Natural variation in cadmium tolerance and its relationship to metal hyperaccumulation for seven populations of Thlaspi caerulescens from western Europe
By N. Roosens, N. Verbruggen, P. Meerts, P. Ximénez-Embún, J. A. Smith. 2003
302 citations recorded by the source corpus.
Subfields: Plant Science, Pollution
View Paper: https://www.semanticscholar.org/paper/dcfc14e9962f81dc2f7b0d5d4119b0397aa5b489
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Citations in the corpus
- Zinc in plants. (2007, background): “Intriguingly, other studies have also shown that high [Cd]ext inhibits Zn accumulation in Ganges, but not in Prayon, whilst high [Zn]ext inhibits Cd accumulation in Prayon, but not in Ganges populations (Lombi et al., 2001; Zhao et al., 2002; Roosens et al., 2003).”
- Mechanism of Zinc absorption in plants: uptake, transport, translocation and accumulation (2016, background): “Generally in Zn hyperaccumulators, [Zn]shoot[ [Zn]root up to 10 fold, although this depends upon [Zn]ext/soil solution (Shen et al. 1997; Zhao et al. 2000; Roosens et al. 2003).”
- Dualities in plant tolerance to pollutants and their uptake and translocation to the upper plant parts (2009, background): “Furthermore Ca uptake in the Prayon ecotype is inhibited by the addition of Cd, which leads to the suggestion that at least two other uptake systems must be involved in Cd uptake (Roosens et al., 2003).”
- Molecular mechanisms of metal hyperaccumulation in plants. (2009, background): “In T. caerulescens the variation in Cd accumulation among local populations is correlated with the variation in Zn accumulation, at least in some studies (Assunção et al., 2003c; Roosens et al., 2003).”
- Opportunities and feasibilities for biotechnological improvement of Zn, Cd or Ni tolerance and accumulation in plants (2011, background): “Cd hyperaccumulation so far has only been observed among populations found in the south of France, in the regionaroundGanges (Meerts and Isacker, 1997; Lombi et al., 2000; Assunção et al., 2003a; Roosens et al., 2003).”
- Comprehending crystalline β-carotene accumulation by comparing engineered cell models and the natural carotenoid-rich system of citrus (2011, unknown): “caerulescens populations from calamine and serpentine sites (Roosens et al., 2003).”
- Metal hyperaccumulation in plants: mechanisms of defence against insect herbivores (2005, background): “Glucosinolates give plants in the Brassicaceae a distinctive flavour ( Renwick 2002; Wittstock & Gershenzon 2002), and experiments by Tolra et al. (2001) show that increases in Zn hyperaccumulation can decrease shoot concentrations of sinalbin, the most abundant glucosinolate in T. caerulescens.”
- Organic Acids Accumulation and Antioxidant Enzyme Activities in Thlaspi caerulescens under Zn and Cd Stress (2006, background): “Comparing T. caerulescens plants under growth and treatment conditions similar to ours it is apparent that our plants accumulated less Cd and Zn than those in other experiments (Assunção et al. 2003a; Roosens et al. 2003).”
- Heavy metal hyperaccumulating plants: how and why do they do it? And what makes them so interesting? (2011, background): “The degree of hyperaccumulation of one or more heavy metals an vary significantly in different species or also in populations and cotypes of the same species [36,37].”
- Toxic metal accumulation, responses to exposure and mechanisms of tolerance in plants. (2006, background): “caerulescens are known that grow better in nutrient solution containing low micromolar concentrations of Cd than in nutrient solution without Cd [11].”
- Mechanisms to cope with arsenic or cadmium excess in plants. (2009, background): “Essential or beneficial functions for Cd or As have not been reported in higher plants, except for some Cd-hyperaccumulating populations of Thlaspi caerulescens, which require Cd for optimum growth [4,5].”