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Hypocholesterolaemic pharmaceutical simvastatin disrupts reproduction and population growth of the amphipod Gammarus locusta at the ng/L range. / Neuparth, T.; Martins, C.; de los Santos, C.B. et al.
In: Aquatic Toxicology, Vol. 155, 19.07.2014, p. 337-347.

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Neuparth, T, Martins, C, de los Santos, CB, Costa, MH, Martins, I, Costa, PM & Santos, MM 2014, 'Hypocholesterolaemic pharmaceutical simvastatin disrupts reproduction and population growth of the amphipod Gammarus locusta at the ng/L range', Aquatic Toxicology, vol. 155, pp. 337-347. https://doi.org/10.1016/j.aquatox.2014.07.009

APA

Neuparth, T., Martins, C., de los Santos, C. B., Costa, M. H., Martins, I., Costa, P. M., & Santos, M. M. (2014). Hypocholesterolaemic pharmaceutical simvastatin disrupts reproduction and population growth of the amphipod Gammarus locusta at the ng/L range. Aquatic Toxicology, 155, 337-347. https://doi.org/10.1016/j.aquatox.2014.07.009

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MLA

VancouverVancouver

Neuparth T, Martins C, de los Santos CB, Costa MH, Martins I, Costa PM et al. Hypocholesterolaemic pharmaceutical simvastatin disrupts reproduction and population growth of the amphipod Gammarus locusta at the ng/L range. Aquatic Toxicology. 2014 Jul 19;155:337-347. doi: 10.1016/j.aquatox.2014.07.009

Author

Neuparth, T. ; Martins, C. ; de los Santos, C.B. et al. / Hypocholesterolaemic pharmaceutical simvastatin disrupts reproduction and population growth of the amphipod Gammarus locusta at the ng/L range. In: Aquatic Toxicology. 2014 ; Vol. 155. pp. 337-347.

RIS

TY - JOUR

T1 - Hypocholesterolaemic pharmaceutical simvastatin disrupts reproduction and population growth of the amphipod Gammarus locusta at the ng/L range

AU - Neuparth, T.

AU - Martins, C.

AU - de los Santos, C.B.

AU - Costa, M.H.

AU - Martins, I.

AU - Costa, P.M.

AU - Santos, M.M.

PY - 2014/7/19

Y1 - 2014/7/19

N2 - Simvastatin (SIM), a hypocholesterolaemic drug, is among the most widely used pharmaceuticals worldwide and is therefore of emerging environmental concern. Despite the ubiquitous nature of SIM in the aquatic ecosystems, significant uncertainties exist about sublethal effects of the drug in aquatic organisms. Therefore, here we aimed at investigating a multi-level biological response in the model amphipod Gammarus locusta, following chronic exposures to low levels of SIM (64 ng/L to 8 μg/L). The work integrated a battery of key endpoints at individual-level (survival, growth and reproduction) with histopathological biomarkers in hepatopancreas and gonads. Additionally, an individual-based population modelling was used to project the ecological costs associated with long-term exposure to SIM at the population level. SIM severely impacted growth, reproduction and gonad maturation of G. locusta, concomitantly to changes at the histological level. Among all analysed endpoints, reproduction was particularly sensitive to SIM with significant impact at 320 ng/L. These findings have important implications for environmental risk assessment and disclose new concerns about the effects of SIM in aquatic ecosystems.

AB - Simvastatin (SIM), a hypocholesterolaemic drug, is among the most widely used pharmaceuticals worldwide and is therefore of emerging environmental concern. Despite the ubiquitous nature of SIM in the aquatic ecosystems, significant uncertainties exist about sublethal effects of the drug in aquatic organisms. Therefore, here we aimed at investigating a multi-level biological response in the model amphipod Gammarus locusta, following chronic exposures to low levels of SIM (64 ng/L to 8 μg/L). The work integrated a battery of key endpoints at individual-level (survival, growth and reproduction) with histopathological biomarkers in hepatopancreas and gonads. Additionally, an individual-based population modelling was used to project the ecological costs associated with long-term exposure to SIM at the population level. SIM severely impacted growth, reproduction and gonad maturation of G. locusta, concomitantly to changes at the histological level. Among all analysed endpoints, reproduction was particularly sensitive to SIM with significant impact at 320 ng/L. These findings have important implications for environmental risk assessment and disclose new concerns about the effects of SIM in aquatic ecosystems.

U2 - 10.1016/j.aquatox.2014.07.009

DO - 10.1016/j.aquatox.2014.07.009

M3 - Article

VL - 155

SP - 337

EP - 347

JO - Aquatic Toxicology

JF - Aquatic Toxicology

SN - 0166-445X

ER -