American Journal of Plant Sciences
Vol.10 No.06(2019), Article ID:93052,22 pages

Cannabis Indoor Growing Conditions, Management Practices, and Post-Harvest Treatment: A Review

Dan Jin1,2*, Shengxi Jin2, Jie Chen1,3

1Biomedical Engineering Department, University of Alberta, Edmonton, Canada

2Labs-Mart Inc., Edmonton, Canada

3Electrical and Computer Engineering Department, University of Alberta, Edmonton, Canada

Copyright © 2019 by author(s) and Scientific Research Publishing Inc.

This work is licensed under the Creative Commons Attribution International License (CC BY 4.0).

Received: March 14, 2019; Accepted: June 15, 2019; Published: June 18, 2019


Cannabis has attracted a new wave of research attention as an herbal medicine. To deliver compliant, uniform, and safe cannabis medicine, growers should optimize growing environments on a site-specific basis. Considering that environmental factors are interconnected, changes in a factor prompts adjustment of other factors. This paper reviews existing work that considers indoor growing conditions (light, temperature, CO2 concentration, humidity, growing media, and nutrient supply), management practices (irrigation, fertilization, pruning & training, and harvest timing), and post-harvest treatment (drying and storage) for cannabis indoor production.


Cannabis, Environmental Factors, Growing Conditions, Post-Harvest Treatment, Indoor Cultivation, Agrology, Agricultural Science

1. Introduction

Cannabis is an annual, non-obligate dioecious plant that is used as a complex botanical medicine containing more than 100 identified cannabinoids [1]. Cannabinoids belong to the chemical classification of terpenophenolics, which are widespread in plants. The most important and frequently detected cannabinoids are tetrahydrocannabinolic acid (THCA), ∆9-tetrahydrocannabinol (∆9-THC), ∆8-tetrahydrocannabinol (∆8-THC), cannabidiolic acid (CBDA), cannabidiol (CBD), cannabigerolic acid (CBGA), cannabigerol (CBG), cannabinolic acid (CBNA), cannabinol (CBN), cannabichromenic acid (CBCA), cannabichromene (CBC), cannabicyclolic acid (CBLA), and cannabicyclol (CBL) [2]. Cannabis can be classified either as drug-type plants that have high THC concentrations or as fibre-type plants that are referred to as hemp. Biosynthetic pathways for cannabinoids have been research hotspots since their discovery. The most widely-accepted biosynthetic pathway was proposed by Taura [3] [4] and Morimoto [5] , in which CBGA is the direct precursor of THCA, CBCA and CBDA, where CBGA is biosynthesised by geranyl diphosphate (GPP) and olivetolic acid [6] [7]. It is crucial to understand how cannabinoids are related with each other when studying cannabis, considering that degradation (including decarboxylation, isomerization, irradiation, and oxidation) can affect the chemical components through improper operations or during long-term storage with unsuitable conditions, which may severely alter experimental results. Biosynthetic pathways for the production of cannabinoids, including degradation products [8] , are demonstrated in Figure 1. Current research tends to focus on THC, which is psychoactive. However, non-psychoactive cannabinoids such as CBD, CBG, and CBC also have broad therapeutic potential [2]. Apart from cannabinoids, terpenoids, which are responsible for cannabis’s distinctive odour, are receiving increasing attention for their suggested synergistic interactions with cannabinoids [9] [10]. Large amounts of active ingredients endow cannabis with a wide range

Figure 1. Relationships between the major cannabinoids found in cannabis [8].

of potential therapeutic uses, including the treatment of nausea or vomiting associated with chemotherapy, anorexia associated with AIDS-related weight loss, spasticity and neuropathic pain associated with multiple sclerosis and intractable cancer pain [11].

Since the turn of the 21st century, cannabis for medical purposes has trended globally and became particularly well established in North America. To achieve a consistent profile of effective components in cannabis as an herbal medicine, significant work has been carried out to investigate the mechanism of cannabinoid production. According to recent studies, genetics, growing conditions, manner of drying and storage, and methods of processing and extraction may affect the concentration and profile of pharmaceutically active ingredients derived from cannabis [12]. Within a specific cultivar, the ratio of THC and CBD remains consistent in both male and female plants [13] [14] as well as in leaves and flowers throughout vegetative growth and flowering stages [15] [16] [17]. However, the density of floral bracts and bracteoles that carry glandular trichomes, where cannabinoids and terpenes are biosynthesized and stored, is higher in female plants than in males [2]. Concentration also varies in different plant parts, decreasing in the order of inflorescences, leaves, stem, seeds, and roots [13] [18]. The ratio of THC to CBD is a qualitative trait and the total yield of THC plus CBD is a quantitative trait [19]. Based on this concept, another study calculated cannabinoid yield in a fixed cultivation area as the product of four components: 1) total dry, above-ground biomass; 2) inflorescence leaves and bracts as a proportion of total plant biomass; 3) total cannabinoids in the inflorescence leaves and bract fraction; and 4) “purity”, the proportion of one cannabinoid out of total cannabinoids [14]. The last component “purity” is a qualitative trait controlled by a simple genetic mechanism that is minimally affected by environmental factors, while the first three components are quantitative traits controlled by different polygenic mechanisms that are heavily affected by the environment [14].

Cannabinoid yield in a fixed area = One cannabinoid Total cannabinoid × Total cannabinoid Yield of inflorescence × Yield of inflorescence Yield of total plant biomass × Yield of total plant biomassin a fixed area

In the modern cannabis industry, strains with high THC potency are predominantly propagated in controlled environment systems, such as growth chambers or greenhouses [20]. The process starts with seeds or cuttings and uses light schedules to trigger and control the duration of the vegetative and flowering stages [12] (Figure 2). Environmental factors, including growing conditions, horticultural management practices, and post-harvest processing (curing, extraction, etc.), combine with genetics to contribute to the variation in medicinal profiles of the final products. The Dutch government has issued a quality

Figure 2. Environmental factors throughout the growing process impact cannabis yield and quality.

assurance system for standardizing cultivation, harvesting and processing of cannabis, including strain, growing medium, light cycle, light intensity, colour temperature of the lighting, humidity, temperature, ventilation, plant age at harvest, time of day for harvesting, drying facility humidity and temperature, drying facility ventilation rates, and drying time [21]. The American Herbal Pharmacopoeia (AHP) has also issued standards of identification, analysis, and quality control of cannabis based on peer-reviewed literature [2]. This article provides a comprehensive review of the current scientific knowledge on horticultural practices for indoor medical cannabis production. Harvest yield and consistency depends on environmental factors, which have interdependencies and interactions. Changes in one factor may have profound effects on how the plants respond to others [22]. Therefore, an integrated approach to analyzing growing practices is required.

1.1. Growing Conditions


Light, both the quality (spectrum) and quantity (intensity), plays an important role in cannabis cultivation in controlled environmental systems, where plants capture energy from light and assimilate CO2 and water into dry matter through photosynthesis.

Light spectrum. Plants utilize light in the visible spectrum between 400 nm and 700 nm, which is typically referred to as photosynthetically active radiation (PAR). Blue light tends to decreases internode length while a low red/far-red ratio promotes stalk elongation [23]. Ultraviolet A light (UVA, 315 - 400 nm) helps reverse damage to DNA caused by Ultraviolet B light (UVB, 280 - 315 nm) [24] [25]. UVB is reported to increase THC levels in plants; THC is thought to be a UVB photo-protectant [26] [27] [28]. Lydon (1987) found a significant linear relationship between THC content (mg/g d.w.) in floral tissue and UVB dose in drug-type plants, whereas other characteristics such as physiology, leaf morphology, and content of other cannabinoids (such as CBD) in drug- and fibre-type plants were unaffected [28]. THC content in floral tissue increased from 25% to 32% when the daily effective UVB dose was raised from 0 kJ/m2 to 13.4 kJ/m2. However, this paper only reviews two chemotypes (one each of drug- and fiber-types) and three levels of daily effective UVB doses (0, 6.7, and 13.4 kJ∙m−2 UVB), thus more data are required to draw firm conclusions.

For indoor cultivation, commonly used lamps include fluorescent lamps (FL), metal halide lamps (MH), and high-pressure sodium lamps (HPS). The ability to transform electrical energy to PAR varies between lamps, as does the spectra emitted. For example, the type of phosphor used to coat the surface of CFLs determines the spectral output. Whereas MH lamps emit insufficient red light to produce heavy flowers, HPS lamps are heavily concentrated in the yellow, orange, and red spectra with a small amount of blue. A combination of several lamps may be utilized to cover desired wavelengths.

More recently, light emitting diode (LED) fixtures with adjustable spectra have been developed. One study compared the effects of three light spectra, including one HPS and two types of LEDs (AP673L and NS1), on the morphology and cannabinoid content of cannabis clones [23]. The spectrum produced by HPS was 96% PAR and was heavily concentrated with green/yellow (68%) and orange/red (21%) and less concentrated in violet/blue (8%). In comparison, the AP673L spectrum was 93% PAR and more concentrated with orange/red (59%) than green/yellow (20%) and produces more violet/blue light (14%). The NS1 spectrum was 94% PAR and spread between green/yellow (37%), orange/red (33%), and violet/blue light (24%). The percentage of UVA was 1% in HPS, 0% in AP673L, and 2% in NS1. At maturity, plants grown under the two LEDs were shorter and more compact than those grown under HPS due to increased red and blue emission. HPS resulted in higher flower yields (26.6 g per plant) compared to LED treatments (23.1 g and 22 g for AP673L and NS1, respectively). These results are comparable to a study by Vanhove et al., (2011), where flower yield per plant was 20.1 g under similar lighting conditions [29]. The author did not volunteer any explanation for the decreased yield of LEDs—results from other studies imply that the high thermal efficiency of LEDs decreased the overall heat load, thereby reducing temperature and decreasing evapotranspiration rate, net photosynthesis (PN), CO2 assimilation, and, ultimately, yield [22]. Although the dry flower yield (g/plant) is higher with HPS, it also resulted in the lowest THC mass proportions (9.5%) while NS1 LED resulted in the highest (15.4%); this may indicate a positive effect from blue and UV-A light, which was more prominent with NS1 than the other lamps. One alternative explanation is that the low red to far-red light ratio in HPS lamps induced shade avoidance syndrome in plants, reducing phytochemical biosynthesis. Interestingly, despite inducing different morphologies and cannabinoid concentrations, the different lamp treatments did not result in significant differences in total cannabinoid yield (3.2 g/plant for HPS and 4.3 g/plant for NS1, p > 0.05). LED technology enables the manipulation and optimization of light spectra and could be a useful tool for modulating cannabinoid profile and improving yields of specific compounds.

In a recent study, subcanopy lighting (SCL) utilizing LED lights improved cannabis flower quality, consistency, and yield [30]. In this study, plants were not exposed to supplemental SCL or exposed to one of the two kinds of supplemental SCL spectra: red/blue (Red-Blue) and red-green-blue (RGB), positioned 15 cm to the side of the plant stem and raised 2 cm off the soil surface during the flowering stage. Both Red-Blue and RGC SCL increased the yield of dry flowers compared to the control due to increased amount of light being delivered to plants. Both Red-Blue and RGCSCL increased yield and concentration of total THC in flowers from the lower plant canopy compared to the control treatment. Red-Blue produced a more homogenous cannabinoid and terpenoid profile throughout the canopy (between the upper and lower canopies).

Light intensity. There is a close relationship between yield and photosynthetic rate [31]. Chandra et al. carried out a series of experiments to study the effects of light intensity, CO2 concentration, and temperature on individual leaves [32] [33] [34]. The PN and water use efficiency (WUE) of a high potency Mexican drug-type variety increased to a point, with increasing PPFD (0, 500, 1000, 1500, and 2000 μmol/m2/s) at 20˚C and 25˚C [32]. At 30˚C, both PN and WUE increased up to 1500 μmol/m2/s PPFD and decreased at higher light intensities. At higher temperatures (35˚C and 40˚C), higher PPFD (2000 μmol/m2/s) showed an adverse effect on PN and WUE [32]. The rates of transpiration (E) were positively correlated with increasing PPFD and temperature (2000 μmol/m2/s and 40˚C), but leaf stomatal conductance (gs) increased with PPFD up to 30˚C only [32]. The maximum of PN (PNmax) for this variety was observed at 30˚C with a PPFD of 1500 μmol/m2/s [32]. In another study, all four drug varieties from Mexico and Switzerland show increasing PN with increasing light intensity with a range of (0, 400, 800, 1200, 1600, and 2000 μmol/m2/s) PPFD at 25˚C ± 3˚C [34]. Although the trend of PN increasing with PPFD is similar for different varieties, the magnitude of increase and PNmax varied considerably with the four varieties studied, with PNmax higher in three Switzerland varieties than one Mexican variety [34]. However, the relationship between higher photosynthesis rate and higher cannabinoid yields has not been conclusively demonstrated [23]. Potter (2009) compared leaf tissue collected from a rare variegated cultivar, which had leaves coloured green and yellow on opposite sides of the midrib, and found that photosynthetic ability has minimal effect on the cannabinoid synthesis on local glandular trichomes [35]. The THC content (w/w%) of yellow leaf tissue was higher than green leaf tissue on the symmetrically opposite side of the same leaf. To investigate the influence of light intensity on cannabinoids and terpene production, further research is required under controlled environments over a longer term and on whole plants.

When CO2, nutrients, water, and temperature are not limiting factors, dry matter production is proportional to the amount of light intercepted by a crop canopy [36]. Because area is a limiting factor for indoor production, the amount of light received per plant is heavily influenced by plant density. With a fixed density, the amount of light received per plant and per square meter is proportional to light intensity at canopy level such that higher light intensity increases yield per plant and per square meter before light saturation occurs. Potter emphasised the close-to-linear correlation between the irradiance level at the commencement of flowering and the subsequent final yield [35]. At the initiation of flowing, the plants maximize light energy usage by developing dense foliar canopies. As a result, increasing PPFD from 78 μmol/m2/s (converted from 17 W/m2 of mercury vapour lamps by an conversion factor of 4.59 [37] ) to 274 µmol/m2/s (converted from 55 W/m2 of HPS lamps by a conversion factor of 4.98 [37] ) at plant canopy resulted in a significant increase (p < 0.01) in yield per square meter. A follow-up study measured yield and THC concentrations under PPFD of 400, 600, and 900 μmol/m2/s (converted from 80, 120, and 180 W/m2of HPS lamps by a conversion factor of 4.98 [37] ) at the canopy and did not find an increase in concentration at brighter conditions. However, the overall floral THC yield (g/m2) increased because plants in brighter conditions yielded more floral material [38]. In contrast, increasing irradiance did not significantly affect THC concentration or yield in leaf tissue; high light intensity at high temperatures may adversely affect PN. Additionally, high light intensity is costly. The same study also investigated mean inflorescence yield per unit of electrical power— results ranged from 0.9, 1.2, to 1.6 g/W, with the highest yield efficiencies occurring at the lowest power consumption levels (600 W/m2, 400 W/m2, 270 W/m2). The result was explained by a decreasing tendency for plants to convert light energy into biomass with increasing light saturation at high irradiance levels. This can be used as a reference for licensed producers and individual growers to balance financial input/output when setting up a growing area. A comparison of effects of lighting intensity on the mean yields of dry cannabis flower under different electrical power consumption (400 W/m2, 510 W/m2, 600 W/m2) in four published European studies suggested that the mean yield of dry cannabis flower is approximately 1 g/W, while electrical energy consumption per gram of yield averaged approximately 1 kWh/g from planting to harvest [39].

With the same light output and room size, increasing plant density beyond a certain point decreases light interception per plant, resulting in decreased yield per plant, but the total room yield remains constant. One study investigated two light intensities (one 600 W HPS lamp per square metervs. one 400 W HPS lamp per square meter), two plant densities (16 plants/m2 density vs. 20 plants/m2), and four varieties in a total of sixteen scenarios. It concluded that all three factors significantly affect yield per plant; however, plant density had no effect on yield per square meter [29]. This indicates that light interception is the limiting factor for total indoor yield. Specifically, yield per plant increased with light wattage, decreased with density, and was significantly different between cultivars. Similar observations were made on yield per area, except that yield per area is independent of plant density. Based on these results, light intensity and plant density are considered as independent additive factors. This topic is of interest to industrial growers, and studies are required to determine the optimized combination of light intensity with plant population to fully utilize light and space resources to maximize yield and profitability. However, there must exist upper and lower thresholds at which plant density will affect yield per area, either in extreme overcrowding or sparseness situations. Such thresholds have not been investigated.

Light regime. Cannabis is a “short-day” plant that naturally flowers in late summer [40] , where it needs uninterrupted and sufficiently long nights to initiate flowering. This process is regulated by a class of photoreceptors in the plants called phytochromes [41]. Phytochromes exist as two photoreversible forms: the red light absorbing form (Pr) and the far-red light absorbing form (Pfr), the latter of which inhibits flowering [41]. In the dark, the active form Pfr slowly reverses back to the state form Pr, but the fewest photons of a flash red light with a peak near 667 nm, which is found in both daylight and lamp light, can convert the Pr to Pfr, subsequently, inhibits flowering [35] [41]. For indoor cultivation, a regimen of 18 hours or 24 hours of continuous light has been used for vegetative growth. A schedule of 12 hours of light and 12 hours of darkness is considered a short day length, and has been widely utilized to initiate flowering—the first flowers are visible one week after the light schedule change [12]. The critical day time length is related closely with a variety’s geographical origin, especially those originating far from the equator [35]. Because day time in all latitudes in the North Hemisphere is longer than 12 hours at summer solstice, 12 hours of darkness will initiate flowering for most varieties. Eleven hours of darkness initiated flowering in tropical varieties, possibly due to plant age instead of light regimen [35].

The effect of light regimen on plant development and cannabinoids profile were studied by Potter by subjecting dozens of cannabis varieties (clone lines) to either 11, 12 or 13 hours of light (short day length) after three weeks of vegetative growth under continuous light for 24 hours [35]. The first part (comparison of 12 and 13 hour of light) of the study was carried out in glasshouses while the second part (comparison of 11 and 12 hours of light) was carried out in an indoor environment. The results are summarized in Table 1. The yield of total floral and foliage material of plants was referred to as Botanical Raw Material (BRM) yield (g/m2). The mean BRM yield (g/m2) and the cannabinoid yield (g/m2) of plants was significantly higher when grown under 12 hours of light compared to 11 hours. There was no benefit in increasing from 12 to 13 hours of light, but there were large decreases in yield in decreasing from 12 to 11 hours of light. Therefore, a 12-hour light regime is the most energy-efficient and economical [35]. It is notable that although there is no significant difference in mean values of all clone lines of some effects investigated, for example, the mean height, the total floral and foliage material (g/m2), and the cannabinoid yield (g/m2), these effects varied with individual clone lines (strains). Each strain requires unique growing conditions and harvest timings that should be investigated and optimized within its specified growing environment.

Table 1. The effect of light regimen on plant development and cannabinoids profile.

aNo significant difference (p > 0.05).

Light cycle in the vegetative stage. Under a continuous light regimen of 24 or 18 hours of light per day, cannabis plants remain vegetative. Vegetative growth shifts to reproductive growth after a two week exposure to 12 continuous hours of light per day [12]. Cuttings from a THC dominant variety were grown indoors by Bedrocan VB (Netherlands) under 18 h of light for 37 days of vegetative stage and 12 h of light for 40 days of flowering stage [42]. One batch was grown under standard conditions and other three batches were grown with one less week of vegetative growth plus one extra week of flowering, one extra week of vegetative growth, one extra week of vegetative growth and one extra week of flowering, respectively. Differences were observed in certain compounds compared with the standard batch. The conclusion was that alterations in growth cycle time appear to cause more differences in chemical profile than growing cuttings in different batches [42].

Light cycle in the flowering stage. A recommended growth period for 200 indoor high-THC cannabis varieties from 20 producers in Europe is between seven to nine weeks in short day length, with a mean recommended duration of 57 days [39]. In order to study the effect of duration of flowering period on cannabinoid yield, 25 THC-dominant clone lines from 14 varieties were sampled in the GM Pharmaceuticals’ glasshouses at the sixth, eighth, and tenth weeks flowering [35]. With a 33% extension in flowering duration from the sixth to eighth week, mean THC yield (g/m2) increased over 50%. With 25% extension in flowering period from the eighth to ten weeks, mean THC yield (g/m2) increased 30%, while the yield increases for approximately half of the clones were less than 25%. The mean THC and CBG content in floral and foliage material continuously increased in the twenty-five clones between the sixth and tenth week of flowering, while the mean proportion of CBG fell as a proportion of total THC and CBG. This suggests that the ratio of these two cannabinoids can be affected by harvest timing. Furthermore, genetics impact THC:CBG ratios more than harvest timing because the THC:CBG ratio of one clone was stable at all harvest timings whereas the average THC:CBG ratios combined from three harvest dates (six, eight, ten weeks) showed significant differences between clone lines. The effect of flowering period length on mixed THC/CBD profiles were studied on five clone lines from five seeds of one variety. THC and CBD content in floral and foliage material continuously increased from the fourth week to eighth week in 12-hour light regime but stopped increasing after the ninth week. For one of the clone lines, the CBD/THC ratio remained constant over the entire flowering stage whereas the ratio fluctuated in other clone lines. Potter concluded that the clone lines with stable CBD/THC ratio can be used as phytopharmaceutical feedstocks and, if such clones are absent, desirable consistent cannabinoid mixtures could only be achieved by blending materials possessing one single dominant cannabinoid. THC dominant Sativex plants grown in the GM Pharmaceuticals’ glasshouses were normally harvested at eight weeks after switch to a 12-hour light regime. While the THC content in floral tissue was relatively stable (13% - 17%) between the fourth week and ninth week with highest value achieved around six weeks in short day length, the floral yield per plant increases steadily until the end of cultivation, which is 400 g/m2 of floral material combined with 200 g/m2 of foliage material.

Another study concluded that the peak total THC content (THC + THCA) in floral material was achieved between the sixth and seventh week after changing to a 12-hour regime in an indoor grow box and the total THC content started to decline at the onset of senescence in all three chemotype I varieties [35]. Aizpurua-Olaizola (2016) observed that plants from chemotypes II and III needed more time to reach peak production of THCA, CBDA, and monoterpenes than plants from chemotype I [17]. Clones from all chemotypes were kept for 42 days for root-growing phase, followed by 60 days for vegetative stages under 18 hours of light and 77 days for flowering phase under 12 hours of light [17]. THCA in flowers of chemotype I plants peaked at the ninth week in short day length (day 165) for indoor growth, while peak content of THCA and CBDA in chemotype II (THC and CBD with equivalent ratio) and chemotype III (CBD dominant) continued to increase until the end of the study (eleventh week, or day 179). The total amount of eight monoterpenes in flowers reached its peak in the ninth week of the flowering phase for chemotype I while the levels continued to increase until the end of the study for chemotype II and III. The amount of sesquiterpenes was stable during the flowering phase. Different maxima may depend on cultivars, cultivation method (from seed or clone), and growing environment (lighting, temperature, humidity, growing medium, nutrients, etc.).

Temperature. Temperature can be a limiting factor for PN: Low temperatures slow PN and excessive heat stops PN. High temperature causes plants to expend energy in cooling by acquiring water and transpiring it through the stomata. Chandra (2011) studied PN in seven cannabis varieties and concluded that the optimal temperatures varied between 25˚C to 30˚C and were variety-specific [33]. The optimum growth temperature is 25˚C - 30˚C for tropical varieties and 25˚C for temperate varieties [2]. In a field experiment on industrial hemp, Sikora calculated accumulative growing degree days (GDD) instead of daily temperatures and found that THC and CBD concentrations are positively correlated with GDD [43]. However, the authors assumed a linear relationship between climate and the content of major cannabinoids, resulting in poor statistical regression between GDD and THC & CBD content. Four varieties from both temperate (Illinois and Nepal) and tropical (Jamaica and Panama) climates yielded higher THC content (mg/g dry weight) in cannabis leaves under cool conditions (23˚C) than under warm conditions (32˚C) [44].

CO2 concentration. Carbon dioxide (CO2) is one of the two limiting factors for PN. A high potency Mexican drug-type variety was exposed to different concentrations of CO2 (250, 350, 450, 550, 650, and 750 µmol/mol) under optimum lightning and temperature conditions (30˚C and 1500 μmol/m2/s PPFD) [32]. Elevated CO2 concentration (750 µmol/mol) increased PN, WUE, and intercellular CO2 concentration (Ci) by 50%, 111%, and 115% respectively and suppressed the rate of transpiration E and gs by 29% and 42% respectively compared to ambient CO2 (Ca: 350 µmol/mol) [32]. Higher PN, WUE, and nearly constant Ci/Ca under elevated CO2 concentrations suggested a potential for better survival, growth, and productivity in CO2 rich environments [32].

Humidity. Compared to relative or absolute humidity, vapor pressure deficit (VPD) more accurately describes the driving force of water loss from plant leaves. VPD combines the relative humidity and air temperature and describes the difference between the actual and maximum amounts of water the air can hold for a given temperature. VPD impacts the opening of leaf stomata, which are responsible for CO2 and water vapor exchange, thereby affecting PN and nutrient transportation. High VPD may induce wilt and necrosis of the leaf tips. For indoor cultivation, ventilation is crucial to control humidity because both high and low VPD can result in reduced yield [22]. At a growing temperature of 25˚C, the recommended relative humidity is 75% for juvenile cannabis plants and 55% - 60% for vegetative growth and flowering [45] , which correspond to VPD of 0.8 kPa and 1.3 - 1.4 kPa respectively. VPD is calculated using the following formula [46] :

VPD = ( 1 R H ) × 610.7 × 10 7.5 T 237.3 + T

where T is the atmospheric temperature in centigrade and RH is relative humidity.

A review of several works reported an increased THC content in drier climates, which was explained as an enhanced THC production in response to stress [27]. A recent experiment confirmed that controlled drought stress may be an effective horticultural management technique to maximize both floral weight and cannabinoid yield in cannabis [47]. An eleven-day drought (withholding irrigation until the drought stress threshold of −1.5 MPa was reached at week seven of the flowering stage) increased the concentration of major cannabinoids THCA and CBDA by 12% and 13%, respectively. In Chemotype II plants, yield per unit growing area of THC was 43% higher, CBDA yield was 47% higher, THC yield was 50% higher, and CBD yield was 67% higher than the control. A follow-up investigation directly contradicted these results: drought stress timing and frequency (in weeks four, five, six, or seven weeks in the flowering stage) did not result in higher floral yield or cannabinoid content compared with the control [47]. The author attributed the differences to the container size and growing medium—the follow-up study used larger growing vessels than the previous trial, so it took longer for a plant to deplete the water already in the vessel to achieve drought conditions. The timing of controlled drought stress was found to influence the content of some terpenoids. Earlier drought stress increased the yield of linalool and cis-ocimene but decreased yield of caryophyllene. Later drought stress increased the yield of alpha-bisabolol and trans-ocimene.

Growing medium. Both soil and soilless (i.e. hydroponics) mediums are used for cannabis production. AHP recommends neutral to alkaline loamy and sandy soil with a pH between 6.5 and 7.2 [2]. One study grew cannabis in eleven different soils that varied in pH and elemental composition [48]. Soil parameters were correlated with the leaves’ elemental and cannabinoid contents. Extractable soil Mg was negatively correlated with THC and CBD concentrations in leaf tissue. Extractable soil P was negatively correlated with CBD concentrations in leaf tissue [48]. Another study showed that there was no difference in floral material yield between two organic coir-based growing media, which had distinct water-holding capacities [49]. However, the lower capacity (U2-HP) growing medium produced 11% higher floral dry weight, 13% higher growth index, 20% higher THC yield, and 20% higher CBGA yield than the one with higher capacity (U2) [49]. The increases may be attributed to the higher irrigation frequency (17 times in U2-HP and 13 times in U2), which was necessary for maintaining moisture (30%), and/or high root zone oxygen, which positively affects plant health, nutrient uptake, root growth, and root-bone disease prevention [49]. Hydroponic systems have greater control over the growing environment by delivering a full range of nutrients to the roots. Active hydroponic systems use pumps and include ebb and flow systems, nutrient film technique, drip irrigation, aeroponics, and deep-water-culture systems. Passive systems use capillary action to drag water to the roots and these include reservoir systems, wick systems, and capillary mats. Commonly used growing media for hydroponic systems include light expanded clay aggregate (referred to as LECA), rock wool, and coconut fibre (coir).

Both soil and hydroponics are widely used for commercial cultivation, and each has its own advantages and disadvantages. Soil has a greater buffer capacity than hydroponics and is simpler to set up. Hydroponic systems allow for comprehensive control, enabling quicker and easier troubleshooting for nutrient delivery. With easy access to nutrients and water, plants are commonly believed to grow faster and have higher yields with hydroponics. However, evidence suggested that yields and potency are not improved by hydroponics compared to soil systems [39]. In addition, a hydroponics system is more complex and requires constant availability of water, electricity, nutrients, and other supplies. The increased complexity without corresponding increases in cannabis productivity or potency led to GW Pharmaceuticals’ rejection of hydroponic growing systems in the Netherlands [12].

1.2. Management Practices

Starting materials

Seeds vs. clones. Two starting materials are available: seeds and clones. Clones are made from tissue cultures by micropropagation or from cuttings of a mother plant. Clones guarantee genetic uniformity, which the pharmaceutical industry values for consistency of quality, safety, and efficacy—qualities that the industry regards as more important than high yield [12]. Clones can also avoid the development of male plants that can be encountered when starting from seeds [2]. To compare the yield and uniformity of plants grown from seeds and clones, Potter grew thirty plants from cuttings and thirty plants from seeds of one variety under identical environmental conditions. The yield of floral and foliage material obtained from plants grown from seeds (494 g/m2) and those grown from cuttings (515 g/m2) were not significantly different (p > 0.05). However, the mean THC content of the cloned plants (14.6% THC w/w) was significantly higher than those grown from seeds (11.1% THC) (p < 0.01). Although the mean CBG and CBC content in floral and foliage has no significant differences (p > 0.05) from plants grown from seeds and grown from cuttings, the CBC potency of seed derived plants was significantly more variable (p < 0.01).The ratios of cannabinoids were also found to be significantly more variable in plants grown from seeds (p < 0.01). However, it was not discussed whether the variability resulted from the uniformity of the heterozygous seeds or homozygous seeds. Furthermore, to achieve maximum rooting success and root quality, cuttings from either apical or basal positions (p > 0.05) should have at least three fully expanded (compared with having two leaves) and uncut leaves (compared with removing the leaf tip), and treated with 0.2% indole-3-butyric (IBA) rooting hormone (compared with treating with 0.2% willow extract gel) [47]. Among these factors, rooting hormone had the greatest effect on both rooting success rate and root quality while removing leaf tips had the second greatest effect on rooting success rate.

Irrigation. Water quality is critical for PN and its products and nutrient transport. For greenhouse crops, the water should be absent of contamination from metals, herbicides, pesticides, and toxicologically hazardous substances [21]. In addition, irrigation water should be tested for the following desirable parameters: alkalinity (expressed as CaCO3 concentration), pH, and electrical conductivity (EC) [50]. The recommended parameters vary greatly among different strains. The optimal EC or pH for cannabis in soil or hydroponic systems has yet to be established through experimentation. General recommendations for irrigation are CaCO3 concentrations between 30 mg/L and 100 mg/L, EC below 1.5 mS/cm, and hardness as Ca and Mg ions between 100 mg/L to 150 mg/L [51]. AHP recommends that the pH in irrigation water should be 6.5 - 7.2 for soil and 5.8 - 6.0 for hydroponics [2]. The pH should be continuously monitored and adjusted whenever it deviates from the set point. Watering frequency and amount can be visually determined or automated to satisfy plant requirements [12] [52] [53].

Nutrient supply. If the growing medium lacks nutrients, it must be supplemented to ensure the plants’ health and yield. Different fertilizers may be used or mixed in accordance with different growth cycles, however, organic fertilizers are not recommended for hydroponic systems because they ferment in the reservoirs, causing microbiological contamination and clogging.

Several studies analyzed the effect of applied fertilizers on morphological and biochemical characteristics of cannabis plants. One study analyzed responses of greenhouse-grown cannabis to N, P, and K at low (0 ppm), medium (25 ppm for N and 50 ppm for P and K), and high concentrations (125 ppm for N and 150 ppm for P and K) [54]. Fertilizers were applied during planting. Mean height (at 28 days and harvest) and tissue yield (combined leaves and flowers) were positively correlated with applied P at three concentrations but were not statistically significant for applied N or K. Although THC and CBD concentrations showed no significant differences after treatment with applied P, N, and K (p > 0.05), total THC yield was significantly positively correlated with applied P due to increased biomass (p < 0.05). In a study where three levels of N fertilizer were applied once each month with totals of 150, 450, and 600 mg/kg, applied N had a positive effect on plant height and a negative effect on THC content (% dry weight) in leaves [55]. Mg and Fe were reported to be important for THC production as enzyme co-factors [27].

Caplan sought to determine the optimal rate of organic fertilizer during vegetative and flowering stages for cannabis grown in coir-based growing media. The study applied liquid fertilizer with a N-P-K ratio of 4:1.3:1.7 at rates of 117, 234, 351, 468, and 585 mg nitrogen per litre of irrigation water (N/L) during vegetative growth and found that the interpolated optimal rate was 389 mg N/L. This optimal rate increased the yield of floral dry weight by 80% as compared to 117 mg N/L [49]. The final yield was positively correlated with growth attributes (growth index [height (cm) × length (cm) × width (cm) × 300−1], leaf number, and branch number) in the vegetative stage [49]. This result suggests that growing larger plants during the vegetative stage by supplying optimal fertilizer rate will increase yield [49]. The study also concluded that fertilization rate had no effect on floral THCA concentrations (10.6% ± 0.31%) or CBN concentrations (0.08% ± 0.018%) but increased THC concentrations, reaching a maximum of 0.31% at 418 mg N/L [49]. Optimal fertilization during the vegetative stage may reduce maturation time [49].

The same study applied five rates of liquid organic fertilizer (57, 113, 170, 226, and 283 mg N/L) with a N-P-K ratio of 2.00:0.87:3.32 during the flowering stage in two coir-based growing media [49]. Fertilizer rate was positively correlated with floral yield. In the medium with lower water-holding capacity (U2-HP), the interpolated optimal rate (261 mg N/L) increased the yield of floral dry weight by 110% compared to the lowest rate (57 mg N/L). Similar results were found for the other medium. Although growth and floral yield are increased with fertilizer rate, concentrations of THC, THCA, and CBGA decreased. The optimal fertilizer rate for U2-HP for maximizing both floral yield and cannabinoid yield was between 212 and 261 mg N/L.

Growing medium management. The condition of the growing medium is dependent on the primary inputs: irrigation and fertilization. Caplan’s experiment showed that growing medium pH decreased over time for all fertilizer rates applied during vegetative growth [49]. The highest floral yield, which supplied 234, 351, and 468 mg N/L, resulted in the lowest pH values, which were between 6.19 and 6.5, with lowest mean pH (6.19) occurring at 351 mg N/L rate on day 17 [49]. The low pH values for organic fertilizers may be caused by NH 4 + nitrification and the excretion of protons by the roots after NH 4 + uptake [49]. This study showed no visual signs of nutrient disorders with pH between 6.2 - 7.1 for the vegetative stage and 6.7 - 7.2 for the flowering stage. EC was positively correlated with fertilization, ranging from 0.9 to 3.9 mS/cm [49]. Floral yield was reduced at 468 and 585 mg N/L, and was attributed to high EC, which was 3.0 ± 0.13 and 3.8 ± 0.13 mS/cm, respectively. Salinity is expressed in EC and can lead to increased osmotic potential and reduced external water potential in the root zone. The pH decreased and EC increased upon higher rates of fertilizer application during flowering [49]. The study concluded that cannabis tolerates EC up to 3.0 mS/cm without reductions in yield.

Pruning and training. Pruning and training enhance yield by maximizing light interception, optimizing nutrient allocation, creating more air circulation, and reducing humidity. Clipping the lower branches on the Bedrocan variety (hybrid “Indica”/“Sativa”), which were grown under 37 days of vegetative stage and 54 days of flowering stage, resulted in lower concentrations for THC, CBG and some terpenes [42]. Additional studies need to be conducted to quantitatively determine the effects of pruning timing and amount on growth and yield.

Another technique uses framed netting to support and position buds in an “opened-up” gesture to provide more light to the lower branches. Knight utilized the ScrOG method, which uses framed netting, to enhance yield of an indoor hydroponic system [56]. An average of 687 g dried inflorescence was achieved per plant using this method. This relatively high yield per plant maybe due to the characteristics of the strains selected and the relatively low plant density (6 plants in 15 m2). The estimated yield per area was 274.8 g/m2 and was comparable to yields reported in other studies [39].

Harvest timing. Because the content of cannabinoids and terpenes change throughout growing and flowering stages, harvest timing affects final chemical composition. To determine specific harvest timing, two methods are commonly used by growers: chemical analysis and visually observation/organoleptic evaluation. The University of Mississippi checks THCA concentrations of raw materials daily to determine optimal harvest time [2]. Whereas chemical analysis is destructive, visual examination is adopted to set harvest timing without disturbing the plants. AHP suggests four physical evaluations. The first evaluation is based on the percentage of senesced stigmas, which appear brown. The percentage at harvest is suggested as 75% [18]. The second evaluation is based on the firmness of the inflorescence—relatively firm resistance when pressed suggested maturity. The third evaluation is based on the color of glandular trichomes. Harvest should occur when there is a shift from a clear to amber or a cloudy white of the first resin heads, which indicates the degradation of THC to CBN. The last evaluation is based on odor, which will reach a peak and give a unique and strain-specific pungent aroma at maturity. These methods can be combined to determine optimal harvest timing [2].

1.3. Post-Harvest

After harvesting cannabis, it is manicured, cured, dried, and stored. Fresh cannabis material typically contains 78-80% moisture [39] and drying is necessary for handling, storage, and avoiding degradation of major cannabinoids before chemical examination. The Office of Medicinal Cannabis of the Dutch Government specifies that the water content of cannabis must be between 5% - 10% directly after packing [57]. Drying crops directly on the ground or under direct sunshine must be avoided [21]. Plants dry within 24 hours to 15% ± 2% moisture when spread evenly to a depth of approximately 15 cm at 40˚C [35]. Moisture content can be checked by measuring weight loss after drying for 24 hours at 105˚C. If the plants are hung to dry, the mean times taken to achieve 15% moisture were 36, 18, and 11 hours at 30˚C, 40˚C, and 50˚C, respectively [35]. When stored in paper bags to dry at 21˚C and 40% RH, fresh floral material cut from stems reached 11% ± 1% moisture in 5 days [47]. The dried material was then cured at 18˚C and 60% RH for 14 days before determining the floral dry weight [47]. Drying at temperature higher than 37˚C for 24 hours may decarboxylate cannabinoid acids [58]. The effect of high drying temperatures on cannabinoids and terpenes requires further investigation. To minimize loss of volatile terpenes during heating, another method for cannabinoid and terpene preservation is freezing by sublimation, which takes 10 to 20 days.

As oxidation occurs with the presence of light, heat, and oxygen, degradation of major cannabinoids is minimized after drying by storage in cool and dark places. Fresh products must be stored between 1˚C and 5˚C and frozen products must be kept at −18˚C to −20˚C for long-term storage [21]. The content of THC stored at −18˚C, 4˚C, and 22˚C ± 1˚C decomposed at rates of 3.83%, 5.38%, and 6.92% per year, respectively [59]. Samples can be stored at −18˚C or 4˚C for about 30 weeks before concentrations of THCA and THC change, however, samples stored at 22˚C ± 1˚C showed some immediate decomposition. Dried samples stored at 50˚C for 24 hours showed slight decarboxylation while those stored at 100˚C and 150˚C showed significant decarboxylation of THCA and decomposition of THC within two hours [60]. The effect of freeze-drying on terpenes has not been well-studied, but reportedly fails to preserve the profile of the fresh plant by changing terpene concentrations [61].

2. Conclusions

Cannabis standardization is required to obtain consistent cannabinoid and terpene profiles and, subsequently, stable efficacy for medical purposes. Growing conditions and management practices should be optimized and standardized to maximize yields; light, temperature, CO2 concentration, irrigation, humidity, nutrients, and growing media combine and interact to affect the final yield.

The effects of LED should be compared with traditional lamps used in cannabis cultivation in terms of cannabis yield and electricity consumption. The effects of near-visible light, especially UV, on yield require additional data to form conclusions. Light intensity studies have been conducted with conclusive results, but comparisons between studies are hampered by the differences in controlled variables between experiments. Optimal light conditions for cannabis should be researched under controlled environments to determine the optimized combination of light intensity with plant density for maximum plant yield. Light interception and plant growing density may affect the development rate of inflorescences, however, current research yields conflicting results. Optimal growing temperatures for cannabis are believed to be associated with the cultivars’ geographic origins. Studies that control for temperature are lacking.

The pH value recommendations in growing media vary in current literature. Watering amount and frequency is not well specified. Fertilizers have many variables and the effects of content, elemental ratio, and frequency of fertilization on yield are unclear. Analyzing the effects of the dozens of interacting variables of the nutrient in growing media will be a significant undertaking and will require large amounts of indoor growing space to control for individual variables. Studies comparing the yield and quality of cannabis cultivation in soil and hydroponic systems are still lacking.

Details on pruning and training are limited. The effects of different pruning and training techniques, including pruning lower leaves during vegetative stage, clipping or inverting the top to make the plant bushy, utilization of framed netting or ScrOG methods needs to be examined in controlled studies. Harvest timing is subjective and must be examined on a case-by-case basis. Due to the large number of variables, it may not be possible to determine exact harvest times for cannabis. The fluctuation of cannabinoids and terpenes throughout a 24-hour cycle needs further research. Post-harvest treatment, especially drying temperature and duration, should be studied for the effects on cannabinoids and terpene loss.

Current industrial practices for growing conditions vary significantly, and certain aspects of harvest can be subjective. Additional research and studies are required to conclusively develop a set of optimal and standardized growing conditions and harvest techniques.


The authors acknowledge Labs-Mart Inc. for providing funding during the preparation of this manuscript. We are also grateful to Dr. Tiequan Zhang from Agriculture and Agri-Food Canada and Dr. Thomas Graham from the University of Guelph for providing valuable comments and suggestions.

Conflicts of Interest

The authors declare no conflicts of interest regarding the publication of this paper.

Cite this paper

Jin, D., Jin, S.X. and Chen, J. (2019) Cannabis Indoor Growing Conditions, Management Practices, and Post-Harvest Treatment: A Review. American Journal of Plant Sciences, 10, 925-946.


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