Chibuike, G. U. & Obiora, S. C. Heavy metal polluted soils: Effect on plants and bioremediation methods. Appl. Environ. Soil Sci. 2014, 1–12. https://doi.org/10.1155/2014/752708 (2014).
Google Scholar
Baek, S. A. et al. Effects of heavy metals on plant growths and pigment contents in Arabidopsis thaliana. Plant Pathol. J. 28, 446–452. https://doi.org/10.5423/PPJ.NT.01.2012.0006 (2012).
Google Scholar
Gong, Z. Z. et al. Plant abiotic stress response and nutrient use efficiency. Sci. China Life Sci. 63, 635–674. https://doi.org/10.1007/s11427-020-1683-x (2020).
Google Scholar
Pravin, U. S., Manisha, P. T. & Ravindra, M. M. Sediment heavy metal contaminants in Vasai Creek of Mumbai: Pollution impacts. Am. Chem. Soc. 2(3), 171–180. https://doi.org/10.5923/j.chemistry.20120203.13 (2012).
Google Scholar
Kim, Y. H. et al. Silicon mitigates heavy metal stress by regulating P-type heavy metal ATPases, Oryza sativa low silicon genes, and endogenous phytohormones. BMC Plant Biol. 14, 1–13. https://doi.org/10.1186/1471-2229-14-13 (2014).
Google Scholar
Mao, F. et al. The metal distribution and the change of physiological and biochemical process in soybean and mung bean plants under heavy metal stress. Int. J. Phytoremed. 20, 1113–1120. https://doi.org/10.1080/15226514.2017.1365346 (2018).
Google Scholar
Reichman, S. M., Menzies, N. W., Asher, C. J. & Mulligan, D. R. Seedling responses of four Australian tree species to toxic concentrations of manganese in solution culture. Plant Soil. 258, 341–350. https://doi.org/10.1023/B:PLSO.0000016564.14512.eb (2004).
Google Scholar
Driscoll, C. T., Mason, R. P., Chan, H. M., Jacob, D. J. & Pirrone, N. Mercury as a global pollutant: Sources, pathways, and effects. Environ. Sci. Technol. 47, 4967–4983. https://doi.org/10.1021/es305071v (2013).
Google Scholar
Liu, Z. C. et al. Effects of different concentrations of mercury on accumulation of mercury by five plant species. Ecol. Eng. 106, 273–278. https://doi.org/10.1016/j.ecoleng.2017.05.051 (2017).
Google Scholar
Hassan, M. J. et al. Effect of cadmium toxicity on growth, oxidative damage, antioxidant defense system and cadmium accumulation in two sorghum cultivars. Plants 9, 1575. https://doi.org/10.3390/plants9111575 (2020).
Google Scholar
Patra, M., Bhowmik, N., Bandopadhyay, B. & Sharma, A. Comparison of mercury, lead and arsenic with respect to genotoxic effects on plant systems and the development of genetic tolerance. Environ. Exp. Bot. 52, 199–223. https://doi.org/10.1016/j.envexpbot.2004.02.009 (2004).
Google Scholar
Zhou, Z. S., Wang, S. J. & Yang, Z. M. Biological detection and analysis of mercury toxicity to alfalfa (Medicago sativa) plants. Chemosphere 70, 1500–1509. https://doi.org/10.1016/j.chemosphere.2007.08.028 (2008).
Google Scholar
Biczak, R. Quaternary ammonium salts with tetrafluoroborate anion: Phytotoxicity and oxidative stress in terrestrial plants. J. Hazard. Mater. 304, 173–185. https://doi.org/10.1016/j.jhazmat.2015.10.055 (2016).
Google Scholar
Elbaz, A., Wei, Y. Y., Meng, Q., Zheng, Q. & Yang, Z. M. Mercury-induced oxidative stress and impact on antioxidant enzymes in Chlamydomonas reinhardtii. Ecotoxicology 19, 1285–1293. https://doi.org/10.1007/s10646-010-0514-z (2010).
Google Scholar
Gao, S. et al. Growth and antioxidant responses in Jatropha curcas seedling exposed to mercury toxicity. J. Hazard. Mater. 182, 591–597. https://doi.org/10.1016/j.jhazmat.2010.06.073 (2010).
Google Scholar
Warren, S. D. et al. Reproduction and dispersal of biological soil crust organisms. Front. Ecol. Evol. 7, 1–17. https://doi.org/10.3389/FEVO.2019.00344 (2019).
Google Scholar
Wu, L. & Zhang, Y. Precipitation and soil particle size co-determine spatial distribution of biological soil crusts in the Gurbantunggut Desert, China. J. Arid. Land. 10, 701–711. https://doi.org/10.1007/s40333-018-0065-3 (2018).
Google Scholar
Hu, R. et al. The mechanism of soil nitrogen transformation under different biocrusts to warming and reduced precipitation: From microbial functional genes to enzyme activity. Sci. Total Environ. 722, 137849. https://doi.org/10.1016/j.scitotenv.2020.137849 (2020).
Google Scholar
Pan, Z. et al. The upside-down water collection system of Syntrichia caninervis. Nat. Plants. 2(7), 16076. https://doi.org/10.1038/nplants.2016.76 (2016).
Google Scholar
Coe, K. K. et al. Strategies of desiccation tolerance vary across life phases in the moss Syntrichia caninervis. Am. J. Bot. 108, 249–262. https://doi.org/10.1002/ajb2.1571 (2020).
Google Scholar
Silva, A. T. et al. To dry perchance to live: Insights from the genome of the desiccation-tolerant biocrust moss Syntrichia caninervis. Plant J. 105, 1339–1356. https://doi.org/10.1111/tpj.15116 (2021).
Google Scholar
Young, K. & Reed, S. Spectrally monitoring the response of the biocrust moss Syntrichia caninervis to altered precipitation regimes. Sci. Rep. 7, 41793. https://doi.org/10.1038/srep41793 (2017).
Google Scholar
Zhang, J. & Zhang, Y. M. Ecophysiological responses of the biocrust moss Syntrichia caninervis to experimental snow cover manipulations in a temperate desert of central Asia. Ecol. Res. 35, 198–207. https://doi.org/10.1111/1440-1703.12072 (2019).
Google Scholar
Zheng, Y. P., Zhao, J. C., Zhang, B. C., Li, L. & Zhang, Y. M. Advances on ecological studies of algae and mosses in biological soil crusts. Chin. J. Bot. 44, 371–378 (2009).
Google Scholar
Mei, L. et al. Mercury-induced phytotoxicity and responses in upland cotton (Gossypium hirsutum L.) seedlings. Plants 10, 1494. https://doi.org/10.3390/plants10081494 (2021).
Google Scholar
Zhao, Z. S. et al. Metabolic adaptations to mercury-induced oxidative stress in roots of Medicago sativa L. J. Inorg. Biochem. 101, 1–9. https://doi.org/10.1016/j.jinorgbio.2006.05.011 (2007).
Google Scholar
Yuniarti, R. & Yuniati, R. Mercury effects on the early seedling of Paraserianthes falcataria (L.) Nielsen grew in hydroponic culture. IOP Conf. Ser. Mater. Sci. Eng. 902, 012073. https://doi.org/10.1088/1757-899X/902/1/012073 (2020).
Google Scholar
Li, Y. et al. Reorganization of photosystem II is involved in the rapid photosynthetic recovery of desert moss Syntrichia caninervis upon rehydration. J. Plant Physiol. 167, 1390–1397. https://doi.org/10.1016/j.jplph.2010.05.028 (2010).
Google Scholar
Deng, B. L., Yang, K. J., Zhang, Y. F. & Li, Z. T. Can heavy metal pollution defend seed germination against heat stress? Effect of heavy metals (Cu2+, Cd2+ and Hg2+) on maize seed germination under high temperature. Environ. Pollut. 216, 46–52. https://doi.org/10.1016/j.envpol.2016.05.050 (2016).
Google Scholar
Khan, K. Y. et al. Study amino acid contents, plant growth variables and cell ultrastructural changes induced by cadmium stress between two contrasting cadmiums accumulating cultivars of Brassica rapa ssp. chinensis L. (pak choi). Ecotoxicol. Environ. Saf. 200, 110748. https://doi.org/10.1016/j.ecoenv.2020.110748 (2020).
Google Scholar
Arnon, D. L. Copper enzymes in isolated chloroplasts.Polyphenoloxidases in Beta vulgaris. Plant Physiol. 24, 1–15 (1949).
Google Scholar
Bates, L. S., Waldren, R. P. & Teare, I. D. Rapid determination of free proline for water-stress studies. Plant Soil. 39, 205–207. https://doi.org/10.1007/BF00018060 (1973).
Google Scholar
Luo, X. L. & Huang, Q. F. Relationships between leaf and stem soluble sugar content and tuberous root starch accumulation in Cassava. J. Agric. Sci. 3, 64–72. https://doi.org/10.5539/jas.v3n2p64 (2011).
Google Scholar
Choudhury, S. & Panda, S. K. Toxic effects, oxidative stress and ultrastructural changes in moss Taxithelium nepalense (Schwaegr.) broth under chromium and lead phytotoxicity. Water Air Soil Pollut. 167, 73–90. https://doi.org/10.1007/s11270-005-8682-9 (2005).
Google Scholar
Kumar, A., Dutt, S., Bagler, G., Ahuja, P. S. & Kumar, S. Engineering a thermo-stable superoxide dismutase functional at sub-zero to >50°C, which also tolerates autoclaving. Sci. Rep. 2, 347–351. https://doi.org/10.1038/srep00387 (2012).
Google Scholar
Pasquariello, M. S. et al. Influence of postharvest chitosan treatment on enzymatic browning and antioxidant enzyme activity in sweet cherry fruit. Postharvest. Biol. Technol. 109, 45–46. https://doi.org/10.1016/j.postharvbio.2015.06.007 (2015).
Google Scholar
Emamverdian, A., Ding, Y. L., Mokhberdoran, F. & Xie, Y. F. Growth responses and photosynthetic indices of bamboo plant (Indocalamus latifolius) under heavy metal stress. Sci. World J. 2018, 1–6. https://doi.org/10.1155/2018/1219364 (2018).
Google Scholar
Sahu, G. K., Upadhyay, S. & Sahoo, B. B. Mercury induced phytotoxicity and oxidative stress in wheat (Triticum aestivum L.) plants. Physiol. Mol. Biol. Plants 18, 21–31. https://doi.org/10.1007/s12298-011-0090-6 (2012).
Google Scholar
Wang, R. Y. et al. Effect of amendments on contaminated soil of multiple heavy metals and accumulation of heavy metals in plants. Environ. Sci. Pollut. Res. 25, 28695–28704. https://doi.org/10.1007/s11356-018-2918-x (2018).
Google Scholar
Esposito, S. et al. In-field and in-vitro study of the moss Leptodictyum riparium as bioindicator of toxic metal pollution in the aquatic environment: Ultrastructural damage, oxidative stress and HSP70 induction. PLoS ONE 13, 1–16. https://doi.org/10.1371/journal.pone.0195717 (2018).
Google Scholar
Qureshi, S. et al. Effect of microbial activity on trace element release from sewage sludge. Environ. Sci. Technol. 37, 3361–3366. https://doi.org/10.1021/es020970h (2003).
Google Scholar
Lebeau, T., Bagot, D., Jézéquel, K. & Fabre, B. Cadmium biosorption by free and immobilised microorganisms cultivated in a liquid soil extract medium: Effects of Cd, pH and techniques of culture. Sci. Total Environ. 291, 73–83. https://doi.org/10.1016/S0048-9697(01)01093-2 (2002).
Google Scholar
Cho, U. H. & Park, J. O. Mercury-induced oxidative stress in tomato seedlings. Plant Sci. 156, 1–9. https://doi.org/10.1016/S0168-9452(00)00227-2 (2000).
Google Scholar
Chen, J. et al. Bioaccumulation and physiological effects of mercury in Pteris vittata and Nephrolepis exaltata. Ecotoxicology 18, 110–121. https://doi.org/10.1007/s10646-008-0264-3 (2009).
Google Scholar
Bellini, E. et al. The moss Leptodictyum riparium counteracts severe cadmium stress by activation of glutathione transferase and phytochelatin synthase, but slightly by phytochelatins. Int. J. Mol. Sci. 21, 1583. https://doi.org/10.3390/ijms21051583 (2020).
Google Scholar
Altaf, M. A. et al. Melatonin mitigates nickel toxicity by improving nutrient uptake fluxes, root architecture system, photosynthesis, and antioxidant potential in tomato seedling. J. Soil Sci. Plant Nutr. 21, 1842–1855. https://doi.org/10.1007/s42729-021-00484-2 (2021).
Google Scholar
Zhang, H. H. et al. Toxic effects of heavy metals Pb and Cd on mulberry (Morus alba L.) seedling leaves: Photosynthetic function and reactive oxygen species (ROS) metabolism responses. Ecotoxicol. Environ. Saf. 195, 110469. https://doi.org/10.1016/j.ecoenv.2020.110469 (2020).
Google Scholar
Hoekstra, F. A., Golovina, E. A. & Buitink, J. Mechanisms of plant desiccation tolerance. Trends Plant Sci. 6, 431–438. https://doi.org/10.1016/S1360-1385(01)02052-0 (2001).
Google Scholar
Xiong, A. S. et al. Expression and function of a modified AP2/ERF transcription factor from Brassica napus enhances cold tolerance in transgenic Arabidopsis. Mol. Biotechnol. 53, 198–206. https://doi.org/10.1007/s12033-012-9515-x (2013).
Google Scholar
Hare, P. D., Cress, W. A. & Staden, J. V. Proline synthesis and degradation: A model system for elucidating stress-related signal transduction. J. Exp. Bot. 50, 413–434. https://doi.org/10.1093/jxb/50.333.413 (1999).
Google Scholar
Székely, G. et al. Duplicated P5CS genes of Arabidopsis play distinct roles in stress regulation and developmental control of proline biosynthesis. Plant J. 53, 11–28. https://doi.org/10.1111/j.1365-313X.2007.03318.x (2008).
Google Scholar
Mishra, P., Bhoomika, K. & Dubey, R. S. Differential responses of antioxidative defense system to prolonged salinity stress in salt-tolerant and salt-sensitive Indica rice (Oryza sativa L.) seedlings. Protoplasma 250, 3–19. https://doi.org/10.1007/s00709-011-0365-3 (2013).
Google Scholar
Mittler, R. ROS are good. Trends Plant Sci. 22, 11–19. https://doi.org/10.1016/j.tplants.2016.08.002 (2017).
Google Scholar
Gill, S. S. & Tuteja, N. Reactive oxygen species and antioxidant machinery in abiotic stress tolerance in crop plants. Plant Physiol. Biochem. 48, 909–930. https://doi.org/10.1016/j.plaphy.2010.08.016 (2010).
Google Scholar
Kolahi, M., Kazemi, E. M., Yazdi, M. & Barnaby, A. G. Oxidative stress induced by cadmium in lettuce (Lactuca sativa Linn.): Oxidative stress indicators and prediction of their genes. Plant Physiol. Biochem. 146, 71–89. https://doi.org/10.1016/j.plaphy.2019.10.032 (2020).
Google Scholar
Merwald, H. et al. UVA-induced oxidative damage and cytotoxicity depend on the mode of exposure. J. Photochem. Photobiol. B Biol. 79, 197–207. https://doi.org/10.1016/j.jphotobiol.2005.01.002 (2005).
Google Scholar
Pazmiño, D. M. et al. Differential response of young and adult leaves to herbicide 2,4-dichlorophenoxyacetic acid in pea plants: Role of reactive oxygen species. Plant Cell Environ. 34, 1874–1889. https://doi.org/10.1111/j.1365-3040.2011.02383.x (2011).
Google Scholar
Ghori, N. H. et al. Heavy metal stress and responses in plants. Int. J. Environ. Sci. Technol. (Tehran) 16, 1807–1828. https://doi.org/10.1007/s13762-019-02215-8 (2019).
Google Scholar
Vezza, M. E., Llanes, A., Travaglia, C., Agostini, E. & Talano, M. A. Arsenic stress effects on root water absorption in soybean plants: Physiological and morphological aspects. Plant Physiol. Biochem. 123, 8–17. https://doi.org/10.1016/j.plaphy.2017.11.020 (2018).
Google Scholar
C, A., Tasdighi, H. & Gholamhoseini, M.,. Evaluation of proline, chlorophyll, soluble sugar content and uptake of nutrients in the German chamomile (Matricaria chamomilla L.) under drought stress and organic fertilizer treatments. Asian Pac. J. Trop. Biomed. 6(10), 886–891. https://doi.org/10.1016/j.apjtb.2016.08.009 (2016).
Google Scholar
Sharma, A. et al. Phytohormones regulate accumulation of osmolytes under abiotic stress. Biomolecules 9(7), 285. https://doi.org/10.3390/biom9070285 (2019).
Google Scholar
Zhang, S. S., Zhang, H. M., Qin, R., Jiang, W. S. & Liu, D. H. Cadmium induction of lipid peroxidation and effects on root tip cells and antioxidant enzyme activities in Vicia faba L. Ecotoxicology 18, 814–823. https://doi.org/10.1007/s10646-009-0324-3 (2009).
Google Scholar
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