Tiago Torres

Dr. Tiago Torres


Research Focus & Metrics

Academic Career Length

12Years (2015-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 April 2015 in Ecotoxicology and Environmental Safety
Verified
Journal Article
Closed access
SRSílvia Ribeiro
Sílvia Ribeiro
TTTiago Torres
Tiago Torres
Rosário MartinsRosário Martins
Rosário Martins
Miguel SantosMiguel Santos
Miguel Santos

1 May 2016 in Aquatic Toxicology
Verified
Journal Article
Closed access
Miguel SantosMiguel Santos
Miguel Santos
RRRaquel Ruivo
Raquel Ruivo
MLMonica Lopes-Marques
Monica Lopes-Marques
TTTiago Torres
Tiago Torres
CSCarmen B De Los Santos
Carmen B De Los Santos
Teresa NeuparthTeresa Neuparth
Teresa Neuparth

Verified
Journal Article
Open access
PDF file
TTTiago Torres
Tiago Torres
Isabel CunhaIsabel Cunha
Isabel Cunha
Rosário MartinsRosário Martins
Rosário Martins
Miguel SantosMiguel Santos
Miguel Santos
Recently, several emerging pollutants, including Personal Care Products (PCPs), have been detected in aquatic ecosystems, in the ng/L or µg/L range. Available toxicological data is limited, and, for certain PCPs, evidence indicates a potential risk for the environment. Hence, there is an urgent need to gather ecotoxicological data on PCPs as a proxy to improve risk assessment. Here, the toxicity of three different PCPs (4-Methylbenzylidene Camphor (4-MBC), propylparaben and triclocarban) was tested using embryo bioassays with Danio rerio (zebrafish) and Paracentrotus lividus (sea urchin). The No Observed Effect Concentration (NOEC) for triclocarban was 0.256 µg/L for sea urchin and 100 µg/L for zebrafish, whereas NOEC for 4-MBC was 0.32 µg/L for sea urchin and 50 µg/L for zebrafish. Both PCPs impacted embryo development at environmentally relevant concentrations. In comparison with triclocarban and 4-MBC, propylparaben was less toxic for both sea urchin (NOEC = 160 µg/L) and zebrafish (NOEC = 1000 µg/L). Overall, this study further demonstrates the sensitivity of embryo bioassays as a high-throughput approach for testing the toxicity of emerging pollutants.


1 November 2018 in Science of The Total Environment
Verified
Journal Article
Closed access
CECarla Escapa
Carla Escapa
TTTiago Torres
Tiago Torres
Teresa NeuparthTeresa Neuparth
Teresa Neuparth
Ricardo N. CoimbraRicardo N. Coimbra
Ricardo N. Coimbra
AGAna Garcia
Ana Garcia
Marta OteroMarta Otero
Marta Otero

18 June 2015 in Journal of Toxicology and Environmental Health, Part A
Verified
Journal Article
Closed access
DLDaniela Lima
Daniela Lima
FCFilipe Castro
Filipe Castro
ICInês Coelho
Inês Coelho
RLRicardo Lacerda
Ricardo Lacerda
Manuel GestoManuel Gesto
Manuel Gesto
Miguel SantosMiguel Santos
Miguel Santos
Both field and experimental data examined the influence of exposure to environmental contaminant tributyltin (TBT) on marine organisms. Although most attention focused on the imposex phenomenon in gastropods, adverse effects were also observed in other taxonomic groups. It has been shown that imposex induction involves modulation of retinoid signaling in gastropods. Whether TBT influences similar pathways in fish is yet to be addressed. In this study, larvae of the model teleost Danio rerio were exposed to natural retinoids, all-trans-retinoic acid, 9-cis-retinoic acid, and all-trans-retinol, as well as to the RXR synthetic pan-agonist methoprene acid (MA) and to TBT. Larvae were exposed to TBT from 5 days post fertilization (dpf) to adulthood, and reproductive capacity was assessed and correlated with mode of action. TBT significantly decreased fecundity at environmentally relevant levels at 1 μg TBT Sn/g in diet. Interestingly, in contrast to previous reports, TBT altered zebrafish sex ratio toward females, whereas MA exposure biased sex toward males. Since fecundity was significantly altered in the TBT-exposed group with up to 62% decrease, the potentially affected pathways were investigated. Significant downregulation was observed in brain mRNA levels of aromatase b (CYP19a1b) in females and peroxisome proliferator activated receptor gamma (PPARg) in both males and females, suggesting an involvement of these pathways in reproductive impairment associated with TBT.