Lighting: spectrum, PPFD and DLI
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Beginner · Light

Lighting: spectrum, PPFD and DLI

A from-zero guide to how grow light actually works: what to measure, what to aim for at each stage, and how to avoid cooking your plants.

Beginner9 diagramsPeer-reviewed · 9 sources~14 min read
01 · Start here

What this is (and why light is the engine)

Light is not just ‘on or off.’ It is the raw fuel a plant turns into sugar, and the single biggest lever on yield and quality you control indoors. This paper assumes you know nothing: it defines every term, gives concrete numbers to aim for at each growth stage, and explains the one switch that makes a plant flower.

Plants eat light. Photosynthesis converts light energy plus CO2 and water into sugar, so more usable light, up to a limit, means more growth[8]. The three numbers that matter most are PPFD (how bright, right now), DLI (how much total light per day), and spectrum (the color mix). Every term is defined the first time it appears.

From light to growth1Light + CO2 + waterphotons hit theleaf2Photosynthesisenergy capturedin the leaf3Sugarsthe plant's food4Growth + budsleaves, stems,flowerIf CO2, water or nutrients run short, extra light stops helping. Light is one input among several.
Figure 1. Light is the input, but it only pays off when CO2, water and nutrients keep pace.
This pairs with the acclimation paper

Read this one for the targets. Read the light acclimation paper for how to ramp up to them safely, so young plants adapt instead of bleaching.

02 · The vocabulary

PAR, PPFD, DLI and umol/J in plain English

Get the gist of these five terms and the rest of the paper falls into place. They all describe the same thing from different angles: how much usable light a plant is getting.

PAR (Photosynthetically Active Radiation)The slice of light from 400 to 700 nm that plants can use for photosynthesis[5]. Lumens and watts do not measure this, which is why a bright-looking bulb can be useless for plants.
PPFD (Photosynthetic Photon Flux Density)How many usable photons land on one square meter each second, in micromoles (umol/m2/s). This is ‘how bright’ at the canopy. Measure it with a quantum/PAR meter, not a phone lux app.
DLI (Daily Light Integral)The total photons delivered over a whole day, in moles per square meter (mol/m2/day). This is the number that actually drives yield. DLI = PPFD x seconds of light per day / 1,000,000[1].
Efficacy (umol/J)How many usable photons a fixture makes per joule of electricity. This is the headline efficiency number when shopping: higher means more light per dollar of power.
PhotoperiodHours of light per 24 hours. ‘18/6’ means 18 on, 6 off.
Same daily dose, different bright/hours mixDLI in mol/m2/day. 400 PPFD over 18h gives the same dose as 600 PPFD over 12h.01223344613.0 mol200x18h25.9 mol400x18h25.9 mol600x12h34.6 mol800x12h38.9 mol900x12h
Figure 2. Worked DLI examples: a lower PPFD over more hours can match a higher PPFD over fewer hours. The daily total is what counts.[1]
Where PAR sits on the spectrumPAR is the 400-700 nm window. Lumens/lux instead peak near green (~555 nm), which is why they mislead.UVBlueGreenRedFar-red280 nm515 nm750 nm
Figure 3. PAR is the 400 to 700 nm band plants use. Lux meters weight toward green, so they are the wrong tool for plant light.[5]
PPFD through the day adds up to DLIIntensity (PPFD) times hours is the day's total light: DLI in mol/m2/day. The area under this curve is what the plant actually gets.02505007501000offmiddayoffPPFD umol/m2/s
Diagram. Intensity over time is DLI: the area under the daily PPFD curve.
03 · Core concept 1

Spectrum: what each color does

Blue light, roughly 400 to 500 nm, keeps plants compact with tight internode spacing and is linked to denser growth and resin in flower[3]. Red light, 600 to 700 nm, is the most photosynthetically efficient band and drives flowering and stretch[7].

‘Full-spectrum white’ LEDs are rated by color temperature in Kelvin. Higher-K and bluer (around 4000 to 6500K) leans veg, lower-K and redder (around 3000 to 3500K) leans flower. A good broad white spectrum works fine across both stages for beginners. The practical takeaway: do not over-optimize spectrum early. Intensity matters far more for yield than chasing a perfect color recipe.

What each part of the spectrum does. Green is not wasted: it reaches lower leaves, but it is a minor lever.
Band (nm)NameMain effectWhen it matters
280-400UVStress response, possible resin; safety hazardOptional, end of flower
400-500BlueCompact growth, tight internodes, thicker leavesVeg
500-600GreenPenetrates deeper into the canopy than expectedMinor lever, all stages
600-700RedHighest photosynthetic efficiency, drives flowering and stretchFlower
700-750Far-redSpeeds the dark response, adds stem stretchFine-tuning only
Beginner rule on spectrum

A quality full-spectrum white LED covers veg and flower. Intensity beats spectrum tuning, so spend your attention on PPFD and DLI before you chase color recipes.

04 · Core concept 2

Intensity and the daily dose: targets by stage

Young tissue cannot process intense light, so targets climb as the plant matures. Clones and seedlings want about 100-300 PPFD (DLI ~10-15 mol)[1], early-to-late veg about 300-600 PPFD (DLI ~20-35 mol), and flower about 700-900 PPFD without added CO2 (DLI ~30-45 mol)[2].

Pushing past about 900 PPFD only pays off if you also raise CO2 to 1000-1200 ppm and tighten temperature and humidity[8]. Otherwise extra light just causes stress and bleaching. Because DLI bundles intensity and hours together, you can hit the same daily dose with lower PPFD over more hours (veg at 18/6) or higher PPFD over fewer hours (flower at 12/12).

Flowering PPFD: where useful ends and risk beginsAbove ~900 PPFD without CO2 and tight climate control, you buy stress and heat, not yield.no-CO2 sweet spotmarginalCO2 + climate only07501500
Figure 4. Flower intensity zones. Most rooms top out around 700-900 PPFD. The 1000-1400 band needs CO2 and serious climate control.[9]
Yield response to DLI: rising, then flat, then stressedDLI (mol/m2/day) on the x-axis. Returns rise, flatten at saturation, then bend down into stress. CO2 shifts the flat point right.0204060805152535455565relative growth
Figure 5. Growth rises with DLI, levels off at light saturation, then falls as stress and bleaching set in. Adding CO2 moves the saturation point to the right.[8]
Stage targets. 600 PPFD x 18h (veg) is roughly the same daily dose as 800 PPFD x 12h (flower).
StagePPFD (umol/m2/s)DLI (mol/m2/day)Photoperiod
Clone / seedling100-300~10-1518/6
Early veg300-450~20-2918/6
Late veg450-600~29-3918/6
Flower (no CO2)700-900~30-4512/12
Flower (CO2 1000-1200 ppm)1000-1400~40-6012/12
05 · Core concept 3

The photoperiod flip that triggers flowering

Photoperiod-type cannabis stays vegetative under long days (commonly 18/6) and is forced to flower by switching to 12 hours light and 12 hours uninterrupted dark[4]. This is ‘the flip.’

The plant does not count light hours. It measures the length of the unbroken dark period using a pigment called phytochrome, which flips between an active form (Pfr) and an inactive form (Pr). Once nights are long enough it produces a flowering signal, florigen, in the leaves[5]. This is why light leaks matter so much: even a phone screen, an indicator LED, or a pinhole in a tent during lights-off can reset phytochrome and stall or revert flowering, cause re-vegging, or trigger hermaphrodites[4].

How the dark period triggers flowering1Lights onPr converts toactive Pfr: 'itis day'2Lights offPfr slowlyreverts to Pr3Long enough nightflorigen signalmade in leaves4Flipgrowing tipsswitch to budproductionA red or far-red light leak re-converts Pr back to Pfr and breaks the cycle, so the plant 'thinks' it is still day.
Figure 6. Phytochrome tracks the dark period. A light leak during lights-off resets the clock and stalls the flip.[4]
Seal your dark period

Light leaks during the dark period are the number one beginner flowering failure: stalled bloom, re-veg, or hermaphrodites. Far-red and red are exactly what phytochrome senses. Seal pinholes, cover indicator LEDs, use light-proof ducting. If you can see in the dark, so can the plant.

Photoperiod: the light schedule flips the planthours of light vs dark over 24hVegetative 18/618h light6h darkFlower 12/1212h light12h dark12 hours of uninterrupted dark triggers and holds flowering. A light leak in the dark can revert or stress the plant.
Diagram. Photoperiod by stage: 18/6 in veg, 12/12 to flower.
06 · The hardware

LED vs HPS vs CMH, and reading efficacy

Modern LED is the efficiency leader at roughly 2.7-3.0 umol/J for good fixtures (budget units 2.0-2.3), runs cooler, and lasts longer[6]. HPS (high-pressure sodium) sits around 1.7-1.9 umol/J and runs hot but is cheap to buy. CMH/LEC (ceramic metal halide) lands lower, around 1.3-1.9 umol/J, but has a pleasant broad spectrum.

Efficacy (umol/J) is the number to compare. A 3.0 umol/J LED makes about 60% more usable light than a ~1.85 umol/J double-ended HPS for the same power bill[6]. For beginners, a reputable full-spectrum LED with a published PPFD map and efficacy at or above ~2.5 umol/J is the safe default. Ignore inflated ‘equivalent watt’ marketing and look at actual PPF (total umol/s) and coverage.

Fixture efficacy (umol/J)Higher is more light per watt. The target line marks a sensible 'good buy' threshold.01233target2.1Budget LED2.85Good LED1.85HPS DE1.7HPS SE1.5CMH
Figure 7. Efficacy by fixture type. Good LED clears the ~2.5 umol/J threshold comfortably; HPS and CMH fall short.[6]
Compare on efficacy and total PPF plus a real PPFD map, never on lumens or 'equivalent watts.'
TypeEfficacy (umol/J)HeatUpfront costBest for
LED2.0-3.0LowHigherDefault choice, all stages
HPS1.7-1.9HighLowBudget builds, red-heavy flower
CMH / LEC1.3-1.9MediumMediumBroad natural spectrum incl. some UV
07 · Do this

Hanging height, coverage, and a stage-by-stage setup

Light obeys the inverse-square law: roughly doubling the distance from the canopy cuts PPFD by about 75%. Height is your coarse intensity dial, the dimmer is the fine dial. Hang about 24 in for seedlings and clones, ~18 in for veg, and ~12-16 in for flower, then fine-tune with the dimmer and a PAR meter.

Verify coverage by taking PPFD readings at nine points: four corners, four edge-midpoints, and the center. Aim for a min-to-average ratio above 0.75 so edge plants are not starved while the center bleaches. Hanging higher trades peak intensity for more even spread, so use a manufacturer PPFD map as your starting point and confirm with real readings at canopy height.

A 9-point PPFD grid (example, umol/m2/s)Average ~640, lowest corner 560: min/avg = 0.875, above the 0.75 floor. A reading under ~480 here would flag a weak corner.0225450675900560Corner640Edge760Center650Edge590Corner
Figure 8. Sample of a 9-point grid. Compare the lowest reading to the average: a min-to-average ratio above 0.75 is acceptable uniformity.
Starting heights. Always confirm against your fixture's PPFD map and a meter at canopy height.
StageHang heightTarget PPFDPhotoperiod
Clone / seedling~24 in100-30018/6
Veg~18 in300-60018/6
Flower~12-16 in700-90012/12
Ramp, do not slam

Pair this with the light acclimation paper: raise the dimmer or lower the fixture over several days rather than jumping a fresh clone to full intensity.

08 · When it goes wrong

Light stress, far-red and UV, and common mistakes

Too much light shows as bleaching (white or yellow bud tips directly under the fixture), upward-cupping or ‘taco’ leaves, and faded color even when nutrients are fine. The fix is to dim or raise the light, not to feed more.

Far-red (~730 nm) can speed the transition to dark via the phytochrome system and slightly stretch plants[4]. UV-B in the final 1-2 weeks is a popular potency play, but the evidence that UV-B reliably raises cannabinoids or yield is mixed[2], and it carries real eye, skin and plant-stress risks. Treat it as optional and advanced.

The biggest avoidable errors: jumping a clone to flower-level PPFD, trusting lux/wattage over a PAR meter, and ignoring light leaks.
SymptomLikely causeWhat to do
Bleached / white tops under the fixtureToo much PPFDRaise or dim the light, do not feed
Taco / upward-cupping leavesLight plus heat stressRaise the light, check leaf-surface temp
Stretchy, pale growthToo little light or hung too farLower the fixture or boost intensity
Stalled flowering, re-vegLight leak during the dark periodSeal the room light-tight
Scorched tops, PPFD looks fineRadiant heat (esp. HPS)Raise the fixture, watch leaf temp
09 · Reality check

Realistic expectations

More light only helps up to the point where something else (CO2, water, nutrients, temperature or genetics) becomes the limiting factor. Past saturation you pay for electricity and heat with no extra yield, and eventually with stress[1].

Yield is capped by the shortest inputYield is held to the level of the lowest stave. Here CO2 is the bottleneck, so adding more light is wasted.0255075100target90Light45CO280Water70Nutrients60Temp75Genetics
Figure 9. The limiting-factor idea: pushing light far above the other inputs wastes effort. Lift the shortest stave first.[8]
What to actually do
  1. Without CO2, ~700-900 PPFD / ~35-45 mol DLI in flower is a sensible ceiling. The 1000-1400 PPFD regime needs CO2, cooling and humidity control: a whole-room commitment, not just a brighter light.
  2. Nail intensity, dose and photoperiod first. Spectrum tweaks like far-red and UV are fine-tuning, not the main lever.
  3. Buy on efficacy and a real PPFD map. Hit the stage targets, seal your dark period, and lighting stops being your bottleneck.

Once lighting is handled, the rest is climate, feed and genetics. Read the light acclimation paper for how to ramp safely, and the flowering stages paper for what happens after the flip.

Related papers

References

  1. Rodriguez-Morrison, V., Llewellyn, D., & Zheng, Y. (2021). Cannabis Yield, Potency, and Leaf Photosynthesis Respond Differently to Increasing Light Levels in an Indoor Environment. Frontiers in Plant Science, 12, 646020. https://doi.org/10.3389/fpls.2021.646020
  2. Llewellyn, D., Golem, S., Foley, E., Dinka, S., Jones, A.M.P., & Zheng, Y. (2022). Indoor grown cannabis yield increased proportionally with light intensity, but ultraviolet radiation did not affect yield or cannabinoid content. Frontiers in Plant Science, 13, 974018. https://doi.org/10.3389/fpls.2022.974018
  3. Magagnini, G., Grassi, G., & Kotiranta, S. (2018). The Effect of Light Spectrum on the Morphology and Cannabinoid Content of Cannabis sativa L. Medical Cannabis and Cannabinoids, 1(1), 19-27. https://doi.org/10.1159/000489030
  4. Kusuma, P., Westmoreland, F.M., Zhen, S., & Bugbee, B. (2021). Photons from NIR LEDs can delay flowering in short-day soybean and Cannabis: Implications for phytochrome activity. PLOS ONE, 16(7), e0255232. https://doi.org/10.1371/journal.pone.0255232
  5. Eichhorn Bilodeau, S., Wu, B.-S., Rufyikiri, A.-S., MacPherson, S., & Lefsrud, M. (2019). An Update on Plant Photobiology and Implications for Cannabis Production. Frontiers in Plant Science, 10, 296. https://doi.org/10.3389/fpls.2019.00296
  6. Nelson, J.A., & Bugbee, B. (2014). Economic Analysis of Greenhouse Lighting: Light Emitting Diodes vs. High Intensity Discharge Fixtures. PLOS ONE, 9(6), e99010. https://doi.org/10.1371/journal.pone.0099010
  7. Westmoreland, F.M., Kusuma, P., & Bugbee, B. (2021). Cannabis lighting: Decreasing blue photon fraction increases yield but efficacy is more important for cost effective production of cannabinoids. PLOS ONE, 16(3), e0248988. https://doi.org/10.1371/journal.pone.0248988
  8. Chandra, S., Lata, H., Khan, I.A., & ElSohly, M.A. (2008). Photosynthetic response of Cannabis sativa L. to variations in photosynthetic photon flux densities, temperature and CO2 conditions. Physiology and Molecular Biology of Plants, 14(4), 299-306. https://doi.org/10.1007/s12298-008-0027-x
  9. Kotiranta, S., Pihlava, J.-M., Kotilainen, T., & Palonen, P. (2024). High light intensity improves yield of specialized metabolites in medicinal cannabis (Cannabis sativa L.), resulting from both higher inflorescence mass and concentrations of metabolites. Industrial Crops and Products, 211, 118210. https://doi.org/10.1016/j.indcrop.2024.118210

Citations marked in-text as [n] map to this list. Peer-reviewed sources except where noted. Cannabis tissue culture is strongly genotype-dependent, verify dilutions, hormone doses and local regulations against the primary sources before relying on them.