Pollen is a male flower gametophyte located in the anthers of stamens in angiosperms and a considerable source of compounds with health protective potential. In the present work, phytochemical screening was carried out as well as analysis of the antioxidant and antibacterial properties of pollen extracts from Micromeria fruticosa, Achillea fragrantissima, and Phoenix dactylifera growing wild in Palestine. Phytochemical screening examined the total flavonol, flavone and phenolic content. The DPPH (1,2-Diphenyl-1-Picrylhydrazyl) and FRAP (ferric reducing antioxidant power) methods were used to assess antioxidant propriety, and disc diffusion, minimum inhibitory and bactericidal concentration tests were used to test the pollen extract’s antibacterial activity against multidrug-resistant (MDR) clinical isolates. The highest level of total phenolic was found in the extract of Micromeria fruticosa (56.78 ± 0.49 mg GAE (Gallic Acid Equivalent)/g). The flavone and flavonol content of samples ranged from 2.48 ± 0.05 to 8.03 ± 0.01 mg QE (Quercetin Equivalent)/g. Micromeria fruticosa pollen with IC50 values of 0.047 and 0.039 mg/mL in the DPPH and FRAP assays, respectively, showed the greatest radical scavenging action. In addition, this pollen showed a mild antibacterial action against the microorganisms studied, with MICs varying from 0.625 to 10 mg/mL and inhibition diameters ranging from 13.66 ± 1.5 to 16.33 ± 1.5 mm.

Anchusa italica Retz has been used for a long time in phytotherapy. The aim of the present study was to determine the antioxidant and antibacterial activities of extracts from the leaves and roots of Anchusa italica Retz. We first determined the content of phenolic compounds and flavonoids using Folin–Ciocalteu reagents and aluminum chloride (AlCl₃). The antioxidant activity was determined using three methods: reducing power (FRAP), 2.2-diphenyl-1-picrylhydrazyl (DPPH), total antioxidant capacity (TAC). The antimicrobial activity was investigated against four strains of Escherichia coli, two strains of Klebsiella pneumoniae and coagulase-negative Staphylococcus, and one fungal strain of Candida albicans. The results showed that the root extract was rich in polyphenols (43.29 mg GAE/g extract), while the leave extract was rich in flavonoids (28.88 mg QE/g extract). The FRAP assay showed a strong iron reduction capacity for the root extract (IC₅₀ of 0.11 µg/mL) in comparison to ascorbic acid (IC₅₀ of 0.121 µg/mL). The DPPH test determined an IC₅₀ of 0.11 µg/mL for the root extract and an IC₅₀ of 0.14 µg/mL for the leaf extract. These values are low compared to those for ascorbic acid (IC₅₀ of 0.16 µg/mL) and BHT (IC₅₀ 0.20 µg/mL). The TAC values of the leaf and root extracts were 0.51 and 0.98 mg AAE/g extract, respectively. In vitro, the extract showed inhibitory activity against all strains studied, with diameters of zones of inhibition in the range of 11.00–16.00 mm for the root extract and 11.67–14.33 mm for the leaf extract. The minimum inhibitory concentration was recorded for the leaf extract against E. coli (ATB:57), corresponding to 5 mg/mL. Overall, this research indicates that the extracts of Anchusa italica Retz roots and leaves exert significant antioxidant and antibacterial activities, probably because of the high content of flavonoids and polyphenols.

Salt stress is one of the most significant abiotic stresses that substantially negatively impact plant growth and productivity. However, a slew of research thus far has investigated the ameliorating properties of arbuscular mycorrhizal (AM) symbiosis and their potential to improve plant tolerance to salt stress. The present study aimed to evaluate and compare the role of mycorrhizal inocula obtained from Sabkha (S-AMF) and non-Sabkha (NS-AMF) habitats of Saudi Arabia on the morphological, physiological, and biochemical behaviors of the Lasiurus scindicus plant. For this reason, arbuscular mycorrhizal fungi (AMF) isolated from Sabkha and non-Sabkha soils were treated with salinity-exposed L. scindicus. The results revealed that the AMF-treated plants had higher growth metrics and increased synthesis of photosynthetic pigments, which were reduced by salt stress. Furthermore, the application of AM symbiosis induced an increase in the activities of the antioxidant system, which resulted in a reduction of the plant oxidative damage. It was also found that the increased accumulation of proline and phenols acted as a protective measure. Moreover, plants inoculated with S-AMF had the highest ameliorating responses on all the studied parameters compared to NS-AMF. This could be attributed to the presence of habitat-specific AMF, which may have induced adaptive plasticity in plants to tolerate or resist extreme salinity. However, further study in exploring the S-AMF diversity is needed to make it an ecofriendly choice for the restoration of salinity-affected ecosystems.

Lasiurus scindicus Henr. is one of the most important forage grass species of the Arabian deserts. Temperature and soil salinity are well known to influence the germination and seedling development of various forage species. Therefore, in the current study, the effect of temperature and salinity and their interaction on the germination parameters, seedling growth, and physiological parameters of L. scindicus were evaluated. For this reason, L. scindicus seeds were treated with five salinity concentrations (i.e., 0, 50, 100, 150, and 200 mM NaCl) and incubated at two temperature levels (T1 = 25/20 °C, D/N and T2 = 35/30 °C, D/N). The results indicated that the salinity and temperature significantly affected the germination indices, seedling growth parameters, chlorophyll, and proline content. The highest germination percentage (GP; 90%) was recorded in the non-saline-treated seeds incubated at T1. The seeds at T2 under the non-saline treatment exhibited an increased germination rate (GR = 17.5%). The interactive effect of salinity and temperature on germination and growth parameters was significant, indicating that the germination response to salinity depends on temperature. The germination of seeds treated with 200 mM NaCl was completely inhibited at both temperatures T1 and T2. However, the ungerminated seeds at both T1 (85%) and T2 (78%) restored their germination abilities after they were transferred to distilled water. Also, the seed vigor index (SVI) constantly showed a decline with the increasing salinity levels especially at T2, which was lowest when seeds were treated with 150 mM salinity. Growth parameters (i.e., aRL, aSL, RDW, SDW, SB, and SLA) and the chlorophyll content showed a similar pattern as that of germination. However, the proline content (shoot proline and root proline) showed a progressive increase with increasing salinity and temperature. All of these characteristics indicate that L. scindicus seeds were not able to germinate under extreme salinity and temperature conditions but remained viable in a state of enforced dormancy. This is most likely an important adaptive strategy of this species for survival in the high-saline changing habitats of the arid region of Saudi Arabia, and thus, it can be an excellent choice for restoring degraded rangelands and salinity-inflicted abundant farmlands for forage agriculture.

The use of contaminated water to irrigate crop plants poses a risk to human health from the bioaccumulation potential of microcystins (MCs) in the edible tissues of vegetable plants. The main objective of this study is to determine the concentration of total microcystins (MC-LR and MC-RR) in leafy green plants (Lactuca sativa L. var. longifolia and Eruca sativa) that have previously been irrigated with polluted water. Integrated water samples were collected by cleaned plastic bottles at a depth of about 30 cm from one of the sources of water used to irrigate agricultural lands for crop plants. At the same time, samples from plants were also collected because this water from the lake farm is used for the irrigation of surrounding vegetable plants such as Lactuca sativa L. var. longifolia and Eruca sativa. The dominant species of cyanobacteria in water samples are Microcystis aeruginosa (Kützing) and Oscillatoria limnetica Lemmermann, which were detected with an average cell count 2,300,000 and 450,000 cells/mL, respectively. These two dominant species in water produced two MCs variants (MC-LR, -RR) that were quantified by high-performance liquid chromatography (HPLC). Dissolve and particulate MCs were detected in the irrigation waters by HPLC with concentrations of 45.04–600 μg/L. MCs in the water samples exceeded the WHO safety limit (1 μg/L) of MC in drinking water. In addition, the total concentration of Microcystin in Lactuca sativa L. var. longifolia and Eruca sativa were 1044 and 1089 ng/g tissues, respectively. The estimated daily intake (EDI) of microcystins by a person (60 kg) consuming 300 g of fresh plants exceeded the total daily intake guidelines (0.04 μg kg⁻¹ body weight) for human food consumption. According to the findings of this study, irrigation water and plants used for human consumption should be tested for the presence of MCs regularly through critical and regularly monitored programs to prevent the accumulation and transfer of such toxins through the food web.

Our objective is to test selected mycorrhizal complexes to verify the contribution of mycorrhizal symbiosis as a biological tool promoting the development of the argan tree under hostile conditions. In addition, this study aims to assess the impact of soil drought caused by stopping watering of young argan plants inoculated with strains of fungal complexes indigenous to the species in comparison to non-inoculated plants. Under conditions of water deficit stress, the most marked reductions in fresh and dry biomass were recorded in non-mycorrhizal plants. The most negative values of leaf water potential Ψf and Ψb were also noted in non-mycorrhizal plants. On the other hand, plants inoculated with mycorrhizal Bouyzakarne inoculum were relatively less affected by watering discontinuation compared to those inoculated with mycorrhizal Argana inoculum. Water stress caused a reduction in potassium and phosphorus content in the leaves and roots of all plants. However, mycorrhizal plants exhibited the highest P and K values compared to non-mycorrhizal ones. Therefore, mycorrhization compensates for the deficit in absorption of inorganic nutrients during drought. Sodium gradually decreased in the leaves but increased in the roots, and this delocalization of Na⁺ ions under water deficit stress resulted in higher concentrations in the roots than in the leaves of all plants. However, the mycorrhizal plants exhibited relatively lower values of root Na⁺ compared to the non-mycorrhizal controls. The water deficit reduced the content of chlorophyll a and b in the leaves and the chlorophyll a/b ratio in stressed plants. The lowest chlorophyll values were recorded in non-mycorrhizal plants. The levels of proline and soluble sugars in the leaves and roots of argan plants increased in all plants, especially with the extension of the duration of stress. However, proline accumulation was higher in mycorrhizal plants, with superiority in plants inoculated with the Bouyzakarne complex in comparison with that of Argana. In contrast, the accumulation of soluble sugars was higher in non-mycorrhizal plants than in mycorrhizal plants. We concluded that with a correct choice of the symbiotic fungi complexes, AMF inoculation biotechnology can benefit argan cultivation, especially under stressful conditions in arid regions with structural drought, where native Arbuscular mycorrhizal fungi levels are low.