Skip to main content
Advertisement
Browse Subject Areas
?

Click through the PLOS taxonomy to find articles in your field.

For more information about PLOS Subject Areas, click here.

  • Loading metrics

Natural zeolite for heavy metal, ammonia removal, and physiological responses in European sea bass (Dicentrarchus labrax) juveniles tanks with different densities

  • Ghada R. Sallam,

    Roles Conceptualization, Data curation, Formal analysis, Methodology, Writing – original draft, Writing – review & editing

    Affiliation Aquaculture Division, Fish Rearing Lab., National Institute of Oceanography and Fisheries (NIOF), Alexandria, Egypt

  • Hadir A. Aly,

    Roles Data curation, Methodology, Writing – review & editing

    Affiliation Aquaculture Division, Fish Rearing Lab., National Institute of Oceanography and Fisheries (NIOF), Alexandria, Egypt

  • Ayman M. Lotfy,

    Roles Data curation, Methodology, Writing – review & editing

    Affiliation Aquaculture Division, Fish Rearing Lab., National Institute of Oceanography and Fisheries (NIOF), Alexandria, Egypt

  • Mohamed M. Abdel-Rahim,

    Roles Data curation, Methodology, Validation, Writing – review & editing

    Affiliation Aquaculture Division, Fish Rearing Lab., National Institute of Oceanography and Fisheries (NIOF), Alexandria, Egypt

  • Walied M. Fayed,

    Roles Data curation, Writing – review & editing

    Affiliation Department of Animal and Fish Production, Faculty of Agriculture (Saba Basha), Alexandria University, Alexandria, Egypt

  • Islam I. Teiba,

    Roles Methodology, Writing – review & editing

    Affiliation Faculty of Agriculture, Tanta University, Tanta, Egypt

  • Kumbukani Mzengereza,

    Roles Writing – review & editing

    Affiliations Department of Fisheries and Aquatic Science, Mzuzu University, Mzuzu, Malawi, African Center of Excellence in Neglected and Underutilized Biodiversity, Mzuzu University, Mzuzu, Malawi

  • Mavuto Tembo,

    Roles Writing – review & editing

    Affiliation African Center of Excellence in Neglected and Underutilized Biodiversity, Mzuzu University, Mzuzu, Malawi

  • Wales Singini,

    Roles Writing – review & editing

    Affiliation African Center of Excellence in Neglected and Underutilized Biodiversity, Mzuzu University, Mzuzu, Malawi

  • Yusuf Jibril Habib,

    Roles Formal analysis, Validation, Writing – review & editing

    Affiliation Department of Medical Analysis, Tishk International University-Erbil, Kurdistan Region, Iraq

  • Akram Ismael Shehata

    Roles Conceptualization, Data curation, Formal analysis, Methodology, Writing – original draft, Writing – review & editing

    akramismael2@gmail.com

    Affiliation Department of Animal and Fish Production, Faculty of Agriculture (Saba Basha), Alexandria University, Alexandria, Egypt

Abstract

The present study aims to investigate the influence of zeolite usage and stocking densities on various parameters, including ammonia removal from water, accumulation of heavy metals in fish organs, water quality, growth performance, feed efficiency, muscle composition, as well as hematological and biochemical parameters in European seabass (Dicentrarchus labrax) over a 90-day duration. A total of 2400 D. labrax with an initial weight of 9.83 ± 2.02 g and initial length of 9.37 ± 0.32 cm were distributed among 24 tanks. The research involved six distinct treatment groups, with two different zeolite levels (0 and 15 ppt) and three stocking density levels (50, 100, and 150 fish/m3), each replicated four times. The results of the research demonstrate a statistically significant improvement (p < 0.05) in water quality measures with the introduction of zeolite. The successful implementation of this amendment mitigated the adverse effects of fish density on water quality parameters. Higher stocking density negatively impacted European sea bass growth, feed utilization, and hemato-biochemical indicators. Zeolite use effectively alleviated these adverse effects, particularly on performance, feed utilization, hematological, and biochemical parameters. The study’s results indicate that the utilization of zeolite has shown to be efficacious in mitigating the accumulation of heavy metals in both water and fish organs, while concurrently augmenting fish attributes. However, the increase in density led to a significant decrease in the accumulation of heavy metals in both water and fish organs. The present study highlights the capacity of natural zeolites to mitigate the negative consequences associated with water quality concerns. The efficiency of these zeolites in limiting the accessibility of heavy metals in polluted water is shown, hence minimizing their accumulation in fish organs. In addition, the improvement of fish performance has the capacity to have a beneficial influence on both the well-being and efficiency of fish in aquaculture. Additional research is essential to fully understand the complex molecular pathways involved in utilizing natural zeolite under different fish densities.

1. Introduction

Feeding the world’s expanding population, which is expected to reach 9.6 billion by 2050, poses a significant problem due to a lack of natural resources required for food production, such as land and water. Because of limited land and water resources, aquaculture’s sustainability will most likely depend on improving production settings, boosting productivity, upgrading aquaculture technology, and lowering production costs. In many nations, aquaculture has emerged as an excellent food production alternative [1, 2]. The aforementioned industry has seen rapid growth because of its pivotal role in addressing the increasing need for animal protein in the human diet [3]. Sustainable aquaculture might help accomplish FAO Sustainable Development Goals to reduce poverty, hunger, food security, nutrition, and sustainable agriculture [1, 4]. Because of subsequent industrial development, the excessively wasteful use of agricultural pesticides in recent and previous decades, and the disregard for safe disposal methods for industrial waste, most of the water resources used for fish farming have been contaminated, particularly by heavy metal pollutants [5].

The use of all accessible water sources, even dubious drinking water, is a novel aquaculture approach. Thus, many aquaculture industry chose groundwater as their primary water supply [6]. Aquaculture in the desert using subsurface brackish or saltwater is a potential option. Desert aquaculture may be a sustainable production industry, particularly in areas where plant cultivation is difficult [79]. However, people who use deep saltwater have a lot of problems, like water that is too hard, has too much ammonia, and not enough air [1012]. That being said, this water supply is susceptible to rapid degradation based on pond biomass or stocking density. Intensified manufacturing techniques are now needed to fulfill the growing demand brought on by population growth. The provided area for aquaculture growth, the scarcity of freshwater, and the restrictive wastewater rules are the main hindrances to long-lasting conventional systems [13, 14]. In order to establish a sustainable sector for dessert aquaculture, several studies have examined ways to improve subterranean seawater quality via the use of different technologies, including activated carbon [15, 16], probiotic and biofloc technology system [17, 18], biological and sand filters [1921], and zeolites [2225]. Fish are near the top of the marine food chain, so heavy metals can usually get into their bodies from food, water, and sediments [2628].

The presence of hazardous heavy metals in fish may negate their good benefits; various deleterious effects of heavy metals on human health have long been recognised [29]. This could include very bad threats like kidney failure, liver damage, heart disease, and even death [30, 31]. Also, stocking density (SD) is an important component influencing the physical and biological properties of fish. Besides that, SD might affect the quality of the water because a high SD can cause a lot of ammonia and other bad things to be in it. Ammonia is the second-most important water quality factor that affects fish performance, especially in systems that use a lot of water [32].

Heavy metals (Zn, Cr, Pb, Cd, Cu, Mn, Fe, etc.) are also a big problem for the environment because they are found in the ocean, groundwater, and wastewater [33], which in turn adversely affects aquaculture projects. As industry trash, a lot of dangerous heavy metals have been dumped into the environment, polluting the land and water badly. Cadmium, copper, nickel, lead, and zinc are some of the most common metals that build up in living organisms and cause a wide range of illnesses and disorders [34]. Additionally, they are frequent pollutants in groundwater in military and industrial locations. There are many methods for extracting dissolved heavy metals, including electrodialysis, sorption, phytoextraction, precipitation, ultrafiltration, and reverse osmosis [3537]. Recent discourse has cantered on the possibility of utilizing other inexpensive products as sorbents for heavy metal removal. Nevertheless, excessive levels of heavy metals and ammonia that cause injury can be remedied in a variety of ways. Mechanical solutions and chemical solutions are two such economically prohibitively expensive methods. The economy and technology are both receptive to alternative approaches. The addition of natural zeolite to aquaculture water is one of the most promising methods for purifying water [12, 25, 38, 39].

Zeolites are hydrated aluminosilicate minerals that occur naturally. They belong to the mineral class known as "tectosilicates." The most prevalent natural zeolites are generated through glass alteration. Many authors have explored the sorption capacity of natural zeolite (clinoptilolite) for inorganic cations [40, 41]. More research is showing that natural zeolite has a lot of potential to be one of the best and most cost-effective ways to remove ammonia and some heavy metals from water. This is because it has special molecular sieve, sorption, and ion exchange properties [33]. Because zeolite exchangeable ions are largely harmless (sodium, calcium, and potassium ions), they are especially well suited for removing unwanted heavy metal ions from industrial effluent waters. Clinoptilolite is the most prevalent natural zeolite, and much study has been done to characterize its chemical, surface, and sorption characteristics [42]. It is possible to get rid of some heavy metals from rainwater with zeolites. When it comes to sorption processes, clinoptilolite samples from different areas behave in different ways. This study looked at how well a natural zeolite called Clinoptillolite from Western Anatolia can soak up some heavy metal cations that are in solution. So, the main goal of this work is to use natural zeolite to change the damaging aquaculture waste water from high SD ponds where European sea bass are raised and that rely on underground salt water.

2. Material and method

2.1. Ethical approval

All guidelines for rearing and using fish were followed and approved according to the Institutional Animal Care and Use Committee (IACUC) at the National Institute of Oceanography and Fisheries, Egypt, which licensed ethical permission (Approval No. NIOF. AQ1. F. 21. R. 005). Furthermore, all research procedures adhered to the ARRIVE guidelines v2.0 [43], ensuring the research protocol aligns with established ethical standards and safeguards the well-being of the fish subjects.

2.2 Experimental location and facilities

Ethics rules from the National Institute of Oceanography and Fisheries, Egypt, were followed during the trial. Two thousand four hundred healthy European sea bass fingerlings were bought from the Marine Finfish Hatchery, K21, which is part of the General Authority for Fish Resources Development (GAFRD) and the Ministry of Agriculture and Land Reclamation in West Alexandria, Egypt. They were then kept at the El-Mothalas Fish Rearing Facility at the El-Max Station for Applied Research, which is part of the National Institute of Oceanography and Fisheries (NIOF) in Alexandria, Egypt. The Mediterranean Sea is 1.2 kilometers away from this spot. Deep wells (about 100 m deep) are the only places that can provide saltwater with a salinity of 32<. Unfortunately, tests on water samples showed that the levels of ammonia and heavy metals were a little higher than what is suggested for marine fish hatcheries [44]. Certain heavy metals include: Iron (99.3 μg/l), cobalt (50 μg/l), copper (5.3 μg/l), manganese (85.2 μg/l), zinc (6.5 μg/l), cadmium (40 μg/l), chrome (66 μg/l), nickel (70,113 μg/l), and lead (28 μg/l) [45].

2.3 Experimental design and fish

After acclimating the fish for fifteen days, 2400 sea bass fingerlings (average initial weight: 9.83 ± 2.02 g and initial length of 9.37 ± 0.32 cm) were relocated to 24 experimental concrete containers (3.75 m3). Three stocking densities (50, 100, and 150 fish/m3) were tested with 15ppt zeolite concentration and control treatments (same densities without zeolite). The selection of the zeolite concentration was determined by findings from a prior study of Mansour et al., [25]. Every week, the zeolite sacs were taken out, cleaned with fresh water, let to air dry, and then reused for a maximum of four weeks before being swapped out for new ones. The natural zeolite (clinoptilolite, denoted as Z) employed in this experiment was sourced from Yemen (http://alixzeolite.com/en/). Its physical and chemical characteristics have been detailed in previous studies [12, 25, 38, 39].

2.4 Feed formulation and feeding protocol

The fish were fed with a home-formulated pelleted diet. In line with recommendations from a prior experiment, considerable effort was invested in meticulously formulating the experimental diet to ensure it comprised 38% crude protein and 12% crude lipid, aligning with the specific nutritional requirements of the target species (D. labrax) [46]. Table 1 displays the formulation and approximate composition (%, on a dry matter (DM) basis) of the diet. Fish were fed to satiety four times per day for ninety days.

thumbnail
Table 1. Composition and proximate analysis of diet used during the study.

https://doi.org/10.1371/journal.pone.0297844.t001

2.5 Sample collection and analytical procedures

2.5.1 Water analysis.

The water quality parameters were monitored, including temperature (~ 26–28°C), pH, dissolved oxygen (DO, mg/L), salinity (~ 28–29 ppt), and total ammonia nitrogen (TAN, ppm) on a daily basis for all treatment groups. A portable PH meter (PH-8424) (HANNA Instrument) was used to test both pH and temperature. The measurement of dissolved oxygen was done using the HI-9142 (HANNA Instrument). The YSI Eco Sense EC300 Conductivity/Salinity meter was used to monitor salinity. Utilizing the YSI Professional Plus and YSI 9300 photometers, total ammonia nitrogen (TAN) was tracked. The U.S. Environmental Protection Agency determined the concentration of un-ionized ammonia-N as a percentage of TAN. (www.epa.gov/oeca/disclaimer.html).

2.5.2 Determination of metal concentrations and quality assurance.

Copper (Cu), lead (Pb), cadmium (Cd), iron (Fe), and zinc (Zn) were analyzed in water (μg/L) and fish organs (mg/g wet weight,wt). Heavy metal levels were measured by sampling each tank’s water three times a week. Using Atomic Absorption Spectrophotometer (AAS), samples were examined. Water examination of heavy metals followed Shkinev et al., [47], whereas fish samples were analyzed using Atta et al., [48]. Fish samples were washed with distilled water and scales were removed. The fish were dissected and the muscle tissue, liver, and gills separated using stainless steel instruments and digested as stated [48, 49]. The procedure included breaking down 1 gram of ingredients using a 1:1 mixture of perchloric acid, nitric acid, and sulfuric acid. The mixture was then heated at 200° C for 30 minutes. Once the digest had cooled to room temperature, it was mixed with pure water to make 50 ml. It was then tested for Cu, Zn, Pb, and Cd using an atomic absorption spectrophotometer (AAS type Agilent AA55) at various wavelengths. The same steps were used to make analytical blanks. The answer was mg/kg of wet weight.

2.6 Growth performance, survival and feed utilization

At day 90 of the experiment, the mean body weight (FBW, g) of the experimental treatments was obtained by randomly weighing 15 fish from each tank and dividing the total weight by the fish count. Furthermore, the condition factor (KF) of both treated and untreated D. labrax juveniles was computed. The data were then used to determine if zeolite improved the growth of D. labrax juveniles. According to Cho and Kaushik [50] and Castell and Tiews [51], the growth performance, feed utilization, survival rate and hepatosomatic index of fish juveniles were determined using the following equations.

  1. Weight gain (WG, g) = final body weight (g)-initial body weight (g)
  2. Average daily gain (ADG, g/fish/d) = (Final Weight—Initial Weight) / Number of Days
  3. Specific growth rate (SGR, %/d) = 100 × [(ln final body weight (g)-ln initial body weight (g))/ duration of rearing (day)], where ln is the natural logarithm.
  4. Survival rate (SR,%) = 100 × (initial number of fish/final number of fish).
  5. Hepatosomatic Index (HSI) = (Liver Weight / Total Body Weight) × 100
  6. Feed intake (FI, g/fish) = Total feed supplied—Remaining feed
  7. Feed conversion rate (FCR) = feed intake (g)/weight gain (g).
  8. Protein efficiency rate (PER) = net weight gained (g)/protein intake amount (g).
  9. Condition factor (KF) = 100W/L3, where W = fish weight; L = fish length.

2.7 Feed and fish proximate chemical analyses

Prior to the commencement of the experiment, a random sample of the feed and the fish under investigation (approximately fifty fish) were retained in order to ascertain their initial body chemistry composition. Following the conclusion of the experiment, 15 fish from each treatment were collected as samples in order to identify any nearby contaminants. Samples of the trial feed and fish underwent thorough chemical analysis following AOAC [52] guidelines to assess their moisture, crude protein, crude lipid, crude fiber, and ash contents in the diet. Additionally, protein, lipid, and ash concentrations were analyzed in the whole body of European sea bass as part of the comprehensive evaluation.

2.8 Blood sample: Hematology

The fish underwent anesthesia using 0.3 ml/l of clove oil prior to blood collection. Subsequently, blood samples were drawn from three fish per replicate and twelve fish per treatment via the caudal vein and collected in plastic tubes. Using a 1 ml syringe, blood samples were obtained at the end of the experiment by puncturing the caudal vein. To examine the hematological profile, samples were obtained in tiny plastic tubes containing ethylene diamine tetra acetic acid (EDTA), an anti-coagulating agent. Using Drabkin’s solution and the cyanmethemoglobin technique, the evaluation of hemoglobin concentration (Hgb) was calculated [53].

2.8.1 Serum constituents.

Blood serum was collected without EDTA, allowed to clot at room temperature, and centrifuged at 3000 rpm for 20 minutes. The serum samples were kept at—20°C until analysis. The concentration of glucose was assessed through colorimetric methods as outlined in the procedure detailed by Trinder [54]. Cholesterol (mg/dl) [55], aspartate aminotransferase activity (AST, EC. 2.6.1.1), alanine aminotransferase activity (ALT, EC. 2.6.1.2) [56], and serum urea level [57] were measured using enzymatic methods. El-Nasr Pharmaceutical Chemicals Co. (Egypt) kits were used to calorimetrically identify serum total protein (g/dl) according to the manufacturer’s instructions and the following references: total protein [58] and albumin content [59]. After subtracting albumin (A) from the total protein level, the A/G ratio was computed to determine globulin (G).

2.9 Statistical analysis

To examine differences among the treatments, all data from the experimental trial were statistically analyzed using R, as described by Assaad et al., [60]. The data were analyzed using two-way analysis of variance (ANOVA) with post hoc analysis and the Tukey’s test, with P < 0.05 set as the criterion of significance. The ANOVA method was used to calculate the influence of the zeolite treatment on the survival rate, water quality, growth, and physiological parameters of juvenile European seabass. The data are shown in a tabular format (meaning standard errors).

3. Results

3.1 Heavy metal concentrations in water samples

The mean levels of certain heavy metals (cadmium, copper, zinc, iron, and lead) in water at varying densities for the control and zeolite groups (Table 2). The results presented in demonstrate the concentrations of heavy metals (Cd, Cu, Zn, Fe, and Pb) in water under different treatments, varying in fish density (50, 100, and 150 fish) and the inclusion of zeolite. The values, expressed in micrograms per liter (μg/L) and presented as means ± standard error (SE), reveal significant variations among treatments. For cadmium (Cd), a clear trend of decreasing concentrations is observed with increasing fish density, further accentuated by the addition of zeolite. Copper (Cu), zinc (Zn), iron (Fe), and lead (Pb) also exhibit notable changes in concentration across treatments. Statistical analysis (P-values) underscores the significance of both fish density and zeolite application in influencing heavy metal concentrations, with interactions between these factors also noted. These findings highlight the potential of fish density management and zeolite supplementation as effective strategies for controlling heavy metal levels in aquatic environments.

thumbnail
Table 2. Heavy metals concentration (μg /L) in water of different treatments (Means± SE).

https://doi.org/10.1371/journal.pone.0297844.t002

3.2 Ammonia removal rate, source and ammonia removal rate, control heavy metal concentration

Table 3 presents the ammonia removal rates (ARRS and ARRC, expressed as percentages of the source and control, respectively) for various heavy metals under different treatments, including those involving fish densities treated both with and without zeolite. The results, presented as means with standard errors, highlight substantial variations in ammonia removal efficiency. Zeolite application at different fish densities significantly enhances ammonia removal rates compared to the control. Notably, the removal rates exhibit a clear dose-dependent relationship, with higher fish densities demonstrating superior ammonia removal. The zeolite-treated groups consistently outperform the control, as evidenced by the significantly higher RRS percentages for Cd, Cu, Zn, Fe, and Pb. Additionally, the ARRC percentages underscore the effectiveness of zeolite in augmenting ammonia removal compared to the control, with significant differences observed across all metals. The interaction effects between treatment and fish density further emphasize the nuanced interplay influencing ammonia removal rates in this experimental setup. Overall, the results underscore the potential of zeolite treatment in enhancing ammonia removal efficiency in aquatic environments.

thumbnail
Table 3. Heavy metals concentration in ammonia removal rate; as % of the source (ARRS) and ammonia removal rate; as % of the control (ARRC) of different treatments (Means± SE).

https://doi.org/10.1371/journal.pone.0297844.t003

3.3 The determination of heavy metal concentrations in European sea bass tissues

Heavy metals like Fe, Cu, Zn, Cd, and Pb (mg/g wet wt.) were found in sea bass fingerlings’ gills, liver, and muscles at different concentrations, with and without zeolite treatment (Table 4). All metal accumulation patterns varied significantly (p < 0.001) among treatments and fish organs. Table 4 reveals that all fish had the least amount of metals (Fe, Cu, and Zn) in their muscles, whereas almost all fish had the most Fe, Cu, and Zn in their liver. Tukey’s test indicated metal variations, such as the highest levels of Fe, Cu, and Zn in the liver in different treatments, whereas muscles had the lowest concentration of all metals. When investigating how metals fluctuate in water based on the density of the fish, Table 4 indicates that adding zeolite significantly decreased heavy metal accumulation (p < 0.001) in all organs of sea bass of all densities. Furthermore, higher fish density is linked to lower heavy metal accumulations in all organs of sea bass.

thumbnail
Table 4. Means± SE of heavy metals concentration (mg/g wet weight) in different organs of European sea bass in different treatments.

https://doi.org/10.1371/journal.pone.0297844.t004

3.4 Efficacy of ammonia removal and water quality

The result of the water quality parameters of European seabass when treated with zeolite as removal of ammonia concentration was shown in Table 5. The data demonstrated that when density increased, dissolved oxygen (DO, mg/L), pH, and nitrate (NO3, mg/L) levels declined considerably (p < 0.05). However, ionized ammonium (NH4, mg/L), unionized ammonia (NH3, mg/L), and nitrite (NO2, mg/L) rise. The results also showed that the zeolite treatment significantly improved (p < 0.05) the water quality parameters by lowering NH4, NH3, and NO2 levels compared to the control treatments. The addition of zeolite resulted in significant DO, pH, and ammonia readings. In addition, for all water quality metrics, there was a substantial relationship between stocking density (SD) and zeolite treatment. The results revealed that pH and DO increased considerably (p < 0.05) from 6.7 and 4.8 with high density in the control treatment to 7.95 and 6.75 with low density in the zeolite treatment. Throughout the research period (Table 5), the overall values of ionized ammonium (NH4), unionized ammonia (NH3), and nitrite (NO2) were substantially different (p < 0.05) among the tested treatments. The addition of natural zeolite had an inverse connection with all ammonia readings. It was found that stocking densities greatly (p < 0.05) raised ammonia levels. The tested zeolite did better than the control treatments when it came to removing ammonia from the source water. The zeolite treatment with a low stocking density had the best results, with a 63% removal rate. With decreasing stocking density, the value of the ammonia removal rate as a proportion of the source water rises.

thumbnail
Table 5. Water quality parameters of European seabass treated with natural zeolite as removal of stressful ammonia concentrations.

https://doi.org/10.1371/journal.pone.0297844.t005

3.5 Efficiency in growth, survival, and food consumption

Table 6 outlines the growth performance and survival rates of European seabass exposed to natural zeolite treatment and a control treatment without zeolite, across varying densities aimed at mitigating elevated ammonia concentrations. The results, with means and standard errors, reveal significant improvements in various growth parameters and survival rates in the zeolite-treated groups compared to the control. The final weight, weight gain, average daily gain (ADG), specific growth rate (SGR), and survival percentage consistently demonstrate substantial enhancements with zeolite application, particularly at higher fish densities. The hepatosomatic index (HSI) and condition factor (KF) also reflect positive trends with zeolite treatment. Statistical analysis indicates highly significant differences (p < 0.001) across treatments for most variables, emphasizing the positive impact of zeolite on the growth and health of European seabass under conditions of ammonia stress. The interaction effects between treatment and fish density further underscore the nuanced dynamics influencing the observed improvements. Overall, these findings highlight the potential of natural zeolite as a beneficial intervention for mitigating the negative effects of ammonia stress on the growth and survival of European seabass.

thumbnail
Table 6. Growth performance and survival rate of European seabass treated with natural zeolite as a removal of stressful ammonia concentrations.

https://doi.org/10.1371/journal.pone.0297844.t006

3.6 Feed utilization and carcass composition percentage of European seabass treated with natural zeolite

Table 7 displays the feed utilization and proximal body analysis of juvenile European sea bass under natural zeolite treatment compared to a control treatment without zeolite, across different densities. The percentage body composition of juvenile D. labrax exhibited significant differences (p < 0.05) in all aspects except for body moisture. The result show that stocking density and zeolite had a significant (p < 0.05) impact on the feed conversion ratio (FCR) and the protein efficiency ratio (PER). The best results were seen when stocking density and zeolite were kept as low as possible. The findings clearly show that adding zeolite has a significant impact on the growth performance, feed utilization, and survival rate of juvenile seabass. The zeolite groups exhibited a statistically significant increase in final body protein levels (p < 0.05), although body ash and lipids were found to be lower compared to the control group. Additionally, research has shown that an increase in density causes a decrease in protein content as well as an increase in lipid and ash contents. The study observed the relationship between zeolite treatment and density, specifically in relation to ash. The results indicated that the maximum value of 18.8 ± 0.36% was seen in the high-density control group, while the lowest value of 11.6 ± 0.439% was observed in the low-density group with zeolite treatment.

thumbnail
Table 7. Feed utilization and carcass composition of European seabass treated with natural zeolite as removal of stressful ammonia concentrations.

https://doi.org/10.1371/journal.pone.0297844.t007

3.7 Hematological analysis

Table 8 displays the hematological parameters of European seabass under natural zeolite treatment and a control treatment without zeolite, across various fish densities, for mitigating stressful ammonia concentrations. The data, expressed as means with standard errors, reveal significant improvements in several hematological indicators in the zeolite-treated groups compared to the control. Zeolite application, particularly at higher fish densities, leads to a significant increase in red blood cell count (RBCs) and hemoglobin levels (Hb), emphasizing the positive impact on oxygen-carrying capacity. Hematocrit (Hct) also exhibits improvements with zeolite treatment. White blood cell count (WBCs) and differential leukocyte percentages (lymphocytes, monocytes, neutrophils) indicate a positive influence on immune response, with higher fish densities showing enhanced immune parameters. Statistical analysis demonstrates highly significant differences (p < 0.001) across treatments for most variables, highlighting the positive effects of zeolite in ameliorating hematological stress induced by ammonia. The interaction effects between treatment and fish density provide valuable insights into the nuanced dynamics influencing these hematological responses. Overall, the results suggest that natural zeolite treatment contributes to improved hematological health in European seabass exposed to ammonia stress.

thumbnail
Table 8. Hematological parameters of European seabass treated with natural zeolite as removal of stressful ammonia concentrations.

https://doi.org/10.1371/journal.pone.0297844.t008

3.8 Serum biochemical values

Table 9 presents the biochemical parameters of European seabass under natural zeolite treatment and a control treatment without zeolite, across various fish densities, for mitigating stressful ammonia concentrations. The results, with means and standard errors, highlight significant improvements in multiple biochemical markers in zeolite-treated groups compared to the control. Notably, cholesterol levels exhibit a dose-dependent decrease with increasing fish density, emphasizing the positive impact of zeolite. The total protein and albumin levels, while showing some variations, do not reach statistical significance. Glucose levels are significantly elevated in zeolite-treated groups, suggesting a potential metabolic response to zeolite application. The albumin/globulin ratio (A/G) significantly increases with zeolite treatment, indicative of improved protein metabolism. Urea, uric acid, and lysozyme levels demonstrate mixed trends across treatments. Importantly, zeolite treatment leads to significant reductions in aspartate aminotransferase (AST) and alanine aminotransferase (ALT), indicating a protective effect on liver function. Statistical analysis underscores the significance of zeolite treatment for most parameters (p < 0.001), with notable interactions between treatment and fish density. These findings suggest that natural zeolite application contributes to favorable biochemical profiles, showcasing its potential in mitigating the biochemical impacts of ammonia stress in European seabass.

thumbnail
Table 9. Biochemical parameters of European seabass treated with natural zeolite as removal of stressful ammonia concentrations.

https://doi.org/10.1371/journal.pone.0297844.t009

4. Discussion

There were two main goals of this study: to find out if natural zeolite could help with two big environmental problems that aquaculture faces: getting rid of heavy metals and reducing ammonia stress in young European sea bass. This investigation specifically targeted underground water sources with varying densities. Naturally-occurring substances known as heavy metals may pose significant threats to both aquatic ecosystems and human health when they are found in water in excessive amounts [61]. In the present study, we observed the mean values of some heavy metals’ values between control and zeolite groups (cadmium, copper, zinc iron, and lead) in water at different densities. It was found that the zeolite group had lower concentrations of Cd, Cu, Zn, and Fe compared to the control group. This happened at different densities. Consistent with our results, studies have shown that natural zeolites can remove heavy metal cations (Mn, Fe, Cd, Zn, Pb, Cu, Co, Cr, Cu, and Pb) from waste and drinking water up to 97% of the time [33].

The potential mechanisms through which zeolite contributes to the removal of heavy metals involve various factors, primarily centered around its exceptional adsorption capacities and interactions with metal ions [62]. Zeolites, owing to their unique crystal structures and high surface areas, possess inherent adsorption sites that attract and retain heavy metal ions. The ion exchange capability of zeolites allows them to selectively replace cations in their structure with heavy metal ions, facilitating the removal of these contaminants from aqueous solutions [63]. Additionally, the surface chemistry of zeolites plays a crucial role in metal adsorption, with active functional groups enhancing binding affinity. Moreover, the specific mineralogical composition of zeolites influences their metal sorption capacities [64]. Previous studies, such as those by Figueiredo and Quintelas [65] and Roshanfekr Rad and Anbia [66], have extensively explored and supported these mechanisms, providing valuable insights into the intricate processes by which zeolites effectively contribute to the removal of heavy metals from various environmental matrices.

Additionally, earlier research has shown zeolite’s capacity to absorb heavy metals from wastewater from industry, municipalities, and agriculture [67]. During the course of the experiment, it was observed that the zeolite group with a density of 150 had depressed levels of Cd and Pb. Consistent with our research findings, previous reports have shown that the inclusion of zeolite in water had a beneficial impact on the elimination of Cd and Pb contaminants from Oreochromis mossambicus [68]. One potential factor contributing to our findings might be the insufficient duration of the study period, which may have hindered the total elimination of Cd and Pb from seabass. Additionally, the density of the seabass population could have had a role in these outcomes. Our findings also showed that the percentage of heavy metal removal (RRS%) from water increased with density. Additionally, the RRS% of Cd, Cu, Zn, and Fe was greatly boosted by the addition of zeolite. Accordingly, when zeolite treatment is applied, the percentage of ammonia removal rate at varying densities increases considerably for all heavy metals (Cd, Cu, Zn, Fe, and Pb) when compared to the control group. Erdem et al. suggested that natural zeolites had significant capabilities for the removal of heavy metals [69].

Our results showed that the addition of zeolite has a substantial and favorable influence on lowering heavy metal accumulation in the liver, gills, and muscles of sea bass across all densities. Furthermore, increasing fish density is related to lower heavy metal accumulations in all organs of sea bass. In agreement with our findings, James and Sampath discovered that the presence of zeolite in water reduced heavy metals such as Cd in the muscle of Oreochromis mossambicus [68]. Similarly, the zeolite-treated group had the lowest accumulation of heavy metals such as Cu in the liver and muscle of Oreochromis niloticus [70]. The results also showed that the zeolite treatment made the water quality better by lowering the levels of NH4, NH3, and NO2 by a lot compared to the control treatments. This led to higher readings for DO, pH, and ammonia. Furthermore, there was a significant relationship between stocking density (SD) and zeolite treatment for all water quality metrics. Saeed et al. came to the same conclusion, showing that adding zeolite greatly decreased the amounts of all inorganic dissolved nitrogen in water, including ammonia (NH3, NH4-N), nitrite (NO2), and nitrate (NO3) [71]. This is consistent with our findings, since NO2 levels fall dramatically as the zeolite level increases. This discovery might be attributed mostly to zeolite’s adsorption ability, which attracted nitrate ions and enhanced nutrient preservation from water [72]. In addition, we noticed an increase in water pH and DO in the treatment group as compared to the control group. Finding high pH levels might have something to do with the fact that zeolites are slightly acidic and sodium-form exchangers prefer hydrogen. This means that high pH levels are found when the exchanger is balanced with electrolyte solutions that aren’t very strong [73].

The incorporation of zeolite into the water or feed used in fish raising has several advantages that have both direct and indirect impacts on the well-being of aquatic organisms. The current investigation documented an enhancement in growth and feed utilization indices (namely, FBW, WG, ADG, SGR%, survival, and KF) of European sea bass as the concentration of zeolite increased. Similar to this study, Ali et al. discovered that adding natural zeolite to tanks for rearing as a water adjuvant increased the ADG and survival rate of Dicentrarchus labrax [12]. Similarly, Rabiatul et al. and Aly et al. found a significant positive correlation between the development efficacy of Oreochromis sp. and D. labrax, and increasing zeolite levels [16, 74]. The feed utilization and carcass composition of European seabass treated with natural zeolite demonstrated that except for body moisture, there were significant variations in the body composition of juvenile D. labrax (p < 0.05). According to the findings, stocking density and zeolite had a significant (p < 0.05) influence on FCR and PER. Recently it has been reported that stocking density had a negative effect, but PER and FCR got much better when the zeolite level went up. However, a substantial rise in body protein was seen, and when zeolite was increased, the negative effects of increased density were lessened. Meanwhile, the quantity of fat and ash decreased [39]. The enhancement of fish growth performance and feed utilization by zeolite can be attributed to its effectiveness in reducing ammonia levels and toxicity, thereby improving water quality. This improvement in water conditions enables the conservation of energy that would otherwise be expended in coping with adverse environmental factors, redirecting it towards growth [75, 76].

The hematological parameters of the fish mirrored the escalating deterioration of the surrounding rearing water, and these measurements can serve as valuable tools for regular assessments of the physiological status of the fish [77, 78]. The current result demonstrated that the incorporation of zeolite had a favorable and advantageous impact on crucial hematological parameters in juvenile D. labrax (European seabass) in comparison to a control group. There are many things that can change the blood parameters of fish, including the season, the quality of the water, the fish’s age, its sex, its nutrition, its health, its genetic makeup, how it was transported and handled, and other environmental conditions, as well as the ways it was sampled and analyzed in the lab [79, 80]. Biochemical parameters are commonly employed for assessing the physiological and overall health condition of aquatic organisms [8183]. Elevated ALT and AST activities are acknowledged as markers reflecting the liver’s health status [8486]. The result of the present study significantly increases the albumin, cholesterol, and urea, as well as liver function enzymes such as AST and ALT, in the European sea bass exposed to the highest density. There are compensatory effects of zeolite on the levels of total protein and globulin at the maximal density of fish rearing. Furthermore, the water interventions resulted in considerable alleviation of cholesterol, urea, AST, and ALT levels in both densities. Similarly, Çoğun and Şahin observed that the administration of zeolite effectively mitigated the elevated levels of serum cortisol, ALT, AST, and cholinesterase in Nile tilapia subjected to lead-induced poisoning [87].

5. Conclusions

The study demonstrates that incorporating zeolite into the water significantly enhances water quality metrics, effectively mitigating the adverse effects of increased aquaculture density on water quality indicators. Elevated stocking densities of European sea bass resulted in a noticeable decline in growth performance, feed utilization, and various hemato-biochemical indices. However, upon introducing zeolite, improvements were observed in feed utilization, hematological parameters, and biochemical aspects of fish growth performance. The study’s findings highlight the efficacy of zeolite (15 ppt) in reducing heavy metal deposition in both water and fish organs, contributing to enhanced fish growth and development. Despite an increase in density, the study reveals a substantial reduction in the buildup of heavy metals in water and fish organs. This research underscores the potential of natural zeolites to alleviate the impact of water quality issues, showcasing their effectiveness in diminishing heavy metal deposition in fish tissues by reducing their availability in polluted water.

Acknowledgments

We extend our thanks to the Administration of the National Institute of Oceanography and Fisheries (NIOF), Egypt, for their invaluable encouragement and support of our teamwork. In addition, we would like to thank the African Center of Excellence in Neglected and Underutilized Biodiversity (ACENUB), MZUZU University, Malawi, for open access support.

References

  1. 1. FAO. The State of Food Security and Nutrition in the World: 2022: Repurposing Food and Agricultural Policies to Make Healthy Diets More Affordable: FAO; 2022.
  2. 2. FAO. The state of world fisheries and aquaculture 2022. Towards blue transformation. Food and Agriculture Organization of the United Nations Rome, Italy; 2022.
  3. 3. Tacon AGJ. Trends in Global Aquaculture and Aquafeed Production: 2000–2017. Rev Fish Sci Aquac. 2020;28(1):43–56. https://doi.org/10.1080/23308249.2019.1649634.
  4. 4. Halwart M. Fish farming high on the global food system agenda in 2020. FAO Aquaculture Newsletter. 2020;(61):II–III.
  5. 5. Emenike EC, Iwuozor KO, Anidiobi SU. Heavy metal pollution in aquaculture: Sources, impacts and mitigation techniques. Biol Trace Elem Res. 2022;200(10):4476–92. pmid:34813030
  6. 6. Stickney RR, Gatlin DM III. Aquaculture: An introductory text: Cabi; 2022.
  7. 7. Soliman NF. Aquaculture in Egypt under changing climate. Alexandria Research Center for Adaptation to Climate Change (ARCA): Alexandria, Egypt. 2017.
  8. 8. Vo TTE, Je S-M, Jung S-H, Choi J, Huh J-H, Ko H-J. Review of photovoltaic power and aquaculture in desert. Energies. 2022;15(9):3288.
  9. 9. Ibrahim LA, Abu-Hashim M, Shaghaleh H, Elsadek E, Hamad AAA, Alhaj Hamoud Y. A comprehensive review of the multiple uses of water in aquaculture-integrated agriculture based on international and national experiences. Water. 2023;15(2):367.
  10. 10. Ficke AD, Myrick CA, Hansen LJ. Potential impacts of global climate change on freshwater fisheries. Rev Fish Biol Fish. 2007;17(4):581–613. https://doi.org/10.1007/s11160-007-9059-5.
  11. 11. Mishra RK. Fresh water availability and its global challenge. BJMAS. 2023;4(3):1–78. https://doi.org/10.37745/bjmas.2022.0208.
  12. 12. Aly HA, Abdel-Rahim MM, Sallam GR, Lotfy AM, Abdelaty BS. Use of natural zeolites as a detoxifier of heavy metals in water and the flesh of reared european seabass dicentrarchus labrax. Croatian Journal of Fisheries. 2020;78(3):121–32. https://doi.org/10.2478/cjf-2020-0012.
  13. 13. Badiola M, Mendiola D, Bostock J. Recirculating Aquaculture Systems (RAS) analysis: Main issues on management and future challenges. Aquac Eng. 2012;51:26–35. https://doi.org/10.1016/j.aquaeng.2012.07.004.
  14. 14. Dalsgaard J, Lund I, Thorarinsdottir R, Drengstig A, Arvonen K, Pedersen PB. Farming different species in RAS in Nordic countries: Current status and future perspectives. Aquac Eng. 2013;53:2–13. https://doi.org/10.1016/j.aquaeng.2012.11.008.
  15. 15. Nootong K, Pavasant P, Powtongsook S. Effects of organic carbon addition in controlling inorganic nitrogen concentrations in a biofloc system. J World Aquac Soc. 2011;42(3):339–46. https://doi.org/10.1111/j.1749-7345.2011.00472.x.
  16. 16. Aly HA, Abdel-Rahim M, Lotfy AM, Abdelaty BS, Sallam GR. The applicability of activated carbon, natural zeolites, and probiotics (EM®) and its effects on ammonia removal efficiency and fry performance of European seabass Dicentrarchus labrax. J Aquac Res Dev. 2016;7(11):459–66. https://doi.org/10.4172/2155-9546.1000459.
  17. 17. Mehrim A. Effect of dietary supplementation of Biogen®(Commercial probiotic) on mono-sex Nile tilapia Oreochromis niloticus under different stocking densities. J Fish Aquat Sci. 2009;4(6):261–73.
  18. 18. Islam MM, Barman A, Khan MI, Mukul SA, Stringer LC. Biofloc aquaculture as an environmentally friendly climate adaptation option. Anthr Sci. 2022;1(1):231–2. https://doi.org/10.1007/s44177-021-00006-w.
  19. 19. Trang NTD, Brix H. Use of planted biofilters in integrated recirculating aquaculture-hydroponics systems in the Mekong Delta, Vietnam. Aquac Res. 2014;45(3):460–9. https://doi.org/10.1111/j.1365-2109.2012.03247.x.
  20. 20. Freitas de Oliveira F, Moreira RG, Schneider RP. Evidence of improved water quality and biofilm control by slow sand filters in aquaculture–A case study. Aquac Eng. 2019;85:80–9. https://doi.org/10.1016/j.aquaeng.2019.03.003.
  21. 21. Bomo AM, Ekeberg D, Stevik TK, Hanssen JF, Frostegård Å. Retention and removal of the fish pathogenic bacterium Yersinia ruckeri in biological sand filters. J Appl Microbiol. 2004;97(3):598–608. https://doi.org/10.1111/j.1365-2672.2004.02342.x.
  22. 22. STEŢCA G, MOREA A. Physiological effects of natural zeolites in fish feed. Bulletin of the University of Agricultural Sciences & Veterinary Medicine Cluj-Napoca Animal Science & Biotechnologies. 2013;70(2).
  23. 23. Ghasemi Z, Sourinejad I, Kazemian H, Rohani S. Application of zeolites in aquaculture industry: a review. Rev Aquac. 2018;10(1):75–95. https://doi.org/10.1111/raq.12148.
  24. 24. Hamed M, Hussein M, Abd-Eltwab A, Salama S. Using the natural zeolite (clinoptiolite) in removing ammonia, heavy metals and improving water quality in fish ponds. Azhar J Agric Res. 2022;47(1):79–88. https://doi.org/10.21608/ajar.2022.266486.
  25. 25. Mansour AT, Fayed WM, Alsaqufi AS, Aly HA, Alkhamis YA, Sallam GR. Ameliorative effects of zeolite and yucca extract on water quality, growth performance, feed utilization, and hematobiochemical parameters of European seabass reared at high stocking densities. Aquac Rep. 2022;26:101321. https://doi.org/10.1016/j.aqrep.2022.101321.
  26. 26. Sharma A, Grewal AS, Sharma D, Srivastav AL. Chapter 3—Heavy metal contamination in water: consequences on human health and environment. In: Shukla SK, Kumar S, Madhav S, Mishra PK, editors. Metals in Water: Elsevier; 2023. p. 39–52.
  27. 27. Pandey G, Madhuri S. Heavy metals causing toxicity in animals and fishes. Res J Anim Vet Fishery Sci. 2014;2(2):17–23.
  28. 28. Khayatzadeh J, Abbasi E, editors. The effects of heavy metals on aquatic animals. The 1st International Applied Geological Congress, Department of Geology, Islamic Azad University–Mashad Branch, Iran; 2010.
  29. 29. Castro R, Lamas J, Morais P, Sanmartín ML, Orallo F, Leiro J. Resveratrol modulates innate and inflammatory responses in fish leucocytes. Vet Immunol Immunopathol. 2008;126(1):9–19. pmid:18644630
  30. 30. Al-Busaidi M, Yesudhason P, Al-Mughairi S, Al-Rahbi WAK, Al-Harthy KS, Al-Mazrooei NA, et al. Toxic metals in commercial marine fish in Oman with reference to national and international standards. Chemosphere. 2011;85(1):67–73. pmid:21700309
  31. 31. Rahman MS, Molla AH, Saha N, Rahman A. Study on heavy metals levels and its risk assessment in some edible fishes from Bangshi River, Savar, Dhaka, Bangladesh. Food Chem. 2012;134(4):1847–54. pmid:23442629
  32. 32. Francis-Floyd R, Watson C, Petty D, Pouder DB. Ammonia in aquatic systems. UF/IFAS University of Florida (UF)/Institute of Food and Agricultural Sciences (IFAS), FA. 2009;16:1–4.
  33. 33. Margeta K, Logar NZ, Šiljeg M, Farkaš A. Natural zeolites in water treatment–how effective is their use. Water treatment. 2013;5:81–112. https://doi.org/10.5772/50738.
  34. 34. Rahman Z, Singh VP. The relative impact of toxic heavy metals (THMs) (arsenic (As), cadmium (Cd), chromium (Cr)(VI), mercury (Hg), and lead (Pb)) on the total environment: an overview. Environ Monit Assess. 2019;191(7):419. pmid:31177337
  35. 35. Altaf M, Yamin N, Muhammad G, Raza MA, Shahid M, Ashraf RS. Electroanalytical techniques for the remediation of heavy metals from wastewater. In: Inamuddin , Ahamed MI, Lichtfouse E, editors. Water Pollution and Remediation: Heavy Metals. Cham: Springer International Publishing; 2021. p. 471–511.
  36. 36. Yılmaz F, Özdemir N, Demirak A, Tuna AL. Heavy metal levels in two fish species Leuciscus cephalus and Lepomis gibbosus. Food Chem. 2007;100(2):830–5. https://doi.org/10.1016/j.foodchem.2005.09.020.
  37. 37. Mulligan CN, Yong RN, Gibbs BF. Remediation technologies for metal-contaminated soils and groundwater: an evaluation. Eng Geol. 2001;60(1):193–207. https://doi.org/10.1016/S0013-7952(00)00101-0.
  38. 38. Abdel-Rahim MM. Sustainable use of natural zeolites in aquaculture: a short review. Oceanogr Fish. 2017;2(4):1–5. https://doi.org/10.19080/OFOAJ.2017.02.555593.
  39. 39. Fayed WM, Sallam GR, Khalid AE, Kashuit AA, Aly HA, Omar EA. Zeolite as a major control factor of water quality problems arising from stocking density of European sea bass (Dicentrarchus labrax) juveniles. Aquac Aquar Conserv Legis. 2019;12(3):953–67.
  40. 40. Armaǧan B, Özdemir O, Turan M, Çelik M. The removal of reactive azo dyes by natural and modified zeolites. J Chem Technol Biotechnol. 2003;78(7):725–32. https://doi.org/10.1002/jctb.844.
  41. 41. Wang S, Peng Y. Natural zeolites as effective adsorbents in water and wastewater treatment. Chem Eng J. 2010;156(1):11–24. https://doi.org/10.1016/j.cej.2009.10.029.
  42. 42. Elnabris KJ, Muzyed SK, El-Ashgar NM. Heavy metal concentrations in some commercially important fishes and their contribution to heavy metals exposure in Palestinian people of Gaza Strip (Palestine). J Assoc Arab Univ Basic Appl Sci. 2013;13(1):44–51. https://doi.org/10.1016/j.jaubas.2012.06.001.
  43. 43. Percie du Sert N, Hurst V, Ahluwalia A, Alam S, Avey MT, Baker M, et al. The ARRIVE guidelines 2.0: Updated guidelines for reporting animal research*. Journal of Cerebral Blood Flow & Metabolism. 2020;40(9):1769–77. pmid:32663096.
  44. 44. Moretti F. Atlas of the European novel: 1800–1900: verso; 1999.
  45. 45. Abdel-Rahim MM, Elhetawy AIG, Refaey WMA, Lotfy AM, El-Zaeem SY, Elebiary EH, et al. Potential benefits of natural bentonite as a water clarifier on ammonia removal, performance, immunity, antioxidant, and histology of Dicentrarchus labrax. Egypt J Aquat Res. 2023;49(2):253–60. https://doi.org/10.1016/j.ejar.2023.04.002.
  46. 46. El-Dahhar A, Samira S, Shimaa A, Mona M. Effect of early weaning diets with different levels of selenium on survival and growth of European sea bass larvae. J Arabian Aquac Soc. 2016;11:35–47. https://doi.org/10.12816/0042803.
  47. 47. Shkinev VM, Gomolitskii VN, Spivakov BY, Geckeler KE, Bayer E. Determination of trace heavy metals in waters by atomic-absorption spectrometry after preconcentration by liquid-phase polymer-based retention. Talanta. 1989;36(8):861–3. pmid:18964820
  48. 48. Atta A, Voegborlo RB, Agorku ES. Total mercury distribution in different tissues of six species of freshwater fish from the Kpong hydroelectric reservoir in Ghana. Environ Monit Assess. 2012;184(5):3259–65. pmid:21713471
  49. 49. Bernhard M. Manual of methods in aquatic environment research. Part 3- Sampling and analyses of biological material(Guidelines for the FAO (GFCM)/UNEP Joint Coordinated Project on Pollution in the Mediterranean). FAO Fish Tech Pap. 1976;(158).
  50. 50. Cho C, Kaushik S. Nutritional energetics in fish: energy and protein utilization in rainbow trout (Salmo gairdneri). Aspects of food production, consumption and energy values. 1990;61:132–72. https://doi.org/10.1159/000417529.
  51. 51. Castell J, Tiews K. Report of the EIFAC, IUNS and ICES Working Group on Standardization of Methodology in Fish Nutrition Research, Hamburg, Federal Republic of Germany, 21–23 March 1979. Documents Techniques de la CECPI (FAO). 1980.
  52. 52. AOAC HW. International A: Official Methods of Analysis of the AOAC International. The Association: Arlington County, VA, USA. 2000.
  53. 53. Goldenfarb PB, Bowyer FP, Hall E, Brosious E. Reproducibility in the Hematology Laboratory: The Microhematocrit Determination. Am J Clin Pathol. 1971;56(1):35–9. pmid:5556212
  54. 54. Trinder P. Determination of glucose concentration in the blood. Ann Clin Biochem. 1969;6:24.
  55. 55. Endo H, Maita M, Takikawa M, Ren H, Hayashi T, Urano N, et al. Enzyme sensor system for determination of total cholesterol in fish plasma. Fish Sci. 2003;69(6):1194–9. https://doi.org/10.1111/j.0919-9268.2003.00745.x.
  56. 56. Reitman S, Frankel S. A colorimetric method for the determination of serum glutamic oxalacetic and glutamic pyruvic transaminases. Am J Clin Pathol. 1957;28(1):56–63. pmid:13458125
  57. 57. Barham D, Trinder P. Enzymatic determination of uric acid. Analyst. 1972;97:142–5.
  58. 58. Bradford MM. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem. 1976;72(1):248–54. pmid:942051
  59. 59. Wotton I, Freeman H. Microanalysis in Medical Biochemistry. Churchill, New York. USA. Wiegertjes, GF, RJM Stet, HK Parmentier and WB Van Muiswinkel, 1996. Immunogenetics of disease resistance in fish; a comparable approach Dev. Comp Immunol. 1982;20:365–81.
  60. 60. Assaad HI, Hou Y, Zhou L, Carroll RJ, Wu G. Rapid publication-ready MS-Word tables for two-way ANOVA. SpringerPlus. 2015;4(1):33. pmid:25635246
  61. 61. Shah AI, editor Heavy metal impact on aquatic life and human health–an over view. IAIA17 conference proceedings| IA’s contribution in addressing climate change 37th annual conference of the international association for impact assessment; 2017.
  62. 62. Ugwu EI, Othmani A, Nnaji CC. A review on zeolites as cost-effective adsorbents for removal of heavy metals from aqueous environment. International Journal of Environmental Science and Technology. 2022;19(8):8061–84.
  63. 63. Ramesh K, Reddy DD. Chapter Four—Zeolites and Their Potential Uses in Agriculture. In: Sparks DL, editor. Advances in Agronomy. 113: Academic Press; 2011. p. 219–41.
  64. 64. Hong M, Yu L, Wang Y, Zhang J, Chen Z, Dong L, et al. Heavy metal adsorption with zeolites: The role of hierarchical pore architecture. Chem Eng J. 2019;359:363–72. https://doi.org/10.1016/j.cej.2018.11.087.
  65. 65. Figueiredo H, Quintelas C. Tailored zeolites for the removal of metal oxyanions: Overcoming intrinsic limitations of zeolites. Journal of Hazardous Materials. 2014;274:287–99. pmid:24794984
  66. 66. Roshanfekr Rad L, Anbia M. Zeolite-based composites for the adsorption of toxic matters from water: A review. Journal of Environmental Chemical Engineering. 2021;9(5):106088. https://doi.org/10.1016/j.jece.2021.106088.
  67. 67. Wen J, Yi Y, Zeng G. Effects of modified zeolite on the removal and stabilization of heavy metals in contaminated lake sediment using BCR sequential extraction. J Environ Manage. 2016;178:63–9. pmid:27136618
  68. 68. James R, Sampath K. Effect of zeolite on the reduction of cadmium toxicity in water and a freshwater fish, Oreochromis mossambicus. Bull Environ Contam Toxicol. 1999;62(2):222–9. https://doi.org/10.1007/s001289900863.
  69. 69. Erdem E, Karapinar N, Donat R. The removal of heavy metal cations by natural zeolites. J Colloid Interface Sci. 2004;280(2):309–14. pmid:15533402
  70. 70. Türkmen M, Dinler ZM. Protective effects of zeolite (clinoptilolite) on copper toxicity in tilapia (Oreochromis niloticus). J Anatol Environ Anim Sci. 2021;6(2):188–94. https://doi.org/10.35229/jaes.844104.
  71. 71. Saeed SM , AF FE-B, Shehab El Din M, Ibrahim IH. Role of natural zeolite in improving water quality, performance and health status of Nile tilapia (Oreochromis niloticus L.) in earthen ponds. Abbassa Int J Aqua. 2015;8(2):361–83.
  72. 72. Mumpton FA. La roca magica: Uses of natural zeolites in agriculture and industry. Proc Natl Acad Sci. 1999;96(7):3463–70. pmid:10097058
  73. 73. Leinonen H, Lehto J. Purification of metal finishing waste waters with zeolites and activated carbons. Waste Manag Res. 2001;19(1):45–57. pmid:11525475
  74. 74. Zain R, Shaari N, Amin M, Jani M. Effects of different dose of zeolite (clinoptilolite) in improving water quality and growth performance of red hybrid tilapia (Oreochromis sp.). ARPN J Eng Appl Sci. 2018;13(24):9421–6.
  75. 75. Chartois H, Delbard C, Le Delliou H, Person-Le Ruyet J. Toxicity of ammonia to turbot juveniles: 1. effects on survival, growth and food utilisation. Aquatic Living Resources. 1997;10(5):307–14. Epub 09/15. https://doi.org/10.1051/alr:1997034.
  76. 76. Sallam GR, Habib YJ, El Basuini MF, Fayed WM, Shehata AI. Synergistic interactions of zeolite, stocking density, and water exchange: A holistic approach to optimizing aquaculture performance of juvenile European seabass (Dicentrarchus labrax). Scientific African. 2024;23:e02043. https://doi.org/10.1016/j.sciaf.2023.e02043.
  77. 77. Foss A, Kristensen T, Åtland Å, Hustveit H, Hovland H, Øfsti A, et al. Effects of water reuse and stocking density on water quality, blood physiology and growth rate of juvenile cod (Gadus morhua). Aquaculture. 2006;256(1):255–63. https://doi.org/10.1016/j.aquaculture.2006.02.032.
  78. 78. Hussein EE, Habiba MM, Ashry AM, Al-Zayat AM, Teiba II, Shehata AI, et al. Effects of dietary supplementation with organic acids mixture on growth, feed efficiency, hematobiochemical parameters, immunity, and intestinal microbiota of Gilthead seabream (Sparus aurata) juveniles. Aquac Rep. 2023;33:101846. https://doi.org/10.1016/j.aqrep.2023.101846.
  79. 79. Rey Vázquez G, Guerrero GA. Characterization of blood cells and hematological parameters in Cichlasoma dimerus (Teleostei, Perciformes). Tissue Cell. 2007;39(3):151–60. https://doi.org/10.1016/j.tice.2007.02.004.
  80. 80. Shadrack RS, Kotra KK, Gereva S, Teiba II, El-Ratel IT, El Basuini MF. Utilizing dietary probiotics can boost amberjack (Seriola dumerili) lysozyme activity, antioxidant capacity, and gut microbiota. Scientific African. 2023;22:e01905. https://doi.org/10.1016/j.sciaf.2023.e01905.
  81. 81. Elhetawy AIG, Abdel-Rahim MM, Sallam AE, Shahin SA, Lotfy AMA, El Basuini MF. Dietary wood and activated charcoal improved ammonium removal, heavy metals detoxification, growth performance, blood biochemistry, carcass traits, and histopathology of European seabass. Aquaculture Nutrition. 2023;2023:8860652. pmid:38023984
  82. 82. Wang T, Wang X, Shehata AI, Wang R, Yang H, Wang Y, et al. Growth performance, physiological and antioxidant capacity responses to dietary fish meal replacement with insect meals for aquaculture: A case study in red claw crayfish (Cherax quadricarinatus). Aquac Res. 2022;53(10):3853–64. https://doi.org/10.1111/are.15892.
  83. 83. Arafa SSI, Omar EA, Yousef MI, Srour TM, Shehata AI. Modulation of growth performance, feed utilization, and physiological traits in redbelly Tilapia (Tilapia zillii) through environmental and sex-based interactions. Journal of Animal Physiology and Animal Nutrition. 2024;n/a(n/a). https://doi.org/10.1111/jpn.13918.
  84. 84. Shehata AI, Alhoshy M, Wang T, Mohsin M, Wang J, Wang X, et al. Dietary supplementations modulate the physiological parameters, fatty acids profile and the growth of red claw crayfish (Cherax quadricarinatus). Journal of Animal Physiology and Animal Nutrition. 2023;107(1):308–28. https://doi.org/10.1111/jpn.13704.
  85. 85. Hussein EE, El Basuini MF, Ashry AM, Habiba MM, Teiba II, El-Rayes TK, et al. Effect of dietary sage (Salvia officinalis L.) on the growth performance, feed efficacy, blood indices, non-specific immunity, and intestinal microbiota of European sea bass (Dicentrarchus labrax). Aquac Rep. 2023;28:101460. https://doi.org/10.1016/j.aqrep.2022.101460.
  86. 86. Mzengereza K, Ishikawa M, Koshio S, Yokoyama S, Yukun Z, Shadrack RS, et al. Effect of Substituting Fish Oil with Camelina Oil on Growth Performance, Fatty Acid Profile, Digestibility, Liver Histology, and Antioxidative Status of Red Seabream (Pagrus major). Animals. 2021;11(7):1990. pmid:34359117
  87. 87. Çoğun HY, Şahin M. The effect of lead and zeolite on hematological and some biochemical parameters in Nile fish (Oreochromis niloticus). Curr Prog Biol Res. 2013;12:277–86. https://doi.org/10.5772/53076.