Next Article in Journal
Chinese Technical Guideline for Deriving Water Quality Criteria for Protection of Freshwater Organisms
Previous Article in Journal
Neurobehavioral Effects of Low-Dose Chronic Exposure to Insecticides: A Review
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Levels of Heavy Metals in Grapevine Soil and Leaf Samples in Response to Seasonal Change and Farming Practice in the Cape Winelands

Department of Horticultural Sciences, Faculty of Applied Sciences, Cape Peninsula University of Technology, P.O. Box 1906, Bellville 7535, South Africa
*
Author to whom correspondence should be addressed.
Toxics 2023, 11(2), 193; https://doi.org/10.3390/toxics11020193
Submission received: 12 January 2023 / Revised: 16 February 2023 / Accepted: 17 February 2023 / Published: 19 February 2023
(This article belongs to the Section Metals and Radioactive Substances)

Abstract

:
Heavy metal toxicity is a major threat to the health of both humans and ecosystems. Toxic levels of heavy metals in food crops, such as grapes, can have devastating effects on plant health and the market value of the produce. Two important factors that may influence the prevalence of heavy metals in grapevines are seasonal change and farming practices. The objectives of this study were (i) to conduct a detailed pioneer screening of heavy metal levels in soils and grapevine leaf tissues in selected wine farms and (ii) to study the influence of season and farming on heavy metal levels in soils and grapevine leaf tissues. Soil and grapevine leaf samples were collected from demarcated areas in selected vineyards in the Cape Winelands region of South Africa. The sampling was conducted in winter and summer from the same sites. The soil and leaf samples were analysed using inductively coupled plasma mass spectrometry (ICP-MS) techniques. The pooled data from the farms practising conventional or organic farming showed that seasonal variation had no significant effect (DF = 1, 22; p > 0.05) on the heavy metal contents in the soil. When the soil data from the winter and summer months were compared separately or pooled, the influence of agricultural practice was well-pronounced in As (DF = 1, 22, or 46; p < 0.05) and Cu (DF = 1, 22, or 46; p <0.05). The agricultural practice greatly influenced (DF = 1, 22; p< 0.05) Cu, As, Cr, and Hg uptake, with little effect on Ni, Co, Cd, and Hg leaf contents. Generally, the heavy metals studied (Cr, Co, Ni, Zn, As, Cd, Hg, and Pb) were substantially below the maximum permitted levels in plant and soil samples, per the recommendations of the WHO and Er indices, respectively. However, moderate contamination of the soils was recorded for Cr, Ni, Zn, and Pb. Remarkably, the Cu levels in the organic vineyard soils were significantly higher than in the conventional vineyards. Furthermore, based on the Igeo index, Cu occurred at moderate to heavy contamination levels.

1. Introduction

Natural and anthropogenic activities are responsible for the build-up of dangerous levels of heavy metals. Many factors affect the prevalence of heavy metals in grapevines [1]. According to Alagic et al. [2], one of the primary sources of heavy metals, such as lead, chromium, arsenic, zinc, cadmium, copper, and nickel, in soils is agricultural practices. The emissions of heavy metals from rapidly expanding industrial areas, mining tails, leaded gasoline and paint, fertilizers, animal manure, wastewater irrigation, and pesticides may contaminate the soil [3,4,5,6], leading to many environmental problems. Heavy metal toxicity is a major threat to the health of both humans and ecosystems; their accumulation in food crops, including grapes, can have devastating effects on plant health and the market value of the produce [2,7]. Briffa et al. [8] reviewed the toxicological effects of heavy metals on humans, including oxidative stress, liver damage, fever, pneumonia, asthma, brain damage, death, and DNA damage.
Soils contaminated with heavy metals have become one of the major environmental problems around the world [9]. Industrial expansion, mine tailing, the combustion of fossil fuels, the spillage of petrochemicals, the disposal of high metal waste (e.g., batteries and metal scraps), atmospheric deposition, and agricultural practices may be the sources of heavy metals [5,6,10,11]. The agroecosystems are exposed to pollutants in fertilizers, biosolids, pesticides, and wastewater. Some farmers mix soil and sewage sludge, which may contain heavy metals [8]. A recent study on the level of atmospheric concentrations of commonly used pesticides successfully quantified carbaryl, chlorpyrifos, terbuthylazine, s-metolachlor, diazinon, tebuconazole, atrazine, simazine, malathion, and metazachlor in three agricultural regions (Grabouw, Hex River Valley and Piketberg) of the Western Cape, South Africa, and the concentrations were generally higher in the summer and during the spraying season [12]. Commonly used fungicides in vineyards, such as the Bordeaux mixture (Ca(OH)2 + CuSO4) and Mancozeb (C4H6MnN2S4)-based products, are important sources of Cu and Zn contamination, respectively. Phosphate fertilizers often contain Cd, Hg, and Pb impurities [13]. Agricultural soils may accumulate high levels of heavy metals, which has dire consequences for the quality and health of plants [14]. While it is helpful to regularly monitor the levels of heavy metals in agricultural soils, it is even more crucial to study the drivers of heavy metals in soils to achieve efficient and durable management of heavy metals.
Mondol et al. [10] determined that environmental changes contribute to the differences in heavy metal uptake from soils. They also concluded that trace elements were higher during the dry season compared to the wet season [15]. Ullah et al. [16] suggest that this might result from lower pollution levels during the wet season as heavy rainfalls flush pollution into canals. A study by Oluyemi et al. [17] at a landfill in Nigeria showed that heavy metals were higher in the dry season than in the wet season. These claims are backed up by Osobamiro and Adewuyi [18], who studied three farm settlements in Ogun-State Southwest, Nigeria and found that heavy metal concentrations were higher in the dry season than during the wet season. The study suggests that high precipitation, leaching, erosion, and plant uptake may account for the reduction in heavy metal levels in the rainy season observed in the results of heavy metals from the three farm settlements.
Land-use patterns, including agricultural practices, profoundly influence soil quality, directly impacting heavy metal accumulation in the soil [19,20,21]. Many wine producers have adopted three farming practices to maximise production: conventional farming, polyculture, and organic farming [22]. In organic wine farming, no pesticides are used. It is a holistic farming system that promotes healthy and productive biodiversity while improving soil health [23]. Polyculture farming is the cultivation of different crops in the same space at the same time [24]. This practice slows down the soil degradation processes while improving soil fertility. Conventional farming involves using synthetic chemical fertilizers, pesticides, herbicides, and other genetically modified organisms in crop production. Conventional farming is one of the primary sources of heavy metals entering the food chain and posing a risk to environmental health [25].
The Cape Winelands is among the most important agriculture-producing regions in South Africa. It contributes approximately ZAR 26,223 million to the annual GDP of South Africa [26]. It is a world-renowned wine-producing region; hence, it is of utmost importance to study the heavy metal occurrence in grapevines of the Cape Winelands. It is essential to understand how ecological factors, especially the season and farming practices, influence the prevalence and accumulation of heavy metals in grapevines. The Cape Winelands region is an excellent model for studying the ecological dynamics of heavy metals. The Cape Winelands include Stellenbosch, Franschhoek, Constantia, Paarl, and Worcester.
The objectives of this study were (i) to conduct a detailed pioneer screening of heavy metal levels in soils and grapevine leaf tissues in selected wine farms and (ii) to study the influence of season and farming on heavy metal levels in soils and grapevine leaf tissues. This study revealed that farming practices influenced heavy metal contamination, especially Cu—its levels in organic vineyard soils were significantly higher than in conventional vineyards. However, generally, eight of the nine heavy metals studied (Cr, Co, Ni, Zn, As, Cd, Hg, and Pb) were substantially below the maximum permitted levels in plant and soil samples.

2. Materials and Methods

2.1. Experimental Design

Soil samples and grapevine leaves were collected from demarcated areas in selected vineyards in the Cape Winelands region of South Africa. The sampling was conducted in the winter and summer from the same sites. A deliberate effort was made to ensure that vineyards with different cultivation practices (organic, conventional, and mixed cropping) were selected for this study.

2.2. Site Characteristics

Six vineyards (sites) located in different regions of the Western Cape were selected for this study: Stellenbosch (A), Eikenbosch (B), Franschhoek (C), Wolseley (D), Robertson (E), and Piketberg (F) (Figure 1). Soils were obtained from vineyards with different cultivation approaches: organic (semi to 100% organic), conventional, and polyculture approaches.

2.3. Soil and Leaf Sampling

At each vineyard, four sampling points 200 m apart were randomly selected, and the sampling points were in the middle of the vineyard’s location for the points. From each sampling point, one kilogram of soil samples was collected after removing surface debris using a garden spade at a depth of 15–20 cm. The soil samples were placed in separate paper bags. Fresh leaf material (100 g) from randomly selected plants at sampling points that were 200 m apart was placed in a paper bag. A total of 48 soil and 48 leaf samples were collected from 6 vineyards in the Western Cape, South Africa. The sampling sites were geo-referenced (Table 1). The collection of samples from the same sampling points was carried out in two seasons (summer and winter). The soil and the leaf samples were analysed at the ICP-MS & XRF Laboratory, Stellenbosch University. Inductively coupled plasma mass spectrometry (ICP-MS) is a powerful technique for elemental trace analysis and is recommended for ultra-trace metals due to its increased sensitivity [27,28,29,30].

2.4. Sample Preparation and Analysis

The samples were air-dried and sieved (2 mm sieve) before testing. The concentrations (units: µg kg−1 or mg kg−1) of the major, minor, and trace elements of (ICP-AES and ICP-MS) Cr, Co, Ni, Cu, Zn, As, Cd, Pb, and Hg combined were determined as described by Berg et al. [31] with slight modifications. Portions of about 0.5 g (dry weight of plant samples) and 0.1 g (soil samples) were digested with 8 mL nitric oxide at 150 °C for 6–8 h. After cooling to room temperature, the samples were filtered, and demineralized water was added to a total volume of 50 mL. Calibration standards for the ICP-MS analysis were prepared from multi-element stock solutions (Spec-troscan, Teknolab As, N-1440 Drsbak). The ICP-MS instrument was calibrated with standard solutions of 50 and 250 ng mL−1. For the major elements, an additional standard of 1000 ng mL−1 was used. All the calibration standards and blanks were matched with the nitric acid concentration of the samples. The certified reference material 1573a (tomato leaves) was used to validate the analytical methods for determining the botanical materials’ major, minor, and trace elements. Accuracy and precision for the soil samples were achieved by using internal quality control standards (WQB-1). The result of the digested solution in mg/L obtained from the ICP was multiplied by the dilution factor in the digestion process using the following formula: mg kg−1 = mg L−1 × [(Final volume mL)/(weight of sample g)]. Analyses were performed on a Plasma Quad I ICP- MS instrument. The ICP-MS was equipped with a peristaltic pump (Ismatec Reglo 100) and a Meinhard nebulizer. The permissible limits for heavy metals in edible plants that were published by the World Health Organization [32,33] and the Food and Agriculture Organization of the United Nations (FAO) were used as standards for the comparison and classification of heavy metal levels into three categories (low, optimum, and high); the levels for the individual heavy metals are as follows: 0.5 µg g−1 arsenic (As), 0.02 µg g−1 cadmium (Cd), 1.3 µg g−1 chromium (Cr), 0.01 µg g−1 cobalt (Co), 10 µg g−1 copper (Cu), and 0.03 µg g−1 mercury (Hg).

2.5. Contamination and Ecological Risk Assessment

Contamination indices were used to evaluate the influence of anthropogenic activities on the accumulation of heavy metals in the farms (geo-accumulation index [Igeo]) and the ecological risks associated with heavy metal levels (contamination factor [Cf] and ecological risks [Er]). The following formula was used [34,35]:
Igeo = log2[Cn/1.5Bn]
where Cn is the measured concentration of metal in the soil and
Bn is the background value of a metal.
The background values (mg kg−1) for Cr (5.82), Cu (2.98), Cd (0.62), Zn (12), Hg (0.15), and Pb (2.99) were from South Africa [36], the value for As (20) was from the Netherlands [37], and the value for Co (18) was from China [38]. To compensate for possible variations in the background values and minor anthropogenic influences, a factor of 1.5 was used [34]. The degree of metal contamination in soils as defined by Muller [39], with seven soil quality levels ranging from 1 (uncontaminated) to 6 (extremely contaminated), was used (Table 2).
The ecological risk index of each heavy metal was determined using the method developed by Hakanson [40] (Table 2). The following equations were used [34,40]:
Cf = Cn/Bn
Er = Tr × Cf
where Tr is the toxic response factor for each given pollutant,
Cf is the contamination factor for each heavy metal,
Cn is the measured level of each heavy metal in the sediment,
Bn is the background level of each heavy metal, and
Er is the ecological risk index.
The toxic response factors [40] are: Cr (2), Co (5), Cu (5), Cd (30), Ni (5), Zn (1), As (10), Hg (40), and Pb (5).

2.6. Statistical Analysis

Heavy metal concentrations in the soils and leaf tissues obtained during the winter and summer months from each farm were compared using a one-way analysis of variance (ANOVA). The heavy metal concentrations in the soils and leaf tissues obtained from farms with different farming practices were compared using a one-way analysis of variance (ANOVA). SPSS was used to process and analyse the data.

3. Results

3.1. Heavy Metals in Soil Samples

3.1.1. Levels of Heavy Metals in Soil Samples

Three of the farm sites (Sites A, B, and E) that were sampled practise conventional farming, and the other three farms practise organic farming (Sites D, E, and F). Meanwhile, four farm sites had polycultures, three of which were conventional farms. The average concentrations of heavy metals in the soil samples from six study sites in the Cape Winelands are given in Table 3. The mean concentration of heavy metal in the soil was highest for chromium (58.738 ± 2.988 mg kg−1), and the lowest was observed for Hg (0.015 ± 0.0002 mg kg−1) at site F. The mean concentrations of Cd and Hg in the soil samples are generally low across all the sites.

3.1.2. Effect of Seasonal Variation on Heavy Metal Deposits in the Soil

The seasonal variations in the distribution of some of the selected heavy metals in soil samples from the Cape Winelands are shown in Figure 2. The levels of Cd and Hg in all the vineyards are generally minimal. Site E recorded the lowest levels of heavy metals in the soil samples analysed. The heavy metal contents of the soil did not vary significantly (DF = 1, 6; p > 0.05) between the winter and summer for all the study sites. Furthermore, when the data from the farms that practice conventional or organic farming were pooled, the seasonal variation had no significant effect (DF = 1, 22; p > 0.05) on the heavy metal contents in the soil.

3.1.3. Effect of Agricultural Practice on Heavy Metal Deposits in the Soil

The impact of agricultural practices (conventional; Sites A, B, and E) and organic practices (sites C, D and F) on heavy metal deposits in the soil is shown in Figure 3. When the soil data from the winter and summer months were compared separately or pooled, the influence of agricultural practice was well-pronounced in As (DF = 1, 22, or 46; p < 0.05) and Cu (DF = 1, 22, or 46; p < 0.05). There were no significant differences in the overall heavy metal deposits in the soil between organic and conventional agricultural practices in both the summer (DF = 1, 16; F = 0.09; p = 0.76) and winter (DF = 1, 16; F = 0.02; F = 0.76). The ecological risk index based on the contamination factors and background levels showed low ecological risk in the vineyards for eight of the nine heavy metals assessed—the Er was below 40, corresponding to low risk (Table 2 and Table 4). Meanwhile, the geo-accumulation index (Er ˂ 0) indicated a low level of soil contamination for Co, As, Cd, and Hg (Table 4), and neither season nor farming practice had a significant effect on soil contamination. However, moderate contamination of the soils was recorded for Cr, Ni, Zn, and Pb (Table 4). The Cu Igeo (2.329 ± 0.674 − 2.669 ± 0.597) and Er (45.068 ± 15.234 − 55.248 ± 17.883) values in the organic farms were relatively higher than the Cu Igeo (1.512 ± 0.297 − 1.661 ± 0.303) and Er (22.249 ± 4.043 − 24.820 ± 5.381) in the conventional farms, suggesting moderate to heavy levels of geochemical contamination and moderate ecological risk (Table 4).

3.2. Heavy Metals in Plant Samples

3.2.1. Levels of Heavy Metals in Plant Samples

The average concentrations of heavy metals in the plant samples from the six study sites in the Cape Winelands are provided in Table 5. The highest mean concentration of heavy metals in the plant samples was observed for Cu (87.098 ± 19.481 mg/kg) at site D, and the lowest was observed for Cd (0.002 ± 0.0004 mg/kg), also at site D. There were significant (DF = 5, 18; p < 0.05) variations in the heavy metal contents (Cr, Cu, As, Cd, Hg, and Pb) in the plant leaves among the sites.

3.2.2. Effect of Agricultural Practice on Heavy Metal Uptake by Plant Samples

Leaf samples from eight cultivars of grapevine plants occurring in the farms were analysed. To determine the impact of agricultural practices on heavy metals, pooled data from conventional (A, B and E) and organic (sites C, D and F) farming sites were statistically compared (Figure 4 and Table 5). The agricultural practice significantly influenced (DF = 1, 22; p < 0.05) Cu, As, Cr, and Hg uptake, with little effect on Ni, Co, Cd, and Hg. Generally, the heavy metals were substantially below the maximum permitted levels in plants.

4. Discussion

A key finding of this study is that the heavy metal contents in soils and grape leaves are below the maximum allowed concentrations of heavy metals in the leaf samples, based on the recommendations of the WHO [33]. Furthermore, the heavy metal concentrations in the soil for eight of the nine heavy metals posed low ecological risk based on the classification of ecological risk heavy metal pollution (40). This is good news for wine consumers and the wine industry in South Africa as the Cape Winelands is the largest wine-producing region on the African continent [41,42]. In addition, the seasonal change did not significantly influence variations in the heavy metals. However, farming practices influenced the accumulations of As and Cu, suggesting that pesticide application is a more important factor influencing heavy metal contents in the Cape Winelands. Cu contamination levels in organic farm soils had higher Igeo values (2.3–2.7), which corresponded to moderately to heavily contaminated soils compared with those in conventional farms. In addition to the over-dependence on agrochemicals, rapid industrialization and urbanization contribute significantly to heavy metal contamination through the high use of metal, leaded gasoline, paint, and petrochemical waste disposal and atmospheric deposition [43,44].
Cu and As varied significantly between the farms that employed organic and conventional farming practices. These two elements are contained in some well-known pesticides used in the cultivation of grapevines [45]. The levels of As were higher in the farms that practice conventional farming. This was expected because many insecticides used to control pests in grapevines have arsenic compounds. The application of foliar fungicides in vineyards and orchards can increase the soil concentration of heavy metals, such as copper (Cu) and zinc (Zn), up to the toxicity threshold for fruit trees and cover crops [13]. However, remarkably, the Cu concentrations in the organic vineyards were higher than in the conventional vineyards in the current study. The Cu Igeo and Er values in the organic farms were higher relative to the conventional farms and corresponded to moderate to heavy contamination and moderate ecological risk, respectively. Vannini et al. [35] also reported similar findings in agricultural soils of the Valdichiana area, Tuscany, Italy; the Cf and Igeo indices for Cu were higher than for the other heavy metals, and they attributed those findings to the increased use of Cu-based products. The accumulation of Cu in soil and plant tissues could be influenced by many factors other than pesticides, such as the mineralization of organic matter, microorganisms, and minerals in the rock. It is worth noting that organic amendments such as compost and manure, which are widely used in organic farming, bind with Cu more tightly than other micronutrients [46]. Previous studies have investigated the levels of heavy metals in grapefruits in Spain and China [47,48].
This study showed that the season did not affect the heavy metal levels. The results from previous studies suggest that heavy metal concentrations in soils, rivers, and leaves vary with the season; generally, higher heavy metal concentrations are more prevalent in the dry season than in the rainy season [17,49]. In a study by Okoro et al. [50] on the concentrations of heavy metals in seawater from Cape Town harbour, South Africa, the authors reported that Sn and Cd occurred at higher levels in the summer, while Hg, Pb, and As were more prevalent in the winter. It is worth noting that the Cape Peninsula region has a Mediterranean climate, characterised by hot and dry summers and cold and rainy winters [51].
Although this study only investigated the concentrations of heavy metals in vineyard soils and grapevine leaves, the results are very relevant because the use of Cu- and Zn-based pesticides in vineyards can increase the levels of these metals in wines and grapes. In the current study, the geochemical analysis showed that in addition to Cu, the heavy metals Ni, Zn, Cr, and Pb showed moderate soil contamination. In a study conducted in Sri Lanka, Prabaga et al. [11] found that most of the accumulated metals are mainly concentrated in the leaves of the grape tree than in the fruit. A survey carried out on the west coast of the Oristano province (Sardinia, Italy) revealed that cobalt occurred at a greater level than the legal limit in one vineyard, and the long-term use of copper-based fungicides in vineyards does not represent a cause of concern for the studied areas [52]. A study that investigated cadmium, copper, lead, and zinc concentrations in wines and alcohol-containing drinks from Italy, Bulgaria, and Poland revealed that these metals occurred in low concentrations; however, the Cu and Zn concentrations were highest in the Italian wines (Cu = 0.13 ± 0.05 mg L−1; Zn = 0.83 ± 0.56 mg L−1) and lowest in the Polish products (Cu = 0.04 ± 0.001 mg L−1; Zn = 0.18 ± 0.16 mg L−1) [53].

5. Conclusions

Four (Co, As, Cd, and Hg) of the nine heavy metals occurred at very low concentrations in the vineyard soils and posed low contamination and ecological risks. However, moderate contamination of the soils was recorded for Cr, Ni, Zn, and Pb. Notably, the Cu levels in the organic vineyard soils were significantly higher than in the conventional vineyards, which is surprising and requires further investigation because Cu-based pesticides are generally not used in organic farming. The season had no significant influence on heavy metal contamination. This study provides comprehensive baseline data on heavy metals in vineyard soils and grapevine leaves in the Cape Winelands. The findings of this study can be applied when adopting farming practices that promote a reduction in metals and also highlight the need for continuous monitoring of toxic metals, even in organic farming, for healthier agroecosystems.

Author Contributions

Conceptualization, A.M., F.N., and L.K.; formal analysis, A.M., E.A.A., and F.N.; investigation, A.M.; resources, F.N. and L.K.; data curation, F.N. and E.A.A.; writing—original draft preparation, A.M.; writing—review and editing, F.N. and E.A.A.; visualization, E.A.A.; supervision, F.N., L.K., and E.A.A.; project administration, F.N. and L.K.; funding acquisition, F.N. and L.K. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by Cape Peninsula University of Technology, grant number URF R166. The APC was funded by CPUT.

Data Availability Statement

The data presented in this study will be openly available in Figshare at DOI: 10.25381/cput.21821703.

Acknowledgments

The authors thank CPUT for funding this project. Terence Mabela, a horticultural technician at the Department of Horticultural Sciences, CPUT, assisted with the sample collection.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Alagić, S.Č.; Tošić, S.B.; Dimitrijević, M.D.; Antonijević, M.M.; Nujkić, M.M. Assessment of the quality of polluted areas based on the content of heavy metals in different organs of the grapevine (Vitis vinifera) cv Tamjanika. Environ. Sci. Pollut. Res. 2015, 22, 7155–7175. [Google Scholar] [CrossRef]
  2. Alagić, S.Č.; Tošić, S.B.; Dimitrijević, M.D.; Petrović, J.V.; Medić, D.V. The Characterization of Heavy Metals in the Grapevine (Vitis vinifera) Cultivar Rkatsiteli and Wild Blackberry (Rubus fruticosus) from East Serbia by ICP-OES and BAFs. Commun. Soil Sci. Plant Anal. 2016, 47, 2034–2045. [Google Scholar] [CrossRef]
  3. Wuana, R.A.; Okieimen, F.E. Heavy metals in contaminated soils: A review of sources, chemistry, risks and best available strategies for remediation. Int. Sch. Res. Not. 2011, 2011, 402647. [Google Scholar] [CrossRef] [Green Version]
  4. Mahar, A.; Wang, P.; Ali, A.; Awasthi, M.K.; Lahori, A.H.; Wang, Q.; Li, R.; Zhang, Z. Challenges and opportunities in the phytoremediation of heavy metals contaminated soils: A review. Ecotoxicol. Environ. Saf. 2016, 126, 111–121. [Google Scholar] [CrossRef]
  5. Ceniceros-Gómez, A.E.; Macías-Macías, K.Y.; de la Cruz-Moreno, J.E.; Gutiérrez-Ruiz, M.E.; Martínez-Jardines, L.G. Characterization of mining tailings in México for the possible recovery of strategic elements. J. S. Am. Earth Sci. 2018, 88, 72–79. [Google Scholar] [CrossRef]
  6. Wang, L.; Ji, B.; Hu, Y.; Liu, R.; Sun, W. A review on in situ phytoremediation of mine tailings. Chemosphere 2017, 184, 594–600. [Google Scholar] [CrossRef]
  7. Onakpa, M.M.; Njan, A.A.; Kalu, O.C. A review of heavy metal contamination of food crops in Nigeria. Ann. Glob. Health 2018, 84, 488. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  8. Briffa, J.; Sinagra, E.; Blundell, R. Heavy metal pollution in the environment and their toxicological effects on humans. Heliyon 2020, 6, e04691. [Google Scholar] [CrossRef]
  9. Li, C.; Zhou, K.; Qin, W.; Tian, C.; Qi, M.; Yan, X.; Han, W. A Review on Heavy Metals Contamination in Soil: Effects, Sources, and Remediation Techniques. Soil Sediment Contam. Int. J. 2019, 28, 380–394. [Google Scholar] [CrossRef]
  10. Bora, F.-D.; Bunea, C.-I.; Rusu, T.; Pop, N. Vertical distribution and analysis of micro-, macroelements and heavy metals in the system soil-grapevine-wine in vineyard from North-West Romania. Chem. Cent. J. 2015, 9, 19. [Google Scholar] [CrossRef] [Green Version]
  11. Prabagar, S.; Dharmadasa, R.M.; Lintha, A.; Thuraisingam, S.; Prabagar, J. Accumulation of heavy metals in grape fruit, leaves, soil and water: A study of influential factors and evaluating ecological risks in Jaffna, Sri Lanka. Environ. Sustain. Indic. 2021, 12, 100147. [Google Scholar] [CrossRef]
  12. Fernandes Veludo, A. Measurement and Analyses of 25 CUPs in the Atmosphere in Three Agricultural Regions of the Western Cape, South Africa. Master’s Thesis, Utrecht University, Utrecht, The Netherlands, 2021. [Google Scholar]
  13. Brunetto, G.; Ferreira, P.A.A.; Melo, G.W.; Ceretta, C.A.; Toselli, M. Heavy metals in vineyards and orchard soils. Rev. Bras. Frutic. 2017, 39, e263. [Google Scholar] [CrossRef] [Green Version]
  14. Liang, Q.; Xue, Z.-J.; Wang, F.; Sun, Z.-M.; Yang, Z.-X.; Liu, S.-Q. Contamination and health risks from heavy metals in cultivated soil in Zhangjiakou City of Hebei Province, China. Environ. Monit. Assess. 2015, 187, 754. [Google Scholar] [CrossRef]
  15. Mondol, M.; Chamon, A.; Faiz, B.; Elahi, S. Seasonal variation of heavy metal concentrations in Water and plant samples around Tejgaon industrial Area of Bangladesh. J. Bangladesh Acad. Sci. 2011, 35, 19–41. [Google Scholar] [CrossRef] [Green Version]
  16. Ullah, S.; Gerzabek, M.; Mondol, M.; Rashid, M.; Islam, M. Heavy metal pollution of soils and water and their transfer into plants in Bangladesh. In Proceedings of the Extended Abstracts: 5th International Conference on the Biogeochemistry of Trace Elements, Vienna, Austria, 11–15 July 1999; pp. 260–261. [Google Scholar]
  17. Oluyemi, E.; Feuyit, G.; Oyekunle, J.; Ogunfowokan, A. Seasonal variations in heavy metal concentrations in soil and some selected crops at a landfill in Nigeria. Afr. J. Environ. Sci. Technol. 2008, 2, 089–096. Available online: http://academicjournals.org/AJest (accessed on 1 December 2020).
  18. Osobamiro, M.T.; Adewuyi, G.O. Levels of heavy metals in the soil: Effects of season, agronomic practice and soil geology. J. Agric. Chem. Environ. 2015, 4, 109–117. [Google Scholar] [CrossRef] [Green Version]
  19. Fu, B.; Chen, L.; Ma, K.; Zhou, H.; Wang, J. The relationships between land use and soil conditions in the hilly area of the loess plateau in northern Shaanxi, China. CATENA 2000, 39, 69–78. [Google Scholar] [CrossRef]
  20. Fu, B.J.; Guo, X.D.; Chen, L.D.; Ma, K.M.; Li, J.R. Soil nutrient changes due to land use changes in Northern China: A case study in Zunhua County, Hebei Province. Soil Use Manag. 2001, 17, 294–296. [Google Scholar] [CrossRef]
  21. Raiesi, F. A minimum data set and soil quality index to quantify the effect of land use conversion on soil quality and degradation in native rangelands of upland arid and semiarid regions. Ecol. Indic. 2017, 75, 307–320. [Google Scholar] [CrossRef]
  22. Forbes, S.L.; Cohen, D.A.; Cullen, R.; Wratten, S.D.; Fountain, J. Consumer attitudes regarding environmentally sustainable wine: An exploratory study of the New Zealand marketplace. J. Clean. Prod. 2009, 17, 1195–1199. [Google Scholar] [CrossRef] [Green Version]
  23. Seufert, V.; Ramankutty, N.; Mayerhofer, T. What is this thing called organic?—How organic farming is codified in regulations. Food Policy 2017, 68, 10–20. [Google Scholar] [CrossRef] [Green Version]
  24. Adamczewska-Sowińska, K.; Sowiński, J. Polyculture Management: A Crucial System for Sustainable Agriculture Development. In Soil Health Restoration and Management; Meena, R.S., Ed.; Springer Singapore: Singapore, 2020; pp. 279–319. [Google Scholar]
  25. Shennan, C.; Krupnik, T.J.; Baird, G.; Cohen, H.; Forbush, K.; Lovell, R.J.; Olimpi, E.M. Organic and Conventional Agriculture: A Useful Framing? Annu. Rev. Environ. Resour. 2017, 42, 317–346. [Google Scholar] [CrossRef]
  26. CWD. Cape Winelands District Annual Report 2020/21; CWD: Cape Town, South Africa, 2021; p. 180.
  27. Ammann, A.A. Inductively coupled plasma mass spectrometry (ICP MS): A versatile tool. J. Mass Spectrom. 2007, 42, 419–427. [Google Scholar] [CrossRef] [PubMed]
  28. Pérez-Álvarez, E.P.; Garcia, R.; Barrulas, P.; Dias, C.; Cabrita, M.J.; Garde-Cerdán, T. Classification of wines according to several factors by ICP-MS multi-element analysis. Food Chem. 2019, 270, 273–280. [Google Scholar] [CrossRef] [PubMed]
  29. Voica, C.; Dehelean, A.; Iordache, A.; Geana, I. Method validation for determination of metals in soils by ICP-MS. Rom. Rep. Phys. 2012, 64, 221–231. [Google Scholar]
  30. Castanheiro, A.; Hofman, J.; Nuyts, G.; Joosen, S.; Spassov, S.; Blust, R.; Lenaerts, S.; De Wael, K.; Samson, R. Leaf accumulation of atmospheric dust: Biomagnetic, morphological and elemental evaluation using SEM, ED-XRF and HR-ICP-MS. Atmos. Environ. 2020, 221, 117082. [Google Scholar] [CrossRef]
  31. Berg, B.; Laskowski, R. Methods in Studies of Organic Matter Decay. In Advances in Ecological Research; Academic Press: Cambridge, MA, USA, 2005; Volume 38, pp. 291–331. [Google Scholar]
  32. WHO. Guidlines for Drinking Water Quality; World Health Organization: Hal Ghaxaq, Malta, 2015. [Google Scholar]
  33. FAO/WHO. Codex Alimentarious Commission on Food Standards Programme. In Proceedings of the Codex Committee on Contaminants in Foods, 5th Session, The Hague, The Netherlands, 23 November–1 December 2006; CF5 INF/1. WHO Press: Geneva, Switzerland, 2011. [Google Scholar]
  34. Mkhize, T.A. Assessment of Heavy Metal Contamination in Soils around Krugersdorp Mining Area, Johannesburg, South Africa. Ph.D. Thesis, University of KwaZulu-Natal, Durban, South Africa, 2020. [Google Scholar]
  35. Vannini, A.; Grattacaso, M.; Canali, G.; Nannoni, F.; Di Lella, L.A.; Protano, G.; Biagiotti, S.; Loppi, S. Potentially Toxic Elements (PTEs) in Soils and Bulbs of Elephant Garlic (Allium ampeloprasum L.) Grown in Valdichiana, a Traditional Cultivation Area of Tuscany, Italy. Appl. Sci. 2021, 11, 7023. [Google Scholar] [CrossRef]
  36. Herselman, J.E. The Concentration of Selected Trace Metals in South African Soils. Ph.D. Thesis, University of Stellenbosch, Stellenbosch, South Africa, 2007. [Google Scholar]
  37. Lijzen, J.; Baars, A.; Otte, P.; Rikken, M.; Swartjes, F.; Verbruggen, E.; Van Wezel, A. Technical Evaluation of the Intervention Values for Soil/Sediment and Groundwater. Human and Ecotoxicological Risk Assessment and Derivation of Risk Limits for Soil, Aquatic Sediment and Groundwater; RIVM Rapport 711701023; National Institute for Public Health and the Environment: Bilthove, The Netherlands, 2001. [Google Scholar]
  38. Li, Y.; Qu, X.; Zhang, M.; Peng, W.; Yu, Y.; Gao, B. Anthropogenic Impact and Ecological Risk Assessment of Thallium and Cobalt in Poyang Lake Using the Geochemical Baseline. Water 2018, 10, 1703. [Google Scholar] [CrossRef] [Green Version]
  39. Muller, G. Index of geoaccumulation in sediments of the Rhine River. Geojournal 1969, 2, 108–118. [Google Scholar]
  40. Hakanson, L. An ecological risk index for aquatic pollution control.a sedimentological approach. Water Res. 1980, 14, 975–1001. [Google Scholar] [CrossRef]
  41. Meadows, M.E. The Cape Winelands. In Landscapes and Landforms of South Africa; Grab, S., Knight, J., Eds.; Springer International Publishing: Cham, Switzerland, 2015; pp. 103–109. [Google Scholar]
  42. Tassiopoulos, D.; Nuntsu, N.; Haydam, N. Wine Tourists in South Africa: A Demographic and Psychographic Study. J. Wine Res. 2004, 15, 51–63. [Google Scholar] [CrossRef]
  43. Zhang, M.-K.; Liu, Z.-Y.; Wang, H. Use of Single Extraction Methods to Predict Bioavailability of Heavy Metals in Polluted Soils to Rice. Commun. Soil Sci. Plant Anal. 2010, 41, 820–831. [Google Scholar] [CrossRef]
  44. Jordanova, V.K.; Delzanno, G.L.; Henderson, M.G.; Godinez, H.C.; Jeffery, C.A.; Lawrence, E.C.; Morley, S.K.; Moulton, J.D.; Vernon, L.J.; Woodroffe, J.R.; et al. Specification of the near-Earth space environment with SHIELDS. J. Atmos. Sol. Terr. Phys. 2018, 177, 148–159. [Google Scholar] [CrossRef] [Green Version]
  45. Li, X.; Dong, S.; Su, X. Copper and other heavy metals in grapes: A pilot study tracing influential factors and evaluating potential risks in China. Sci. Rep. 2018, 8, 17407. [Google Scholar] [CrossRef] [Green Version]
  46. Schulte, E.; Kelling, A. Understanding Plant Nutrients: Soil and Applied Copper. Univ. Wis. Ext. 2004, A2527. Available online: http://corn.agronomy.wisc.edu/Management/pdfs/a2527.pdf (accessed on 11 January 2023).
  47. Laczi, E.; Luca, E.; Dumitraş, A.; Hoaghia, A.; Boancă, P. Irrigation and Fertilization Management Effect on Chinese Cabbage Chemical Composition. Commun. Soil Sci. Plant Anal. 2017, 48, 63–72. [Google Scholar] [CrossRef]
  48. González-Martín, M.I.; Revilla, I.; Betances-Salcedo, E.V.; Vivar-Quintana, A.M. Pesticide residues and heavy metals in commercially processed propolis. Microchem. J. 2018, 143, 423–429. [Google Scholar] [CrossRef]
  49. Raji, M.I.O.; Ibrahim, Y.K.E.; Tytler, B.A.; Ehinmidu, J.O. Assessment and Seasonal Variations of Heavy Metals and Mineral Elements in River Sokoto, North-western Nigeria. Niger. J. Basic Appl. Sci. 2016, 24, 9–14. [Google Scholar] [CrossRef] [Green Version]
  50. Okoro, H.; Ximba, B.J.; Tamba, O.; Fatoki, O.S.; Adekola, F.A.; Snyman, R.G.; Yahya, W.B. Distribution and seasonal variations of selected heavy metals in seawater from Cape Town harbour of Western Cape Province, Republic of South Africa. Zimb. J. Sci. Technol. 2017, 11, 82–97. [Google Scholar]
  51. CSIR. Environmental Baseline Description; Western Cape Government: Cape Town, South Africa, 2014; pp. 50–163.
  52. Fabrizio, D.; Stefania, F. Heavy Metal Pollution in Soil: A Survey on West-Central Sardinian Long-Term Vineyards (Italy); Agricultural Research Agency of Sardinia (AGRIS): Bonassai, Italy, 2012. [Google Scholar]
  53. Formicki, G.; Stawarz, R.; Greń, A.; Muchacka, R. Cadmium, copper, lead and zinc concentrations in low quality wines and alcohol containing drinks from Italy, Bulgaria and Poland. J. Microbiol. Biotechnol. Food Sci. 2012, 1, 753–757. [Google Scholar]
Figure 1. A map of the sampled vineyard sites in the Cape Winelands region; the map was created using QGIS and Google Earth software.
Figure 1. A map of the sampled vineyard sites in the Cape Winelands region; the map was created using QGIS and Google Earth software.
Toxics 11 00193 g001
Figure 2. Seasonal fluctuation of heavy metals in soil samples from different grapevine sites (AF) in the Cape Winelands.
Figure 2. Seasonal fluctuation of heavy metals in soil samples from different grapevine sites (AF) in the Cape Winelands.
Toxics 11 00193 g002
Figure 3. Influence of agricultural practices on heavy metal deposits in soils during the winter (A) and summer (B) in vineyards in the Cape Winelands.
Figure 3. Influence of agricultural practices on heavy metal deposits in soils during the winter (A) and summer (B) in vineyards in the Cape Winelands.
Toxics 11 00193 g003
Figure 4. Influence of agricultural practices on heavy metal uptake by plant samples from vineyards of the Cape Winelands.
Figure 4. Influence of agricultural practices on heavy metal uptake by plant samples from vineyards of the Cape Winelands.
Toxics 11 00193 g004
Table 1. The coordinates of sampled vineyards in the Cape Winelands, the location, the sampled grapevine cultivars, and the farming practices.
Table 1. The coordinates of sampled vineyards in the Cape Winelands, the location, the sampled grapevine cultivars, and the farming practices.
CoordinatesSiteTownGrapevine Cultivars SampledFarming Practice
Y = −34.0170461
X = 18.7550072
A *StellenboschCabernet sauvignon and Cabernet francConventional
Y = −33.8347509
X = 18.591131
B *EikenboschSauvignon blanc and Cabernet francConventional
Y = −33.9205238
X = 19.1186237
C *FranschhoekMerlot and Cabernet sauvignonSem-organic
Y = −33.4056598
X = 19.2374146
DWolseleyShiraz, Sèmillon, Merlot, and Sauvignon blancOrganic (certified)
Y = −33.836914
X = 19.9131483
E *RobertsonChardonnay, Sauvignon, and Sauvignon blancConventional
Y = −32.96663
X = 18.75134
FPiketbergCabernet sauvignon, Cabernet sauvignon, Merlot, and ShirazOrganic (certified)
* Evidence of polyculture farming observed.
Table 2. Classes of metal contamination, Igeo [39], and the ecological risk for metal pollution, Er, [40].
Table 2. Classes of metal contamination, Igeo [39], and the ecological risk for metal pollution, Er, [40].
Igeo ClassIgeo ValueSoil Quality Based on Igeo ValueErEcological Risk of Single Metal
0<0UncontaminatedEr ˂ 40Low risk
10–1Uncontaminated to moderately contaminated40 ≤ Er ˂ 80Moderate risk
21–2Moderately contaminated80 ≤ Er ˂ 160Considerable risk
32–3Moderately contaminated to heavily contaminated160 ≤ Er ˂ 320High risk
43–4Heavily contaminatedEr ≥ 320Very high risk
54–5Heavily to extremely contaminated
6>5Extremely contaminated
Table 3. Average concentrations of selected heavy metals in soil samples from different sites collected in summer and winter.
Table 3. Average concentrations of selected heavy metals in soil samples from different sites collected in summer and winter.
SitesHeavy Metal Concentrations (SEM) mg kg−1 in Soils
* FPCrCoNiCuZnAsCdHgPb
A ***C42.933 ± 1.6225.399 ± 0.96415.568 ± 0.65418.471 ± 2.50827.171 ± 0.91323.177 ± 1.9170.019 ± 0.0020.042 ± 0.000517.488 ± 0.763
B ***C48.849 ± 14.9485.673 ± 1.59213.155 ± 3.6099.343 ± 0.89120.271 ± 2.88429.166 ± 11.4420.024 ± 0.0040.030 ± 0.01111.929 ± 1.498
C ***O^13.505 ± 0.7491.987 ± 0.0014.695 ± 0.15810.719 ± 1.87635.406 ± 18.0014.074 ± 1.7520.044 ± 0.0250.032 ± 0.000419.285 ± 3.452
DO34.763 ± 14.7382.267 ± 0.8357.931 ± 1.80041.275 ± 7.36525.167 ± 6.4779.751 ± 0.1260.027 ± 0.0130.018 ± 0.0107.896 ± 0.270
E ***C23.586 ± 2.5784.129 ± 0.08711.112 ± 1.28114.266 ± 1.10123.690 ± 1.3534.900 ± 0.8260.022 ± 0.00040.019 ± 0.00310.376 ± 0.557
FO58.738 ± 2.98810.550 ± 0.704726.812 ± 0.36937.687 ± 0.07144.980 ± 1.6516.455 ± 0.5150.032 ± 0.0050.015 ± 0.000217.550 ± 1.821
** FAO/WHO-ML 100505010050203.0-100
* FP = Farming practice—Conventional(c)/Organic(o)/Semi-organic (^), SEM = Standard Error of Mean, ** ML = Maximum level permitted in soil by [33]; *** = sites which also practised polyculture; - = data not available
Table 4. Contamination factor (Cf), ecological risk index (Er), and geo-accumulation Index (Igeo) (Mean ± SE) of heavy metals occurring in the soils of the vineyards in the Cape Winelands.
Table 4. Contamination factor (Cf), ecological risk index (Er), and geo-accumulation Index (Igeo) (Mean ± SE) of heavy metals occurring in the soils of the vineyards in the Cape Winelands.
Heavy MetalSeasonFarming PracticeCfErIgeo
WinterConventional5.992 ± 0.91611.984 ± 1.8321.964 ± 0.222
Cr Organic4.899 ± 2.1149.798 ± 4.2281.447 ± 0.604
SummerConventional7.223 ± 2.12314.446 ± 4.2462.126 ± 0.466
Organic7.358 ± 2.56714.716 ± 5.1352.034 ± 0.672
WinterConventional0.236 ± 0.0061.179 ± 0.029−2.670 ± 0.035
Co Organic0.285 ± 0.1901.424 ± 0.951−3.059 ± 0.952
Conventional0.327 ± 0.0531.636 ± 0.267−2.239 ± 0.256
SummerOrganic0.264 ± 0.1241.319 ± 0.618−2.815 ± 0.654
WinterConventional3.582 ± 0.45217.908 ± 2.2611.232 ± 0.187
Ni Organic3.571 ± 2.02017.853 ± 10.1000.804 ± 0.779
SummerConventional4.161 ± 0.64920.805 ± 3.2451.432 ± 0.249
Organic4.095 ± 2.01120.475 ± 10.0551.085 ± 0.728
WinterConventional4.449 ± 0.80922.249 ± 4.0431.512 ± 0.297
Cu Organic9.014 ± 3.04745.068 ± 15.2342.329 ± 0.674
SummerConventional4.964 ± 1.07624.820 ± 5.3811.661 ± 0.303
Organic11.049 ± 3.57655.248 ± 17.8832.669 ± 0.597
WinterConventional1.908 ± 0.2311.908 ± 0.2310.324 ± 0.188
Zn Organic2.344 ± 0.8402.344 ± 0.8400.476 ± 0.474
SummerConventional2.044 ± 0.1492.044 ± 0.1490.439 ± 0.102
Organic3.520 ± 0.5243.520 ± 0.5241.198 ± 0.218
WinterConventional0.809 ± 0.2828.091 ± 2.822−1.135 ± 0.643
As Organic0.348 ± 0.0673.479 ± 0.669−2.157 ± 0.260
SummerConventional1.099 ± 0.52810.990 ± 5.276−0.980 ± 0.988
Organic0.328 ± 0.1113.281 ± 1.115−2.432 ± 0.640
WinterConventional0.036 ± 0.0041.097 ± 0.134−5.379 ± 0.173
Cd Organic0.037 ± 0.0111.121 ± 0.339−5.451 ± 0.414
SummerConventional0.034 ± 0.0011.029 ± 0.042−5.453 ± 0.059
Organic0.073 ± 0.0202.179 ± 0.617−4.483 ± 0.407
WinterConventional0.186 ± 0.0497.436 ± 1.961−3.105 ± 0.357
Hg Organic0.122 ± 0.0464.865 ± 1.837−3.844 ± 0.572
SummerConventional0.221 ± 0.0578.834 ± 2.267−2.890 ± 0.456
Organic0.168 ± 0.0356.720 ± 1.387−3.232 ± 0.339
WinterConventional4.242 ± 0.67121.209 ± 3.3541.466 ± 0.215
Pb Organic5.139 ± 1.46025.693 ± 7.3011.639 ± 0.463
SummerConventional4.622 ± 0.81323.110 ± 4.0651.578 ± 0.257
Organic4.835 ± 1.10624.176 ± 5.5301.598 ± 0.376
Table 5. Average concentrations of selected heavy metals in grapevine leaf samples from different sites (vineyards) in the Cape Winelands.
Table 5. Average concentrations of selected heavy metals in grapevine leaf samples from different sites (vineyards) in the Cape Winelands.
SitesHeavy Metal Concentration (SEM) mg kg−1
* FPCrCoNiCuZnAsCdHgPb
A ***C0.959 ± 0.057 ab0.240 ± 0.053 a0.566 ± 0.049 a4.230 ± 0.328 a27.906 ± 2.230 ab0.318 ± 0.046 ab0.007 ± 0.001 ab0.017 ± 0.002 ab0.373 ± 0.045 ab
B ***C1.335 ± 0.164 a0.269 ± 0.047 a0.574 ± 0.047 a4.256 ± 0.458 a23.987 ± 3.138 ab0.454 ± 0.102 a0.008 ± 0.0008 ab0.017 ± 0.001 ab0.619 ± 0.057 a
C ***O^0.620 ± 0.081 b0.107 ± 0.011 a0.431 ± 0.058 a3.957 ± 0.364 a32.289 ± 5.858 a0.119 ± 0.030 b0.018 ± 0.005 a0.018 ± 0.002 ab0.307 ± 0.063 b
DO0.572 ± 0.063 b0.103 ± 0.018 a0.461 ± 0.069 a87.098 ± 19.481 b24.192 ± 2.730 b0.125 ± 0.022 b0.002 ± 0.0004 b0.020 ± 0.0005 ab0.295 ± 0.083 b
E ***C0.699 ± 0.069 b0.200 ± 0.044 a0.821 ± 0.203 a6.082 ± 0.885 a24.789 ± 1.437 ab0.106 ± 0.009 b0.016 ± 0.006 ab0.014 ± 0.002 a0.165 ± 0.035 b
FO0.973 ± 0.131 ab0.298 ± 0.106 aa1.104 ± 0.372 a60.603 ± 7.971 bc16.848 ± 1.937 ab0.117 ± 0.021 b0.004 ± 0.001 ab0.023 ± 0.003 b0.197 ± 0.034 b
** FAO/WHO-ML 1.350101099.40.00050.020.12
* FP = Farming practice—Conventional(c)/Organic(o)/Semi-organic (^), SEM = Standard Error of Mean, ** ML = Maximum level permitted in edible plants by [33]; *** = sites with evidence of polyculture farming; means with the same lowercase letters (a or b or c) are not significantly different.
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Mahlungulu, A.; Kambizi, L.; Akinpelu, E.A.; Nchu, F. Levels of Heavy Metals in Grapevine Soil and Leaf Samples in Response to Seasonal Change and Farming Practice in the Cape Winelands. Toxics 2023, 11, 193. https://doi.org/10.3390/toxics11020193

AMA Style

Mahlungulu A, Kambizi L, Akinpelu EA, Nchu F. Levels of Heavy Metals in Grapevine Soil and Leaf Samples in Response to Seasonal Change and Farming Practice in the Cape Winelands. Toxics. 2023; 11(2):193. https://doi.org/10.3390/toxics11020193

Chicago/Turabian Style

Mahlungulu, Amanda, Learnmore Kambizi, Enoch Akinbiyi Akinpelu, and Felix Nchu. 2023. "Levels of Heavy Metals in Grapevine Soil and Leaf Samples in Response to Seasonal Change and Farming Practice in the Cape Winelands" Toxics 11, no. 2: 193. https://doi.org/10.3390/toxics11020193

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop