In the expanding North American medical cannabis industry, growers lack reliable and systematically investigated information on the horticultural management of their crops, especially with regard to nutrient management and growing substrates. To evaluate organic substrates and their optimal nutrient management, five rates that supplied 57, 113, 170, 226, and 283 mg N/L of a liquid organic fertilizer (2.00N–0.87P–3.32K) were applied to container-grown plants [Cannabis sativa L. ‘WP:Med (Wappa)’] in two coir-based organic substrates. The trial was conducted in a walk-in growth chamber and the two substrates used were ABcann UNIMIX 2-HP (U2-HP) with lower container capacity (CC) and ABcann UNIMIX 2 (U2) with higher CC. U2-HP produced 11% higher floral dry weight (yield), 13% higher growth index (GI), 20% higher ∆9-tetrahydrocannabinol (THC) concentration, 57% higher THC yield (per plant), 22% higher Δ9-tetrahydrocannabidiolic acid (THCA) yield, and 20% higher cannabigerolic acid (CBGA) yield than U2. Increasing fertilizer rate led to increased growth and yield but also to a dilution of THC, THCA, and CBGA. In U2-HP, to maximize both yield and cannabinoid yield, the optimal organic fertilizer rates were those which supplied 212–261 mg N/L. For U2, the highest applied rate, that supplied 283 mg N/L, maximized yield; although lower rates delivered higher cannabinoid concentrations in dry floral material. The results on these substrates and recommended fertilizer rates can serve as a guide when using other organic fertilizers and substrates; although results may differ with cannabis variety.

Cannabis producers, especially those with organic operations, lack reliable information on the fertilization requirements for their crops. To determine the optimal organic fertilizer rate for vegetative-stage cannabis (Cannabis sativa L.), five rates that supplied 117, 234, 351, 468, and 585 mg N/L of a liquid organic fertilizer (4.0N–1.3P–1.7K) were applied to container-grown plants with one of two coir-based organic substrates. The trial was conducted in a walk-in growth chamber and the two substrates used were ABcann UNIMIX 1-HP with lower water-holding capacity (WHC) and ABcann UNIMIX 1 with higher WHC. No differences in growth or floral dry weight (yield) were found between the two substrates. Pooled data from both substrates showed that the highest yield was achieved at a rate that supplied 389 mg N/L (interpolated from yield-fertilizer responses) which was 1.8 times higher than that of the lowest fertilizer rate. The concentration of ∆9-tetrahydrocannabinol (THC) in dry floral material was maximized at a rate that supplied 418 mg N/L, and no fertilizer rate effects were observed on Δ9-tetrahydrocannabidiolic acid (THCA) or cannabinol (CBN). The highest yield, cannabinoid content, and plant growth were achieved around an organic fertilizer rate that supplied 389 mg N/L during the vegetative growth stage when using the two coir-based organic substrates.

Additional index words. Cannabis sativa, marijuana, deficit irrigation, plant water potential, medicinal crops, volumetric soil moisture content Abstract. Controlled application of drought can increase secondary metabolite concentrations in some essential oil-producing crops. To evaluate the effects of drought on cannabis (Cannabis sativa L.) inflorescence dry weight and cannabinoid content, drought stress was applied to container-grown cannabis plants through gradual growing substrate drying under controlled environment. Fertigation was withheld during week 7 in the flowering stage until midday plant water potential (WP) was approximately L1.5 MPa (drought stress threshold). This occurred after 11 days without fertigation. A well-irrigated control was used for comparison. Leaf net photosynthetic rate (P n ), plant WP, wilting (leaf angle), and volumetric moisture content (VMC) were monitored throughout the drying period until the day after the drought group was fertigated. At the drought stress threshold, P n was 42% lower and plant WP was 50% lower in the drought group than the control. Upon harvest, drought-stressed plants had increased concentrations of major cannabinoids tetrahydrocannabinol acid (THCA) and cannabidiolic acid (CBDA) by 12% and 13%, respectively, compared with the control. Further, yield per unit growing area of THCA was 43% higher than the control, CBDA yield was 47% higher, Δ 9 -tetrahydrocannabinol (THC) yield was 50% higher, and cannabidiol (CBD) yield was 67% higher. Controlled drought stress may therefore be an effective horticultural management technique to maximize both inflorescence dry weight and cannabinoid yield in cannabis, although results may differ by cannabis cultivar or chemotype.

This study evaluated the influence of several factors and their interactive effects on the propagation success of stem cuttings of cannabis (Cannabis sativa L.). Factors included (i) leaf number (two or three), (ii) leaf tip removal (one-third of leaf tips removed), (iii) basal/apical position of stem cutting on the stock plant, and (iv) rooting hormone [0.2% indole-3-butyric (IBA) acid gel or 0.2% willow (Salix alba L.) extract gel]. Cuttings were placed in a growth chamber for twelve days and then assessed on their rooting success rate and root quality using a relative root quality scale. The IBA gel delivered a 2.1× higher rooting success rate and 1.6× higher root quality than the willow extract. Removing leaf tips reduced rooting success rate from 71% to 53% without influencing root quality. Cuttings with three leaves had 15% higher root quality compared with those with two, but leaf number did not influence rooting success rate. Position of cutting had little effect on rooting success or quality. To achieve maximum rooting success and root quality, cuttings from either apical or basal positions should have at least three fully expanded uncut leaves and the tested IBA rooting hormone is preferred to the willow-based product.

Background The taxonomic classification of Cannabis genus has been delineated through three main types: sativa (tall and less branched plant with long and narrow leaves), indica (short and highly branched plant with broader leaves) and ruderalis (heirloom type with short stature, less branching and small thick leaves). While still under discussion, particularly whether the genus is polytypic or monotypic, this broad classification reflects putative geographical origins of each group and putative chemotype and pharmacologic effect. Methods Here we describe a thorough investigation of cannabis accessions using a set of 23 highly informative and polymorphic SNP (Single Nucleotide Polymorphism) markers associated with important traits such as cannabinoid and terpenoid expression as well as fibre and resin production. The assay offers insight into cannabis population structure, phylogenetic relationship, population genetics and correlation to secondary metabolite concentrations. We demonstrate the utility of the assay for rapid, repeatable and cost-efficient genotyping of commercial and industrial cannabis accessions for use in product traceability, breeding programs, regulatory compliance and consumer education. Results We identified 5 clusters in the sample set, including industrial hemp (K5) and resin hemp, which likely underwent a bottleneck to stabilize cannabidiolic acid (CBDA) accumulation (K2, Type II & III). Tetrahydrocannabinolic acid (THCA) resin (Type I) makes up the other three clusters with terpinolene (K4 - colloquial “sativa” or “Narrow Leaflet Drug” (NLD), myrcene/pinene (K1) and myrcene/limonene/linalool (K3 - colloquial “indica”, “Broad Leaflet Drug” (BLD), which also putatively harbour an active version of the cannabichrometic acid Synthase gene (CBCAS). Conclusion The final chemical compositions of cannabis products have key traits related to their genetic identities. Our analyses in the context of the NCBI Cannabis sativa Annotation Release 100 allows for hypothesis testing with regards to secondary metabolite production. Genetic markers related to secondary metabolite production will be important in many sectors of the cannabis marketplace. For example, markers related to THC production will be important for adaptable and compliant large-scale seed production under the new US Domestic Hemp Production Program.