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Article

Radiation Hazard from Natural Radioactivity in the Marine Sediment of Jeddah Coast, Red Sea, Saudi Arabia

1
Environmental Science Department, Faculty of Meteorology, Environment and Arid Land Agriculture, King Abdulaziz University (KAU), Jeddah 21589, Saudi Arabia
2
Geology Department, Faculty of Science, Ain Shams University, Cairo 11566, Egypt
*
Author to whom correspondence should be addressed.
J. Mar. Sci. Eng. 2022, 10(8), 1145; https://doi.org/10.3390/jmse10081145
Submission received: 4 July 2022 / Revised: 14 August 2022 / Accepted: 16 August 2022 / Published: 19 August 2022
(This article belongs to the Special Issue Environmental Radioactivity in the Ocean)

Abstract

:
Marine sediment samples were collected along the Jeddah coast, Red Sea, Saudi Arabia, in order to assess radiation hazards and the exposure to human and marine living organisms. Using collaborative techniques, grain size, mineralogical characteristics, and natural radioactivity were investigated. To examine the influence of sediment characteristics over the distribution of the measured radionuclides, resulting data were statistically processed by using multivariate analyses. 238U, 232Th, and 40K levels were specified to be 19.50, 9.38, and 403.31 Bq kg−1, respectively. Radionuclides distributions were affected by sediment mud content, organic matter, and heavy minerals index. The calculated radiation risk parameters are within the safe range and lower than the global average. Natural radiation from these marine sediments is normal and poses no significant radiological risk to the public or marine living organisms. The natural radioactivity of the marine sediment in this Jeddah coastline will have to be monitored on a regular basis to avoid overexposure to the residents.

1. Introduction

Scientists, international organizations, and laypeople are increasingly agreeing that human exposure to ionizing radiation represents a terrible and unavoidable environmental issue. Public exposure to radiation come from naturally occurring (primordial) and artificial (fall-out) radionuclides, with the majority from natural sources [1,2,3]. Naturally occurring radionuclides such as Uranium-238 (238U), Thorium-232 (232Th), and Potassium-40 (40K) are abundant in the Earth’s continental crust [4,5]. These radionuclides can be found in different environmental components, including rocks, soil, stream sediment, groundwater, surface water, marine sediment and water, and biota [6,7,8,9,10,11].
The coastal ecosystem supports a diverse range of inorganic and bio-resources, many of which, in common fishery, are commercially, culturally, scientific, aesthetically, and recreationally important to the people of the entire region. The study of various bio-resources and associated geological processes of the coastal zone improves the proper understanding of the relationship between biotic and non-biotic components and their mutual dependence on maintaining ecosystem integrity [12,13]. Marine sediments play an important role in the ecology and environment of coastal ecosystems and marine environments. They are constantly changing and are the most dynamic part of these ecosystems [14,15]. Numerous marine contaminants, including radionuclides, are stored in marine sediments. Anthropogenic activities have contributed to the radioactivity level in marine ecosystems. Industrial discharges, nuclear accidents, and the discharge of nuclear waste have been recognized as main sources of elevated radioactivity levels in many marine ecosystems [16,17,18]. Lin et al. [19] recorded anthropogenic uranium imprints in the Baltic Sea sediments due to human nuclear-related activities. Al-Qasmi et al. [20] ascribed the enrichment of 238U, 236U, and 234U in the marine sediment from Loch Etive, Scotland, to the uranium released from the phosphate plant and Sellafield nuclear-fuel reprocessing facility. Pappa et al. [21] reported enhanced values of 226Ra and 235U in Stratoni port, Greece, due to mining-related activities. Aközcan et al. [22] recorded an extraordinary increase in the background levels of 226Ra and 40K in Bafa Lake, Turkey; these hot spots were attributed to industrial and agricultural activities. Diab et al. [23] noticed a slight increase in 238U and 232Th levels due to oil exploration and production activities in Egypt’s Gulf of Suez. Influences of the Chernobyl disaster are still noted in the marine sediments of numerous European countries such as the Gulf of Bothnia [24], Swedish coast [25], Amvrakikos Gulf (Greece) [26], Vefsnfjord (Norway) [27], Black Sea [28], and Baltic Sea [19]. Radionuclides released from the Fukushima accident have been transported long distances within the Pacific Ocean and are stored in marine sediments [29,30].
These radionuclides can accumulate in marine biota via sediment and water and demonstrate biomagnifications through trophic levels. Consequently, these radioactive elements enter the food chain through the direct consumption of marine foods [4,7,13,31,32]. Radionuclides in marine sediments are frequently used as radiotracers to better understand sedimentological, morphodynamics, and oceanographic processes and to reconstruct pollution events in the past [18,33]. The detection of radionuclides in sediments contributes significantly to human background radiation exposure and provides vital information on human and ecosystem health effects of natural radioactivity [4,23,34]. In addition, it can provide a critical foundation for evaluating any inadvertent release of radioelements for the better management and conservation of marine resources [18].
Lately, considerable emphasis has been dedicated to the development of a scientific database of radiation baselines in the Middle East, particularly in Arab nations, considering their ambitious intentions to construct nuclear and renewable energy capacities. For example, the United Arab Emirates launched the Arabian Gulf region’s first nuclear program by constructing four nuclear reactors [35,36]. Egypt has begun restarting its ambitious program to construct nuclear power reactors [37]. Saudi Arabia’s nuclear energy ambitions are in the initial stages, and the country recently revealed a proposal for nuclear power development that will be completed by 2040 [36,38,39]. The construction of a nuclear research reactor in Saudi Arabia is almost finished. Saudi Arabia’s Red Sea coastline contains many promising sites for nuclear power plant construction [36,40]. The baseline data could be used to analyze any changes in the radiation background level caused by radioactive substances-related activities.
The Red Sea is a complicated marine ecosystem that has unique biodiversity, as well as a vital maritime lane that connects the world’s major oceans for global trade and commerce [41,42]. Saudi Arabia has rapidly progressed from a developing state with serious limitations to an ambitious industrialized country. Saudi Arabia’s Red Sea coastline is densely populated and is thought to be more conducive to many different types of sustainable economic-development and blue economy activities [41]. Influences of large-scale human activities on the Red Sea’s environmental compartments have heightened in recent years, and these influences are now of significant concern [41,43,44,45]. There is a scarcity of data on the radioactivity level in Saudi Arabia’s coastal regions along the Red Sea [41]. Environmental radioactivity studies were concentrated in the Arabian Gulf [46,47,48,49]. The study area chosen for this study represents a result of recent industry developments in the Jeddah coastline over the last two decades. There are no available data about the natural radioactivity levels in Jeddah area. Thus, the present study attempt to (1) determine the levels of natural radioactivity in Jeddah coastline marine sediments, (2) compare the obtained results with literature, and (3) investigate the radiation hazard for members of the public and marine non-human biota due to exposure to natural radiation. This study will contribute to the radiation data bank of Saudi Arabia.

2. Materials and Methods

2.1. The Study Area

The study area covers the coastal of Jeddah, Red Sea, Saudi Arabia, between latitudes 20°56′50″ and 21°11′30″ N and longitudes 39°8′40″ and 39°19′40″ E (Figure 1). Jeddah city is considered one of the most significant and largest (1765 km2) urban and industrial areas along Saudi Arabia’s Red Sea coastline. It is characterized by an arid climate with sparse rainfall [43,50].
Jeddah is part of the eastern Red Sea shelf region, bordered on land by the rough Arabian Shield mountains. These mountains represent Neoproterozoic basement rocks, which include Precambrian calc-alkaline volcanic, volcaniclastic, intrusive, and metamorphic rocks. Tertiary clastic succession, basaltic lavas, and gabbro dikes cover these basement rocks. Quaternary surficial deposits cover the coastal plain, including coral reefs and carbonate, alluvial deposits, sabkha, and sand dunes [15,51].
The Red Sea is unique among the world’s seas in that it has a few permanent streams flowing into it and receives extremely scanty irregular rainfall. Terrigenous sediments are contributed by mostly northwesterly winds and occasional rainstorms. Aeolian and biogenic materials contribute significantly to the marine realm in arid regions such as Saudi Arabia, where riverine sediments are rare or completely absent [50,52].

2.2. Sampling and Sample Treatment

Eighteen sampling sites representing the surface marine sediments (0–10 cm depth) were selected for this study (Figure 1). Approximately 500 g of sediment samples was collected during March 2020 using a Van-Veen grab sampler by combining three subsamples from each site. In order to prevent cross-contamination, the collected samples were transferred to new, clean, and labelled plastic jars using a clean stainless-steel shovel. The samples were immediately stored in ice boxes under −4 °C until transportation to the lab. The sediment samples were blended, homogenized, and dried at room temperature before being placed in an electric oven (105 °C; 24 h) to dispose of the moisture and to achieve a constant weight [9,28,32]. These samples were then divided into several portions for various laboratory examinations.

2.3. Sediment Granulometry and Mineralogy

Utilizing loss in ignition methods [53], organic matter content (OM%) was determined in the sediment. Following digestion in HCl (1 N), the gravimetric technique was used to calculate CaCO3 concentrations [54]. Wet sieving was used to calculate the proportions of the different particle size grades (sand 2.00–0.063 mm and mud < 0.063 mm) [55]. Heavy minerals were separated using heavy liquid technique (Bromoform) and examined using a polarizing microscope [56,57]. The mineralogical compositions of the bulk powdered sediment samples were determined by using the X-ray diffraction technique (XRD). The qualitative chemical composition of selected heavy mineral grains were examined utilizing environmental scanning electron microscope (ESEM) and energy dispersive spectrometer (EDS) techniques (SEM/EDX, XL 30 ESEM, Philips Co., Amsterdam, The Netherlands). Extensive technical descriptions of OM% and CaCO3%, grain size and heavy minerals determination and the specification of SEX/EDX and XRD instruments are provided in Table S1 (in Supplementary Materials).

2.4. Radiometric Analysis

Dried and homogenized marine sediment samples were weighed and instantly placed into a 100 mL plastic standard cylinder and firmly sealed using Teflon tape around their screw necks, and wide Vinyl tape was used around their caps and secured for 30 days until examination. The radiogenic gases 222Rn and 220Rn are prevented from escaping by the in-growth of U and Th decay, which additionally allows for secular equilibrium between 238U, 232Th, and their decay products [58]. A well-calibrated sodium-iodide and thallium-activated gamma-ray spectrometry scintillation detector (3″ × 3″ NaI (Tl)) was used to specify the amounts of 238U (234Th-0.0633 MeV), 232Th (212Pb-0.2386 MeV) and 40K (1.461 MeV) activity concentrations in the collected marine sediment samples. This detector is sealed with a photomultiplier tube in aluminum housing. The tube is adequately protected against induced X-rays by a cylindrical copper (0.6 cm thickness) and isolated from environmental radiation by a chamber of lead bricks and lead cover (5 cm). Standard point sources (60Co and 137Cs) were used to calibrate the detector’s energy. Every sample has been counted for 1000 s. Additional details for the exact calculation of the activity concentration can be obtained from the literature [4,5].
Samples preparation, grain size analysis and heavy minerals separation were conducted at the Geology Department, Faculty of Science, Ain Shams University Laboratories. The XRD analysis were carried out at the Central Laboratories Sector of The Egyptian Mineral Resources Authority. SEM/EDX and radiometric analysis were performed at the Egyptian Nuclear Materials Authority.

2.5. Calculation of the Radiation Hazard Indices

The radium equivalent activity index (Raeq) [1,59], external hazard index (Hex) [1,60], absorbed dose rate (D) [1], annual effective dose (AEDE) [1], and excess lifetime cancer risk (ELCR) [6,61,62] have all been calculated in order to evaluate the external radiation hazards brought on by the activity concentration of the measured radionuclides in the marine sediment of the Jeddah Coast, Red Sea, Saudi Arabia. Table S2 (in Supplementary Materials) provides an overview of the descriptions and formulas used to calculate external hazard indicators.
The total dose rate (TD) per organism to biota (non-human) in the marine environments was calculated utilizing the ERICA Tool software (ERICA tool version 2.0.185, https://erica-tool.com/, accessed on 3 July 2022) [63]. The ERICA software is a dosimetry model that calculates the internal and external absorbed dose rates to (marine living organisms across a broad range of body masses and habitats for all radioactive elements of concern (238U and 232Th). The ERICA tool is thoroughly described in the literature [63,64]; more details can be found in Table S1.

2.6. Statistical Analyses

To reveal and emphasize the interrelationship between the investigated radionuclide (238U, 232Th, and 40K) activity concentrations and sediment properties (grain size, CaCO3, OM, and Heavy Minerals index), a multivariate Pearson’s correlation coefficient matrix (PCC), hierarchical cluster analysis (HCA) in Q mode, and principal component analysis (PCA) were performed using SPSS (version 21.0, New York, NY, USA) and OriginLab (version OriginPro 2021, Northampton, MA, USA).

3. Results and Discussion

3.1. Textural Attributes

Findings of grain-size analysis of the collected marine sediment samples are provided in Table 1. Their CaCO3 contents varied from 6.80 to 62.80%, these sediments are generally rich in carbonate. The organic matter content (OM%) of these sediments ranged from 0.00 to 1.20%. The low OM observed in these sediments can be explained by the deposition of siliciclastic terrigenous materials, which are low in OM or by rapid degradation of recently formed, easily decomposable endogenic biological activity [65]. Compared to mud fraction (silt and clay), sand fractions were found to be dominant in all studied samples (23.00–92.80%). On the other hand, the mud fraction has no clear trend. It is obvious that these sediments are composed mainly of carbonate and sand with minor amounts of mud and OM. The carbonate content in these coastal sediments is sourced from the erosions of carbonate-rich coastal rocks and the mixing of sediments with shell fragments and other calcareous debris [44,66,67].

3.2. Mineralogy

The mineral composition of representative bulk sediment samples (Figure S1) revealed the dominance of silicate minerals (quartz, albite, and amphiboles) and non-silicate minerals (calcite, aragonite, and gypsum). The heavy minerals indices of the studied marine sediments range from 0.48% and 15.16% (mean 5.81%).
The light minerals fractions of these marine sediments consist mostly of quartz and feldspar grains (mainly albite). Both opaque and non-opaque minerals varieties identified within the heavy mineral assemblage. The opaque minerals are mostly magnetite, ilmenite, and chromite (Figure 2). The non-opaque minerals assemblages consist of amphiboles, pyroxenes, epidote, zircon, sphene, garnet, monazite, tourmaline, and kyanite (Figure 3). Andalusite, rutile, and staurolite were recorded in a few samples in minor amounts. Interestingly, monazite grains show U and Th concentrations in their chemical composition (Figure 4). Monazite is thought to be the primary source of natural radioactivity in marine and beach sand [68,69,70,71,72].
The heavy mineral assemblages of Jeddah coastal marine sediments are, to a large extent similar, suggesting inheritance from the same source rocks. The nature of these assemblages indicates a variety of probable source rocks, including sedimentary, igneous, and metamorphic, with a relatively short distance of transportation. This explains the distinctly low roundness of the heavy grains (Figure 3) and the considerable amounts of feldspars grains. The distinctly high proportions of amphiboles and pyroxenes in the marine sediments studied indicate a major role of the surrounding basement. The potential contribution of a metamorphic rock source has pointed to the presence of garnet, kyanite, staurolite, and andalusite [57,73]. These results are consistent with many research studies [52,66,74].

3.3. Activity Concentrations

Table 1 lists the measured activity concentrations of 238U, 232Th, and 40K in the investigated marine sediment. These values are presented by graduated symbols method in Figure 5. The activity concentrations of the measured radionuclide have the order of 40K > 238U > 232Th. The results clearly reveal that the observed concentration of 40K greatly surpasses those of both 238U and 232Th. This indicates that 40K in common is a more prevalent radioactive element in these marine sediments. Potassium is more abundant in magmatic rocks as a major constituent of several rock-forming minerals than U and Th [75,76,77]. The activity concentration of 238U, 232Th, and 40K varied site-by-site, because the physical, chemical, geochemical, and mineralogical components of the marine sediment vary greatly [78,79]. The mean concentration values of 238U, 232Th, and 40K are 19.50 Bq kg−1, 9.38 Bq kg−1, and 403.31 Bq kg−1; respectively. These mean values are significantly lower than the world average [6] (Table 2). The current investigation revealed that 238U, 232Th, and 40K levels in marine sediment of Jeddah coastline are remarkably natural.
We attempted to compile a recent comparison of natural radiation levels in marine sediment from various regions of Saudi Arabia and those worldwide. Table 2 showed that the mean values of 238U in the Jeddah marine sediment were lower than that reported in Saudi Arabia and other countries except for the Arabian Gulf [48], Addurrah beach [49], Egyptian Gulf of Suez [23], Egyptian Mediterranean Sea [69], and Turkey [80]. The mean activity concentrations of 232Th in Jeddah marine sediments were lower than all other locations in the world except for the Arabian Gulf [48], Farasan Island [46], Oman [81], and Turkey [80]. Conversely, the 40K mean values were higher than all other locations in the world except Addurrah beach [49], Serbia [82], Cyprus [4], and Bangladesh [32]. It is worth noting that U and Th series disequilibria were well documented [31,83]. The presented values of 226Ra and 228Ra (Table 2) do not assume that there are 238U/226Ra and 232Th/228Ra equilibria in those samples; they are merely displayed for simple comparisons.
Table 2. Comparison of 238U, 232Th, and 40K mean activity concentration in marine sediment and sand samples reported for different region in Saudi Arabia and worldwide.
Table 2. Comparison of 238U, 232Th, and 40K mean activity concentration in marine sediment and sand samples reported for different region in Saudi Arabia and worldwide.
LocationSamples238U Series *232Th Series **40KReference
Saudi Arabia
JeddahMarine Sediment (N = 18)19.509.38403.31Present study
Arabian GulfMarine Sediment (N = 9)3.50 *5.90 **113.50[48]
Arabian GulfMarine Sediment (N = 12)26.40 *16.30351.00[47]
Arabian GulfBeach sand (N = 12)22.70 *14.80392.00[47]
Farasan IslandMarine Sediment (N = 8)35.461.8434.34[46]
Gulf of Aqaba (Addurrah beach)Marine Sediment (N = 19)16.9722.48641.08[49]
Worldwide
World average 3245412[6]
Egypt (Gulf of Suez)Shore Sediment (N = 36)13.7914.55128.67[23]
Egypt (Red Sea)Marine Sediment (N = 84)23.80 *19.60374.90[84]
Egypt (Mediterranean Sea)Beach sand (N = 12)8.80 *30.80106.9[69]
OmanMarine Sediment (N = 11)20.492.2644.83[81]
Iran (Caspian Sea)Marine Sediment (N = 8)34.40 *11.40310.00[9]
Serbia (Boka Kotorska Bay)Marine Sediment (N = 12)37.0035.00580.00[82]
Cyprus (East coast region)Marine Sediment (N = 15)23.00 *19.00628.10[4]
China (Beibu Gulf)Marine Sediment (N = 50)25.9037.6263[85]
India (Tamilnadu)Beach sand (N = 101)47.0426.63372.49[86]
Bangladesh (Bay of Bengal)Offshore Sediment (N= 6)31.2051.90686.40[32]
Turkey (Kocaeli- black sea)Beach sand (N = 20)8.858.93219.41[80]
Ghana (Tema Harbour)Marine Sediment (N = 21)34.0030.00320.00[31]
Nigeria (Akwa Ibom)Beach Sediment (N = 15)23.0036.00145.00[2]
* 226Ra activity concentration. ** 228Ra activity concentration.

3.4. Multivariate Statistical Analyses

A comparative PCC (Table 3) analysis was conducted to pinpoint the direct association between the specific characteristics of the considered marine sediments and 238U, 232Th, and 40K. Correlations of 0.20–0.39, 0.40- 0.59, 0.60–0.79, and 0.80–1.00 are considered weak, moderate, strong, and very strong, respectively [87]. 238U has significant strong positive correlations with mud content (Pearson’s R = 0.678) and weak positive correlation with OM (Pearson’s R = 0.357), indicating the effect of fine particles and OM on the distribution of 238U [37]. 238U has moderate positive correlations with 232Th (Pearson’s R = 0.419), this is due to the co-existence of U and Th radionuclides in nature [69,85,88], which is reflected by the presence of both radioelements in the SEM/EDX of monazite grain (Figure 4). 232Th has significant strong positive correlations with heavy minerals index (Pearson’s R = 0.696). On the other hand, 40K has moderate positive correlations with sand content (Pearson’s R = 0.510).
The observed HCA results (Figure 6) were remarkably similar to the PCC results. It revealed that there are two groups of variables. Cluster (1) is related to 40K and sand. This suggests that 40K is more linked with sand in the considered marine sediments. Cluster (2) splits into two subclusters: A (238U, 232Th, HI, and Mud) and B (CaCO3). This indicates that 238U and 232Th are more associated with HI and, to a lesser extent, mud content. In addition, no possible association is noted between CaCO3 and the measured radionuclides.
Figure 7 present the 3D loading of PCA component; three components (PC1 (38.92), PC2 (30.04%), and PC3 (12.47%)) were extracted. The 3D plots of the extracted three components positively confirms the findings of PCC and HCA analyses.

3.5. Radiation Hazard

3.5.1. Radiation Hazard for Humans

The calculated values of the radiological hazard parameters for the investigated marine sediments are shown in Table 4. In order to establish homogeneity with regard to radiation dose from the measured naturally occurring radionuclides, the radium equivalent activity index (Raeq) was calculated [1,59]. The obtained Raeq values ranged from 43.526 to 87.620 Bq kg−1 (mean 63.969 Bq kg−1). These levels are considerably below 370 Bq kg−1, which is the suggested maximum value [1,59]. Gamma radiation from emitting natural radionuclides in the studied marine sediment has an external hazard index (Hex) that ranges from 0.118 to 0.237 (mean 0.173). All calculated Hex values in this investigation are below the safety level of one [60], which is regarded as negligible. Absorbed dose rate (D) is the exposure of an individual to external, terrestrial radiation while engaged in outdoor activity. The calculated D values varied from 21.196 to 42.137 nGy h−1 (mean 31.493 nGy h−1). These values were below the world average (57 nGy h−1) [1] in all studied marine sediment samples. Figure 8 shows the contributions of 238U, 232Th, and 40K to the obtained D values contained in each sediment sampling site. Evidently, the contribution of 40K is the greater one, and the contribution of the measured radionuclides in D values varies from one site to another.
The annual effective doses (AEDEs) for inhabitants were calculated based on D values. AEDE values ranged from 0.026 to 0.052 mSv yr−1 (mean 0.039 mSv yr−1). These values were lower than the worldwide average (0.07 mSv yr−1) [1] in all the studied sediment samples. Long-term exposure to ionizing radiation typically leads to further risks described as excess lifetime cancer risk (ELCR). To obtain a better insight of the health effects of external exposure to the measured natural radionuclides in Jeddah coast marine sediments, ELCR factors were calculated using AEDE values. The obtained values ranged from 0.091 × 10−3 to 0.181 × 10−3 (mean 0.135 × 10−3). The ELCR-calculated values are lower than the world’s average (0.29 × 10−3) [6,61]. This demonstrates that public exposure to the investigated marine sediments in Jeddah coastal area cannot cause cancer over the course of their lives. Figure 9 depicts the GIS-based distribution pattern maps of the calculated radiological risk parameters.

3.5.2. Radiation Hazard for Non-Human Biota

Using the ERICA Tool [63,64], the TD to non-human biota (marine organisms) as a result of exposure to 238U and 232Th in Jeddah coast marine sediments was estimated and is displayed in Table 5. As shown, the expected TD values were far below the background dose rates. The estimated TD values from Jeddah coast marine sediments radionuclide concentrations to non-human biota are not considerable biological hazards. The assessed TD values for phytoplankton and polychaete worms were considerably greater than other organisms. This indicates that sediment radioactivity may end up causing phytoplankton and polychaete worms to receive the highest dose rates. As the base of the food chain, phytoplankton can be regarded as a significant bioindicator for continuous monitoring of radiological hazard in aquatic ecosystems [31].

4. Conclusions

From textural and mineralogical attributes, the Jeddah coastal marine sediments are a mixture of materials of marine and continental origin. These sediments are dominated by sand fraction and CaCO3 with low OM content. The identified non-opaque heavy minerals are amphiboles, pyroxenes, epidote, zircon, sphene, garnet, monazite, tourmaline, and kyanite with minor amounts of andalusite, rutile, and staurolite. The measured activity concentrations have the order of 40K > 238U > 232Th. The mean concentration values of 238U, 232Th, and 40K are 19.50 Bq kg−1, 9.38 Bq kg−1, and 403.31 Bq kg−1, respectively. The radionuclide distributions were influenced by sediment mud content, organic matter, and heavy minerals index. The calculated Raeq, Hex, D, AEDE, and ELCR are within the safe range and lower than the global average. The estimated TD per organism was far below the background dose rates. Natural radiation from these marine sediments is normal and poses no significant radiological risk to the public or non-human biota. The natural radioactivity of the marine sediment in this Jeddah coastline must be monitored on a regular basis to avoid unnecessary radiation exposure to the residents. Additional studies on natural radioactivity in marine water and other radionuclides level such as 137Cs could provide improved insights into the status of natural radioactivity in this area. This research can assist regulatory bodies and government agencies in planning for urban and industrial expansion while keeping environmental radiation in mind.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/jmse10081145/s1, Table S1 Extensive technical descriptions of OM % and CaCO3%, grain size and heavy minerals determination, and the specification of SEX/EDX and XRD instruments and ERICA tool. Table S2: Summary of the external hazard radiological parameters. Figure S1. X-ray diffractograms of bulk marine sediment samples.

Author Contributions

Conceptualization, B.A.A.-M. and A.G.; methodology, B.A.A.-M. and A.G.; software, A.G.; validation, B.A.A.-M. and A.G.; formal analysis, A.G.; investigation, B.A.A.-M. and A.G.; resources, B.A.A.-M.; data curation, A.G.; writing—original draft preparation, A.G.; writing—review and editing, B.A.A.-M. and A.G.; project administration, B.A.A.-M.; funding acquisition, B.A.A.-M. All authors have read and agreed to the published version of the manuscript.

Funding

This research work was funded by Institutional Fund Projects under grant no. (IFPIP: 126-155-1442).

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Acknowledgments

This research work was funded by Institutional Fund Projects under grant no. (IFPIP: 126-155-1442). Therefore, the authors gratefully acknowledge technical and financial support from the Ministry of Education and King Abdulaziz University, DSR, Jeddah, Saudi Arabia. The authors also thank Omnia El Sayed (Ain Shams University) for providing Landsat data and helping in the application of the GIS technique. Moreover, we are indebted to Moataz Khalifa (Menoufia University), Mostafa Eid, Aya Osham, and Easra S. Ahmed (Ain Shams University) for their technical assistance.

Conflicts of Interest

The authors declare no conflict of interest. The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript; or in the decision to publish the results.

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Figure 1. The study area and sampling site’s locations.
Figure 1. The study area and sampling site’s locations.
Jmse 10 01145 g001
Figure 2. SEM/EDX of (a) ilmenite (sample 3) and (b) chromite (sample 3).
Figure 2. SEM/EDX of (a) ilmenite (sample 3) and (b) chromite (sample 3).
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Figure 3. Photomicrographs of identified heavy minerals.
Figure 3. Photomicrographs of identified heavy minerals.
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Figure 4. SEM/EDX of monazite (sample 1).
Figure 4. SEM/EDX of monazite (sample 1).
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Figure 5. Distribution pattern maps of 238U, 232Th, and 40K activity concentrations.
Figure 5. Distribution pattern maps of 238U, 232Th, and 40K activity concentrations.
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Figure 6. Q-Mode dendrogram of HCA analysis.
Figure 6. Q-Mode dendrogram of HCA analysis.
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Figure 7. PCA variable 3D loading.
Figure 7. PCA variable 3D loading.
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Figure 8. The contributions of 238U, 232Th, and 40K to D values.
Figure 8. The contributions of 238U, 232Th, and 40K to D values.
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Figure 9. Distribution pattern maps of radiological risk parameters.
Figure 9. Distribution pattern maps of radiological risk parameters.
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Table 1. Grain size data, heavy minerals index, and activity concentration of the measured radionuclides.
Table 1. Grain size data, heavy minerals index, and activity concentration of the measured radionuclides.
Sample
No.
CaCO3
%
OM
%
Sand%
(2.00–0.063 mm)
Mud%
(<0.063 mm)
Heavy
Minerals%
238U
(Bq kg−1)
232Th
(Bq kg−1)
40K
(Bq kg−1)
144.000.2050.605.204.9639.7212.64387.38
221.400.0078.600.003.9412.434.14387.45
37.600.0077.8014.606.4424.358.28433.87
418.000.0075.806.2010.0824.8612.13356.39
538.800.2056.804.208.1212.478.26472.61
625.000.0075.000.005.3012.228.34470.02
717.000.0074.009.0015.1637.2916.17315.07
86.800.0092.800.406.0612.928.54454.53
919.200.2075.804.806.3212.438.22449.36
1062.801.2023.0013.002.4437.778.82338.31
1154.600.4039.405.604.3824.748.55250.51
1256.800.4038.404.404.0212.358.17253.09
1350.200.0048.601.208.9012.4716.17317.65
1415.400.4084.200.0010.9012.4112.24557.83
1550.400.2049.000.404.0612.384.04374.47
1642.400.0057.200.400.4824.958.05537.17
1747.800.0052.000.200.5612.938.08444.20
1848.200.0051.200.602.5412.288.05459.69
Min.6.800.0023.000.000.4812.224.04250.51
Max.62.801.2092.8014.6015.1639.7216.17557.83
Mean34.800.1861.123.905.8119.509.38403.31
Table 3. PCC analysis.
Table 3. PCC analysis.
CaCO3OMSandMudHI238U232Th40K
CaCO310.488−0.969−0.052−0.5440.101−0.123−0.425
OM 1−0.5970.437−0.1720.357−0.073−0.278
Sand 1−0.1980.477−0.2680.0690.510
Mud 10.2270.6780.217−0.381
HI 10.1540.696−0.114
238U 10.419−0.312
232Th 1−0.186
40K 1
WeakModerateStrongVery Strong
Table 4. Calculated radiological parameters in Jeddah Coast sediment.
Table 4. Calculated radiological parameters in Jeddah Coast sediment.
Sample No.RaeqHexDAEDEELCR × 10–3
187.6200.23742.1370.0520.181
248.1760.13024.3970.0300.105
369.5890.18834.3390.0420.147
469.6390.18833.6700.0410.145
560.6780.16430.4600.0370.131
660.3350.16330.2820.0370.130
784.6670.22940.1300.0490.172
860.1320.16230.0810.0370.129
958.7780.15929.4430.0360.126
1076.4340.20636.8850.0450.158
1156.2530.15227.0390.0330.116
1243.5260.11821.1960.0260.091
1360.0580.16228.7760.0350.124
1472.8690.19736.3890.0450.156
1546.9910.12723.7750.0290.102
1677.8300.21038.7920.0480.167
1758.6880.15829.3770.0360.126
1859.1820.16029.7020.0360.127
Min43.5260.11821.1960.0260.091
Max87.6200.23742.1370.0520.181
Mean63.9690.17331.4930.0390.135
Table 5. Estimated TD for marine organism in Jeddah Coastline marine sediment.
Table 5. Estimated TD for marine organism in Jeddah Coastline marine sediment.
Sample
No.
Benthic
Fish
CrustaceanMacroalgaeMollusca–BivalvePelagic
Fish
PhytoplanktonPolychaete WormZooplankton
12.84 × 10–33.14 × 10–32.85 × 10–21.45 × 10–21.72 × 10–31.08 × 10–13.70 × 10–11.23 × 10–3
28.90 × 10–49.90 × 10–48.92 × 10–34.55 × 10–35.40 × 10–43.43 × 10–21.16 × 10–13.90 × 10–4
31.75 × 10–31.93 × 10–31.75 × 10–28.91 × 10–31.05 × 10–36.77 × 10–22.27 × 10–17.60 × 10–4
41.85 × 10–32.04 × 10–31.79 × 10–29.17 × 10–31.08 × 10–37.73 × 10–22.32 × 10–18.60 × 10–4
59.60 × 10–41.06 × 10–39.05 × 10–34.64 × 10–35.40 × 10–44.37 × 10–21.16 × 10–14.80 × 10–4
69.50 × 10–41.04 × 10–38.88 × 10–34.55 × 10–35.30 × 10–44.33 × 10–21.14 × 10–14.70 × 10–4
72.74 × 10–33.02 × 10–32.69 × 10–21.37 × 10–21.61 × 10–31.11 × 10–13.48 × 10–11.25 × 10–3
81.00 × 10–31.10 × 10–39.38 × 10–34.81 × 10–35.60 × 10–44.52 × 10–21.21 × 10–15.00 × 10–4
99.60 × 10–41.06 × 10–39.02 × 10–34.62 × 10–35.40 × 10–44.35 × 10–21.16 × 10–14.80 × 10–4
102.65 × 10–32.93 × 10–32.70 × 10–21.37 × 10–21.63 × 10–39.60 × 10–23.52 × 10–11.10 × 10–3
111.78 × 10–31.97 × 10–31.78 × 10–29.06 × 10–31.07 × 10–36.91 × 10–22.31 × 10–17.80 × 10–4
129.50 × 10–41.05 × 10–38.96 × 10–34.60 × 10–35.40 × 10–44.32 × 10–21.15 × 10–14.70 × 10–4
131.09 × 10–31.20 × 10–39.25 × 10–34.79 × 10–35.40 × 10–46.13 × 10–21.17 × 10–16.50 × 10–4
141.02 × 10–31.13 × 10–39.11 × 10–34.70 × 10–35.40 × 10–45.24 × 10–21.16 × 10–15.60 × 10–4
158.90 × 10–49.80 × 10–48.88 × 10–34.53 × 10–35.40 × 10–43.40 × 10–21.15 × 10–13.90 × 10–4
161.79 × 10–31.97 × 10–31.79 × 10–29.12 × 10–31.08 × 10–36.84 × 10–22.32 × 10–17.70 × 10–4
179.90 × 10–41.09 × 10–39.37 × 10–34.80 × 10–35.60 × 10–44.42 × 10–21.21 × 10–14.90 × 10–4
189.50 × 10–41.04 × 10–38.91 × 10–34.57 × 10–35.30 × 10–44.28 × 10–21.15 × 10–14.70 × 10–4
Min8.90 × 10–49.80 × 10–48.88 × 10–34.53 × 10–35.30 × 10–43.40 × 10–21.14 × 10–13.90 × 10–4
Max2.84 × 10–33.14 × 10–32.85 × 10–21.45 × 10–21.72 × 10–31.11 × 10–13.70 × 10–11.25 × 10–3
Mean1.45 × 10–31.60 × 10–31.41 × 10–27.19 × 10–38.40 × 10–46.03 × 10–21.82 × 10–16.70 × 10–4
Background
Dose Rates
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MDPI and ACS Style

Al-Mur, B.A.; Gad, A. Radiation Hazard from Natural Radioactivity in the Marine Sediment of Jeddah Coast, Red Sea, Saudi Arabia. J. Mar. Sci. Eng. 2022, 10, 1145. https://doi.org/10.3390/jmse10081145

AMA Style

Al-Mur BA, Gad A. Radiation Hazard from Natural Radioactivity in the Marine Sediment of Jeddah Coast, Red Sea, Saudi Arabia. Journal of Marine Science and Engineering. 2022; 10(8):1145. https://doi.org/10.3390/jmse10081145

Chicago/Turabian Style

Al-Mur, Bandar A., and Ahmed Gad. 2022. "Radiation Hazard from Natural Radioactivity in the Marine Sediment of Jeddah Coast, Red Sea, Saudi Arabia" Journal of Marine Science and Engineering 10, no. 8: 1145. https://doi.org/10.3390/jmse10081145

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