associated with the ripening of vegetables, for example lycopene for tomato.
  • the invention proposes in particular to implement such a method to evaluate the maturation or quality or composition of the grape by measuring the content of at least one compound of the Anthocyanin or Flavonoid type in the skin of a fruit, and particular of a grain or a bunch of grapes.
  • the invention thus makes it possible to better know the state or the needs of a culture at different times of its evolution or in different plots, in particular for a spatially or temporally heterogeneous culture. This knowledge makes it possible to organize the various operations at the right moment, such as size, harvest, phytotherapy treatment or nutrient intake.
  • the invention may be implemented to analyze on the fly a plurality of plants to be evaluated, as and when a displacement of the measuring device in crops, or conversely after harvesting.
  • This evaluation can also make it possible to adjust, in real time, the nature of a current operation or the amount of treatment or nutrient implemented.
  • a use of the invention may be the adjustment of a fertilizer treatment depending on the condition of the plants evaluated, or the adjustment of a phytotherapeutic treatment depending on the detection of pathogens and their quantity.
  • Another use of the invention may be to control the quality of products after harvest, and to control a selection or treatment during packaging.
  • FIGURE 1 schematically shows a device according to one embodiment of the invention
  • FIGURE 2 is a perspective view, on the side of the measurement face, of a device according to one embodiment of the invention.
  • FIG. 3 is a simplified sectional side view of a device according to one embodiment of the invention.
  • FIG. 4 represents a spectral diagram of the wavelengths implemented in a device according to one embodiment of the invention;
  • FIGURE 5 is a diagram illustrating an implementation of a system according to one embodiment of the invention.
  • FIGURE 1 to FIGURE 3 represents a preferred embodiment of the invention as it has now been realized and tested.
  • This embodiment is based on a portable housing 10 powered by a remote battery 121 or integrated in the handle, having a measurement face 14 and a user interface comprising a screen 152 and control members such as buttons or buttons 101 and 102.
  • This housing can be held by a portion forming a handle 12 containing the removable battery 121 or the connector of the remote portable battery.
  • This housing 10 also comprises a cylindrical portion 13 extending towards the opposite side to the interface and carrying the measuring face at its end.
  • the measurement face 14 is surrounded by a more or less opaque and possibly removable cover 130, which makes it possible to reduce the interference of the ambient light and to give a reference as to the optimum measurement distance with respect to the measuring face 14.
  • This measurement face comprises a set of detectors 40 covering the fluorescence wavelengths to be measured. In the embodiment described here, this set 40 comprises three detectors 41, 42 and 43 adjacent to each other and grouped together in an equilateral triangle in the center of the measurement face 14. These three detectors are oriented in directions parallel to each other around the other. a detection axis 140, or very slightly convergent around this detection axis 140.
  • Each of these detectors 41, 42 and 43 comprises a detection element, here a silicon photodiode 420 of approximately 2 cm ⁇ 2 cm, and detects the light in a determined wavelength band, respectively blue-green, red and far-red.
  • This detection band is obtained by a color filter or high pass and an interference filter.
  • the combination of these two types of filters allows a better filtration which may be necessary, in particular to prevent the detectors from receiving radiation emitted by the excitation sources. It should be noted that the detectors receive directly the fluorescence to be measured, without using collecting, converging or collimated optics.
  • Each detector requires only one detection element, the photodiode 420 (FIGURE 3), chosen sufficiently large to obtain a good sensitivity that makes it possible to dispense with collection optics. This detection element thus receives a radiation 49 coming from the whole of the target zone 91 illuminated by the excitation emitters.
  • This arrangement makes it possible to use relatively simple detection elements, and to avoid the need for collection optics. Beyond saving on the cost of optics, it avoids the constraints of space, adjustment and depth of field.
  • the measuring face 14 has a concave conical peripheral surface bearing several sets of emitters, which can emit excitation light in different wavelengths, distributed in a circle around the set of detectors.
  • These emitters comprise a set of ultraviolet emitters comprising six UV emitters 21 to 26, distributed at 120 ° in three groups of two adjacent emitters, on a circle around the set of detectors 40.
  • Each of these sources comprises a source, here a ultraviolet LED diode 27, placed in a parabolic reflector 281 forming a beam of about 30 °.
  • the reflectors are mounted on a base 282 determining the position of their beam with respect to the detection axis 140.
  • the UV emitters can also use a dioptric or catadioptric device to improve the convergence of the emitted beam.
  • the emitters also comprise a set of visible light emitters 30, comprising three emitters 31, 32 and 33 distributed at 120 ° around the set of detectors 40 in the same circle as the set of UV emitters 20 and intercalated with the UV emitters.
  • Each of these visible light emitters comprises a source comprising a matrix of LED diodes of red, green and blue interposed colors, integrated in a common component 34 about 4.5 cm side and a power of 3x15W, and covered with a transparent plastic plate forming a matrix of convergent microlenses.
  • This common component 34 is mounted on a shim 36 forming a radiator, the shape of which determines the orientation of the source with respect to the detection axis 140.
  • the transmitter also comprises a broadband pass-through color filter, making it possible to restrict the emissions in the wavelengths used for fluorescence detection, especially towards far red.
  • sources of monochrome excitation can also be used, for example amber-colored sources in the form of a monochromatic LED matrix of high power, of the order of 200W continuously.
  • the excitation emitters are oriented so as to obtain uniform illumination of the target zone 91, even when it is a heterogeneous and / or three-dimensional object.
  • the beams of the emitters are oriented to converge to the axis or axes A41, A42 and A43 of the detectors 41, 42 and 43. More In particular, the axes A22, A32 of the excitation beams are concurrent with each other and with the detection axis 140 at the same point P140, at an optimum distance for the measurement. In the embodiment described, the point of convergence P140 is between 10 and 20 cm of the set 40 of detectors, for example around 15 cm.
  • the emitted beams are not collimated and have a certain opening or divergence makes it possible to limit the constraints on the measurement distance.
  • the target here a bunch of grapes 9
  • the target here a bunch of grapes 9
  • the fluorescence 49 emitted towards the detectors will thus be sufficiently stable and homogeneous to provide faithful measurements of the measured zone 91.
  • the measurements using the UV emitters are made at a distance of about 15 cm, the measurements using only the emitters in visible light can be carried out at greater distances, or even around Im, for example for a measurement of anthocyanins.
  • the beams of the emitters may be oriented so as to be parallel to the detection axis, for example for measurement applications at a large distance.
  • FIG. 3 illustrates more particularly the structure of the device in this embodiment of the invention.
  • the cylindrical portion 13 of the housing encloses a substantially annular electronic card 131, comprising the power supply circuits of the excitation sources, the excitation pulse management circuit and a circuit producing a current generator.
  • the detectors, and the electronics that go with them, are grouped in a cylindrical detection module 400, placed on the measuring face 14 at the center of the circle formed by the excitation emitters and extending in the direction of the target at analyze.
  • the outer face of this cylinder carries the three detectors 41, 42 and 43. This arrangement makes it possible to place the detectors substantially at the same level as the ends of the emitters so that they have a wide reception field and thus makes it possible to approach of the target.
  • the detection module 400 comprises three substantially analogous, substantially circular, small electronic cards 141, 142, 143, stacked along its longitudinal axis, fixed and spaced apart by columns 144.
  • the first small electronic card 141 located on the side of the outer face of the detection module 400, carries the detection elements, here silicon photodiodes.
  • the silicon photodiode 420 receives the light to be detected through a colored or high-pass filter 421 and an interference filter 422 detachably fixed by a locking nut 423 in a cylindrical opening 25.4 mm, thus able to receive standard filters of one inch or 25mm.
  • the second small electronic card 142 carries the circuits and amplifiers that produce the rejection of the ambient light by a feedback loop.
  • the third small circuit board 143 carries circuits and components containing in particular sample-and-hold devices.
  • the detection module 400 constitutes a compact assembly that can be removed from the housing 10, for example for maintenance or to be replaced by a camera module or a module including one or more optical guides. This detection module is connected, through the opening of the large electronic card 131, to a processing module 151 located on the interface side and comprising all or part of the processing means: in particular an acquisition unit and calculation means.
  • This processing module is comprised in a portion 15 of the housing carrying the screen 152 and can be tilted for good readability, and retracted in a housing 105 inside the housing 10.
  • This processing module may comprise a detachable connection him allowing to be exchanged easily, for example for an update or a change of function.
  • the electronics 131 linked to the excitation, that 141 to 143 related to the detection, and the processing module 151 are thus arranged in different and separate electronic modules, allowing simplified maintenance. These modules are further separated by a certain distance, here two centimeters and typically at least 1.5 cm, which allows better dissipate the heat generated and limit the risk of interference between the circuits they comprise.
  • the detection is synchronized to the excitation that is emitted by the excitation transmitters.
  • An IkHz excitation frequency with 20 microsecond pulses has been used successfully, and allows for real-time processing as a field trip.
  • the different fluorescence measurements required to establish the content or the programmed index are interleaved within the measurement period.
  • management and processing means are arranged to: - emit a control signal for controlling the transmitters by pulses,
  • an amplification carries out the rejection of the ambient light by a feedback loop, control, for example by the same control signal, the treatment of the fluorescence peak detected, for example, by means of sample-and-hold devices;
  • synchronous detection using phase modulation between excitation and detection is provided.
  • the management and processing means are then arranged to:
  • FIGURE 4 shows the spectral pattern of excitation wavelengths 61, 62 and 63 and fluorescence detection 65, 66 and 67 in the embodiment being tested.
  • the device of the invention has many applications, especially in the field of agriculture or maintenance of green spaces and scientific research on plants.
  • This combination made it possible to monitor and evaluate grape evolution and phenolic ripening by measuring anthocyanins for red grapes and flavonoids for white grapes.
  • the measurements based on the blue-green fluorescence under UV excitation can also be correlated with the results based on other fluorescences (for example FRF G / FRF R ) to monitor the absence or presence of pathogens before or during harvest.
  • other embodiments which comprise a system 5 including one or more analysis devices 511 to 514, mounted on a structure 52 of shape and size intended to be towed by a vehicle 53 along a large area of plant, for example to monitor and continuously analyze a row of vine 50, on several levels and on both sides.
  • These analysis devices 511 to 514 may each comprise only part of the means implemented, for example only the emitters and detectors part as well as their management means, and be centralized on a single processing module 51.
  • This processing module 51 can also be integrated with, or communicate with, one or more computerized means such as geolocation means 531, or measurement control means 532, or control means 533 for a processing performed as and to measure, or communication means 534 with one or more other systems.
  • computerized means such as geolocation means 531, or measurement control means 532, or control means 533 for a processing performed as and to measure, or communication means 534 with one or more other systems.
  • culture should not be taken too restrictively and may include plants that are monitored and / or maintained, even if they do not produce crops, such as grass, or have not been artificially planted as a monitored or maintained natural area.

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  • Health & Medical Sciences (AREA)
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  • Physics & Mathematics (AREA)
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  • Analytical Chemistry (AREA)
  • Biochemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • General Physics & Mathematics (AREA)
  • Immunology (AREA)
  • Pathology (AREA)
  • Investigating, Analyzing Materials By Fluorescence Or Luminescence (AREA)
EP08805884A 2007-06-01 2008-05-29 Appareil d'analyse de vegetaux sur le terrain, procede de suivi de l'etat ou de l'evolution d'une culture et procede de gestion d'un traitement de vegetaux Withdrawn EP2167941A1 (fr)

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FR0703923A FR2916850B1 (fr) 2007-06-01 2007-06-01 Appareil d'analyse de vegetaux sur le terrain, procede de suivi ou cartographie de l'etat ou de l'evolution d'une culture et procede de gestion d'un traitement de vegetaux
PCT/FR2008/050941 WO2008152308A1 (fr) 2007-06-01 2008-05-29 Appareil d'analyse de vegetaux sur le terrain, procede de suivi de l'etat ou de l'evolution d'une culture et procede de gestion d'un traitement de vegetaux

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EP2167941A1 true EP2167941A1 (fr) 2010-03-31

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US (1) US8476603B2 (zh)
EP (1) EP2167941A1 (zh)
CN (1) CN101715551B (zh)
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CA (1) CA2688260A1 (zh)
FR (1) FR2916850B1 (zh)
WO (1) WO2008152308A1 (zh)

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Publication number Publication date
CN101715551B (zh) 2013-01-30
US20100181496A1 (en) 2010-07-22
CN101715551A (zh) 2010-05-26
AU2008263727A1 (en) 2008-12-18
FR2916850B1 (fr) 2013-02-01
CA2688260A1 (fr) 2008-12-18
FR2916850A1 (fr) 2008-12-05
WO2008152308A8 (fr) 2009-02-19
US8476603B2 (en) 2013-07-02
WO2008152308A1 (fr) 2008-12-18

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