| Rogge W F, Hildemann L M, Mazurek M A, et al. Sources of fine organic aerosol. 3. Road dust, tire debris, and organometallic brake lining dust:Roads as sources and sinks[J]. Environmental Science & Technology, 1993, 27(9):1892-1904 |
| Knight L J, Parker-Jurd F N F, Al-Sid-Cheikh M, et al. Tyre wear particles:An abundant yet widely unreported microplastic?[J]. Environmental Science and Pollution Research International, 2020, 27(15):18345-18354 |
| Wagner S, Hüffer T, Klöckner P, et al. Tire wear particles in the aquatic environment-A review on generation, analysis, occurrence, fate and effects[J]. Water Research, 2018, 139:83-100 |
| Chibwe L, Parrott J L, Shires K, et al. A deep dive into the complex chemical mixture and toxicity of tire wear particle leachate in fathead minnow[J]. Environmental Toxicology and Chemistry, 2022, 41(5):1144-1153 |
| Tian Z Y, Zhao H Q, Peter K T, et al. A ubiquitous tire rubber-derived chemical induces acute mortality in coho salmon[J]. Science, 2021, 371(6525):185-189 |
| Mohajerani A, Kurmus H, Conti D, et al. Environmental impacts and leachate analysis of waste rubber incorporated in construction and road materials:A review[J]. The Science of the Total Environment, 2022, 835:155269 |
| Jin J, van Swaaij A P J, Noordermeer J W M, et al. On the various roles of 1,3-diphenyl guanidine in silica/silane reinforced sbr/br blends[J]. Polymer Testing, 2021, 93:106858 |
| Zahn D, Mucha P, Zilles V, et al. Identification of potentially mobile and persistent transformation products of REACH-registered chemicals and their occurrence in surface waters[J]. Water Research, 2019, 150:86-96 |
| Johannessen C, Helm P, Lashuk B, et al. The tire wear compounds 6PPD-quinone and 1,3-diphenylguanidine in an urban watershed[J]. Archives of Environmental Contamination and Toxicology, 2022, 82(2):171-179 |
| Schulze S, Zahn D, Montes R, et al. Occurrence of emerging persistent and mobile organic contaminants in European water samples[J]. Water Research, 2019, 153:80-90 |
| Scheurer M, Sandholzer A, Schnabel T, et al. Persistent and mobile organic chemicals in water resources:Occurrence and removal options for water utilities[J]. Water Supply, 2022, 22(2):1575-1592 |
| Xie L, Nakajima F, Kasuga I, et al. Simultaneous screening for chemically diverse micropollutants in public water bodies in Japan by high-performance liquid chromatography-Orbitrap mass spectrometry[J]. Chemosphere, 2020, 1:128524 |
| Hou F, Tian Z Y, Peter K T, et al. Quantification of organic contaminants in urban stormwater by isotope dilution and liquid chromatography-tandem mass spectrometry[J]. Analytical and Bioanalytical Chemistry, 2019, 411(29):7791-7806 |
| Tang J, Tang L, Zhang C, et al. Different senescent HDPE pipe-risk:Brief field investigation from source water to tap water in China (Changsha City)[J]. Environmental Science and Pollution Research International, 2015, 22(20):16210-16214 |
| Johannessen C, Metcalfe C D. The occurrence of tire wear compounds and their transformation products in municipal wastewater and drinking water treatment plants[J]. Environmental Monitoring and Assessment, 2022, 194(10):731 |
| Zhang H Y, Huang Z, Liu Y H, et al. Occurrence and risks of 23 tire additives and their transformation products in an urban water system[J]. Environment International, 2023, 171:107715 |
| Tang S Q, Sun X F, Qiao X H, et al. Prenatal exposure to emerging plasticizers and synthetic antioxidants and their potency to cross human placenta[J]. Environmental Science & Technology, 2022, 56(12):8507-8517 |
| Bempong M A, Hall E V. Reproductive toxicology of 1,3-diphenylguanidine:Analysis of induced sperm abnormalities in mice and hamsters and reproductive consequences in mice[J]. Journal of Toxicology and Environmental Health, 1983, 11(4-6):869-878 |
| Ma Y B, Han J, Guo Y Y, et al. Disruption of endocrine function in in vitro H295R cell-based and in in vivo assay in zebrafish by 2,4-dichlorophenol[J]. Aquatic Toxicology, 2012, 106-107:173-181 |
| Yang C, Lim W, Song G. Reproductive toxicity due to herbicide exposure in freshwater organisms[J]. Comparative Biochemistry and Physiology Part C:Toxicology & Pharmacology, 2021, 248:109103 |
| Gu J, Li L Z, Yin X G, et al. Long-term exposure of zebrafish to bisphenol F:Adverse effects on parental reproduction and offspring neurodevelopment[J]. Aquatic Toxicology, 2022, 248:106190 |
| Qiao Y J, He J Y, Han P, et al. Long-term exposure to environmental relevant triclosan induces reproductive toxicity on adult zebrafish and its potential mechanism[J]. The Science of the Total Environment, 2022, 826:154026 |
| Howe K, Clark M D, Torroja C F, et al. The zebrafish reference genome sequence and its relationship to the human genome[J]. Nature, 2013, 496(7446):498-503 |
| Spence R, Gerlach G, Lawrence C, et al. The behaviour and ecology of the zebrafish, Danio rerio[J]. Biological Reviews of the Cambridge Philosophical Society, 2008, 83(1):13-34 |
| Segner H. Zebrafish (Danio rerio) as a model organism for investigating endocrine disruption[J]. Comparative Biochemistry and Physiology Toxicology & Pharmacology, 2009, 149(2):187-195 |
| Scholz S, Fischer S, Gündel U, et al. The zebrafish embryo model in environmental risk assessment-Applications beyond acute toxicity testing[J]. Environmental Science and Pollution Research, 2008, 15(5):394-404 |
| Fraysse B, Mons R, Garric J. Development of a zebrafish 4-day embryo-larval bioassay to assess toxicity of chemicals[J]. Ecotoxicology and Environmental Safety, 2006, 63(2):253-267 |
| Kalueff A V, Echevarria D J, Homechaudhuri S, et al. Zebrafish neurobehavioral phenomics for aquatic neuropharmacology and toxicology research[J]. Aquatic Toxicology, 2016, 170:297-309 |
| Huang T, Zhao Y H, He J, et al. Endocrine disruption by azole fungicides in fish:A review of the evidence[J]. Science of the Total Environment, 2022, 822:153412 |
| He J H, Gao J M, Huang C J, et al. Zebrafish models for assessing developmental and reproductive toxicity[J]. Neurotoxicology and Teratology, 2014, 42:35-42 |
| David R M, Jones H S, Panter G H, et al. Interference with xenobiotic metabolic activity by the commonly used vehicle solvents dimethylsulfoxide and methanol in zebrafish (Danio rerio) larvae but not Daphnia magna[J]. Chemosphere, 2012, 88(8):912-917 |
| 国家质量监督检验检疫总局, 中国国家标准化管理委员会. 化学品鱼类急性毒性试验:GB/T 27861-2011[S]. 北京:中国标准出版社, 2012 |
| Organisation for Economic Co-operation and Development (OECD). Test No. 236:Fish embryo acute toxicity (FET) test[R]. Paris:OECD, 2013 |
| Maes J, Verlooy L, Buenafe O E, et al. Evaluation of 14 organic solvents and carriers for screening applications in zebrafish embryos and larvae[J]. PLoS One, 2012, 7(10):e43850 |
| 国家质量监督检验检疫总局, 中国国家标准化管理委员会. 危险化学品鱼类急性毒性分级试验方法:GB/T 21281-2007[S]. 北京:中国标准出版社, 2008 |
| Sendra M, Pereiro P, Yeste M P, et al. Surgical face masks as a source of emergent pollutants in aquatic systems:Analysis of their degradation product effects in Danio rerio through RNA-Seq[J]. Journal of Hazardous Materials, 2022, 428:128186 |
| Su Z Q, Łabaj P P, Li S, et al. A comprehensive assessment of RNA-seq accuracy, reproducibility and information content by the Sequencing Quality Control Consortium[J]. Nature Biotechnology, 2014, 32(9):903-914 |
| Kikuchi M, Nishimura T, Ishishita S, et al. foxl3, a sexual switch in germ cells, initiates two independent molecular pathways for commitment to oogenesis in medaka[J]. Proceedings of the National Academy of Sciences of the United States of America, 2020, 117(22):12174-12181 |
| Kurokawa H, Saito D, Nakamura S, et al. Germ cells are essential for sexual dimorphism in the medaka gonad[J]. Proceedings of the National Academy of Sciences of the United States of America, 2007, 104(43):16958-16963 |
| Yokoi H, Yan Y L, Miller M R, et al. Expression profiling of zebrafish sox9 mutants reveals that Sox9 is required for retinal differentiation[J]. Developmental Biology, 2009, 329(1):1-15 |
| Nakamura S, Watakabe I, Nishimura T, et al. Analysis of medaka sox9 orthologue reveals a conserved role in germ cell maintenance[J]. PLoS One, 2012, 7(1):e29982 |
| Ren F, Miao R, Xiao R, et al. m6A reader Igf2bp3 enables germ plasm assembly by m6A-dependent regulation of gene expression in zebrafish[J]. Science Bulletin, 2021, 66(11):1119-1128 |
| Webster K A, Schach U, Ordaz A, et al. Dmrt1 is necessary for male sexual development in zebrafish[J]. Developmental Biology, 2017, 422(1):33-46 |
| Liu X J, Wang H, Gong Z Y. Tandem-repeated zebrafish zp3 genes possess oocyte-specific promoters and are insensitive to estrogen induction[J]. Biology of Reproduction, 2006, 74(6):1016-1025 |
| Mold D E, Dinitz A E, Sambandan D R. Regulation of zebrafish zona pellucida gene activity in developing oocytes[J]. Biology of Reproduction, 2009, 81(1):101-110 |
| Chu L H, Li J Z, Liu Y, et al. Gonadotropin signaling in zebrafish ovary and testis development:Insights from gene knockout study[J]. Molecular Endocrinology, 2015, 29(12):1743-1758 |
| Wu K, Song W Y, Zhang Z W, et al. Disruption of dmrt1 rescues the all-male phenotype of the cyp19a1a mutant in zebrafish-a novel insight into the roles of aromatase/estrogens in gonadal differentiation and early folliculogenesis[J]. Development, 2020, 147(4):dev182758 |
| Lin S W, Ge W. Differential regulation of gonadotropins (FSH and LH) and growth hormone (GH) by neuroendocrine, endocrine, and paracrine factors in the zebrafish-An in vitro approach[J]. General and Comparative Endocrinology, 2009, 160(2):183-193 |
| Miller W L, Auchus R J. The molecular biology, biochemistry, and physiology of human steroidogenesis and its disorders[J]. Endocrine Reviews, 2011, 32(1):81-151 |
| Zhai G, Shu T T, Xia Y G, et al. Androgen signaling regulates the transcription of anti-Müllerian hormone via synergy with SRY-related protein SOX9A[J]. Science Bulletin, 2017, 62(3):197-203 |
| Shu T T, Zhai G, Pradhan A, et al. Zebrafish cyp17a1 knockout reveals that androgen-mediated signaling is important for male brain sex differentiation[J]. General and Comparative Endocrinology, 2020, 295:113490 |
| Mindnich R, Deluca D, Adamski J. Identification and characterization of 17 beta-hydroxysteroid dehydrogenases in the zebrafish, Danio rerio[J]. Molecular and Cellular Endocrinology, 2004, 215(1-2):19-30 |
| Tokarz J, Möller G, de Angelis M H, et al. Zebrafish and steroids:What do we know and what do we need to know?[J]. The Journal of Steroid Biochemistry and Molecular Biology, 2013, 137:165-173 |
| Trant J M, Gavasso S, Ackers J, et al. Developmental expression of cytochrome P450 aromatase genes (CYP19a and CYP19b) in zebrafish fry (Danio rerio)[J]. The Journal of Experimental Zoology, 2001, 290(5):475-483 |
| Chiang E F, Yan Y L, Tong S K, et al. Characterization of duplicated zebrafish cyp19 genes[J]. The Journal of Experimental Zoology, 2001, 290(7):709-714 |
| Tang H P, Chen Y, Liu Y, et al. New insights into the role of estrogens in male fertility based on findings in aromatase-deficient zebrafish[J]. Endocrinology, 2017, 158(9):3042-3054 |
| Hossain M S, Larsson A, Scherbak N, et al. Zebrafish androgen receptor:Isolation, molecular, and biochemical characterization[J]. Biology of Reproduction, 2008, 78(2):361-369 |
| Crowder C M, Lassiter C S, Gorelick D A. Nuclear androgen receptor regulates testes organization and oocyte maturation in zebrafish[J]. Endocrinology, 2018, 159(2):980-993 |
| Chen Y, Tang H P, Wang L, et al. Fertility enhancement but premature ovarian failure in esr1-deficient female zebrafish[J]. Frontiers in Endocrinology, 2018, 9:567 |
| Hou L P, Shu H, Lin L L, et al. Modulation of transcription of genes related to the hypothalamic-pituitary-gonadal and the hypothalamic-pituitary-adrenal axes in zebrafish (Danio rerio) embryos/larvae by androstenedione[J]. Ecotoxicology and Environmental Safety, 2018, 156:403-408 |
| Brion F, Tyler C R, Palazzi X, et al. Impacts of 17beta-estradiol, including environmentally relevant concentrations, on reproduction after exposure during embryo-larval-, juvenile- and adult-life stages in zebrafish (Danio rerio)[J]. Aquatic Toxicology, 2004, 68(3):193-217 |
| Huang C B, Li X D. Maternal cypermethrin exposure during the perinatal period impairs testicular development in C57BL male offspring[J]. PLoS One, 2014, 9(5):e96781 |