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Article

Use of Interspecies Correlation Estimation (ICE) Models to Derive Water Quality Criteria of Microplastics for Protecting Aquatic Organisms

1
National Marine Hazard Mitigation Service, Ministry of Natural Resource of the People’s Republic of China, Beijing 100194, China
2
Department of Water Ecology and Environment, Institute of Water Resources and Hydropower Research, Beijing 100038, China
*
Author to whom correspondence should be addressed.
Int. J. Environ. Res. Public Health 2022, 19(16), 10307; https://doi.org/10.3390/ijerph191610307
Submission received: 15 July 2022 / Revised: 15 August 2022 / Accepted: 15 August 2022 / Published: 19 August 2022

Abstract

:
Microplastics (MPs) in the water environment pose a potential threat to aquatic organisms. The Species Sensitivity Distribution (SSD) method was used to assess the ecological risks of microplastics on aquatic organisms in this study. However, the limited toxicity data of aquatic organisms made it impossible to derive water quality criteria (WQC) for MPs and difficult to implement an accurately ecological risk assessment. To solve the data gaps, the USEPA established the interspecies correlation estimation (ICE) model, which could predict toxicity data to a wider range of aquatic organisms and could also be utilized to develop SSD and HC5 (hazardous concentration, 5th percentile). Herein, we collected the acute toxicity data of 11 aquatic species from 10 families in 5 phyla to fit the metrical-based SSDs, meanwhile generating the ICE-based-SSDs using three surrogate species (Oncorhynchus mykiss, Hyalella Azteca, and Daphnia magna), and finally compared the above SSDs, as well as the corresponding HC5. The results showed that the measured HC5 for acute MPs toxicity data was 112.3 μg/L, and ICE-based HC5 was 167.2 μg/L, which indicated there were no significant differences between HC5 derived from measured acute and ICE-based predicted values thus the ICE model was verified as a valid approach for generating SSDs with limited toxicity data and deriving WQC for MPs.

1. Introduction

Significant evidence shows that Microplastics (MPs) have entered the water environment and threaten the well-being of aquatic species [1,2,3]. Microplastics are defined as plastic particles, fragments, fibers, and films up to 5 mm in size [4,5,6,7]. Previous studies have concluded that MPs had a variety of toxic effects on aquatic organisms, such as lethal toxicity, enzyme toxicity, genetic toxicity, thyroid toxicity, and reproductive toxicity, etc. [8,9,10]. Results showed that MPs might impose potential risks to the aquatic ecosystem, including oceans [11]. The bulletin of China’s marine ecological environment in 2021 showed that the average density of floating MPs on the sea surface was 0.44 pieces/m3. This pollution cannot be ignored [12]. The fundamental reason for the difficulty in conducting a comprehensive aquatic risk assessment for MPs is the lack of toxicity data [13].
Species Sensitivity Distribution (SSD) is an important instrument for developing Water Quality Criteria (WQC). However, due to the complexity of test protocols and species availability, results for certain species were unlikely to be obtained. In response to the data gap, the US EPA developed the interspecies correlation estimation (ICE) model, which is based on a log–log correlation between abundant chemical toxicity values for a series of species [14], at least 1258 chemicals, and 5487 test results of 180 species in an acute toxicity dataset [15]. Moreover, the ICE model could accurately predict the toxicity and produce protective toxicity estimates [16], such as species sensitivity distribution (SSD) and HC5 (hazard concentration, 5th percentile), for evaluating the contaminant threat to species of interest [17,18,19,20]. The ICE will help overcome the lack of toxicity data to ensure that there is enough data for WQC studies [9,21].
In this study, we collected the acute toxicity data of 11 aquatic species from 10 families in 5 phyla to fit the metrical-based SSDs, meanwhile generating the ICE-based-SSDs using three surrogate species (Oncorhynchus mykiss, Hyalella Azteca, and Daphnia magna), and finally compared the above SSDs, as well as the corresponding HC5. Moreover, the WQC of MPs for aquatic organisms was derived using a battery of toxicity data (11 aquatic species from 10 families in 5 phyla) according to the US EPA guidelines.
The objectives of this study were to (i) derive measure-based and ICE-based WQC for MPs and to (ii) compare measured-based-SSDs with original and improved ICE-based-SSDs for MPs. Our study could provide valuable information on pollution management and environmental risk assessment for MPs in the ambient aquatic environment.

2. Materials and Methods

2.1. Measured Toxicity Data Collection and Processing

ECOTOX (http://cfpub.epa.gov/ecotox, accessed on 1 March 2022) and two supplemental online databases, CNKI (http://www.cnki.net, accessed on 1 March 2022) and ELSEVIER (http://www.sciencedirect.com, accessed on 1 March 2022), were used to obtain MP toxicity data. The data were checked and processed in accordance with EPA requirements in the United States [22]. “MPs”, “Microplastics”, “aquatic life/organisms”, “toxicity”, and “ecotoxicity” were the important terms.
Data were submitted to stringent quality control procedures and subjected to rigorous quality assurance guidelines (Yan et al., 2013). To begin with, the values of 48-h LC50 or EC50 for Daphnia and 96-h LC50 or EC50 for other species were discovered in databases or literature for aquatic acute toxicity. Second, the data’s key toxicological endpoints were immobility, respiratory inhibition, and mortality. Finally, the vast majority of exposure tests were either flow-through or static/renewal. All of the tests were carried out in accordance with ASTM standards [21]. The detailed information about the Measured toxicity data is listed in Table 1. The acute toxicological data of 11 aquatic species from 10 families in 5 phyla were collected. The most sensitive species were Tetraselmis chuii, i.e., a kind of algae. As we all know, algae are one of the important components of marine primary productivity [23] and can take the lead in sensing microplastic pollution in water. The least sensitive species were Vibrio fischeri, the EC50 was 1.00 × 106 μg/L.

2.2. ICE Data Set

The ICE software and more powerful ICE models for aquatic and terrestrial species were created by the US EPA and made accessible on the internet (https://www3.epa.gov/webice/, accessed on 1 March 2022). In this study, the Web-ICE platform was employed. Through a user-friendly interface, the Web-ICE delivered interspecies extrapolation models for acute toxicity. The following requirements were satisfied with the test results of the database: Fish with an LC50/EC50 of 96 h; most invertebrates with a LC50/EC50 of 48 h; fish weighing 0.1–0.2 g; fish less than 1 months old or less than 30 mm in length. Furthermore, MPs’ toxicological endpoints in fish and invertebrates are limited to those associated with death, such as immobility, respiratory suppression, and fatal impacts.
Based on geometric means from the measured database, the Web-ICE was seeded with acute toxicity values for Oncorhynchus mykiss, Hyalella Azteca, and Daphnia magna (6.03 × 105 μg/L, 2.18 × 105 μg/L, and 7.70 × 102 μg/L, respectively) to predict toxicity values.

2.3. Data Analysis

Log-logistic, log-normal, and Burr III were usually used to fit SSDs [34]. Based on previous studies, we found that log-logistic fitted the toxicity data well and could make it statistically more meaningful. Thus, in this study, log-logistic was used to generate SSDs. The equation is shown as follows:
Y = 1/(1 + exp ((α − X) / β))
where the cumulative probability of species is defined as Y, which is the order of the data point divided by one plus the total number plus one of the data points; X is the LC50 or EC50 by log-transformed. Where α and β are parameters, which represent the location (or intercept) and the slope of the curve, respectively. Moreover, we used a two-sample Kolmogorov–Smirnov test (K-S test) to analyze the difference between the predicted data group and the measured data group [35]. The main data analysis software was Origin 8.0 and SPSS 20.0.
According to the US EPA guidelines, the criteria used to pick the predicted toxicity data are briefly listed as follows: (1) mean square error (MSE) < 0.22; (2) taxonomic distance ≤ 4; (3) cross-validation success rate > 85%; (4) degree of freedom (df) > 8; (5) R2 value > 0.6; (6) p-values < 0.01. The statistical parameters were critical to assessing the accuracy of the model [34,35,36].

3. Results and Discussion

3.1. Estimated Toxicity Using Web-ICE

By running the Web-ICE program, we obtained 133 predicted toxicity values, and only 19 toxicity data were adopted based on the aforementioned ICE criteria, including amphibians, invertebrates, and fish (see Table 2). One hundred and fourteen toxicity data did not meet one or more conditions, such as MSE > 0.22 or R2 value ≤ 0.6, or cross-validation success rate ≤ 85%.
Fifty-one toxicity values of different species were predicted by Web-ICE for D. magna. Forty-two invalid data were excluded, and only seven species were effective. They were Thamnocephalus platyurus, Daphnia pulex, Simocephalus serrulatus, Utterbackia imbecillis, Amblema plicata, Megalonaias nervosa, and Margaritifera falcata. For O. mykiss, 9 effective data came from a total of 62 data. For H. azteca, three effective data came from a total of 20 data.

3.2. ICE-and Measure-Based SSD

SSDs were generated by log-logistic, which was constructed using measured toxicity data and ICE predicted toxicity data from three surrogate species (Figure 1). The cumulative probability means the sensitivity of species. The results showed that species in the first quartile of the SSD curve were assumed to be the most sensitive, while those in the second and third quartiles were supposed to be moderately tolerant, and those in the fourth quartile were thought to be the most tolerant [36,37,38]. The ranking results of the predicted and the metrical species distributions were quite different, the most sensitive species based on the metrical SSD curves were Tetraselmis chuii, Pseudokirchneriella subcapitata, and Daphnia magna (a total of 11, a quartile of 3), while the most sensitive species in ICE-based SSD curves were Amblema plicata, Americamysis bahia, Megalonaias nervosa, Ceriodaphnia dubia, Utterbackia imbecillis, and Daphnia pulex (a total of 19, a quartile of 5). The most tolerant species were a little different between the two ICE models. The most tolerant species predicted by original ICE models were Salmo trutta, Oncorhynchus tshawytscha, and Oncorhynchus kisutch (a total of 12, a quartile of 3), while the most sensitive species predicted by improved ICE models were Oncorhynchus tshawytscha, Ictalurus punctatus, Oncorhynchus kisutch, Pimephales promelas, and Carassius auratus (a total of 21, a quartile of 5). Dyer et al. [19] used ICE and ranked the predicted species. The result suggested that those more sensitive to a wide range of chemicals were cold-water fish species Moreover, Raimondo et al. [38] also concluded that trout was the most sensitive species to pesticides via ICE predicted values. That is not consistent with this study, the sensitivity of various species to specific chemicals was also observed to be significantly different [37].
In addition, the most sensitive species and the most tolerant species were both predicted by improved ICE models, which showed a much wider range of predictions than the original ICE models [34,35,36,37]. Although HC5 values obtained from ICE- and measure-based SSD were different, the Kolmogorov–Smirnov test indicated that the two SSDs showed no significant difference (ks = 0.902, n1 = 11, n2 = 19, p = 0.183 > 0.05).

3.3. Aquatic Life Criteria Derivation

In this study, the HC5 of MPs from ICE- and measure-based SSD were obtained to be 167.2 μg/L and 112.3 μg/L, respectively, which were similar to those reported in previous studies [39,40]. The comparison results suggested the possibility of extrapolation utilizing ICE in terms of statistical analysis and effect evaluation. As a result, the use of ICE models to produce relatively accurate estimates of chemical toxicity and protective criteria was encouraging, and it might be utilized as a potential alternative to current water quality derivation techniques in the absence of appropriate empirical toxicity data [41,42,43].
While there are solid ecological reasons to avoid using non-China specifics in the development of China-specific water quality criteria, considerable new research on the evaluation of ecological features as elements worth protecting may lead to reconsideration of such eliminations. If attributes are protected, the location of the species endemicity is irrelevant. This is crucial to assessing danger at a given location. We envisage the creation and deployment of ICE models that include a wide range of species from throughout the world, providing the most rigorous technique for developing environmental criteria regardless of location.

4. Conclusions

This study compared HC5 obtained from ICE-based and metrical acute toxicity values of MPs for aquatic species to assess the accuracy of ICE-generated SSDs. There was no significant difference between the ICE-based and measured-based SSDs, showing that ICE might be a viable method for predicting acute toxicity data for aromatic chemicals. Furthermore, the collection of toxicity data from experiments usually suffered from a long cycle and high cost. Compared with the experimental measurement, the cost of the prediction via ICE models is fairly low, which would save significant time and expense. Thus, in ecological risk assessment, the ICE models are advocated as a good option.

Author Contributions

Conceptualization, formal analysis, supervision, J.W.; methodology, data curation, software, L.G.; formal analysis, X.Z.; supervision, editing, D.W.; formal analysis Y.L. All authors have read and agreed to the published version of the manuscript.

Funding

This research was supported by the National Natural Science Foundation of China (No. 52000181) and the IWHR Research & Development Support Program (WE110145B0062021).

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Data are available on request due to privacy and ethical restrictions.

Acknowledgments

The authors thank the editors and anonymous experts for their comments, which have greatly improved the study.

Conflicts of Interest

The author states that there is no conflict of interest.

References

  1. Ammendolia, J.; Saturno, J.; Brooks, A.L.; Jacobs, S.; Jambeck, J. An emerging source of plastic pollution: Environmental presence of plastic personal protective equipment (PPE) debris related to COVID-19 in a metropolitan city. Environ. Pollut. 2020, 269, 116160. [Google Scholar] [CrossRef] [PubMed]
  2. Briain, O.; Mendes, A.; Mccarron, S.; Healy, M.G.; Morrison, L. The role of wet wipes and sanitary towels as a source of white microplastic fibres in the marine environment. Water Res. 2020, 182, 116021. [Google Scholar] [CrossRef]
  3. Canning-Clode, J.; Sepúlveda, P.; Almeida, S.; Monteiro, J.G. Will COVID-19 Containment and Treatment Measures Drive Shifts in Marine Litter Pollution? Front. Mar. Sci. 2020, 7, 691. [Google Scholar] [CrossRef]
  4. Cecchi, T. Analysis of volatiles organic compounds in Venice lagoon water reveals COVID 19 lockdown impact on microplastics and mass tourism related pollutants. Sci. Total Environ. 2021, 783, 146951. [Google Scholar] [CrossRef] [PubMed]
  5. Chen, X.; Chen, X.; Liu, Q.; Zhao, Q.; Xiong, X.; Wu, C. Used disposable face masks are significant sources of microplastics to environment. Environ. Pollut. 2021, 285, 117485. [Google Scholar] [CrossRef]
  6. De-la-Torre, G.E.; Aragaw, T.A. What we need to know about PPE associated with the COVID-19 pandemic in the marine environment. Mar. Pollut. Bull. 2021, 163, 111879. [Google Scholar] [CrossRef]
  7. Expósito, N.; Rovira, J.; Sierra, J.; Folch, J.; Schuhmacher, M. Microplastics levels, size, morphology and composition in marine water, sediments and sand beaches. Case study of Tarragona coast (western Mediterranean). Sci. Total Environ. 2021, 786, 147453. [Google Scholar] [CrossRef]
  8. Fadare, O.O.; Okoffo, E.D. COVID-19 face masks: A potential source of microplastic fibers in the environment. Sci. Total Environ. 2020, 737, 140279. [Google Scholar] [CrossRef]
  9. Elgarahy, A.M.; Akhdhar, A.; Elwakeel, K.Z. Microplastics prevalence, interactions, and remediation in the aquatic environment: A critical review. J. Environ. Chem. Eng. 2021, 5, 106224. [Google Scholar] [CrossRef]
  10. Han, J.; He, S. Need for assessing the inhalation of micro(nano)plastic debris shed from masks, respirators, and home-made face coverings during the COVID-19 pandemic. Environ. Pollut. 2021, 268, 115728. [Google Scholar] [CrossRef]
  11. Ho, W.K.; Leung, S.Y. The Crucial Role of Heavy Metals on the Interaction of Engineered Nanoparticles with Polystyrene Microplastics. Water Res. 2021, 201, 117317. [Google Scholar] [CrossRef] [PubMed]
  12. Krv, A.; Hbs, B.; Vpr, B.; Bs, A.; Jba, C.; Bkda, B.; Sg, B. Challenges and strategies for effective plastic waste management during and post COVID-19 pandemic. Sci. Total Environ. 2021, 750, 141514. [Google Scholar]
  13. Liang, H.; Ji, Y.; Ge, W.; Wu, J.; Song, N.; Yin, Z.; Chai, C. Release kinetics of microplastics from disposable face masks into the aqueous environment. Sci. Total Environ. 2022, 816, 151650. [Google Scholar] [CrossRef]
  14. Wu, J.; Liu, Z.; Yan, Z.; Yi, X. Derivation of water quality criteria of phenanthrene using interspecies correlation estimation models for aquatic life in China. Environ. Sci. Pollut. Res. Int. 2015, 22, 9457–9463. [Google Scholar] [CrossRef] [PubMed]
  15. Raimondo, S.; Vivian, D.; Barron, M. Web-Based Interspecies Correlation Estimation (Web-ICE) for Acute Toxicity: User Manual; Version 3.1; Office of Research and Development, US Environmental Protection Agency: Gulf Breeze, FL, USA, 2010.
  16. Wang, X.; Fan, B.; Fan, M.; Belanger, S.; Li, J.; Chen, J.; Gao, X.; Liu, Z. Development and use of interspecies correlation estimation models in China for potential application in water quality criteria. Chemosphere 2020, 240, 124848. [Google Scholar] [CrossRef] [PubMed]
  17. Dyer, S.D.; Versteeg, D.J.; Belanger, S.E.; Chaney, J.G.; Mayer, F.L. Interspecies correlation estimates predict protective environmental concentrations. Environ. Sci. Technol. 2006, 40, 3102–3111. [Google Scholar] [CrossRef]
  18. Raimondo, S.; Mineau, P.; Barron, M. Estimation of chemical toxicity to wildlife species using interspecies correlation models. Environ. Sci. Technol. 2007, 41, 5888–5894. [Google Scholar] [CrossRef]
  19. Dyer, S.D.; Versteeg, D.J.; Belanger, S.E.; Chaney, J.G.; Raimondo, S.; Barron, M.G. Comparison of species sensitivity distributions derived from interspecies correlation models to distributions used to derive water quality criteria. Environ. Sci. Technol. 2008, 42, 3076–3083. [Google Scholar] [CrossRef]
  20. Golsteijn, L.; Hendriks, H.W.; van Zelm, R.; Ragas, A.M.; Huijbregts, M.A. Do interspecies correlation estimations increase the reliability of toxicity estimates for wildlife? Ecotoxicol. Environ. Saf. 2012, 80, 238–243. [Google Scholar] [CrossRef]
  21. ASTM. Chronic toxicity of the bromoxynil formulation Buctril to Daphnia magna exposed continuously and intermittently. Arch. Environ. Contam. Toxicol. 1993, 25, 152–159. [Google Scholar]
  22. USEPA. Guidelines for Deriving Numerical National Water Quality Criteria for the Protection of Aquatic Organisms and Their Uses (PB 85-227049); Office of Research and Development, Environmental Research Laboratories, US Environmental Protection Agency: Duluth, MN, USA; Narragansett, RI, USA; Corvallis, OR, USA, 1985.
  23. Md Refat Jahan, A.; De la Torre, B.; Pizzaro-Ortega, B.; Dioses-Salinas, B.; Al-Nahian, C. Personal protective equipment (PPE) pollution driven by the COVID-19 pandemic in Cox’s Bazar, the longest natural beach in the world. Mar. Pollut. Bull. 2021, 169, 112497. [Google Scholar]
  24. Prata, J.C.; Silva, A.; Walker, T.R.; Duarte, A.C.; Santos, T.R. COVID-19 Pandemic Repercussions on the Use and Management of Plastics. Environ. Sci. Technol. 2020, 54, 7760–7765. [Google Scholar] [CrossRef] [PubMed]
  25. Shen, M.; Zeng, Z.; Song, B.; Yi, H.; Hu, T.; Zhang, Y.; Zeng, G.; Xiao, R. Neglected microplastics pollution in global COVID-19: Disposable surgical masks. Sci. Total Environ. 2021, 790, 148130. [Google Scholar] [CrossRef] [PubMed]
  26. Shruti, V.C.; Pérez-Guevara, F.; Kutralam-Muniasamy, G. Wet wipes contribution to microfiber contamination under COVID-19 era: An important but overlooked problem. Environ. Chall. 2021, 5, 100267. [Google Scholar] [CrossRef]
  27. Su, Y.; Zhang, Z.; Zhu, J.; Shi, J.; Shi, H. Microplastics act as vectors for antibiotic resistance genes in landfill leachate: The enhanced roles of the long-term aging process. Environ. Pollut. 2021, 270, 116278. [Google Scholar] [CrossRef]
  28. Sullivan, G.L.; Delgado-Gallardo, J.; Watson, T.M.; Sarp, S. An investigation into the leaching of micro and nano particles and chemical pollutants from disposal face masks—Linked to the COVID-19 pandemic. Water Res. 2021, 196, 117033. [Google Scholar] [CrossRef]
  29. Tagorti, G.; Kaya, B. Genotoxic effect of microplastics and COVID-19: The hidden threat. Chemosphere 2022, 286, 131898. [Google Scholar] [CrossRef]
  30. Thiele, C.J.; Hudson, M. Uncertainty about the risks associated with microplastics among lay and topic-experienced respondents. Sci. Rep. 2021, 11, 7155. [Google Scholar] [CrossRef]
  31. Wang, Z.; An, C.; Chen, X.; Lee, K.; Feng, Q. Disposable masks release microplastics to the aqueous environment with exacerbation by natural weathering. J. Hazard. Mater. 2021, 417, 126036. [Google Scholar] [CrossRef]
  32. Eriksson, A.N.M.; Rigaud, C.; Krasnov, A.; Wincent, E.; Vehniäinen, E.-R. Exposure to retene, fluoranthene, and their binary mixture causes distinct transcriptomic and apical outcomes in rainbow trout (Oncorhynchus mykiss) yolk sac alevins. Aquat. Toxicol. 2022, 244, 106083. [Google Scholar] [CrossRef]
  33. Baker, J.E.; Eisenreich, S.J.; Eadie, B.J. Sediment trap fluxes and benthic recycling of organic carbon, polycyclic aromatic hydrocarbons, and polychlorobiphenyl congeners in Lake Superior. Environ. Sci. Technol. 1991, 25, 500–509. [Google Scholar] [CrossRef]
  34. Cheung, K.C.; Leung, H.M.; Kong, K.Y.; Wong, M.H. Residual levels of DDTs and PAHs in freshwater and marine fish from Hong Kong markets and their health risk assessment. Chemosphere 2007, 66, 460–468. [Google Scholar] [CrossRef]
  35. Zhang, H.; Pan, L.; Tao, Y. Toxicity assessment of environmental pollutant phenanthrene in clam Venerupis philippinarum using oxidative stress biomarkers. Environ. Toxicol. Pharmacol. 2014, 37, 697–704. [Google Scholar] [CrossRef] [PubMed]
  36. Shi, Z.; Wang, C.; Zhao, Y. Effects of surfactants on the fractionation, vermiaccumulation, and removal of fluoranthene by earthworms in soil. Chemosphere 2020, 250, 126332. [Google Scholar] [CrossRef] [PubMed]
  37. Lee, J.H.; Landrum, P.F.; Koh, C.-H. Toxicokinetics and time-dependent PAH toxicity in the amphipod Hyalella azteca. Environ. Sci. Technol. 2002, 36, 3124–3130. [Google Scholar] [CrossRef]
  38. Macıas-Zamora, J.V.; Mendoza-Vega, E.; Villaescusa-Celaya, J.A. PAHs composition of surface marine sediments: A comparison to potential local sources in Todos Santos Bay, BC, Mexico. Chemosphere 2002, 46, 459–468. [Google Scholar] [CrossRef]
  39. Rostami, M.; Rostami, S. Effect of salicylic acid and mycorrhizal symbiosis on improvement of fluoranthene phytoremediation using tall fescue (Festuca arundinacea Schreb). Chemosphere 2019, 232, 70–75. [Google Scholar] [CrossRef]
  40. Callen, M.S.; Lopez, J.M.; Iturmendi, A.; Mastral, A.M. Nature and sources of particle associated polycyclic aromatic hydrocarbons (PAH) in the atmospheric environment of an urban area. Environ. Pollut. 2013, 183, 166–174. [Google Scholar] [CrossRef]
  41. Chen, H.Y.; Teng, Y.G.; Wang, J.S. Source apportionment of polycyclic aromatic hydrocarbons (PAHs) in surface sediments of the Rizhao coastal area (China) using diagnostic ratios and factor analysis with nonnegative constraints. Sci. Total Environ. 2012, 414, 293–300. [Google Scholar] [CrossRef]
  42. Meier, J.R.; Snyder, S.; Sigler, V.; Altfater, D.; Gray, M.; Batin, B.; Baumann, P.; Gordon, D.; Wernsing, P.; Lazorchak, J. An integrated assessment of sediment remediation in a midwestern U.S. stream using sediment chemistry, water quality, bioassessment, and fish biomarkers. Environ. Toxicol. Chem. 2013, 32, 653–661. [Google Scholar] [CrossRef]
  43. Maletic, S.P.; Beljin, J.M.; Roncevic, S.D.; Grgic, M.G.; Dalmacija, B.D. State of the art and future challenges for polycyclic aromatic hydrocarbons is sediments: Sources, fate, bioavailability and remediation techniques. J. Hazard Mater. 2019, 365, 467–482. [Google Scholar] [CrossRef] [PubMed]
Figure 1. Comparison of SSDs constructed using measured toxicity data and ICE predicted toxicity data from 3 surrogate species.
Figure 1. Comparison of SSDs constructed using measured toxicity data and ICE predicted toxicity data from 3 surrogate species.
Ijerph 19 10307 g001
Table 1. Toxicity data of microplastic to aquatic species (LC50/EC50).
Table 1. Toxicity data of microplastic to aquatic species (LC50/EC50).
PhylumFamilySpeciesLC50/EC50 (μg/L)Reference
ArthropodaDaphnidaeDaphnia magna7.70 × 102[23]
Ceriodaphnia dubia9.58 × 102[24]
ThamnocephalidaeThamnocephalus platyurus5.20 × 103[25]
HarpacticidaeTigriopus japonicus2.15 × 103[26]
HyalellidaeHyalella azteca2.18 × 105[27]
ChordataSalmonidaeOncorhynchus mykiss6.03 × 105[28]
GobiidaePomatoschistus microps3.05 × 105[29]
ChlorophytaChlorodendraceaePseudokirchneriella subcapitata5.80 × 102[30]
Tetraselmis chuii1.45 × 102[31]
ProteobacteriaVibrionaceaeVibrio fischeri1.00 × 106[32]
EchinodermataParechinidaeParacentrotus lividus2.61 × 103[33]
Table 2. Summary of the regression parameters of surrogate-predicted species using ICE models.
Table 2. Summary of the regression parameters of surrogate-predicted species using ICE models.
Surrogate SpeciesPredicted SpeciesEstimated
Toxicity (mg/L)
Cross-Validation Success (%)MSER2Taxonomic Distance
Daphnia magna
Thamnocephalus platyurus724.26910.050.984
Daphnia pulex628.65900.120.971
Simocephalus serrulatus755.41870.210.882
Utterbackia imbecillis580.281000.110.964
Amblema plicata279.27900.180.944
Megalonaias nervosa437.8910.160.963
Margaritifera falcata787.86900.140.953
Oncorhynchus mykiss
Salmo salar61,347.21930.120.952
Salvelinus fontinalis60,703.33920.110.942
Salmo trutta61,269.36960.10.952
Oncorhynchus tshawytscha60,424.03940.070.961
Oncorhynchus kisutch79,193.941000.040.981
Oncorhynchus clarkii44,376.05950.090.941
Lepomis cyanellus85,160.741000.130.944
Salvelinus namaycush28,786.62960.080.932
Perca flavescens50,142.3880.140.944
Hyalella azteca
Gammarus pseudolimnaeus2161.171000.030.993
Pimephales promelas3457.14970.220.854
Americamysis bahia350.71860.200.864
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Wu, J.; Zhao, X.; Gao, L.; Li, Y.; Wang, D. Use of Interspecies Correlation Estimation (ICE) Models to Derive Water Quality Criteria of Microplastics for Protecting Aquatic Organisms. Int. J. Environ. Res. Public Health 2022, 19, 10307. https://doi.org/10.3390/ijerph191610307

AMA Style

Wu J, Zhao X, Gao L, Li Y, Wang D. Use of Interspecies Correlation Estimation (ICE) Models to Derive Water Quality Criteria of Microplastics for Protecting Aquatic Organisms. International Journal of Environmental Research and Public Health. 2022; 19(16):10307. https://doi.org/10.3390/ijerph191610307

Chicago/Turabian Style

Wu, Jiangyue, Xiaohui Zhao, Lin Gao, Yan Li, and Dan Wang. 2022. "Use of Interspecies Correlation Estimation (ICE) Models to Derive Water Quality Criteria of Microplastics for Protecting Aquatic Organisms" International Journal of Environmental Research and Public Health 19, no. 16: 10307. https://doi.org/10.3390/ijerph191610307

APA Style

Wu, J., Zhao, X., Gao, L., Li, Y., & Wang, D. (2022). Use of Interspecies Correlation Estimation (ICE) Models to Derive Water Quality Criteria of Microplastics for Protecting Aquatic Organisms. International Journal of Environmental Research and Public Health, 19(16), 10307. https://doi.org/10.3390/ijerph191610307

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