The main characteristic of Cannabis sativa L. is the production of compounds of medicinal interest known as phytocannabinoids. Environmental factors and crop management practices are directly related to the yield of these compounds. Knowing how these factors influence the production of phytocannabinoids is essential to promote greater metabolite yield and stability. In this review, we aim to examine current cannabis agronomic research topics to identify the available information and the main gaps that need to be filled in future research. This paper introduces the importance of C. sativa L., approaching state-of-the-art research and evaluating the influence of crop management and environment conditions on yield and phytocannabinoid production, including (i) pruning; (ii) light and plant density; (iii) ontogeny; (iv) temperature, altitude, and CO2 concentration; (v) fertilization and substrate; and (vi) water availability, and presents concluding remarks to shed light on future directions.
Recent advancements in high-throughput phenotyping have led to the use of drones with RGB sensors for evaluating plant traits. This study explored the relationships between vegetation indices (VIs) with grain yield and morphoagronomic and physiological traits in maize genotypes. Eight maize hybrids, including those from the UENF breeding program and commercial varieties, were evaluated using a randomized block design with four replications. VIs were obtained at various stages using drones and Pix4D Mapper 4.7.5 software. Analysis revealed significant differences in morphoagronomic traits and photosynthetic capacity. At 119 days after planting (DAP), the RGB vegetation index VARI showed a significant correlation (r = 0.99) with grain yield. VARI also correlated with female flowering (r = −0.87), plant height (r = −0.79), 100-grain weight (r = −0.77), and anthocyanin concentration (r = −0.86). PCA showed a clear separation between local and commercial hybrids, explaining 46.7% of variance at 91 DAP, 52.3% at 98 DAP, 64.2% at 112 DAP, and 66.1% at 119 DAP. This study highlights the utility of VIs in maize phenotyping and genotype selection during advanced reproductive stages.
17 February 2024 in Plant Physiology and Biochemistry
Coffea canephora has two botanical varieties, Robusta and Conilon. Intraspecific variability was hypothesized and projected for the selection of C. canephora plants able to maintain production in the context of global climate changes. For that, architectural, C-assimilation and biomass analyses were performed on 17-month-old Robusta (clones ‘A1’ and ‘3 V’) and Conilon (clones ‘14’ and ‘19’) varieties grown in non-limiting soil, water, and mineral nutrient conditions. Nondestructive coffee plant architecture coding, reconstruction, and plant photosynthesis estimations were performed using a functional-structural plant modeling platform OpenAlea. 3D reconstructions and inclusion of parameters calculated and estimated from light response curves, such as dark respiration (Rd), maximum rate of carboxylation of RuBisCO, and photosynthetic electron transport allowed the estimation of instantaneous and daily plant photosynthesis. The virtual orchard leaf area index was low, and light was not a limiting factor in early C. canephora development stages. Under such conditions, Robusta assimilated more CO2 at the plant and orchard scale and produced higher total biomass than Conilon. Lower plant daily photosynthesis and total biomass were correlated to higher Rd in Conilon than in Robusta. Among the architectural traits, leaf inclination, size, and allometry were most highly correlated with plant assimilation and biomass. Relative allocation in leaf biomass was higher in ‘19’ Conilon than in young Robusta plants, indicating intraspecific biomass partitioning. Similarly, variation in relative distribution of the root biomass and the root volume reflected clonal variation in soil occupation, indicating intraspecific variability in space occupation competitiveness. C. canephora denoted high root allocation in both Conilon and Robusta clones. However, relevant differences at sub-specific levels were found, indicating the high potential of C. canephora to cope with drought events, which are expected to occur more frequently in the future, due to climate changes. The methodology developed here has the potential to be used for other crops and tree species.
Coffea canephora genotypes adopt distinct strategies to cope with drought and rehydration. We hypothesized that the greater drought tolerance of genotype ‘3V’ compared to ‘A1’, previously reflected in physiological and anatomical leaf traits after two water-stress (WS) cycles, could also be observed in P–V curve responses, root and branch anatomy, leaf midrib elongation (CVL), and root distribution. The ‘3V’ and ‘A1’ plants were grown under well-watered (WW) conditions and two cycles of water stress (WS). The ‘3V’ was more sensitive to WS, with reduced branch xylem vessel density (BXVD), while ‘A1’ demonstrated increased BXVD. Root xylem vessel area (RXVA) decreased to a greater extent in ‘3V’ than in ‘A1’, and both genotypes showed increased bulk elastic modulus. Regardless of water conditions, ‘A1’ maintained a higher relative leaf water content at the turgor loss point (RWCTLP). Morphological acclimation did not occur in the second WS cycle. The ‘3V’ plants developed greater root mass in deeper soil layers than ‘A1’ under the WS condition. These findings suggest that ‘A1’ follows a conservative drought-avoidance strategy with lower physio-morphological plasticity, while ‘3V’ exhibits greater drought tolerance. Such responses highlighted coordinated physiological, morphological, and anatomical adaptations of the above- and below-ground organs for resource acquisition and conservation under WS.
Understanding the dynamics of physiological changes involved in the acclimation responses of plants after their exposure to repeated cycles of water stress is crucial to selecting resilient genotypes for regions with recurrent drought episodes. Under such background, we tried to respond to questions as: (1) Are there differences in the stomatal-related and non-stomatal responses during water stress cycles in different clones of Coffea canephora Pierre ex A. Froehner? (2) Do these C. canephora clones show a different response in each of the two sequential water stress events? (3) Is one previous drought stress event sufficient to induce a kind of “memory” in C. canephora? Seven-month-old plants of two clones (’3V’ and ‘A1’, previously characterized as deeper and lesser deep root growth, respectively) were maintained well-watered (WW) or fully withholding the irrigation, inducing soil water stress (WS) until the soil matric water potential (Ψmsoil) reached ≅ −0.5 MPa (−500 kPa) at a soil depth of 500 mm. Two sequential drought events (drought-1 and drought-2) attained this Ψmsoil after 19 days and were followed by soil rewatering until a complete recovery of leaf net CO2 assimilation rate (Anet) during the recovery-1 and recovery-2 events. The leaf gas exchange, chlorophyll a fluorescence, and leaf reflectance parameters were measured in six-day frequency, while the leaf anatomy was examined only at the end of the second drought cycle. In both drought events, the WS plants showed reduction in stomatal conductance and leaf transpiration. The reduction in internal CO2 diffusion was observed in the second drought cycle, expressed by increased thickness of spongy parenchyma in both clones. Those stomatal and anatomical traits impacted decreasing the Anet in both drought events. The ‘3V’ was less influenced by water stress than the ‘A1’ genotype in Anet, effective quantum yield in PSII photochemistry, photochemical quenching, linear electron transport rate, and photochemical reflectance index during the drought-1, but during the drought-2 event such an advantage disappeared. Such physiological genotype differences were supported by the medium xylem vessel area diminished only in ‘3V’ under WS. In both drought cycles, the recovery of all observed stomatal and non-stomatal responses was usually complete after 12 days of rewatering. The absence of photochemical impacts, namely in the maximum quantum yield of primary photochemical reactions, photosynthetic performance index, and density of reaction centers capable of QA reduction during the drought-2 event, might result from an acclimation response of the clones to WS. In the second drought cycle, the plants showed some improved responses to stress, suggesting “memory” effects as drought acclimation at a recurrent drought.