Uploaded August 2024 | Updated September 2026, 2 weeks ago
Visual Trichome Evaluation to Determine Peak Harvest Time
Professor DeBacco
Why Look at the Trichomes?
Trichomes provide an indication of the plants ripeness and cannabinoid and terpen concentrations.
Visual evaluations may not provide an exact number, it can indicate when the greatest concentrations of these compounds are likely to occur in the plant.
A plant sample chemically analyzed is the “best” method, this is time consuming and costly so out of reach by most growers. So, the visual inspection can get very close to peak harvest with minimal cost helping growers maximize their production.
Different Types of Trichomes
Bulbous
Smallest (20 micrometers) and need an aid to be seen
Can synthesize cannabinoids and terpenes
Swell in size as they fill with oil
Sessile
Larger than bulbous (75 micrometers) but still hard to see with the naked eye
Develop early 3-week old plants
Stalked
Very large (500 micrometers) and can be seen with the naked eye
The ‘prized’ trichomes that appear during flowering
Most likely to get damaged
What We Are Looking At…
(A) An individual inflorescence, with majority of the organs covered in stalked glandular trichomes.
Arrow indicates cluster of calyces and bracts covered with trichomes.
(B) Dark field micrograph of stalked glandular trichomes protruding from calyx epidermis. Biosynthesis of secondary metabolites occurs in the secretory disk cells lining the base of the globular trichome head. The metabolites are stored in the clear subcuticular cavity above the secretory disk cells; this cavity will turn milky white to dark brown over the course of flower maturity.
(C) Graphic illustration of stalked glandular trichome structure
Color Differences of Trichomes
Clear- “Empty” not ready for harvest
Cloudy- Increased levels of cannabinoids and terpens
Amber- “Converting” in this stage desirable compounds may be changing to less desirable compounds
Can Pistils be Used?
Pistils can provide a quick guide, but it is the trichomes where the cannabinoids and terpenes are stored so this is the plant part that should be observed with attention to detail.
Traditional Method
Loupe
Works great and still recommended, but it is hard to share what is seen.
Max-see Camera Used
Compact handheld camera/microscope that can connect to an electronic device.
Actual Images from Class…
All of the following images were taken of the Abacus plants from class week 6-8 of flower with the help of a student’s Max-see camera.
Thanks Aaron!
Pistil Trichomes
While there are some trichomes that have developed on the pistils these are not the ones to focus on.
Not all trichomes contain the desirable compounds
The Brown/Amber color of the pistil is an indication that this flower is nearing harvest time, but it is the inspection of the trichomes that makes the final decision on when to harvest.
Close, But Not Yet…
Here the stalked capitate trichomes can be seen.
However, most are clear indicating it is a little early to harvest.
There is some initial cloudy trichomes, but the overall population must be taken into consideration.
Previously Clear Now Cloudy
This indicates an increase the amount of cannabinoids the plant is producing.
Notice Some Purple to the Stalks
This is based mainly on the genetics and not environmental factors, it is possible for the grower to enhance the color based on various plant stressors.
Temperature
Light spectrum
Light Intensity
Purple Concentration
The purple pigment is a sign of Anthocyanin production.
This water-soluble pigment is in a larger class of compounds known as flavonoids.
While anecdotal, some people report better symptom relief with anthocyanins.
Peak Cloudiness
This would be the earliest recommended harvest, but typically the goal is to see a few ambers before harvesting.
First Ambers Can Be Seen
Typically this marks the “optimum time” to harvest.
Link to Lecture Slides: drive.google.com/file/d/1Igw7_UgnDOKwHQ5CCYXoYNR7EZ9NzaWv/view?usp=drive_link
*Due to the description character limit the full work cited for "Visual Trichome Evaluation o Determine Peak Harvest Time" can be viewed at... docs.google.com/document/d/1HCphYjf-hETABf0oBNnwgIo2QgqVGg8H/edit?usp=drive_link&ouid=104237452697237972847&rtpof=true&sd=true
Visual Trichome Evaluation to Determine Peak Harvest Time
Professor DeBacco
Why Look at the Trichomes?
Trichomes provide an indication of the plants ripeness and cannabinoid and terpen concentrations.
Visual evaluations may not provide an exact number, it can indicate when the greatest concentrations of these compounds are likely to occur in the plant.
A plant sample chemically analyzed is the “best” method, this is time consuming and costly so out of reach by most growers. So, the visual inspection can get very close to peak harvest with minimal cost helping growers maximize their production.
Different Types of Trichomes
Bulbous
Smallest (20 micrometers) and need an aid to be seen
Can synthesize cannabinoids and terpenes
Swell in size as they fill with oil
Sessile
Larger than bulbous (75 micrometers) but still hard to see with the naked eye
Develop early 3-week old plants
Stalked
Very large (500 micrometers) and can be seen with the naked eye
The ‘prized’ trichomes that appear during flowering
Most likely to get damaged
What We Are Looking At…
(A) An individual inflorescence, with majority of the organs covered in stalked glandular trichomes.
Arrow indicates cluster of calyces and bracts covered with trichomes.
(B) Dark field micrograph of stalked glandular trichomes protruding from calyx epidermis. Biosynthesis of secondary metabolites occurs in the secretory disk cells lining the base of the globular trichome head. The metabolites are stored in the clear subcuticular cavity above the secretory disk cells; this cavity will turn milky white to dark brown over the course of flower maturity.
(C) Graphic illustration of stalked glandular trichome structure
Color Differences of Trichomes
Clear- “Empty” not ready for harvest
Cloudy- Increased levels of cannabinoids and terpens
Amber- “Converting” in this stage desirable compounds may be changing to less desirable compounds
Can Pistils be Used?
Pistils can provide a quick guide, but it is the trichomes where the cannabinoids and terpenes are stored so this is the plant part that should be observed with attention to detail.
Traditional Method
Loupe
Works great and still recommended, but it is hard to share what is seen.
Max-see Camera Used
Compact handheld camera/microscope that can connect to an electronic device.
Actual Images from Class…
All of the following images were taken of the Abacus plants from class week 6-8 of flower with the help of a student’s Max-see camera.
Thanks Aaron!
Pistil Trichomes
While there are some trichomes that have developed on the pistils these are not the ones to focus on.
Not all trichomes contain the desirable compounds
The Brown/Amber color of the pistil is an indication that this flower is nearing harvest time, but it is the inspection of the trichomes that makes the final decision on when to harvest.
Close, But Not Yet…
Here the stalked capitate trichomes can be seen.
However, most are clear indicating it is a little early to harvest.
There is some initial cloudy trichomes, but the overall population must be taken into consideration.
Previously Clear Now Cloudy
This indicates an increase the amount of cannabinoids the plant is producing.
Notice Some Purple to the Stalks
This is based mainly on the genetics and not environmental factors, it is possible for the grower to enhance the color based on various plant stressors.
Temperature
Light spectrum
Light Intensity
Purple Concentration
The purple pigment is a sign of Anthocyanin production.
This water-soluble pigment is in a larger class of compounds known as flavonoids.
While anecdotal, some people report better symptom relief with anthocyanins.
Peak Cloudiness
This would be the earliest recommended harvest, but typically the goal is to see a few ambers before harvesting.
First Ambers Can Be Seen
Typically this marks the “optimum time” to harvest.
Link to Lecture Slides: drive.google.com/file/d/1Igw7_UgnDOKwHQ5CCYXoYNR7EZ9NzaWv/view?usp=drive_link
*Due to the description character limit the full work cited for "Visual Trichome Evaluation o Determine Peak Harvest Time" can be viewed at... docs.google.com/document/d/1HCphYjf-hETABf0oBNnwgIo2QgqVGg8H/edit?usp=drive_link&ouid=104237452697237972847&rtpof=true&sd=true







![Preparing Solutions Understanding pH and Water Potential
Molarity, Molality, and Normality
Use molarity when dealing with solution chemistry where volume is easy to measure.
Use molality when temperature varies or when studying boiling/freezing point changes.
Use normality when the reaction involves charge or proton transfer, and equivalents matter.
Molarity (M)
Molarity is the concentration of a solution expressed as moles of solute per liter of solution.
Formula:
𝑀=moles of solute /liters of solution
Key Features:
Depends on volume, which changes with temperature.
Commonly used in aqueous solutions, titrations, and equilibrium calculations.
Molality (m)
Molality (m): is the concentration expressed as moles of solute per kilogram of solvent.
Formula:
𝑚=moles of solute /kg of solvent
Key Features:
Depends on mass, not volume → temperature‑independent.
Used in colligative properties (boiling point elevation, freezing point depression).
Normality (N)
Normality (N): measures concentration in equivalents per liter of solution.
Formula:
𝑁=𝑀×(number of equivalents )
What Counts as an “Equivalent”? Depends on the reaction type:
Acid–base: H⁺ or OH⁻ donated/accepted
Redox: electrons transferred
Precipitation: charge equivalents
Example: 1 M H₂SO₄ → 2 equivalents of H⁺ → 2 N
Core Differences
Molarity: moles of solute per liter of solution
Temperature‑dependent (volume changes)
Most common in equilibrium, kinetics, and titrations
Molality: moles of solute per kilogram of solvent
Temperature‑independent (mass does not change)
Used for colligative properties
Normality: equivalents per liter of solution
Reaction‑specific (acid–base, redox, precipitation)
Useful when stoichiometry involves equivalents rather than moles
Preparing Solutions
Preparing solutions: Always specify if molarity is for the hydrate/salt form (ex. MgCl₂·6H₂O)
Dilutions: C₁V₁ = C₂V₂ (valid for molarity in dilute aqueous solutions).
Understanding the C₁V₁ = C₂V₂ Equation
Dilution is about making a solution less concentrated by adding solvent (usually water). The equation:
𝐶_1 𝑉_1=𝐶_2 𝑉_2
C₁ = initial concentration
V₁ = volume you need to take from the stock
C₂ = final concentration
V₂ = final total volume after dilution
Why it works: The number of moles stays the same before and after dilution
*only the volume changes.
Step‑by‑Step: How to Prepare a Diluted Solution
Identify C₁, V₂, and C₂.
Solve for V₁ using
𝑉_1=(𝐶_2 𝑉_2)/𝐶_1
Measure V₁ of the stock solution.
Transfer to a volumetric flask.
Add solvent until you reach V₂.
Definition of pH
pH=−log10[H+]
Each 1‑unit change in pH = 10‑fold change in [H+]
Temperature Dependence
Kw increases with temperature
Neutral pH drops as temperature rises
At 37 °C, neutral pH ≈ 6.8
Important for interpreting physiological pH (blood ≈ 7.4 is still alkaline relative to neutrality)
Strong Acids and Bases
Strong acids and strong bases dissociate completely in water
Examples:
HCl → H⁺ + Cl⁻
NaOH → Na⁺ + OH⁻
In dilute solutions: [H⁺] ≈ initial concentration
Osmosis in Cells
Water moves from higher Ψ → lower Ψ across membranes.
If a cell is placed in a solution with lower Ψ → water leaves → plasmolysis
If placed in higher Ψ → water enters → turgor pressure increases
Pressure Potential (Ψp): The Push of Water
Pressure potential is the physical pressure exerted on water.
In turgid plant cells, Ψp is positive (cell wall pushes back).
In xylem, Ψp can be negative due to tension from transpiration.
Pressure can raise water potential, helping water move upward.
Movement Through Plant Tissues
Water potential gradients drive:
Root uptake
Xylem transport
Leaf transpiration
Water moves from soil (highest Ψ) → roots → stem → leaves → air (lowest Ψ).
Turgor Pressure and Cell Function
Turgor pressure maintains:
Leaf rigidity
Growth
Stomatal opening
Low Ψ in the environment → loss of turgor → wilting.
Water Potential and the Cohesion–Tension Mechanism
Transpiration creates negative pressure potential in leaves:
Water evaporates
Pulls water upward through xylem
Cohesion keeps the column intact
Adhesion helps water stick to xylem walls
This entire process is driven by Ψ gradients.
Gravity is overcome by pressure potential + solute potential + transpiration tension.
Typical Ψ values in a transpiring plant
Soil: Ψ ≈ –0.1 MPa
Root xylem: Ψ ≈ –0.3 MPa
Stem xylem: Ψ ≈ –0.6 MPa
Leaf mesophyll: Ψ ≈ –1.5 MPa
Air (dry): Ψ ≈ –100 MPa or lower
This enormous gradient explains how water is pulled upward against gravity.
Link to Lecture Slides: https://drive.google.com/file/d/1mpj28HsfUezYR-QpF3iSDAS9juxqPJPj/view?usp=drive_link
Due to the description character limit the full work cited for Preparing Solutions Understanding pH and Water Potential can be viewed at... https://docs.google.com/document/d/1ARYz5HO1Do9joQZ0suC1PpF0xjbx3FSS/edit?usp=drive_link&ouid=104237452697237972847&rtpof=true&sd=true Preparing Solutions Understanding pH and Water Potential](https://i.ytimg.com/vi/WbINsHL1wbE/mqdefault.jpg)


