Skip to main content

Advertisement

Log in

Responses of Niger [Guizotia abyssinica (L.f.) Cass.] to cadmium and nickel stress

  • Research Articles
  • Published:
Vegetos Aims and scope Submit manuscript

Abstract

Niger (Guizotia abyssinica (L.f.) Cass) is an incredibly useful but underutilized oil crop commonly grown in East Africa, mainly in Ethiopia, and the Indian subcontinent. Various abiotic stresses of the present-day environment significantly reduce crop productivity. Of them, heavy-metal stress is one of the major causes of osmotic stress that leads to oxidative stress. The present study aims to elucidate and understand the influence of nickel and cadmium chloride stress on seed germination, chlorophyll content, protein content, hydrogen peroxide production, proline accumulation, and antioxidant enzyme activity in niger. The germination rate of sterilized seeds exposed to 0, 25, 50, 75, 100, and 150 ppm of nickel and cadmium chloride was recorded 24 h after treatments. Four-week-old seedlings were also treated with heavy metals and biochemical observations were recorded on the 15th day after treatment. A direct relationship was noted between heavy metal stress and the hydrogen peroxide and proline content of niger. The extent of oxidative stress was significantly higher, as compared to the control, in all the treatments. The majority of the antioxidants exhibited a significantly negative relationship with chlorophyll and protein content of niger. Furthermore, a higher concentration of heavy metal stress results in decreased germination rate, chlorophyll content and triggers antioxidant enzyme activity. Thus, oxidative stress in niger caused by a high level of nickel and cadmium, which could result in membrane damage via the production of reactive oxygen species was compensated by the active defense mechanism via high proline accumulation and antioxidant enzyme activity.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3

Similar content being viewed by others

Data availability

The data that support the findings of this study are available from the corresponding author upon reasonable request.

References

  • Ahmad A, Siddiqi TO, Iqbal M (2011) Medicinal plants in changing environment. Capital Publishing Company, New Delhi, India (ISBN: 81/85589-14-3)

    Google Scholar 

  • Akhtar T, Zia-ur-Rehman M, Naeem A, Nawaz R, Ali S, Murtaza G, Rizwan M (2017) Photosynthesis and growth response of maize (Zea mays L.) hybrids exposed to cadmium stress. Environ Sci Pollut Res 24(6):5521–5529. https://doi.org/10.1007/s11356-016-8246-0

    Article  CAS  Google Scholar 

  • Alemayehu T (2001) The impact of uncontrolled waste disposal on surface water quality in Addis Ababa Ethiopia. SINET Ethiop J Sci 24(1):93–104. https://doi.org/10.4314/sinet.v24i1.18177

    Article  Google Scholar 

  • Alia BB, Pardha Saradhi P, Mohanty P (1993) Proline in relation to free radical production in seedlings of Brassica juncea raised under sodium chloride stress. Plant Soil 155(156):497500

    Google Scholar 

  • Anjum NA, Umar S, Iqbal M (2014) Assessment of cadmium accumulation, toxicity, and tolerance in Brassicaceae and Fabaceae plants—implications for phytoremediation. Environ Sci Pollut Res 21(17):10286–10293. https://doi.org/10.1007/s11356-014-2889-5

    Article  CAS  Google Scholar 

  • Anjum SA, Tanveer M, Hussain S, Bao M, Wang L, Khan I, Shahzad B (2015) Cadmium toxicity in Maize (Zea mays L.): consequences on antioxidative systems, reactive oxygen species and cadmium accumulation. Environ Sci Pollut Res 22(21):17022–17030. https://doi.org/10.1007/s11356-015-4882-z

    Article  CAS  Google Scholar 

  • Ansari MKA, Ahmad A, Umar S, Zia MH, Iqbal M, Owens G (2015) Genotypic variation in phytoremediation potential of Indian mustard exposed to nickel stress: A hydroponic study. Int J Phytorem 17:135–144. https://doi.org/10.1080/15226514.2013.862206

    Article  CAS  Google Scholar 

  • Aref IM, Khan PR, Khan S, El-Atta H, Ahmed AI, Iqbal M (2016) Modulation of antioxidant enzymes in Juniperus procera needles in relation to habitat environment and dieback incidence. Trees Struct Funct 30:1669–1681. https://doi.org/10.1007/s00468-016-1399-0

    Article  Google Scholar 

  • Arnon DI (1949) Copper enzymes in isolated chloroplasts Polyphenoloxidase in Beta vulgaris. Plant Physiol 24(1):1–15. https://doi.org/10.1104/2Fpp.24.1.1

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Arora M, Kiran B, Rani S, Rani A, Kaur B, Mittal N (2008) Heavy metal accumulation in vegetables irrigated with water from different sources. Food Chem 111(4):811–815. https://doi.org/10.1016/j.foodchem.2008.04.049

    Article  CAS  Google Scholar 

  • Asada K, Takahashi M (1987) Production and scavenging of active oxygens in chloroplasts. Photoinhibition 1987:227–287

    Google Scholar 

  • Ashraf M (2009) Biotechnological approach of improving plant salt tolerance using antioxidants as markers. Biotechnol Adv 27(1):84–93

    Article  CAS  PubMed  Google Scholar 

  • Azad HN, Shiva AH, Malekpour R (2011) Toxic effects of lead on growth and some biochemical and ionic parameters of sunflower (Helianthus annuus L.) seedlings. Curr Res J Biol Sci 3:398–403

    CAS  Google Scholar 

  • Bagheri R, Bashir H, Ahmad J, Iqbal M, Qureshi MI (2015) Spinach (Spinacia oleracea L.) modulates its proteome differentially in response to salinity, cadmium and their combination stress. Plant Physiol Biochem 97:235–245. https://doi.org/10.1016/j.plaphy.2015.10.012

    Article  CAS  PubMed  Google Scholar 

  • Baker AJM, Brooks R (1989) Terrestrial higher plants which hyperaccumulate metallic elements A review of their distribution, ecology and phytochemistry. Biorecovery 1(2):81–126

    CAS  Google Scholar 

  • Bashir H, Qureshi MI, Ibrahim AM, Iqbal M (2015) Chloroplast and photosystems: impact of cadmium and iron deficiency. Photosynthetica 53(3):321–335. https://doi.org/10.1007/s11099-015-0152-z

    Article  CAS  Google Scholar 

  • Bates LS, Waldren RP, Teare ID (1973) Rapid determination of free proline for water-stress studies. Plant Soil 39(1):205–207. https://doi.org/10.1007/BF00018060

    Article  CAS  Google Scholar 

  • Chakraborty U, Pradhan B (2012) Oxidative stress in five wheat varieties (Triticum aestivum L.) exposed to water stress and study of their antioxidant enzyme defense system, water stress responsive metabolites and H2O2 accumulation. Braz J Plant Physiol 24:117–130

    Article  CAS  Google Scholar 

  • Chandlee JM, Scandalios JG (1984) Analysis of variants affecting the catalase developmental program in maize scutellum. Theor Appl Genet 69(1):71–77. https://doi.org/10.1007/BF00262543

    Article  CAS  PubMed  Google Scholar 

  • DaCosta M, Huang B (2007) Changes in antioxidant enzyme activities and lipid peroxidation for bentgrass species in response to drought stress. J Am Soc Hortic Sci 132(3):319–326

    Article  CAS  Google Scholar 

  • De Maria S, Puschenreiter M, Rivelli AR (2013) Cadmium accumulation and physiological response of sunflower plants to Cd during the vegetative growing cycle. J Plant Soil Environ 59:254–261. https://doi.org/10.17221/788/2012-PSE

    Article  Google Scholar 

  • Dirbaba N, Yan X, Wu H, Colebrooke L, Wang J (2018) Occurrences and ecotoxicological risk assessment of heavy metals in surface sediments from Awash River Basin. Ethiop Water 10(5):535. https://doi.org/10.3390/w10050535

    Article  CAS  Google Scholar 

  • Dutta PC, Helmersson S, Kebedu E, Alemaw G, Appelqvist LÅ (1994) Variation in lipid composition of niger seed (Guizotia abyssinica Cass) samples collected from different regions in Ethiopia. J Am Oil Chem Soc 71(8):839–843. https://doi.org/10.1007/BF02540459

    Article  CAS  Google Scholar 

  • Gajewska E, Skłodowska M, Słaba M, Mazur J (2006) Effect of nickel on antioxidative enzyme activities, proline and chlorophyll contents in wheat shoots. Biol Plant 50(4):653–659. https://doi.org/10.1007/s10535-006-0102-5

    Article  CAS  Google Scholar 

  • Gill RA, Zhang N, Ali B, Farooq MA, Xu J, Gill MB, Mao B, Zhou W (2016) Role of exogenous salicylic acid in regulating physio-morphic and molecular changes under chromium toxicity in black-and yellow-seeded Brassica napus L. Environ Sci Pollut Res 23:20483–20496

    Article  CAS  Google Scholar 

  • Hossain Z, Mandal AKA, Datta SK, Biswas AK (2007) Development of NaCl-tolerant line in Chrysanthemum morifolium Ramat through shoot organogenesis of selected callus line. J Biotechnol 129(4):658–667

    Article  CAS  PubMed  Google Scholar 

  • Husen A, Iqbal M, Khanam N, Aref IM, Sohrab SS, Masresha G (2019) Modulation of salt-stress tolerance of Niger (Guizotia abyssinica), an oilseed plant, by application of salicylic acid. J Environ Biol 40(1):96–104

    Article  CAS  Google Scholar 

  • Iqbal M, Khudsar T (2000) Heavy metal stress and forest cover: Plant performance as affected by cadmium toxicity. In: Kohli RK, Singh HP, Vij SP, Dhir KK, Batish DR, Khurana DK (eds) Man and Forests: 85–112, DNES, IUFRO, ISTS & Punjab University. Chandigarh, India

    Google Scholar 

  • Iqbal M, Srivastava PS, Siddiqi TO (2000) Environmental hazards: plants and people. CBS Publishers, New Delhi, India (ISBN: 81-239-0644-7)

    Google Scholar 

  • Júnior CAL, Mazzafera P, Arruda MAZ (2014) A comparative ionomic approach focusing on cadmium effects in sunflowers (Helianthus annuus L.). Environ Exp Bot 107:180–186. https://doi.org/10.1016/j.envexpbot.2014.06.002

    Article  CAS  Google Scholar 

  • Júnior CAL, Oliveira SR, Mazzafera P, Arruda MAZ (2016) Expanding the information about the influence of cadmium on the metabolism of sunflowers: Evaluation of total, bioavailable, and bioaccessible content and metallobiomolecules in sunflower seeds. Environ Exp Bot 125:87–97

    Article  Google Scholar 

  • Kearsey MJ, Pooni HS (1996) The Genetical analysis of quantitative traits. Chapman and Hall, Birmingham, UK

    Book  Google Scholar 

  • Leonard SS, Harris GK, Shi X (2004) Metal-induced oxidative stress and signal transduction. Free Rad Biol Med 37:1921–1942. https://doi.org/10.1016/j.freeradbiomed.2004.09.010

    Article  CAS  PubMed  Google Scholar 

  • Lowry OH, Rosebrough NJ, Farr AL, Randall RJ (1951) Estimations of protein with the folin phenol reagent. J Biol Chem 193:262–275

    Article  Google Scholar 

  • Mahmood T, Islam KR, Muhammad S (2007) Toxic effects of heavy metals on early growth and tolerance of cereal crops. Pak J Bot 39(2):451–462

    Google Scholar 

  • Matysik J, Bhalu B, Mohanty P (2002) Molecular mechanisms of quenching of reactive oxygen species by proline under stress in plants. Curr Sci 82(5):525–532

    CAS  Google Scholar 

  • Mehindirata S, Ali ST, Mahmooduzzafar S, T.O. & Iqbal, M. (1999) Cadmium-induced changes in foliar responses of Solanum melongena L. Phytomorphology 49:295–302

    Google Scholar 

  • Mehindirata S, Mahmooduzzafar S, T.O. & Iqbal, M. (2000) Cadmium-induced changes in growth and structure of root and stem of Solanum melongena L. Phytomorphology 50:243–251

    Google Scholar 

  • Mekonnen KN, Ambushe AA, Chandravanshi BS, Redi-Abshiro M, McCrindle RI (2014) Assessment of potentially toxic elements in Swiss chard and sediments of Akaki River Ethiopia. Toxicol Environ Chem 96(10):1501–1515. https://doi.org/10.1080/02772248.2015.1025788

    Article  CAS  Google Scholar 

  • Nagella P, Hosakatte NM, Ravishankar KV, Hahn EJ, Paek KY (2008) Analysis of genetic diversity among Indian niger [Guizotia abyssinica (L. f.) Cass.] cultivars based on randomly amplified polymorphic DNA markers. Electron J Biotechnol 11(1):140–144. https://doi.org/10.4067/S0717-34582008000100014

    Article  Google Scholar 

  • Naik HNK, Devaraj RV (2016) Effect of salinity stress on antioxidant defense system of Niger (Guizotia abyssinica Cass.). Am J Plant Sci 7(6):980–990

    Article  CAS  Google Scholar 

  • Naik KH, Devaraj VR (2017) Induction of antioxidant system in niger (Guizotia abyssinica Cass.) under drought stress. Af J Agric Res 12(41):3037–3044. https://doi.org/10.5897/AJAR2017.12709

    Article  CAS  Google Scholar 

  • Pandey N, Sharma CP (2002) Effect of heavy metals Co2+, Ni2+ and Cd2+ on growth and metabolism of cabbage. Plant Sci 163:753–758. https://doi.org/10.1016/S0168-9452(02)00210-8

    Article  CAS  Google Scholar 

  • Parida BK, Chhibba IM, Nayyar VK (2003) Influence of nickel-contaminated soils on fenugreek (Trigonella corniculata L.) growth and mineral composition. Sci Hort 98:113–119. https://doi.org/10.1016/S0304-4238(02)00208-X

    Article  CAS  Google Scholar 

  • Patil PP, Ghane SG, Barmukh RB, Teixeira da Silva JA, Nikam TD (2010) Differential response of niger (Guizotia abyssinica Cass.) cultivars to salinity stress in relation to seed germination, oxidative stress, osmotic adjustment and antioxidant enzyme activities. Plant Stress 4(1):56–63

    Google Scholar 

  • Prasad, M. N., & Strzalka, K. (Eds.). (2013). Physiology and biochemistry of metal toxicity and tolerance in plants. Springer Science & Business Media.

  • Rahman S, Iqbal M, Husen A (2023) Medicinal Plants and Abiotic Stress: An Overview. Their Response to Abiotic Stress, Medicinal Plants, pp 1–34

    Google Scholar 

  • Ramadan MF, Morsel JT (2002) Proximate neutral lipid composition of niger. Czech J Food Sci 20:98–104

    Article  CAS  Google Scholar 

  • Recatalá L, Sánchez J, Arbelo C, Sacristán D (2010) Testing the validity of a Cd soil quality standard in representative Mediterranean agricultural soils under an accumulator crop. Sci Total Environ 409(1):9–18. https://doi.org/10.1016/j.scitotenv.2010.09.021

    Article  CAS  PubMed  ADS  Google Scholar 

  • Rivelli AR, Puschenreiter M, De Maria S (2014) Assessment of cadmium uptake and nutrient content in sunflower plants grown under Cd stress. Plant Soil Environ 60(2):80–86. https://doi.org/10.17221/520/2013-PSE

    Article  CAS  Google Scholar 

  • Roy M, McDonald LM (2015) Metal uptake in plants and health risk assessments in metal-contaminated smelter soils. Land Degrad Dev 26(8):785–792. https://doi.org/10.1002/ldr.2237

    Article  Google Scholar 

  • Rylott EL, Bruce NC (2022) Plants to mine metals and remediate land: Engineered plants can clean up pollution and recover technology-critical metals. Science 377(6613):1380–1381. https://doi.org/10.1126/science.abn6337

    Article  CAS  PubMed  ADS  Google Scholar 

  • Sairam RV, Prakash CS (2005) Can agricultural biotechnology contributes to global food security. In Vitro Cell Dev Biol Plant 41:424–430. https://doi.org/10.1079/IVP2005663

    Article  Google Scholar 

  • Saleem M, Asghar HN, Khan MY, Zahir ZA (2015) Gibberellic acid in combination with pressmud enhances the growth of sunflower and stabilizes chromium (VI)-contaminated soil. Environ Sci Pollut Res 22(14):10610–10617. https://doi.org/10.1007/s11356-015-4275-3

    Article  CAS  Google Scholar 

  • Sarma H (2011) Metal hyperaccumulation in plants: a review focusing on phytoremediation technology. J Environ Sci Technol 4(2):118–138

    Article  MathSciNet  CAS  Google Scholar 

  • SAS, I. (2002). SAS software. SAS Institute Inc 9, NC, USA.

  • Seregin IV, Kozhevnikova AD (2006) Physiological role of nickel and its toxic effects on higher plants. Russ J Plant Physiol 53(2):257–277. https://doi.org/10.1134/S1021443706020178

    Article  CAS  Google Scholar 

  • Sinha VB, Grover A, Singh S, Pande V, Ahmed Z (2014) Overexpression of Ran gene from Lepidium latifolium L. (LlaRan) renders transgenic tobacco plants hypersensitive to cold stress. Mol Biol Rep 41(9):5989–5996. https://doi.org/10.1007/s11033-014-3476-z

    Article  CAS  PubMed  Google Scholar 

  • Sinha VB, Grover A, Yadav PV, Pande V (2018) Salt and osmotic stress response of tobacco plants overexpressing Lepidium latifolium L. Ran GTPase gene. Ind J Plant Physiol 23(3):494–498. https://doi.org/10.1007/s40502-018-0396-2

    Article  CAS  Google Scholar 

  • Sofo A, Scopa A, Nuzzaci M, Vitti A (2015) Ascorbate peroxidase and catalase activities and their genetic regulation in plants subjected to drought and salinity stresses. Int J Mol Sci 16(6):13561–13578. https://doi.org/10.3390/ijms160613561

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Umar, S., Moinuddin, I. M., & Iqbal, M. (2005). Heavy metal: availability, accumulation and toxicity in plants. Physiology of abiotic stress in plants. Agrobios (India), Jodhpur, 325–348.

  • Velikova V, Yordanov I, Edreva A (2000) Oxidative stress and some antioxidant systems in acid rain-treated bean plants: protective role of exogenous polyamines. Plant Sci 151(1):59–66. https://doi.org/10.1016/S0168-9452(99)00197-1

    Article  CAS  Google Scholar 

  • Vincevica-Gaile Z, Klavins M (2012) Transfer of metals in food chain: An example with copper and lettuce. Environ Clim Technol 10(1):21–24

    Google Scholar 

  • Wang YC, Lee CM, Lee LC, Tung LC, Hsieh-Li HM, Lee-Chen GJ, Su MT (2011) Mitochondrial dysfunction and oxidative stress contribute to the pathogenesis of spinocerebellar ataxia type 12 (SCA12). J Biol Chem 286(24):21742–21754

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Wondimu T, Alamerew S, Ayana A, Garedew W (2014) Variablitiy and association of quantitative traits in Achote (Coccinia abyssinica (Lam) Cogn) in Ethiopia. Int J Plant Breed Genet 8(1):1–12

    Article  Google Scholar 

  • Yabe J, Ishizuka M, Umemura T (2010) Current levels of heavy metal pollution in Africa. J Vet Med Sci 72(10):1257–1263. https://doi.org/10.1292/jvms.10-0058

    Article  CAS  PubMed  Google Scholar 

  • Yunus M, Iqbal M (1996) Plant Response to Air Pollution. John Wiley & Sons, Chichester, U.K.

    Google Scholar 

Download references

Acknowledgements

The first author is highly indebted to the Ministry of Science and Higher Education (MoSHE-Ethiopia) for sponsorship and permission to join the graduate school and the Ethiopian embassy in New Delhi, India is warmly acknowledged. We are grateful to the Biotechnology Department of Sharda University, Greater Noida, for continuous technical help and support.

Funding

This work was funded and supported by the Ministry of Science and Higher Education (MoSHE-Ethiopia). The author, TAA has received financing from the MoSHE-Ethiopia for academic and scientific endeavors. We attest that neither the writing of the manuscript nor its publication received any kind of financial or other support.

Author information

Authors and Affiliations

Authors

Contributions

“Both authors contributed to the concept and design of the study, material preparation, data collection, and analysis. The first draft of the manuscript written by AAT. Final manuscript was examined, discussed and approved by both authors.”

Corresponding author

Correspondence to Aderajew Adgo Tesema.

Ethics declarations

Conflict of interest

The authors declare none.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Tesema, A.A., Mekonen, D.A. Responses of Niger [Guizotia abyssinica (L.f.) Cass.] to cadmium and nickel stress. Vegetos 37, 239–249 (2024). https://doi.org/10.1007/s42535-023-00591-8

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s42535-023-00591-8

Keywords

Navigation