Halpern, B. S. et al. A global map of human impact on marine ecosystems. Science 319, 948–952, https://doi.org/10.1126/science.1149345 (2008).
Jambeck, J. R. et al. Plastic waste inputs from land into the ocean. Science 347, 768–771, https://doi.org/10.1126/science.1260352 (2015).
Lu, Y. et al. Major threats of pollution and climate change to global coastal ecosystems and enhanced management for sustainability. Environ. Pollut. 239, 670–680, https://doi.org/10.1016/j.envpol.2018.04.016 (2018).
Nguyen, X. V., Tran, M. H., Le, T. D. & Papenbrock, J. An assessment of heavy metal contamination on the surface sediment of seagrass beds at the Khanh Hoa Coast, Vietnam. B. Environ. Contam. Tox. 99, 728–734, https://doi.org/10.1007/s00128-017-2191-6 (2017).
Le, X. S. & Nguyen, V. B. Assessment of heavy metal concentration (copper, lead and zinc) in the seawater environment in typical coastal island communes. Vietnam Environment Administration Magazine – Ministry of Natural Resources and Environment, Vietnam III, 49–55 (2018).
Dinh, K. V. Vietnam’s fish kill remains unexamined. Science 365, 333–333, https://doi.org/10.1126/science.aay6007 (2019).
Colin, S. P. & Dam, H. G. Testing for resistance of pelagic marine copepods to a toxic dinoflagellate. Evol. Ecol. 18, 355–377, https://doi.org/10.1007/s10682-004-2369-3 (2005).
Klerks, P. L. & Weis, J. S. Genetic adaptation to heavy metals in aquatic organisms: A review. Environ. Pollut. 45, 173–205, https://doi.org/10.1016/0269-7491(87)90057-1 (1987).
Dam, H. G. Evolutionary adaptation of marine zooplankton to global change. Annu. Rev. Mar. Sci. 5, 349–370, https://doi.org/10.1146/annurev-marine-121211-172229 (2013).
Krause, K. E., Dinh, K. V. & Nielsen, T. G. Increased tolerance to oil exposure by the cosmopolitan marine copepod Acartia tonsa. Sci. Total Environ. 607–608, 87–94, https://doi.org/10.1016/j.scitotenv.2017.06.139 (2017).
Wang, M. H., Zhang, C. & Lee, J. S. Quantitative shotgun proteomics associates molecular-level cadmium toxicity responses with compromised growth and reproduction in a marine copepod under multigenerational exposure. Environ. Sci. Technol. 52, 1612–1623, https://doi.org/10.1021/acs.est.8b00149 (2018).
Tran, T. T., Janssens, L., Dinh, K. V. & Stoks, R. Transgenerational interactions between pesticide exposure and warming in a vector mosquito. Evol. Appl. 11, 906–917, https://doi.org/10.1111/eva.12605 (2018).
Dao, T. -S., Vo, T. -M.-C., Wiegand, C., Bui, B. -T. & Dinh, K. V. Transgenerational effects of cyanobacterial toxins on a tropical micro-crustacean Daphnia lumholtzi across three generations. Environ. Pollut. 243, 791–799, https://doi.org/10.1016/j.envpol.2018.09.055 (2018).
Donelson, J. M., Munday, P. L., McCormick, M. I. & Pitcher, C. R. Rapid transgenerational acclimation of a tropical reef fish to climate change. Nat. Clim. Chang. 2, 30–32 (2012).
Doan, X. N. et al. Extreme temperature impairs growth and productivity in a common tropical marine copepod. Sci. Rep. 9, 4550, https://doi.org/10.1038/s41598-019-40996-7 (2019).
Kelly, M. W., Pankey, M. S., DeBiasse, M. B. & Plachetzki, D. C. Adaptation to heat stress reduces phenotypic and transcriptional plasticity in a marine copepod. Funct. Ecol. 31, 398–406, https://doi.org/10.1111/1365-2435.12725 (2017).
Moe, S. J. et al. Combined and interactive effects of global climate change and toxicants on populations and communities. Environ. Toxicol. Chem. 32, 49–61, https://doi.org/10.1002/etc.2045 (2013).
Dinh Van, K. et al. Susceptibility to a metal under global warming is shaped by thermal adaptation along a latitudinal gradient. Glob. Change Biol. 19, 2625–2633, https://doi.org/10.1111/gcb.12243 (2013).
Stoks, R., Debecker, S., Dinh, K. V. & Janssens, L. Integrating ecology and evolution in aquatic toxicology: insights from damselflies. Freshw. Sci. 34, 1032–1039, https://doi.org/10.1086/682571 (2015).
Janssens, L., Dinh, K. V., Debecker, S., Bervoets, L. & Stoks, R. Local adaptation and the potential effects of a contaminant on predator avoidance and antipredator responses under global warming: a space-for-time substitution approach. Evol. Appl. 7, 421–430, https://doi.org/10.1111/eva.12141 (2014).
Vera-Chang, M. N. et al. Transgenerational hypocortisolism and behavioral disruption are induced by the antidepressant fluoxetine in male zebrafish Danio rerio. Proc. Natl. Acad. Sci. USA 115, E12435–E12442, https://doi.org/10.1073/pnas.1811695115 (2018).
Dinh Van, K., Janssens, L., Debecker, S. & Stoks, R. Temperature- and latitude-specific individual growth rates shape the vulnerability of damselfly larvae to a widespread pesticide. J. Appl. Ecol. 51, 919–928 (2014).
Noyes, P. D. & Lema, S. C. Forecasting the impacts of chemical pollution and climate change interactions on the health of wildlife. Curr. Zool. 61, 669–689, https://doi.org/10.1093/czoolo/61.4.669 (2015).
Grønning, J. B., Doan, N. X., Dinh, T. N., Dinh, K. V. & Nielsen, T. G. Ecology of Pseudodiaptomus annandalei in tropical aquaculture ponds with emphasis on the limitation of production. J. Plankton Res. 41, 741–758 (2019).
Doan, N. X. et al. Temperature- and sex-specific grazing rate of a tropical copepod Pseudodiaptomus annandalei to food availability: implications for live feed in aquaculture. Aquacult. Res. 49, 3864–3873, https://doi.org/10.1111/are.13854 (2018).
Chew, L. L., Chong, V. C., Tanaka, K. & Sasekumar, A. Phytoplankton fuel the energy flow from zooplankton to small nekton in turbid mangrove waters. Mar. Ecol. Prog. Ser. 469, 7–24, https://doi.org/10.3354/meps09997 (2012).
Prato, E., Parlapiano, I. & Biandolino, F. Sublethal effects of copper on some biological traits of the amphipod Gammarus aequicauda reared under laboratory conditions. Chemosphere 93, 1015–1022, https://doi.org/10.1016/j.chemosphere.2013.05.071 (2013).
Schwarz, J. A., Mitchelmore, C. L., Jones, R., O’Dea, A. & Seymour, S. Exposure to copper induces oxidative and stress responses and DNA damage in the coral Montastraea franksi. Comp. Biochem. Phys. C Toxicol. & Pharmacol. 157, 272–279, https://doi.org/10.1016/j.cbpc.2012.12.003 (2013).
Holan, J. R., King, C. K., Sfiligoj, B. J. & Davis, A. R. Toxicity of copper to three common subantarctic marine gastropods. Ecotox. and Environ. Safe. 136, 70–77, https://doi.org/10.1016/j.ecoenv.2016.10.025 (2017).
Caldwell, G. S., Lewis, C., Pickavance, G., Taylor, R. L. & Bentley, M. G. Exposure to copper and a cytotoxic polyunsaturated aldehyde induces reproductive failure in the marine polychaete Nereis virens (Sars). Aquat. Toxicol. 104, 126–134, https://doi.org/10.1016/j.aquatox.2011.03.018 (2011).
Biandolino, F., Parlapiano, I., Faraponova, O. & Prato, E. Effects of short- and long-term exposures to copper on lethal and reproductive endpoints of the harpacticoid copepod Tigriopus fulvus. Ecotox. and Environ. Safe. 147, 327–333, https://doi.org/10.1016/j.ecoenv.2017.08.041 (2018).
Kwok, K. W. H. & Leung, K. M. Y. Toxicity of antifouling biocides to the intertidal harpacticoid copepod Tigriopus japonicus (Crustacea, Copepoda): Effects of temperature and salinity. Mar. Pollut. Bull. 51, 830–837, https://doi.org/10.1016/j.marpolbul.2005.02.036 (2005).
Dinh, K. V., Olsen, M. W., Altin, D., Vismann, B. & Nielsen, T. G. Impact of temperature and pyrene exposure on the functional response of males and females of the copepod Calanus finmarchicus. Environ. Sci. Pollut. Res. 26, 29327–29333, https://doi.org/10.1007/s11356-019-06078-x (2019).
Amiard, J. C., Amiard-Triquet, C., Barka, S. & Pellerin, J. & Rainbow, P. S. Metallothioneins in aquatic invertebrates: Their role in metal detoxification and their use as biomarkers. Aquat. Toxicol. 76, 160–202, https://doi.org/10.1016/j.aquatox.2005.08.015 (2006).
Ki, J. S. et al. Gene expression profiling of copper-induced responses in the intertidal copepod Tigriopus japonicus using a 6K oligochip microarray. Aquat. Toxicol. 93, 177–187, https://doi.org/10.1016/j.aquatox.2009.04.004 (2009).
Kim, B.-M. et al. Heavy metals induce oxidative stress and trigger oxidative stress-mediated heat shock protein (hsp) modulation in the intertidal copepod Tigriopus japonicus. Comp. Biochem. Phys. C Toxicol. & Pharmacol. 166, 65–74, https://doi.org/10.1016/j.cbpc.2014.07.005 (2014).
Xu, K. et al. Effects of low concentrations copper on antioxidant responses, DNA damage and genotoxicity in thick shell mussel Mytilus coruscus. Fish Shellfish Immun. 82, 77–83, https://doi.org/10.1016/j.fsi.2018.08.016 (2018).
Dipinto, L. M., Coull, B. C. & Chandler, G. T. Lethal and sublethal effects of the sediment-associated PCB aroclor 1254 on a meiobenthic copepod. Environ. Toxicol. Chem. 12, 1909–1918, https://doi.org/10.1002/etc.5620121017 (1993).
Medina, M., Barata, C., Telfer, R. & Baird, D. J. Age- and sex-related variation in sensitivity to the pyrethroid cypermethrin in the marine copepod Acartia tonsa Dana. Arch. Environ. Con. Tox. 42, 17–22 (2002).
Kadiene, E. U., Bialais, C., Ouddane, B., Hwang, J. S. & Souissi, S. Differences in lethal response between male and female calanoid copepods and life cycle traits to cadmium toxicity. Ecotoxicology 26, 1227–1239, https://doi.org/10.1007/s10646-017-1848-6 (2017).
McManus, G. B., Wyman, K. D., Peterson, W. T. & Wurster, C. F. Factors affecting the elimination of PCBs in the marine copepod Acartia tonsa. Estuar. Coast. Shelf Sci. 17, 421–430, https://doi.org/10.1016/0272-7714(83)90127-0 (1983).
Toxværd, K., Dinh, K. V., Henriksen, O., Hjorth, M. & Nielsen, T. Impact of pyrene exposure during overwintering of the Arctic copepod Calanus glacialis. Environ. Sci. Technol. 52, 10328–10336, https://doi.org/10.1021/acs.est.8b03327 (2018).
Koski, M., Stedmon, C. & Trapp, S. Ecological effects of scrubber water discharge on coastal plankton: Potential synergistic effects of contaminants reduce survival and feeding of the copepod Acartia tonsa. Mar. Environ. Res. 129, 374–385, https://doi.org/10.1016/j.marenvres.2017.06.006 (2017).
Hansen, B. H. et al. Maternal polycyclic aromatic hydrocarbon (PAH) transfer and effects on offspring of copepods exposed to dispersed oil with and without oil droplets. J. Toxicol. Environ. Health A Curr. Issues 80, 881–894, https://doi.org/10.1080/15287394.2017.1352190 (2017).
Byrne, M., Foo, S. A., Ross, P. M. & Putnam, H. M. Limitations of cross- and multigenerational plasticity for marine invertebrates faced with global climate change. Glob. Change Biol. 26, 80–102, https://doi.org/10.1111/gcb.14882 (2020).
Brander, S. M., Biales, A. D. & Connon, R. E. The role of epigenomics in aquatic toxicology. Environ. Toxicol. Chem. 36, 2565–2573, https://doi.org/10.1002/etc.3930 (2017).
Ivanina, A. V. & Sokolova, I. M. Interactive effects of metal pollution and ocean acidification on physiology of marine organisms. Curr. Zool. 61, 653–668, https://doi.org/10.1093/czoolo/61.4.653 (2015).
Blewett, T. A., Simon, R. A., Turko, A. J. & Wright, P. A. Copper alters hypoxia sensitivity and the behavioural emersion response in the amphibious fish Kryptolebias marmoratus. Aquat. Toxicol. 189, 25–30, https://doi.org/10.1016/j.aquatox.2017.05.007 (2017).
Fitzgerald, J. A. et al. Sublethal exposure to copper supresses the ability to acclimate to hypoxia in a model fish species. Aquat. Toxicol. 217, https://doi.org/10.1016/j.aquatox.2019.105325 (2019).
Froehlich, H. E., Gentry, R. R. & Halpern, B. S. Global change in marine aquaculture production potential under climate change. Nat. Ecol. Evol. 2, 1745–1750, https://doi.org/10.1038/s41559-018-0669-1 (2018).
Sommer, U., Peter, K. H., Genitsaris, S. & Moustaka-Gouni, M. Do marine phytoplankton follow Bergmann’s rule sensu lato? Biol. Rev. 92, 1011–1026, https://doi.org/10.1111/brv.12266 (2017).
Daufresne, M., Lengfellner, K. & Sommer, U. Global warming benefits the small in aquatic ecosystems. Proc. Natl. Acad. Sci. USA 106, 12788–12793, https://doi.org/10.1073/pnas.0902080106 (2009).
Horne, C. R., Hirst, A. G., Atkinson, D., Neves, A. & Kiorboe, T. A global synthesis of seasonal temperature-size responses in copepods. Global Ecol. Biogeogr. 25, 988–999, https://doi.org/10.1111/geb.12460 (2016).
Pan, Y. J. et al. Effects of cold selective breeding on the body length, fatty acid content, and productivity of the tropical copepod Apocyclops royi (Cyclopoida, Copepoda). J. Plankton Res. 39, 994–1003, https://doi.org/10.1093/plankt/fbx041 (2017).
Gibbin, E. M. et al. Can multi-generational exposure to ocean warming and acidification lead to the adaptation of life history and physiology in a marine metazoan? J. Exp. Biol. 220, 551–563, https://doi.org/10.1242/jeb.149989 (2017).
Cheung, W. W. L. et al. Shrinking of fishes exacerbates impacts of global ocean changes on marine ecosystems. Nat. Clim. Chang. 3, 254–258, https://doi.org/10.1038/nclimate1691 (2013).
Kiørboe, T. & Sabatini, M. Scaling of fecundity, growth and development in marine planktonic copepods. Mar. Ecol. Prog. Ser. 120, 285–298, https://doi.org/10.3354/meps120285 (1995).
Merilä, J. & Hendry, A. P. Climate change, adaptation, and phenotypic plasticity: the problem and the evidence. Evol. Appl. 7, 1–14, https://doi.org/10.1111/eva.12137 (2014).
Donelson, J. M., Salinas, S., Munday, P. L. & Shama, L. N. S. Transgenerational plasticity and climate change experiments: Where do we go from here? Glob. Change Biol. 24, 13–34, https://doi.org/10.1111/gcb.13903 (2018).
Calosi, P. et al. Adaptation and acclimatization to ocean acidification in marine ectotherms: an in situ transplant experiment with polychaetes at a shallow CO2 vent system. Philos. T. R. Soc. B 368, https://doi.org/10.1098/rstb.2012.0444 (2013).
Lee, Y. H., Jeong, C. B., Wang, M. H., Hagiwara, A. & Lee, J. S. Transgenerational acclimation to changes in ocean acidification in marine invertebrates. Mar. Pollut. Bull. 153, https://doi.org/10.1016/j.marpolbul.2020.111006 (2020).
Yao, Y., Wang, J., Yin, J. & Zou, X. Marine heatwaves in China’s marginal seas and adjacent offshore waters: past, present, and future. J. Geophys. Res. Oceans 125, e2019JC015801 (2020).
Smale, D. A. et al. Marine heatwaves threaten global biodiversity and the provision of ecosystem services. Nat. Clim. Chang. 9, 306–312, https://doi.org/10.1038/s41558-019-0412-1 (2019).
Crain, C. M., Kroeker, K. & Halpern, B. S. Interactive and cumulative effects of multiple human stressors in marine systems. Ecol. Lett. 11, 1304–1315, https://doi.org/10.1111/j.1461-0248.2008.01253.x (2008).
Vietnamese Ministry of Natural Resources and Environment. (ed Ministry of Natural Resources and Environment) 10 (Hanoi, 2015).
Cai, M. G. et al. Lost but can’t be neglected: Huge quantities of small microplastics hide in the South China Sea. Sci. Total Environ. 633, 1206–1216, https://doi.org/10.1016/j.scitotenv.2018.03.197 (2018).
Landis, W. G. et al. Global climate change and contaminants, a call to arms not yet heard? Integr. Environ. Assess. 10, 483–484, https://doi.org/10.1002/ieam.1568 (2014).
Barlow, J. et al. The future of hyperdiverse tropical ecosystems. Nature 559, 517–526, https://doi.org/10.1038/s41586-018-0301-1 (2018).
Worm, B. et al. Impacts of biodiversity loss on ocean ecosystem services. Science 314, 787–790, https://doi.org/10.1126/science.1132294 (2006).
Hwang, J. S. et al. Patterns of zooplankton distribution along the marine, estuarine, and riverine portions of the Danshuei ecosystem in northern Taiwan. Zool. Stud. 49, 335–352 (2010).
Dhanker, R., Kumar, R. & Hwang, J. S. Predation by Pseudodiaptomus annandalei (Copepoda: Calanoida) on rotifer prey: Size selection, egg predation and effect of algal diet. J. Exp. Mar. Biol. Ecol. 414, 44–53, https://doi.org/10.1016/j.jembe.2012.01.011 (2012).
Golez, M. S. N., Takahashi, T., Ishimaru, T. & Ohno, A. Post-embryonic development and reproduction of Pseudodiaptomus annandalei (Copepoda: Calanoida). Plankt. Biol. Ecol. 51, 15–25 (2004).
Colin, S. P. & Dam, H. G. Latitudinal differentiation in the effects of the toxic dinoflagellate Alexandrium spp. on the feeding and reproduction of populations of the copepod Acartia hudsonica. Harmful Algae 1, 113–125, https://doi.org/10.1016/S1568-9883(02)00007-0 (2002).
Guillard, R. R. & Ryther, J. H. Studies of marine planktonic diatoms: I. Cyclotella nana Hustedt, and Detonula confervacea (Cleve) Gran. Can. J. Microbiol. 8, 229–&, https://doi.org/10.1139/m62-029 (1962).
IPCC. Climate change 2013: The physical science basis: Contribution of Working Group I to the Fourth Assessment Report of the Intergovernmental Panel on Climate Change. (Cambridge University Press, 2013).
Quinn, G. P. & Michael, K. J. Experimental design and data analysis for biologists. 537 (Cambridge University Press, 2002).
Warton, D. I. & Hui, F. K. C. The arcsine is asinine: the analysis of proportions in ecology. Ecology 92, 3–10, https://doi.org/10.1890/10-0340.1 (2011).
Dinh, K. V. et al. Delayed effects of chlorpyrifos across metamorphosis on dispersal-related traits in a poleward moving damselfly. Environ. Pollut. 218, 634–643, https://doi.org/10.1016/j.envpol.2016.07.047 (2016).
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