Abstract
Shrimp and Crab, important sources of protein, are currently being adversely affected by the rising industrialization, which has led to higher levels of heavy metals. The goal of this study was to evaluate the health risks of contamination associated with nine heavy metals (Cd, Pb, Cu, Cr, Zn, Ni, As, Al, and Fe) in two species of shrimp (Macrobrachium rosenbergii and Metapenaeus monoceros) and one species of crab (Scylla serrata) that were collected from the Khulna, Satkhira, and Bagerhat areas of Bangladesh. Inductively coupled plasma-optical emission spectrometry (ICP-OES) was used for the study. The results showed that all metal concentrations in shrimp and crab samples were below the recommended level, indicating that ingestion of these foods would not pose any substantial health risks to individuals. To evaluate the non-carcinogenic health risks, the target hazard quotient (THQ) and hazard index (HI) were determined, and the target cancer risk (TR) was utilized to evaluate the carcinogenic health risks. From the health point of view, this study showed that crustaceans obtained from the study sites were non – toxic (THQ and HI < 1), and long-term, continuous intake is unlikely to pose any significant health hazards (TR = 10−7-10−5) from either carcinogenic or non-carcinogenic effects.
Keywords: Bioaccumulation, Metal toxicity, Estimated daily intake, Human health hazard, Target cancer risk, ICP-OES
Graphical Abstract
Highlights
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Presence of heavy metals in shrimp and crab was measured.
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Target Cancer Risk from consuming fish were evaluated.
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Shrimps and crabs were found to be safe for consumption.
1. Introduction
In recent time, an upsurge trend was found in shrimp consumption. The movement was toward a greater awareness of a balanced diet and the nutritional value of seafood consumption, such as the advantages of consuming seafood that is high in protein, vitamin D, vitamin B3, and zinc [1]. Being one of Bangladesh's top export sectors, processed frozen shrimp generates roughly $448 million annually. 80% of Bangladesh's frozen food exports are comprised of shrimp, which also accounts for 2.5% of the global shrimp market [2]. In contrast to the possible health benefits of eating fish, chemical contaminants found in these food items have become a matter of concern, especially for people who eat fish frequently [3], [4]. Heavy metal buildup in the body's tissues can lead to chronic sickness and have negative effects on the wider population [5]. Chronic exposure to heavy metals such as Cd, Pb, Cu, Cr, Zn, Ni, As, Al, and Fe above their acceptable threshold has negative effects on both humans and animals and can pose serious health risk, including neurological issues, headaches, liver damage, gastrointestinal distress, increase red blood cells, reduce lung functions, induce renal tumors, reduce cognitive development, high blood pressure, kidney dysfunctions, osteomalacia and reproductive deficiencies [6], [7], [8], [9]. Water, sediment, and fish feed are the three main ways that shrimp and crabs can become contaminated with heavy metals. Industrial wastes, geochemical structures, and metal mining created a potential source of heavy metal contamination in the aquatic environment [10], [11].
Global attention has been drawn to the problem of trace metal contamination of aquatic environments, particularly in developing nations like Bangladesh [12]. This issue has become a challenge for scientists around the world [13], [14]. Numerous academic studies discovered a substantial association between fish and sediments [15], [16]. Industrial activities, mining, and the dumping of toxic metal-containing effluents that have not been fully treated are the major human-caused sources of heavy metal pollution of water, sediment, and aquatic life [17], [18]. Metal contamination has been on the rise due to the quick development of industry and agriculture, which is dangerous for humans, fish, and invertebrates [19]. Because of the city's tens of thousands of industrial facilities and sewerage systems, which routinely discharge massive amounts of hazardous waste into these rivers, river pollution is becoming more and more severe [13], [20]. Many fields in Bangladesh's southern region are swamped by this river water during the rainy season. As a result, contaminated shrimp and crabs, and water are introduced into the farms with heavy metals. Prawns are omnivores, thus, to promote quicker growth, industrially produced feed that fits their dietary requirements are used. Rice bran, fish meal, soy meal, shrimp meal, silkworms, flour, beef liver and earthworms are frequently used to make these meals [21]. Alarmingly, Bangladesh uses the protein concentrate made from tannery solid wastes for organic fertilizers, poultry feed, and fish feed [22], which might contaminate industrial feeds with heavy metals. By eating shrimp, this heavy metal is eventually transferred to the human body. Neurotoxicity and carcinogenicity are typically the primary negative health impacts of exposure to these heavy metals, even at low concentrations [23].
Some studies have been conducted on trace metals concentration in aquatic elements e.g., water, sediments, fish etc. in some important rivers of Bangladesh. [16], [20], [24]. Studies found out that urban and industrial development increase the metal contamination in aquatic environment and organisms [13], [25]. In recent time, many industries have been established in and about Khulna city, and the number is continually increasing now-a-days. So, the amount of contaminated wastewater in adjacent rivers is increasing drastically. As a result, the increase in heavy metal concentration in aquatic animal might be increasing. It should be monitored continuously to ensure the heavy metal concentration in shrimp and crab, whether it is below safe level or not. To the best of our knowledge, no detailed study has been conducted on the trace metal concentration in shrimp and crab so far. So, metal toxicity data to calculate the risk assessment is very insufficient. Similarly, there is a shortage of detailed information to assess health risk for the shrimp and crab consumers in Bangladesh. Therefore, the present study aimed to find out the concentration of Cd, Pb, Cu, Cr, Zn, Ni, As, Al, and Fe in two mostly consumed shrimp and one crab species and to assess the human health risk due to consumption. In addition, the carcinogenic and non-carcinogenic health implications of the consumption of those were evaluated.
2. Materials and methods
2.1. Collection and preparation of samples
Two cultured shrimp species Macrobrachium rosenbergii and Metapenaeus monoceros, and a crab species (Scylla serrata) were collected from Khulna Division (Satkhira, Khulna, and Bagerhat district) of Bangladesh (Fig. 1). Total 315 samples (5 replicate samples of each species from each farm) were collected from seven different farms and from three districts. The study region was chosen because of the significant role it plays in the shrimp and prawn aquaculture industry as well as the export of frozen fishery products [26].
Shrimp and crab samples were collected and kept in an ice box to maintain a temperature of 4–5 ºC and delivered to the laboratory for analysis within 24 h. Samples were then washed thoroughly with running water, dried and stored at − 20 ºC until chemical analysis.
Using stainless steel scalpels, frozen shrimp samples were dissected at ∼ 25 ºC. Fresh weights (f.w.) were recorded together with the collection of edible tissues. Before use, all glassware for heavy metal analysis washed with detergent, rinsed in distilled water, steeped in 5% nitric acid for more than 24 h, rinsed with deionized water, and allowed to air-dry at ∼ 25 ºC.
2.2. Analysis of metals by ICP-OES
Concentrations of metals were analyzed using an inductively coupled plasma-optical emission spectrometry (ICP-OES) (SN: P70407, PRODIGY 7, Teledyne Leeman Labs, USA) following the method used by Khan, Jeong [27] with little modification. Before analysis the shrimp and crab were thawed and 1 g sample was taken from each shrimp and crab. Samples were digested for 12 h with 25 mL of HNO3 (68%) and 2.0 mL of H2O2 (32%), acting as a catalyst, on a hot plate [28]. The temperature of the heating plate was ramped from 50 °C up to 160 °C. A roughly 5–7 mL of a colorless watery appearance indicates the end of digestion. After digestion the samples were cooled and filtered with the Whatman No. 42 filter paper. The filtrates were then dissolved and diluted with ultrapure deionized water to 50 mL. To quantify the concentration of Cd, Pb, Cu, Cr, Zn, Ni, As, Al, and Fe all digested samples and blanks were examined in triplicate.
Argon gas was initially used to torch the coil and high frequency electric current was then delivered to the work coil at the torch tube's tip to create plasma. Plasma was produced by ionizing argon gas using the electromagnetic field produced by the high frequency current in the torch tube [29]. The energy utilized in the excitation-emission of the sample came from the high electron density and temperature (10000 K) of this plasma. Through the little tube in the middle of the torch tube, solution samples were injected into the plasma in an atomized condition [29]. The wavelengths used for the detection and quantification of Cd, Pb, Cu, Cr, Zn, Ni, As, Al, and Fe were 226.502, 283.305, 324.754, 206.149, 213.856, 231.604, 228.812, 396.152, and 259.940 nm, respectively. The concentrations of metals in shrimp and crab were expressed as mg/kg fresh weight.
2.3. Estimated daily intake (EDI)
EDI was calculated by the method shown by [30] and expressed in mg/day. The average metal content of each sample was computed, then multiplied by the appropriate consumption rate to create an estimate of EDI [31]. The daily intake rate was determined by Eq. (1).
(1) |
Where MC is the metal concentration in the shrimp and crab samples (mg/kg fw), and IR is the ingestion rate, which was taken as 49.5 g fw/day-person [32].
2.4. Target hazard quotient (THQ)
THQ is an estimation of the non-carcinogenic risk level due to heavy metals exposure. THQ was calculated by using Eq. (2) as per the standard assumption of USEPA Region III Risk-Based Concentration Table [33].
(2) |
Where, EF represents exposure frequency (350 days/year), ED represents exposure duration (30 years for noncancer risk, as used, IR is the ingestion rate (49.5 g/day) [32], BW is the typical adult body weight of 70 kg, MC is the dry weight of heavy metal concentration in shrimp (mg/kg), and ATn is the typical average exposure time for non-carcinogens (EF × ED) (365 days/year X number of exposure years, assuming 30 years, 10, 950 days) [33], [34]. RfD is the oral reference dosage (mg/kg-day) of a certain metal to which the human population may be continually exposed over the course of their lives without an appreciable risk of deleterious effects. and the values of RfD used in this study were recommended by US EPA and other studies [35], [36], [37], [38], [39], [40]. If the THQ value is less than or equal to 1, it means that there is a low likelihood that the exposed population will face any long-term health risks. In contrast, if the THQ is greater than 1, there may be a health concern, necessitating the implementation of relevant actions and safety precautions [41].
2.5. Hazard index
The hazard index (HI) was expressed as the sum of the individual metal THQ values [36]. A HI < 1 is considered safe and HI > 1 is considered hazardous, and THQ (Cd) is the target hazard quotient for Cd intake, and so on.
2.6. Target cancer risk
The term "target cancer risk" (TR) was used to describe the escalating likelihood that a person may get cancer over the course of their lifetime as a result of exposure to a suspected carcinogen [42]. USEPA Region III Risk-Based Concentration Table provides the approach to assess TR [36].
(3) |
Where ATc is the average period of carcinogens (365 days per year for 70 years), according to USEPA, and CPSo is the carcinogenic potency slope for the oral route (mg/kg bw/day) [36]. The values of CPSo for As, Pb, Cr and Ni were known from USPEA, hence TR values for these metal intakes were computed.
2.7. Data Analysis
One-way analysis of variance was used to look at the differences between the mean values that were statistically significant. Using the statistical program SPSS (SPSS 11.0, IBM, Armonk, NY, USA), the multiple-comparison tests were performed using Tukey's honestly significant difference test. All measurements were carried out at least five times [43].
3. Results and discussion
The present study was conducted to determine the concentration of nine heavy metals, namely Cadmium (Cd), Lead (Pb), Copper (Cu), Chromium (Cr), Zinc (Zn), Nickel (Ni), Arsenic (As), Aluminium (Al), and Iron (Fe) associated human health risk from the consumption of two shrimp (Macrobrachium rosenbergii, Metapenaeus monoceros) and a crab (Scylla serrata) species. Among the shrimp and crab species, concentrations of the above-mentioned heavy metals were observed. Average concentration of heavy metals found in crustaceans are listed in Table 1.
Table 1.
Location | Species | Heavy Metal Concentration (mg/kg f.w.) |
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Cd | Pb | Cu | Cr | Zn | Ni | As | Al | Fe | ||
Khulna | Macrobrachium rosenbergii | 0.062 ± 0.012a | 0.088 ± 0.006ab | 0.019 ± 0.013a | 0.059 ± 0.014b | 0.178 ± 0.056b | 0.065 ± 0.019a | 0.104 ± 0.003a | 0.120 ± 0.057a | 0.034 ± 0.019a |
Metapenaeus monoceros | 0.060 ± 0.021a | 0.093 ± 0.002a | 0.016 ± 0.009a | 0.050 ± 0.008b | 0.127 ± 0.108b | 0.079 ± 0.021a | 0.112 ± 0.014a | 0.079 ± 0.064a | 0.034 ± 0.02a | |
Scylla serrata | 0.058 ± 0.003a | 0.079 ± 0.002b | 0.031 ± 0.003a | 0.098 ± 0.007a | 0.548 ± 0.007a | 0.073 ± 0.038a | 0.108 ± 0.015a | 0.093 ± 0.059a | 0.058 ± 0.006a | |
Bagerhat | Macrobrachium rosenbergii | 0.057 ± 0.014a | 0.087 ± 0.008a | 0.019 ± 0.012b | 0.091 ± 0.029a | 0.215 ± 0.052b | 0.079 ± 0.028a | 0.115 ± 0.009a | 0.086 ± 0.033a | 0.045 ± 0.029a |
Metapenaeus monoceros | 0.062 ± 0.009a | 0.082 ± 0.007a | 0.008 ± 0.013b | 0.074 ± 0.01a | 0.124 ± 0.065b | 0.102 ± 0.035a | 0.113 ± 0.021a | 0.082 ± 0.056a | 0.033 ± 0.014a | |
Scylla serrata | 0.057 ± 0.019a | 0.081 ± 0.006a | 0.056 ± 0.008a | 0.077 ± 0.000a | 0.474 ± 0.028a | 0.099 ± 0.01a | 0.128 ± 0.005a | 0.093 ± 0.019a | 0.074 ± 0.002a | |
Satkhira | Macrobrachium rosenbergii | 0.066 ± 0.017a | 0.091 ± 0.007a | 0.019 ± 0.012a | 0.087 ± 0.025a | 0.277 ± 0.104b | 0.089 ± 0.028a | 0.109 ± 0.019a | 0.087 ± 0.034a | 0.052 ± 0.007a |
Metapenaeus monoceros | 0.060 ± 0.009a | 0.080 ± 0.006a | 0.015 ± 0.013a | 0.057 ± 0.026a | 0.266 ± 0.114b | 0.089 ± 0.026a | 0.107 ± 0.004a | 0.108 ± 0.074a | 0.059 ± 0.031a | |
Scylla serrata | 0.056 ± 0.011a | 0.086 ± 0.003a | 0.013 ± 0.012a | 0.092 ± 0.029a | 0.805 ± 0.235a | 0.051 ± 0.045a | 0.107 ± 0.022a | 0.118 ± 0.009a | 0.083 ± 0.004a |
Data presented as mean ± Std, different letters in the same column within each location indicates significant difference.
3.1. Concentration of heavy metals
Heavy metal concentrations in shrimp and crab species were determined by ICP-OES and expressed as mg/kg. On a wet weight basis, the concentrations of every metal were calculated. A comparison of heavy metals (mg/kg) concentrations in shrimp and crab samples from previous studies has presented in Table 2.
Table 2.
Location | Cd | Pb | Cu | Cr | Zn | Ni | AS | Fe | References |
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Buriganga river, Bangladesh | 8.03–13.52 | 3.36–6.34 | 8.25–11.21 | [20] | |||||
Buriganga river, Bangladesh | 1.50 | 0.51 | 575 | 2.50 | 195 | 0.60 | 1.20 | [78] | |
Satkhira farm, Bangladesh |
0.60 × 10−1 | 0.96 | 0.20 | [40] | |||||
Kalpakkam, India | 0.8–6.5 | 17.6–117.0 | [79] | ||||||
Tumkur, India | 0.80 | 33 | 55 | 3 | 600 | [79] | |||
Ganga, West Bengal, India | 0.60 × 10−2- 0.02 | 1.1–5.4 | 4.90–12.2 | [80] | |||||
Ganga, Kolkata | 4.60 × 10−2 | 3.50 | 0.96 | 7.70 × 10−2 | 12.59 | [81] | |||
St. Martins Island | 0.50 | 0.50 | 5 | 1 | 50 | 5 | [54] | ||
Khulna division, Bangladesh | 5.60 × 10−2 − 6.57 × 10−2 | 7.91 × 10−2 − 9.28 × 10−2 | 0.82 × 10−2 − 5.56 × 10−2 | 5.00 × 10−2 − 9.84 × 10−2 | 12.68 × 10−2 − 80.52 × 10−2 | 5.15 × 10−2 − 10.23 × 10−2 | 10.38 × 10−2 − 12.80 × 10−2 | 3.28 × 10−2 − 8.334 × 10−2 | Present study for Shrimp and crab |
Maximum level (mg/ kg wet weight) | 0.50 | 0.50 | 5 | 0.50 | 50 | 5 | [50], [54] |
3.1.1. Cadmium
At a minimum dose of 1 mg/kg, Cadmium (Cd) can cause chronic poisoning [44]. Fish should only have a Cd value of 0.05 mg/kg or less, according to FAO/WHO [45]. The standard for Cd in seafood set by the Australian National Health and Medical Research Council (ANHMRC) is 2.0 mg/kg [46]. The main sources of Cd contamination in marine species are the use of uncontrolled fertilizers, long-term discharge of untreated industrial wastes and the potential increase in Cd concentration in farm water. [40]. In the current study, Cd levels in samples of shrimp from various locations ranged from 5.7 × 10−2 to 6.6 × 10−2 mg/kg. The highest and lowest Cd concentrations were found in M. rosenbergii tissues from Satkhira (6.6 ×10−2 mg/kg) and Bagerhat (5.7 ×10−2) (mg/kg) regions, respectively (Table 1). However, lowest concentration of Cd was found in the crab samples from the Satkhira regions (5.6 ×10−2 mg/kg), whereas highest concentration was found from the Khulna regions (5.8 ×10−2 mg/kg) (Table 1). Cd levels in the chosen samples from all sites were found to be lower than the permitted limits [45]. Previous studies show that crustaceans in the Buriganga River have a high Cd content of 1.51 mg/kg, [47]. An earlier investigation revealed that the Cd levels in fish samples from the Bangshi River between two separate seasons ranged from 0.09 to 0.87 mg/kg [16], [40].
3.1.2. Lead
Lead (Pb) concentrations in shrimp tissues ranged from 8.0 × 10−2 to 9.3 × 10−2 mg/kg, with M. monoceros from Satkhira regions having the lowest concentration (8.0 ×10−2 mg/kg) and M. monoceros from Khulna regions having the highest concentration (9.3 ×10−2 mg/kg) (Table 1). Highest Pb concentration in the crab samples was found from Satkhira regions (8.6 ×10−2 mg/kg), while lowest Pb concentration was found in the Khulna regions 7.9 × 10−2 mg/kg (Table 1). These levels were well below the maximum allowable threshold (0.50 mg/kg) [48]. All shrimp and crab samples showed lower values than the suggested level. Studies showed that M. rosenbergii from the Buriganga river had Pb pollution of 0.51 mg/kg [38], [40]. Due to the bottom-dwelling nature of the M. monoceros and M. rosenbergii, these species constantly came into contact with sediments, thus sediment pollution might be a major contributing factor for Pb contamination. The discharge of industrial effluents from a range of companies, including poultry farms, oil refineries, textile manufacturers, and other sources can also cause Pb to enter rivers [40].
3.1.3. Copper
All living organisms require Copper (Cu) for appropriate growth and metabolism [49]. However, at large concentrations, Cu becomes poisonous. It has been reported that Cu concentrations should not exceed 5 mg/kg in the food product [50]. In the examined samples, concentration of Cu was found comparatively at a lower amount. Cu values in the shrimp samples ranged from 0.8 × 10−2 to 1.9 × 10−2 mg/kg, with M. rosenbergii having the maximum concentration of 1.9 × 10−2 mg/kg from the Khulna and Satkhira regions, and M. monoceros having the minimum concentration of 0.8 × 10−2 mg/kg from the Bagerhat regions (Table 1). Thus, the Cu contents in the experimental specimens were lower than the recommended levels. The enrichment of Cu in macrobenthic fauna might be through Cu input in water and sediments from nearby industry.
3.1.4. Chromium
The maximum tolerable concentration of Chromium (Cr) varies between 0.5 [50] and 1.0 mg/kg [51]. The crustacean samples included in the preliminary analysis had Cr values ranging from 5.0 × 10−2 to 9.8 × 10−2 mg/kg. Highest Cr content was found in M. rosenbergii from Bagerhat (9.1 ×10−2 mg/kg), whereas, lowest concentration was found in M. monoceros from Khulna district5.0 × 10−2 mg/kg (Table 1). Highest and lowest levels of Cr was found in S. serrata from Khulna district (9.8 ×10−2 mg/kg) and Bagerhat districts (7.7 ×10−2 mg/kg) respectively (Table 1). In the current study, we found a lower level of Cr than those reported in other studies in shrimp and mollusks (bivalve) [52]. Study findings imply that Cr pollution exceed the safe limit of FAO's acceptable guideline for Cr concentration in shrimp was exceeded in an Indian river [53].
3.1.5. Zinc
Zinc (Zn), as a cofactor for roughly 300 enzymes for all marine organisms, is a vital mineral for both humans and animals [54]. Zn is a constituent of various enzymes and is crucial for a number of biological processes that need to be maintained at quite high levels. Zn toxicity resulting from excessive consumption may lead to electrolyte imbalance, nausea, and anemia [55]. The highest and lowest concentration of Zn was found in M. rosenbergii (27.7 ×10−2 mg/kg) and M. monoceros (12.4 ×10−2 mg/kg) from Satkhira and Bagerhat respectively. On the other hand, the maximum amount of Zn was 80.5 × 10−2 mg/kg in S. serrata from the Satkhira area, while the lowest amount was 47.4 × 10−2 mg/kg from the Bagerhat area (Table 1). The FAO's recommended maximum limit for zinc is 30 mg/kg [56]. All shrimp and crab samples had Zn amounts below the recommended levels. Therefore, it can be concluded that there is no risk to human health from this metal.
3.1.6. Nickel
Ni levels in the shrimp samples ranged from 6.5 × 10−2 to 10.2 × 10−2 mg/kg. M. monoceros, obtained from the Bagerhat regions, had the highest concentration (10.2 ×10−2 mg/kg), while M. rosenbergii, collected from the Khulna regions, had the minimum concentration (6.5 ×10−2 mg/kg). S. serrata from Satkhira and Bagerhat district had the lowest concentration of 5.1 × 10−2 mg/kg and highest concentration of 9.9 × 10−2 mg/kg Ni, respectively (Table 1). The WHO maximum recommended level of Ni is 0.2 mg/kg [57]. No Ni concentrations in all samples exceeded the allowable limit.
3.1.7. Arsenic
Both organic and inorganic types of arsenic (As) can be found in our diet, however inorganic As is more harmful than organic As. The types of As that are present are challenging to accurately assess. It is believed that 10% of all arsenic is inorganic [58]. S. serrata from the Bagerhat region had the highest concentration of As (12.80 ×10−2 mg/kg), while from the Satkhira region had the lowest value (10.72 ×10−2 mg/kg). The maximum As concentration was found in M. rosenbergii from Khulna regions (10.4 ×10−2 mg/kg), while the lowest concentration was found from Bagerhat of 11.5 × 10−2 mg/kg (Table 1). The findings revealed that the shrimp and crab had comparatively higher concentrations of As than other metal tested. The maximum permitted concentration of arsenic in crustaceans is 5 mg/kg [50], [54]. Our findings showed that the As concentration was below the safe level. Recent studies, however, contend that at very low quantities, As disrupts the endocrine system. Chronic exposure to inorganic arsenic may have negative consequences on the liver, gastrointestinal tract, respiratory tract, skin, hematological system, cardiovascular system, neurological system, and skin [59]. Acute high level As exposure can also cause vomiting, diarrhea, anemia, liver damage, and even death. Long-term exposure is thought to increase the risk of developing cancer, hypertension, some types of diabetes, and skin disease [60].
3.1.8. Aluminum
In most cases, Aluminum (Al) exposure through the mouth is safe. Some studies indicate that persons who are exposed to high quantities of aluminum may get Alzheimer's disease [61]. The M. monoceros from the Bagerhat region had the lowest concentration of Al (8.2 ×10−2 mg/kg), whereas M. rosenbergii from Khulna region had the highest concentration of Al (12.0 ×10−2 mg/kg). The highest and lowest Al concentration in S. serrata was found in Satkhira regions (11.8 ×10−2 mg/kg), and Khulna regions (9.3 ×10−2 mg/kg), respectively (Table 1). Previous research has connected neurotoxicity (bad health effects on the central or peripheral nervous system or both), [61] Alzheimer's disease, and breast cancer to regular exposure to high quantities of Al.
3.1.9. Iron
The human body requires iron for proper functioning. Suggested level of heavy metal concentration for Iron (Fe) in white shrimp is 0.50 mg/kg [62]. It functions as an electron transporter inside cells, a component of important protein frameworks in various tissues, and a carrier of oxygen from the lungs to the tissues through red platelet hemoglobin. S. serrata from Satkhira had the highest content of Fe (8.3 ×10−2 mg/kg), whereas from Bagerhat had the lowest concentration (7.4 ×10−2 mg/kg). M. monoceros from Bagerhat had the lowest concentration of 3.3 × 10−2 mg/kg and from Satkhira had the highest concentration of 5.9 × 10−2 mg/kg (Table 1). The study's finding is far safe to the recommended level. The gastrointestinal (GI) mucosa can be severely damaged by Fe ingestion, which can produce nausea, vomiting, abdominal discomfort, hematemesis, and diarrhea. Patients may also experience hypovolemia due to considerable fluid and blood loss.
3.2. Estimated Daily Intake (EDI)
Estimated daily intake (EDI) of trace metals in shrimp and crab has been evaluated in this study. Table 3 lists the EDI of few hazardous heavy metals from ingestion of crustaceans by Bangladeshi adults typically living in the coastal area. EDI to RfD ratio is a significant measure of health risk. RfD is the estimation of the amount of daily exposure to which the general population might be continuously exposed over the course of a lifetime without a significant risk of adverse consequences [63]. New York State Department of Health claims if the derived heavy metal's EDI to RfD ratio is equal to or less than the RfD, the risk is small [64]. However if the ratio is > 1–5, > 5–10, and > 10 x the Rfd, the risk is low, moderate, and significant, respectively [63]. As a result, EDI can be used as a benchmark to assess the possible health effects of the chemical at various levels. The likelihood of negative consequences in a human population rises as the frequency and/or size of exposures that exceed the RfD [54].
Table 3.
Location | Variety | Estimated daily intake (EDI) (mg/person/ day) |
||||||||
---|---|---|---|---|---|---|---|---|---|---|
Cd | Pb | Cu | Cr | Zn | Ni | As | Al | Fe | ||
Khulna | Macrobrachium rosenbergii | 3.05 × 10−3 | 4.38 × 10−3 | 0.94 × 10−3 | 2.93 × 10−3 | 8.81 × 10−3 | 3.20 × 10−3 | 5.14 × 10−3 | 5.97 × 10−3 | 1.68 × 10−3 |
Metapenaeus monoceros | 2.98 × 10−3 | 4.59 × 10−3 | 0.81 × 10−3 | 2.48 × 10−3 | 6.28 × 10−3 | 3.95 × 10−3 | 5.53 × 10−3 | 3.89 × 10−3 | 1.68 × 10−3 | |
Scylla serrata | 2.88 × 10−3 | 3.92 × 10−3 | 1.52 × 10−3 | 4.87 × 10−3 | 27.14 × 10−3 | 3.62 × 10−3 | 5.36 × 10−3 | 4.59 × 10−3 | 2.86 × 10−3 | |
Bagerhat | Macrobrachium rosenbergii | 2.83 × 10−3 | 4.31 × 10−3 | 0.99 × 10−3 | 4.52 × 10−3 | 10.64 × 10−3 | 3.96 × 10−3 | 5.72 × 10−3 | 4.28 × 10−3 | 2.24 × 10−3 |
Metapenaeus monoceros | 3.08 × 10−3 | 4.08 × 10−3 | 0.41 × 10−3 | 3.66 × 10−3 | 6.12 × 10−3 | 5.06 × 10−3 | 5.61 × 10−3 | 4.04 × 10−3 | 1.62 × 10−3 | |
Scylla serrata | 2.83 × 10−3 | 3.99 × 10−3 | 2.75 × 10−3 | 3.81 × 10−3 | 23.48 × 10−3 | 4.90 × 10−3 | 6.34 × 10−3 | 4.62 × 10−3 | 3.69 × 10−3 | |
Satkhira | Macrobrachium rosenbergii | 3.25 × 10−3 | 4.48 × 10−3 | 0.98 × 10−3 | 4.28 × 10−3 | 13.71 × 10−3 | 4.39 × 10−3 | 5.39 × 10−3 | 4.31 × 10−3 | 2.59 × 10−3 |
Metapenaeus monoceros | 2.98 × 10−3 | 3.97 × 10−3 | 0.73 × 10−3 | 2.82 × 10−3 | 13.17 × 10−3 | 4.39 × 10−3 | 5.29 × 10−3 | 5.36 × 10−3 | 2.96 × 10−3 | |
Scylla serrata | 2.78 × 10−3 | 4.28 × 10−3 | 0.66 × 10−3 | 4.57 × 10−3 | 39.86 × 10−3 | 2.55 × 10−3 | 5.31 × 10−3 | 5.82 × 10−3 | 4.13 × 10−3 |
However, we have not reached an absolute conclusion that all doses below the RfD are "acceptable" (or without risk) and all doses above the RfD are "unacceptable" (or cause adverse effects) [54], [65]. The daily consumption of a heavy metal determines how harmful it is to people [66]. The average EDIs of all tested metals in the two species of shrimp and one species of crab were lower than the tolerable daily intake limit that indicates that the average consumption of the species in the coastal area would not result in health risk (Table 3). Although the shrimp and crab species examined for this study were deemed acceptable for everyday human consumption, they may pose health hazards if consumed continuously and excessively over 30 years.
3.3. Health risk assessment
Consuming shrimp and crab could expose human to heavy metals in a way that negatively impacts human's health. Therefore, a health risk assessment is unquestionably required for people who regularly consume shrimp and crab.
3.3.1. Target hazard quotient and hazard index
Table 4 provides estimated target hazard quotients (THQ) and hazard index (HI) for Cd, Pb, Cu, Cr, Zn, Ni, As, Al, and Fe consuming from Macrobrachium rosenbergii, Metapenaeus monoceros, and Scylla serrata cultivated at Khulna Division (Satkhira, Khulna, and Bagerhat district) of Bangladesh. USEPA states that ≤ 1 is the permissible value for THQ [33]. The outcome revealed that each metal's THQ value was less than 1, indicating that consuming shrimp and crab would not expose people to any non-carcinogenic health risks if they only intake one heavy metals individually. Moreover, all metals taken into account together had HI less than the permissible level of 1 for shrimp and crab.
Table 4.
Location | Variety | Target Hazard Quotient (THQ) |
Hazard Index (HI) | ||||||||
---|---|---|---|---|---|---|---|---|---|---|---|
Cd | Pb | Cu | Cr | Zn | Ni | As | Al | Fe | |||
Khulna | Macrobrachium rosenbergii | 4.18 × 10−2 | 1.49 × 10−2 | 3.23 × 10−4 | 1.34 × 10−2 | 4.02 × 10−4 | 2.19 × 10−3 | 2.35 × 10−1 | 8.17 × 10−5 | 3.28 × 10−5 | 0.01 |
Metapenaeus monoceros | 4.08 × 10−2 | 1.57 × 10−2 | 2.79 × 10−4 | 1.13 × 10−2 | 2.87 × 10−4 | 2.71 × 10−3 | 2.53 × 10−1 | 5.34 × 10−5 | 3.29 × 10−5 | 0.01 | |
Scylla serrata | 3.95 × 10−2 | 1.34 × 10−2 | 5.20 × 10−4 | 2.22 × 10−2 | 1.24 × 10−3 | 2.48 × 10−3 | 2.45 × 10−1 | 6.30 × 10−5 | 5.59 × 10−5 | 0.02 | |
Bagerhat | Macrobrachium rosenbergii | 3.88 × 10−2 | 1.47 × 10−2 | 3.38 × 10−4 | 2.06 × 10−2 | 4.86 × 10−4 | 2.71 × 10−3 | 2.61 × 10−1 | 5.86 × 10−5 | 4.39 × 10−5 | 0.01 |
Metapenaeus monoceros | 4.22 × 10−2 | 1.39 × 10−2 | 1.39 × 10−4 | 1.67 × 10−2 | 2.80 × 10−4 | 3.47 × 10−3 | 2.56 × 10−1 | 5.53 × 10−5 | 3.17 × 10−5 | 0.01 | |
Scylla serrata | 3.88 × 10−2 | 1.37 × 10−2 | 9.43 × 10−4 | 1.74 × 10−2 | 1.07 × 10−3 | 3.36 × 10−3 | 2.89 × 10−1 | 6.33 × 10−5 | 7.21 × 10−5 | 0.02 | |
Satkhira | Macrobrachium rosenbergii | 4.45 × 10−2 | 1.53 × 10−2 | 3.37 × 10−4 | 1.96 × 10−2 | 6.26 × 10−4 | 3.01 × 10−3 | 2.46 × 10−1 | 5.90 × 10−5 | 5.07 × 10−5 | 0.01 |
Metapenaeus monoceros | 4.08 × 10−2 | 1.36 × 10−2 | 2.49 × 10−4 | 1.29 × 10−2 | 6.02 × 10−4 | 3.01 × 10−3 | 2.41 × 10−1 | 7.34 × 10−5 | 5.80 × 10−5 | 0.01 | |
Scylla serrata | 3.80 × 10−2 | 1.47 × 10−2 | 2.25 × 10−4 | 2.09 × 10−2 | 1.82 × 10−3 | 1.75 × 10−3 | 2.42 × 10−1 | 7.97 × 10−5 | 8.08 × 10−5 | 0.03 |
3.3.2. Target cancer risk (TR)
According to the USFDA [67], the majority (around 90%) of As exposure occurs through seafood. As exposure has been linked to a number of health effects. The inorganic As is regarded as a carcinogen and has been linked to lung, skin, liver, gall bladder, and skin cancers. Kidney failure, hypertension, and gastrointestinal disorders are some of harmful effects of cadmium's toxicity. Pregnant women's Cd intoxication has been linked to shorter pregnancies, smaller babies, and more lately, children's immune and/or endocrine system abnormalities [68]. The major harmful effect of Pb exposure has been linked to delay in neurobehavioral development [69]. The neurological system's efficiency may suffer with prolonged exposure. EPA reports that heavy metal may potentially cause cancer in humans [70]. Moreover, Pb exposure can cause significant damage to the brain, liver, and kidneys as well as eventual mortality [71]. In addition, high exposure of Pb in men can damage the sperm-producing organs [72].
For As, Pb, Cr, and Ni a carcinogenic potency slope factors are available. As is categorized as an established carcinogen (USEPA group A) and based on animal studies, Pb can also be categorized as probable carcinogen (USEPA group B2) [73]. Table 5 shows the TRs for As, Pb, Cr, and Ni in adults from crustacean’s ingestion exposure. The TR values for As, Pb, Cr, and Ni ranged from 4.53 × 10−5 to 5.58 × 10−5, 1.96 × 10−7 to 2.29 × 10−7, 8.60 × 10−6 to 1.43 × 10−5, and 2.54 × 10−5 to 5.05 × 10−5 respectively in shrimp and crab (Table 5). Cancer risks below 10−6 are typically regarded as insignificant, those above 10−4 are generally seen as unacceptable, and those that fall between 10−6 and 10−4 are generally regarded as allowable [33], [74]. For all shrimp and crab samples, the TR for As, Pb, Cr, and Ni was between 10−7and 10−5. Additional sources of metal exposure, such as consuming other foods (such as ground water, wheat, rice, pulses, meat, and eggs), inhaling dust, and so on, could not be considered in this study. Moreover, Mercury (Hg) contamination can be a potential health threat nowadays [75], [76]. Acute exposure to this heavy metal can cause insomnia, neuromuscular changes, headaches and changes in nerve responses [77], therefore, these need to be considered in future study.
Table 5.
Location | Variety | Target cancer risk (TR) |
|||
---|---|---|---|---|---|
As | Pb | Cr | Ni | ||
Khulna | Macrobrachium rosenbergii | 4.53 × 10−5 | 2.18 × 10−7 | 8.60 × 10−6 | 3.19 × 10−5 |
Metapenaeus monoceros | 4.87 × 10−5 | 2.29 × 10−7 | 7.27 × 10−6 | 3.95 × 10−5 | |
Scylla serrata | 4.72 × 10−5 | 1.96 × 10−7 | 1.43 × 10−5 | 3.61 × 10−5 | |
Bagerhat | Macrobrachium rosenbergii | 5.03 × 10−5 | 2.15 × 10−7 | 1.33 × 10−5 | 3.95 × 10−5 |
Metapenaeus monoceros | 4.94 × 10−5 | 2.03 × 10−7 | 1.07 × 10−5 | 5.05 × 10−5 | |
Scylla serrata | 5.58 × 10−5 | 1.99 × 10−7 | 1.12 × 10−5 | 4.89 × 10−5 | |
Satkhira | Macrobrachium rosenbergii | 4.75 × 10−5 | 2.24 × 10−7 | 1.26 × 10−5 | 4.38 × 10−5 |
Metapenaeus monoceros | 4.66 × 10−5 | 1.98 × 10−7 | 8.28 × 10−6 | 4.38 × 10−5 | |
Scylla serrata | 4.67 × 10−5 | 2.13 × 10−7 | 1.34 × 10−5 | 2.54 × 10−5 |
4. Conclusions
This study was conducted to learn more about the levels of heavy metals in shrimp and crab from Bangladesh's southern-western region. Cadmium had absolutely distinct bioaccumulation resulted in higher average concentration in crab than in shrimp samples. Being a favored cuisine in this area, shrimp consumption may cause chronic illnesses including renal failure and other chronic diseases owing to excessive consumption if crustaceans contain significantly higher amount of heavy metals. However, the investigation revealed a minimum heavy metal content which is below the maximum recommended level. Our research provides a new perspective on eating shrimp and crab from these areas that poses nearly no health danger. Long-term cancer risk is negligible for people who regularly consume shrimps and crabs with lower concentrations of heavy metals than that identified in the current study.
Ethical Approval
Appropriate ethical approval was obtained from the Ethical Approval committee of Jashore University of Science and Technology.
Declarations
All authors have read, understood, and have complied as applicable with the statement on “Ethical responsibilities of authors” as found in the Instruction of Authors.
Funding
This work was supported by the Shahjalal University of Science and Technology’s Research Centre, Sylhet, Bangladesh.
CRediT authorship contribution statement
Shafi Ahmed: Conceptualization; Methodology; Software; Validation; Formal Analysis; Investigation; Resources; Data Curation; Writing – Original Draft Preparation; Supervision. Md. Farid Uddin: Formal Analysis; Writing – Original Draft Preparation. Md. Sakib Hossain: Formal Analysis; Writing – Review & Editing; Investigation; Visualization. Abdullah Jubair: Writing – Review & Editing; Investigation; Visualization. Md. Nahidul Islam: Methodology; Software; Validation; Data Curation; Writing – Original Draft Preparation; Writing – Review & Editing; Supervision. Mizanur Rahman: Conceptualization; Writing – Review & Editing; Supervision; Project Administration; Funding Acquisition.
Declaration of Competing Interest
The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
Handling Editor: Prof. L.H. Lash
Contributor Information
Md. Nahidul Islam, Email: nahidul.islam@bsmrau.edu.bd.
Mizanur Rahman, Email: mizan-fet@sust.edu.
Data Availability
Data will be made available on request.
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Associated Data
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Data Availability Statement
Data will be made available on request.