A root growth module was adapted and implemented into the HYDRUS software packages to model root growth as a function of different environmental stresses. The model assumes that various environmental factors, as well as soil hydraulic properties, can influence root development under suboptimal conditions. The implementation of growth and stress functions in the HYDRUS software opens the opportunity to derive parameters of these functions from laboratory or field experimental data using inverse modeling. One of the most important environmental factors influencing root growth is soil temperature. The effects of temperature in the root growth module was the first part of the newly developed HYDRUS add-on to be validated by comparing modeling results with measured rooting depths in an aeroponic experimental system with bell pepper (Capsicum annuum L.). The experiment was conducted at root zone temperatures of 7, 17, and 27°C. Inverse optimization was used to estimate a single set of parameters that was found to well reproduce measured time series of rooting depths for all temperature treatments. A sensitivity analysis showed that parameters such as the maximum rooting depth and cardinal temperatures had only a small impact on the model output and can thus be specified using values from the literature without significantly increasing prediction uncertainties. On the other hand, parameters that define the growth rate or the shape of the temperature stress function had a high influence. The root growth module that considers temperature stress only slightly increased the complexity of the standard HYDRUS models.Water uptake by root systems can greatly affect water flow through the soil (Hao et al., 2005;Yu et al., 2007). The spatial pattern of root water uptake is determined by the spatial distribution of the root system, the knowledge of which is essential for predicting the spatial distribution of water contents and water fluxes in soils. The spatial distribution of roots and their growth are sensitive to various physical, chemical, and biological factors, as well as to soil hydraulic properties that influence the availability of water and oxygen for plants. It is thus important to describe root growth under the influence of various environmental factors to accurately simulate agricultural systems.Various attempts have been made in the past to develop root growth models that account for the influence of various environmental factors such as temperature (Stone et al
Two bell pepper (Capsicum annuum) cultivars, differing in their response to chilling, were exposed to three levels of root-zone temperatures. Gas exchange, shoot and root phenology, and the pattern of change of the central metabolites and secondary metabolites caffeate and benzoate in the leaves and roots were profiled. Low root-zone temperature significantly inhibited gaseous exchange, with a greater effect on the sensitive commercial pepper hybrid (Canon) than on the new hybrid bred to enhance abiotic stress tolerance (S103). The latter was less affected by the treatment with respect to plant height, shoot dry mass, root maximum length, root projected area, number of root tips and root dry mass. More carbon was allocated to the leaves of S103 than nitrogen at 17°C, while in the roots at 17°C, more nitrogen was allocated and the ratio between C/N decreased. Metabolite profiling showed greater increase in the root than in the leaves. Leaf response between the two cultivars differed significantly. The roots accumulated stress-related metabolites including γ-aminobutyric acid (GABA), proline, galactinol and raffinose and at chilling (7°C) resulted in an increase of sugars in both cultivars. Our results suggest that the enhanced tolerance of S103 to root cold stress, reflected in the relative maintenance of shoot and root growth, is likely linked to a more effective regulation of photosynthesis facilitated by the induction of stress-related metabolism.
Fluctuations of winter and summer and day and night temperatures strongly influence shoot and root growth, as well as the whole plant tolerance to extreme soil temperatures. We compared the response of a commercial pepper (Capsicum annuum L.) hybrid (Romance, Rijk Zwaan) to a range of soil temperatures when grafted to a new rootstock hybrid (S101, Syngenta), self-grafted, or ungrafted. The new rootstock hybrid was bred for enhancing abiotic stress tolerance. Plants were grown during winter and summer seasons in a plastic greenhouse with natural ventilation. Minirhizotron cameras and in-growth cores were used to investigate grafted bell pepper root dynamics and root and shoot interactions in response to extreme (low and high air and soil) temperatures. Soil and air temperatures were measured throughout the experiment. The variations of the grafted peppers and the ungrafted aboveground biomass exposed to low and high temperatures during winter and summer were higher in the Romance grafted on the S101 rootstock than in the self-grafted and ungrafted Romance. The plot of rootstock S101 accumulated Cl, and the rootstock efficiently allocated C into the leaves, stems, and roots and N into the leaves, stems, and fruits. These traits of rootstock S101 can be used to improve the tolerance of other pepper cultivars to low and high soil temperatures, which could lengthen the pepper growing season, as well as provide highly interesting information to plant breeders.Abbreviations: DAT, days after transplanting; EC, electrical conductivity; ROM, Romance hybrid.Bell pepper yield is severely reduced by abiotic stresses, including low soil water content and low and high root zone temperatures. These stresses affect root and shoot interactions by reducing plant growth and development, causing wilt and necrosis, and retarding the rate of branching and fruit ripening (Ahn et al., 1999). The long bell pepper production season in Mediterranean-like climates usually includes exposure to high and low temperatures during the summer and winter seasons, respectively, making it impossible to take advantage of the plants' full potential. A simple option to ensure continuous production is to breed new cultivars that are better adapted to high and low temperatures. However, due to the lack of practical selection methods, such as genetic markers, it is still a slow and inefficient process . Currently, grafting is regarded as an alternative to the relatively slow breeding methods and is aimed at increasing the environmental-stress tolerance of fruit vegetables (Flores et al., 2010) and enabling the use of the extensive genetic diversity of the Capsicum species scion and rootstock accessions.
Low temperature is a prominent limiting factor for tropical originated crops production in temperate regions, particularly during cool-season production. The diverse response of two rootstocks (Canon-sensitive and S103-tolerant to low root-zone temperature) was studied when exposed to aeroponically different temperature regimes at the root zone: constant low temperature of 14°C low root-zone temperature (LRZT), transient exposure to LRZT of 27–14−27°C and control temperature of 27°C. Gas exchange, shoot dry mass, and root morphology were measured. Shifts in central and secondary metabolite levels in the leaves and roots were examined by gas chromatography-mass spectrometry (GC-MS). Low root-zone temperature inhibited photosynthesis and transpiration of both grafted bell pepper plants; however, self-grafted Canon physiology was impeded to a greater extent compared with Canon grafted onto rootstock S103. Rootstock S103 demonstrated higher sink potential contributing to milder reduction of photosynthesis and transpiration during stress compared with self-grafted Canon. This reduction of gas exchange led to a significant reduction of root maximum length and root dry mass in self-grafted Canon in response to the stress at 14°C compared with Canon grafted onto rootstock S103. In response to stress, GC-MS metabolite profiling showed enhance metabolism in both cultivars’ leaves, as well as in the roots irrespective of the developmental stage of the plant. This evidence combined indicates enhance gas exchange and carbon assimilation when bell pepper is grafted on S103 under low root-zone temperature.
Green roofs in the Mediterranean region are often exposed to high levels of radiation, extreme temperatures, and an inconsistent water supply. To withstand these harsh conditions in shallow soils and poorly aerated growth media, plants must be armored with adaptations. Strategies that have evolved in desert plants can play significant roles in the use of plants for green covers. In the following, we will specifically focus on (1) heat and radiation, (2) drought, and (3) salinity. Further, we will discuss (4) interactions between neighboring plants. Finally, we will (5) propose a design for diverse green roofs that includes horticultural and medicinal products and provides diverse habitats. Many desert plants have developed morphological and anatomical features to avoid photo-inhibition, which can be advantageous for growth on green roofs. Plants exhibiting C4photosynthesis or crassulacean acid metabolism (CAM) photosynthesis have a protected hydraulic system that enables growth under dry conditions. Furthermore, dew and high levels of relative humidity can provide reliable water sources under limited precipitation. Halophytes are protected against salinity, ionic specific stress, and nutritional imbalances, characteristics that can be advantageous for green roofs. Under limited space, competition for resources becomes increasingly relevant. Allelopathy can also induce the germination and growth inhibition of neighboring plants. Many desert plants, as a result of their exposure to environmental stress, have developed unique survival adaptations based on secondary metabolites that can be used as pharmaceuticals. A systematic survey of plant strategies to withstand these extreme conditions provides a basis for increasing the number of green roof candidates.
The objective of this study is to identify cowpea genotypes that are tolerant to both phosphorous and drought stresses on highly weathered soil. It is hypothesized that (1) genotypes that have the highest grain yield under optimum conditions do not perform best under P or water stress and (2) genotypes that have the highest grain yield under P stress conditions also perform well under water or combined water and P stress. An experiment was conducted in the humid forest zone of Ghana during two dry seasons (2017 and 2018). Ten cowpea genotypes were evaluated in response to four combinations of P fertilizer and drought treatments. The treatments included 0 kg P ha−1 + water stress (0P + WS; control treatment); 60 kg P ha−1 + water stress (60P + WS); 0 kg P ha−1 + no water stress (0P + NWS); 60 kg P ha−1 + no water stress (60P + NWS; optimum condition) in both field experiments. The experiment was laid out in a split plot arrangement with three replications. The grain yield of the cowpea genotypes during 2017 growing cycle ranged between 1094 and 3600 kg ha−1, and in 2018 between 928 and 3125 kg ha−1. In both growing cycles, genotypes Asontem and GH5344 had the highest grain yield under optimum conditions (60 kg P ha−1 + water). Under combined P and water stress, Hans adua, GH6060 and Asontem were the best three genotypes with grain yield ranging between 1678 and 1478 kg ha−1 and this observation was made during both growing cycles. In conclusion, the genotypes showed a variable response to the different treatments in this study. Hypothesis 1 (genotypes that have the highest grain yield under optimum conditions do not perform best under water or P stress conditions) was not confirmed as the genotypes GH2309 and GH6060 (ranking 3rd and 4th under optimum conditions) were among the three best cultivars both under water or P stress conditions. Hypothesis 2.1 (genotypes that have the highest grain yield under P stress conditions perform well under water stress conditions) was confirmed for all genotypes studied except for the genotype Asontem. Hypothesis 2.2 (genotypes that have the highest grain yield under P stress conditions perform also well under combined water and P stress) was true since the best four genotypes under P stress where the best four genotypes under combined water and P stress (0P + WS). GH6060, Hans adua and Asontem are most adapted to combined water and P stress and need to be further explored to ascertain their potential as drought and phosphorus deficiency-tolerant genotypes.
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