Windenergie op zee: een groene toekomst met een grijs randje?

Jens
Broeckx

© Foto: Hans Hillewaert / CC BY-SA 4.0

Eerder dit jaar kondigden negen Europese landen, waaronder België, trots een mega-investering van 1.000 miljard euro in windenergie op de Noordzee aan. Het doel is om tegen 2050 acht keer zoveel windenergie op te wekken als nu.

Het project wordt geprezen als politiek, economisch en ecologisch voordelig. Meer onafhankelijkheid van landen als Rusland, Saoedi-Arabië en de Verenigde Staten is een belangrijke aanleiding, net als de beloofde 91.000 extra jobs in de windenergiesector. Bovendien ligt de CO2-uitstoot veel lager dan die van fossiele energie. Eén factor blijft onderbelicht: de impact op lokale ecosystemen.

Meer windenergie op zee betekent meer infrastructuur in een ruwe omgeving. Zout zeewater veroorzaakt corrosie, die de levensduur van windturbines sterk verkort. Daar bestaat een oplossing voor: opofferingsanodes. Die lossen langzaam op, zodat de turbine zelf gespaard blijft. Bij dat proces komen verschillende metalen vrij in het mariene milieu. Van sommige, zoals zink en aluminium, is de impact redelijk goed in te schatten, want zij zijn al uitgebreid onderzocht. Over andere metalen was tot voor kort nauwelijks iets bekend.

Dat geldt voor indium en gallium. Deze metalen worden steeds belangrijker voor moderne technologieën en komen ook voor in de anodes, maar over hun effecten op het mariene milieu en de organismen die daar leven was bijna niets geweten. De masterthesis van Jens Broeckx (onderzoeksgroep ECOSPHERE, Universiteit Antwerpen) brengt daar verandering in. Twee diersoorten werden blootgesteld aan verschillende concentraties van beide metalen: het wadkreeftje, een kleine kreeftachtige die in de zeebodem leeft, en de zebravis, een veelgebruikt modelorganisme dat in de waterkolom voorkomt. Zo konden effecten in zowel de bodem als het water onder de loep worden genomen.

Geruststellend, of toch niet?© Foto: Jens Broeckx

Op het eerste gezicht zijn de resultaten geruststellend. Zowel de wadkreeftjes als de zebravissen stierven niet, en ontwikkelingsstoornissen gelinkt aan de metalen werden niet vastgesteld. Dit gold zelfs voor concentraties die vele malen hoger liggen dan wat men vandaag in de Noordzee meet.

Toch zijn de metalen niet helemaal onschuldig. Naarmate de concentraties stegen, stapelden ze zich op in de dieren. De chronische effecten hiervan worden pas na langere tijd zichtbaar. Metalen die zich ophopen in organismen worden bovendien via de voedselketen doorgegeven aan andere dieren, en kunnen uiteindelijk op ons bord belanden.

Geen sterfte betekent dus niet dat de metalen geen effect hebben. Zo bond indium zich bijna volledig aan het sediment waarin de wadkreeftjes leefden. In het water was er nauwelijks indium te detecteren, maar de dieren namen het wel op via het sediment.

Dat resultaat legt een belangrijke blinde vlek in de milieumonitoring bloot. Vaak worden enkel de metaalconcentraties in de waterkolom gemeten, waardoor ten onrechte kan worden besloten dat er niets aan de hand is. Ondertussen nemen de concentraties in het sediment en in de dieren gestaag toe. Wat dat op langere termijn betekent, is nog niet onderzocht.

Niet elk metaal gedraagt zich hetzelfde

Opvallend is ook het grote verschil tussen indium en gallium. Indium was bijna afwezig in de waterkolom, gallium daarentegen kwam er volop voor. Die chemische verschillen bepaalden wat de dieren opnamen: de zebravissen namen amper indium op, simpelweg omdat het in hun leefomgeving nauwelijks voorkwam, maar wel veel gallium, aangezien dat voor hen beschikbaar was.

Bij de zebravissen werd een onverwacht verband gevonden: hoe meer indium in de omgeving, hoe minder gallium ze opnamen. Dat wijst wellicht op concurrentie via een nog onbekend mechanisme, mogelijk gelinkt aan het transport van ijzer in het lichaam. Een precieze verklaring vraagt verder onderzoek.

Een extra hindernis voor de energietransitie

De resultaten van deze studie betekenen echter niet dat windenergie op zee plots een kritieke bedreiging vormt voor het mariene milieu. De geteste concentraties veroorzaakten geen acute effecten bij de wadkreeftjes en zebravissen. Wat de studie wel aantoont, is hoe weinig we weten over metalen die vrijkomen door energie-infrastructuur op zee. De effecten zijn vandaag misschien beperkt, maar door de aangekondigde investering wordt onderzoek hiernaar dringender.

Hoe zorgen we ervoor dat de energietransitie niet alleen klimaatvriendelijk is, maar ook ecologisch verantwoord?

Broeckx pleit voor meer aandacht voor sediment in de milieumonitoring rond windmolenparken. Dieren die op of in de zeebodem leven, kunnen aan metalen worden blootgesteld zonder dat waterstalen dit aangeven.

Deze studie is pas het begin. Langere blootstellingsperiodes, meer organismen, andere metalen en preciezere metingen zijn nodig om uit te maken hoe schadelijk de opgehoopte metalen op termijn zijn.

Achter dit onderzoek schuilt een bredere vraag: hoe zorgen we ervoor dat de energietransitie niet alleen klimaatvriendelijk is, maar ook ecologisch verantwoord? De Europese leiders die de deal ondertekenden, moeten die vraag meenemen in de uitwerking van hun plan voor de toekomst van de Noordzee.

Bibliografie

  1. Ahmadi, H., Granger, D. A., Hamilton, K. R., Blair, C., & Riis, J. L. (2021). Censored data considerations and analytical approaches for salivary bioscience data. Psychoneuroendocrinology, 129, 105274. https://doi.org/10.1016/j.psyneuen.2021.105274
  2. Barnes, R. S. K. (1994). The Brackish-Water Fauna of Northwestern Europe. Cambridge University Press, pp. 176-177. https://doi.org/10.1002/aqc.3270050208
  3. Bat, L., & Raffaelli, D. (1998). Sediment toxicity testing: a bioassay approach using the amphipod Corophium volutator and the polychaete Arenicola marina. Journal of Experimental Marine Biology and Ecology, 226(2), 217–239. https://doi.org/10.1016/s0022-0981(97)00249-9
  4. Batley, G. E., & Campbell, P. G. C. (2022). Metal contaminants of emerging concern in aquatic systems. Environmental Chemistry, 19(1), 23–40. https://doi.org/10.1071/en22030
  5. Bell, A. M., Von Der Au, M., Regnery, J., Schmid, M., Meermann, B., Reifferscheid, G., Ternes, T., & Buchinger, S. (2020). Does galvanic cathodic protection by aluminum anodes impact marine organisms? Environmental Sciences Europe, 32(1). https://doi.org/10.1186/s12302-020-00441-3
  6. Bergman, J., Svenningsson, A., Liv, P., Bergenheim, T., & Burman, J. (2020). Location matters: highly divergent protein levels in samples from different CNS compartments in a clinical trial of rituximab for progressive MS. Fluids and Barriers of the CNS, 17(1), 49. https://doi.org/10.1186/s12987-020-00205-4
  7. Betoulle, S., Etienne, J., & Vernet, G. (2002). In vivo and in vitro modulation of carp (Cyprinus carpio L.) phagocyte oxidative burst activity by gallium. Journal of Toxicology and Environmental Health, 65(8), 603–615. https://doi.org/10.1080/152873902317349754
  8. Bobba, S., Carrara, S., Huisman, J., Mathieux, F., & Pavel, C. (2020). Critical Raw Materials for Strategic Technologies and Sectors in the EU: A Foresight Study. European Commission. https://doi.org/10.2873/58081
  9. Bower, C.E., & Holm-Hansen, T. (1980). A Salicylate–Hypochlorite method for determining ammonia in seawater. Canadian Journal of Fisheries and Aquatic Sciences, 37(5), 794–798. https://doi.org/10.1139/f80-106
  10. Brun, N. R., Christen, V., Furrer, G., & Fent, K. (2014). Indium and Indium Tin Oxide Induce Endoplasmic Reticulum Stress and Oxidative Stress in Zebrafish (Danio rerio). Environmental Science & Technology, 48(19), 11679–11687. https://doi.org/10.1021/es5034876
  11. Bryant, V., Newbery, D., McLusky, D., & Campbell, R. (1985). Effect of temperature and salinity on the toxicity of nickel and zinc to two estuarine invertebrates (Corophium volutator, Macoma balthica). Marine Ecology Progress Series, 24, 139–153. https://doi.org/10.3354/meps024139
  12. Butcher, T, & Brown, T. (2014). Gallium. In Critical Metals Handbook, Gunn, G. (Ed.). John Wiley & Sons. https://doi.org/10.1002/9781118755341.ch7
  13. Calabrese, E. J., & Baldwin, L. A. (2003). Hormesis: The Dose-Response Revolution. The Annual Review of Pharmacology and Toxicology, 43(1), 175–197. https://doi.org/10.1146/annurev.pharmtox.43.100901.140223
  14. Ciarelli, S., Vonck, W. A., & Van Straalen, N. M. (1997). Reproducibility of spiked-sediment bioassays using the marine benthic amphipod, Corophium volutator. Marine Environmental Research, 43(4), 329–343. https://doi.org/10.1016/s0141-1136(96)00095-5
  15. Chitambar, C. R. (2010). Medical applications and toxicities of gallium compounds. International Journal of Environmental Research and Public Health, 7(5), 2337–2361. https://doi.org/10.3390/ijerph7052337
  16. Chitambar, C. R. (2016). Gallium and its competing roles with iron in biological systems. Biochimica Et Biophysica Acta (BBA) - Molecular Cell Research, 1863(8), 2044–2053. https://doi.org/10.1016/j.bbamcr.2016.04.027
  17. Conradi, M., & Depledge, M. (1999). Effects of zinc on the life-cycle, growth and reproduction of the marine amphipod Corophium volutator. Marine Ecology Progress Series, 176, 131–138. https://doi.org/10.3354/meps176131
  18. Correia, A. D., Costa, F. O., Neuparth, T., Diniz, M. E., & Costa, M. H. (2001). Sub-lethal effects of copper spiked sediments on the marine amphipod Gammarus locusta: evidence of hormesis. Ecotoxicology and Environmental Restoration, 4(2), 32-38. https://www.researchgate.net/publication/236620372_Sub-lethal_Effects_of_Copper-Spiked_Sediments_on_the_Marine_Amphipod_Gammarus_locusta_Evidence_of_Hormesis
  19. De Backer, A., Van Ael, E., Vincx, M., & Degraer, S. (2009). Behaviour and time allocation of the mud shrimp, Corophium volutator, during the tidal cycle: a laboratory study. Helgoland Marine Research, 64(1), 63–67. https://doi.org/10.1007/s10152-009-0167-6
  20. De Borger, E., Tiano, J., Braeckman, U., Ysebaert, T., & Soetaert, K. (2020). Biological and biogeochemical methods for estimating bioirrigation: a case study in the Oosterschelde estuary. Biogeosciences, 17(6), 1701–1715. https://doi.org/10.5194/bg-17-1701-2020
  21. Degraer, S., Brabant, R., Rumes, B., & Vigin, L. (2022). Environmental Impacts of Offshore Wind Farms in the Belgian Part of the North Sea: Getting ready for offshore wind farm expansion in the North Sea. Memoirs on the Marine Environment. Royal Belgian Institute of Natural Sciences. https://odnature.naturalsciences.be/downloads/mumm/windfarms/winmon_report_2022_final.pdf
  22. Ebeling, A., Wippermann, D., Zimmermann, T., Klein, O., Kirchgeorg, T., Weinberg, I., Hasenbein, S., Plaß, A., & Pröfrock, D. (2023). Investigation of potential metal emissions from galvanic anodes in offshore wind farms into North Sea sediments. Marine Pollution Bulletin, 194, 115396. https://doi.org/10.1016/j.marpolbul.2023.115396
  23. Ebeling, A., Wippermann, D., Zimmermann, T., Klein, O., Kirchgeorg, T., Weinberg, I., Plass, A., Hasenbein, S., & Pröfrock, D. (2025). Coupling metal concentrations and drift simulations for tracing emissions from offshore wind farms. Marine Pollution Bulletin, 214, 117810. https://doi.org/10.1016/j.marpolbul.2025.117810
  24. Elizalde-Velázquez, G. A., & Herrera-Vázquez, S. E. (2023). Zebrafish as Model Organism in Aquatic Ecotoxicology: Current trends and future perspectives. In Zebrafish Research - An Ever-Expanding Experimental Model, Disner, G. E. (Ed.). IntechOpen. https://doi.org/10.5772/intechopen.1002731
  25. Eriksson, S. P., & Weeks, J. M. (1994). Effects of copper and hypoxia on two populations of the benthic amphipod Corophium volutator (Pallas). Aquatic Toxicology, 29(1–2), 73–81. https://doi.org/10.1016/0166-445x(94)90049-3
  26. Farrell, E. M., Beermann, J., Neumann, A., & Wrede, A. (2022). The interplay of temperature and algal enrichment intensifies bioturbation of the intertidal amphipod Corophium volutator. Journal of Experimental Marine Biology and Ecology, 559, 151837. https://doi.org/10.1016/j.jembe.2022.151837
  27. Fasmina, M., Jayamanne, S. C., Liyanage, N. P., Perera, J. & De Silva, D. (2021). Determination of the Toxicity Cause by Trace Metals on Zebrafish (Danio rerio) Embryo. Journal of Aquaculture and Fish Health, 10(2), 176. https://doi.org/10.20473/jafh.v10i2.21496
  28. Fish, J. D., & Mills, A. (1979). The reproductive biology of Corophium volutator and C. arenarium (Crustacea: Amphipoda). Journal of the Marine Biological Association of the United Kingdom, 59(2), 355–368. https://doi.org/10.1017/s002531540004265x
  29. Fox, M., Ohlauson, C., Sharpe, A. D., & Brown, R. J. (2014). The use of a Corophium volutator chronic sediment study to support the risk assessment of medetomidine for marine environments. Environmental Toxicology and Chemistry, 33(4), 937–942. https://doi.org/10.1002/etc.2515
  30. Harris, W. R., & Messori, L. (2002). A comparative study of aluminum(III), gallium(III), indium(III), and thallium(III) binding to human serum transferrin. Coordination Chemistry Reviews, 228(2), 237–262. https://doi.org/10.1016/s0010-8545(02)00037-1
  31. Haynes, W. (2013). Holm’s Method. In Encyclopedia of Systems Biology, Dubitzky, W., Wolkenhauer, O., Cho, K. H., & Yokota, H. (Ed.). Springer Nature. https://doi.org/10.1007/978-1-4419-9863-7_1214
  32. Held, A., Kramer, G.N., Lamberty, A., Robouch, P., & Wätjen, U. (2006). The certification of the mass fractions of As, Cd, Co, Cr, Cu, Fe, Hg, Mn, Ni, Sb, Sc, Se, Sn, Th, Tl, U, V and Zn in three sediments: BCR-277R estuarine sediment, BCR-280R lake sediment and BCR-320R channel sediment. European Commission; Joint Research Centre; Institute for Reference Materials and Measurements. https://doi.org/10.2787/16519
  33. Hengstmann, E., Corella, P. Z., Alter, K., Belzunce-Segarra, M. J., Booth, A. M., Castro-Jiménez, J., Czerner, N., De Cauwer, K., Deviller, G., Gomiero, A., Goseberg, N., Hasenbein, S., Kirchgeorg, T., Mason, C., Pape, W., Parmentier, K., Plaß, A., Pröfrock, D., Sarhadi, A., Vanavermaete, D., van der Molen, J., Vinagre, P. A., Wood, D., Weinberg, I., Windt, C., Zonderman, A., Kenyon, J., & De Witte, B. (2025). Chemical emissions from offshore wind farms: From identification to challenges in impact assessment and regulation. Marine Pollution Bulletin, 215, 117915. https://doi.org/10.1016/j.marpolbul.2025.117915
  34. Henn, K., & Braunbeck, T. (2010). Dechorionation as a tool to improve the fish embryo toxicity test (FET) with the zebrafish (Danio rerio). Comparative Biochemistry and Physiology Part C Toxicology & Pharmacology, 153(1), 91–98. https://doi.org/10.1016/j.cbpc.2010.09.003
  35. Hirata, S., Toshimitsu, H., & Aihara, M. (2006). Determination of arsenic species in marine samples by HPLC-ICP-MS. Analytical Sciences, 22(1), 39–43. https://doi.org/10.2116/analsci.22.39
  36. Ikhazuagbe, I. H., Ofoka, E. A., Odofin, O. L., Erumiseli, O., Edoka, O. E., Ezennubia, K. P., Ogbunike, P. M., Annan, E., Okonkwo, S. S., & Dike, J. C. (2025). Antibacterial activity and mechanistic insights of gallium-based nanoparticles: an emerging frontier in metal-based antimicrobials. RSC Advances, 15(38), 31122–31153. https://doi.org/10.1039/d5ra04216j
  37. Jiang, W., Lin, S., Chang, C. H., Ji, Z., Sun, B., Wang, X., Li, R., Pon, N., Xia, T., & Nel, A. E. (2015). Implications of the Differential Toxicological Effects of III–V Ionic and Particulate Materials for Hazard Assessment of Semiconductor Slurries. ACS Nano, 9(12), 12011–12025. https://doi.org/10.1021/acsnano.5b04847
  38. Kaldellis, J., & Apostolou, D. (2017). Life cycle energy and carbon footprint of offshore wind energy. Comparison with onshore counterpart. Renewable Energy, 108, 72–84. https://doi.org/10.1016/j.renene.2017.02.039
  39. Kater, B. J., Hannewijk, A., Postma, J. F., & Dubbeldam, M. (2000). Seasonal changes in acute toxicity of cadmium to amphipod Corophium volutator. Environmental Toxicology and Chemistry, 19(12), 3032–3035. https://doi.org/10.1002/etc.5620191224
  40. Kimmel, C. B., Ballard, W. W., Kimmel, S. R., Ullmann, B., & Schilling, T. F. (1995). Stages of embryonic development of the zebrafish. Developmental Dynamics, 203(3), 253–310. https://doi.org/10.1002/aja.1002030302
  41. Kirchgeorg, T., Weinberg, I., Hörnig, M., Baier, R., Schmid, M., & Brockmeyer, B. (2018). Emissions from corrosion protection systems of offshore wind farms: Evaluation of the potential impact on the marine environment. Marine Pollution Bulletin, 136, 257–268. https://doi.org/10.1016/j.marpolbul.2018.08.058
  42. Klein, O., Zimmermann, T., Ebeling, A., Kruse, M., Kirchgeorg, T., & Pröfrock, D. (2022). Occurrence and Temporal Variation of Technology-Critical Elements in North Sea Sediments—A determination of preliminary reference values. Archives of Environmental Contamination and Toxicology, 82(4), 481–492. https://doi.org/10.1007/s00244-022-00929-4
  43. Kremling, K., Andreae, M.O., Brügmann, L., van den Berg, C.M.G., Prange, A., Schirmacher, M., Koroleff, E., Kremling, K., & Kus, J. (1999). Determination of trace elements. In Methods of Seawater Analysis, Grasshoff, K., Kremling, K., & Ehrhardt, M. (Ed.). Wiley. https://doi.org/10.1002/9783527613984.ch12
  44. Ladenberger, A., Demetriades, A., Reimann, C., Birke, M., Sadeghi, M., Uhlbäck, J., Andersson, M., & Jonsson, E. (2015). GEMAS: Indium in agricultural and grazing land soil of Europe — Its source and geochemical distribution patterns. Journal of Geochemical Exploration, 154, 61–80. https://doi.org/10.1016/j.gexplo.2014.11.020
  45. Le, P. T. T., & Boyd, C. E. (2012). Comparison of phenate and salicylate methods for determination of total ammonia nitrogen in freshwater and saline water. Journal of the World Aquaculture Society, 43(6), 885–889. https://doi.org/10.1111/j.1749-7345.2012.00616.x
  46. Lee, H., Morrison, C., Doriean, N. J., Welsh, D. T., & Bennett, W. W. (2024). Trace metal distribution in seagrass-vegetated sediments of an urbanized estuary in Queensland, Australia. Marine Pollution Bulletin, 208, 116981. https://doi.org/10.1016/j.marpolbul.2024.116981
  47. Lewis, E., & Perkin, R. (1981). The practical salinity scale 1978: conversion of existing data. Deep Sea Research Part A. Oceanographic Research Papers, 28(4), 307–328. https://doi.org/10.1016/0198-0149(81)90002-9
  48. Liang, S. X. T., Wong, L. S., Dhanapal, A. C. T. A., & Djearamane, S. (2020). Toxicity of metals and metallic nanoparticles on nutritional properties of microalgae. Water Air & Soil Pollution, 231(2). https://doi.org/10.1007/s11270-020-4413-5
  49. Lv, P., & Liu, F. (2023). Heme-deficient primitive red blood cells induce HSPC ferroptosis by altering iron homeostasis during zebrafish embryogenesis. Development, 150(20). https://doi.org/10.1242/dev.201690
  50. Majid, S., Smeets, K., Vergauwen, L., Pilehvar, A., Knapen, D., & Blust, R. (2025). Insights into the combined toxicity of copper and cadmium in zebrafish (Danio rerio) embryos and adults. Ecotoxicology and Environmental Safety, 299, 118368. https://doi.org/10.1016/j.ecoenv.2025.118368
  51. Manna, S., & Firdous, S. M. (2025). Unravelling the developmental toxicity of heavy metals using zebrafish as a model: a narrative review. BioMetals, 38(2), 419–463. https://doi.org/10.1007/s10534-025-00671-z
  52. Meadows, P. S., & Reid, A. (1966). The behaviour of Corophium volutator (Crustacea: Amphipoda). Journal of Zoology, 150(4), 387–399. https://doi.org/10.1111/j.1469-7998.1966.tb03013.x
  53. Mejías, O., Poulet, T., Behnoudfar, P., Jackson, L., Freeman, J., Jones, T. R., Howard, D. L., & Parbhakar-Fox, A. (2025). Fate, distribution, and transport dynamics of indium in a polymetallic mine waste environment: An integrated mineralogical characterisation and geochemical modelling study. The Science of the Total Environment, 998, 180268. https://doi.org/10.1016/j.scitotenv.2025.180268
  54. Moeller, T. (1941). Contributions to the Chemistry of Indium. II. The hydrolysis of indium trichloride solutions. Journal of the American Chemical Society, 63(5), 1206–1207. https://doi.org/10.1021/ja01850a013
  55. Nguyen, C. H., Field, J. A., & Sierra-Alvarez, R. (2019). Microbial toxicity of gallium- and indium-based oxide and arsenide nanoparticles. Journal of Environmental Science and Health Part A, 55(2), 168–178. https://doi.org/10.1080/10934529.2019.1676065
  56. Nielsen, M., & Kofoed, L. (1982). Selective Feeding and Epipsammic Browsing by the Deposit-Feeding Amphipod Corophium volutator. Marine Ecology Progress Series, 10, 81–88. https://doi.org/10.3354/meps010081
  57. OECD (2025). Test No. 236: Fish Embryo Acute Toxicity (FET) Test. In OECD guidelines for the testing of chemicals. Section 2: Effects on biotic systems. https://doi.org/10.1787/9789264203709-en
  58. Olivares, C. I., Field, J. A., Simonich, M., Tanguay, R. L., & Sierra-Alvarez, R. (2016). Arsenic (III, V), indium (III), and gallium (III) toxicity to zebrafish embryos using a high-throughput multi-endpoint in vivo developmental and behavioral assay. Chemosphere, 148, 361–368. https://doi.org/10.1016/j.chemosphere.2016.01.050
  59. Peters, C., & Ahlf, W. (2005). Reproduction of the estuarine and marine amphipod Corophium volutator (Pallas) in laboratory for toxicity testing. Chemosphere, 59(4), 525–536. https://doi.org/10.1016/j.chemosphere.2005.01.053
  60. Porteus, C. S., Waples, E., Dempsey, A., Paull, G., & Wilson, R. W. (2024). A survey of water chemistry used in zebrafish facilities and their effects on early zebrafish development. F1000Research, 13, 168. https://doi.org/10.12688/f1000research.134520.2
  61. Posit Team (2026). RStudio: Integrated Development Environment for R. Posit Software. http://www.posit.co
  62. R Core Team (2024). R: A Language and Environment for Statistical Computing. R Foundation for Statistical Computing. https://www.R-project.org
  63. Radowitz, B. (2020). Dipping into lakes: why offshore wind has moved into inland waters. Recharge. https://www.rechargenews.com/wind/dipping-into-lakes-why-offshore-wind-has-moved-into-inland-waters/2-1-907526
  64. Reese, A., Voigt, N., Zimmermann, T., Irrgeher, J., & Pröfrock, D. (2020). Characterization of alloying components in galvanic anodes as potential environmental tracers for heavy metal emissions from offshore wind structures. Chemosphere, 257, 127182. https://doi.org/10.1016/j.chemosphere.2020.127182
  65. Ringering, K., Kouhail, Y., Yecheskel, Y., Dror, I., & Berkowitz, B. (2018). Mobility and retention of indium and gallium in saturated porous media. Journal of Hazardous Materials, 363, 394–400. https://doi.org/10.1016/j.jhazmat.2018.09.079
  66. Rombough, P. (2002). Gills are needed for ionoregulation before they are needed for O2 uptake in developing zebrafish, Danio rerio. Journal of Experimental Biology, 205(12), 1787–1794. https://doi.org/10.1242/jeb.205.12.1787
  67. Rueda-Bayona, J. G., Eras, J. J. C., & Chaparro, T. R. (2022). Impacts generated by the materials used in offshore wind technology on Human Health, Natural Environment and Resources. Energy, 261, 125223. https://doi.org/10.1016/j.energy.2022.125223
  68. Salminen, R., Batista, M. J., Bidovec, M., Demetriades, A., De Vivo, B., De Vos, W., Duris, M., Gilucis, A., Gregorauskiene, V., Halamic, J., Heitzmann, P., Lima, A., Jordan, G., Klaver, G., Klein, P., Lis, J., Locutura, J., Marsina, K., Mazreku, A., O’Connor, P. J., Olsson, S. Å., Ottesen, R.-T., Petersell, V., Plant, J. A., Reeder, S., Salpeteur, I., Sandström, H., Siewers, U., Steenfelt, A. & Tarvainen, T. (2005). Geochemical Atlas of Europe. Part 1: Background Information, Methodology and maps. Geological Survey of Finland. https://edepot.wur.nl/486313
  69. Satymov, R., Bogdanov, D., & Breyer, C. (2025). Techno-economics of offshore wind power in global resolution. Applied Energy, 393, 125980. https://doi.org/10.1016/j.apenergy.2025.125980
  70. Savenko, A. V., & Savenko, V. S. (2010). Gallium (III) speciation in seawater. Geochemistry International, 48(9), 950–952. https://doi.org/10.1134/s0016702910090090
  71. Scarlett, A., Rowland, S., Canty, M., Smith, E., & Galloway, T. (2007). Method for assessing the chronic toxicity of marine and estuarine sediment-associated contaminants using the amphipod Corophium volutator. Marine Environmental Research, 63(5), 457–470. https://doi.org/10.1016/j.marenvres.2006.12.006
  72. Schipper, C. A., Burgess, R. M., & van den Dikkenberg, L. C. (2006). Sediment toxiciteittest met de slijkgarnaal Corophium volutator. Rijksinstituut voor Kust en Zee, 6, 18 pp. https://doi.org/10.13140/RG.2.2.12730.59847
  73. Schiwy, S., Herber, A., Hollert, H., & Brinkmann, M. (2020). New Insights into the Toxicokinetics of 3,4-Dichloroaniline in Early Life Stages of Zebrafish (Danio rerio). Toxics, 8(1), 16. https://doi.org/10.3390/toxics8010016
  74. Scholz, S., Fischer, S., Gündel, U., Küster, E., Luckenbach, T., & Voelker, D. (2008). The zebrafish embryo model in environmental risk assessment—applications beyond acute toxicity testing. Environmental Science and Pollution Research, 15(5), 394–404. https://doi.org/10.1007/s11356-008-0018-z
  75. Schulze, Y., Ghiaci, P., Zhao, L., Biver, M., Warringer, J., Filella, M., & Tamás, M. J. (2023). Chemical-genomic profiling identifies genes that protect yeast from aluminium, gallium, and indium toxicity. Metallomics, 15(6). https://doi.org/10.1093/mtomcs/mfad032
  76. Schwarz-Schampera, U. (2014). Indium. In Critical Metals Handbook, Gunn, G. (Ed.). John Wiley & Sons. https://doi.org/10.1002/9781118755341.ch9
  77. Snell, J., Emteborg, H., & Schimmel, H. (2012a). The Certification of the Mass Fractions of Elements in Fish Muscle: Certified Reference Material ERM® - BB422. European Commission; Joint Research Centre; Institute for Reference Materials and Measurements. https://doi.org/10.2787/69685
  78. Snell, J., De Vos, E., Emteborg, H., & Schimmel, H. (2012b). The Certification of the Mass Fractions of Elements in Mussel Tissue: Certified Reference Material ERM® - CE278k. European Commission; Joint Research Centre; Institute for Reference Materials and Measurements. https://doi.org/10.2787/6829
  79. Spitsbergen, J. M., & Kent, M. L. (2003). The State of the Art of the Zebrafish Model for Toxicology and Toxicologic Pathology Research—Advantages and Current Limitations. Toxicologic Pathology, 31, 62–87. https://doi.org/10.1080/01926230390174959
  80. Tchounwou, P. B., Yedjou, C. G., Patlolla, A. K., & Sutton, D. J. (2012). Heavy metal toxicity and the environment. Proceedings of the Fourth International Symposium on Polarization Phenomena in Nuclear Reactions, 101, 133–164. https://doi.org/10.1007/978-3-7643-8340-4_6
  81. Thain, J., & Roddie, B. (2001). Biological effects of contaminants: Corophium sp. sediment bioassay and toxicity test. ICES Techniques in Marine Environmental Sciences, 28, 21 pp. https://doi.org/10.17895/ices.pub.5079
  82. Tsai, P., Wu, S., Chiang, C., Lee, M., Chen, H., Chen, W., Chen, C., Yang, S., Yeh, C., & Kuan, Y. (2020). Evaluation of cytotoxicity, apoptosis, and genotoxicity induced by indium chloride in macrophages through mitochondrial dysfunction and reactive oxygen species generation. Ecotoxicology and Environmental Safety, 193, 110348. https://doi.org/10.1016/j.ecoenv.2020.110348
  83. USGS (2026). Mineral commodity summaries 2026. U.S. Geological Survey. https://doi.org/10.3133/mcs2026
  84. Vijver, M. G., Van Gestel, C. a. M., Lanno, R. P., Van Straalen, N. M., & Peijnenburg, W. J. G. M. (2004). Internal metal sequestration and its ecotoxicological relevance: A review. Environmental Science & Technology, 38(18), 4705–4712. https://doi.org/10.1021/es040354g
  85. Watson, G. J., Banfield, G., Watson, S. C. L., Beaumont, N. J., & Hodkin, A. (2025). Offshore wind energy: assessing trace element inputs and the risks for co-location of aquaculture. Npj Ocean Sustainability, 4(1). https://doi.org/10.1038/s44183-024-00101-6
  86. Westerfield, M. (2000). The Zebrafish Book: A guide for the laboratory use of zebrafish (Danio rerio). University of Oregon Press. https://zfin.org/zf_info/zfbook/zfbk.html
  87. White, S. J. O., Hussain, F. A., Hemond, H. F., Sacco, S. A., Shine, J. P., Runkel, R. L., Walton-Day, K., & Kimball, B. A. (2016). The precipitation of indium at elevated pH in a stream influenced by acid mine drainage. The Science of the Total Environment, 574, 1484–1491. https://doi.org/10.1016/j.scitotenv.2016.08.136
  88. Yandem, G., & Jabłońska-Czapla, M. (2024). Review of indium, gallium, and germanium as emerging contaminants: occurrence, speciation and evaluation of the potential environmental impact. Archives of Environmental Protection, 50(3), 84–99. https://doi.org/10.24425/aep.2024.151688
  89. Yang, J. (2014). Comparative acute toxicity of gallium(III), antimony(III), indium(III), cadmium(II), and copper(II) on freshwater swamp shrimp (Macrobrachium nipponense). Biological Research, 47(1), 13. https://doi.org/10.1186/0717-6287-47-13
  90. Yang, J. L., & Chen, L. H. (2017). Toxicity of antimony, gallium, and indium toward a teleost model and a native fish species of semiconductor manufacturing districts of Taiwan. Journal of Elementology, 23(1), 191–199. https://doi.org/10.5601/jelem.2017.22.3.1470
  91. Zheng, J., Yuan, S., Wu, C., & Li, W. (2016). Chronic waterborne zinc and cadmium exposures induced different responses towards oxidative stress in the liver of zebrafish. Aquatic Toxicology, 177, 261–268. https://doi.org/10.1016/j.aquatox.2016.06.001
Universiteit of Hogeschool
Universiteit Antwerpen
Thesis jaar
2026
Promotor(en) en begeleiders
Lieven Bervoets, Moses Ndugwa