Next Article in Journal
Solid-Phase Synthesis for Constructing Thiazolotriazinone-Based Compounds Library
Previous Article in Journal
Enhanced Amitriptyline Degradation by Electrochemical Activation of Peroxydisulfate: Mechanisms of Interfacial Catalysis and Mass Transfer
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

An Assessment of the Public Health Risk Associated with Consumption of Imported Fish Based on the Intake of Essential and Harmful Elements

by
Agata Witczak
1,*,
Artur Ciemniak
1,
Beata Więcaszek
2,
Sławomir Keszka
3,
Mikołaj Protasowicki
1 and
Kamila Pokorska-Niewiada
1,*
1
Department of Toxicology, Dairy Technology and Food Storage, West Pomeranian University of Technology in Szczecin, Papieża Pawła VI 3, 71-459 Szczecin, Poland
2
Department of Hydrobiology, Ichthyology and Reproductive Biotechnology, West Pomeranian University of Technology in Szczecin, Kazimierza Królewicza 4, 71-550 Szczecin, Poland
3
Border Veterinary Inspection Post in the Port of Szczecin, 70-606 Szczecin, Poland
*
Authors to whom correspondence should be addressed.
Molecules 2025, 30(18), 3836; https://doi.org/10.3390/molecules30183836
Submission received: 5 August 2025 / Revised: 12 September 2025 / Accepted: 19 September 2025 / Published: 22 September 2025
(This article belongs to the Special Issue Chemical Analysis of Pollutant in the Environment)

Abstract

Despite its many important health benefits, fish consumption is associated with a growing risk of toxicity due to increasing levels of environmental pollution. Therefore, this study compared the potential risks to human health associated with the consumption of imported fish and locally produced fish, which may be contaminated with toxic elements. A selection of the most commonly consumed fish in Poland, imported and domestic, was assayed for 11 trace elements in muscle tissue using ICP-AES, CV-AAS and GF-AAS. In general, the levels of toxic elements decreased according to the following sequence: As > Hg > Cd > Pb; however, the values of lead were slightly higher than those of cadmium in cod. All imported fish contained significantly more cadmium than the Polish species. Our assessment of EDI, THQ, TTHQ, TWI, PTMI and BMDL01 indicates that typical levels of consumption of fish do not pose a risk based on the assumed intake. The highest TTHQ was observed in tilapia, but it did not exceed 0.169. This was well below the acceptable value. Hence, the consumption of these fish does not appear to entail any non-carcinogenic or carcinogenic health risks. In addition, the estimated consumer risk parameters indicate no risk to consumer health in the short term; however, the presence of these elements may present a long-term hazard due to the potential for bioaccumulation. Continuous monitoring of trace element concentrations, especially toxic ones, is recommended for the protection of communities in both local and global contexts. Our findings provide a clearer picture of the health risk associated with the consumption of fish in the Polish market.

1. Introduction

For health-conscious consumers, one of the most desirable foods is fish. The chemical composition of raw fish is as follows: 0–0.5% carbohydrates, 16–21% protein, 1.2–1.5% minerals, 0.2–25% fat and 66–81% water. The muscle tissue is a source of long-chain omega-3 polyunsaturated fatty acids (n-3 LC-PUFA), amino acids, fat-soluble vitamins (A and D) and essential elements such as calcium, zinc and iron. As these compounds are frequently absent from diets leading to various health problems, even in developed countries [1,2,3], dieticians often recommend increasing the share of fish in the diet, both for preventive purposes and for treating diet-related diseases, such as diabetes [4,5]. Although fish are a valuable source of nutrients, they also absorb pollutants from their environment (polycyclic aromatic hydrocarbons, polychlorinated biphenyls, dioxins, microplastics, lead, cadmium, arsenic and mercury). Many of these pollutants demonstrate high persistence, biomagnification, bioaccumulation and non-biodegradability in food chains; as such, they can have considerable negative effects on aquatic ecosystems [3,6,7,8]. After consumption, the compounds acquired from fish can accumulate in the tissues and internal organs of the human body, with various positive and negative effects: The essential trace elements are needed for the activity of various enzymes, while the toxic elements can act as cofactors, initiators or promoters of various diseases. Considering the adverse, and even harmful, effects of certain elements on the human body, food safety organizations, such as the FAO, are introducing oral reference doses for most heavy metals and metalloids in food. The US EPA (Environmental Protection Agency) has developed an Integrated Risk Assessment program aimed at protecting human health from contamination from various sources [9,10,11]. Various factors are also introduced to determine consumer risk associated with consuming contaminated products (e.g., EDI, EWI, THQ, TTHQ, PTWI, BMDL, etc.). This complicates the analysis of results and contributes to inconsistent health risk assessments. Furthermore, combinations of elements can have synergistic or antagonistic effects, potentially resulting in a significantly higher impact [12,13,14].
Many authors have addressed the problem of trace element contamination in fish sold in local markets around the world [15,16,17,18]. However, the greatest concern is caused by imported fish, especially from Asia. Concerns primarily revolve around farming methods, feed quality and the use of substances that enhance fish production, which are banned in Europe. The most frequently mentioned species is the pangasius, whose farming is associated with the Mekong River, one of the most polluted rivers in the world [19,20]. In response to growing concerns about the safety of pangasius species originating from Vietnam, the European Commission in 2023, citing the applicable regulations [21], ruled that pangasius species originating from Vietnam did not pose a risk to food safety in the EU [22].
Geochemical properties and the cleanliness of ecosystems can influence the bioaccumulation of metals in fish [23,24,25]. No consistent pattern of metal content was observed among species or across locations.
One of the leading exporters of food and fish products is China. It provides approximately 260,000 tons of frozen fish fillets and fish products to Poland per year, placing the country among its leading European importers [26,27]. These fish include Nile tilapia (Orechromis niloticus niloticus), panga (Pangasius pangasius), Pacific cod (Gadus macrocephalus), pollock (Pollachius virens) and yellow-leafed sole (Limanda aspera). These imports are primarily driven by the lower cost of fish from the region.
The main aim of this study was to compare the levels of essential and harmful elements in samples of fish species imported to Poland with those caught in the country. All fish were frozen. The findings were used to determine the extent to which an edible portion of 100 g of fish product covers the recommended daily intake of essential trace elements. The study also aimed to assess the risk to human health associated with regular consumption of these species, which is an important consideration for consumer health.

2. Results and Discussion

Fish meat could be considered a cornerstone of a healthy human diet, with its consumption lowering the risk of coronary cardiac disease, hypertension and cancer. This is mainly due to its nutrient content, with the key elements presented in Table 1.
The lowest zinc content (0.94 mg/kg w.w.) was found in panga, and the highest (8.40 mg/kg w.w.) was found in rainbow trout (Table 1). The Polish trout, salmon and bream were found to contain significantly higher zinc levels than imported species (Appendix A).
Zinc is essential for the catalytic activity of many enzymes and plays an important role in enhancing immune function, protein and DNA synthesis, supporting wound healing and enabling cell signaling and division [28]. Both excess zinc and its deficiency in the diet can have serious health consequences. In Poland, the recommended intake is 8 mg/day for women and 11 mg/day for men [29]; similar values are recommended by the National Institutes of Health (NIH) [28]. Of all the fish analyzed, a portion of rainbow trout covers over 3% (for women) and almost 2.5% (for men) of these values (Table 2).
The nickel content in the analyzed fish did not exceed 0.37 mg/kg w.w., with significantly lower amounts being found in all imported fish compared to the Polish fish (Table 1). Nickel is not one of the most important elements in the human body, and its deficiency is rarely observed, as it is present in almost all types of food. However, lower levels can increase perinatal mortality and reduce growth rate and cause problems with iron absorption [30].
Table 1. Mean content (x ± SD) of trace elements in imported (A) and Polish (B) fish fillets (mg/kg w.w.). Comparison of the content of selected elements in the analyzed fish species with previous data.
Table 1. Mean content (x ± SD) of trace elements in imported (A) and Polish (B) fish fillets (mg/kg w.w.). Comparison of the content of selected elements in the analyzed fish species with previous data.
Nile TilapiaPangaAlaska
Pollock
HakeYellowfin SolePacific CodFlounderMackerelRainbow TroutSalmonBream
Mean, mean ± SD, or range of analyzed elements * (mg/kg w.w.)
Zn3.89 ± 0.74
2.59–5.38
6.28 ± 0.39 [26]
58.3 ± 0.6 [31]
14.0 ** [32]
1.31–3.9 [33]
3.6–11.0 [34]
2.08 ± 1.13
0.94–5.92
3.57 ± 0.02 [35]
2.31 ± 0.65
1.11–3.41
3.44 ** [36]
2.18 ± 0.30
1.77–2.80
3.34 ± 0.38 [37]
3.21 ** [36]
3.30 ** [38]
2.72 ± 0.23
2.34–3.03
3.19 ± 0.45
2.63–3.72
0.35 ± 0.01 [39]
3.47 ± 0.32
3.14–3.88
2.41 ± 0.88 [40]
4.62 ± 0.71 [41]
1.83 ± 0.54
1.38–2.49
0.27 ± 0.005 [39]
2.0 ± 0.3 [42]
8.74 ** [36]
8.95 ± 4.30 [40]
66.8 ± 1.6 [31]
7.54 ± 1.00
6.10–8.40
5.6 ± 1.9 [26]
4.7–8.6 [43]
16.98 ** [44]
4.86 ± 0.76
4.18–5.58
1.7–9.9 [43]
1.96 ± 0.04 [45]
3.20 ** [36]
5.60 ± 0.54
5.06–6.25
2.3–3.5 [46]
Ni0.073 ± 0.06
0.03–0.37
<0.01–0.07 [34]
5.75 ± 1.04 [26]
0.03 ± <0.01 [35]
0.08 ± 0.03
0.04–0.14
0.10–0.17 [47]
0.08 ± 0.03
0.02–0.13
0.090 ** [36]
0.08 ± 0.06
<LOD–0.17
<0.05 ** [38]
0.035 ** [36]
0.09 ± 0.04
0.05–0.14
0.10 ± 0.03
0.10–0.11
0.10 ± 0.01 [39]
0.33 ± 0.02
0.31–0.35
0.02 ± 0.02 [41]
0.04 ± 0.06 [40]
0.33 ± 0.03
0.30–0.36
0.070 ** [36]
0.82 ± 0.15 [42]
0.16 ± 0.12 [40]
0.03 ± 0.01 [39]
0.04 ± <0.01 [31]
0.27 ± 0.02
0.25–0.30
2.38 ± 0.28 [26]
5.25 ** [44]
0.33 ± 0.02
0.31–0.36
0.038 ** [36]
0.32 ± 0.02
0.29–0.34
<LOD–0.13 [46]
Fe1.84 ± 0.29
1.04–2.29
<LOQ–91.5 [48]
2.4–17.0 [34]
28.0 ** [32]
1.14 ± 0.39
0.31–1.78
9.35 ± 0.03 [35]
1.45 ± 0.45
0.96–2.58
1.35 ** [36]
1.42 ± 0.20
1.06–1.70
1.35 ** [36]
1.7 ** [38]
1.32 ± 0.42
0.85–1.77
1.53 ± 0.15
1.31–1.62
2.37 ± 0.10 [39]
1.73 ± 0.28
1.35–1.96
3.52 ± 1.51
[40,41]
1.61 ± 0.35
1.17–1.90
8.98 ** [36]
9.22 ± 0.11 [40,42]
3.16 ± 0.12 [39]
1.57 ± 0.08
1.48–1.67
40.02 ** [44]
3.09–5.59 [43]
1.48 ± 0.10
1.35–1.60
1.87 ** [36]
2.6 ± 0.21 [45]
2.46–11.90 [43]
1.41 ± 0.10
1.32–1.56
1.3–1.5 [46]
Mn0.12 ± 0.03
0.08–0.21
<LOQ–17.7 [48]
0.05–1.41 [33]
0.40 ± 0.02 [26]
1.0 ** [32]
0.07 ± 0.03
0.02–0.12
0.14–0.20 [47]
0.22 ± 0.01 [35]
0.05 ± 0.01
0.02–0.07
0.059 ** [36]
0.05 ± 0.01
0.02–0.07
0.09 ** [38]
0.054 ** [36]
0.06 ± 0.03
0.02–0.08
0.06 ± 0.01
0.05–0.07
0.12 ± 0.01
0.11–0.14
0.19 ± 0.12 [41]
0.07 ± 0.09 [40]
0.07 ± 0.01
0.06–0.07
0.16 ** [36]
0.46 ± 0.11 [42]
0.03 ± 0.03 [40]
0.08 ± 0.01
0.07–0.09
1.37 ± 0.12 [26]
0.25–0.36 [43]
0.09 ± 0.01
0.08–0.09
0.110 ** [36]
0.14–0.87 [43]
0.09 ± <0.01
0.09–0.10
0.11–0.39 [46]
Cr0.08 ± 0.03
0.04–0.13
0.007–0.8 [34]
3.6 ± 0.45 [39]
0.03 ± 0.06 [35]
2.79 ± 0.95 [49]
0.09 ± 0.04
0.04–0.17
0.08 ± 0.04
0.02–0.15
0.22 ** [36]
0.09 ± 0.03
0.04–0.13
0.10 ** [38]
0.114 ** [36]
0.08 ± 0.01
0.06–0.10
0.08 ± 0.01
0.07–0.09
0.08 ** [50]
0.1 ± <0.01
0.09–0.10
0.32 ± 0.04 [40]
0.01 ± 0.01
0.08–0.11
0.18 ** [36]
0.87 ± 0.11 [42]
0.44 ± 0.04 [40]
0.03 ± <0.01 [31]
0.13 ± 0.04
0.10–0.17
3.14 ** [44]
0.13 ± <0.01
0.012–0.013
0.314 ** [36]
0.11 ± <0.01
0.012–0.014
0.02–0.11 [46]
Cu0.15 ± 0.07
0.06–0.33
<LOQ–42.9 [48]
0.23–0.47 [33]
0.2–9.0 [34]
1.6 ** [32]
0.19 ± 0.04
0.09–0.25
0.16–0.23 [47]
0.64 ± 0.01 [35]
0.20 ± 0.10
0.07–0.39
0.227 ** [36]
0.13 ± 0.04
0.08–0.19
0.12 ± 0.04 [37]
0.16 ** [38]
0.136 ** [36]
0.15 ± 0.02
0.12–0.18
0.20 ± 0.01
0.9–0.21
0.127 ± 0.01 [39]
0.19 ± 0.02
0.02–0.22
0.33 ± 0.16 [41]
0.19 ± 0.02
0.17–0.21
1.03 ** [36]
0.72 ± 0.02 [42]
0.28 ± 0.003 [39]
0.21 ± 0.01
0.20–0.23
2.06 ** [44]
0.19–0.55 [43]
0.21 ± 0.01
0.20–0.21
0.580 ** [36]
0.98 ± 0.02 [45]
0.12–0.90 [43]
0.21 ± <0.01
0.20–0.21
0.11–0.24 [46]
Al0.24 ± 0.05
0.13–0.32
0.3–8.7 [34]
0.14 ± 0.03
0.09–0.19
0.24 ± 0.09
0.10–0.42
2.53 ** [36]
0.19 ± 0.06
0.01–0.28
0.834 ** [36]
0.18 ± 0.03
0.1–0.22
0.14 ± 0.02
0.11–0.15
0.12 ± 0.01
0.11–0.13
1.72 ± 0.58 [41]
0.13 ± 0.01
0.12–0.14
1.16 ** [36]
0.11 ± 0.02
0.08–0.13
1.89–2.75 50]
0.11 ± 0.03
0.07–0.15
0.529 ** [36]
0.23–3.72 [43]
0.11 ± 0.01
0.10–0.13
Li0.03 ± 0.02
0.01–0.08
0.004–0.013 [34]
0.04 ± 0.02
0.01–0.08
0.03 ± 0.01
0.01–0.05
0.014 ** [36]
0.02 ± 0.01
0.01–0.04
0.017 ** [36]
0.04 ± 0.02
0.02–0.07
0.04 ± 0.02
0.02–0.06
0.05 ± 0.01
0.04–0.06
0.017 ± 0.007 [41]
0.05 ± 0.02
0.04–0.07
0.018 ** [36]
0.06 ± 0.01
0.04–0.07
0.06 ± 0.01
0.01–0.07
0.005 ** [36]
0.05 ± 0.01
0.04–0.06
0.01–0.05 [46]
As0.21 ± 0.08
0.11–0.39
0.01–0.06 [34]
<0.001 ** [35]
0.24 ± 0.08
0.11–0.39
<0.017 ** [47]
0.17 ± 0.05
0.08–0.26
0.18 ± 0.05
0.09–0.29
7.86 ± 2.83 [37]
0.23 ± 0.02
0.20–0.27
0.16 ± 0.03
0.12–0.19
1.59 ** [50]
0.21 ± 0.07
0.12–0.28
5.29 ± 1.87 [40]
0.13 ± 0.03
0.10–0.16
2.51 ± 0.75 [40]
<LOD [31]
0.14 ± 0.01
0.13–0.15
0.16 ± 0.05
0.09–0.22
0.10 ± 0.03
0.05–0.12
0.0–0.3 [51]
Pb0.026 ± 0.009
0.013–0.047
<LOQ–0.3 [48]
0.34–2.7 [33]
0.001–0.041 [34]
0.094 ± 0.055 [35]
3.49 ± 1.86 [49]
0.024 ± 0.010
0.010–0.014
0.12–0.17 [47]
0.019 ± 0.005
0.011–0.031
0.010 ** [36]
0.017 ± 0.004
0.012–0.024
0.016 ± 0.005 [37]
0.002 ± 0.001 [52]
0.010 ** [36]
0.013 ± 0.04
0.007–0.016
0.011 ± 0.002
0.010–0.014
0.024 ** [50]
0.202 ± 0.01 [39]
0.010 ± 0.003
0.125–0.276
0.053 ± 0.052 [41]
0.021 ± 0.059 [40]
0.008 ± 0.003
0.103–0.163
0.009 ** [36]
0.122 ± 0.021 [42]
0.075 ± 0.024 [40] 0.457 ± 0.016 [39]
0.046 ± 0.004 [31]
0.009 ± 0.002
0.129–0.152
<LOD [44]
0.017–0.035 [43]
0.010 ± 0.003
0.093–0.222
0.005 ** [36]
<0.01–0.02 [43]
0.011 ± 0.004
0.053–0.123
0–0.115 [7,51]
0–0.02 ** [46]
Cd0.040 ± 0.013
0.011–0.073
0.09–1.17 [33]
<0.0025 [34]
0.051 ± 0.004 [26]
0.003 ± <0.001 [31]
0.40 ± 0.01 [49]
0.043 ± 0.011
0.026–0.072
<0.006 [47]
0.032 ± 0.007
0.020–0.048
0.036 ± 0.008
0.021–0.048
0.01 ± 0.01 [37]
0.003 ± 0.001 [52]
0.032 ± 0.010
0.013–0.045
0.010 ± 0.006
0.005–0.018
<0.002 [53]
0.030 ± 0.001
[39]
0.011 ± 0.002
0.008–0.012
0.009 ± 0.006
[41]
0.002 ± <0.001
[40]
0.011 ± 0.004
0.006–0.016
0.007 ± 0.002 [42]
0.003 ± 0.003 [40] 0.488 ± 0.012 [39]
<LOD [31]
0.013 ± 0.004
0.008–0.017
0.007 ± 0.001 [26]
<LOD [44]
<LOD–0.012 [43]
0.020 ± 0.006
0.012–0.027
<LOD–0.008 [43]
0.019 ± 0.004
0.016–0.024
<LOD–0.060 [7,52]
<LOD–0.003 [46]
Hg0.055 ± 0.082
0.025–0.058
<LOD–0.16 [48]
0.001–0.16 [34]
0.054 ± 0.010
0.031–0.070
0.10–0.69 [54]
0.002–0.018 [47]
0.043 ± 0.008
0.028–0.058
0.037 ** [55]
0.040 ± 0.011
0.031–0.070
0.44 ± 0.06 [56]
0.023 ± 0.002 [52]
0.041 ** [55]
0.045 ± 0.005
0.036–0.051
0.031 ± 0.009
0.022–0.043
0.049 ** [55]
0.128 ** [50]
0.058 ± 0.002
0.055–0.060
0.036 ± 0.017 [41]
0.016 ± 0.017 [40]
0.056 ** [55]
0.037 ± 0.004
0.033–0.040
0.152 ± 0.096 [40]
0.058 ** [55]
0.035 ± 0.003
0.033–0.038
0.010 ** [55]
0.041 ± 0.002
0.039–0.042
0.029 ± 0.007
0.023–0.039
<LOD–0.391 [7,51]
<LOD–0.01 [46]
Bold: The present findings, * The given value depends on the information given in the manuscripts of other authors, ** No information on standard deviation.
Table 2. Coverage of the daily requirement for micronutrients (%) according to Polish regulations [29].
Table 2. Coverage of the daily requirement for micronutrients (%) according to Polish regulations [29].
Zn
Mean ± SD
(Range)
Fe
Mean ± SD
(Range)
Mn
Mean ± SD
(Range)
Cu
Mean ± SD
(Range)
Women Men Women Men Women Men Men/Women
Polish
Recommendations
RDA
8.0 mg/day
RDA
11.0 mg/day
RDA
18.0 mg/day
RDA
10.0 mg/day
AI
1.8 mg/day
AI
2.3 mg/day
RDA
0.9 mg/day
Nile tilapia1.7 ± 0.3
(1.1–2.3)
1.2 ± 0.2
(0.8–1.7)
0.36 ± 0.06
(0.20–0.44)
0.64 ± 0.10
(0.36–0.80)
0.23 ± 0.06
(0.17–0.41)
0.18 ± 0.05
(0.13–0.32)
0.58 ± 0.28
(0.24–1.27)
Pacific cod1.4 ± 0.2
(1.1–1.6)
1.0 ± 0.1
(0.8–1.2)
0.30 ± 0.03
(0.25–0.31)
0.53 ± 0.05
(0.46–0.56)
0.12 ± 0.02
(0.10–0.14)
0.09 ± 0.02
(0.08–0.11)
0.78 ± 0.05
(0.72–0.82)
Panga0.9 ± 0.5
(0.4–2.6)
0.7 ± 0.4
(0.3–1.9)
0.22 ± 0.08
(0.06–0.34)
0.40 ± 0.14
(0.11–0.62)
0.14 ± 0.06
(0.03–0.23)
0.11 ± 0.05
(0.03–0.18)
0.72 ± 0.15
(0.36–0.96)
Alaska pollock1.0 ± 0.3
(0.5–1.5)
0.7 ± 0.2
(0.4–1.1)
0.28 ± 0.09
(0.19–0.50)
0.50 ± 0.16
(0.33–0.90)
0.10 ± 0.02
(0.04–0.14)
0.08 ± 0.02
(0.03–0.11)
0.76 ± 0.36
(0.26–1.49)
Yellowfin sole1.2 ± 0.1
(1.0–1.3)
0.9 ± 0.1
(0.7–1.0)
0.26 ± 0.08
(0.16–0.34)
0.46 ± 0.15
(0.29–0.61)
0.11 ± 0.06
(0.04–0.16)
0.08 ± 0.04
(0.03–0.13)
0.57 ± 0.08
(0.45–0.69)
North-Pacific hake0.9 ± 0.1
(0.8–1.2)
0.7 ± 0.1
(0.6–0.9)
0.27 ± 0.04
(0.21–0.33)
0.49 ± 0.07
(0.37–0.59)
0.10 ± 0.03
(0.04–0.13)
0.08 ± 0.02
(0.03–0.10)
0.49 ± 0.15
(0.32–0.72)
Flounder1.5 ± 0.1
(1.7–1.7)
1.1 ± 0.1
(1.0–1.2)
0.33 ± 0.05
(0.26–0.38)
0.60 ± 0.10
(0.47–0.68)
0.22 ± 0.03
(0.21–0.26)
0.17 ± 0.02
(0.16–0.21)
0.74 ± 0.07
(0.67–0.84)
Mackerel0.8 ± 0.2
(0.6–1.1)
0.6 ± 0.2
(0.4–0.8)
0.31 ± 0.07
(0.23–0.37)
0.56 ± 0.12
(0.41–0.66)
0.13 ± 0.01
(0.12–0.14)
0.10 ± 0.01
(0.10–0.11)
0.73 ± 0.06
(0.67–0.81)
Rainbow trout3.3 ± 0.4
(2.7–3.7)
2.4 ± 0.3
(1.9–2.7)
0.30 ± 0.02
(0.29–0.32)
0.55 ± 0.03
(0.52–0.58)
0.16 ± 0.01
(0.14–0.16)
0.12 ± 0.01
(0.11–0.13)
0.83 ± 0.05
(0.79–0.90)
Salmon2.1 ± 0.3
(1.8–2.4)
1.5 ± 0.2
(1.3–1.8)
0.29 ± 0.02
(0.26–0.31)
0.52 ± 0.03
(0.47–0.56)
0.17 ± 0.01
(0.17–0.18)
0.13 ± 0.01
(0.13–0.14)
0.79 ± 0.02
(0.77–0.81)
Bream2.4 ± 0.2
(2.2–2.7)
1.8 ± 0.2
(1.6–2.0)
0.27 ± 0.02
(0.25–0.30)
0.49 ± 0.04
(0.46–0.54)
0.18 ± <0.01
(0.17–0.18)
0.14 ± 0.01
(0.14–0.14)
0.79 ± 0.02
(0.78–0.81)
SD—standard deviation; RDA—recommended dietary allowance [29]; AI—adequate intake [29].
The iron content ranged from 0.31 to 2.29 mg/kg w.w. and did not differ significantly between the analyzed fish species (Table 1, Appendix A). Iron is an essential component of hemoglobin and myoglobin and occurs in the diet as heme and non-heme forms; the heme form is found only in meat and seafood [29]. Our data indicate that a portion of the tested fish will cover about 0.3% of the iron requirement in women and a little over 0.6% in men (Table 2).
Significantly higher levels of manganese were observed in tilapia and flounder than in the other species (Table 1). Manganese is a cofactor of many enzymes, including manganese superoxide dismutase, pyruvate carboxylase and arginase [53]. Consuming a portion of these fish will cover approximately 0.2% of the requirement in both women and men (Table 2).
Additionally, significantly higher amounts of chromium were found in rainbow trout than in the other species (Table 1). Chromium takes part in the metabolism of carbohydrates, lipids and proteins by enhancing the action of insulin [57].
The copper content varied widely between 0.062 and 0.386 mg/kg w.w. (Table 1), with no statistically significant differences observed between species. Copper is a cofactor of various enzymes involved, inter alia, in energy production, iron metabolism, neuropeptide activation, connective tissue synthesis and neurotransmitter synthesis [58].
The aluminum content ranged from 0.072 to 0.416 mg/kg, with two imported species (tilapia and pollock) containing significantly more aluminum than the others (Table 1). The highest lithium content was found in salmon, and the lowest in hake; the levels in both species differed significantly (p < 0.05) from those found in the others (Table 1).
The concentration of arsenic in Nile tilapia sold in Bangkok markets was 0.50 mg/kg [59], while in this study, it was half as high. For arsenic and mercury, only single significant relationships were found between species.
Fish are a potential source of mercury in the human diet. Therefore, the European Commission has set the maximum level of this element in muscle at 0.50 mg/kg [21]. This study indicates that the tested fish are safe in this regard. Considering the safety of sensitive individuals—children, pregnant women, breastfeeding mothers and the elderly—special attention should be paid to elevated levels of this element, even if they are within the permissible range. However, there are reports by Rodriguez et al. [54] and Ferrantelli et al. [60] indicating elevated mercury levels in pangasius fillets. Moreover, Ferantelli et al. [60] indicate that elevated mercury levels in pangasius may result from the origin, breeding, feeding, storage and processing of these fish. They also note that the quality of water used during fillet freezing may contribute to the presence of high Hg levels.
For lead, significantly higher concentrations were observed in the tissues of pollock and pangasius (Appendix A). Similarly, lead accumulation in Baltic cod and rainbow trout in the present study was almost 10 times higher than the results reported by Staszowska et al. [61] for the same fish species.
Despite the low levels of toxic elements found in local fish in this study, significant levels of lead have been reported in rainbow trout (from Polish farms) and cod from the Baltic Sea [18]. This confirms the need for ongoing monitoring of fish contamination with toxic elements.
All imported fish contained significantly more cadmium than the Polish species. While toxic elements were found in the analyzed fish, their concentrations were much lower than the maximum limits given by the FAO/WHO and the European Union for heavy metals in fish [10,21,28]. Cadmium levels in bream from Slovakia were three times lower (0.0007 mg/kg) than those analyzed in this study, while mercury concentrations in fish from Slovakia were five times higher (0.155 mg/kg). It is important to note that this is the Zemplínska Šírava reservoir, one of the most polluted in Europe, due in part to the presence of polychlorinated biphenyls [62].
In general, the levels of toxic elements decreased according to the following sequence: As > Hg > Cd > Pb; however, the values of lead were slightly higher than those of cadmium in cod (Table 1). The differences in metal accumulation among species could be related to their unique physiology and ecological niche [63].
Based on the results, it can be concluded that the diversity of origins of fish used for human consumption significantly influences their composition, including heavy metal content. The differences in the chemical composition of the meat of the above-mentioned fish species are certainly due to their diverse origins. Breeding conditions vary dramatically, depending on the species’ sensitivity to water parameters.
It is widely believed that eating fish can play a significant part in maintaining good health. Fish meat consists of high-quality protein containing all the essential amino acids, as well as a number of polyunsaturated omega-3 fatty acids, vitamins and minerals, particularly zinc and iron. However, many of these essential trace elements are only available in the head, bones and viscera, and hence are only acquired when consuming small fish whole [64,65]. Fish are generally consumed in insufficient quantities to ensure a significant share of the daily requirement for trace elements (Table 2). Current recommendations for fish consumption vary across Europe and range from 100 to 482 g/person/week for adults [3,66,67]. However, most countries recommend higher fish consumption, i.e., at least two portions per week. The Polish Institute of Food and Nutrition [68] and the EUMOFA report [69] that Poland is characterized by low fish consumption among the European Union countries. Alarmingly, young people in Poland are reported to consume only 13.4 g of fish per week, with the main reason being a fear of contamination [67].
Our assessment of EDI, THQ, TTHQ, TWI, PTMI and BMDL01 indicates that typical levels of consumption of fish do not pose a risk based on the assumed intake (Table 3 and Table 4, Figure 1). Previous studies based on the same indicators have also found there to be negligible risk, e.g., in Brazil [70] and in Iran (Hg, Cd and Pb) [71]. A study of fish from Lake Temsah (Suez Canal region, Egypt) did not indicate any significant potential risk to health (EDI < 1) [8], nor did a study of the consumption of rainbow trout from Samsun fish markets (Turkey) (TTHQ = 0.084) [72]. However, there are regions where fish consumption may pose a risk of contamination with toxic elements. An Iranian study indicated a risk of mercury, cadmium and lead poisoning among fish caught from the Caspian Sea region (TTHQ = 0.975), and mercury poisoning in fish caught in the Persian Gulf and Oman (THQ = 1.347) [71]. It has also been found that fish commonly purchased in shops in Nigeria, Osun State, may contain toxic levels of cadmium for both adults (EDI = 1.708) and children (EDI = 7.471) [73].
Information about food potentially contaminated with toxic elements should be provided to consumers to prevent negative health consequences. Government authorities responsible for food safety should regularly monitor levels of toxic element contamination in newly introduced food products. Following European Commission guidelines, special attention should also be paid to groups of people at increased risk of poisoning from toxic elements. This includes children, pregnant women, breastfeeding mothers and the elderly. Expanding information campaigns and preventing misinformation about fish from foreign markets is also recommended. It should be emphasized that knowledge of the location of the waters from which the fish were caught, and the environmental conditions prevailing in those locations is crucial. It is also important to pay attention to the characteristics of the fish, its diet and lifespan, as toxic elements have the potential to bioaccumulate and bioconcentrate.

3. Materials and Methods

3.1. Characteristics of the Tested Material

The research material included eleven species of fish. Six species were imported from China and Vietnam, viz. Nile tilapia (Orechromis niloticus niloticus), panga (Pangasius pangasius), Alaska pollock (Gadus chalcogrammus), North-Pacific hake (Merluccius productus), yellowfin sole (Limanda aspera) and Pacific cod (Gadus macrocephalus). In addition, five species were purchased from various batches in retail trade in Poland, Szczecin, viz. flounder (Platichthys flesus), mackerel (Scomber scombrus), rainbow trout (Oncorhynchus mykiss), salmon (Salmo salar) and bream (Abramis brama). Individual batches of fish (the number of batches for each fish species and the number of samples are in Table 5) came from different producers (the list of producers is known to the authors). To ensure representativeness, the batches of fish for testing were selected randomly. Each batch weighed about 2.5 kg. A total of 790 samples, 10 from each batch, were tested. The characteristics of the collected material are presented in Table 5.
All fish, both domestic and foreign, were purchased gutted. They were not euthanized in the authors’ laboratory. Therefore, ethics committee approval was not required.

3.2. Determination of Elements

Muscle samples weighing 1 g ± 0.001 g were ground and mineralized in a CEM MDS-2000 microwave oven (SpectraLab Scientific Inc., Markham, ON, Canada) with the addition of 3 mL of EMSURE, 65% nitric acid (Merck KGaA, Darmstadt, Germany). After mineralization, the samples were filtered and transferred to polyethylene bottles using deionized water. The bottles were weighed and filled with deionized water (0.05 μS cm−1; Barnstead™ Gen-Pure™ Pro, Thermo Scientific, Erlangen, Germany) to a mass of 25.0 g ± 0.1 g. The levels of Zn, Ni, Fe, Mn, Cr, Cu, Al and Li were determined using the ICP-AES method (Jobin Yvon JY-24, Longjumeau, France) fitted with a Meinhard (Singapore) TR 50-C1 nebulizer. The generator operated with an output power of 1000 W; frequency, 40.68 MHz; and the plasma gas and the nebulizer gas were argon with flow rates of 12.0 L/min., nebulizer flow rate of 0.7 L/min and sample solution flow rate of 1.0 mL/min.
The arsenic content was also determined with an ICP-AES using the hydride generation system. The solutions of the analyzed samples and the NaBH4 and HCl reagents were introduced simultaneously using two dual-channel peristaltic pumps [74].
The following wavelengths were used for the analyses (nm): Zn—213.9; Ni—231.6; Fe—238.2; Mn—257.6; Cr—357.9; Cu—324.7; Al—396.2; Li—670.8 and As—193.8.
Cadmium and lead contents were determined by GF-AAS with Zeeman background correction (4110 ZL Perkin Elmer, Waltham, MA, USA). While in the furnace, the samples underwent five temperature stages from 110 to 2500 °C, with atomization at 1600 °C (Pb) and 1550 °C (Cd). The following settings were applied: slit width, 0.7 mm; lamp current, 10 mA (Pb) and 4 mA (Cd).
Mercury (Hg) content was determined by CV-AAS using a Bacharach Coleman MAS-50 mercury analyzer (Bacharach Inc., Pittsburgh, PA, USA) at a wavelength of λ = 253.7 nm. All samples were analyzed in three analytical replicates.
The precision of the analytical method was verified with the MODAS-3 certified reference material (Consortium “MODAS”, Warsaw, Poland). The quality was verified based on LOD, LOQ and recovery (Table 6).

3.3. Evaluation of Element Concentrations in Relation to Nutrient Requirement

To determine the extent to which the daily consumption of the analyzed fish met the demand for the studied nutrients, the findings were compared with the recommended values for the Polish population. These are as follows: zinc and iron—8 mg/day for women and 11 mg/day for men; copper—0.9 mg/day, lithium—1 mg/day, manganese (AI)—1.8 mg/day for women and 2.3 mg/day for men [29]. Referring to the most recent Statistical Yearbook of Agriculture, it was assumed that an adult weighing 70 kg consumes 13.4 g/day of fish [75].

3.4. Assessment of Concentrations of Harmful Elements in Relation to Standards and Risk Factors

To assess the possible health effects resulting from the consumption of imported fish, the EDI, EWI and THQ (Equations (1)–(3)) of the component nutrients were calculated [76,77]. These indicators determine potential non-cancer risks to human health. A THQ score above 1 indicates potential systemic effects. If the EDI ≥ RfD, the exposed human population will experience a health risk.
EDI (Estimated Daily Intake, Equation (1))
E D I = M S × C B W μ g / k g   b w d a y
MS—the daily food ingestion rate in grams per day (13.4 g/day) [75]; C—fresh weight concentration of trace elements in fish (mg/kg); BW—reference body weight (70 kg).
THQ (Target Hazard Quotient, Equation (2))
T H Q = E F × E D × M S × C R f D × B W × A T × 10 3
EF—exposure frequency to trace elements (365 days/year); ED—exposure duration (70 years); MS—food ingestion rate, 13.4 g/day [75]; C—concentration of trace element in fish (mg/kg); RfD—oral reference dose of trace element (mg/kg BW/day) (Zn = 0.3; Ni = 0.02; Fe = 0.7; Mn = 0.14; Cr = 0.003; Cu = 0.04; Li = 0.02; Cd = 0.001) [76,78]; BW—reference body weight of 70 kg; AT—averaged exposure time to non-carcinogenic trace elements (365 days × 70 years).
TTHQ (Total Target Hazard Quotient), i.e., total THQ of all elements analyzed (Equation (3))
T T H Q = T H Q Z n + T H Q N i + T H Q F e + T H Q M n + T H Q C r + T H Q C u + T H Q A l + T H Q L i + T H Q A s + T H Q C d + T H Q ( H g )
TWI (Tolerable Weekly Intake, Equation (4))
%   T W I = E D I × 7 × 100 T W I
where the TWI value for Cd = 2.5 μg/kg BW per week.
Due to the damage caused to human health, the committee JECFA [79] established a PTMI for cadmium of 25 μg/kg BW (Equation (5)).
PTMI (Provisional Tolerable Monthly Intake, Equation (5))
%   P T M I = E D I × 30 × 100 P T M I
where the PTMI value for cadmium = 25 μg/kg BW per month [16]
The committee JECFA [79] also determined a BMDL value for Pb of BMDL01—1.5 μg/kg/BW per day for adult consumers (Equation (6)).
BMDL (Benchmark Dose Lower Confidence Limit, Equation (6))
% B M D L 0.1 = E D I × 100 B M D L 0.1
where the BMDL0.1 for Pb, for effects on systolic blood pressure in adults, =1.50 μg/kg BW per day.

3.5. Statistical Analysis

The descriptive statistics are presented as mean ± SD (in tables). All statistical analyses were performed using the Statistica 13.0 software package (Statsoft, Cracow, Poland). Analysis of variance with ANOVA test was preceded by Levene’s test of homogeneity of variance and the Kologorov–Smirnov test of distribution normality. The arithmetical mean, standard deviation, and the significance of differences (Duncan’s test) were calculated. The level of significance was assumed to be α = 0.05. The correlation between the parameters was determined using Pearson’s correlation statistics.

4. Conclusions

Following WHO and EU guidelines, the authors suggest that the prevailing belief in Poland that some imported fish are contaminated with heavy metals may be unfounded. Although some differences in mineral content between imported and local fish were observed in this study, all metals appear to be present at safe levels, including toxic metals. On the other hand, although the risk factors are <1, the relatively higher levels of cadmium in imported species merit explicit discussion as a potential long-term risk. Similarly, mercury and arsenic levels in fish muscle vary significantly depending on the catch location and species. Disseminating such information could influence consumer choices and contribute to a greater interest in local fish species. Furthermore, it would encourage caution when trying local delicacies in areas with higher levels of environmental pollution. However, it should be noted that the results obtained are only partially conclusive, as the conclusions are based solely on information provided by vendors (catchment area). To assess the actual risk of metal contamination in fish, other factors must be taken into account, such as the age and sex of the fish, living conditions, pollution of the aquatic environment and diet, which also play a role in the bioaccumulation of elements.

Author Contributions

Conceptualization, A.W. and B.W.; methodology, A.C.; research material, S.K. and B.W.; validation, K.P.-N. and A.W.; investigation, A.C.; data curation, K.P.-N.; writing—original draft preparation, K.P.-N. and A.C.; writing—review and editing, A.W. and K.P.-N.; visualization, K.P.-N.; supervision, A.W. and M.P. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Data are contained within the article.

Acknowledgments

The authors are very grateful to Krzysztof Formicki, Dean of the Faculty of Food Sciences and Fisheries, West Pomeranian University of Technology, Szczecin, Poland, for support.

Conflicts of Interest

The authors declare no conflicts of interest.

Abbreviations

The following abbreviations are used in this manuscript:
AIAdequate Intake
BMDLBenchmark Dose Lower Confidence Limit
CV-AASCold Vapor Atomic Absorption Spectrometry
EDIEstimated Daily Intake
EUMOFAEuropean Observatory on the Market in Fisheries and Aquaculture
FAO/WHOFood and Agriculture Organization (FAO) and the World Health Organization (WHO)
GF-AASGraphite Furnace–Atomic Absorption Spectrometry
ICP-AESInductively Coupled Plasma Atomic Emission Spectrophotometry
JECFAJoint FAO/WHO Expert Committee on Food Additives
LODLimits of Detection
LOQLimits of Quantification
NaBH4Sodium borohydride
NIHNational Institutes of Health
PTMIProvisional Tolerable Monthly Intake
RDARecommended Dietary Allowance
RfDReference Dose
SDStandard Deviation
THQTarget Hazard Quotient
TTHQTotal Target Hazard Quotient
TWITolerable Weekly Intake
w.w.Wet weight

Appendix A

Table A1. Significant differences (marked in bold) in the content of elements between individual fish species (p < 0.05).
Table A1. Significant differences (marked in bold) in the content of elements between individual fish species (p < 0.05).
Zn
Fish Species
Nile TilapiaPacific CodPangaAlaska PollockYellowfin SoleNorth-Pacific HakeFlounderMackerelRainbow TroutSalmon
Pacific cod0.1420
Panga0.00020.0252
Alaska pollock0.00100.06420.6285
Yellowfin sole0.01520.29330.19920.3674
North-Pacific hake0.00040.03820.82410.76660.2612
Flounder0.35300.52910.00480.01640.11270.0083
Mackerel0.00000.00620.58620.33940.07990.47420.0008
Rainbow trout0.00000.00000.00000.00000.00000.00000.00000.0000
Salmon0.03010.00040.00000.00000.00000.00000.00280.00000.0000
Bream0.00020.00000.00000.00000.00000.00000.00000.00000.00000.0975
Ni
Fish species
Nile tilapiaPacific codPangaAlaska pollockYellowfin soleNorth-Pacific hakeFlounderMackerelRainbow troutSalmon
Pacific cod0.3042
Panga0.90500.3355
Alaska pollock0.89910.34890.9988
Yellowfin sole0.49530.67770.54030.5566
North-Pacific hake0.81590.37990.89420.90040.6007
Flounder0.00000.00000.00000.00000.00000.0000
Mackerel0.00000.00000.00000.00000.00000.00000.9770
Rainbow trout0.00000.00000.00000.00000.00000.00000.00980.0091
Salmon0.00000.00000.00000.00000.00000.00000.93600.95420.0087
Bream0.00000.00000.00000.00000.00000.00000.48800.48620.04090.4910
Fe
Fish species
Nile tilapiaPacific codPangaAlaska pollockYellowfin soleNorth-Pacific hakeFlounderMackerelRainbow troutSalmon
Pacific cod0.1579
Panga0.00160.0904
Alaska pollock0.08440.70570.1676
Yellowfin sole0.02300.36410.36410.5568
North-Pacific hake0.06460.61420.20390.87360.6424
Flounder0.55860.36210.00970.22170.08030.1797
Mackerel0.26200.70670.04320.48170.22050.40900.5410
Rainbow trout0.20490.84380.06420.59050.28840.50830.44470.8360
Salmon0.10950.81070.13330.86820.47410.76210.27190.56530.6843
Bream0.06350.60580.19620.85990.64000.97560.17690.40210.50060.7511
Mn
Fish species
Nile tilapiaPacific codPangaAlaska pollockYellowfin soleNorth-Pacific hakeFlounderMackerelRainbow troutSalmon
Pacific cod0.0004
Panga0.00390.5127
Alaska pollock0.00000.53330.2293
Yellowfin sole0.00010.65060.29900.8204
North-Pacific hake0.00000.57740.25480.92100.8849
Flounder0.77340.00110.00820.00010.00020.0001
Mackerel0.00220.61730.83990.29530.37310.32410.0051
Rainbow trout0.02030.23650.54140.08380.11770.09590.03640.4478
Salmon0.06290.10240.28650.02800.04300.03320.09980.22670.5983
Bream0.09350.06620.20830.01550.02530.01890.13710.15940.46530.7986
Cr
Fish species
Nile tilapiaPacific codPangaAlaska pollockYellowfin soleNorth-Pacific hakeFlounderMackerelRainbow troutSalmon
Pacific cod0.8799
Panga0.56920.6407
Alaska pollock0.97220.89480.5716
Yellowfin sole0.97720.89560.57760.9930
North-Pacific hake0.58000.63960.97410.57550.5862
Flounder0.39020.44990.73200.39330.39720.7211
Mackerel0.42710.48620.78150.42810.43360.77290.9280
Rainbow trout0.00990.01300.03950.00970.01010.03960.07280.0668
Salmon0.01460.01860.05190.01410.01480.05280.08870.08430.8721
Bream0.09070.10830.22490.08910.09200.22670.32860.31770.35730.4105
Cu
Fish species
Nile tilapiaPacific codPangaAlaska pollockYellowfin soleNorth-Pacific hakeFlounderMackerelRainbow troutSalmon
Pacific cod0.2130
Panga0.29640.7273
Alaska pollock0.26120.86930.8319
Yellowfin sole0.91800.18850.28240.2338
North-Pacific hake0.49430.06270.10560.08290.5291
Flounder0.28770.80470.89840.91960.26050.0952
Mackerel0.29120.77530.93420.88480.26810.09860.9564
Rainbow trout0.12850.73780.52120.63970.11060.03140.58640.5613
Salmon0.18680.90430.65750.79340.16320.05230.73250.70330.8055
Bream0.18980.92170.67100.80660.16660.05350.74560.71700.79640.9754
Al
Fish species
Nile tilapiaPacific codPangaAlaska pollockYellowfin soleNorth-Pacific hakeFlounderMackerelRainbow troutSalmon
Pacific cod0.0008
Panga0.00080.9534
Alaska pollock0.96970.00070.0008
Yellowfin sole0.05580.14370.13530.0520
North-Pacific hake0.06500.12450.12390.05630.8903
Flounder0.00010.62440.60210.00010.06320.0511
Mackerel0.00030.80340.77470.00030.10070.08420.7823
Rainbow trout0.00000.45920.43700.00000.03680.02810.75880.5904
Salmon0.00010.50770.48490.00010.04400.03420.82520.64660.9148
Bream0.00010.50680.48650.00010.04280.03350.82840.64580.90560.9837
Li
Fish species
Nile tilapiaPacific codPangaAlaska pollockYellowfin soleNorth-Pacific hakeFlounderMackerelRainbow troutSalmon
Pacific cod0.8431
Panga0.71300.8418
Alaska pollock0.59420.49530.4105
Yellowfin sole0.83620.98070.84920.4995
North-Pacific hake0.16510.12840.10010.34600.1332
Flounder0.08180.11180.13680.02690.10730.0018
Mackerel0.08540.11740.14990.02820.11500.00190.9928
Rainbow trout0.02910.04330.05930.00740.04250.00030.62220.6033
Salmon0.00340.00580.00910.00050.00570.00000.23660.22120.4334
Bream0.19150.24610.28370.07760.23620.00820.61260.63100.35280.1065
As
Fish species
Nile tilapiaPacific codPangaAlaska pollockYellowfin soleNorth-Pacific hakeFlounderMackerelRainbow troutSalmon
Pacific cod0.2318
Panga 0.43630.0561
Alaska pollock0.28220.84160.0777
Yellowfin sole0.60390.09970.75470.1316
North-Pacific hake0.37330.67360.11900.79700.1907
Flounder0.99280.23870.42170.29810.58410.4005
Mackerel0.04500.37820.00550.31180.01280.22380.0469
Rainbow trout0.10470.61610.01810.52190.03690.39640.10870.6591
Salmon0.22360.98870.05460.84100.09680.66960.23360.39090.6310
Bream0.00620.11740.00040.09110.00110.05740.00660.43600.25240.1243
Pb
Fish species
Nile tilapiaPacific codPangaAlaska pollockYellowfin soleNorth-Pacific hakeFlounderMackerelRainbow troutSalmon
Pacific cod0.0009
Panga0.50720.0076
Alaska pollock0.08770.10900.2533
Yellowfin sole0.00420.63040.02430.2258
North-Pacific hake0.05260.17410.17320.76020.3246
Flounder0.00070.90720.00600.09350.57170.1532
Mackerel0.00010.58390.00140.03750.33460.06900.6459
Rainbow trout0.00030.72900.00300.06060.44100.10530.80020.8080
Salmon0.00060.85970.00520.08600.53980.14300.94160.68080.8427
Bream0.00120.91840.00910.12130.67900.18850.83840.53290.67060.7943
Cd
Fish species
Nile tilapiaPacific codPangaAlaska pollockYellowfin soleNorth-Pacific hakeFlounderMackerelRainbow troutSalmon
Pacific cod0.0000
Panga0.51820.0000
Alaska pollock0.22940.00060.0782
Yellowfin sole0.22640.00060.07640.9522
North-Pacific hake0.55330.00000.24510.49150.4852
Flounder0.00000.91100.00000.00070.00070.0000
Mackerel0.00000.91560.00000.00070.00080.00010.9887
Rainbow trout0.00000.68350.00000.00200.00200.00020.73630.7438
Salmon0.00150.15310.00010.04300.03860.00840.16550.17330.2628
Bream0.00130.16430.00010.04260.04160.00800.17050.18330.26280.9407
Hg
Fish species
Nile tilapiaPacific codPangaAlaska pollockYellowfin soleNorth-Pacific hakeFlounderMackerelRainbow troutSalmon
Pacific cod0.0539
Panga0.04790.0001
Alaska pollock0.96650.05500.0510
Yellowfin sole0.68510.02220.09370.6767
North-Pacific hake0.64200.12160.02010.65550.4199
Flounder0.00670.00000.41790.00700.01740.0019
Mackerel0.31760.31200.00360.32210.18130.53340.0002
Rainbow trout0.18420.49390.00100.18750.09500.34060.00000.6924
Salmon0.69590.10950.02340.70580.46010.91930.00240.49920.3141
Bream0.02520.72200.00000.02600.00910.06580.00000.19430.33040.0576

References

  1. EFSA (European Food Safety Authority). Dietary Reference Values for nutrients Summary report. EFSA Support. Publ. 2017, 2017, e15121. [Google Scholar] [CrossRef]
  2. Kotlęga, D.; Peda, B.; Palma, J.; Zembroń-Łacny, A.; Gołąb-Janowska, M.; Masztalewicz, M.; Nowacki, P.; Szczuko, M. Free Fatty Acids Are Associated with the Cognitive Functions in Stroke Survivors. Int. J. Environ. Res. Public Health 2021, 18, 6500. [Google Scholar] [CrossRef] [PubMed]
  3. Noreen, S.; Hashmi, B.; Aja, P.M.; Atoki, A.V. Health benefits of fish and fish by-products—A nutritional and functional perspective. Front. Nutr. 2025, 12, 1564315. [Google Scholar] [CrossRef] [PubMed]
  4. Skałecki, P.; Florek, M.; Kędzierska-Matysek, M.; Poleszak, E.; Domaradzki, P.; Kaliniak-Dziura, A. Mineral and trace element composition of the roe and muscle tissue of farmed rainbow trout (Oncorhynchus mykiss) with respect to nutrient requirements: Elements in rainbow trout products. J. Trace Elem. Med. Biol. 2020, 62, 126619. [Google Scholar] [CrossRef]
  5. Abera, B.; Adimas, M. Health benefits and health risks of contaminated fish consumption: Current research outputs, research approaches, and perspectives. Heliyon 2024, 10, e33905. [Google Scholar] [CrossRef]
  6. Herrera-Herrera, C.; Fuentes-Gandara, F.; Zambrano-Arévalo, A.; Higuita, F.B.; Hernández, J.P.; Marrugo-Negrete, J. Health Risks Associated with Heavy Metals in Imported Fish in a Coastal City in Colombia. Biol. Trace Elem. Res. 2019, 190, 526–534. [Google Scholar] [CrossRef]
  7. Stanek, M.; Janicki, B. Distribution of heavy metals in the meat, gills and liver of common bream (Abramis brama L.) caught from Żnińskie Duże Lake (Poland). J. Elem. 2016, 21, 1141–1150. [Google Scholar] [CrossRef]
  8. Younis, A.M.; Hanafy, S.; Elkady, E.M.; Alluhayb, A.H.; Alminderej, F.M. Assessment of health risks associated with heavy metal contamination in selected fish and crustacean species from Temsah Lake, Suez Canal. Sci. Rep. 2024, 14, 18706. [Google Scholar] [CrossRef]
  9. Dourson, M.L. Let the IRIS Bloom:Regrowing the integrated risk information system (IRIS) of the U.S. Environmental Protection Agency. Regul. Toxicol. Pharmacol. RTP 2018, 97, A4–A5. [Google Scholar] [CrossRef]
  10. USEPA. Integrated Risk Information System (IRIS). United States Environmental Protection. Available online: https://www.epa.gov/iris (accessed on 13 April 2025).
  11. Díaz, G.E.E.; Orellana, F.R.S.; Vega, R.E.Y.; Valdiviezo-Rivera, J.S.; Ríos-Touma, B.P. Trace Metal Contamination in Commercial Fish from the Ecuadorian Amazon: Preliminary Health Risk Assessment in a Local Market. Fishes 2025, 10, 392. [Google Scholar] [CrossRef]
  12. Jamil Emon, F.; Rohani, M.F.; Sumaiya, N.; Tuj Jannat, M.F.; Akter, Y.; Shahjahan, M.; Abdul Kari, Z.; Tahiluddin, A.B.; Goh, K.W. Bioaccumulation and Bioremediation of Heavy Metals in Fishes—A Review. Toxics 2023, 11, 510. [Google Scholar] [CrossRef]
  13. Radwan, M.; Abbas, M.M.M.; Afifi, M.A.M.; Mohammadein, A.; Al Malki, J.S. Fish Parasites and Heavy Metals Relationship in Wild and Cultivated Fish as Potential Health Risk Assessment in Egypt. Front. Environ. Sci. 2022, 10, 890039. [Google Scholar] [CrossRef]
  14. Canli, M.; Atli, G. The relationships between heavy metal (Cd, Cr, Cu, Fe, Pb, Zn) levels and the size of six Mediterranean fish species. Environ. Pollut. 2003, 121, 129–136. [Google Scholar] [CrossRef] [PubMed]
  15. Varol, M.; Kaçar, E. Analysis of metal(loid)s and minerals in tissues of fish from a reservoir on the Euphrates River by ICP-MS/MS: Health risks, nutritional benefits and correlations with fish size. Food Chem. Toxicol. 2025, 204, 115652. [Google Scholar] [CrossRef]
  16. Dogruyol, H.; Can Tunçelli, İ.; Özden, Ö.; Erkan, N.; Karakulak, F.S. Bioaccumulation of Mercury, Cadmium, Lead, and Arsenic in Whiting and Tub Gurnard From the Sea of Marmara: Implications for Human Health. Food Sci. Nutr. 2025, 13, e70370. [Google Scholar] [CrossRef]
  17. Yildiz, H.; Bayrakli, B.; Altuntas, M.; Celik, I. Concentrations, selenium-mercury balance, and potential health risk assessment for consumer of whiting (Merlangius merlangus euxinus L., 1758) from different regions of the southern Black Sea. Environ. Sci. Pollut. Res. Int. 2023, 30, 65059–65073. [Google Scholar] [CrossRef]
  18. Jarosz-Krzemińska, E.; Mikołajczyk, N.; Adamiec, E. Content of toxic metals and As in marine and freshwater fish species available for sale in EU supermarkets and health risk associated with its consumption. J. Sci. Food Agric. 2021, 101, 2818–2827. [Google Scholar] [CrossRef] [PubMed]
  19. Nghia, N.D.; Lunestad, B.T.; Trung, T.S.; Son, N.T.; Maage, A. Heavy metals in the farming environment and in some selected aquaculture species in the Van Phong Bay and Nha Trang Bay of the Khanh Hoa Province in Vietnam. Bull. Environ. Contam. Tox. 2009, 82, 75–79. [Google Scholar] [CrossRef] [PubMed]
  20. Sakultantimetha, A.; Bangkedphol, S.; Lauhachinda, N.; Homchan, U.; Songsasen, A. Environmental fate and transportation of cadmium, lead and manganese in a river environment using the EPISUITE Program. Agric. Nat. Resour. 2009, 43, 620–627. [Google Scholar]
  21. Commission Regulation (EC). No 1881/2006 of 19 December 2006 Setting Maximum Levels for Certain Contaminants in FOODSTUFFS. Available online: https://eur-lex.europa.eu/legal-content/EN/TXT/PDF/?uri=CELEX:32006R1881 (accessed on 28 April 2025).
  22. Zambelli, S. Question for Written Answer E-000134/23 to the Commission. 2023. Available online: https://www.europarl.europa.eu/RegData/questions/reponses_qe/2023/000134/P9_RE(2023)000134_EN.pdf (accessed on 10 May 2025).
  23. Ristea, E.; Pârvulescu, O.C.; Lavric, V.; Oros, A. Assessment of Heavy Metal Contamination of Seawater and Sediments Along the Romanian Black Sea Coast: Spatial Distribution and Environmental Implications. Sustainability 2025, 17, 2586. [Google Scholar] [CrossRef]
  24. Siddique, A.B.; Al Helal, A.S.; Patindol, T.A.; Lumanao, D.M.; Longatang, K.J.G.; Rahman, M.A.; Catalvas, L.P.A.; Tulin, A.B.; Shaibur, M.R. Assessment of Heavy Metal Contamination and Ecological Risk in Urban River Sediments: A Case Study from Leyte, Philippines. Pollutants 2025, 5, 7. [Google Scholar] [CrossRef]
  25. Özçelik, Ş.; Tekin-Özan, S. Evaluation of selected heavy metal and selenium pollution in water and sediments of Lake Eğirdir (Isparta/Türkiye) using statistical analysis and pollution indices. Oceanol. Hydrobiol. Stud. 2024, 53, 186–207. [Google Scholar] [CrossRef]
  26. Łuszczek-Trojnar, E.; Błoniarz, P.; Winiarski, B.; Drąg-Kozak, E.; Popek, W. Comparison of cadmium, zinc, manganese and nickel concentrations in fillets of selected species of food fish. Sci. Ann. Pol. Soc. Anim. Prod. 2015, 11, 75–84. (In Polish) [Google Scholar]
  27. Witczak, A.; Harada, D.; Aftyka, A.; Cybulski, J. Endocrine-disrupting organochlorine xenobiotics in fish products imported from Asia—An assessment of human health risk. Environ. Monit. Assess. 2021, 193, 132. [Google Scholar] [CrossRef]
  28. NIH (National Institutes of Health). Available online: https://ods.od.nih.gov/factsheets/Zinc-HealthProfessional/#en (accessed on 14 July 2025).
  29. Rychlik, E.; Stoś, K.; Woźniak, A.; Mojska, H. Normy Żywienia dla Populacji Polski; Narodowy Instytut Zdrowia Publicznego PZH—Państwowy Instytut Badawczy: Warszawa, Poland, 2024; ISBN 978-83-65870-78-0. (In Polish) [Google Scholar]
  30. Begum, W.; Rai, S.; Banerjee, S.; Bhattacharjee, S.; Mondal, M.H.; Bhattarai, A.; Saha, B. A comprehensive review on the sources, essentiality and toxicological profile of nickel. RSC Adv. 2022, 12, 9139. [Google Scholar] [CrossRef]
  31. Gaidam, M.B.; Sadauki, M.A.; Dauda, A.B.; Idris, B.M.G.; Yagana, A.; Ali, J.; Bichi, A.H. Analysis if heavy metals in some fresh and marine water fish species sold in Damaturu Metropolies. LSIJ 2023, 1, 29–37. [Google Scholar]
  32. Bayissa, T.N.; Geerardyn, M.; Gobena, S.; Vanhauteghem, D.; Du Laing, G.; Wakijra Kabeta, M.; Janssens, G.P.J. Impact of species and their edible parts on the macronutrient and mineral composition of fish from the same aquatic environment, the Gilgel Gibe Reservoir, Ethiopia. J. Anim. Physiol. Anim. Nutr. 2022, 106, 220–228. [Google Scholar] [CrossRef]
  33. El-Sappah, A.H.; Seif, M.M.; Abdel-Kader, H.H.; Soaud, S.A.; Elhamid, M.A.A.; Abdelghaffar, A.M.; El-Sappah, H.H.; Sarwar, H.; Yadav, V.; Maitra, P.; et al. Genotoxicity and Trace Elements Contents Analysis in Nile Tilapia (Oreochromis niloticus) Indicated the Levels of Aquatic Contamination at Three Egyptian Areas. Front. Vet. Sci. 2022, 9, 818866. [Google Scholar] [CrossRef] [PubMed]
  34. Simukoko, C.K.; Mwakalapa, E.B.; Bwalya, P.; Muzandu, K.; Berg, V.; Mutoloki, S.; Polder, A.; Lyche, J.L. Assessment of heavy metals in wild and farmed tilapia (Oreochromis niloticus) on Lake Kariba, Zambia: Implications for human and fish health. Food Addit. Contam. Part A Chem. Anal. Control Expo. Risk Assess. 2022, 39, 74–91. [Google Scholar] [CrossRef] [PubMed]
  35. Artar, E.; Olgunoglu, M.P.; Olgunoglu, I.A. Mineral Contents and Fatty Acids Compositions of Fillets of Female and Male Pangas (Pangasıus hypophthalmus, Sauvage 1878) Cultured in Turkey. Prog. Nutr. 2022, 24, e2022056. [Google Scholar] [CrossRef]
  36. Guérin, T.; Chekri, R.; Vastel, C.; Sirot, V.; Volatier, J.L.; Leblanc, J.C.; Noël, L. Determination of 20 trace elements in fish and other seafood from the French market. Food Chem. 2011, 127, 934–942. [Google Scholar] [CrossRef]
  37. Bergés-Tiznado, M.E.; Bojórquez-Sánchez, C.; Acosta-Lizárraga, L.G.; Zamora-García, O.G.; Márquez-Farías, J.F.; Páez-Osuna, F. Tissue dynamics of potential toxic elements in the Pacific hake (Merluccius productus): Distribution and the public health risk assessment. Environ. Sci. Pollut. Res. 2022, 29, 77945–77957. [Google Scholar] [CrossRef]
  38. Antovic, I.; Sukovic, D.; Andjelic, S.; Svrkota, N. Heavy metals and radionuclides in muscles of Fish species in the south Adriatic—Montenegro. RAP Conference Proceedings. Bull. Vet. Inst. Pulawy 2019, 4, 589–595. [Google Scholar] [CrossRef]
  39. Ogundiran, M.A.; Adewoye, S.O.; Ayandiran, T.A.; Dahunsi, S. Heavy metal, proximate and microbial profile of some selected commercial marine fish collected from two markets in south western Nigeria. Afr. J. Biotechnol. 2014, 13, 1147–1153. [Google Scholar] [CrossRef]
  40. Copat, C.; Grasso, A.; Fiore, M.; Cristaldi, A.; Zuccarello, P.; Signorelli, S.S.; Conti, G.O.; Ferrante, M. Trace elements in seafood from the Mediterranean sea: An exposure risk assessment. Food Chem. Toxicol. 2018, 115, 13–19. [Google Scholar] [CrossRef]
  41. Pokorska, K.; Protasowicki, M.; Bernat, K.; Kucharczyk, M. Content of metals in flounder, Platichthys flesus L., and Baltic herring, Clupea harengus membras L., from the southern Baltic Sea. Arch. Pol. Fish. 2012, 20, 51–53. [Google Scholar] [CrossRef]
  42. Demirezen, D.; Uruç, K. Comparative study of trace elements in certain fish, meat and meat products. Meat Sci. 2006, 74, 255–260. [Google Scholar] [CrossRef]
  43. Rajkowska-Myśliwiec, M.; Pokorska-Niewiada, K.; Witczak, A.; Balcerzak, M.; Ciecholewska-Juśko, D. Health benefits and risks associated with element uptake from grilled fish and fish products. J. Sci. Food Agric. 2022, 102, 957–964. [Google Scholar] [CrossRef] [PubMed]
  44. Al-Dahhan, W.H.; Ahmad, S.M.; Mansour, O.; Jebali, J.; Yousif, E.A. Determination of Heavy Metals in Some Types of Imported Fish from Local Markets. ANJS 2022, 25, 14–19. [Google Scholar] [CrossRef]
  45. Atanassoff, A.; Nikolov, G.; Staykov, Y.; Zhelyazkov, G.; Sirakov, I. Proximate and mineral analysis of Atlantic Salmon (Salmo salar) cultivated in Bulgaria. Biotechnol. Anim. Husb. 2013, 29, 571–579. [Google Scholar] [CrossRef]
  46. Lidwin-Kaźmierkiewicz, M.; Pokorska, K.; Protasowicki, M.; Rajkowska, M.; Wechterowicz, Z. Content of selected essential and toxic metals in meat of freshwater fish from West Pomerania, Poland. Pol. J. Food Nutr. Sci. 2009, 59, 219–224. [Google Scholar]
  47. Kilercioglu, S.; Kosker, A.R.; Evliyaoglu, E. Public health risk assessments associated with heavy metal levels in panga fish fillets imported from Vietnam. Int. J. Agric. Environ. Food Sci. 2022, 6, 568–578. [Google Scholar] [CrossRef]
  48. Al-Sisi, M.; Elhawat, N.; Alshaal, T.; Eissa, F. Assessment of trace element occurrence in Nile Tilapia from the Rosetta branch of the River Nile, Egypt: Implications for human health risk via lifetime consumption. Ecotoxicol. Environ. Saf. 2024, 285, 117079. [Google Scholar] [CrossRef] [PubMed]
  49. Ekweozor, I.K.E.; Ugbomeh, A.P.; Ogbuehi, K.A. Zn, Pb, Cr and Cd concentrations in fish, water and sediment from the Azuabie Creek, Port Harcourt. J. Appl. Sci. Environ. Manag. 2017, 21, 87–91. [Google Scholar] [CrossRef]
  50. Burger, J.; Gochfeld, M.; Shukla, T.; Jeitner, C.; Burke, S.; Donio, M.; Shukla, S.; Snigaroff, R.; Snigaroff, D.; Stamm, T.; et al. Heavy Metals in Pacific Cod (Gadus macrocephalus) from the Aleutians: Location, Age, Size, and Risk. J. Toxicol. Environ. Health Part A 2007, 70, 1897–1911. [Google Scholar] [CrossRef] [PubMed]
  51. Szkoda, J.; Żmudzki, J.; Nawrocka, A.; Kmiecik, M. Toxic elements in free-living freshwater fish, water and sediments in Poland. Bull. Vet. Inst. Pulawy 2014, 58, 589–595. [Google Scholar] [CrossRef]
  52. Djedjibegovic, J.; Marjanowic, A.; Tahirovic, D.; Caklovica, K.; Turalic, A.; Lugusic, A.; Omeragic, E.; Sober, M.; Caklovica, F. Heavy metals in commercial fish and seafood products and risk assessment in adult population in Bosnia and Herzegovina. Sci. Rep. 2020, 10, 13238. [Google Scholar] [CrossRef]
  53. Li, L.; Yang, X. The Essential Element Manganese, Oxidative Stress, and Metabolic Diseases: Links and Interactions. Oxidative Med. Cell. Longev. 2018, 2018, 7580707. [Google Scholar] [CrossRef]
  54. Rodríguez, M.; Gutiérrez, Á.J.; Rodríguez, N.; Rubio, C.; Paz, S.; Martín, V.; Revert, C.; Hardisson, A. Assessment of mercury content in Panga (Pangasius hypophthalmus). Chemosphere 2018, 196, 53–57. [Google Scholar] [CrossRef]
  55. Brodziak-Dopierała, B.; Fischer, A. Analysis of the Mercury Content in Fish for Human Consumption in Poland. Toxics 2023, 11, 717. [Google Scholar] [CrossRef]
  56. Acosta-Lizárraga, L.G.; Bergés-Tiznado, M.E.; Bojórquez-Sánchez, C.; Osuna-Martínez, C.C.; Páez-Osuna, F. Bioaccumulation of mercury and selenium in tissues of the mesopelagic fish Pacific hake (Merluccius productus) from the northern Gulf of California and the risk assessment on human health. Chemosphere 2020, 255, 126941. [Google Scholar] [CrossRef]
  57. Balali-Mood, M.; Naseri, K.; Tahergorabi, Z.; Khazdair, M.R.; Sadeghi, M. Toxic Mechanisms of Five Heavy Metals: Mercury, Lead, Chromium, Cadmium, and Arsenic. Front. Pharmacol. 2021, 12, 643972. [Google Scholar] [CrossRef]
  58. Wysocka, D.; Snarska, A.; Sobiech, P. Copper—An essential micronutrient for calves and adult cattle. J. Elem. 2019, 24, 101–110. [Google Scholar] [CrossRef]
  59. Sirisangarunroj, P.; Monboonpitak, N.; Karnpanit, W.; Sridonpai, P.; Singhato, A.; Laitip, N.; Ornthai, N.; Yafa, C.; Judprasong, K. Toxic Heavy Metals and Their Risk Assessment of Exposure in Selected Freshwater and Marine Fish in Thailand. Foods 2023, 12, 3967. [Google Scholar] [CrossRef]
  60. Ferrantelli, V.; Giangrosso, G.; Cicero, A.; Naccari, C.; Macaluso, A.; Galvano, F.; D’Orazio, N.; Arcadipane, G.E.; Naccari, F. Evaluation of mercury levels in Pangasius and Cod fillets traded in Sicily (Italy). Food Addit. Contam. Part A 2012, 29, 1046–1051. [Google Scholar] [CrossRef]
  61. Staszowska A, Skałecki P, Florek M and Litwińczuk A, Impact of fish species and their living environment on concentration of lead and estimated intake thereof from muscle tissue. Food Sci. Technol. Qual. 2013, 20, 60–68. (In Polish) [CrossRef]
  62. Brázová, T.; Syrota, Y.; Oros, M.; Uhrovič, D. Heavy Metal Accumulation in Freshwater Fish: The Role of Species, Age, Gender, and Parasites. Bull. Environ. Contam. Toxicol. 2025, 114, 92. [Google Scholar] [CrossRef] [PubMed]
  63. Gholamhosseini, A.; Shiry, N.; Soltanian, S.; Banaee, M. Bioaccumulation of metals in marine fish species captured from the northern shores of the Gulf of Oman, Iran. Reg. Stud. Mar. Sci. 2021, 41, 101599. [Google Scholar] [CrossRef]
  64. Kawarazuka, N.; Béné, C. The potential role of small fish species in improving micronutrient deficiencies in developing countries: Building evidence. Public Health Nutr. 2011, 14, 1927–1938. [Google Scholar] [CrossRef]
  65. Phogat, S.; Dahiya, T.; Jangra, M.; Kumari, A.; Kumar, A. Nutritional Benefits of Fish Consumption for Humans: A Review. Int. J. Environ. Clim. Change 2022, 12, 1443–1457. [Google Scholar] [CrossRef]
  66. Lofstedt, A.; de Roos, B.; Fernandes, P.G. Less than half of the European dietary recommendations for fish consumption are satisfied by national seafood supplies. Eur. J. Nutr. 2021, 60, 4219–4228. [Google Scholar] [CrossRef] [PubMed]
  67. Utri-Khodadady, Z.; Skolmowska, D.; Głąbska, D. Determinants of Fish Intake and Complying with Fish Consumption Recommendations—A Nationwide Cross-Sectional Study among Secondary School Students in Poland. Nutrients 2024, 16, 853. [Google Scholar] [CrossRef]
  68. Jarosz, M.; Rychlik, E.; Stoś, K.; Charzewska, J. Nutrition Recommendations for Polish Population. In Normy Żywienia Dla Populacji Polski i ich Zastosowanie; NIZP-PZH; Narodowy Instytut Zdrowia Publicznego—Państwowy Zakład Higieny: Warsaw, Poland, 2020; Volume 83, pp. 1–465. (In Polish) [Google Scholar]
  69. EUMOFA—European Market Observatory for Fisheries and Aquaculture. The EU Fish Market, 2023rd ed.; Publications Office of the European Union: Luxemburg, 2023; Available online: https://eumofa.eu/documents/20124/35668/EFM2023_EN.pdf/95612366-79d2-a4d1-218b-8089c8e7508c?t=1699541180521 (accessed on 10 May 2025).
  70. Ferreira, W.Q.; Alves, B.S.; Dantas, K. Health risk assessment attributed the consumption of fish and seafood in Belém, Pará, Brazil. J. Trace Elem. Miner. 2023, 6, 100103. [Google Scholar] [CrossRef]
  71. Hashempour-Baltork, F.; Jannat, B.; Tajdar-Oranj, B.; Aminzare, M.; Sahebi, H.; Mirza Alizadeh, A.; Hosseini, H. A comprehensive systematic review and health risk assessment of potentially toxic element intakes via fish consumption in Iran. Ecotoxicol. Environ. Saf. 2023, 1, 114349. [Google Scholar] [CrossRef]
  72. Yardım, Ö.; Bat, L. Human Health Risk Assessment of Heavy Metals Via Dietary Intake of Rainbow Trout from Samsun Fish Markets. J. Anatol. Environ. Anim. Sci. 2020, 5, 260–263. [Google Scholar] [CrossRef]
  73. Adebiyi, F.M.; Ore, O.T.; Owolafe, O.S. Human health risk assessment of potentially toxic metals in fish (Cynoglossus sp.) commonly consumed in Nigeria. Discov. Toxicol. 2024, 1, 7. [Google Scholar] [CrossRef]
  74. Rajkowska-Myśliwiec, M.; Ciemniak, A.; Karp, G. Arsenic in Rice and Rice-Based Products with Regard to Consumer Health. Foods 2024, 13, 3153. [Google Scholar] [CrossRef]
  75. Statistical Yearbook of the Republic of Poland; Statistics Poland: Warsaw, Poland, 2024. (In Polish)
  76. US EPA. Risk-Based Concentration Table; United States Environmental Protection Agency: Washington, DC, USA, 2000. [Google Scholar]
  77. US EPA. Quantitative Risk Assessment Calculations; Environmental Protection Agency: Washington, DC, USA, 2015. [Google Scholar]
  78. Ravanbakhsh, M.; Javid, A.Z.; Hadi, M.; Fard, N.J.H. Heavy metals risk assessment in fish species (Johnius belangerii (C) and Cynoglossus arel) in Musa Estuary. Persian Gulf. Environ. Res. 2020, 188, 109560. [Google Scholar] [CrossRef] [PubMed]
  79. JECFA. Evaluations of the Joint FAO/WHO Expert Committee on Food Additives (JECFA). Includes All Updates Up to the 89th JECFA (June 2020). 2021. Available online: https://apps.who.int/food-additives-contaminants-jecfa-database/search.aspx?fcc=2 (accessed on 17 July 2025).
Figure 1. Total target hazard quotient of all samples.
Figure 1. Total target hazard quotient of all samples.
Molecules 30 03836 g001
Table 3. Potential human health risk assessment (EDI, THQ).
Table 3. Potential human health risk assessment (EDI, THQ).
EDI
Fish Species ZnNiFeMnCrCuAlLiAsPbCdHg
Nile tilapiax1.930.040.920.0590.0390.0750.1210.0170.1040.0130.0200.021
Pacific codx1.580.050.760.0310.0410.1000.0670.0180.0790.0050.0050.015
Pangax1.030.040.570.0360.0450.0930.0680.0190.1200.0120.0220.027
Alaska pollockx1.150.040.720.0260.0400.0970.1200.0150.0830.0090.0160.021
Yellowfin solex1.350.050.660.0270.0400.0730.0900.0180.1150.0060.0160.022
North-Pacific hakex1.080.040.710.0260.0450.0620.0920.0100.0880.0090.0180.020
Flounderx1.720.170.860.0570.0480.0950.0590.0260.1050.0050.0050.029
Mackerelx0.910.170.800.0340.0470.0940.0630.0260.0620.0040.0050.018
Rainbow troutx3.750.130.780.0400.0650.1060.0540.0280.0700.0050.0060.017
Salmonx2.410.160.740.0440.0630.1020.0560.0320.0800.0050.0100.020
Breamx2.780.160.700.0460.0560.1020.0560.0240.0480.0060.0100.014
THQ
Fish species ZnNiFeMnCrCuAlLiAsPbCdHg
Nile tilapiax0.0060.0020.001<0.0010.0130.0020.0300.0010.035 0.0200.013
Pacific codx0.0050.0030.001<0.0010.0140.0020.0170.0010.026 0.0050.010
Pangax0.0030.0020.001<0.0010.0150.0020.0170.0010.040 0.0220.017
Alaska pollockx0.0040.0020.001<0.0010.0130.0020.0300.0010.028 0.0160.013
Yellowfin solex0.0040.0020.001<0.0010.0130.0020.0230.0010.038 0.0160.014
North-Pacific hakex0.0040.0020.001<0.0010.0150.0020.0230.0010.029 0.0180.012
Flounderx0.0060.0080.001<0.0010.0160.0020.0150.0010.035 0.0050.018
Mackerelx0.0030.0080.001<0.0010.0160.0020.0160.0010.021 0.0050.011
Rainbow troutx0.0120.0070.001<0.0010.0220.0030.0140.0010.023 0.0060.011
Salmonx0.0080.0080.001<0.0010.0210.0030.0140.0020.027 0.0100.013
Breamx0.0090.0080.001<0.0010.0190.0030.0140.0010.016 0.0100.009
Table 4. Coverage of % TWI, % PTMI, % BMDL0.1.
Table 4. Coverage of % TWI, % PTMI, % BMDL0.1.
CdCdPb
Fish Species% TWI
x ± SD
% PTMI
x ± SD
% BMDL0.1
x ± SD
Nile tilapia5.53 ± 1.822.37 ± 0.780.87 ± 0.30
Pacific cod1.39 ± 0.870.59 ± 0.370.36 ± 0.06
Panga6.05 ± 1.522.59 ± 0.650.78 ± 0.33
Alaska pollock4.48 ± 1.001.92 ± 0.430.62 ± 0.16
Yellowfin sole4.43 ± 1.391.90 ± 0.600.43 ± 0.12
North-Pacific hake5.04 ± 1.092.16 ± 0.470.57 ± 0.12
Flounder1.48 ± 0.260.64 ± 0.110.34 ± 0.09
Mackerel1.47 ± 0.550.63 ± 0.240.27 ± 0.09
Rainbow trout1.76 ± 0.540.75 ± 0.230.30 ± 0.07
Salmon2.74 ± 0.841.17 ± 0.360.33 ± 0.08
Bream2.68 ± 0.501.15 ± 0.210.37 ± 0.12
Table 5. Characteristics of the tested material.
Table 5. Characteristics of the tested material.
SpeciesAmount of Material
Tested
Amount of Analysed
Samples
Country of
Origin
Fat Content % aDry Weight
% a
Nile tilapia18 180China1.39 ± 0.4718.39 ± 1.71
Panga27 270Vietnam1.09 ± 0.7310.36 ± 2.19
Alaska Pollock12 120China0.67 ± 0.098.60 ± 1.42
North-Pacific hake3 12China2.05 ± 0.126.81 ± 1.02
Yellowfin sole9 90China1.07 ± 0.1711.25 ± 1.13
Pacific cod13 130China0.50 ± 0.0616.79 ± 0.29
Flounder10 100Poland2.08 ± 0.0520.08 ± 1.22
Mackerel30 300Poland13.01 ± 0.1127.14 ± 2.06
Rainbow trout12 120Poland4.7 ± 0.1224.03 ± 1.33
Salmon880Poland13.5 ± 0.3218.5 ± 0.1.12
Bream22220Poland3.5 ± 0.3217.51 ± 0.98
a Arithmetic mean ± standard deviation.
Table 6. LOD, LOQ values and recovery of analyzed samples.
Table 6. LOD, LOQ values and recovery of analyzed samples.
Trace
Element
LOD µg/kgLOQ µg/kgRecovery %Trace ElementLOD µg/kgLOQ µg/kgRecovery %
Zn20.462.898.8Al5.518.896.9
Ni1.44.196.9Li1.34.097.6
Fe19.860.498.4As0.31.095.9
Mn1.23.997.7Pb0.83.199.2
Cr1.44.598.2Cd0.311.198.9
Cu8.626.199.1Hg1.65.296.7
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

Witczak, A.; Ciemniak, A.; Więcaszek, B.; Keszka, S.; Protasowicki, M.; Pokorska-Niewiada, K. An Assessment of the Public Health Risk Associated with Consumption of Imported Fish Based on the Intake of Essential and Harmful Elements. Molecules 2025, 30, 3836. https://doi.org/10.3390/molecules30183836

AMA Style

Witczak A, Ciemniak A, Więcaszek B, Keszka S, Protasowicki M, Pokorska-Niewiada K. An Assessment of the Public Health Risk Associated with Consumption of Imported Fish Based on the Intake of Essential and Harmful Elements. Molecules. 2025; 30(18):3836. https://doi.org/10.3390/molecules30183836

Chicago/Turabian Style

Witczak, Agata, Artur Ciemniak, Beata Więcaszek, Sławomir Keszka, Mikołaj Protasowicki, and Kamila Pokorska-Niewiada. 2025. "An Assessment of the Public Health Risk Associated with Consumption of Imported Fish Based on the Intake of Essential and Harmful Elements" Molecules 30, no. 18: 3836. https://doi.org/10.3390/molecules30183836

APA Style

Witczak, A., Ciemniak, A., Więcaszek, B., Keszka, S., Protasowicki, M., & Pokorska-Niewiada, K. (2025). An Assessment of the Public Health Risk Associated with Consumption of Imported Fish Based on the Intake of Essential and Harmful Elements. Molecules, 30(18), 3836. https://doi.org/10.3390/molecules30183836

Article Metrics

Back to TopTop