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Article

Consuming Blackberry as a Traditional Nutraceutical Resource from an Area with High Anthropogenic Impact

1
Department of Food Engineering, University of Oradea, Oradea, Bihor 410048, Romania
2
Technological High School Ștefan Manciulea, Blaj, Alba 515400, Romania
3
Transilvania University of Brașov, Faculty of Silviculture and Forest Engineering, 500123 Brașov, Romania
4
Department of Forestry and Forest Engineering, University of Oradea, Oradea, Bihor 410048, Romania
5
Plant Protection Department, University of Agricultural Sciences and Veterinary Medicine, Cluj-Napoca, Cluj 400372, Romania
*
Author to whom correspondence should be addressed.
Forests 2019, 10(3), 246; https://doi.org/10.3390/f10030246
Submission received: 31 January 2019 / Revised: 23 February 2019 / Accepted: 5 March 2019 / Published: 11 March 2019
(This article belongs to the Special Issue Forest, Foods and Nutrition)

Abstract

:
The most serious quality issue of natural resources for human consumption or medicinal purposes is the contamination with pollutants harmful to consumers. Common blackberry (Rubus fruticosus L.) is a sought-after nutraceutical and an important component in herbal medicine in many places around the globe. The present study aims to analyze the level of heavy metal bioaccumulation in blackberry organs, as well as its spatial distribution in two consecutive years immediately after the interruption of the extended activity of the industrial source of pollution. The research was conducted in one of the most polluted areas in Romania and Eastern Europe, within a 26 km radius of the source of pollution. The Pb, Cd, Cu, and Zn concentrations in the leaves, flowers, and unwashed blackberry fruits were analyzed spectrophotometrically through flame atomic absorption spectroscopy (FAAS). The results show that blackberry is an important bioaccumulator of these heavy metals—71% of the Pb concentration values and 100% of the Cd concentration values exceeded the World Health Organization thresholds by up to 29 and 15 times, respectively. Also, the leaves are the largest reservoirs of Pb and Zn (the median values: 51.4 mg/kg dry weight and 105.2 mg/kg d.w., respectively), and the flowers contained the largest quantities of Cd and Cu (2.54 mg/kg d.w. and 11.3 mg/kg d.w., respectively). The Pb concentrations decreased by a power function in relation to the distance from the source of pollution. The implications of these results on the safety of the use of blackberry are discussed. The urgent necessity for food education of the local population which consumes contaminated nutraceutical products is emphasized.

1. Introduction

In spite of all the qualitative changes which human activity has experienced over time, the attraction for products provided directly and generously by nature has not diminished [1]. The diversity of uses which every natural resource offers is the most convincing evidence of its value. For instance, blackberry is simultaneously edible, medicinal, and melliferous, thus it can be classified as a highly interesting nutraceutical (Table 1).
Since the time of Hippocrates [11], the belief that food has therapeutic properties has gradually consolidated [12] and has engaged a rich terminology, with interchangeable notions that have created confusion and controversies [13]. A nutraceutical is a hybrid concept better located at the boundary between food and drug [14]. It was introduced by DeFelice in 1989 and brought about a revolution in nutrition [15]. In contrast to other food-derived products claimed to have benefits on human health, nutraceuticals have a proven clinic efficiency in preventing and even treating certain pathological conditions [16]. At least in Europe, the lack of nutraceuticals identity and insufficient clinical evidence from in vivo experiments has kept down the formulation of shared regulatory framework for nutraceuticals [17] that would guarantee consumers the efficacy and safety of this pharma-food.
Despite increasing research on the properties of bioactive compounds [18], nutraceuticals, as rich substance mixtures [17], require: (1) a supplementary chemometric effort to identify the dietary markers which enable the quality control of the products [19] and (2) robust clinical evidence to support their use [20] and thus the transition from potential nutraceutical to established nutraceutical [15].
Taking into account the blackberry, the most important bioactive ingredients are: (1) the ellagitannins, which, besides their usual antidiarrheal and antidysenteric astringency, inhibit the growth of cancerous cells [3,21,22,23] and (2) the anthocyanins and other polyphenols, with their significant antiradical, antioxidant, and chemoprotective activities [8,21,22,23,24,25,26,27,28,29,30,31,32,33,34,35].
In many places around the world, especially in rural and tribal areas, exploiting natural, food, and medicinal resources is a survival issue, therefore a social factor [36] or, in any case, an alternative source of income. In 2005, 14,837 t of wild blackberries were harvested, in addition to 154,578 t of cultivated blackberries [37]. In Romania, 1 ha of forest land can yield up to 12.5 t of blackberries per year [9]. In our researched area, there are over 17,400 people who have access to contaminated natural products. With the cease of pollutant activity, 80% of employees were fired in 2009 and directed towards other fields. Consequently, the interest for the exploitation of the agricultural, medicinal, and nutritional potential of the area increased.
The large number of uses of vegetal products and their composition raises the often-times vital issue of product safety. The contamination with pollutants, either local, regional, or cross-border, endangers the health of consumers of such bio-products. Heavy metals, resulting from metallurgical activities by means of the refining and burning of fossil fuels or fertilizing agricultural soils, enter the food chain via the air, water, and soil, manifesting toxicity even in very small concentrations [38,39]. For instance, lead, cadmium, and zinc poisoning attacks the nervous system, causing a decrease in intellectual performance, as well as aggressiveness, delinquency, and narcomania in youths [40,41,42,43,44,45]. Blackberry is more prone to cadmium accumulation than other fruit [46].
Impact studies on historical pollution of the chemical composition of blackberry were carried out in Sudety Mountains SW, Poland [47]; Pirdop, Bulgaria [48]; Vladivostok, Russia [49]; Lori region, Armenia [50]; Berlin, Germany [46]; Middle Spis, Slovakia [51]; and Moldova Nouă, Romania [52]. The level of heavy metal contamination in leaves, fruits, and products derived from blackberries (blackberry leaf tea, blackberry wine) was also determined [53,54].
Our research aims to determine the recent pollution level through the concentration of certain heavy metals in blackberry vegetal material (Rubus fruticosus L.), and to characterize its spatial distribution in relation to the distance from the source of pollution and the site geomorphology. The investigations were carried out in one of the most polluted areas in Romania and Eastern Europe. The age and seriousness of the pollution in these areas prompted a variety of impact studies on the environment and the living organisms—revised by Smejkal [55] and Micu [56]. However, blackberry was not analyzed in these studies, in spite of its wide popularity among local and national consumers [9].

2. Materials and Methods

2.1. The History of the Pollution

The source of the pollution whose effects are analyzed in this article is the industrial park in the town Copşa Mică (46°06′59.10″ N and 24°13′15.43″ E), in the center of Romania. Until now, it produced large quantities of carbon black (for 58 years: 1935–1993), metallurgical and refined zinc, electrolytic lead, bismuth, antimony, iron, cadmium powder, sulphuric acid, sulfur dioxide, sulfates, sulfurs, carbon monoxide, nitrogen oxides, volatile arsenic compounds, and ammonia (for 70 years: 1939–2009).
The location of the industrial park on the wide valley of the Târnava river, which channels the local circulation of air mass, allowed the pollutants to distribute over large distances. The hydrographic fragmentation of the territory extended the pollution transversally to the secondary valleys. At the nearest weather station, according to the climatic data provided by the National Meteorological Agency [57], the mean annual temperature is 8.4 °C, the mean annual rainfall is 625.6 mm·year−1, the annual wind frequency is 65.5%, and the speed of the wind with the highest frequency is 3.1 m·s−1. The low amount of rainfall leads to the persistence of pollutants in the atmosphere and the high percentage of atmospheric calm allows air mass stagnation and pollutant deposition.
The plant material was collected in two consecutive years, starting with the year when the activity on the polluting industrial platform ceased. In the two years of sampling the mean temperatures were 9.4 and 9.1 °C and the rainfall levels were 648.4 and 782.3 mm·year−1, respectively [57].

2.2. Sampling Design

The distribution of pollutants in blackberry organs was examined in nine sampling plots, eight of which were grouped in the first 8 km from the source of pollution (Figure 1), and one control plot, located 26 km from the industrial park in Copşa Mică (type of site D). The target was the study of pollution in various topoclimates. Each plot was identified geographically and geomorphologically, using Global Positioning System coordinates, the side aspect, the exposure to the circulation of polluted air (Table 2), and the distance to the main flue-gas stack for emissions—which is 250 m tall.
The vegetal material samples were collected according to the regulations of the United Nations Economic Commission for Europe-International Co-operative Programme on Assessment and Monitoring of Air Pollution Effects on Forests- [58]. At least five blackberry dominant bushes were chosen from every sampling plot. The material (20–30 g leaves, flowers/sampling plot and 100–200 g fruits/plot) was collected systematically from the four cardinal sides of the bush. Only healthy samples were considered [59], and great care was taken to avoid touching or contaminating them with the tools used. The flowers were collected no later than 2–3 days after bloom or in the budding stage, to prevent loss of pollen due to insect pollination. The leaves were collected in the second half of the growing season, but before the autumnal senescence, when the heavy metal concentration peaks [60]. The ripe fruits were harvested in the firm stage.

2.3. Processing the Material

The vegetal material was not washed, so as to identify the total pollutant concentrations in the state in which the resource is used [61]. For instance, the blackberry long-lived leaves are eaten by game, particularly by cervids [9], and blackberries are not washed before consumption. To avoid pollen removal, which bioconcentrates an important fraction of heavy metals, the flowers were not washed either.
The laboratory investigations followed Kelp’s [62] recommendations. The samples were oven-dried to a constant mass at 60 °C, which did not affect the sanogenetic qualities of the product [9]. Mineralization was achieved after wet digestion [58], using the Berghof MWS-2 microwave oven. The mixture of 0.3–0.5 g dried plant powder, 2 mL concentrated HNO3 (65% concentration, Merck extra pure), and 3 mL H2O2 (30% concentration, Merck, Darmstadt, Germany) were introduced in the microwave system (Berghof MWS-2, Eningen, Germany). Mineralization was carried out in three steps, at temperatures of 145, 180, and 100 °C (Table 3).
After mineralization, samples were filtered through a 0.45 mm filter and brought to a volume of 50 mL in a volumetric flask with ultrapure water with a specific resistance of 18.2 MΩ/cm obtained from a Direct Q3UV Smart (Millipore SAS, Molsheim, France). The digested samples were analyzed by flame atomic absorption spectroscopy (FAAS) with ZEEnit 700 Atomic Absorption Spectrometer (Analytik Jena AG, Jena, Germany). Calibrating standard solutions of Cd, Cu, Pb, and Zn were prepared daily by the accurate dilution of the respective stock standard solutions (1000 mg/L). Ultrapure water with a specific resistance of 18.2 MΩ/cm obtained from a Direct Q3UV Smart (Millipore SAS, Molsheim, France) was used to prepare the standard solutions. For quality control purpose, blanks and triplicates samples (n = 3) were analyzed during the procedure. The variation coefficient was under 5%. The operation conditions were those recommended for each metal in the instrument’s method (Table 4).
The sensitivity of the FAAS method was estimated using the limit of detection (LOD) and the limit of quantification (LOQ). The LOD and LOQ (Table 5) were calculated based on the standard deviation of the response and the slope [63,64,65,66]. A total number of 171 spectrometric determinations were carried out.

2.4. Data Processing

Data analysis was performed using Microsoft EXCEL 2007 and STATISTICA 8.0. The results were related to the World Health Organization [67] limits for heavy metals in products with ecosanogenetic qualities (Table 6).

3. Results and Discussions

3.1. The Level of Heavy Metal Contamination in Blackberry

The concentrations of the studied microelements were found to be strongly scattered around the mean (high coefficients of variation—Table 7). Thus, the arithmetic mean was no longer relevant and was replaced with the median to express the central tendency. Most of the lead and cadmium concentration values greatly exceeded the toxicity thresholds (Table 7). Furthermore, these thresholds were exceeded in the control plot as well, which was believed to be unaffected by the influence of the pollution caused by the industrial park in Copşa Mică. As such, 40% of the measured lead concentrations, 100% of the cadmium concentrations, and 67% of the copper concentrations in the control plot exceeded the WHO permissible limit. This result is proof of the area expansion of heavy metal pollution. The other sampling plots are located up to 8 km from the source of pollution and have pollutant concentrations which exceeded the permissible limit for lead by up to 29.1 times, the permissible limit for cadmium by up to 14.9 times, and the permissible limit for copper by up to 38.8 times. Approximately a quarter of the values of lead concentration exceeded the permissible limit by at least 5 times. More than half of the values of cadmium concentration exceeded the permissible limit by at least 5 times.
Based on the blackberry average yield in Romania [9], this means that a hectare of blackberry shrubs from the Copșa Mică area sequesters yearly through leaves, flowers, and fruits: 2.17 kg Pb, 0.17 kg Cd, 7.52 kg Zn, and 0.77 kg Cu.
The fact that these discovered values are greater than those highlighted in pollution literature is worrisome for the local consumers. Gasser et al. [70] processed the database of the German Medicines Manufacturers’ Association and indicated that the following values of Cd and Pb concentrations range in blackberry leaves: <0.07–0.32 mg/kg dry weight and <0.4–2.8 mg/kg d.w., respectively. Shikhova [49] highlighted average concentrations of 15.07 mg/kg d.w. Pb in Rubus sachalinensis H. Lév. from the suburban forest phytocenosis in Vladivostok. After analyzing samples of Rubus fruticosus harvested from different sampling plots in Berlin, von Hoffen and Säumel [46] found average cadmium concentrations of 0.0081 mg/kg d.w., and lead concentrations of 0.0595 mg/kg d.w.
Investigations of heavy metal content in blackberry were also carried out in areas with historical pollution of mining or metallurgical origin. Micu et al. [52] identified average concentrations of 12 ppm Cu, 0.03 mg/kg d.w. Cd, and 19 mg/kg d.w. Pb in the blackberry leaves on the spoil heaps of Moldova Nouă (Romania). Wisłocka et al. [47] found in washed Rubus idaeus L. leaves grown on uranium mine dumps in the Sudety Mountains range heavy metal concentrations of 17.6–41.0 mg/kg d.w. for Pb, 0.40–1.60 mg/kg d.w. for Cd, 1.20–10.50 mg/kg d.w. for Cu, and 27–88 mg/kg d.w. for Zn, which were consistent with their concentrations in the soil. In the Middle Spis (Slovakia), which was affected by acid and heavy metal pollution for decades, Vollmannova et al. [51] found the following range of toxic metal concentrations: 0.30–1.19 mg/kg d.w. Pb, 0.18–0.42 mg/kg d.w. Cd, 5.50–6.50 mg/kg d.w. Cu, and 16.1–30.7 mg/kg d.w. Zn in dry blackberry leaves, as well as 0.03 mg/kg d.w. Pb, 0.03–0.05 mg/kg d.w. Cd, 0.48–0.99 mg/kg d.w. Cu, and 2.08–3.13 mg/kg d.w. Zn in fresh blackberries. Compared to our results, the investigations carried out by Teofilova et al. [48] in the area of the copper foundry in Pirdop (Bulgaria) reported higher average values of copper content (62.5 mg/kg d.w.), the same values for zinc (80 mg/kg d.w.), and lower values for lead (8.5 mg/kg d.w.) and cadmium (0.275 mg/kg d.w.) in blackberry fruits.
The large discrepancy with the literature data is partly due to the way our samples were prepared, i.e., without pre-washing. We intended to quantify the total bioaccumulation of heavy metals in the blackberry organs, as they are used directly by consumers (humans, cervids, bees) and thus the input to the trophic chain through the contaminants is more widely dispersed in the ecosystem structure. The data from the literature of other species reveal that, by washing, the heavy metal concentrations were reduced by 3.09–85.79% for Pb, 4.00–86.11% for Cd, 0.78–84.85% for Zn, and 0.76–86.41% for Cu, varying by species, organ harvested, culture system, sampling period, and degree and type of pollution [71,72,73,74,75,76]. We assume that even in the case of blackberry, as a species with hirsute organs, the deposition of heavy metals at least at the surface of the leaves is considerable. It has been shown that Pb and Cd concentrations are 10 times higher in hirsute plants than in those with a smooth surface [77].
The non-parametric Kruskal–Wallis test (Table 8) led to the stratification of the values of metal concentration according to the blackberry organs.
The values in the content of lead, cadmium, zinc, and copper in fruits are noticeably different compared to those in flowers and leaves (Figure 2). Of the sampled blackberry organs, the fruits retained the smallest metal quantities, except for copper—the copper content had the highest variation in the fruits. The leaves contained 4.5 times more lead than the fruits. The flowers contained 3 times more cadmium and 3.8 times more zinc than the fruits. The flowers contained 2.2 times more copper than the leaves (Figure 2).
This means that the risk to consumers of such resources, quantified for a portion of 100 grams of fresh blackberries, with an average moisture content of 91.4% (own data), consists in the ingestion of 8.51 mg Pb, 0.74 mg Cd, 19.64 mg Zn, and 5.71 mg Cu.
Yedoyan and Yedoyan [50] found notable differences between blackberry organs which were polluted anthropogenically, especially in terms of lead and copper content. For instance, the root was found to be an important copper reservoir.
Concerning other species besides blackberry, from the Copșa Mică area, Alexa et al. [78] spectrometrically measured the heavy metal content. The comparisons emphasized the fact that trees are more important heavy metal bioaccumulators than blackberry. In June 2001, in full industrial season, up to 620 mg/kg d.w. lead and up to 8.5 mg/kg d.w. cadmium were found in locust leaves [78].
The net differentiation of blackberry organs in heavy metals storage is the consequence of their different and asynchronous lifespan, the morphological characteristics of their surface, and the exposure to the pollutant flow. Blackberry leaves—long-living, hirsute on both sides, and more exposed to atmospheric pollutants—are the largest reservoirs of heavy metals (Figure 2). The consistency and morphology of the floral tissue and the synchronization of the flowering stage with the rainiest months reduce the retention of heavy metals in flowers compared to leaves. Blackberries themselves, sheltered by leaves and slowly ripening, accumulate smaller amounts of heavy metals (Figure 2).
The unnoticeable differences of heavy metal concentrations between the two years of sampling (Table 8) suggest a long-lasting soil pollution and a strong sequestration of these pollutants in the blackberry organs, which goes beyond the rainfall increase in the second year.

3.2. The Spatial Variability of the Heavy Metal Content in Blackberry

The factors of influence on the metal content in the vegetal material were identified by using the non-parametric Kruskal–Wallis test, when the majority of dependent variables had non-Gaussian distributions. The results show that only the lead content is more sensitive to location change (Table 8). It decreases by a power function according to the distance from the source of pollution (Figure 3). In the first 3 km, the higher dispersion of lead concentrations and the more pronounced decay with the distance in the case of the leaves were noted. The matrix of the sign test (not listed) indicated that, in fact, the variation of lead content according to altitude is due only to the lowest altitude, which had the largest lead quantities. The zinc and copper concentrations were changeless from one sampling plot to another. The cadmium concentration depended on the exposure of the location to the local circulation of polluted air. The differences between the sampled years were not statistically significant (Table 8).

3.3. Safety in Herbal Medicine

In spite of the growing popularity of natural products, one must be realistic and admit that none can be completely free from various contaminants. The risk of contaminated nutraceuticals intake is much higher in the absence of specific legislation, as manufacturers are not compelled to oversee the nature, safety, and therapeutic and nutritional efficacy of these products [11]. Furthermore, the preference for nutraceuticals is fueled by consumers’ false belief that the natural product is inevitably healthy and safe [19].
Food products consumed by people undoubtedly contain metals and metalloids [38,79]. Even if it comes up in a biotope where the anthropogenic pressure is low, the collected raw material may be contaminated due to certain non-hygienic harvesting techniques or poor storage and conditioning. Heavy metals can bioaccumulate in plants in concentrations which exceed the maximum limits permitted by the environmental regulations, where they can reach the human or animal organism directly or indirectly through the food chain. A lot of metals give rise to toxicity even with reduced concentrations.
Important lead, cadmium, and zinc concentrations were found in consumer finished food or medicinal products, such as tea and blackberry wine [53,54]. Small quantities of these metals in Rubus species were found in Himalaya as well [34].
The smaller the quantities of non-essential heavy metals in traditional nutraceutical products, the lower will be the risk to the consumers health Small quantities of non-essential heavy metals in traditional nutraceutical products as their absence eliminates the risk of noxious effects on health [80]. Consequently, it is necessary to implement a qualitative assessment of wild resources consumed directly or used in ethnomedicine, before using or processing them, by determining the heavy metal content [81].
Resources, such as blackberry in Copşa Mică, are consumed by the local population in raw or processed forms. At the observed lead and cadmium concentrations (Table 7, Figure 2), the therapeutic value of the blackberry active ingredients decreases.
The International Agency for Research on Cancer classifies the anorganic compounds of Pb into group 2A—probably carcinogenic to humans. The symptoms of lead poisoning are abdominal pain, constipation, nausea, cramps, vomiting, anorexia, and weight loss [82]. Chronic exposure to high levels of Pb produces significant accumulations in the bones, as well as disorders of the central nervous system, hepatic and renal disorders, gout, and high blood pressure. Furthermore, it affects the optimal functions of the male and female reproductive system, with negative effects on pregnancy [83,84,85,86,87,88].
As a non-essential metal, Cd accumulates in the environment continuously, with one of its main sources being the atmospheric deposit. Chronic exposure to Cd causes kidney failure, increased risk of pre-diabetes and diabetes, high blood pressure, osteoporosis, and cancer [89,90,91,92]. In our researched area children represent the age range most exposed to the risk of contamination by eating blackberries. The poor education of some people maintains this risk. Hence, an acute need for food education for all social categories from the area is felt.

4. Conclusions

Blackberry is a popular nutraceutical, but unfortunately it is also an important heavy metal bioaccumulator. The extended industrial activity (which began in 1935) of metallurgical and chemical production in Copşa Mică led to the remnant contamination of blackberry with lead, cadmium, zinc, and copper. Shortly after the interruption of the pollution emission, the lead concentrations in blackberry were found to exceed the recommended threshold by up to 29 times in 71% of cases. Furthermore, all the cadmium concentrations exceeded the WHO threshold by up to 15 times, and 83% of the values of copper concentration exceeded the permissible limit by up to 39 times. The organs of blackberry store these elements differently—the flowers and leaves are the largest bioaccumulators. The lead bioaccumulation was found to have a definite spatial distribution. Conversely, the zinc and copper concentrations were changeless from one sampling plot to another. The results indicate a wide geographic expansion of pollution with these metals, within a radius of at least 26 km.

Author Contributions

Conceived and designed the experiment: G.G., F.D., and I.A.V. Performed the experiment: G.G. and T.M. Analyzed the data: F.D. and T.M. Interpreted the results: I.A.V., F.D., and G.G. Conceived the paper, wrote the first draft and edited the manuscript: F.D., M.M.V., and S.B. Supervised the manuscript: F.D.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Ekor, M. The Growing Use of Herbal Medicines: Issues Relating to Adverse Reactions and Challenges in Monitoring Safety. Front. Pharmacol. 2014, 4, 177. [Google Scholar] [CrossRef] [PubMed]
  2. Butură, V. Encyclopaedia of Romanian Ethnobotany; Științifică și Enciclopedică Publishing House: Bucharest, Romania, 1979; pp. 159–202. [Google Scholar]
  3. Lim, T.K. Edible Medicinal and Non-Medicinal Plants—Fruits; Springer: Berlin, Germany, 2012; pp. 559–569. [Google Scholar]
  4. Alonso, R.; Cavidad, I.; Calleja, J.M. A preliminary study of hypoglycemic activity of Rubus fruticosus. Planta Med. 1980, 40, 102–106. [Google Scholar] [CrossRef] [PubMed]
  5. Leonti, M.; Casu, L.; Sanna, F.; Bonsignore, L. A comparison of medicinal plant use in Sardinia and Sicily-De Materia Medica revisited? J. Ethnopharmacol. 2009, 121, 55–67. [Google Scholar] [CrossRef] [PubMed]
  6. Guarrera, P.M. Food medicine and minor nourishment in the folk traditions of Central Italy (Marche, Abruzzo and Latium). Fitoterapia 2003, 74, 515–544. [Google Scholar] [CrossRef]
  7. Lust, J. The Herb Book; Dover Publications Inc.: New York, NY, USA, 2014; pp. 298–300. [Google Scholar]
  8. Chevallier, A. Encyclopedia of Herbal Medicine, 3rd ed.; Dorling Kindersley Publishing: New York, NY, USA, 2016; pp. 264–265. [Google Scholar]
  9. Beldeanu, E.C. Forest Species of Sanogenic Interest; Transilvania University Press: Braşov, Romania, 2004; pp. 145–147. [Google Scholar]
  10. Sher, H. Ethnoecological evaluation of some medicinal and aromatic plants of Kot Malakand Agency, Pakistan. Sci. Res. Essays 2011, 6, 2164–2173. [Google Scholar]
  11. Daliu, P.; Santini, A.; Novellino, E. From pharmaceuticals to nutraceuticals: Bridging disease prevention and management. Expert Rev. Clin. Pharmacol. 2018, 28, 1–7. [Google Scholar] [CrossRef] [PubMed]
  12. Santini, A.; Novellino, E.; Armini, V.; Ritieni, A. State of the art of Ready-to-Use Therapeutic Food: A tool for nutraceuticals addition to foodstuff. Food Chem. 2013, 140, 843–849. [Google Scholar] [CrossRef] [PubMed]
  13. Santini, A.; Novellino, E. To Nutraceuticals and Back: Rethinking a Concept. Foods 2017, 6, 74. [Google Scholar] [CrossRef] [PubMed]
  14. Santini, A.; Novellino, E. Nutraceuticals: Shedding light on the grey area between pharmaceuticals and food. Expert Rev. Clin. Pharmacol. 2018, 11, 545–547. [Google Scholar] [CrossRef] [PubMed]
  15. De Felice, S.L. The nutraceutical revolution: Its impact on food industry R&D. Trends Food Sci. Technol. 1995, 6, 59–61. [Google Scholar]
  16. Santini, A.; Tenore, G.C.; Novellino, E. Nutraceuticals: A paradigm of proactive medicine. Eur. J. Pharm. Sci. 2017, 96, 53–61. [Google Scholar] [CrossRef] [PubMed]
  17. Santini, A.; Cammarata, S.M.; Capone, G.; Ianaro, A.; Tenore, G.C.; Pani, L.; Novellino, E. Nutraceuticals: Opening the debate for a regulatory framework. Br. J. Clin. Pharmacol. 2018, 84, 659–672. [Google Scholar] [CrossRef] [PubMed]
  18. Yeung, A.W.K.; Tzvetkov, N.T.; El-Tawil, O.S.; Bungǎu, S.G.; Abdel-Daim, M.M.; Atanasov, A.G. Antioxidants: Scientific Literature Landscape Analysis. Oxid. Med. Cell. Longev. 2019, 2019, 8278454. [Google Scholar] [CrossRef] [PubMed]
  19. Durazzo, A.; D’Addezio, L.; Camilli, E.; Piccinelli, R.; Turrini, A.; Marletta, L.; Marconi, S.; Lucarini, M.; Lisciani, S.; Gabrielli, P.; et al. From Plant Compounds to Botanicals and Back: A Current Snapshot. Molecules 2018, 23, 1844. [Google Scholar] [CrossRef] [PubMed]
  20. Andrew, R.; Izzo, A.A. Principles of pharmacological research of nutraceuticals. Br. J. Pharmacol. 2017, 174, 1177–1194. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  21. Seeram, N.P.; Adams, L.S.; Zhang, Y.; Lee, R.; Sand, D.; Scheuller, H.S.; Heber, D. Blackberry, black raspberry, blueberry, cranberry, red raspberry, and strawberry extracts inhibit growth and stimulate apoptosis of human cancer cells in vitro. J. Agric. Food Chem. 2006, 54, 9329–9339. [Google Scholar] [CrossRef] [PubMed]
  22. Dai, J.; Patel, J.D.; Mumper, R.J. Characterization of blackberry extract and its antiproliferative and anti-inflammatory properties. J. Med. Food 2007, 10, 258–265. [Google Scholar] [CrossRef] [PubMed]
  23. Hager, T.J.; Howard, L.R.; Liyanage, R.; Lay, J.O.; Prior, R.L. Ellagitannin composition of blackberry as determined by HPLC-ESI-MS and MALDI-TOF-MS. J. Agric. Food Chem. 2008, 56, 661–669. [Google Scholar] [CrossRef] [PubMed]
  24. Heinonen, I.M.; Meyer, A.S.; Frankel, E.N. Antioxidant activity of berry phenolics on human low-density lipoprotein and liposome oxidation. J. Agric. Food Chem. 1998, 46, 4107–4112. [Google Scholar] [CrossRef]
  25. Wang, S.Y.; Lin, H.S. Antioxidant activity in fruits and leaves of blackberry, raspberry and strawberry varies with cultivar and developmental stage. J. Agric. Food Chem. 2000, 48, 140–146. [Google Scholar] [CrossRef] [PubMed]
  26. Moyer, R.A.; Hummer, K.E.; Finn, C.E.; Frei, B.; Wrolstad, R.E. Anthocyanins, phenolics, and antioxidant capacity in diverse small fruits: Vaccinium, Rubus, and Ribes. J. Agric. Food Chem. 2002, 50, 519–525. [Google Scholar] [CrossRef] [PubMed]
  27. Ding, M.; Feng, R.; Wang, S.Y.; Bowman, L.; Lu, Y.; Qian, Y.; Castranova, V.; Jiang, B.H.; Shi, X. Cyanidin-3-glucoside, a natural product derived from blackberry, exhibits chemopreventive and chemotherapeutic activity. J. Biol. Chem. 2006, 281, 17359–17368. [Google Scholar] [CrossRef] [PubMed]
  28. Pantelidis, G.E.; Vasilakakis, M.; Manganaris, G.A.; Diamantidis, G.R. Antioxidant capacity, phenol, anthocyanin and ascorbic acid contents in raspberries, blackberries, red currants, gooseberries and cornelian cherries. Food Chem. 2007, 102, 777–783. [Google Scholar] [CrossRef]
  29. Elisia, I.; Kitts, D.D. Anthocyanins inhibit peroxyl radical-induced apoptosis in Caco-2 cells. Mol. Cell. Biochem. 2008, 312, 139–145. [Google Scholar] [CrossRef] [PubMed]
  30. Bowen-Forbes, C.S.; Zhang, Y.; Nair, M.G. Anthocyanin content, antioxidant, anti-inflammatory and anticancer properties of blackberry and raspberry fruits. J. Food Compos. Anal. 2010, 23, 554–560. [Google Scholar] [CrossRef]
  31. Jing, P.; Giusti, M. Contribution of berry anthocyanins to their chemopreventive properties. In Berries and Cancer Prevention; Stoner, G.D., Seeram, N.P., Eds.; Springer: New York, NY, USA, 2011; pp. 1–38. [Google Scholar]
  32. Kolevski, G.; Ivic-Kolevska, S. Antioxidants in fruits and human medical research: An overview. J. Hyg. Eng. Des. 2012, 1, 271–274. [Google Scholar]
  33. Tavares, L.; Figueira, I.; McDougall, G.J.; Vieira, H.L.A.; Stewart, D.; Alves, P.M.; Ferreira, R.B.; Santos, C.N. Neuroprotective effects of digested polyphenols from wild blackberry species. Eur. J. Nutr. 2013, 52, 225–236. [Google Scholar] [CrossRef] [PubMed]
  34. Ahmad, M.; Masood, S.; Sutana, S.; Ben Hadda, T.; Bader, A.; Zafar, M. Antioxidant and nutraceutical value of wild medicinal Rubus berries. Pak. J. Pharm. Sci. 2015, 28, 241–247. [Google Scholar] [PubMed]
  35. Predná, L.; Habánová, M. Antioxidant potential in selected species of small berry fruits. Acta Fytotech. Zootech. 2015, 18, 116–118. [Google Scholar] [CrossRef]
  36. Bhattarai, N.; Karki, M. Medicinal and aromatic plants: Ethnobotany and conservation status. In Encyclopedia of Forest Sciences; Burley, J., Evans, J., Youngquist, J.A., Eds.; Elsevier Ltd.: Kidlington, UK, 2004; pp. 523–532. [Google Scholar]
  37. Strik, B.C. Berry crops: Worldwide area and production systems. In Berry Fruit: Value-Added Products for Health Promotion, 1st ed.; Zhao, Y., Ed.; CRC Press: Boca Raton, FL, USA, 2007; pp. 3–51. [Google Scholar]
  38. Farmaki, E.G.; Thomaidis, N.S. Current status of the metal pollution of the environment of Greece—A review. Glob. NEST J. 2008, 10, 366–375. [Google Scholar]
  39. Mohammed, A.S.; Kapri, A.; Goel, R. Heavy metal pollution: Source, impact and remedies. In Biomanagement of Metal-Contaminated Soils, Environmental Pollution; Khan, M.S., Zaidi, A., Goel, R., Musarrat, J., Eds.; Springer: Dordrecht, The Netherlands, 2011; Volume 20, pp. 1–29. [Google Scholar]
  40. Dietrich, K.N.; Ris, M.D.; Succop, P.A.; Berger, O.G.; Bornschein, R.L. Early exposure to lead and juvenile delinquency. Neurotoxicol. Teratol. 2001, 23, 511–518. [Google Scholar] [CrossRef]
  41. Needleman, H.L.; McFarland, C.; Ness, R.B.; Fienberg, S.E.; Tobin, M.J. Bone lead levels in adjudicated delinquents - a case control study. Neurotoxicol. Teratol. 2002, 24, 711–717. [Google Scholar] [CrossRef]
  42. Kim, S.; Moon, C.; Eun, S.; Ryu, P.; Jo, S. Identification of ASK1, MKK4, JNK, c-Jun, and caspase-3 as a signaling cascade involved in cadmium-induced neuronal cell apoptosis. Biochem. Biophys. Res. Commun. 2005, 328, 326–334. [Google Scholar] [CrossRef] [PubMed]
  43. Monroe, R.K.; Halvorsen, S.W. Cadmium blocks receptor-mediated Jak/STAT signaling in neurons by oxidative stress. Free Radic. Biol. Med. 2006, 41, 493–502. [Google Scholar] [CrossRef] [PubMed]
  44. Zhu, L.; Ji, X.J.; Wang, H.D.; Pan, H.; Chen, M.; Lu, T.J. Zinc neurotoxicity to hippocampal neurons in vitro induces ubiquitin conjugation that requires p38 activation. Brain Res. 2012, 1438, 1–7. [Google Scholar] [CrossRef] [PubMed]
  45. Caito, S.; Aschner, M. Developmental neurotoxicity of lead. Adv. Neurobiol. 2017, 18, 3–12. [Google Scholar] [PubMed]
  46. von Hoffen, L.P.; Säumel, I. Orchards for edible cities: Cadmium and lead content in nuts, berries, pome and stone fruits harvested within the inner city neighbourhoods in Berlin, Germany. Ecotoxicol. Environ. Saf. 2014, 101, 233–239. [Google Scholar] [CrossRef] [PubMed]
  47. Wisłocka, M.; Krawczyk, J.; Klink, A.; Morrison, L. Bioaccumulation of heavy metals by selected plant species from uranium mining dumps in the Sudety Mts., Poland. Pol. J. Environ. Stud. 2006, 15, 811–818. [Google Scholar]
  48. Teofilova, T.; Kodzabashev, N.; Gherasimov, S.; Markova, E. Comparative characterization of the heavy metal contents in samples from two regions in Bulgaria with different anthropogenic load. Nat. Montenegrina 2010, 9, 897–912. [Google Scholar]
  49. Shikhova, N.S. Some regularities in the accumulation of lead in urban plants (by example of Vladivostok). Contemp. Probl. Ecol. 2012, 5, 215–222. [Google Scholar] [CrossRef]
  50. Yedoyan, R.; Yedoyan, T.V. The study of heavy metals (Ni, Zn, Cu, Pb) in the vegetative organs, harvest and growing soil of potatoes, wheat, and wild blackberry. Food Environ. Saf. J. Fac. Food Eng. 2012, 11, 38–42. [Google Scholar]
  51. Vollmanova, A.; Zupka, S.; Bajcan, D.; Medvecky, M.; Daniel, J. Dangerous heavy metals in soil and small forest fruit as a result of old environmental loads. In Proceedings of the 14th International Conference on Environmental Science and Technology, Rhodes, Greece, 3–5 September 2015; pp. 698–703. [Google Scholar]
  52. Micu, L.M.; Petanec, D.I.; Iosub-Ciur, M.D.; Andrian, S.; Popovici, R.A.; Porumb, A. The heavy metals content in leave of the forest fruits (Hippophae rhamnoides and Rubus fruticosus) from the tailings dumps mining. Rev. Chim. 2016, 67, 64–68. [Google Scholar]
  53. Kekedy-Nagy, L.; Ionescu, A. Characterization and classification of tea herbs based on their metal content. Acta Univ. Sapientiae Agric. Environ. 2009, 1, 11–19. [Google Scholar]
  54. Amidžić, D.; Klarić, I.; Velić, D.; Vedrina Dragojević, I. Evaluation of mineral and heavy metal contents in Croatian blackberry wines. Czech J. Food Sci. 2011, 29, 260–267. [Google Scholar] [CrossRef] [Green Version]
  55. Smejkal, G. The Forest and the Industrial Pollution; Ceres: Bucharest, Romania, 1982; p. 195. [Google Scholar]
  56. Micu, M.O. The Influence of Pollution in the Area Copşa Mică and Its Ecological Implications. Ph.D. Thesis, Transilvania University of Brașov, Braşov, Romania, 2001. [Google Scholar]
  57. National Meteorological Agency. Catalog. Available online: http://www.meteoromania.ro/catalog/?tip=1&cod_geo=614436&cod_clasa=CLIMATOLOGICA&cod_subclasa=1|18&pas=5&tipulLor=LUNARE&pagina=2 (accessed on 22 February 2019).
  58. Stefan, K.; Raitio, H.; Bartels, U.; Fürst, A.; Rautio, P. Sampling and analysis of needles and leaves—Manual part IV. In Manual on Methods and Criteria for Harmonized Sampling, Assessment, Monitoring and Analysis of the Effects of Air Pollution on Forests; UNECE-ICP Forests Programme Co-ordinating Centre: Hamburg, Germany, 2005; pp. 1–25. [Google Scholar]
  59. Luyssaert, S.; Raitio, H.; Vervaeke, P.; Mertens, J.; Lust, N. Sampling procedure for the foliar analysis of decidous trees. J. Environ. Monit. 2002, 4, 858–864. [Google Scholar] [CrossRef] [PubMed]
  60. Djingova, F.; Kuleff, I. Instrumental techniques for trace analysis. In Trace Elements: Their Distribution and Effects in the Environment; Markert, B., Friese, K., Eds.; Elsevier Science Ltd.: London, UK, 2000; pp. 137–185. [Google Scholar]
  61. Hansen, M.D.; Nøst, T.H.; Heimstad, E.S.; Evenset, A.; Dudarev, A.A.; Rautio, A.; Myllynen, P.; Dushkina, E.V.; Jagodic, M.; Christensen, G.N.; et al. The impact of a Nickel-Copper smelter on concentrations of toxic elements in local wild food from the Norwegian, Finnish, and Russia border regions. Int. J. Environ. Res. Public Health 2017, 14, 694. [Google Scholar] [CrossRef] [PubMed]
  62. Council of Europe. Kelp, Monograph 1426, 6th ed.; Council of Europe: Strasbourg, France, 2007; Volume 2. [Google Scholar]
  63. Sun, H.; Li, L. Investigation of Distribution for Trace Lead and Cadmium in Chinese Herbal Medicines and Their Decoctions by Graphite Furnace Atomic Absorption Spectrometry. Am. J. Anal. Chem. 2011, 2, 217–222. [Google Scholar] [CrossRef]
  64. Thomsen, V.; Schatzlein, D.; Mercuro, D. Limits of Detection in Spectroscopy. Spectroscopy 2003, 18, 112–114. [Google Scholar]
  65. Chan, C.C. Analytical method validation: Principles and practices. In Pharmaceutical Manufacturing Handbook: Regulations and Quality; Gad, S.C., Ed.; John Wiley & Sons: Hoboken, NJ, USA, 2008; pp. 727–742. [Google Scholar]
  66. Frank, V.; Tölgyessy, J. The chemistry of soil. In Chemistry and Biology of Water, Air and Soil: Environmental Aspects; Tölgyessy, J., Ed.; Elsevier: Amsterdam, The Netherlands, 1993; pp. 621–698. [Google Scholar]
  67. World Health Organization. WHO Guidelines for Assessing Quality of Herbal Medicines with Reference to Contaminants and Residues; World Health Organization: Geneva, Switzerland, 2007. [Google Scholar]
  68. Kabelitz, L. Heavy metals in herbal drugs. Pharm. Ind. 1998, 60, 444–451. [Google Scholar]
  69. European Commission. Regulation (EC) No 396/2005 of the European Parliament and of the Council of 23 February 2005 on Maximum Residue Levels in or on Food and Feed of Plant and Animal Origin and Amending Council Directive 91/414/EEC; European Commission: Brussels, Belgium, 2005; pp. 1–16. [Google Scholar]
  70. Gasser, U.; Klier, B.; Kühn, A.V.; Steinhoff, B. Current findings on the heavy metal content in herbal drugs. Pharm. Sci. Notes 2009, 1, 37–50. [Google Scholar]
  71. Mohite, R.D.; Basavaiah, N.; Singare, P.U.; Reddy, A.V.R.; Singhal, R.K.; Blaha, U. Assessment of Heavy Metals Accumulation in Washed and Unwashed Leafy Vegetables Sector-26 Vashi, Navi Mumbai, Maharashtra. J. Chem. Biol. Phy. Sci. Sec. D 2016, 6, 1130–1139. [Google Scholar]
  72. Ataabadi, M.; Hoodaji, M.; Najafi, P. Assessment of washing procedure for determination some of airborne metal concentrations. Afr. J. Biotechnol. 2012, 11, 4391–4395. [Google Scholar] [CrossRef]
  73. Aksoy, A.; Åžahin, U. Elaeagnus angustifolia L. as a biomonitor of heavy metal pollution. Turk. J. Bot. 1999, 23, 83–87. [Google Scholar]
  74. Yusuf, K.A.; Oluwole, S.O. Heavy Metal (Cu, Zn, Pb) Contamination of Vegetables in Urban City: A Case Study in Lagos. Res. J. Environ. Sci. 2009, 3, 292–298. [Google Scholar] [CrossRef]
  75. Felix-Henningsen, P.; Urushadze, T.; Steffens, D.; Kalandadze, B.; Narimanidze, E. Uptake of heavy metals by food crops from highly-polluted Chernozem-like soils in an irrigation district south of Tbilisi, eastern Georgia. Agron. Res. 2010, 8, 781–795. [Google Scholar]
  76. Aghaei, A.; Khademi, H.; Eslamian, S. Comparison of Three Tree Leaves as Biomonitors of Heavy Metals Contamination in Dust, A Case Study of Isfahan. Helix Int. J. 2017, 7, 1873–1887. [Google Scholar]
  77. Hoffman, D.J.; Rattner, B.A.; Burton, G.A.; Cairns, J. Handbook of Ecotoxicology; CRC Press: Boca Raton, FL, USA, 2003; p. 1315. [Google Scholar]
  78. Alexa, B.; Cotârlea, I.; Bărbătei, R. The Pollution of Forests in Mediaş Forest District and the Ecological Restoration Done; Constant Publishing House: Sibiu, Romania, 2004; p. 145. [Google Scholar]
  79. Mantovi, P.; Bonazzi, G.; Maestri, E.; Marmiroli, N. Accumulation of copperand zinc from liquid manure in agricultural soils and crop plants. Plant Soil 2003, 50, 249–257. [Google Scholar] [CrossRef]
  80. Sadhu, A.; Upadhyay, P.; Singh, P.K.; Agrawal, A.; Ilango, K.; Karmakar, D.; Singh, G.P.I.; Dubey, G.P. Quantitative analysis of heavy metals in medicinal plants collected from environmentally diverse locations in India for use in a novel phytopharmaceutical product. Environ. Monit. Assess. 2015, 187, 542. [Google Scholar] [CrossRef] [PubMed]
  81. Nookabkaew, S.; Rangkadilok, N.; Satayavivad, J. Determination of trace elements in herbal tea products and their infusions consumed in Thailand. Agric. Food Chem. 2006, 54, 6939–6944. [Google Scholar] [CrossRef] [PubMed]
  82. World Health Organization. IARC Monographs on the Evaluation of the Carcinogenic Risk of Chemicals to Humans—Inorganic and Organic Lead Compounds; World Health Organization: Lyon, France, 2006; Volume 87. [Google Scholar]
  83. Goyer, R. Lead toxicity: Current concerns. Environ. Health Perspect. 1993, 100, 177–187. [Google Scholar] [CrossRef] [PubMed]
  84. Silbergeld, E.K.; Sauk, J.; Somerman, M.; Todd, A.; McNeill, F.; Fowler, B.; Fontaine, A.; van Buren, J. Lead in bone: Storage site, exposure source, and target organ. Neurotoxicology 1993, 14, 225–236. [Google Scholar] [PubMed]
  85. Sakai, T. Biomarkers of lead exposure. Ind. Health 2000, 38, 127–142. [Google Scholar] [CrossRef] [PubMed]
  86. Kalia, K.; Flora, S.J. Strategies for safe and effective therapeutic measures for chronic arsenic and lead poisoning. J. Occup. Health 2005, 47, 1–21. [Google Scholar] [CrossRef] [PubMed]
  87. Navas-Acien, A.; Guallar, E.; Silbergeld, E.K.; Rothenberg, S.J. Lead exposure and cardiovascular disease - a systematic review. Environ. Health Perspect. 2007, 115, 472–482. [Google Scholar] [CrossRef] [PubMed]
  88. Flora, S.J.S.; Pachauri, V.; Saxena, G. Arsenic, cadmium and lead. In Reproductive and Developmental Toxicology; Gupta, R.C., Ed.; Academic: New York, NY, USA, 2011; Volume 33, pp. 415–438. [Google Scholar]
  89. Schwartz, G.G.; Ilyasova, D.; Ivanova, A. Urinary cadmium, impaired fasting glucose, and diabetes in the NHANES III. Diabetes Care 2003, 26, 468–470. [Google Scholar] [CrossRef] [PubMed]
  90. Eum, K.D.; Lee, M.S.; Paek, D. Cadmium in blood and hypertension. Sci. Total Environ. 2008, 407, 147–153. [Google Scholar] [CrossRef] [PubMed]
  91. World Health Organization. IARC Monographs on the Evaluation of the Carcinogenic Risk of Chemicals to Humans—Beryllium, Cadmium, Mercury, and Exposures in the Glass Manufacturing Industry; World Health Organization: Lyon, France, 1993; Volume 58. [Google Scholar]
  92. World Health Organization. IARC Monographs on the Evaluation of the Carcinogenic Risk of Chemicals to Humans—Arsenic, Metals, Fibres and Dusts; World Health Organization: Lyon, France, 2012; Volume 100. [Google Scholar]
Figure 1. The sampling plots area: the circle marks the source of pollution; the squares mark the sample plots (numbered from 1 to 8 and identified with the type of site).
Figure 1. The sampling plots area: the circle marks the source of pollution; the squares mark the sample plots (numbered from 1 to 8 and identified with the type of site).
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Figure 2. The stratification of heavy metal content according to the sampled blackberry organs.
Figure 2. The stratification of heavy metal content according to the sampled blackberry organs.
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Figure 3. The variation of lead content in relation to the distance from the main source of pollution (control plot is excluded).
Figure 3. The variation of lead content in relation to the distance from the main source of pollution (control plot is excluded).
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Table 1. The spectrum of traditional uses of blackberry.
Table 1. The spectrum of traditional uses of blackberry.
ResourceUtilizationInformation Source
Part of PlantSpeciesRangeProductUses/Disease
Whole plantRubus fruticosusRomanian folk medicinetea, decoctionleukorrhea[2]
Rubus sp.Native American folk medicineextract from fruit, root, and leaveshair and fabric dye[3]
Aerial partsRubus fruticosusEuropevarioushypoglycemia[4]
StemRubus sp.Native American practicesropetransport[3]
Young shootsRubus fruticosus, R. ulmifolius SchottSardinian and Sicilian traditional medicinedecoctionmenstrual pain[5]
Rubus fruticosusRomanian folk medicinedecoctionbronchitis, diarrhea, dysentery[2]
LeavesRubus fruticosus, R. ulmifoliusSardinian and Sicilian traditional medicinefresh leaves for chewingstrengthening spongy gums[5]
Rubus fruticosusCentral Italy folk medicinemacerationcicatrizant for skin, fungal infections, skin abscesses[6]
Rubus villosus Aiton.around the worldleaves for chewingbleeding gums[7]
Rubus fruticosusEuropean folk medicinemouthwash, decoctionstrengthening spongy gums, mouth ulcers, sore throats, diarrhea, hemorrhoids[8]
FruitsRubus sp.around the worldjam, syrup, jelly, marmalade, cake stuffing, wine, liqueur, ice cream, in yoghurt, drink and chewing gum dye[3,9]
Rubus fruticosusRomanian folk medicinedecoction in lardtuberculosis[2]
wineleukorrhea
Rubus fruticosusAncient Greeksfresh fruitgout[3]
Fruits and leavesRubus fruticosusPakistani traditional medicinevariousskin diseases, itching, scabies, eczema[10]
RootsRubus villosusaround the worlddried root tea used for edema, leaves and roots used for diarrhea, enteritis, chronic appendicitis, leukorrhea, expectorant properties[7]
Table 2. Classification of sampled sites according to the location in relation to the source of pollution.
Table 2. Classification of sampled sites according to the location in relation to the source of pollution.
Type of SiteSite Description
ASite located in the main valley (where the source of pollution is found) with frontal exposure to the source of pollution (slope facing the flue-gas stack).
BSite located in the main valley (where the source of pollution is found) with tangential exposure to the source of pollution (slope not facing the flue-gas stack).
CSite located in a secondary valley with frontal exposure to the local circulation of air mass.
DSite located in a secondary valley, partially protected from the source of pollution.
Table 3. The settings for mineralization of samples.
Table 3. The settings for mineralization of samples.
Temperature (°C)145180100
Power (%)759040
Time (min)51010
Table 4. Instrumental parameters for metal determination by flame atomic absorption spectroscopy (FAAS).
Table 4. Instrumental parameters for metal determination by flame atomic absorption spectroscopy (FAAS).
Standard ConditionsElement
CdCuPbZn
Wavelength, λ (nm)228.8324.8283.3213.9
Slit width (nm)1.21.21.20.5
Hollow-cathode lamp current (mA)3334
Background correctionDeuteriumDeuteriumDeuteriumDeuterium
FlameC2H2/airC2H2/airC2H2/airC2H2/air
Fuel flow (N L/h)50506550
Table 5. Limit of detection (LOD) and limit of quantification (LOQ) of the flame atomic absorption spectroscopy method.
Table 5. Limit of detection (LOD) and limit of quantification (LOQ) of the flame atomic absorption spectroscopy method.
ParameterElement
CdZnPbCu
Linear working range (mg/L)0–10–10–10–3
Limit of detection (mg/L)0.0120.0130.0830.036
Limit of quantification (mg/L)0.0390.0420.2760.119
Table 6. Tolerable limits for heavy metals in food supplements and herbal drugs.
Table 6. Tolerable limits for heavy metals in food supplements and herbal drugs.
ReferencePb (mg/kg)Cd (mg/kg)Zn (mg/kg)Cu (mg/kg)
[68]10.00.5--
[67]10.00.3--
[62]54--
[69]---5 (berries and small fruits)
[62]50,5--
Table 7. Statistics of heavy metal content in the blackberry samples from Copsa Mică area, Romania.
Table 7. Statistics of heavy metal content in the blackberry samples from Copsa Mică area, Romania.
MetalThe Significance of the Differences between Individual Values *RangeArithmetic MeanMedianCoefficient of Variation (%)Relative Frequency (%) of Values Which Exceed the World Health Organization ThresholdThe Significance of the Differences between Blackberry Organs ** (Kruskal–Wallis Test)
tpHp
Pb (mg/kg dry weight)4.64<0.0011.67–291.3934.7220.27141.5970.514.27<0.001
Cd (mg/kg d.w.)11.49<0.0010.32–4.461.861.6157.08100.08.180.02
Zn (mg/kg d.w.)10.01<0.00110.91–193.5476.0370.2965.49-23.05<0.001
Cu (mg/kg d.w.)7.84<0.0011.23–34.088.517.1869.8983.39.340.01
* All values of heavy metals concentrations either from leaves, either from fruits or flowers were merged; ** The differences refer to the concentrations of Pb, Cd, Zn and Cu grouped according to the three blackberry organs (leaves, fruits, flowers).
Table 8. The significance of the differences between the heavy metal concentration values by some nonbiological factors.
Table 8. The significance of the differences between the heavy metal concentration values by some nonbiological factors.
Independent VariableDependent Variable
PbCdZnCu
p from Kruskal–Wallis Test (0.05 is the Threshold Value for Statistical Significance) *
Distance from source of pollution0.0050.130.360.80
Altitude0.010.310.270.07
Aspect0.080.920.590.70
Exposure to air circulation0.090.010.150.48
Year of sampling0.260.410.89-
* Kruskal-Wallis p-values for the effects of independent nonbiological factors on heavy metal concentration in blackberry organs sampled across air pollution gradients in Copșa Mică area, Romania.

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Vlad, I.A.; Goji, G.; Dinulică, F.; Bartha, S.; Vasilescu, M.M.; Mihăiescu, T. Consuming Blackberry as a Traditional Nutraceutical Resource from an Area with High Anthropogenic Impact. Forests 2019, 10, 246. https://doi.org/10.3390/f10030246

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Vlad IA, Goji G, Dinulică F, Bartha S, Vasilescu MM, Mihăiescu T. Consuming Blackberry as a Traditional Nutraceutical Resource from an Area with High Anthropogenic Impact. Forests. 2019; 10(3):246. https://doi.org/10.3390/f10030246

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Vlad, Ioana Andra, Győző Goji, Florin Dinulică, Szilard Bartha, Maria Magdalena Vasilescu, and Tania Mihăiescu. 2019. "Consuming Blackberry as a Traditional Nutraceutical Resource from an Area with High Anthropogenic Impact" Forests 10, no. 3: 246. https://doi.org/10.3390/f10030246

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