Please wait a minute...
Frontiers of Environmental Science & Engineering

ISSN 2095-2201

ISSN 2095-221X(Online)

CN 10-1013/X

Postal Subscription Code 80-973

2018 Impact Factor: 3.883

Front. Environ. Sci. Eng.    2019, Vol. 13 Issue (1) : 8    https://doi.org/10.1007/s11783-019-1099-2
RESEARCH ARTICLE
Influence of reclaimed water discharge on the dissemination and relationships of sulfonamide, sulfonamide resistance genes along the Chaobai River, Beijing
Ning Zhang1,2, Xiang Liu1(), Rui Liu1, Tao Zhang3, Miao Li1(), Zhuoran Zhang1, Zitao Qu4, Ziting Yuan5, Hechun Yu5
1. School of Environment, Tsinghua University, Beijing 100084, China
2. Division of Environment and Resources Research, Transport Planning and Research Institute, Ministry of Transport, Beijing 100028, China
3. Chinese Academy for Environmental Planning, Beijing 100012, China
4. Institute of Chemistry, Industrial Chemistry, Technical University of Munich (Asian Campus), Singapore 139660, Singapore
5. School of Water Resources and Environment, China University of Geosciences (Beijing), Beijing 100083, China
 Download: PDF(620 KB)   HTML
 Export: BibTeX | EndNote | Reference Manager | ProCite | RefWorks
Abstract

Reclaimed water threatens the ecological safety of the Chaobai River.

SMX, TMP, and SDZ were the first three abundant antibiotics in the research area.

SRGs and intI1 were widespread with high abundance after reclaimed water recharge.

The SRGs values followed the sequence: Summer>autumn>spring>winter.

Strong correlations were detected between SRGs and environmental factors.

Reclaimed water represents an important source of antibiotics and antibiotic resistance genes, threatening the ecological safety of receiving environments, while alleviating water resource shortages. This study investigated the dissemination of sulfonamide (SAs), sulfonamide resistance genes (SRGs), and class one integrons (intI1) in the surface water of the recharging area of the Chaobai River. The three antibiotics sulfamethoxazole, trimethoprim, and sulfadiazine had the highest abundance. The highest absolute abundances were 2.91×106, 6.94×106, and 2.18×104 copies/mL for sul1, sul2, and intI1 at the recharge point, respectively. SRGs and intI1 were widespread and had high abundance not only at the recharging point, but also in remote areas up to 8 km away. Seasonal variations of SRGs abundance followed the order of summer>autumn>spring>winter. Significant correlations were found between SRGs and intI1 (R2 = 0.887 and 0.786, p<0.01), indicating the potential risk of SRGs dissemination. Strong correlations between the abundance of SRGs and environmental factors were also found, suggesting that appropriate environmental conditions favor the spread of SRGs. The obtained results indicate that recharging with reclaimed water causes dissemination and enrichment of SAs and SRGs in the receiving river. Further research is required for the risk assessment and scientific management of reclaimed water.

Keywords Sulfonamide residues      Sulfonamide resistance genes      Reclaimed water recharge      Surface water      Class one integrons     
Corresponding Author(s): Xiang Liu,Miao Li   
Issue Date: 29 December 2018
 Cite this article:   
Ning Zhang,Xiang Liu,Rui Liu, et al. Influence of reclaimed water discharge on the dissemination and relationships of sulfonamide, sulfonamide resistance genes along the Chaobai River, Beijing[J]. Front. Environ. Sci. Eng., 2019, 13(1): 8.
 URL:  
https://academic.hep.com.cn/fese/EN/10.1007/s11783-019-1099-2
https://academic.hep.com.cn/fese/EN/Y2019/V13/I1/8
Fig.1  Location of the study area with the distribution of river water monitoring points along the Chaobai River. (a) location of the Chaobai and the Wenyu Rivers; (b) location of the surface water monitoring points.
Fig.2  Levels of sulfonamides antibiotics (SAs) in surface water (ng/mL): (a) column charts of each location are arranged in order of March 7, 2017; June 9, 2017; September 19, 2017 and December 15, 2016; (b) the total concentration of SAs varies along the river.
Fig.3  Abundance of sulfonamide resistance genes in all samples: (a) absolute abundance of sul1, (b) relative abundance of sul1, (c) absolute abundance of sul2, (d) relative abundance of sul2
Fig.4  Abundance of class 1 integron in all samples. (a) Absolute abundance of class I integron, (b) relative abundance of class I integron
Fig.5  Heat map about resistance genes profile of all samples. Each row is labeled with the sample site, each column is the abundance of sul1, sul2, intI1 in different seasons of all site respectively. (a) absolute abundance (copies/mL), (b) relative abundance
Fig.6  Redundancy analysis (RDA) of average SRGs and the environmental variables in all water samples. Circle symbols represent the SRGs concentration of all samples, environmental variables in red arrows represent intI1, water qualities. The lengths of arrows reveal the strength of the correlation and the angles between arrows indicate the relationship of different parameters. The percentage of horizontal axis is 77.4%, vertical axis is 17.9.
Season ARGs intI1 SDZ SMX TMP SDM SML STZ pH TOC TP TN
Spring sul1 0.877** 0.615* 0.562* 0.658*
sul2 0.700** 0.748* 0.645*
sul 0.884** 0.627* 0.558* 0.663*
Summer sul1 0.807** 0.837** 0.685**
sul2 0.902** 0.568* 0.579*
sul 0.871** 0.685** 0.601*
Autumn sul1 0.817** 0.878** 0.805** 0.797** 0.731**
sul2 0.583* 0.712** 0.659* 0.676** 0.580*
sul 0.587* 0.715** 0.662** 0.678** 0.583*
Winter sul1 0.968** 0.905** 0.697** 0.896** 0.860** 0.765**
sul2 0.960** 0.740** 0.928** 0.799** 0.605*
sul 0.974** 0.896** 0.684** 0.906** 0.860** 0.755**
Tab.1  Relationship between absolute abundance of SRGs and intI1, SAs, environment factors
Season ARGs intI I SDZ SMX TMP SDM SML STZ pH TOC TP TN
Spring sul1 -0.640* 0.672**
sul2 0.576* -0.637*
sul -0.634* 0.670**
Summer sul1 0.818** 0.871** -0.612* 0.592*
sul2 -0.566*
sul 0.760** 0.682** -0.578*
Autumn sul1 0.973** -0.634*
sul2 0.943** 0.834** 0.740** 0.775**
sul 0.931** 0.838** 0.723** 0.790**
Winter sul1 0.953** 0.732** 0.905** 0.716** 0.782**
sul2 0.905** 0.599* 0.856** 0.881** 0.742** 0.769** 0.942**
sul 0.957** 0.740** 0.900** 0.726** 0.792**
Tab.2  Calculated heat duties of heat equipment and power duty of pump P1 shown in Fig. 1
1 G C AAmos, EGozzard, C ECarter, AMead, M J Bowes, P M Hawkey, L Zhang, A CSinger, W HGaze, E M HWellington (2015). Validated predictive modelling of the environmental resistome. The ISME Journal, 9(6): 1467–1476
https://doi.org/10.1038/ismej.2014.237 pmid: 25679532
2 Y MAwad, K R Kim, S C Kim, K Kim, S RLee, S SLee, Y SOk (2015). Monitoring antibiotic residues and corresponding antibiotic resistance genes in an agroecosystem. Journal of Chemistry, 2015: 974843
https://doi.org/10.1155/2015/974843
3 FBalzer, S Zühlke, SHannappel (2016). Antibiotics in groundwater under locations with high livestock density in Germany. Water Science and Technology: Water Supply, 16(5): 1361–1369
https://doi.org/10.2166/ws.2016.050
4 FBaquero, J L Martinez, R Cantón (2008). Antibiotics and antibiotic resistance in water environments. Current Opinion in Biotechnology, 19(3): 260–265
https://doi.org/10.1016/j.copbio.2008.05.006 pmid: 18534838
5 WBen, J Wang, RCao, MYang, Y Zhang, ZQiang (2017). Distribution of antibiotic resistance in the effluents of ten municipal wastewater treatment plants in China and the effect of treatment processes. Chemosphere, 172: 392–398
https://doi.org/10.1016/j.chemosphere.2017.01.041 pmid: 28088530
6 GCambray, A M Guerout, D Mazel (2010). Integrons. Annual Review of Genetics, 44(1): 141–166
https://doi.org/10.1146/annurev-genet-102209-163504 pmid: 20707672
7 BChen, X Liang, XHuang, TZhang, XLi (2013). Differentiating anthropogenic impacts on ARGs in the Pearl River Estuary by using suitable gene indicators. Water Research, 47(8): 2811–2820
https://doi.org/10.1016/j.watres.2013.02.042 pmid: 23521975
8 CChen, J Li, PChen, RDing, P Zhang, XLi (2014). Occurrence of antibiotics and antibiotic resistances in soils from wastewater irrigation areas in Beijing and Tianjin, China. Environmental Pollution, 193: 94–101
https://doi.org/10.1016/j.envpol.2014.06.005 pmid: 25016103
9 D JChen, M P Hu, J H Wang, Y Guo, R ADahlgren (2016). Factors controlling phosphorus export from agricultural/forest and residential systems to rivers in eastern China, 1980–2011. Journal of Hydrology (Amsterdam), 533: 53–61
https://doi.org/10.1016/j.jhydrol.2015.11.043
10 SCoutu, V Wyrsch, H KWynn, LRossi, D ABarry (2013). Temporal dynamics of antibiotics in wastewater treatment plant influent. Science of the Total Environment, 458–460: 20–26
https://doi.org/10.1016/j.scitotenv.2013.04.017 pmid: 23639908
11 NCzekalski, E Gascón Díez, HBürgmann (2014). Wastewater as a point source of antibiotic-resistance genes in the sediment of a freshwater lake. The ISME Journal, 8(7): 1381–1390
https://doi.org/10.1038/ismej.2014.8 pmid: 24599073
12 NDevarajan, A Laffite, C KMulaji, J POtamonga, P TMpiana, J IMubedi, KPrabakar, B WIbelings, JPoté (2016). Occurrence of antibiotic resistance genes and bacterial markers in a tropical river receiving hospital and urban wastewaters. PLoS One, 11(2): e0149211
https://doi.org/10.1371/journal.pone.0149211 pmid: 26910062
13 ADi Cesare, E M Eckert, M Rogora, GCorno (2017). Rainfall increases the abundance of antibiotic resistance genes within a riverine microbial community. Environmental Pollution, 226: 473–478
https://doi.org/10.1016/j.envpol.2017.04.036 pmid: 28438356
14 JDu, H Ren, JGeng, YZhang, KXu, L Ding (2014). Occurrence and abundance of tetracycline, sulfonamide resistance genes, and class 1 integron in five wastewater treatment plants. Environmental Science and Pollution Research International, 21(12): 7276–7284
https://doi.org/10.1007/s11356-014-2613-5 pmid: 24566967
15 PGao, D Mao, YLuo, LWang, B Xu, LXu (2012). Occurrence of sulfonamide and tetracycline-resistant bacteria and resistance genes in aquaculture environment. Water Research, 46(7): 2355–2364
https://doi.org/10.1016/j.watres.2012.02.004 pmid: 22377146
16 M RGillings, W H Gaze, A Pruden, KSmalla, J MTiedje, Y GZhu (2015). Using the class 1 integron-integrase gene as a proxy for anthropogenic pollution. The ISME Journal, 9(6): 1269–1279
https://doi.org/10.1038/ismej.2014.226 pmid: 25500508
17 EGullberg, S Cao, O GBerg, CIlbäck, LSandegren, DHughes, D IAndersson (2011). Selection of resistant bacteria at very low antibiotic concentrations. PLoS Pathogens, 7(7): e1002158
https://doi.org/10.1371/journal.ppat.1002158 pmid: 21811410
18 M TGuo, Q B Yuan, J Yang (2015). Distinguishing effects of ultraviolet exposure and chlorination on the horizontal transfer of antibiotic resistance genes in municipal wastewater. Environmental Science & Technology, 49(9): 5771–5778
https://doi.org/10.1021/acs.est.5b00644 pmid: 25853586
19 L YHe, Y S Liu, H C Su, J L Zhao, S S Liu, J Chen, W RLiu, G GYing (2014). Dissemination of antibiotic resistance genes in representative broiler feedlots environments: Identification of indicator ARGs and correlations with environmental variables. Environmental Science & Technology, 48(22): 13120–13129
https://doi.org/10.1021/es5041267 pmid: 25338275
20 B DJanke, J C Finlay, S E Hobbie, L A Baker, R W Sterner, D Nidzgorski, B NWilson (2014). Contrasting influences of stormflow and baseflow pathways on nitrogen and phosphorus export from an urban watershed. Biogeochemistry, 121(1): 209–228
https://doi.org/10.1007/s10533-013-9926-1
21 LJiang, X Hu, TXu, HZhang, DSheng, DYin (2013). Prevalence of antibiotic resistance genes and their relationship with antibiotics in the Huangpu River and the drinking water sources, Shanghai, China. Science of the Total Environment, 458– 460: 267–272
https://doi.org/10.1016/j.scitotenv.2013.04.038 pmid: 23664984
22 LJiang, X Hu, DYin, HZhang, ZYu (2011). Occurrence, distribution and seasonal variation of antibiotics in the Huangpu River, Shanghai, China. Chemosphere, 82(6): 822–828
https://doi.org/10.1016/j.chemosphere.2010.11.028 pmid: 21131021
23 Y NJiao, H Chen, R XGao, Y GZhu, CRensing (2017). Organic compounds stimulate horizontal transfer of antibiotic resistance genes in mixed wastewater treatment systems. Chemosphere, 184: 53–61
https://doi.org/10.1016/j.chemosphere.2017.05.149 pmid: 28578196
24 K GKarthikeyan, M TMeyer (2006). Occurrence of antibiotics in wastewater treatment facilities in Wisconsin, USA. Science of the Total Environment, 361(1–3): 196–207
https://doi.org/10.1016/j.scitotenv.2005.06.030 pmid: 16091289
25 S CKim, K Carlson (2007). Temporal and spatial trends in the occurrence of human and veterinary antibiotics in aqueous and river sediment matrices. Environmental Science & Technology, 41(1): 50–57
https://doi.org/10.1021/es060737+ pmid: 17265926
26 UKlümper, A Dechesne, LRiber, K KBrandt, AGülay, S JSørensen, B FSmets (2017). Metal stressors consistently modulate bacterial conjugal plasmid uptake potential in a phylogenetically conserved manner. The ISME Journal, 11(1): 152–165
https://doi.org/10.1038/ismej.2016.98 pmid: 27482924
27 RKoczura, J Mokracka, ATaraszewska, NŁopacinska (2016). Abundance of class 1 integron-integrase and sulfonamide resistance genes in river water and sediment is affected by anthropogenic pressure and environmental factors. Microbial Ecology, 72(4): 909–916
https://doi.org/10.1007/s00248-016-0843-4 pmid: 27599709
28 KKümmerer (2009). Antibiotics in the aquatic environment: A review—Part I. Chemosphere, 75(4): 417–434
https://doi.org/10.1016/j.chemosphere.2008.11.086 pmid: 19185900
29 MLaht, A Karkman, VVoolaid, CRitz, T Tenson, MVirta, VKisand (2014). Abundances of tetracycline, sulphonamide and beta-lactam antibiotic resistance genes in conventional wastewater treatment plants (WWTPs) with different waste load. PLoS One, 9(8): e103705
https://doi.org/10.1371/journal.pone.0103705 pmid: 25084517
30 MLamshöft, P Sukul, SZühlke, MSpiteller (2007). Metabolism of 14C-labelled and non-labelled sulfadiazine after administration to pigs. Analytical and Bioanalytical Chemistry, 388(8): 1733–1745
https://doi.org/10.1007/s00216-007-1368-y pmid: 17619182
31 JLi, W Cheng, LXu, P JStrong, HChen (2015). Antibiotic-resistant genes and antibiotic-resistant bacteria in the effluent of urban residential areas, hospitals, and a municipal wastewater treatment plant system. Environmental Science and Pollution Research International, 22(6): 4587–4596
https://doi.org/10.1007/s11356-014-3665-2 pmid: 25323405
32 A LLing, N R Pace, M T Hernandez, T M LaPara (2013). Tetracycline resistance and Class 1 integron genes associated with indoor and outdoor aerosols. Environmental Science & Technology, 47(9): 4046–4052
https://doi.org/10.1021/es400238g pmid: 23517146
33 YLuo, D Mao, MRysz, QZhou, H Zhang, LXu, P J JAlvarez (2010). Trends in antibiotic resistance genes occurrence in the Haihe River, China. Environmental Science & Technology, 44(19): 7220–7225
https://doi.org/10.1021/es100233w pmid: 20509603
34 LMa, A D Li, X L Yin, T Zhang (2017). The prevalence of integrons as the carrier of antibiotic resistance genes in natural and man-made environments. Environmental Science & Technology, 51(10): 5721–5728
https://doi.org/10.1021/acs.est.6b05887 pmid: 28426231
35 LMa, X X Zhang, F Zhao, BWu, SCheng, LYang (2013). Sewage treatment plant serves as a hot-spot reservoir of integrons and gene cassettes. Journal of Environmental Biology, 34(2 Spec No suppl): 391–399
pmid: 24620610
36 YMa, M Li, MWu, ZLi, X Liu (2015). Occurrences and regional distributions of 20 antibiotics in water bodies during groundwater recharge. Science of the Total Environment, 518– 519: 498–506
https://doi.org/10.1016/j.scitotenv.2015.02.100 pmid: 25777955
37 NMakowska, R Koczura, JMokracka (2016). Class 1 integrase, sulfonamide and tetracycline resistance genes in wastewater treatment plant and surface water. Chemosphere, 144: 1665–1673
https://doi.org/10.1016/j.chemosphere.2015.10.044 pmid: 26519797
38 DMao, Y Luo, JMathieu, QWang, L Feng, QMu, CFeng, P J Alvarez (2014). Persistence of extracellular DNA in river sediment facilitates antibiotic resistance gene propagation. Environmental Science & Technology, 48(1): 71–78
https://doi.org/10.1021/es404280v pmid: 24328397
39 EMarti, J Jofre, J LBalcazar (2013). Prevalence of antibiotic resistance genes and bacterial community composition in a river influenced by a wastewater treatment plant. PLoS One, 8(10): e78906
https://doi.org/10.1371/journal.pone.0078906 pmid: 24205347
40 J LMartinez (2009). The role of natural environments in the evolution of resistance traits in pathogenic bacteria. Proceedings of the Royal Society of London, B: Biological Sciences, 276(1667): 2521–2530
41 J LMartinez, T M Coque, F Baquero (2015). What is a resistance gene? Ranking risk in resistomes. Nature Reviews. Microbiology, 13(2): 116–123
https://doi.org/10.1038/nrmicro3399 pmid: 25534811
42 DMazel (2006). Integrons: Agents of bacterial evolution. Nature Reviews. Microbiology, 4(8): 608–620
https://doi.org/10.1038/nrmicro1462 pmid: 16845431
43 JMokracka, R Koczura, AKaznowski (2012). Multiresistant Enterobacteriaceae with class 1 and class 2 integrons in a municipal wastewater treatment plant. Water Research, 46(10): 3353–3363
https://doi.org/10.1016/j.watres.2012.03.037 pmid: 22507248
44 GNa, W Zhang, SZhou, HGao, Z Lu, XWu, RLi, L Qiu, YCai, ZYao (2014). Sulfonamide antibiotics in the Northern Yellow Sea are related to resistant bacteria: implications for antibiotic resistance genes. Marine Pollution Bulletin, 84(1–2): 70–75
https://doi.org/10.1016/j.marpolbul.2014.05.039 pmid: 24928456
45 S RPartridge, GTsafnat, ECoiera, J RIredell (2009). Gene cassettes and cassette arrays in mobile resistance integrons. FEMS Microbiology Reviews, 33(4): 757–784
https://doi.org/10.1111/j.1574-6976.2009.00175.x pmid: 19416365
46 LProia, D von Schiller, A Sànchez-Melsió, SSabater, C MBorrego, SRodríguez-Mozaz, J LBalcázar (2016). Occurrence and persistence of antibiotic resistance genes in river biofilms after wastewater inputs in small rivers. Environmental Pollution, 210: 121–128
https://doi.org/10.1016/j.envpol.2015.11.035 pmid: 26708766
47 APruden, M Arabi, H NStorteboom (2012). Correlation between upstream human activities and riverine antibiotic resistance genes. Environmental Science & Technology, 46(21): 11541–11549
https://doi.org/10.1021/es302657r pmid: 23035771
48 LRizzo, C Manaia, CMerlin, TSchwartz, CDagot, M CPloy, IMichael, DFatta-Kassinos (2013). Urban wastewater treatment plants as hotspots for antibiotic resistant bacteria and genes spread into the environment: A review. Science of the Total Environment, 447: 345–360
https://doi.org/10.1016/j.scitotenv.2013.01.032 pmid: 23396083
49 SRodriguez-Mozaz, S Chamorro, EMarti, BHuerta, MGros, A Sànchez-Melsió, C MBorrego, DBarceló, J LBalcázar (2015). Occurrence of antibiotics and antibiotic resistance genes in hospital and urban wastewaters and their impact on the receiving river. Water Research, 69: 234–242
https://doi.org/10.1016/j.watres.2014.11.021 pmid: 25482914
50 N ASabri, H Schmitt, BVan der Zaan, H WGerritsen, TZuidema, H H MRijnaarts (2018). Prevalence of antibiotics and antibiotic resistance genes in a wastewater effluent-receiving river in the Netherlands. Journal of Environmental Chemical Engineering (Online),(accessed March 2, 2018)
51 JTolls (2001). Sorption of veterinary pharmaceuticals in soils: A review. Environmental Science & Technology, 35(17): 3397–3406
https://doi.org/10.1021/es0003021 pmid: 11563639
52 JWang, W Ben, YZhang, MYang, Z Qiang (2015). Effects of thermophilic composting on oxytetracycline, sulfamethazine, and their corresponding resistance genes in swine manure. Environmental Science. Processes & Impacts, 17(9): 1654–1660
https://doi.org/10.1039/C5EM00132C pmid: 26216606
53 NWu, M Qiao, BZhang, W DCheng, Y GZhu (2010). Abundance and diversity of tetracycline resistance genes in soils adjacent to representative swine feedlots in China. Environmental Science & Technology, 44(18): 6933–6939
https://doi.org/10.1021/es1007802 pmid: 20707363
54 JXu, Y Xu, HWang, CGuo, H Qiu, YHe, YZhang, XLi, W Meng (2015). Occurrence of antibiotics and antibiotic resistance genes in a sewage treatment plant and its effluent-receiving river. Chemosphere, 119: 1379–1385
https://doi.org/10.1016/j.chemosphere.2014.02.040 pmid: 24630248
55 W HXu, G Zhang, S CZou, X DLi, Y CLiu (2007). Determination of selected antibiotics in the Victoria Harbour and the Pearl River, South China using high-performance liquid chromatography-electrospray ionization tandem mass spectrometry. Environmental Pollution, 145(3): 672–679
https://doi.org/10.1016/j.envpol.2006.05.038 pmid: 16996177
56 YXu, C Guo, YLuo, JLv, Y Zhang, HLin, LWang, J Xu (2016). Occurrence and distribution of antibiotics, antibiotic resistance genes in the urban rivers in Beijing, China. Environmental Pollution, 213: 833–840
https://doi.org/10.1016/j.envpol.2016.03.054 pmid: 27038570
57 J FYang, G G Ying, J L Zhao, R Tao, H CSu, Y SLiu (2011). Spatial and seasonal distribution of selected antibiotics in surface waters of the Pearl Rivers, China. Journal of Environmental Science and Health. Part. B, Pesticides, Food Contaminants, and Agricultural Wastes, 46(3): 272–280
https://doi.org/10.1080/03601234.2011.540540 pmid: 21462055
58 XYuan, Z Qiang, WBen, BZhu, J Qu (2015). Distribution, mass load and environmental impact of multiple-class pharmaceuticals in conventional and upgraded municipal wastewater treatment plants in East China. Environmental Science. Processes & Impacts, 17(3): 596–605
https://doi.org/10.1039/C4EM00596A pmid: 25614232
59 XZhang, B Wu, YZhang, TZhang, LYang, H H Fang, T Ford, SCheng (2009). Class 1 integronase gene and tetracycline resistance genes tetA and tetC in different water environments of Jiangsu Province, China. Ecotoxicology (London, England), 18(6): 652–660
https://doi.org/10.1007/s10646-009-0332-3 pmid: 19495963
60 X XZhang, T Zhang (2011). Occurrence, abundance, and diversity of tetracycline resistance genes in 15 sewage treatment plants across China and other global locations. Environmental Science & Technology, 45(7): 2598–2604
https://doi.org/10.1021/es103672x pmid: 21388174
61 X MZhan, L W Xiao (2017). Livestock Waste 2016-International Conference on Recent Advances in Pollution Control and Resource Recovery for the Livestock Sector. Frontiers of Environmental Science & Engineering, 11(3): 16
https://doi.org/10.1007/s11783-017-0958-y
62 JZhang, Z Wei, H FJia, XHuang (2017). Factors influencing water quality indices in a typical urban river originated with reclaimed water. Frontiers of Environmental Science & Engineering, 11(4):8
63 YZhang, A Li, TDai, FLi, H Xie, LChen, DWen (2018). Cell-free DNA: A neglected source for antibiotic resistance genes spreading from WWTPs. Environmental Science & Technology, 52(1): 248–257
https://doi.org/10.1021/acs.est.7b04283 pmid: 29182858
64 SZou, W Xu, RZhang, JTang, Y Chen, GZhang (2011). Occurrence and distribution of antibiotics in coastal water of the Bohai Bay, China: Impacts of river discharge and aquaculture activities. Environmental Pollution, 159(10): 2913–2920
https://doi.org/10.1016/j.envpol.2011.04.037 pmid: 21576000
[1] Supplementary Material Download
[1] Mengli Wang, Ruying Li, Qing Zhao. Distribution and removal of antibiotic resistance genes during anaerobic sludge digestion with alkaline, thermal hydrolysis and ultrasonic pretreatments[J]. Front. Environ. Sci. Eng., 2019, 13(3): 43-.
[2] Bo Zhang, Xilai Zheng, Tianyuan Zheng, Jia Xin, Shuai Sui, Di Zhang. The influence of slope collapse on water exchange between a pit lake and a heterogeneous aquifer[J]. Front. Environ. Sci. Eng., 2019, 13(2): 20-.
[3] Boran Wu, Xiaoli Chai, Youcai Zhao, Xiaohu Dai. Designing an in situ remediation strategy for polluted surface water bodies through the specific regulation of microbial community[J]. Front. Environ. Sci. Eng., 2019, 13(1): 4-.
[4] Wentao Zhao, Ying Guo, Shuguang Lu, Pingping Yan, Qian Sui. Recent advances in pharmaceuticals and personal care products in the surface water and sediments in China[J]. Front. Environ. Sci. Eng., 2016, 10(6): 2-.
[5] Haifeng JIA,Shidong LIANG,Yansong ZHANG. Assessing the impact on groundwater safety of inter-basin water transfer using a coupled modeling approach[J]. Front. Environ. Sci. Eng., 2015, 9(1): 84-95.
[6] Juan XIE,Xinyu ZHANG,Zhiwei XU,Guofu YUAN,Xinzhai TANG,Xiaomin SUN,D.J. BALLANTINE. Total phosphorus concentrations in surface water of typical agro- and forest ecosystems in China, 2004–2010[J]. Front.Environ.Sci.Eng., 2014, 8(4): 561-569.
[7] Yongjun LIU, Aining ZHANG, Xiaoyan MA, Xiaochang WANG. Genotoxicity evaluation of surface waters located in urban area of Xi’an City using Vicia faba bioassays[J]. Front Envir Sci Eng, 2013, 7(6): 860-866.
[8] Huining ZHANG, Xiaohu Zhang, Shuting ZHANG, Bo WEI, Qipei JIANG, Xin YU. Detecting Cryptosporidium parvum and Giardia lamblia by coagulation concentration and real-time PCR quantification[J]. Front Envir Sci Eng, 2013, 7(1): 49-54.
[9] Yongming ZHANG, Rong YAN, Zhen ZOU, Jiewei WANG, Bruce E. RITTMANN. Improved nitrogen removal in dual-contaminated surface water by photocatalysis[J]. Front Envir Sci Eng, 2012, 6(3): 428-436.
[10] Wenfeng SUN, Ruibao JIA, Baoyu GAO. Simultaneous analysis of five taste and odor compounds in surface water using solid-phase extraction and gas chromatography-mass spectrometry[J]. Front Envir Sci Eng, 2012, 6(1): 66-74.
[11] Lutz AHRENS, Merle PLASSMANN, Zhiyong XIE, Ralf EBINGHAUS. Determination of polyfluoroalkyl compounds in water and suspended particulate matter in the river Elbe and North Sea, Germany[J]. Front Envir Sci Eng Chin, 2009, 3(2): 152-170.
Viewed
Full text


Abstract

Cited

  Shared   
  Discussed