Literature DB >> 27508251

Data on metal contents (As, Ag, Sr, Sn, Sb, and Mo) in sediments and shells of Trachycardium lacunosum in the northern part of the Persian Gulf.

Vahid Noroozi Karbasdehi1, Sina Dobaradaran2, Iraj Nabipour3, Hossein Arfaeinia4, Roghayeh Mirahmadi1, Mozhgan Keshtkar1.   

Abstract

In this data article, by using inductively coupled plasma optical spectrometry (ICP-OES), we aimed to (1) determine the concentration levels of As, Ag, Sr, Sn, Sb, and Mo in the sediments and the shells of Trachycardium lacunosum simultaneously in two separated areas (unpolluted and polluted areas) (2) comparison between the metal contents of sediments in the unpolluted and polluted areas as well as shells. Analysis of data showed that sediment as well as shell samples in polluted area contained significantly higher concentration levels of all measured metals compared with unpolluted area.

Entities:  

Keywords:  Heavy metal; Persian Gulf; Sediment; Trachycardium lacunosum

Year:  2016        PMID: 27508251      PMCID: PMC4961305          DOI: 10.1016/j.dib.2016.06.065

Source DB:  PubMed          Journal:  Data Brief        ISSN: 2352-3409


Specifications Table Value of the data Data can be used as a base-line data for metal concentration levels in marine environments and understanding industrial activities effects on these environments. Data shown here can be useful for policy makers, managers, and all related stakeholders, companies, agencies, and institutes working in the fields of environment by imposing proper measures to protect environment. Data shown here may serve as benchmarks for other groups working or studying in the field of effluent disposal, pollution control, aquatic ecosystem, toxicology.

Data

In the unpolluted area the concentration levels of As, Ag, Sr, Sn, Sb, and Mo in sediment samples ranged from 0.07–0.81 (Mean: 0.3), 0.4–0.9 (Mean: 0.65), 85–172 (Mean: 134.3), 1.3–3.6 (Mean: 2.63), 2–9.4 (Mean: 3.79) 0.24–0.85 (Mean: 0.45) µg g−1 respectively while in the polluted area the concentration levels of As, Ag, Sr, Sn, Sb and Mo ranged from 11.2–16.3 (Mean: 13.4), 1.1–1.7 (Mean: 1.33), 249–1354 (Mean: 715), 4.12–8.32 (Mean: 5.3), 5.9–20.7 (Mean: 16.16), 1.29–9.52 (Mean: 4.7) µg g−1 respectively (Table 1 and Fig. 1). In the unpolluted area the concentration levels of As, Ag, Sr, Sn, Sb, and Mo in shell samples ranged from 0.01–0.06 (Mean: 0.035), 0.001–0.008 (Mean 0.004), 21–45 (Mean: 27.8), 0.1–1.6 (Mean: 0.71), 0.5–2.7 (Mean: 1.33), 0.01–0.05 (Mean: 0.03) µg g−1 respectively while in the polluted area the concentration levels of As, Ag, Sr, Sn, Sb and Mo ranged from 1.32–6.6 (Mean: 4.15), 011–0.33 (Mean: 0.17), 78–185 (Mean: 131.7), 2.1–3.3 (Mean: 2.5), 3.9–13.8 (Mean: 8.3), 0.7–9.4 (Mean: 4.7) µg g−1 respectively (Table 2 and Fig. 2).
Table 1

Concentration levels of metals (µg g−1 dw) in sediment samples in polluted and unpolluted areas.

AreaStationASAgSrSnSbMo
10.130.6952.32.10.5
20.160.71212.120.35
30.200.6992.23.10.24
40.200.61452.24.20.36
50.250.71522.23.70.41
60.330.81363.12.80.61
70.520.81373.26.40.74
80.700.91282.17.80.71
90.810.4853.49.40.39



Unpolluted area100.790.61543.38.10.42
110.460.41263.62.10.54
120.100.51263.52.20.57
130.140.61462.12.60.85
140.070.71372.52.20.24
150.170.81522.44.70.36
160.140.91631.92.10.35
170.210.51723.42.10.24
180.140.61323.22.20.24
190.130.71461.32.20.41



Mean±SD0.3±0.240.65±0.15134.3±22.72.63±0.673.79±2.380.45±0.18
2012.51.13254.235.91.5
2112.31.14524.519.31.65
2213.51.24894.7819.41.75
2314.21.212345.36161.71
2411.21.32498.2317.43.25
2511.31.18956.3214.82.75
2612.61.411247.3216.94.53
2714.31.512435.615.35.21
2815.31.48654.2315.33.22



Polluted area2911.21.68754.5616.46.52
3013.81.76524.12177.21
3111.61.34524.2518.46.32
3212.61.33654.3420.78.21
3312.51.22635.3216.45.32
3414.61.59658.3216.24.38
3516.21.613547.5413.61.29
3611.71.55624.2317.87.98
3715.31.37864.1214.88.31
3816.31.18964.2115.39.52
3914.91.12544.3316.23.22



Mean±SD13.4±1.71.33±0.192715±357.65.30±1.4516.16±2.994.7±2.6
Fig. 1

Comparison of metals concentration levels in the sediment samples in polluted and unpolluted areas.

Table 2

Concentration levels of metals (µg g−1 dw) in shell samples in polluted and unpolluted areas.

AreaStationASAgSrSnSbMo
10.020.002350.30.90.01
20.030.001220.11.20.03
30.010.001210.21.10.02
40.040.003250.22.20.03
50.060.001311.22.70.04
Unpolluted area120.020.006221.51.30.05
130.030.006230.12.20.05
140.060.007260.51.20.03
150.040.008350.40.70.02
160.020.006451.60.50.04
170.030.001221.41.30.03
180.040.002260.21.20.04
190.050.003281.50.80.03
Mean±SD0.035±0.0160.004±0.00327.8±7.040.71±0.621.33±0.650.032±0.012
202.50.121502.63.90.7
223.30.231853.17.41.7
233.20.21972.45.31.8
244.20.331443.212.43.3
251.30.221252.311.82.6
262.90.211253.310.94.4
274.70.11852.64.35.6
285.30.121622.26.33.4
Polluted area291.60.131682.59.46.3
312.60.151392.29.46.9
326.60.251452.36.78.3
334.50.26992.36.45.7
346.60.11782.36.24.6
356.20.121353.25.61.3
365.70.12852.25.87.2
375.30.131852.113.88.3
384.30.141362.211.39.4
393.90.151282.312.23.6
Mean±SD4.15±1.60.17±0.06131.7±32.82.5±0.48.28±3.124.73±2.63
Fig. 2

Comparison of metals concentration levels in the shell samples in polluted and unpolluted areas.

Experimental design, materials and methods

Study area description

Two different areas were selected in the Asaluyeh as sampling points including polluted area (Nayband Bay) and unpolluted area (Lavar-e-Saheli) (Fig. 3).
Fig. 3

The map and locations of sampling station.

Sample collection

Samples from surface sediments (0–10 cm) and shells of Trachycardium lacunosum in selected polluted and unpolluted areas were collected. 20 sediment samples and 18 shell samples in polluted area and 19 sediment samples and 13 shell samples in unpolluted area were collected during summer 2013. After transferring the collected sediment samples to the laboratory, the samples were dried at 105 °C for 24 h, homogenized, and packed in polyethylene bags and stored at −20 °C prior to analysis. The shell samples washed under a jet of tap water to remove algae, sand, clay and other impurities, and then dried at 105 °C for 24 h and stored at −20 °C prior to analysis.

Reagents

All the employed oxidants and mineral acids including HNO3, H2O2, HF, HClO4 and HCl were of suprapure quality (Merck, Darmstadt, Germany). All glassware and plastic were cleaned by soaking overnight in a 10% (w/v) HNO3 solution and then rinsed with deionized water before use. All solutions were prepared by using ultrapure water (18.2 MΩ cm).

Digestion and analytical procedures

The sediment samples (0.5 g) were digested with 2 ml HNO3 (65%), 6 ml HCl (37%) in a microwave digestion system for 30 min and then diluted to 25 ml with ultrapure water and stored in polyethylene bottle until analysis. 0.5 g of powdered shell was completely digested in a Teflon cup using a mixture of conc. HNO3, HClO4 and HF with the ratio 3:2:1 respectively. Acids were slowly added to dried sample and left overnight before further process. Then, the samples were heated at 200 °C then left to cool and filtered. The filtered solution was justified to a volume of 25 ml. Blank digest was also performed in the same way. ICP-OES instrumental method [1], [2], [3] was used to determine the concentration level of metals including As, Ag, Sr, Sn, Sb and Mo (Table 3).
Table 3

ICP-OES instrumental operating details.

Parameters
Company, modelSPECTRO (Germany), Spectro arcos
RF generator power (W)1400
Frequency of RF generator (MHz)27.12 MHz
Type of detectorCharge coupled devices (CCD)
Torch typeFlared-end EOP torch 2.5 mm
Plasma, auxiliary, and nebulizer gasHigh purity (99.99%) argon
Plasma gas flow rate (L min−1)14.5
Auxiliary gas flow rate (L min−1)0.9
Nebulizer gas flow rate (L min−1)0.85
Sample uptake time (s)240 total
Delay time of (s)
Rinse time of (s)45
Initial stabilization time (s)Preflush: 45
Time between replicate analysis (s)
Measurement replicate3
Pump rate30 RPM
Element (λ nm−1)Ag 328.068; As 189.042; Sr 346.446
Sn 189.991; Sb 206.833; Mo 204.598
Subject areaToxicology
More specific subject areaHeavy metal contents in marine environment
Type of dataTable and figure
How data was acquiredICP-OES (SPECTRO (Germany), Spectro arcos)
Data formatRaw, analyzed
Experimental factorsAll sediment samples were dried at 105 °C for 24 h, homogenized, and packed in polyethylene bags and stored at −20 °C prior to analysis. The shell samples washed under a jet of tap water to remove algae, sand, clay and other impurities, and then dried at 105 °C for 24 h and stored at −20 °C prior to analysis
Experimental featuresEvaluate the metal contents of As, Ag, Sr, Sn, Sb, and Mo in sediments and shells of Trachycardium lacunosum in the northern part of the Persian Gulf
Data source locationBushehr, Asaluyeh bay, along the Persian Gulf, Iran
Data accessibilityData is with this article
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