Fast and non-invasive phenotyping of plant health/stress status using a LED induced chlorophyll fluorescence transient imager

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Fast and non-invasive phenotyping of plant health/stress status using a LED induced chlorophyll fluorescence transient imager Henk Jalink, Wageningen UR Greenhouse Horticulture, The Netherlands EPSO: The European Plant Science Organisation EPSO Workshop on Plant Phenotyping November 02-03, 2009 Forschungszentrum Jülich, Germany Forschungszentrum Jülich, Germany ICG-3: Phytosphere Jülich Plant Phenotyping Centre (JPPC) Website: http://www.jppc.de http://www.plantphenomics.com/phenotyping2009

Fast and non-invasive phenotyping of plant health/stress status using a LED induced chlorophyll fluorescence transient imager Henk Jalink Wageningen UR Greenhouse Horticulture, The Netherlands

What is needed: Technologies to characterize plant performance and dynamics High throughput techniques to measure plant at desired scenarios

What is needed: Technologies to characterize plant performance and dynamics High throughput techniques to measure plant at desired scenarios Objective: Develop an imaging sensor that monitors the health and dynamic response of whole plants

Advantage of chlorophyll fluorescence: only plant tissue is visible; no background LED imager

Spectral properties of chlorophyll Fluorescence a b Laser a fluorescence Camera Absorbance b Chlorophyll-a 400 450 500 550 600 650 700 750 800 Wavelength [nm]

Plant recognition using color Easy for computer to recognize the plant Difficult for computer to recognize the plant

Color and fluorescence image of a plant Difficult for computer to recognize the plant Easy for computer to recognize the plant on fluorescence

Color and fluorescence image of a plant Integration time of 0.1 s

MIPS TM robot arm with colour and CF camera Robot arm for scanning plants MIPS TM camera with laser for CF image Light source for colour image Table with plants

Outgrowth of Phytophthora on potato leaf in petri dish Basic fluorescence Maximal fluorescence Water control Photosynthetic activity Pathogen Calculated infected area (gray color)

Outgrowth of Phytophthora on potato leaf Research on pathogenisis Q.E. (%) 80 70 60 50 40 30 Start of growth Research on resistance of cultivars 50 40 30 20 10 Infected area (%) 20 0 0 15 30 45 60 75 90 105 120 135 150 Time (hrs) Growth rate

Herbicide formulation testing on PA 2 droplets of herbicide

Counting pixels with PA < 40% Number of pixels with PA< 40% 1400 1200 1000 800 600 400 200 With additive better uptake of herbicide Control Glyphosate Glyphosate+POE (15) tallowamine 0 0 20 40 60 80 Time after treatment (h)

Some conclusions MIPS system is too slow for high throughput and screening: about 20 sec MIPS can not measure at elevated light levels Needed: a fast methodology that is able to saturate the photosynthesis within a sec

LED Induced Fluorescence Transient Imager for Measuring Stress CCD-camera 14 bit LED s 5000 Watt 1000 µmol/m 2 s at 40x40 cm 2 Background light

Methodology of the LED Induced Fluorescence Transient Imager CF induction (Kautsky) curve of a corn leaf F(t) = F 0 + (F max -F 0 )*(1 e -t/τ ) Asymptote 50 successive images Linear on log-scale: approximate by exponential curve Sinsawat, 1999 PhD thesis ETH

Led pulse of 15 ms; good contrast 1

Led pulse of 15 ms 2

Led pulse of 15 ms 3

Led pulse of 15 ms 4

Led pulse of 15 ms 5

Led pulse of 15 ms 6

Led pulse of 15 ms 7

Led pulse of 15 ms 8

Led pulse of 15 ms 9

Hardly any contrast due to saturation of photosynthesis 10

Time response of healthy tissue Normal functioning photosynthesis

Time response of partly inhibited photosynthesis Partly inhibited photosynthesis

Time response of fully inhibited photosynthesis Fully inhibited photosynthesis

Creating images of PA and τ by fitting each pixel F(t) = F 0 + (F max -F 0 )*(1 e -t/τ ) F max Photosynthetic activity = (F max F 0 )/F max F 0 τ: time constant Two independent parameters from which images can be calculated

Image of the photosynthetic activity, PA High PA Healthy Low PA

Image of the time constant, τ Slow τ Healthy Fast τ

Robotized LED imager for phenotyping at different scenarios LED imager on robot arm Climate room Fully programmable 30 images within one second Calculation of PA- and τ- image Growth of projected leaf area Can run for weeks

Drought stress: measurement in the dark (adaptation) Control Drought Saintpaulia (African violet) PA Dark

Drought stress: measurement in the light (adaptation) Control Drought Saintpaulia (African violet) PA 90 µmol/m 2 s

Black nightshade stressed and healthy

Black nightshade healthy and heavily stressed PA τ Healthy PA τ Stressed

Wilting of a detached leaf of black nightshade plant PA PA PA PA t=0 t=15 min. t=30 min. t=60 min. τ τ τ τ At t=1 min. a leaf is detached

Screening potato genotypes on salinity stress τ Stressed Control

Summary Stress of whole plants can be visualized on PA and τ Changes in PA- and τ-image can depend on the type of stress Only stress that influences the photosynthetic apparatus like diseases, herbicides, light stress and drought Non-invasive, quantitative, accurate and objective Plants can be monitored continuously at different scenarios Within a time frame of 300 ms: high throughput

Future development New camera system for fluorescence and reflection imaging Camera with 8 position filter wheel White LED s for reflection imaging Pulsed high intensity red LED s for imaging Kautsky curve LED s for fluorescence imaging of chlorophyll and anthocyanins content

Time for discussion Dr. Henk Jalink Wageningen UR Greenhouse Horticulture Visiting address: Building 107, Droevendaalsesteeg 1, 6708 PB Wageningen Mail address: P.O. Box 644, NL 6700 AP Wageningen, The Netherlands Phone: +31 (0) 317 48 08 44 Fax: +31 (0) 317 41 80 94 Mailto: henk.jalink@wur.nl http://www.greenhousehorticulture.wur.nl