Dynamic Plant Phenometrics System for Photosynthetic Response Analysis

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Solution Overview

Problem

Current methods for studying plant responses to dynamic environmental conditions, such as fluctuating light, temperature, and drought, are limited by laboratory-based constant conditions, which fail to detect novel biochemical and regulatory mechanisms crucial for survival in nature.

Innovation Solution

A system and method that simulates dynamic environmental conditions using LED light sources capable of mimicking natural light fluctuations, combined with sensors and data processing units to assess chlorophyll fluorescence and other photosynthetic parameters in real-time, allowing for continuous, non-invasive monitoring of plant responses.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If constant laboratory conditions are used for studying plant responses, then experimental control and reproducibility are improved, but the ability to detect novel biochemical and regulatory mechanisms is worsened

Engineering Contradiction:
Improveexperimental controlVSAvoidnovel biochemical mechanisms
Core Design Contradiction:
ReliabilityVSLoss of information

Solution Approach 1:

The system transitions from static constant conditions to dynamic fluctuating conditions by implementing programmable environmental parameters that mimic natural field variations. The growth chamber can rapidly change light intensity, temperature, humidity, and CO2 levels according to predefined protocols, enabling detection of plant responses to realistic environmental dynamics while maintaining experimental control.

Inventive Principle:
Principle #15Dynamics

Solution Approach 2:

The system systematically varies multiple environmental parameters (light intensity, temperature, humidity, CO2 concentration) simultaneously according to natural field patterns. This multi-parameter dynamic approach reveals biochemical and regulatory mechanisms that remain undetectable under constant conditions, as demonstrated by the detection of novel photoprotective responses in the patent examples.

Inventive Principle:
Principle #35Parameter changes

2Loss of information

If dynamic environmental conditions are simulated, then detection of novel mechanisms is improved, but system complexity increases

Engineering Contradiction:
Improvenovel mechanisms detectionVSAvoidsystem complexity
Core Design Contradiction:
Loss of informationVSDevice complexity

Solution Approach 1:

The growth chamber system integrates multiple environmental control functions (lighting, temperature, humidity, CO2) into a single unified platform. The programmable controller coordinates all parameters simultaneously, and the imaging system captures multiple plant responses (growth, fluorescence, pigment changes) in parallel, reducing overall system complexity despite the dynamic multi-parameter nature.

Inventive Principle:
Principle #6Universality (Multi-functionality)

Solution Approach 2:

The system incorporates continuous monitoring of environmental parameters and plant responses with automated data acquisition and analysis. Sensors track light intensity, temperature, humidity, and CO2 levels in real-time, while imaging systems monitor plant fluorescence and growth. This feedback loop enables automated adjustment and maintains experimental control despite the dynamic conditions.

Inventive Principle:
Principle #23Feedback

3Loss of information

If real-time monitoring is implemented, then understanding of dynamic plant responses is improved, but measurement complexity increases

Engineering Contradiction:
Improvereal-time response dataVSAvoidmeasurement complexity
Core Design Contradiction:
Loss of informationVSDifficulty of detecting and measuring

Solution Approach 1:

The system combines multiple measurement modalities (fluorescence imaging, growth imaging, environmental sensing) into a single integrated platform. The programmable controller coordinates all measurements simultaneously, and data from all sensors are processed together, reducing the complexity that would arise from separate measurement systems.

Inventive Principle:
Principle #5Merging (Combining)

Solution Approach 2:

The system uses non-invasive optical methods (fluorescence imaging, reflectance imaging) to create optical copies or proxies of plant physiological states. These optical measurements serve as indirect but accurate representations of complex biochemical processes, simplifying the measurement of plant responses without direct intervention.

Inventive Principle:
Principle #26Copying

Applied Scientific Principles

This section explains which scientific principles are used to turn an abstract innovation direction into a practical engineering solution.

Function Achieved in This Case

Enables the detection of otherwise undetectable properties and differences in plant responses to dynamic conditions, improving our understanding of photosynthetic productivity and robustness, and predicting field outcomes for mutant or variant strains.

Implementation Method 1

LED light sources capable of mimicking natural light fluctuations

Methodology Applied
Scientific EffectLight Emitting Diode: Light Emitting Diode

Implementation Method 2

measuring chlorophyll fluorescence and photochemical quantum yield in photosynthetically active biological samples wherein lightpulses are used for detecting the fluorescence yield

Methodology Applied
Scientific EffectFluorescence: Fluorescence

Implementation Method 3

lightpulses are used for detecting the fluorescence yield and achieving the maximum fluorescence yield

Methodology Applied
Scientific EffectPhotoluminescence: Photoluminescence

Data Source

PatentEP2856118B1Plant phenometrics system and method
Publication Date: 2017.10.25 BOARD OF TRUSTEES OPERATING MICHIGAN STATE UNIV
  • EP2856118B1 patent drawing
  • EP2856118B1 patent drawing
  • EP2856118B1 patent drawing

AI summary

Chlorophyll fluorescence may be studied in response to a variety of environmental cues or conditions by growing phototrophic organisms under actinic illumination. Such illumination may be punctuated or disrupted to gain information about the photosynthetic properties or performance of the phototrophic organism. Instruments or devices for carrying out the method are also described.