Morphophysiological, biochemical, and nutrient response of spinach (Spinacia oleracea L.) by foliar CeO
Antioxidants
Cerium oxide nanoparticle
Chlorophyll contents
Growth parameters
Nutrient contents
Journal
Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288
Informations de publication
Date de publication:
25 Oct 2024
25 Oct 2024
Historique:
received:
05
06
2024
accepted:
17
10
2024
medline:
26
10
2024
pubmed:
26
10
2024
entrez:
25
10
2024
Statut:
epublish
Résumé
Nanomaterials offer considerable benefits in improving plant growth and nutritional status owing to their inherent stability, and efficiency in essential nutrient absorption and delivery. Cerium oxide nanoparticles (CeO
Identifiants
pubmed: 39455820
doi: 10.1038/s41598-024-76875-z
pii: 10.1038/s41598-024-76875-z
doi:
Substances chimiques
Cerium
30K4522N6T
ceric oxide
619G5K328Y
Carbon Dioxide
142M471B3J
Antioxidants
0
Chlorophyll
1406-65-1
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
25361Subventions
Organisme : This work was financial supported under project No. (RSP2024R48), King Saud University, Riyadh, Saudi Arabia.
ID : RSP2024R48
Informations de copyright
© 2024. The Author(s).
Références
Corwin, D. L. Climate change impacts on soil salinity in agricultural areas. Eur. J. Soil Sci. 72(2), 842–862. https://doi.org/10.1111/ejss.13010 (2021).
doi: 10.1111/ejss.13010
Wu, W., Takahashi, K., Zhou, L. & Jin, S. Income inequality and the distributional effects of elevated carbon dioxide on dietary nutrient deficiency. J. Clean. Prod. 265, 121606 (2020).
doi: 10.1016/j.jclepro.2020.121606
Lamichaney, A. et al. Effect of elevated carbon-dioxide on plant growth, physiology, yield and seed quality of chickpea (Cicer arietinum L.) in Indo-Gangetic plains. Physiol. Mol. Biol. Plants. 27, 251–263 (2021).
doi: 10.1007/s12298-021-00928-0
pubmed: 33707867
pmcid: 7907398
Kaur, H. et al. Effect of elevated CO
Dong, J. et al. Sustainable vegetable production under changing climate: The impact of elevated CO
doi: 10.1016/j.jclepro.2019.119920
Kundu, P., Goel, K. & Zinta, G. Nutritional imbalance in plants under rising atmospheric CO
Yang, X. et al. Effects of elevated CO
doi: 10.1007/s12298-021-00928-0
pubmed: 36241499
Becker, C. & Kläring, H. P. CO
doi: 10.1016/j.foodchem.2015.12.059
pubmed: 26776031
AbdElgawad, H. et al. Soil arsenic toxicity differentially impacts C3 (barley) and C4 (maize) crops under future climate atmospheric CO
doi: 10.1016/j.jhazmat.2021.125331
pubmed: 34030395
Chater, C. C., Caine, R. S., Fleming, A. J. & Gray, J. E. Origins and evolution of stomatal development. Plant Physiol. 174(2), 624–638. https://doi.org/10.1104/pp.17.00183 (2017).
doi: 10.1104/pp.17.00183
pubmed: 28356502
pmcid: 5462063
Zhang, J. et al. Insights into the molecular mechanisms of CO
doi: 10.1016/j.cub.2018.10.015
pubmed: 30513335
Chumley, H. & Hewlings, S. The effects of elevated atmospheric carbon dioxide [CO
doi: 10.1080/01904167.2020.1739303
Wang, X. & Liu, F. Effects of elevated CO
doi: 10.3390/plants10051027
pubmed: 34065412
pmcid: 8161111
Rajashekar, C. B. Elevated CO
doi: 10.4236/ajps.2018.92012
Dong, J., Gruda, N., Lam, S. K., Li, X. & Duan, Z. Effects of elevated CO
doi: 10.3389/fpls.2018.00924
pubmed: 30158939
pmcid: 6104417
Wang, J. et al. Changes in plant nutrient status following combined elevated [CO
doi: 10.3389/fpls.2023.1132414
pubmed: 36909423
pmcid: 9992424
Gohari, G. et al. Protective effects of cerium oxide nanoparticles in grapevine (Vitis vinifera L.) cv. Flame Seedless under salt stress conditions. Ecotoxicol. Environ. Saf. 220, 112402. https://doi.org/10.1016/j.ecoenv.2021.112402 (2021).
doi: 10.1016/j.ecoenv.2021.112402
pubmed: 34090105
Dimkpa, C. O. et al. Zinc oxide nanoparticles alleviate drought-induced alterations in sorghum performance, nutrient acquisition, and grain fortification. Sci. Total Environ. 688, 926–934. https://doi.org/10.1016/j.scitotenv.2019.06.392 (2019).
doi: 10.1016/j.scitotenv.2019.06.392
pubmed: 31726574
Liu, R. & Lal, R. Potentials of engineered nanoparticles as fertilizers for increasing agronomic productions. Sci. Total Environ. 514, 131–139. https://doi.org/10.1016/j.scitotenv.2019.06.392 (2015).
doi: 10.1016/j.scitotenv.2019.06.392
pubmed: 25659311
Shyam, R. & Aery, N. C. Effect of cerium on growth, dry matter production, biochemical constituents and enzymatic activities of cowpea plants [Vigna unguiculata (L.) Walp.]. J. Soil. Sci. Plant. Nutr. 12(1), 1–14. https://doi.org/10.4067/S0718-95162012000100001 (2012).
doi: 10.4067/S0718-95162012000100001
Jahani, S., Saadatmand, S., Mahmoodzadeh, H. & Khavari-Nejad, R. A. Effect of foliar application of cerium oxide nanoparticles on growth, photosynthetic pigments, electrolyte leakage, compatible osmolytes and antioxidant enzymes activities of Calendula officinalis L. Biologia. 74, 1063–1075. https://doi.org/10.2478/s11756-019-00239-6 (2019).
doi: 10.2478/s11756-019-00239-6
Skiba, E., Pietrzak, M., Glińska, S. & Wolf, W. M. The combined effect of ZnO and CeO
doi: 10.3390/cells10113105
pubmed: 34831328
pmcid: 8624121
Lee, S. S. et al. Antioxidant properties of cerium oxide nanocrystals as a function of nanocrystal diameter and surface coating. ACS Nano. 7(11), 9693–9703. https://doi.org/10.1021/nn4026806 (2013).
doi: 10.1021/nn4026806
pubmed: 24079896
Du, W. et al. Physiological and biochemical changes imposed by CeO
doi: 10.1021/acs.est.5b03055
pubmed: 26368651
Liu, D. et al. The effects of cerium on the growth and some antioxidant metabolisms in rice seedlings. Environ. Sci. Pollut. Res. 19, 3282–3291. https://doi.org/10.1007/s11356-012-0844-x (2012).
doi: 10.1007/s11356-012-0844-x
Giraldo, J. P. et al. Plant nanobionics approach to augment photosynthesis and biochemical sensing. Nat. Mater. 13(4), 400–408. https://doi.org/10.1038/nmat3890 (2014).
doi: 10.1038/nmat3890
pubmed: 24633343
Wu, H., Tito, N. & Giraldo, J. P. Anionic cerium oxide nanoparticles protect plant photosynthesis from abiotic stress by scavenging reactive oxygen species. ACS Nano. 11(11), 11283–11297. https://doi.org/10.1021/acsnano.7b05723 (2017).
doi: 10.1021/acsnano.7b05723
pubmed: 29099581
Abbas, Q. et al. Biochar-assisted transformation of engineered-cerium oxide nanoparticles: Effect on wheat growth, photosynthetic traits and cerium accumulation. Ecotoxicol. Environ. Saf. 187, 109845. https://doi.org/10.1016/j.ecoenv.2019.109845 (2020).
doi: 10.1016/j.ecoenv.2019.109845
pubmed: 31654865
Rico, C. M. et al. Cerium oxide nanoparticles impact yield and modify nutritional parameters in wheat (Triticum aestivum L.). J. Agric. Food Chem. 62(40), 9669–9675. https://doi.org/10.1021/jf503526r (2014).
doi: 10.1021/jf503526r
pubmed: 25220448
Liu, Y. et al. Foliar-applied cerium oxide nanomaterials improve maize yield under salinity stress: Reactive oxygen species homeostasis and rhizobacteria regulation. Environ. Pollut. 299, 118900. https://doi.org/10.1016/j.envpol.2022.118900 (2022).
doi: 10.1016/j.envpol.2022.118900
pubmed: 35085650
Skiba, E., Pietrzak, M., Gapińska, M. & Wolf, W. M. Metal homeostasis and gas exchange dynamics in Pisum sativum L. exposed to cerium oxide nanoparticles. Int. J. Mol. Sci. 21(22), 8497. https://doi.org/10.3390/ijms21228497 (2020).
doi: 10.3390/ijms21228497
pubmed: 33187383
pmcid: 7696629
Alsherif, E. A. & AbdElgawad, H. Elevated CO
doi: 10.3390/plants12071535
pubmed: 37050160
pmcid: 10096617
Jiang, F. et al. Effects of TiO
doi: 10.1371/journal.pone.0178088
pubmed: 28558015
pmcid: 5448767
Ayub, M. A. et al. Divergent effects of cerium oxide nanoparticles alone and in combination with cadmium on nutrient acquisition and the growth of maize (Zea mays). Front. Plant Sci. 14, 1151786. https://doi.org/10.3389/fpls.2023.1151786 (2023).
doi: 10.3389/fpls.2023.1151786
pubmed: 37063213
pmcid: 10098090
Du, W. et al. Elevated CO
doi: 10.1016/j.scitotenv.2016.10.197
pubmed: 27838053
Saleh, A. M. et al. NiO-nanoparticles induce reduced phytotoxic hazards in wheat (Triticum aestivum L.) grown under future climate CO
doi: 10.1016/j.chemosphere.2019.01.023
pubmed: 33395791
Pagano, L. et al. Exposure of Cucurbita pepo to binary combinations of engineered nanomaterials: Physiological and molecular response. Environ. Sci. Nano. 4(7), 1579–1590. https://doi.org/10.1039/C7EN00219J (2017).
doi: 10.1039/C7EN00219J
Ramaiyan, B., Kour, J., Nayik, G. A., Anand, N. & Alam, M. S. Spinach (Spinacia oleracea L.). In Antioxidants in Vegetables and Nuts-Properties and Health Benefits, 159–173. https://doi.org/10.1007/978-981-15-7470-2_8 (2020).
Thomas, R. M. et al. Effect of salinity on growth of Nile tilapia (Oreochromis niloticus) and spinach (Spinacia oleracea) in aquaponic system using inland saline groundwater. Aquac. Res. 52(12), 6288–6298. https://doi.org/10.1111/are.15492 (2021).
doi: 10.1111/are.15492
Whiting, D., Wilson, C. & Card, A. Estimating soil texture: sandy, loamy or clayey? Gardening series. Colorado master gardener; no. 7.723 (2005).
Lu, R. K. Methods of Soil and Agro-chemical Analysis 127–332 (China Agricultural Science and Technology Press, 2000).
Mehlich, A. Mehlich 3 soil test extractant: A modification of Mehlich 2 extractant. Commun. Soil Sci. Plant Anal. 15(12), 1409–1416. https://doi.org/10.1080/00103628409367568 (1984).
doi: 10.1080/00103628409367568
Park, J. H., Choppala, G. K., Bolan, N. S., Chung, J. W. & Chuasavathi, T. Biochar reduces the bioavailability and phytotoxicity of heavy metals. Plant Soil 348, 439–451. https://doi.org/10.1007/s11104-011-0948-y (2011).
doi: 10.1007/s11104-011-0948-y
Yin, Y. et al. Elevated CO
doi: 10.1016/j.jhazmat.2016.12.044
pubmed: 28040633
Arnon, D. I. Copper enzymes in isolated chloroplasts. Polyphenoloxidase in Beta vulgaris. Plant Physiol. https://doi.org/10.1104/p.24.1.1 (1949).
doi: 10.1104/p.24.1.1
pubmed: 16654194
pmcid: 437905
Zhang, X. Z. The measurement and mechanism of lipid peroxidation and SOD, POD and CAT activities in biological system. In Res. Method. of Crop Physiol. 208–211 (1992).
Nakano, Y. & Asada, K. Hydrogen peroxide is scavenged by ascorbate-specific peroxidase in spinach chloroplasts. Plant Cell Physiol. 22(5), 867–880. https://doi.org/10.1093/oxfordjournals.pcp.a076232 (1981).
doi: 10.1093/oxfordjournals.pcp.a076232
Aebi, H. [13] Catalase in vitro. In Methods Enzymol. vol. 105, 121–126. https://doi.org/10.1016/S0076-6879(84)05016-3 (Academic Press, 1984).
Jaleel, C. A., Manivannan, P., Sankar, B., Kishorekumar, A. & Panneerselvam, R. Calcium chloride effects on salinity-induced oxidative stress, proline metabolism and indole alkaloid accumulation in Catharanthus roseus. Comptes R. Biol. 330(9), 674–683. https://doi.org/10.1016/j.crvi.2007.07.002 (2007).
doi: 10.1016/j.crvi.2007.07.002
Patterson, B. D., MacRae, E. A. & Ferguson, I. B. Estimation of hydrogen peroxide in plant extracts using titanium (IV). Anal. Biochem. 139(2), 487–492. https://doi.org/10.1016/0003-2697(84)90039-3 (1984).
doi: 10.1016/0003-2697(84)90039-3
pubmed: 6476384
Liu, J. J., Wei, Z. & Li, J. H. Effects of copper on leaf membrane structure and root activity of maize seedling. Bot. Stud. 55(1), 1–6. https://doi.org/10.1186/s40529-014-0047-5 (2014).
doi: 10.1186/s40529-014-0047-5
pubmed: 28510906
pmcid: 5432845
Zhang, W. et al. Uptake and accumulation of bulk and nanosized cerium oxide particles and ionic cerium by radish (Raphanus sativus L.). J. Agric. Food. Chem. 63(2), 382–390. https://doi.org/10.1021/jf5052442 (2015).
doi: 10.1021/jf5052442
pubmed: 25531028
Salehi, H., Chehregani, A., Lucini, L., Majd, A. & Gholami, M. Morphological, proteomic and metabolomic insight into the effect of cerium dioxide nanoparticles to Phaseolus vulgaris L. under soil or foliar application. Sci. Total Environ. 616, 1540–1551. https://doi.org/10.1016/j.scitotenv.2017.10.159 (2018).
doi: 10.1016/j.scitotenv.2017.10.159
pubmed: 29066204
Azhar, W. et al. Ethylene mediates CuONP-induced ultrastructural changes and oxidative stress in Arabidopsis thaliana leaves. Environ. Sci. Nano. 7(3), 938–953. https://doi.org/10.1039/C9EN01302D (2020).
doi: 10.1039/C9EN01302D
Lizzi, D. et al. Germination and early development of three spontaneous plant species exposed to nanoceria (nCeO
doi: 10.3390/nano10122534
Wang, Y. et al. Effects of cerium oxide on rice seedlings as affected by co-exposure of cadmium and salt. Environ. Pollut. 252, 1087–1096. https://doi.org/10.1016/j.envpol.2019.06.007 (2019).
doi: 10.1016/j.envpol.2019.06.007
pubmed: 31252106
Rico, C. M. et al. Effect of cerium oxide nanoparticles on the quality of rice (Oryza sativa L.) grains. J. Agric. Food Chem. 61(47), 11278–11285. https://doi.org/10.1021/jf404046v (2013).
doi: 10.1021/jf404046v
pubmed: 24188281
Alsherif, E. & AbdElgawad, H. Physiological and biochemical responses of wheat plant to selenium nanoparticles under elevated CO
doi: 10.3389/fpls.2023.1183185
pubmed: 37521939
pmcid: 10373590
Broberg, M. C., Högy, P., Feng, Z. & Pleijel, H. Effects of elevated CO
doi: 10.3390/agronomy9050243
AbdElgawad, H. et al. The impact of chromium toxicity on the yield and quality of rice grains produced under ambient and elevated levels of CO
doi: 10.3389/fpls.2023.1019859
pubmed: 36959941
pmcid: 10027917
Jurkow, R., Sękara, A., Pokluda, R., Smoleń, S. & Kalisz, A. Biochemical response of oakleaf lettuce seedlings to different concentrations of some metal (oid) oxide nanoparticles. Agron. 10(7), 997. https://doi.org/10.3390/agronomy10070997 (2020).
doi: 10.3390/agronomy10070997
Hezaveh, T. A., Pourakbar, L., Rahmani, F. & Alipour, H. Interactive effects of salinity and ZnO nanoparticles on physiological and molecular parameters of rapeseed (Brassica napus L.). Commun. Soil. Sci. Plant Anal. 50(6), 698–715. https://doi.org/10.1080/00103624.2019.1589481 (2019).
doi: 10.1080/00103624.2019.1589481
Alsaeedi, A. et al. Silica nanoparticles boost growth and productivity of cucumber under water deficit and salinity stresses by balancing nutrients uptake. Plant Physiol. Biochem. 139, 1–10. https://doi.org/10.1016/j.plaphy.2019.03.008 (2019).
doi: 10.1016/j.plaphy.2019.03.008
pubmed: 30870715
Rizwan, M. et al. Effect of metal and metal oxide nanoparticles on growth and physiology of globally important food crops: A critical review. J. Hazard. Mater. 322, 2–16. https://doi.org/10.1016/j.jhazmat.2016.05.061 (2017).
doi: 10.1016/j.jhazmat.2016.05.061
pubmed: 27267650
Gulzar, S. et al. Effects of melatonin and Trichoderma harzianum on pak choi yield, chlorophyll contents and antioxidant defense system under clubroot disease. S. Afr. J. Bot. 158, 292–300. https://doi.org/10.1016/j.sajb.2023.05.021 (2023).
doi: 10.1016/j.sajb.2023.05.021
Thompson, M., Gamage, D., Hirotsu, N., Martin, A. & Seneweera, S. Effects of elevated carbon dioxide on photosynthesis and carbon partitioning: a perspective on root sugar sensing and hormonal crosstalk. Front. physiol. 8, 578. https://doi.org/10.3389/fphys.2017.00578 (2017).
doi: 10.3389/fphys.2017.00578
pubmed: 28848452
pmcid: 5550704
Khamis, G., Reyad, A. M. & AbdElgawad, H. Elevated CO
doi: 10.3389/fpls.2023.1244019
pubmed: 37780499
pmcid: 10534994
Al Jaouni, S. et al. Elevated CO
doi: 10.1016/j.jplph.2018.03.016
pubmed: 29626813
Gong, X. et al. Cerium relieves the inhibition of photosynthesis of maize caused by manganese deficiency. Biol. Trace Elem. Res. 141, 305–316. https://doi.org/10.1007/s12011-010-8716-z (2011).
doi: 10.1007/s12011-010-8716-z
pubmed: 20480399
Daler, S. Improving grapevine (Vitis vinifera L., cv. Superior Seedless) drought tolerance with cerium oxide nanoparticles: Agronomic and molecular insights. Sci. Hortic. 338, 113606. https://doi.org/10.1016/j.scienta.2024.113606 (2024).
doi: 10.1016/j.scienta.2024.113606
Taylor, N. S. et al. Molecular toxicity of cerium oxide nanoparticles to the freshwater alga Chlamydomonas reinhardtii is associated with supra-environmental exposure concentrations. Nanotoxicology. 10(1), 32–41. https://doi.org/10.3109/17435390.2014.1002868 (2016).
doi: 10.3109/17435390.2014.1002868
pubmed: 25740379
Kamali-Andani, N., Fallah, S., Peralta-Videa, J. R. & Golkar, P. A comprehensive study of selenium and cerium oxide nanoparticles on mung bean: Individual and synergistic effect on photosynthesis pigments, antioxidants, and dry matter accumulation. Sci. Total Environ. 830, 154837. https://doi.org/10.1016/j.scitotenv.2022.154837 (2022).
doi: 10.1016/j.scitotenv.2022.154837
pubmed: 35346715
Li, J. et al. Growth and photosynthetic inhibition of cerium oxide nanoparticles on soybean (Glycine max). Bull. Environ. Contam. Toxicol. 105, 119–126. https://doi.org/10.1007/s00128-020-02892-z (2020).
doi: 10.1007/s00128-020-02892-z
pubmed: 32468075
AbdElgawad, H., Hassan, Y. M., Alotaibi, M. O., Mohammed, A. E. & Saleh, A. M. C3 and C4 plant systems respond differently to the concurrent challenges of mercuric oxide nanoparticles and future climate CO
doi: 10.1016/j.scitotenv.2020.142356
pubmed: 33370918
Lal, M. K. et al. From source to sink: mechanistic insight of photoassimilates synthesis and partitioning under high temperature and elevated CO
doi: 10.1007/s11103-022-01274-9
pubmed: 35610527
Wang, Z., Wang, C. & Liu, S. Elevated CO
doi: 10.1111/1365-2745.13988
Sekhar, K. M., Reddy, K. S. R. & Reddy, A. R. Photosynthesis and carbon sequestration efficacy of Conocarpus erectus L. (Combretaceae) grown under elevated CO
doi: 10.1007/s40502-022-00702-8
Driesen, E., Van den Ende, W., De Proft, M. & Saeys, W. Influence of environmental factors light, CO
doi: 10.3390/agronomy10121975
Mirza, N., Mahmood, Q., Maroof Shah, M., Pervez, A. & Sultan, S. Plants as useful vectors to reduce environmental toxic arsenic content. Sci. World. J. https://doi.org/10.1155/2014/921581 (2014).
doi: 10.1155/2014/921581
Djanaguiraman, M., Nair, R., Giraldo, J. P. & Prasad, P. V. V. Cerium oxide nanoparticles decrease drought-induced oxidative damage in sorghum leading to higher photosynthesis and grain yield. ACS Omega. 3(10), 14406–14416. https://doi.org/10.1021/acsomega.8b01894 (2018).
doi: 10.1021/acsomega.8b01894
pubmed: 30411067
pmcid: 6217696
Prakash, V., Peralta-Videa, J., Tripathi, D. K., Ma, X. & Sharma, S. Recent insights into the impact, fate and transport of cerium oxide nanoparticles in the plant-soil continuum. Ecotoxicol. Environ. Saf. 221, 112403. https://doi.org/10.1016/j.ecoenv.2021.112403 (2021).
doi: 10.1016/j.ecoenv.2021.112403
pubmed: 34147863
AbdElgawad, H., Zinta, G., Beemster, G. T., Janssens, I. A. & Asard, H. Future climate CO
doi: 10.3389/fpls.2016.00556
pubmed: 27200030
pmcid: 4852726
Cao, Z. et al. The impact of cerium oxide nanoparticles on the physiology of soybean (Glycine max (L.) Merr.) under different soil moisture conditions. Environ. Sci. Pollut. Res. 25(1), 930–939. https://doi.org/10.1007/s11356-017-0501-5 (2018).
doi: 10.1007/s11356-017-0501-5
Rizwan, M. et al. Effect of metal and metal oxide nanoparticles on growth and physiology of globally important food crops: a critical review. J. Hazard Mater. 322, 2–16. https://doi.org/10.1016/j.jhazmat.2016.05.061 (2017).
doi: 10.1016/j.jhazmat.2016.05.061
pubmed: 27267650
Ma, X., Wang, Q., Rossi, L. & Zhang, W. Cerium oxide nanoparticles and bulk cerium oxide leading to different physiological and biochemical responses in Brassica rapa. Environ. Sci. Technol. 50(13), 6793–6802. https://doi.org/10.1021/acs.est.5b04111 (2016).
doi: 10.1021/acs.est.5b04111
pubmed: 26691446
Corral-Diaz, B. et al. Cerium oxide nanoparticles alter the antioxidant capacity but do not impact tuber ionome in Raphanus sativus (L.). Plant. Physiol. Biochem. 84, 277–285. https://doi.org/10.1016/j.plaphy.2014.09.018 (2014).
doi: 10.1016/j.plaphy.2014.09.018
pubmed: 25439500
Korsvik, C., Patil, S., Seal, S. & Self, W. T. Superoxide dismutase mimetic properties exhibited by vacancy engineered ceria nanoparticles. Chem. Commun. 10, 1056–1058. https://doi.org/10.1039/B615134E (2007).
doi: 10.1039/B615134E
Hussain, I. et al. Exogenous application of phytosynthesized nanoceria to alleviate ferulic acid stress in Solanum lycopersicum. Sci. Hortic. 214, 158–164. https://doi.org/10.1016/j.scienta.2016.11.032 (2017).
doi: 10.1016/j.scienta.2016.11.032
Rico, C. M., Johnson, M. G., Marcus, M. A. & Andersen, C. P. Intergenerational responses of wheat (Triticum aestivum L.) to cerium oxide nanoparticles exposure. Environ. Sci. Nano. 4(3), 700–711. https://doi.org/10.1039/C7EN00057J (2017).
doi: 10.1039/C7EN00057J
pubmed: 30147938
pmcid: 6104651
Zhao, L. et al. Influence of CeO
doi: 10.1021/jf404328e
pubmed: 24245665
Hong, J. et al. Evidence of translocation and physiological impacts of foliar applied CeO
doi: 10.1021/es404931g
pubmed: 24625209
Giri, A., Armstrong, B. & Rajashekar, C. B. Elevated carbon dioxide level suppresses nutritional quality of lettuce and spinach. Am. J. Plant Sci. 7(01), 246. https://doi.org/10.4236/ajps.2016.71024 (2016).
doi: 10.4236/ajps.2016.71024
Roy, S. & Mathur, P. Delineating the mechanisms of elevated CO
doi: 10.1007/s00299-021-02738-w
pubmed: 34169360
Soares, J. et al. Growth and nutritional responses of bean and soybean genotypes to elevated CO
doi: 10.3390/plants8110465
pubmed: 31671712
pmcid: 6918337
Ayyaz, A. et al. Calcium nanoparticles and abscisic acid improve drought tolerance, mineral nutrients uptake and inhibitor-mediated photosystem II performance in Brassica napus. J. Plant Growth Regul. 43(2), 516–537. https://doi.org/10.1007/s00344-023-11108-7 (2024).
doi: 10.1007/s00344-023-11108-7
Sega, D., Baldan, B., Zamboni, A. & Varanini, Z. FePO
doi: 10.3389/fpls.2020.586470
pubmed: 33101351
pmcid: 7554371
Hong, J. et al. Foliar application of nanoparticles: mechanisms of absorption, transfer, and multiple impacts. Environ. Sci. Nano. 8(5), 1196–1210. https://doi.org/10.1039/D0EN01129K (2021).
doi: 10.1039/D0EN01129K
Liu, M. et al. Influence of surface charge on the phytotoxicity, transformation, and translocation of CeO
doi: 10.1021/acsami.9b01627
pubmed: 30993970
Gui, X. et al. Phytotoxicity of CeO
doi: 10.1007/s11356-017-8880-1
Dai, Y. et al. Transfer of CeO
doi: 10.1016/j.jhazmat.2023.131137
pubmed: 36913748
Singh, A. et al. In-depth exploration of nanoparticles for enhanced nutrient use efficiency and abiotic stresses management: present insights and future horizons. Plant Stress. https://doi.org/10.1016/j.stress.2024.100576 (2024).
doi: 10.1016/j.stress.2024.100576