Abstract
Sometimes free-living nematodes in conventional water treatment processes are not eliminated and cause adverse health effects in water consumer. So, the efficiency of UV lamps (125 W) with irradiation intensity 1020 μW cm−2 on inactivation of free-living nematode Rhabditida released in water samples has been investigated along with the investigation of the effects of turbidity and change of temperature and exposure time in constant of pH 8 ± 0.2. The results showed that UV radiation could disabled the larval and adult nematodes after 12 and 15 min in the presence of turbidity 5 NTU, respectively. Also, increased turbidity up to 50 NTU decreased the inactivation efficiency of larval and adult nematodes from 100% to 73% and 64%, respectively. In addition, with increased temperature, the inactivation efficiency increased significantly in a short time. The results showed a significant relationship between increasing exposure time and temperature and turbidity reduction with UV radiation efficiency in the inactivation of the nematode (P < 0.00). It was also found that the efficiency of the lamp on nematode larvae was more than the adult nematode. Therefore, UV radiation can well inactivate larvae and then adult free-living nematode Rhabditida in water.
Keywords: Ultraviolet, Water treatment, Nematode, Rhabditida, Disinfection
Specifications Table
| Subject area | Environmental Sciences |
| More specific subject area | Biology |
| Type of data | Tables |
| How data was acquired | In this descriptive and analytical study, the efficiency of UV lamps (125 W) with irradiation intensity 1020 μW cm−2 on inactivation of free-living nematode Rhabditida released in water samples has been investigated along with the investigation of the effects of turbidity and change of temperature and exposure time (pH was constant 8 ± 0.2). Free-living nematode Rhabditida were prepared and cultured in the laboratory of Gonabad University of Medical Sciences. UV lamp was prepared before each use for 3 to 5 min to warm up and reach a steady state. To move nematodes to the sample containers under the process, the plates containing cultured nematodes were rinsed by 20 ml of phosphate-buffered saline of pH 8 ± 0.2 so that the nematodes were separated from the culture medium and entered into the reactor container. |
| Data format | Raw, analyzed |
| Experimental factors | In all experiments, there was control sample and experiments were performed with three replications. |
| Experimental features | The relationship between inactivation rate and other parameters was evaluated using linear regression test. |
| Data source location | Gonabad, Mashhad province, Iran |
| Data accessibility | Data are included in this article |
Value of the data
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Nematodes can also pass live through the bed and enter into the water-supply networks in and endanger human health as carriers of pathogens, therefore, searching for a sure solution to remove them is essential. The results of this study focus on this issue.
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There are various ways to disinfect water resources. Using chlorination has declined because this type of disinfection tends to produce toxic compounds resulting from the use of its components. Therefore, we have to look for other methods of disinfection (for example using ultraviolet radiation). The results of this study emphasize this topic.
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Until now in some studies the effects of UV irradiation, temperature, turbidity to inactivation the different microorganism such as nematodes are investigated. But the data from present study specifically studies inactivation of free-living nematode Rhabditida from the water using UV radiation was investigated.
1. Data
The average chemical quality of water used for growing nematodes are shown in Table 1.
Table 1.
The chemical quality properties of subterranean Gonabad water.
| Total hardness | Calcium hardness | Hardness of magnesium | Ca | Na | Mg | pH |
|---|---|---|---|---|---|---|
| 423.5 ± 19.71 | 130.95 ± 3.79 | 292.55 ± 21.31 | 52.38 ± 1.51 | 214 ± 16.24 | 70.21 ± 5.11 | 7.73 |
Inactivation efficiency of larval and adult nematode up to 15 min of exposure in turbidity 5 NTU is shown in Table 2 (Turbidity 5 NTU, pH 8 ± 0.2). The investigation of results presented in Table 2 showed that with increasing time of exposure to UV lamps, the efficiency of inactivating the larval and adult nematodes increased. Larval and adult nematodes were inactivated 100% after 12 and 15 min of exposure respectively.
Table 2.
The inactivation efficiency of nematodes at different UV irradiation time.
| Time[1] | Larval (%) | Adult (%) |
|---|---|---|
| 1 | 4 | 2 |
| 2 | 16 | 11 |
| 3 | 23 | 17 |
| 4 | 32 | 27 |
| 5 | 47 | 39 |
| 6 | 55 | 43 |
| 8 | 72 | 56 |
| 10 | 89 | 78 |
| 12 | 100 | 91 |
| 15 | 100 | 100 |
Table 3 shows the inactivation efficiency of nematodes in different turbidity at a constant temperature of 20 °C and pH 8 ± 0.2 after a 15 min exposure to UV radiation. Data reported in Table 3 also involve change of control samples. Results of Table 3 show that during the 15 min exposure to UV radiation, increased turbidity up to 15 NTU had no effect on the rate of inactivation of both types of nematodes and they were inactivated 100%, but then with increasing turbidity up to 50 NTU, the inactivation efficiency of the larval and adult nematodes decreased 73% and 64% respectively. Table 3 also shows that the percentage of the inactivation of larval nematodes even in the presence of different levels of turbidity was higher than adult nematodes.
Table 3.
The inactivation efficiency of nematodes at different turbidity at a constant.
| Turbidity (NTU) | Adult (%) | Larval (%) |
|---|---|---|
| 5 | 100 | 100 |
| 6 | 100 | 100 |
| 7 | 100 | 100 |
| 8 | 100 | 100 |
| 9 | 100 | 100 |
| 10 | 100 | 100 |
| 15 | 100 | 100 |
| 20 | 94 | 100 |
| 25 | 90 | 100 |
| 30 | 87 | 92 |
| 40 | 79 | 87 |
| 50 | 64 | 73 |
Table 4 shows the effect of temperature on the rate of inactivation of nematodes during the 2 min exposure time at the presence of turbidity 5 NTU and pH 8 ± 0.2. Results of Table 4 show that increased temperature had increased efficiency of inactivating the nematodes and the effect of temperature on inactivation of larval nematodes has been more than adult nematodes so that at 45 °C, the inactivation of larval and adult nematodes was equivalent to 92 and 75%.
Table 4.
The inactivation efficiency of nematodes at different temperature.
| Temperature (°C) | Larval (%) | Adult (%) |
|---|---|---|
| 20 | 16 | 11 |
| 25 | 22.4 | 14.5 |
| 30 | 24.9 | 18.3 |
| 35 | 49.4 | 32.8 |
| 40 | 73.2 | 53.5 |
| 45 | 92 | 75 |
2. Experimental design, materials and methods
To perform this analytical and descriptive study, Ultraviolet light (254 nm type C Arda Company, Iran- 125 W), flow of 25.3 amps, and intensity of 1020 μW cm−2, length of 65 mm, diameter of 10 mm, and arc length of 31 mm was used. The experiment started by placing the lam inside a quartz tube deployed in a 1000 ml glass reactor (mirror to the inside of the container) [2]. The effect of changes in temperature parameters in the range of 20 to 45 °C and turbidity in the range of 5 to 25 NTU within 1 to 15 min on inactivation of larval and adult free-living nematode Rhabditida in natural water samples taken from the subterranean Gonabad water (Ghasabe) was investigated. Free-living nematode Rhabditida were prepared and cultured in the laboratory of Gonabad University of Medical Sciences. UV lamp was prepared before each use for 3 to 5 min to warm up and reach a steady state. To move nematodes to the sample containers under the process, the plates containing cultured nematodes were rinsed by 20 ml of phosphate-buffered saline of pH 8 ± 0.2 so that the nematodes were separated from the culture medium and entered into the reactor container. In all experiments, there was control sample and experiments were performed with three replications [3], [4]. Except when studying the effect of temperature, using circulating water-cooling system, the water temperature was kept constant on 20° during the test [5]. At the end, the relationship between inactivation rate and other parameters was evaluated using linear regression test by SPSS software (version.21).
Acknowledgements
We would like to thank and appreciate Gonabad University of Medical Sciences and all colleagues who have collaborated on writing this paper.
Footnotes
Transparency document associated with this article can be found in the online version at doi:10.1016/j.dib.2018.02.074
Transparency document. Supplementary material
Supplementary material
References
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