ETAA

Evolution of Tolerance to an Anti-Androgen

 Coordinatore  

 Organization address address: "University House, Winston Churchill Avenue"
city: PORTSMOUTH
postcode: PO1 2UP

contact info
Titolo: Dr.
Nome: Elizabeth
Cognome: Bartle
Email: send email
Telefono: +44 23 92843304

 Nazionalità Coordinatore Non specificata
 Totale costo 100˙000 €
 EC contributo 100˙000 €
 Programma FP7-PEOPLE
Specific programme "People" implementing the Seventh Framework Programme of the European Community for research, technological development and demonstration activities (2007 to 2013)
 Code Call FP7-PEOPLE-2012-CIG
 Funding Scheme MC-
 Anno di inizio 2012
 Periodo (anno-mese-giorno) 2012-08-01   -   2016-07-31

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    UNIVERSITY OF PORTSMOUTH HIGHER EDUCATION CORPORATION

 Organization address address: "University House, Winston Churchill Avenue"
city: PORTSMOUTH
postcode: PO1 2UP

contact info
Titolo: Dr.
Nome: Elizabeth
Cognome: Bartle
Email: send email
Telefono: +44 23 92843304

UK (PORTSMOUTH) coordinator 100˙000.00

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 Word cloud

Esplora la "nuvola delle parole (Word Cloud) per avere un'idea di massima del progetto.

strategies    impact    exposure    influence    risk    fish    inform    chemicals    determine    populations    environmental    contaminants    eacs    population    evolutionary    experiments    responses   

 Obiettivo del progetto (Objective)

'The research outlined in this proposal investigates the potential for exposure to endocrine active chemicals (EACs) to influence evolutionary processes within fish populations. The EACs are globally recognised as a prevalent group of environmental contaminants that are known to induce reproductive abnormalities in a range of vertebrates. Although the impact of exposure to these chemicals is well documented, at the level of the individual, it is not yet clear how, or if, these contaminants have the potential to influence evolutionary processes. Such information is urgently needed to understand the implications of exposure to EACs for wild populations and to better inform risk management strategies. The research proposed here adopts a quantitative genetics approach to determine whether an EAC can generate selection within an exposed population and whether the population can respond to this selection. Specifically experiments will be conducted to (1) estimate additive genetic variation for plasticity in phenotypic responses to flutamide; (2) assess the response to selection over four rounds of truncation selection; (3) determine whether there is evidence for correlated responses to selection in traits that are not under direct selection. The results from these experiments will inform on the potential for EACs to impact the health and viability of fish populations and will further inform risk management strategies for EACs. The results will be published in leading journals in the environmental sciences and presented at international meetings. This will provide an excellent foundation on which to develop collaborative scientific networks and attract future competitive research funding to both identify the genes underlying the tolerant phenotype and to assess the potential costs associated with tolerance.'

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