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Article

Comparison of Agronomic Parameters and Nutritional Composition on Red and Green Amaranth Species Grown in Open Field Versus Greenhouse Environment

by
Gudani Millicent Managa
and
Lufuno Ethel Nemadodzi
*
Department of Agriculture and Animal Health, University of South Africa, Science Campus, Florida, Johannesburg 1709, South Africa
*
Author to whom correspondence should be addressed.
Agriculture 2023, 13(3), 685; https://doi.org/10.3390/agriculture13030685
Submission received: 27 February 2023 / Revised: 5 March 2023 / Accepted: 13 March 2023 / Published: 15 March 2023
(This article belongs to the Special Issue Green and Sustainable Agricultural Ecosystem)

Abstract

:
Previously, researchers have not paid attention to indigenous African leafy vegetables such as nightshade and kale, however, amaranth species have recently gained popularity due to their adaptability to various climatic conditions and their cultivation in both open fields and hydroponics. Amaranth species are ranked among the underutilized leafy vegetables with medicinal properties, economic values, nutritional and health benefits. This study aimed to compare the growth parameters and nutritional composition of two consumed red (Amaranthus Cruentus L.) and green (Amaranthus Graecizans L.) amaranth species in South Africa, cultivated in an open field versus a greenhouse. The findings showed a high chlorophyll content and large leaf area under open field conditions on red and green species. The number of leaves and stem height were higher in the greenhouse cultivation system. In open field cultivation, minerals such as calcium, magnesium, phosphorus, iron, zinc, aluminium, copper and manganese for both species were significantly higher whilst potassium, sodium, boron, sulphur were significantly higher in the greenhouse production. The sufficient total nitrogen and ash were recorded in the open field production, and no significant difference was observed between the open field and greenhouse on moisture and ash content of A. Cruentus. In conclusion, A. Cruentus and A. Graecizansn grown in an open field had higher proximate and mineral composition over the greenhouse cultivation system.

1. Introduction

Amaranthus, known as amaranth, is a short-lived annual, dicotyledonous and herbaceous plant, widely distributed throughout the world, which belongs to the Amaranthacea family [1,2]. According to [3], Amaranthacea comprises 65 genera and 900 species, the majority being native to Africans, found in tropical and subtropical regions, and Central and South America. However, most are considered cosmopolitan in distribution and are often introduced to a particular region or place [4]. Amaranth can further be distinguished by two morphological types, described as red and green morphs amaranth [2]. It is one of the underutilized, yet important multipurpose plants previously known as a weed. Although some species are still considered weeds, it has become popular and exploited all over the world as a grain or leafy vegetable for food, forage for animals and as an ornamental [5,6].
Over the years, the A. cruentus species was described as a grain amaranth whilst A. greazicans was reported as a weed’s amaranth species [7]. To date, A. cruentus and A. greazicans are the most common species produced for leafy vegetables [8] and according to [9] they are among the commonly used and consumed edible species of amaranth in South Africa.
In South Africa, amaranth is commonly known as “vowa” by the VhaVenda tribe, “theepe” by the BaPedi tribe, “cheke” by the VaTsonga tribe and pigweed/cockscomb and/or hell’s curse in English [10]. Utilization of amaranth is reported in many parts of Limpopo, followed by KwaZulu-Natal, and the North–West and Mpumalanga provinces [11] of South Africa. According to [12], the young, fresh and succulent leaves of amaranth are handpicked weekly in the summer after the first rains, mostly by older women. In Africa, amaranth is considered an indigenous vegetable that is cooked on its own or in combination with other leafy vegetables and is consumed with other stable foods such as porridge [13]. For instance, the VhaVenda tribe cooks Amaranthus with pumpkin leaves (Cucurbita pepo L.), jew mallow/Bush okra (Corchorus olitorius), nightshade (Solanum nigrum L.) and blackjack (Quercus marilandica). Cooked leaves may also be dried in the shade or refrigerated and stored for consumption during off seasons [14] in winter and/or in drought periods.
Amaranth leaves are reported to have a low content of saturated fats and an absence of cholesterol, therefore, they can be considered as an alternative source of protein in a human diet in comparison with animal protein [15] that is 13–18% higher when compared with wheat (14%) and cereals such as corn (10.3%) [6]. In addition, amaranth leaves are reported to contain dietary minerals such as Ca, K, Cu, Mg, P, Mg, Fe and Zn [16,17,18] including vitamins such as β-catotene, vitamin B6, vitamin C, riboflavin and folate [19,20,21]. Ref. [22] reported that the consumption of amaranth leaves is vital, since one cup of cooked, boiled and drained amaranth leaves contains 90% vitamin C, 73% vitamin A, 28% calcium and 28% iron of the daily nutrient requirement.
Food insecurity and hunger remains to be a global challenge, with many countries still food insecure or vulnerable to food insecurity [23]. Hence, the 2030 Agenda for Sustainable Development and the United Nations Decade of Action on Nutrition (2016–2025) both call on all countries and stakeholders to collaborate to combat hunger and prevent malnutrition in different forms by 2030 [24]. Despite being classified as food secure at the national level, according to [25] approximately 16 million people in South Africa are food insecure, with the majority living in rural areas, and this trend has been constant in recent years [18]. Due to nutrient deficiencies such as vitamin A, iron, zinc and vitamin C [26], the current focus is on indigenous and traditional food crops and their positive impact on the sustainability of our food and agricultural systems as measures to address food insecurity [27]. Amaranth is one of these traditional food crops identified for its exceptional nutritional value and widespread benefits as a sustainable food source, implying that its inclusion in daily diets can help increase the household food supply and improve household food security [28].
Amaranthus is a C4 fast-growing plant [29] with a low production cost that makes it one of the cheapest green leafy vegetables in the tropical market, often referred to as the poor man’s vegetable [30]. Amaranths have a high capacity of osmotic adjustment [6] and a C4 photosynthetic pathway that allows efficient use of CO2 in a large range of temperature and moisture stress environments, which is considered a major factor in their wide geographical distribution. In addition, [31] and [32] indicated that various species can grow under varied soil, optimally in warm conditions and are tolerant to drought, plant diseases and adverse climatic conditions [20]. However, [9] reported that in South Africa and other African countries, amaranth is hardly cultivated because people believe that leafy vegetables grow naturally and can be collected in the fields and/or in the household backyards.
In the past years, due to the lack of formal certified seed suppliers of amaranth, in the Bushbuckridge area of the Limpopo and Mpumalanga provinces where it is commonly consumed, women normally harvest and store amaranth seed, which they later broadcast in their fields when a decline in the population is observed [9].
In the recent years, an interesting approach has developed of using greenhouses as a strategy to produce high-potential crops such as amaranth throughout the year, in different soil types and under different agroclimatic conditions with a minimal management of production inputs [6,19]. Ref. [33] indicated that should appropriate measures be taken, greenhouses have the potential to increase agricultural production by accelerating crop development and increasing the biomass per unit of cultivated area when compared to open field conditions. Furthermore, greenhouses allow crops to develop with little risk to production, protecting plants in contrast to open field crops, which are more vulnerable to environmental changes and rely on natural factors [6]. Various factors such as environmental stress can affect the chemical composition of amaranth, thus stimulating the production of antioxidant compounds [34]. The cultivation of the amaranth plant does not extensively vary in South Africa, the main reason for cultivation being for household food security and replenishment of the seed bank [35]. It is crucial to find ways to increase productivity by growing Amaranthus species in the hydroponics and to monitor other important aspects such as the chemical composition of the harvested amaranth leaves. Therefore, the potential to advance the production and consumption of amaranth is fundamental. This study aimed to compare the agronomical parameters and nutritional composition of two different commonly consumed amaranth species (Amaranthus Cruentus L.) and (Amaranthus Graecizans L.) in South Africa cultivated in an open field vs. a greenhouse. The hypothesis of the study was that different cropping system will have no impact on the physiology and the nutritional composition of the red and green Amaranthus species.

2. Materials and Methods

2.1. Study Sites

Location and cropping systems:
Greenhouse: The pot experiment was conducted in the greenhouse with a minimum and maximum air temperature range of 7.4 to 44.9 °C. It was situated at the University of South Africa, Florida Science Campus, Rooderpoot (Latitude: −26°9′29.274″; Longitude: 27°55′17.663″). The average relative humidity inside the greenhouse was 68% [36] during the planting period (October 2021 to February 2022). The plastic pots (18 cm diameter, 14.5 cm height and 18 cm width) were used for growing the seeds. Open field: The experiment was conducted in Itsani village, located about 6 km southwest of Thohoyandou, in the Thulamela Local Municipality of the Vhembe District (Latitude: −22.94786, Longitude: 30.47276) situated in the Limpopo Province of South Africa. During the summer planting period, the temperatures ranged from 26–32 °C with an average rain fall of ±500 mm annually, mostly experienced during the summer months of October to March. The production cycle was about 4 months during the summer seasons of October 2021 to December 2021 for both cropping systems.

2.1.1. Treatments

The two Amaranth species Amaranthus Cruentus L. and Amaranthus Graecizans L. used in this study were obtained from a local reputable seeds’ supplier. For each cropping system, greenhouse and open field planting was conducted through direct sowing in a sandy loam soil. Pots were arranged at 0.3 m (inter) × 0.25 m (intra) spacing on the greenhouse benches as prescribed by [37] with a crop density established at 30 plants per m2 per accession, totalling to 60 pot plants. In this study, cultivation was done without the application of fertilizers as prescribed by [9]. In both cultivation systems, irrigation was done every second day after sowing and was stopped a week before harvest.

2.1.2. Sample Preparation

Healthy edible leaves of the two Amaranth species A. Cruentus and A. Graecizans from each cropping system were randomly harvested at the 8-leaf stage reached 60–95 days after planting as prescribed by [38,39]. The harvested leaves from the open field cropping system were transported on the same day, by placing them inside a cooler box with ice packs to prevent degeneration of quality (wilting, yellowing and spoilage) to the University of South Africa laboratory, Science Campus, Florida. Leaves from each cropping system were removed from the stems, washed thoroughly with tap water to remove any soil debris and air-dried (30 ± 2) on absorbent paper towel at room temperature for 4 days until sufficiently crisped, as prescribed by [40]. Dried leaves from each cropping system were grounded into fine powder using a Russel Hobbs Blender (500W, Shanghai, China), Zhongshan Jast Electrical Appliance, Co., Ltd. in order to produce a homogeneous powder, and powdered samples were used for the nutritional analysis.

2.2. Procedures

2.2.1. Agronomic Parameters

To determine the agronomic parameters, 25 plants per amaranth species from each cropping system were randomly sampled. The total number of green-emerged leaves was counted for each of the randomly selected plants to record the total number of leaves per plant. The plant height was manually measured in centimetres (cm) using a measuring tape, with an accuracy of 0.01 mm placed vertically on the substrate surface and the measurement was taken at the apical meristem. The length and width of leaves were measured with a tape measure to calculate the leaf area using a liner equation as prescribed by [3] using the formula below:
Leaf area (cm2) = 0.654 × (L × W)
where: 0.654 = leaf shape coefficient; L = length of leaf (cm); W = width of leaf (cm) measured at half length.
In addition, leaf chlorophyll content on the middle leaves found between the bottom and top leaves of 20 plants was measured and replicated three times using a non-destructive method with a Spad 502 chlorophyll meter, KONIKA MINOLTA, Japan.

2.2.2. Chemical Analysis

The nutritional traits of leaves were determined by chemical analysis which included the total nitrogen, moisture, ash and minerals from all the samples. The total nitrogen was determined by the dry combustion method using a Carlo Erba NA 1500 C/N/S Analyser (Carlo Erba NA, Stanford, CA, USA) as described by [41,42]. Moisture and ash were carried out according to the standardized methods of [43], where the ash content was determined by the incineration of a dried powdered sample in a muffle furnace (Zhengzhou Protech Technology Co., Zhengzhou, China) at 550 °C for 12 h until the ash turned white. Moisture was determined by drying in a forced-air drying oven (air re-circulating oven, Carbolite, UK) (934.01) at 105 ± 1 °C for 4 h. Mineral elements comprising calcium, potassium, magnesium, sodium, phosphorus, iron, zinc, aluminium, boron, copper, manganese and sulphur concentrations were determined according to the method by the Association of Official Agricultural Chemists [43] after a cooling period. This process involved inductively coupled plasma spectroscopy and the results of the nutritional analysis were reported on a dry weight basis.

2.3. Statistical Analysis

Data were subjected to a one-way analysis of variance (ANOVA) performed with Genstat 64-bit Release 20.1 (PC/Windows 8–10) software. Where significance differences were observed, means separation was conducted by an LSD test at a 5% significance level.

3. Results

3.1. Agronomic Parameters

Amaranthus Graecizans cultivated in open field conditions had the highest leaf chlorophyll content of 67.9 nm and b leaf area of 4591 cm2. On the contrary, amaranth grown in the greenhouse exhibited a lower chlorophyll content and leaf area of 43.3 nm and 1317 cm2, respectively. Notably, A. Graecizans cultivated in the greenhouse had a significant number of leaves per plant (39.33) and showed a faster and more robust development with taller and thicker stems (70.80 cm) when compared to open field grown plants which had 23.00 leaves and a 59. 00 stem height, respectively. The variation in agronomic parameters between the red and green Amaranthus species grown in two cultivation systems including the analysis of variance (ANOVA) of leaf chlorophyll content, leaf area, number of leaves and stem height showed a significant difference (p ≤ 0.01) between the two-cropping environment: open field vs. greenhouse conditions as shown in Table 1 below, and Figure 1 respectively.
The findings presented in Table 2 show that A. Cruentus in open field cultivation had a significantly higher leaf chlorophyll content of (46.37 nm) whilst the least leaf chlorophyll content of (27.27 nm) was recorded from A. Cruentus grown in the greenhouse. The analysis of variance of leaf area, number of leaves and stem height did not show a significant difference (p ≤ 0.01) between the open field and greenhouse-grown A. Cruentus (* see Table 2 and Figure 2).

3.2. Proximate Composition

Table 3 outlines the proximate composition of A. Graecizans grown in the open field vs. greenhouse, where there was a significant difference (p ≤ 0.01) amongst the two cultivation environments. A. Graecizans grown in the open field exhibited the highest total nitrogen (5.50), moisture content (6.26) and ash content (18.40), whilst A. Graecizans cultivated in the greenhouse had the least proximate composition content (* see Table 3 and Figure 3). On the contrary, A. Cruentus had the highest content of total nitrogen (5.23) detected in the open field. However, the amount of moisture and ash content in this accession was not significantly different (p ≤ 0.01) amongst the two cropping systems as shown in Table 4 and Figure 4.

3.3. Mineral Composition

Our study revealed that there was a significant difference (p ≤ 0.01) in the content of calcium, magnesium, phosphors, iron, zinc, aluminium, copper and manganese, with higher values in the open field cultivation as shown in Table 5 and Figure 5. On the contrary, the content of potassium, sodium, boron and sulphur were significantly higher in the greenhouse cultivation. The means of the analysis of variance of A. Cruentus showed significant differences (p ≤ 0.01) (* see Table 6) among the two cultivation systems. The highest content of Ca, Mg, P, Fe, Zn, Al, B, Cu and Mn were observed in plant material from the open field cultivation. However, the content of sodium detected in A. Cruentus did not differ significantly (p ≤ 0.01) between both the open field and greenhouse cultivations. Notably, the greenhouse cultivation system exhibited significant variations in the content of potassium and sulphur as compared to the open field cropping system as shown in Table 6 and Figure 6.

4. Discussion

The recent interest in Amaranthus species stems from its high level of genetic diversity, phenotypic plasticity, extreme adaptability to adverse growing conditions and climate resilience [44]. Amaranth is one of the easiest plants to grow in agriculturally marginalized lands and can be a solution for improving food security and food nutritional quality [45]. Several studies were conducted on the production of various Amaranthus species, all of which were grown in the open field, however there are few studies on amaranth cultivation in the greenhouse with no and/or few scientific literature recorded. A study by [46] on the chlorophyll content evaluated in GA-2 and RA Amaranthus species in open-field and greenhouse cultivations, revealed that field-grown plants possessed a significantly higher amount of chlorophyll content. Their findings are in agreement with the results of our study, where the open field cultivation had the highest leaf chlorophyll content and leaf area for the Amaranthus species. In addition, a study to observe the performance and fruit quality of Cucumis melo in both the greenhouse and field conditions revealed that the field experiment and inoculation used improved the fruit production and quality [47]. Leaf color is regarded as the primary and immediate indicator of plant performance and purchasing power of consumers [48]. Traits such as leaf size, leaf color, type and intensity of greenness are associated with yield and can be useful in the selection for breeding, as enhancements of these traits also improves marketability and consumer preference [13]. In our study, a low chlorophyll content on the leaves was observed in the greenhouse-grown Amaranthus species, which may be associated with factors such as plant nutrition deficiency and environmental stresses [49] that may have affected the greenness of the leaves, resulting in low branching and pale green small leaves with short/medium plant heights. Broader vegetable leaves are also expected to increase light interception, potentially leading to an increased production of photosynthates. However, [50] disagree on the basis that the higher the number of the leaves yield to shorter/smaller leaf areas or leaf area index, which could imply that most leaves are shaded, thereby yielding little photosynthesis [51].
Amaranthus, unlike Swiss chard and cabbage, cannot withstand low temperatures. All amaranth species prefer warm temperatures and can thrive above 25 °C-day temperatures, however, not lower than 15 °C for the night temperature [22]. In our study, lower night temperatures of 7.4 °C in a greenhouse cultivation could have been the reason for the low leaf chlorophyll content and number of leaves due to chilling injuries, thereby making the amaranth leaves fibrous and bent as reported by [18]. Moreover, due to the closed environment and the design, the relative humidity and day temperatures were higher in the greenhouse conditions than in the open field. This was observed in the present study where the temperature in the greenhouse reached a maximum of 44.9 °C during the day contrary to the maximum temperature of 32 °C in the open field where the study was conducted.
The number of leaves per plant is an important variable to consider when comparing the potentials of plants [52]. From our study, greenhouse-grown A. cruentus had 27.33 recorded as the number of leaves, which was similar to that obtained by [53], which ranged from 18.92–37.11 in salinity tolerance. On the contrary, the results obtained by [6] are not in agreement with our findings, where A. hypochondriacus reported an average of 35 leaves in an open field cultivation system.
The stem height of A. Graecizans grown in a greenhouse cultivation had a significantly taller stem height (* see Table 1), however, a non-significant difference was observed in the leaf area, number of leaves and stem height of A. cruentus plants grown in both two-cropping environments as shown in Table 2. A similar observation of taller stem heights in greenhouse-grown plants was made in a study by [46] using photosynthetic phenomics of field- and greenhouse-grown Amaranthus species. Greenhouse-grown plants (GA-2 and CC) were generally taller than the field grown plants, which is in agreement with the experiment measurements on the availability of PAR in the greenhouse.
Ref. [6] compared the growth of amaranth (Amaranthus hypochondriacus) between greenhouse and open field systems, and the findings revealed that the average height of the greenhouse plants was greater than reported in various open field studies. In a different experiment by [54], which included the application of salicylic acid foliar as a treatment, the highest growth parameters such as the number of leaves and stem height of tomato plants were recorded in the greenhouse cultivation. Similar findings were observed by [55] who concluded that the yield performances (plant height, leaf weight, stem weight) of Amaranthus PLR 1 was better under a polyhouse and under a shade net as compared to open conditions during the rainy and summer seasons. In another study, the stem height growth of different Amaranthus species was observed to be slow in an open field experiment [56]. However, notably in the study by [37] on the comparison of the growth and nutritional composition of selected exotic and indigenous Amaranthus cultivars under the root-knot nematode infestations, the exotic cultivar ‘Tanzania’ had a higher plant height/stem diameter in the field conditions.
Plant/stem height is reported to be a quantitative character controlled by numerous genes and is easily affected by environmental conditions [57]. As a result, [58] reported that under the outdoor environment, high wind speed could cause slight bending of the plants, and this could lead to variations in the height measurements. Should the height range from 50 to 150 cm, it could easily and strongly be branched from the lower part, which supports the findings observed in this study as shown in Table 1.
Greenhouses are known to provide favorable plant conditions. On the contrary, in the open field, environmental conditions are much more variable, forcing plants to adapt in order to survive. In this study, concentrations of the various proximate and mineral composition were found to be largely influenced by the cultivation system. For instance, the open field cropping system had a significant impact on both the red and green species of Amaranthus analyzed. The findings showed that a significant amount of Ca, Mg, P, Fe, Zn, Al, B, Cu and Mn minerals was recorded in amaranth grown in the open field, whilst K, Na, B and S were observed in the greenhouse-grown A. Graecizans species (* see Table 5). In Table 6, the open-field-grown A. Cruentus amaranth species showed a great amount of minerals in its composition, such as Ca, Mg, P, Fe, Zn, Al, B, Cu and Mn, while K and S were found in the greenhouse-grown A. Cruentus plants. However, there was no significant difference between the two cropping systems on sodium content.
A study by [59] suggested that a greater amount of calcium and iron was found in the leaves of amaranth plants which grow under warm to hot conditions, compared to those which grow under cool conditions (greenhouse), in consideration of the plant age. In addition, high levels of calcium and iron have been reported in green accessions of amaranth compared to light green accessions [13]. In the present study, high levels of calcium were reported in the open-field-grown A. Graecizans plants, which is a green accession of amaranth.
The results from the current study on mineral composition are in accordance with the findings of [60], which revealed that compared to the field-grown mature foliage of tropical spinach (Amaranthus sp.) and Roselle (Hibiscus sabdariffa L.), greenhouse-grown micro/baby-greens were lower in Ca but higher in P, K, Mg, Fe, Mn and Zn. On the contrary, a study by [61] evaluating the minerals and ascorbic acid concentrations of greenhouse- and field-grown bell pepper, cucumber and tomato revealed that K, P and Mg concentrations in greenhouse-grown bell pepper, cucumber and tomato were greater than expected levels and lower in the open field cultivations. Field-grown vegetables had lower contents of Cu, Mn, Fe, Zn and ascorbic acid compared to greenhouse-grown vegetables. According to [61], the reason for the elevated concentrations of K, P and Mg in the greenhouse-grown cucumber, tomato and bell pepper might be attributed to poor fertilizer management and a high application of manure and synthetic fertilizers. Similarly, green morph amaranth was found to contain an abundant moisture content, with notable levels of inorganic minerals including K, Ca, Mg, Fe, Mn, Cu and Zn.
Ref. [62] indicated that the high ash content can be an indication of calcium, aluminium, manganese or iron deposition on the activated carbon or the presence of sand. According to [63], low sodium content makes it acceptable for people with high blood pressure and kidney problems. At the same time, sodium is a vital intracellular and extracellular cation which assists in the regulation of plasma volume and acid-based balance during nerve and muscle contraction [64]. Moreover, several minerals were noted to be a key for regulating water balance in different compartments of the body; the most important of these are sodium, potassium and chloride [65].
Whilst Fe is an important element in the biofortification of crops, it is responsible for the formation of chlorophyll in plants [66] and is essential for blood production in humans. An abundance of calcium and gluten-free proteins makes amaranth a suitable diet for newly diagnosed celiac patients, to aid in bone metabolism and relieve complications in the intestine [67]. According to [68], the consumption of African leafy vegetables can contribute to 50–75% of the recommended daily intake of more than 400 g per person, to protect against micronutrient deficiencies (vitamin A, iron and zinc) mostly in children and pregnant women and non-communicable diseases. It is evident that the consumption of indigenous leafy vegetables, i.e., Amaranthus species, can play a significant role in households’ livelihoods through improving food and nutrition as a provision of an important source of essential minerals. As a result, the pharmacological evaluation of seeds and leaf extracts of amaranth revealed the potency of its bioactive compounds in suppressing terminal diseases [27] such as diabetes, hyperlipidaemia, anti-helminthic, antimalarial, anti-inflammatory and antifungal characteristics, and malnutrition related matters [69]. Future studies are recommended in which organic and chemical fertilizers in both open and greenhouse cultivation systems should be used, to determine the production and nutritional composition potential of commonly consumed amaranth species.

5. Conclusions

Amaranthus is a leafy vegetable of interest to answer a mounting demand for food and plays an important role in sustaining food security and alleviation of malnutrition in South Africa. Similar to maize, wheat, sorghum, barley, rice and soybean, amaranth has a high potential for economic exploitation and because of its easy growing habit and nutritional value for both grains and leaves, it is considered a new promising food for the future. The results of this study demonstrated that its growth parameters and nutrient accumulation is greatly influenced by the planting conditions and amaranth species. In the conditions evaluated, the growth parameters, proximate composition and essential minerals of open field cultivated amaranth plants of both species performed better than greenhouse-grown ones. The differences observed could be attributed to both environmental and genetic factors, which may have influenced the plant physiological parameters and nutritional composition of the amaranth species. Amaranth species have a higher nutrition composition than commonly domesticated vegetables such as cabbage, spinach and Swiss chard, and can provide essential minerals, proximate composition and energy/nutrition requirements to the daily diet of vulnerable groups in rural communities. Therefore, this implies that choosing a suitable condition to grow Amaranthus will influence the important nutrients needed for human health. From the findings of this study, it is concluded that Amaranthus species grown in the open field had high mineral compositions for minerals such as Ca, P, Mg, Fe, Zn, etc. whilst K, B, Na and S were highly prevalent in the greenhouse cultivation. If Amaranth species is to be grown for medicinal and/or health purposes, open field cultivation would be ideal. On the other hand, greenhouse cultivation would be ideal for higher yields due to the high number of leaves recorded on both species (A. Graecizans L. and A. Cruentus L.).

Author Contributions

Conceptualization, G.M.M. and L.E.N.; methodology, L.E.N.; software, L.E.N.; validation, G.M.M. and L.E.N.; formal analysis, L.E.N.; investigation, G.M.M.; resources, G.M.M. and L.E.N.; data curation, G.M.M.; writing—original draft preparation, G.M.M.; writing—review and editing, G.M.M. and L.E.N.; visualization, L.E.N.; supervision, L.E.N. project administration, G.M.M. and L.E.N.; funding acquisition, G.M.M. and L.E.N. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

The study was conducted in accordance with the Department of Agriculture and Animal Health, and approved by the UNISA-CAES Health Ethics Committee) of University of South Africa (REC Reference#:2021/CAES_HREC/131 issued on 6 September 2021).

Data Availability Statement

Data supporting will be provided upon request when under review.

Acknowledgments

The authors would love to extend massive gratitude and appreciation to the University of South Africa, Horticulture Center managerial staff for permitting us to conduct the experiment, providing us with the necessities and assisting whenever needed. We also extend our appreciation to the Agricultural Research Council for Soil, Climate and Water for analyzing the nutritional composition of Amaranthus species.

Conflicts of Interest

The authors declare no conflict of interest. Both authors have read and agreed to the published version of the manuscript.

References

  1. Martínez-Núñez, M.; Ruiz-Rivas, M.; Vera-Hernández, P.F.; Bernal-Muñoz, R.; Luna-Suárez, S.; Rosas-Cárdenas, F.F. The phenological growth stages of different amaranth species grown in restricted spaces based in BBCH code. S. Afr. J. Bot. 2019, 124, 436–443. [Google Scholar] [CrossRef]
  2. Sarker, U.; Hossain, M.; Oba, S. Nutritional and antioxidant components and antioxidant capacity in green morph Amaranthus leafy vegetable. Sci. Rep. 2020, 10, 1336. [Google Scholar] [CrossRef] [Green Version]
  3. Ribeiro, J.E. Optimizing harvesting procedures of Amaranthus hybridus L. and A. tricolor L. under different watering regimes during hot and cool seasons in Southern Mozambique. Ph.D. Thesis, Stellenbosch University, Stellenbosch, South Africa, 2017. [Google Scholar]
  4. Sandoval-Ortega, M.H.; Siqueiros-Delgado, M.E.; Sosa-Ramírez, J.; Cerros-Tlatilpa, R. Amaranthaceae (Caryophyllales) richness and distribution in the state of Aguascalientes, Mexico. Bot. Sci. 2017, 95, 203–220. [Google Scholar] [CrossRef] [Green Version]
  5. Tongos, M.D. Growth rate of vegetable amaranth (Amaranthus Cruentus L.) as influenced by row spacing and nitrogen fertilizer in Mubi, Northern Guinea Savannah zone, Nigeria. Int. J. Innov. Agric. Biol. Res. 2016, 4, 8–20. [Google Scholar]
  6. Chávez-Servín, J.L.; Cabrera-Baeza, H.F.; Jiménez-Ugalde, E.A.; Mercado-Luna, A.; de la Torre-Carbot, K.; Escobar-García, K.; Barreyro, A.A.; Serrano-Arellano, J.; García-Gasca, T. Comparison of chemical composition and growth of amaranth (Amaranthus hypochondriacus) between greenhouse and open field systems. Int. J. Agric. Biol. 2017, 19, 577–583. [Google Scholar] [CrossRef]
  7. Das, S. Systematics and taxonomic delimitation of vegetable, grain and weed amaranths: A morphological and biochemical approach. Genet. Resour. Crop Evol. 2012, 59, 289–303. [Google Scholar] [CrossRef]
  8. Alegbejo, J.O. Nutritional value and utilization of Amaranthus (Amaranthus spp.)—A review. 2013. Bayero J. Pure Appl. Sci. 2013, 6, 136–143. [Google Scholar] [CrossRef] [Green Version]
  9. Jansen van Rensburg, W.S.; van Averbeke, W.; Slabbert, R.; Faber, M.; van Jaarsveld, P.; van Heerden, I.; Wenhold, F.; Oelofse, A. African leafy vegetables in South Africa. Water South Afr. 2007, 33, 317–326. [Google Scholar] [CrossRef] [Green Version]
  10. Otang-Mbeng, W.; Mashabela, M.N. A review of beneficial phytochemicals and postharvest studies on some indigenous leafy vegetables from the Mpumalanga Province of South Africa. Med. Plant. 2020, 12, 533–544. [Google Scholar] [CrossRef]
  11. Omotayo, A.O.; Ndhlovu, P.T.; Tshwene, S.C.; Aremu, A.O. Utilization pattern of indigenous and naturalized plants among some selected rural households of North -West Province, South Africa. Plants 2020, 2, 953. [Google Scholar] [CrossRef]
  12. Faber, M.; Oelofse, A.; Van Jaarsveld, P.J.; Wenhold, F.A.M.; Jansen van Rensburg, W.S. African leafy vegetables consumed by households in the Limpopo and KwaZulu-Natal provinces in South Africa. S. Afr. J. Clin. Nutr. 2010, 23, 30–38. [Google Scholar] [CrossRef] [Green Version]
  13. Nyonje, W.A.; Yang, R.Y.; Wu, W.J.; Makokha, A.O.; Owino, W.O.; Abukutsa-Onyango, M.O. Enhancing the nutritional quality of vegetable amaranth through specific food preparation methods. J. Food Res. 2021, 10, 42–55. [Google Scholar] [CrossRef]
  14. Sangija, F.; Martin, H.; Matemu, A. African nightshades (Solanum nigrum complex): The potential contribution to human nutrition and livelihoods in sub-Saharan Africa. Compr. Rev. Food Sci. Food Saf. 2021, 20, 3284–3318. [Google Scholar] [CrossRef] [PubMed]
  15. Adeniji, O.T.; Aloyce, A. Farmers’ participatory identification of horticultural traits: Developing breeding objectives for vegetable amaranth in Tanzania. J. Crop Improv. 2013, 27, 309–318. [Google Scholar] [CrossRef]
  16. Venskutonis, P.R.; Kraujalis, P. Nutritional components of amaranth seeds and vegetables: A review on composition, properties, and uses. Compr. Rev. Food Sci. Food Saf. 2013, 12, 381–412. [Google Scholar] [CrossRef]
  17. Akin-Idowu, P.; Odunola, O.A.; Gbadegesin, M.A.; Ademoyegun, O.T.; Aduloju, A.O.; Olagunju, Y.O. Nutritional evaluation of five species of grain amaranth-an underutilized crop. Int. J. Sci. Res. 2017, 18, 27. [Google Scholar] [CrossRef] [Green Version]
  18. Emmanuel, O.C.; Babalola, O.O. Amaranth production and consumption in South Africa: The challenges of sustainability for food and nutrition security. Int. J. Agric. Sustain. 2022, 20, 449–460. [Google Scholar] [CrossRef]
  19. Mampholo, M.B.; Sivakumar, D.; Van Rensburg, J. Variation in bioactive compounds and quality parameters in different modified atmosphere packaging during postharvest storage of traditional leafy vegetables (Amaranthus Cruentus L. and Solanum retroflexum). J. Food Qual. 2015, 38, 1–12. [Google Scholar] [CrossRef]
  20. Ruth, O.N.; Unathi, K.; Nomali, N.; Chinsamy, M. Underutilization versus nutritional-nutraceutical potential of the Amaranthus food plant: A mini-review. Appl. Sci. 2021, 11, 6879. [Google Scholar] [CrossRef]
  21. Zuwariah, I.; Syahida, M.; Faridah, H.; Rodhiah, R.; Mohd Fakhri, H. Screening of vitamin, mineral and antioxidants in selected vegetables, fruit and grains for the elderly. Food Res. 2021, 5, 122–131. [Google Scholar]
  22. Achigan-Dako, E.G.; Sogbohossou, O.E.; Maundu, P. Current knowledge on Amaranthus spp.: Research avenues for improved nutritional value and yield in leafy amaranths in sub-Saharan Africa. Euphytica 2014, 197, 303–317. [Google Scholar] [CrossRef]
  23. WFP; WHO; UNICEF. The State of Food Security and Nutrition in the World; Food and Agriculture Organization of the United Nations: Rome, Italy, 2022. [Google Scholar]
  24. Chadare, F.J.; Affonfere, M.; Aidé, E.S.; Fassinou, F.K.; Salako, K.V.; Pereko, K.; Deme, B.; Failler, P.; Kakaï, R.G.; Assogbadjo, A.E. Current state of nutrition in West Africa and projections to 2030. Glob. Food Secur. 2022, 32, 100602. [Google Scholar] [CrossRef]
  25. Shisana, O.; Labadarios, D.; Rehle, T.; Simbayi, L.; Zuma, K.; Dhansay, A.; Reddy, P.; Parker, W.; Hoosain, E.; Naidoo, P.; et al. The South African National Health and Nutrition Examination Survey, SANHANES-1: The Health and Nutritional Status of the Nation; HSRC Press: Cape Town, South Africa, 2013. [Google Scholar]
  26. Van der Merwe, J.D.; Cloete, P.C.; Van der Hoeven, M. Promoting food security through indigenous and traditional food crops. Agroecol. Sustain. Food Syst. 2016, 40, 830–847. [Google Scholar] [CrossRef]
  27. Jimoh, M.O.; Afolayan, A.J.; Lewu, F.B. Suitability of Amaranthus species for alleviating human dietary deficiencies. S. Afr. J. Bot. 2018, 115, 65–73. [Google Scholar] [CrossRef]
  28. Ramdwar, M.N.; Chadee, S.T.; Stoute, V.A. Estimating the potential consumption level of amaranth for food security initiatives in Trinidad, West Indies. Cogent Food Agric. 2017, 3, 1321475. [Google Scholar] [CrossRef]
  29. Pulvento, C.; Sellami, M.H.; Lavini, A. Yield and quality of Amaranthus hypochondriacus grain amaranth under drought and salinity at various phenological stages in southern Italy. J. Sci. Food Agric. 2022, 102, 5022–5033. [Google Scholar] [CrossRef]
  30. Rastogi, A.; Shukla, S. Amaranth: A new millennium crop of nutraceutical values. Crit. Rev. Food Sci. Nutr. 2013, 53, 109–125. [Google Scholar] [CrossRef] [PubMed]
  31. Robert, Y.N.; Hiroe, K.; Yotaro, K. Antioxidant activity of various extracts and fractions of Chenopodium quinoa and Amaranthus spp. seeds, analytical, nutritional and clinical methods. Food Chem. 2008, 106, 760–766. [Google Scholar]
  32. Barrio, D.A.; Añón, M.C. Potential antitumor properties of a protein isolate obtained from the seeds of Amaranthus mantegazzianus. Eur. J. Nutr. 2010, 49, 73–82. [Google Scholar] [CrossRef] [PubMed]
  33. Fuller, R.; Zahnd, A. Solar greenhouse technology for food security: A case study from Humla District, NW Nepal. Mt. Res. Dev. 2012, 32, 411–419. [Google Scholar] [CrossRef]
  34. Khandaker, L.; Akond, A.M.; Ali, M.B.; Oba, S. Biomass yield and accumulations of bioactive compounds in red amaranth (Amaranthus tricolor L.) grown under different colored shade polyethylene in spring season. Sci. Hortic. 2010, 123, 289–294. [Google Scholar] [CrossRef]
  35. Allemann, I.; Cawood, M.E.; Allemann, J. Influence of abiotic stress on Amaranthus cruentus allelopathic properties. S. Afr. J. Bot. 2016, 100, 306. [Google Scholar] [CrossRef]
  36. Mthimunye, L.M.; Managa, G.M.; Nemadodzi, L.E. The Influence of Lablab Purpureus Growth on Nitrogen Availability and Mineral Composition Concentration in Nutrient Poor Savanna Soils. Agron. J. 2023, 13, 622. [Google Scholar] [CrossRef]
  37. Makhado, M.V. Productivity and malnutrition elements in local and exotic Amaranthus cultivars. Ph.D. Thesis, University of Limpopo, Polokwane, South Africa, 2021. [Google Scholar]
  38. Van Averbeke, W.; Netshithuthuni, C. Effect of irrigation scheduling on leaf yield of non-heading Chinese cabbage (Brassica rapa L. subsp. chinensis). S. Afr. J. Plant Soil. 2010, 27, 322–327. [Google Scholar] [CrossRef]
  39. Medoua, G.N.; Oldewage-Theron, W.H. Effect of drying and cooking on nutritional value and antioxidant capacity of morogo (Amaranthus hybridus) a traditional leafy vegetable grown in South Africa. J. Food Sci. Technol. 2014, 51, 736–742. [Google Scholar] [CrossRef] [Green Version]
  40. Kachiguma, N.A.; Mwase, W.; Maliro, M.; Damaliphetsa, A. Chemical and mineral composition of amaranth (Amaranthus L.) species collected from central Malawi. J. Food Res. 2015, 4, 92. [Google Scholar] [CrossRef]
  41. Matejovic, I. Total nitrogen in plant material determinated by means of dry combustion: A possible alternative to determination by Kjeldahl digestion. Commun. Soil Sci. Plant Anal. 1995, 26, 2217–2229. [Google Scholar] [CrossRef]
  42. Nemadodzi, L.E.; Araya, H.; Nkomo, M.; Ngezimana, W.; Mudau, N.F. Nitrogen, phosphorus, and potassium effects on the physiology and biomass yield of baby spinach (Spinacia oleracea L.). J. Plant Nutr. 2017, 40, 033–2044. [Google Scholar] [CrossRef]
  43. Association of official agricultural chemists (AOAC). Official Methods of Analysis, 19th ed.; AOAC International: Gaithersburg, MD, USA, 2012. [Google Scholar]
  44. Jamalluddin, N.; Symonds, R.C.; Mayes, S.; Ho, W.K.; Massawe, F. Diversifying crops for food and nutrition security: A case of vegetable amaranth, an ancient climate-smart crop. In Food Security and Nutrition; Academic Press: Amsterdam, Switzerland, 2021; pp. 125–146. [Google Scholar]
  45. Aderibigbe, O.R.; Ezekiel, O.O.; Owolade, S.O.; Korese, J.K.; Sturm, B.; Hensel, O. Exploring the potentials of underutilized grain amaranth (Amaranthus spp.) along the value chain for food and nutrition security: A review. Crit. Rev. Food Sci. Nutr. 2022, 62, 656–669. [Google Scholar] [CrossRef]
  46. Sooriyapathirana, S.D.S.S.; Ranaweera, L.T.; Jayarathne, H.S.M.; Gayathree, T.H.I.; Rathnayake, P.G.R.G.; Karunarathne, S.I.; Thilakarathne, S.M.N.K.; Salih, R.; Weebadde, C.K.; Weebadde, C.P. Photosynthetic phenomics of field-and greenhouse-grown Amaranths vs. sensory and species delimits. Plant Phenomics 2021, 2539380, 2–13. [Google Scholar] [CrossRef]
  47. Copetta, A.; Todeschini, V.; Massa, N.; Bona, E.; Berta, G.; Lingua, G. Inoculation with arbuscular mycorrhizal fungi improves melon (Cucumis melo) fruit quality under field conditions and plant performance in both field and greenhouse. Plant Biosyst. -Int. J. Deal. All Asp. Plant Biol. 2021, 155, 1063–1074. [Google Scholar] [CrossRef]
  48. Moser, R.; Raffaelli, R.; Thilmany-McFadden, D. Consumer preferences for fruit and vegetables with credence-based attributes: A Review. Int. Food Agribus. Manag. 2011, 14, 121–142. [Google Scholar]
  49. Giordano, M.; Petropoulos, S.A.; Rouphael, Y. Response and defence mechanisms of vegetable crops against drought, heat and salinity stress. Agriculture 2021, 11, 463. [Google Scholar] [CrossRef]
  50. Gerrano, A.S.; Jansen van Rensburg, W.S.; Adebola, P.O. Genetic diversity of Amaranthus species in South Africa. S. Afr. J. Plant Soil 2015, 32, 39–46. [Google Scholar] [CrossRef]
  51. Srinivasan, V.; Kumar, P.; Long, S.P. Decreasing, not increasing, leaf area will raise crop yields under global atmospheric change. Glob. Chang. Biol. 2017, 23, 1626–1635. [Google Scholar] [CrossRef] [PubMed]
  52. Wang, C.; He, J.; Zhao, T.H.; Cao, Y.; Wang, G.; Sun, B.; Yan, X.; Guo, W.; Li, M.H. The smaller the leaf is, the faster the leaf water loses in a temperate forest. Front. Plant Sci. 2019, 10, 58. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  53. Omamt, E.N.; Hammes, P.S.; Robbertse, P.J. Differences in salinity tolerance for growth and water-use efficiency in some amaranth (Amaranthus spp.) genotypes. N. Z. J. Crop Hortic. Sci. 2006, 34, 11–22. [Google Scholar] [CrossRef]
  54. Khandaker, L.; Akond, A.M.; Oba, S. Foliar application of salicylic acid improved the growth, yield and leaf’s bioactive compounds in red Amaranth (L.). J. Fruit Ornam. Plant Res. 2011, 74, 77–86. [Google Scholar] [CrossRef]
  55. Ashok, A.D.; Sakthivel, K. Functional performance of PLR 1 Amaranthus under different protected environmental conditions. Int. J. Curr. Microbiol. Appl. Sci. 2020, 9, 510–514. [Google Scholar] [CrossRef]
  56. Tanzin, T. Assessment of growth and yield potential of different vegetable amaranth type In Kleve, Germany. Ph.D. Thesis, Hochschule Rhein-Waal, Hochschule Rhein-Waal University of Applied Sciences, Kleve, Germany, 2018. [Google Scholar]
  57. Yang, Q.; Lin, G.; Lv, H.; Wang, C.; Yang, Y.; Liao, H. Environmental and genetic regulation of plant height in soybean. BMC Plant Biol. 2021, 21, 1–15. [Google Scholar] [CrossRef] [PubMed]
  58. Ogwu, M.C. Value of Amaranthus (L.) species in Nigeria. In Nutritional Value of Amaranth; Waisundara, V., Ed.; IntechOpen: London, UK, 2020; pp. 1–21. [Google Scholar]
  59. Modi, A.T. Growth temperature and plant age influence on nutritional quality of Amaranthus leaves and seed germination capacity. Water S. Afr. 2007, 33, 369–376. [Google Scholar] [CrossRef] [Green Version]
  60. Ayeni, A. Nutrient content of micro/baby-green and field-grown mature foliage of tropical spinach (Amaranthus sp.) and roselle (Hibiscus sabdariffa L.). Foods 2021, 10, 2546. [Google Scholar] [CrossRef] [PubMed]
  61. Aghili, P.; Imani, A.A.; Shahbazi, H.; Alaei, Y. Study of correlation and relationships between seed yield and yield components in Lentil (Lens culinaris Medik). Ann. Biol. Res. 2012, 3, 5042–5045. [Google Scholar]
  62. Zulkania, A.; Hanum, G.F.; Rezki, A.S. The potential of activated carbon derived from bio-char waste of bio-oil pyrolysis as adsorbent. MATEC Web Conf. EDP Sci. 2018, 154, 01029. [Google Scholar] [CrossRef] [Green Version]
  63. Nerbass, F.B.; Calice-Silva, V.; Pecoits-Filho, R. Sodium intake and blood pressure in patients with chronic kidney disease: A salty relationship. Blood Purif. 2018, 45, 166–172. [Google Scholar] [CrossRef]
  64. Gagnon, K.B.; Delpire, E. Sodium transporters in human health and disease. Front. Physiol. 2021, 11, 588664. [Google Scholar] [CrossRef]
  65. Oyeyinka, B.O.; Afolayan, A.J. Comparative evaluation of the nutritive, mineral, and antinutritive composition of Musa sinensis L. (Banana) and Musa paradisiaca L. (Plantain) fruit compartments. Plants 2019, 8, 598. [Google Scholar] [CrossRef] [Green Version]
  66. Pofu, K.M.; Mashela, P.W.; Laurie, S.M.; Oelofse, D. Host-status of sweet potato cultivars to South Africa root-knot nematodes. Acta Agric. Scand. Sec.–B Soil Plant Sci. 2017, 67, 62–66. [Google Scholar] [CrossRef]
  67. Cardo, A.; Churruca, I.; Lasa, A.; Navarro, V.; Vázquez-Polo, M.; Perez-Junkera, G.; Larretxi, I. Nutritional imbalances in adult celiac patients following a gluten-free diet. Nutrients 2021, 13, 2877. [Google Scholar] [CrossRef]
  68. Van Jaarsveld, P.; Faber, M.; Van Heerden, I.; Wenhold, F.; van Rensburg, W.J.; Van Averbeke, W. Nutrient content of eight African leafy vegetables and their potential contribution to dietary reference intakes. J. Food Compos. Anal. 2014, 33, 77–84. [Google Scholar] [CrossRef] [Green Version]
  69. Idris, O.A.; Wintola, O.A.; Afolayan, A.J. Phytochemical and antioxidant activities of Rumex crispus L. in treatment of gastrointestinal helminths in Eastern Cape Province, South Africa. Asian Pac. J. Trop. Biomed. 2017, 7, 1071–1078. [Google Scholar] [CrossRef]
Figure 1. A comparative diagram showing the differences in growth parameters of A. Graecizans L. under open field (Blue) versus greenhouse (Orange) conditions, a referrer to open field whilst b referrers to greenhouse.
Figure 1. A comparative diagram showing the differences in growth parameters of A. Graecizans L. under open field (Blue) versus greenhouse (Orange) conditions, a referrer to open field whilst b referrers to greenhouse.
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Figure 2. A comparative diagram showing the differences in growth parameter of A. Cruentus L. under open field (Blue) versus greenhouse (Orange) a referrer to open field whilst b referrers to greenhouse.
Figure 2. A comparative diagram showing the differences in growth parameter of A. Cruentus L. under open field (Blue) versus greenhouse (Orange) a referrer to open field whilst b referrers to greenhouse.
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Figure 3. A comparative diagram showing the differences in proximate composition of A. Graecizans L. under open field (blue) versus greenhouse (orange) conditions a referrer to open field whilst b referrers to greenhouse.
Figure 3. A comparative diagram showing the differences in proximate composition of A. Graecizans L. under open field (blue) versus greenhouse (orange) conditions a referrer to open field whilst b referrers to greenhouse.
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Figure 4. A comparative diagram showing the differences in proximate composition of A. Cruentus L. under open field (blue) versus greenhouse (orange) conditions a referrer to open field whilst b referrers to greenhouse.
Figure 4. A comparative diagram showing the differences in proximate composition of A. Cruentus L. under open field (blue) versus greenhouse (orange) conditions a referrer to open field whilst b referrers to greenhouse.
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Figure 5. A comparative diagram showing the differences in mineral composition of A. Graecizans L. under open field (blue) versus greenhouse (orange) conditions, a referrer to open field whilst b referrers to greenhouse.
Figure 5. A comparative diagram showing the differences in mineral composition of A. Graecizans L. under open field (blue) versus greenhouse (orange) conditions, a referrer to open field whilst b referrers to greenhouse.
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Figure 6. A comparative diagram showing the differences in mineral composition of A. Cruentus L. under open field (blue) versus greenhouse (orange) conditions, a referrer to open field whilst b referrers to greenhouse.
Figure 6. A comparative diagram showing the differences in mineral composition of A. Cruentus L. under open field (blue) versus greenhouse (orange) conditions, a referrer to open field whilst b referrers to greenhouse.
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Table 1. Comparison of agronomic parameters of A. Graecizans L. grown in open field vs. greenhouse.
Table 1. Comparison of agronomic parameters of A. Graecizans L. grown in open field vs. greenhouse.
Relative Chlorophyll Content (nm) (3× Replications)Leaf Area (cm2)Number of LeavesStem Height (cm)
Treatments
Open field67.9 a4591 a23.00 b59.00 b
Greenhouse43.3 b1317 b39.33 a70.80 a
rep3333
d.f.4444
SEM1.92154.20.6240.363
SED2.72218.00.8820.513
LSD (5%)7.55605.42.4491.425
F probability≤0.001≤0.001≤0.001≤0.001
SEM is the standard error of means, SED is the standard error of difference, LSD is the t-test least significant difference. SEM is the standard error of means. SED is the standard error of difference. LSD is the t-test least significant difference at the 5% level. Means within columns followed by the same lower-case letter did not differ significantly.
Table 2. Comparison of agronomic parameters A. Cruentus L. in the open field vs. greenhouse.
Table 2. Comparison of agronomic parameters A. Cruentus L. in the open field vs. greenhouse.
Relative Chlorophyll Content (3× Replications)
(nm)
Leaf Area
(cm2)
Number of LeavesStem Height (cm)
Treatments
Open field46.37 a7622 a16.33 a84.8 ab
Greenhouse27.27 b5394 ab27.33 ab106.3 a
rep3333
d.f.4444
SEM1.100788.61.2022.56
SED1.5551115.21.7003.63
LSD (5%)4.3183096.24.71910.07
F probability<0.0010.1160.0030.004
SEM is the standard error of means. SED is the standard error of difference. LSD is the t-test least significant difference at the 5% level. Means within columns followed by the same lower-case letter did not differ significantly.
Table 3. Proximate composition of amaranth leaves from A. Graecizans L. in the open field vs. greenhouse on a dry weight basis (%).
Table 3. Proximate composition of amaranth leaves from A. Graecizans L. in the open field vs. greenhouse on a dry weight basis (%).
Total NitrogenMoistureAsh
Treatments
Open field5.50 a6.26 a18.40 a
Greenhouse3.63 b5.57 a14.27 b
rep333
d.f.444
SEM0.06210.07510.143
SED0.08780.10620.203
LSD (5%)0.24380.29500.563
F probability<0.0010.003<0.001
SEM is the standard error of means. SED is the standard error of difference. LSD is the t-test least significant difference at the 5% level. Means within columns followed by the same lower-case letter did not differ significantly.
Table 4. Proximate composition of A. Cruentus L. in the open field vs. greenhouse on a dry weight basis (%).
Table 4. Proximate composition of A. Cruentus L. in the open field vs. greenhouse on a dry weight basis (%).
Total Nitrogen Moisture Ash
Treatments
Open field523 a5.61 a19.50 a
Greenhouse3.37 b5.26 a16.17 a
rep333
d.f.444
SEM0.02190.13410.295
SED0.03090.18960.418
LSD (5%)0.08580.52651.160
F probability<0.0010.1390.001
SEM is the standard error of means. SED is the standard error of difference. LSD is the t-test least significant difference at the 5% level. Means within columns followed by the same lower-case letter did not differ significantly.
Table 5. Comparison of minerals composition of amaranth leaves A. Graecizans L. in the open field vs. greenhouse on a dry weight basis.
Table 5. Comparison of minerals composition of amaranth leaves A. Graecizans L. in the open field vs. greenhouse on a dry weight basis.
CalciumPotassiumMagnesiumSodiumPhosphorusIronZincAluminiumBoronCopperManganeseSulphur
Treatments%%%mg/kg%mg/kgmg/kgmg/kgmg/kgmg/kgmg/kg%
Open field2.41 a4.34 b1.66 a522.4 b0.82 a1174.7 a85.5 a705 a38.37 b15.57 a137.00 a0.56 b
Greenhouse1.72 b4.76 a1.03 b659.8 a0.50 b434.3 b88.4 b237 b59.90 a8.48 b37.60 b0.78 a
Rep333333333333
d.f.444444444444
SEM0.009430.011060.004713.510.002758.381.8620.11.3560.4021.1550.000943
SED0.013330.015630.006674.970.0038911.852.6328.51.9180.5681.6330.001333
LSD (5%)0.037020.043410.0185113.800.0107932.917.2979.05.3241.5774.5340.003702
F probability<0.001<0.001<0.001<0.001<0.001<0.0010.336<0.001<0.001<0.001<0.001<0.001
SEM is the standard error of means. SED is the standard error of difference. LSD is the t-test least significant difference at the 5% level. Means within columns followed by the same lower-case letter did not differ significantly.
Table 6. Comparison of mineral composition of A. Cruentus L. in open field vs. greenhouse on a dry weight basis.
Table 6. Comparison of mineral composition of A. Cruentus L. in open field vs. greenhouse on a dry weight basis.
CalciumPotassiumMagnesiumSodiumPhosphorusIronZincAluminiumBoronCopperManganeseSulphur
Treatments%%%mg/kg%mg/kgmg/kg mg/kgmg/kgmg/kg mg/kg%
Open field2.40 a4.02 b1.71 a392.0 a0.73 a2633 a83.10 a1547 a36.20 a17.30 a194.63 a0.52 b
Greenhouse2.03 b5.07 a1.23 b341.0 a b0.47 b460 b71.87 b255 b77.90 b10.27 b60.27 b0.66 a
Rep333333333333
d.f.444444444444
SEM0.012470.02170.012027.880.0034093.40.37762.51.1420.1971.2590.00337
SED0.017640.03070.0170011.150.00481132.10.53388.41.6150.2791.7800.00477
LSD (5%)0.048970.08530.0471930.960.01335366.81.481245.54.4820.7744.9420.01325
F probability<0.001<0.001<0.0010.010<0.001<0.001<0.001<0.001<0.001<0.001<0.001<0.001
SEM is the standard error of means. SED is the standard error of difference. LSD is the t-test least significant difference at the 5% level. Means within columns followed by the same lower-case letter did not differ significantly.
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Managa, G.M.; Nemadodzi, L.E. Comparison of Agronomic Parameters and Nutritional Composition on Red and Green Amaranth Species Grown in Open Field Versus Greenhouse Environment. Agriculture 2023, 13, 685. https://doi.org/10.3390/agriculture13030685

AMA Style

Managa GM, Nemadodzi LE. Comparison of Agronomic Parameters and Nutritional Composition on Red and Green Amaranth Species Grown in Open Field Versus Greenhouse Environment. Agriculture. 2023; 13(3):685. https://doi.org/10.3390/agriculture13030685

Chicago/Turabian Style

Managa, Gudani Millicent, and Lufuno Ethel Nemadodzi. 2023. "Comparison of Agronomic Parameters and Nutritional Composition on Red and Green Amaranth Species Grown in Open Field Versus Greenhouse Environment" Agriculture 13, no. 3: 685. https://doi.org/10.3390/agriculture13030685

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