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Home All issues Volume 32 (2025) OCL, 32 (2025) 25 Full HTML
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OCL
Volume 32, 2025
Innovative Cropping Systems / Systèmes innovants de culture oléoprotéagineux
Article Number 25
Number of page(s) 10
Section Agronomy
DOI https://doi.org/10.1051/ocl/2025024
Published online 28 August 2025

© F. Benakashani et al., Published by EDP Sciences, 2025

Licence Creative CommonsThis is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Highlights

Trifolium alexandrinum living mulch reduces weeds by 47-74% in saline-grown Nigella sativa while increasing oil yield by 45.7% and maintaining lipid quality (31.1-34.3%). This first IWM protocol for black cumin in salt-affected soils offers herbicide-free production on marginal lands.

1 Introduction

Grain oils have various applications in food, cosmetic, and pharmaceutical industries. They are important for human health and nutrition, as they provide fatty acids and oil-soluble vitamins. They also have some functions and biological activities that help humans prevent some diseases (Hamed et al., 2017). They reduce the risk of heart disease, diabetes, auto-immunity and many other chronic diseases. Grains of Nigella sativa L., an annual herbaceous plant from Ranunculaceae, contain 30–48% valuable plant oil rich in thymoquinone and unsaturated fatty acids (Randhawa and Alghamdi, 2011). Grains of this plant have been traditionally used to treat fever, headache, anxiety, diarrhea, gastrointestinal disorders, asthma, hypertension, diabetes and stroke for years (Randhawa and Alghamdi, 2011). The protective and therapeutic effects of N. sativa oil have been well documented (Al-Okbi et al., 2015). Besides bioactive compounds such as phenolics with high antioxidative activity (Mariod et al., 2009; Meziti et al., 2012; Dalli et al., 2021), N. sativa grains also contain sterols and tocols (Ketenoglu et al., 2020).

N. sativa originates from Southwest Asia, North Africa and Southern Europe (Sultana et al., 2015; Kooti et al., 2017). It is now cultivated in South Asia, including Pakistan and India, the Middle East such as Saudi Arabia and Syria, the Mediterranean region like Turkey and Southern Europe, and extends to other areas (Sultana et al., 2015). N. sativa can tolerate salinity stress (Papastylianou et al., 2018). This makes it a valuable plant for agricultural development and land use in arid and semi-arid areas where soil and water salinity are problems. To grow functional industrial plants in salt-affected lands, we need to understand the specific needs of the crops in these areas and manage various factors, such as water resources, mineral nutrients, pests and diseases, and weeds.

Weeds are a major threat to crop production, with yield reductions ranging from 30 to 90%, depending on weed species, crop type, and management practices (Chauhan, 2022). Weeds can affect the growth and production of secondary metabolites in medicinal plants due to competition, allelopathic effects, and as a biological stress factor. The impact of weeds on the secondary metabolites of medicinal plants can be very significant and varied. These impacts can be either positive or negative, depending on the type of weed and the medicinal plant involved (Gaba et al., 2014; Macías et al., 2019; Shan et al., 2023).

Herbicides are commonly used to control weeds in arable crops and medicinal plants such as N. sativa (Zia UI Hag et al., 2024). However, they can affect the quality of medicinal plants and harm the environment. Therefore, there is a need to reduce the use of herbicides in growing medicinal plants. Although hand weeding can be extremely effective in managing weeds, especially for targeted elimination, it is often constrained by high costs associated with labor and time (Kudsk and Mathiassen, 2020; Peerzada et al., 2022). A better approach to reduce weed competition is to fill the ecological niches that weeds would occupy. “Living mulches” are cover crops that grow at the same time and place as the main crops (Bhaskar et al., 2021). Living mulches have many benefits over dead mulches, i.e. straw and hay. Living mulches enhance the competitive ability of crops by suppressing weeds from 34% to 96% (Ghosheh et al., 2005; Mohammadi, 2010). Furthermore, living mulches positively influence the soil ecosystem by impacting both surface and subterranean layers, thereby enhancing soil biological activity (Nakamoto and Tsukamoto, 2006). Living mulches can either reduce (Carof et al., 2007; Jędrszczyk and Poniedziałek, 2007) or increase (Adamczewska-Sowińska et al., 2009) the productivity of the main crop. These different outcomes depend partly on the species, sowing date, and management method of living mulches. We conducted this study to assess the feasibility of growing N. sativa in salt-affected soils by evaluating its oil yield and composition. Furthermore, since this plant has low competitive power against weeds, we investigated the effect of growing barley (Hordeum vulgare L.) and berseem clover (Trifolium alexandrinum L.) as living mulches on weed control, yield and oil quality of N. sativa in the field.

2 Materials and methods

2.1 Experimental site

We carried out the experiments at the research farm of the Abouraihan College of Agricultural Technologies (35° 28´ N, 51° 36´ E and 1020 masl), University of Tehran, Iran. This site is in an arid region according to the de Martonne climate classification. It has hot and dry summers and mild winters with an annual rainfall and temperature of 141 mm and 15.6 °C, respectively (Tab. 1). The soil type and properties in this experimental field are shown in Table 2.

Table 1

Mean temperature and precipitation in the experimental site during the growing season

Table 2

Physiochemical properties of the soil of the experimental site in depth of 0–30 cm.

2.2 Experimental treatments and agronomic practices

We conducted the experiment in a completely randomized block design with six treatments and four replications. We repeated the experiments in two consecutive years 2017 and 2018. The treatments included two living mulch species: barley and berseem clover, and two living mulch mowing times: (1) mowing after N. sativa establishment at the 6-leaf stage (Ct1) and (2) mowing before the N. sativa flowering stage (Ct2). We also had two control treatments: weed-free (WF): full weeding during the growth stages of N. sativa, and weed-infested (WI): no weeding during the growth of N. sativa. The barley cultivar used (Hordeum vulgare L. cv. 'Baharan'/'Bahman') was a high-yielding six-row winter barley developed by the Iranian Seed and Plant Improvement Institute for semi-cold climates with clay-loam soils typical of the region. For berseem clover (Trifolium alexandrinum L.), locally adapted ecotypes from Isfahan province were used as representative genotypes of central Iran's agricultural ecosystems.

The moldboard plowing (25–30 cm) in the spring was followed by twice disking before planting. Each plot was 4 m in length and 2 m in wide with 4 rows at a distance of 50 cm. A 50 cm space was considered between each experimental unit and each replication. The seedbed preparation operations were the same in both years. The seeds of N. sativa (local landraces which were obtained from Isfahan region of Iran) were sown by hand on 14 April 2017 and 16 April 2018. Seeds were planted using a 50 cm row spacing and 5 cm in-row spacing (400,000 seeds ha−1). Due to a 60% germination percentage, the final plant density achieved was 240,000 plants ha−1. Seeds of the living mulch plants were planted simultaneously with N. sativa. They were planted manually and randomly between N. sativa rows and covered with sand. The seed rates used for barley and berseem clover were 150 kg ha−1 and 30 kg ha−1, respectively. The first irrigation was performed immediately after planting. Until the establishment of N. sativa, irrigation was done weekly, and then, the irrigation interval was considered 10 days. No chemical fertilizers or pesticides were used in the field. A picture of the N. sativa plant is provided in Supplementary Figure S1, showing key morphological features.

2.3 Weed assessment

At the end of Nigella sativa's flowering stage, weed sampling was conducted using three randomly placed 50 cm × 50 cm quadrats per plot. To avoid margin effects, quadrats were placed no closer than 1 m from plot edges. Within replicates, sampling locations were systematically varied to ensure that every plot was adequately sampled and representative coverage is achieved. We examined weed species composition, total weed density and weed biomass. To evaluate the biomass per unit area, the weeds were cut from the ground surface and dried at 75 °C for 73 h.

2.4 Yield related traits and fatty acids profile

Seeds were harvested at physiological maturity which took place 97 ± 3 days after sowing. These seeds were then shade-dried at a temperature of 25 ± 2°C until moisture content reached 8%. For oil extraction, 10 g of the seeds from each treatment from both years were mixed, grounded and put in extraction paper bags. The samples were placed in a distillation flask in a Soxhlet extraction unit and 300 ml of petroleum benzene was added. The boiling temperature range of the Soxhlet apparatus was kept at 40–60 °C for 4 h (Akbari et al., 2020; Movahhedy-Dehnavy et al., 2009). The extracted oil was filtered and dehydrated and the oil content of the seeds was calculated as the percentage of seed dry weight (Ashraf et al., 2006; Movahhedy-Dehnavy et al., 2009; Hosseini et al., 2019).

To determine the fatty acid composition of the oil, the samples were prepared according to the method described by Metcalfe et al. (1966). The samples were analyzed by a gas chromatograph (Unicam 4600, Cambridge, England) equipped with an FID detector after derivatization to fatty methyl esters (FAME). The capillary column was BPX70 (30 m × 0.22 mmi.d.) with a 0.25 μm film thickness (from SGE). The column and the injector temperature were 180 and 240 °C, respectively. The detector temperature was 200 °C (Movahhedy-Dehnavy et al., 2009). FAMEs were identified and quantified based on the comparison of the retention times of the samples with those of standards from Aldrich or Sigma (USA). The percentage of each identified fatty acid was calculated based on the total value of the fatty acids. The value of each sample was determined based on the average of two injections (Movahhedy-Dehnavy et al., 2009).

To compare the N. sativa oil characteristics obtained from different treatments, total values of unsaturated, mono unsaturated, poly unsaturated and saturated fatty acids were calculated. Double bond index (DBI) as an indicator of the unsaturation fatty acid fraction and Iodine value (IV) was also determined for each treatment. DBI and IV were calculated based on Eq. 1 and 2, respectively (Akbari et al., 2020).

DBI = 0 × ([ 14:0 ] + [ 15:0 ] + [ 16:0 ] + [ 18:0 ] + [ 20:0 ]) + 1× ([ 16:1 ] + [ 18:1 ] + [ 20:1 ]) + 2 × ([ 18:2 ] + [ 20:2 ]) + 3 × ([ 18:3 ]) + 4 × ([ 20:4 ]),(1)

IV = (%oleic acid × 0.8601) + (% linoleic acid × 1.7321) + (% eicosenoic acid × 0.7854),(2)

2.5 Statistical analyses

Analysis of variance (ANOVA) on density and dry mass of weeds; and one thousand seed weight and oil yield of N. sativa data was performed using the general linear model (GLM) procedure in the RStudio software. The least significant differences test was applied to compare means at a 5% probability level. Bartlett's test was used to test for homogeneity of variances of the experimental errors of the results of the two years, and considering that the difference between the error variances was not significant, the combined variance analysis was performed for two years of experiment. The year-specific data presented in Supplementary Table S1, also show consistent trends between the two growing seasons. The Shapiro–Wilk test was used to assess data normality and the Breusch–Pagan test was used for homoscedasticity.

3 Results

3.1 Weed composition

Table 3 shows the common weed species and their relative frequency in the experimental field in both years. Amaranthus retroflexus, Chenopodium album and Portulaca oleracea accounted for 86% of the weeds in the N. sativa plots.

Table 3

Weed species and their relative frequency in the experimental field.

3.2 Weed density

The ANOVA showed that weed density was significantly affected by the weed management systems (Tab. 4). Living mulches reduced weed densities significantly (Fig. 1A). The lowest weed density was observed in TCt2 and TCt1 (berseem clover living mulch: mowing before the N. sativa flowering stage and mowing after N. sativa establishment, respectively) which reduced weed density by 74.3% and 70.8% compared with the weed-infested treatment (WI), respectively. In HCt1 (barley living mulch, mowing after black cumin establishment) and HCt2 (barley living mulch, mowing before the N. sativa flowering stage) plots, weed density decreased by 52.0% and 46.8% compared with the WI treatment, respectively.

thumbnail Fig. 1

The effects of weed management systems on density (A) and dry mass (B) of weeds in the black cumin field in two cropping years. The values represent the means of 2017 and 2018. WF: weed free plot; WI: weed infest plot; HCt1: H. vulgare living mulch, mowing after black cumin establishment; HCt2: H. vulgare living mulch, mowing before the black cumin flowering stage. TCt1; T. alexandrinum living mulch, mowing after black cumin establishment; TCt2: T. alexandrinum living mulch, mowing before the black cumin flowering stage.

3.3 Weed growth

Weed management systems had a significant effect on weed dry mass (Tab. 4). Weed dry mass decreased by 74.3% and 70.3% in TCt2 and TCt1 treatments, respectively, compared to the WI treatment (Fig. 1B). HCt1 and HCt2 reduced weed dry mass by 50% compared with the WI treatment (Fig. 1B).

3.4 Grain weight of N. sativa

The weed management systems affected 1000-grain weight of N. sativa significantly (Table 4). The TCt1 (berseem clover mowing after N. sativa establishment) had the highest 1000-grain weight of N. sativa (1.71 g) while WI (weed-infested) had the lowest 1000-grain weight (1.41 g) (Fig. 1A). Likewise, the highest seed yield was recorded for the TCt1 treatment as (366.15 kg ha−1) and the lowest yield was recorded for WI treatment (268.85 kg ha−1) (Supplementary Figure S2). TCt1 increased 1000-grain weight by 7.7% compared with WF (weed-free). There was no significant difference between HCt2 (barley mowing before the black cumin flowering stage) and WF (Fig. 1A).

Table 4

Combined analysis of variance (mean squares) for the effect of treatments on density and biomass of weeds, and yield indices of black cumin.

3.5 N. sativa oil yield

The ANOVA indicated that, the weed management systems significantly affect the oil content of N. sativa seeds (Tab. 4). The lowest oil content was observed in the seeds of plants in the weed infested (WI) plots. The weed management systems increased the percentage of oil content compared with WI and weed free (WF) treatments. The highest oil content was observed in the HCt2 treatment, which was 2.9% more than the WF treatment (Fig. 2C).

The effect of weed management systems on the oil yield of N. sativa plots was significant (Tab. 4). The lowest oil yield was detected in the WI plot. The highest oil yield was obtained from TCt1 and HCt1 treatments (Fig. 2B). The oil yield in TCt1 plots was increased by 12.4% and 45.7%, compared to those in WF and the WI plots, respectively.

thumbnail Fig. 2

The effects of weed management systems on thousand seed weight (A), oil percentage (B), and oil yield (C) of black cumin in two cropping years. The values represent the means of 2017 and 2018. WF: weed free plot; WI: weed infest plot; HCt1: H. vulgare living mulch, mowing after black cumin establishment; HCt2: H. vulgare living mulch, mowing before the black cumin flowering stage. TCt1; T. alexandrinum living mulch, mowing after black cumin establishment; TCt2: T. alexandrinum living mulch, mowing before the black cumin flowering stage.

3.6 Fatty acid composition

Table 5 represents the fatty acid profile of N. sativa oil in response to different weed management systems at two years of the experiment. Six unsaturated fatty acids including linoleic, oleic, palmitoleic, ɑ-linolenic, arachidonic, and eicosenoic fatty acids, and five saturated fatty acids including myristic, palmitic, stearic, arachidic, and pentadecanoic were identified and quantified in N. sativa oil (Tab. 5). Linoleic acid (52.8%), oleic acid (23.1%) and palmitic acid (12.9%) were the main components of the N. sativa oil.

The weed management systems significantly affect the profile of fatty acids in N. sativa oil (Tab. 5). Living mulch treatments increased the amount of linoleic and oleic acids. The highest content of linoleic acid was obtained in the HCt2 treatment which showed a 1.85% increase compared to the WF treatment. Oleic acid in the HCt1 and HCt2 plots was 10.34% and 4.84% higher than the WF treatment, respectively.

Unsaturated (ΣUFA) and saturated (ΣSFA) fatty acids accounted for 79.5% and 20.5% of the total fatty acids of N. sativa oil, respectively (Tab. 6). The living mulch treatments, increased ΣUFA in N. sativa oil up to 3.25% compared with that in the WF treatment. The highest amount of ΣUFA with 80.9% belonged to the TCt1 plot (Tab. 6). A noteworthy point is that the amount of ΣUFA in the WI treatment was also higher than the WF treatment. In contrast, the presence of living mulches decreased the ΣSFA. Among the investigated treatments, TCt1 with 12.8% less saturated fatty acids compared with WF, had the least ΣSFA content. In HCt1 and HCt2 plots, 6.85% less ΣSFA were obtained, compared with the WF plot.

Table 5

The effects of weed management systems on fatty acid composition of black cumin oil. The values represent the means of 2017 and 2018.

Table 6

Comparison of saturated fatty acids (ΣSFA), unsaturated fatty acids (ΣUFA), double bond index (DBI) and iodine value (IV) of Nigella sativa L. seed oil in different weed management systems at two years of experiment.

4 Discussion

The results of our two-year experiment showed that the living mulches played a significant role in controlling salt-tolerant weeds in the N. sativa field. With the application of living mulches, a 61% reduction in weed population was observed. Verret et al. (2017) meta-analyses revealed that intercropping living mulches, relay cropping, or co-planting of cover crops can reduce weed population by 82% compared to the WI plots. It has been reported that living mulch could decrease weed densities in cereal crops by up to 55% (Bhaskar et al., 2014; Den Hollander et al., 2007; Gerhards, 2018). Mulching, by intercepting the light, suppresses the germination and growth of weeds. By absorbing red light, living mulch reduces the ratio of red to far-red light on the soil surface, which prevents the reception of environmental signals for the germination of weed seeds (Mechergui et al., 2021).

The oil content of N. sativa (31.1–34.3%) was in the range reported in previous studies (Ashraf et al., 2006; Seyyedi et al., 2016). These results indicated that N. sativa produces a comparable yield in saline soils and therefore, it can be utilized in the rehabilitation and exploitation of salt affected lands. However, weed infestation reduced the 1000-grain weight and the N. sativa oil content of the seeds that eventually led to a decrease in the oil yield per unit area. Meena et al. (2019) and Mehni et al. (2020) also reported the effect of weeds on reducing the N. sativa yield. The reduction of N. sativa oil content in the presence of weeds was also reported by other researchers (Kirici et al., 2021; Seyyedi et al., 2016; Hossein et al., 2019). Weeds affect growth and productivity of the crop by competition with the crop for limited common resources (Meena et al., 2014). These results emphasized the low competition capacity of N. sativa with weeds. Due to its slow growth, short height, and open canopy structure, the plant exhibits little competitive power compared to most weeds, so that contamination by weeds can destroy 60–80% of the N. sativa crop (Kifelew et al., 2017). Tweaking essential elements of a nutrition program, like the ratios of nutrients and their timing, may control weed competition and help to increase oil yield by enhancing crop growth (Seyyedi et al., 2016). However, an effective weed management program is required to obtain maximum yield in N. sativa farms.

The main weed species in this study included A. retroflexus (Redroot pigweed), C. album (lamb’s quarters), and P. oleracea (purslane). Although the weed composition is affected by various factors such as production sites, year and management practices (Tursun et al., 2007), these species were reported by Seyyedi et al. (2016) in a two-year cultivation of N. sativa in the northeastern part of Iran. This similarity in the results was due to the climatic similarity of the experimental sites and the spread and adaptability of these weeds in arid and semi-arid areas.

A. retroflexus is one of the most important weed species in arid and semi-arid regions (Amini et al., 2014). A C4 photosynthesis system is one of the factors that give this plant the ability to survive and grow in arid environments and salt-affected soils. This plant causes a significant decrease in the yield of agricultural plants and creates problems in harvesting operations (Aguyoh and Masiunas, 2003; Amini et al., 2014). C. album is an annual species that has an almost global distribution and is one of the most important weeds in the world. It is a difficult weed in many agricultural systems because of high seed production and an extended germination period (DeGreeff et al. 2018). A. retroflexus and C. album are fast-growing and allelopathic plants that can drastically reduce the yield of crops in infested fields (Bajwa et al., 2019). P. oleracea (Portulacaceae) is considered one of the 10 most aggressive weeds in the world (CABI, 2022). This plant is an annual weed that exhibits both C4 and CAM photosynthesis systems and therefore shows great compatibility with dry and saline soils (Ozturk et al., 2021). This plant grows in different types of soils and soil pH from acidic to alkaline and tolerates dry and saline soils (Yao et al., 2010). C. album is an intermediate form of C3-C4 (Yorimitsu et al., 2019), possibly an evolutionary step that facilitates range expansion under climate change. P. oleracea severely reduces the yield of monocot and dicot crops (Silva et al., 2007). Various allelochemicals have been identified in this plant (Zhu et al., 2012) that can suppress the germination and growth of crops (Silva et al., 2007). In addition, its leaf and root extracts impair the antioxidant defense system and damage photosynthetic pigments in other plants (El-Shora and Abd El-Gawad, 2015). The adaptation of these three species to arid and saline soils caused them to prevail over other weeds and black cumin. Due to their ability to tolerate salinity, such plants can show a higher competitive ability than agricultural plants in soils that have the potential for salinity stress and cause a decrease in crop growth and yield.

The use of berseem clover as a cover crop (until the establishment of N. sativa) effectively controlled the weeds. Proper density of berseem clover reduced weed emergence and growth by minimizing empty niches that are conducive to weed growth. The greater effectiveness of clover in limiting weeds compared to barley was probably due to the greater shade area of clover. The higher biomass of berseem clover compared to barley showed the higher competition capability of this plant with other species. Our results are in line with Wang et al. (2016) and Bhaskar et al. (2021) who stated that the application of legumes as living mulch is an effective ecological approach to weed suppression and soil fertility improvement. Clover is an ideal living mulch plant because of its nitrogen-fixing ability, long-term perennial growth, and weed suppression potential (Fracchiolla et al. 2022). However, the rapid establishment, high competition ability, and allelopathic properties make barley a desirable plant for weed suppression (Kremer and Ben-Hammouda, 2009). Its rapid establishment and competition capacity largely depend on the absorption of soil moisture during the early stages of growth. Shading and release of allelopathic chemicals could be the reasons for weed growth inhibition in Barley plots (Asghari and Tewari, 2007).

N. sativa yield in presence of the living mulches was higher than the weed-infested and weed free plots. It is well established that mixed cultivation compared to monoculture, improves performance and maximizes the use of resources and more appropriate use of them in the agricultural ecosystem, due to the increase in diversity (Huss et al., 2022). As a result, using living mulches increases yield by reducing the consumption of expensive inputs. Usually, such improvements are obtained in crops where the length of the growing period of plants is different (Ahmed et al., 2020). Cultivation of plants with different morphological and physiological characteristics together facilitates the optimal use of environmental factors (Dong et al., 2018). Our results showed that in the N. sativa mixed cultivation, the use of berseem clover had more beneficial effects than barley. These results can be due to the ability of leguminous plants to fix nitrogen and increase the availability of this element in the soil, which causes the improvement of soil fertility and ultimately the plant productivity (Campiglia et al., 2010). A weed-free system, while eliminating competition, lacks these positive ecological interactions. Therefore, the observed superiority of berseem clover as a cover crop (until the establishment of N. sativa) over the weed-free control in grain yield may be attributed to the mentioned cases. It was also reported that the yield of cereals in the cultivation system with living mulch was 14–22% higher than the system without living mulch (Bhaskar et al., 2014). The use of living mulch also increased the percentage of seed oil. Seed oil content of fennel (Foeniculum vulgare L.) increased by intercropping with legume plants (Rezaei-Chiyaneh et al. 2020). Due to the increase in seed yield and the percentage of oil in seed, oil yield per unit area also increased in living mulch plots.

The yield of N. sativa oil in the plots where the clover was cut in the early growth stages was higher than the plots where the clover was kept until N. sativa flowering stage. These results showed that if berseem clover is permitted to grow until the flowering period of N. sativa, it will contest with N. sativa for resources like nutrients, water, or light for a prolonged duration, which subsequently decreases the yield of black seed oil. In contrast, cutting clover early minimizes this competition. This interpretation aligns with our results, where early cutting of berseem clover improved oil yield by 7.42% compared to plots where clover was retained longer. While the open canopy structure of barley makes it less competitive with the main crop. In this study, the fatty acid composition of the N. sativa oil was similar to the values reported by Tulukcu (2011) and Soleimanifar et al. (2019). Linoleic acid (52.1–53.4%) was the predominant fatty acid in the oil of N. sativa seeds. This is an essential polyunsaturated omega-6 fatty acid which constitutes more than 50% of the total fatty acids in the oil of N. sativa (Ashraf et al., 2006). Yimer et al. (2019) reported that linoleic acid content in the oil of N. sativa was 64.6%. Matthäus and ÖzCaN (2011) also reported the linoleic acid content of N. sativa between 56.7% and 58.9%. Oleic acid was the second predominant fatty acid in the N. sativa oil (22.5–24.9%). The oleic acid content of N. sativa has been reported 18.7 and 23.7% in previous studies (Matthäus and ÖzCaN, 2011). The fatty acid composition of the oil seed of N. sativa varied by the climatic conditions and genotypes (Amin et al., 2010). However, the present study showed that the N. sativa cultivation in saline soil does not significantly change the fatty acid profile of this plant.

Our results indicated that the weed management systems did not affect the relative content of the dominant fatty acids of the N. sativa oil. However, the percentage of unsaturated fatty acids in black cumin oil in the presence of living mulches and weeds was higher than the plots without living mulch and the weed-free plots. The results revealed that the presence of another plant species (weed or living mulch) increases the ΣUFA in N. sativa oil. Crops and weeds may coexist without economic loss of yield, and some relationships between crops and weeds may have beneficial effects (Koehler et al., 2020). The yield of N. sativa oil and the content of each fatty acids in its oil are under the influence of environmental conditions (Bayati et al., 2020). Different plants in the vicinity of each other do not compete for the absorption of a specific element. In other words, the effect of interspecific competition is equal or less than intraspecific competition (Adler et al., 2018). When interspecific competition is weaker than intraspecific competition, each species in a community limits growth of its own population more than its competitors. The result is negative frequency dependence: the rarer a species becomes in a community, the more its population growth rate increases, protecting it from competitive exclusion. A variety of symbiotic mechanisms, such as differential responses to spatial and temporal environmental changes, resource partitioning, and species-specific natural enemies, lead to differences and negative frequency dependence (Adler et al. 2007). One of the ways that two plants are complementary is the time difference in the growth period of the plants. If the length of growth of plants is different from each other, they will provide their required materials (aerial and terrestrial) at different times (Dong et al., 2018).

5 Conclusion

N. sativa exhibited a low competitive ability with weeds since the presence of weeds reduced its seed and oil production capacity. Although weed infestation did not affect the relative amounts of fatty acids in the N. sativa oil, it decreased oil yield per unit area by reducing the grain weight and the percentage of oil in the seed. Amaranthus retroflexus, Chenopodium album and Portulaca oleracea were the major weeds in the experimental site. These are highly salt and drought tolerant plants that may cause serious problems in agricultural lands in the future. Berseem clover and barley as living mulch showed acceptable performance in controlling the dominant weeds. These plants performed well in the hot and dry condition and the salt-affected soil of the site. Berseem clover was more effective in controlling weeds than barley, thereby of its dense cover over the soil and nitrogen fixation activity. However, the results indicated that berseem clover may compete with the main crop in the long term. Thus, berseem clover cultivation as a living mulch and mowing it after N. sativa establishment is recommended to manage weeds of N. sativa and improve its productivity.

Conflicts of interest

The authors have no conflicts of interest to declare.

Supplementary Material

Figure S1. Image of a complete N. sativa plant, its flowers and seeds. (https://commons.wikimedia.org/wiki/File:Nigella_sativa).

Figure S2. The effects of weed management systems on seed yield of black cumin in two cropping years. The values represent the means of 2017 and 2018. WF: weed free plot; WI: weed infest plot; HCt1: H. vulgare living mulch, mowing after black cumin establishment; HCt2: H. vulgare living mulch, mowing before the black cumin flowering stage. TCt1; T. alexandrinum living mulch, mowing after black cumin establishment; TCt2: T. alexandrinum living mulch, mowing before the black cumin flowering stage.

Table S1. Year-wise treatment effects on weed parameters and yield indices of black cumin. Values represent Mean ± Standard Deviation and different lowercase letters indicate significant differences (P±0.05) among treatments within each year and parameter.

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Cite this article as: Benakashani F, Tavakoli H, Soltani E. 2025. Living mulches as a strategy for weed control and improved Nigella sativa L. production in salt-affected soils. OCL 32: 25. https://doi.org/10.1051/ocl/2025024

All Tables

Table 1

Mean temperature and precipitation in the experimental site during the growing season

In the text
Table 2

Physiochemical properties of the soil of the experimental site in depth of 0–30 cm.

In the text
Table 3

Weed species and their relative frequency in the experimental field.

In the text
Table 4

Combined analysis of variance (mean squares) for the effect of treatments on density and biomass of weeds, and yield indices of black cumin.

In the text
Table 5

The effects of weed management systems on fatty acid composition of black cumin oil. The values represent the means of 2017 and 2018.

In the text
Table 6

Comparison of saturated fatty acids (ΣSFA), unsaturated fatty acids (ΣUFA), double bond index (DBI) and iodine value (IV) of Nigella sativa L. seed oil in different weed management systems at two years of experiment.

In the text

All Figures

thumbnail Fig. 1

The effects of weed management systems on density (A) and dry mass (B) of weeds in the black cumin field in two cropping years. The values represent the means of 2017 and 2018. WF: weed free plot; WI: weed infest plot; HCt1: H. vulgare living mulch, mowing after black cumin establishment; HCt2: H. vulgare living mulch, mowing before the black cumin flowering stage. TCt1; T. alexandrinum living mulch, mowing after black cumin establishment; TCt2: T. alexandrinum living mulch, mowing before the black cumin flowering stage.
In the text
thumbnail Fig. 2

The effects of weed management systems on thousand seed weight (A), oil percentage (B), and oil yield (C) of black cumin in two cropping years. The values represent the means of 2017 and 2018. WF: weed free plot; WI: weed infest plot; HCt1: H. vulgare living mulch, mowing after black cumin establishment; HCt2: H. vulgare living mulch, mowing before the black cumin flowering stage. TCt1; T. alexandrinum living mulch, mowing after black cumin establishment; TCt2: T. alexandrinum living mulch, mowing before the black cumin flowering stage.
In the text

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