This work assessed in situ, copper (Cu) uptake and phytotoxicity for durum wheat (Triticum turgidum durum L.) cropped in a range of Cucontaminated, former vineyard soils (pH 4.2-7.8 and total Cu concentration 32-1,030 mg Cu kg −1 ) and identified the underlying soil chemical properties and related root-induced chemical changes in the rhizosphere. Copper concentrations in plants were significantly and positively correlated to soil Cu concentration (total and EDTA). In addition, Cu concentration in roots which was positively correlated to soil pH tended to be larger in calcareous soils than in non-calcareous soils. Symptoms of Cu phytotoxicity (interveinal chlorosis) were observed in some calcareous soils. Iron (Fe)-Cu antagonism was found in calcareous soils. Rhizosphere alkalisation in the most acidic soils was related to decreased CaCl 2 -extractable Cu. Conversely, waterextractable Cu increased in the rhizosphere of both non-calcareous and calcareous soils. This work suggests that plant Cu uptake and risks of Cu phytotoxicity in situ might be greater in calcareous soils due to interaction with Fe nutrition. Larger water extractability of Cu in the rhizosphere might relate to greater Cu uptake in plants exhibiting Cu phytotoxic symptoms.
This work investigated how copper (Cu) phytotoxicity affected iron (Fe) nutrition and root elongation in hydroponically grown durum wheat (Triticum turgidum durum L.
Zwitterionic,
cationic, and anionic per- and polyfluoroalkyl substances
(PFAS) are increasingly reported in terrestrial and aquatic environments,
but their inputs to agricultural lands are not fully understood. Here,
we characterized PFAS in 47 organic waste products (OWP) applied in
agricultural fields of France, including historical and recent materials.
Overall, 160 PFAS from 42 classes were detected from target screening
and homologue-based nontarget screening. Target PFAS were low in agriculture-derived
wastes such as pig slurry, poultry manure, or dairy cattle manure
(median ∑46PFAS: 0.66 μg/kg dry matter). Higher
PFAS levels were reported in urban and industrial wastes, paper mill
sludge, sewage sludge, or residual household waste composts (median
∑46PFAS: 220 μg/kg). Historical municipal
biosolids and composts (1976–1998) were dominated by perfluorooctanesulfonate
(PFOS), N-ethyl perfluorooctanesulfonamido acetic
acid (EtFOSAA), and cationic and zwitterionic electrochemical fluorination
precursors to PFOS. Contemporaneous urban OWP (2009–2017) were
rather dominated by zwitterionic fluorotelomers, which represented
on average 55% of ∑160PFAS (max: 97%). The fluorotelomer
sulfonamidopropyl betaines (X:2 FTSA-PrB, median: 110 μg/kg,
max: 1300 μg/kg) were the emerging class with the highest occurrence
and prevalence in contemporary urban OWP. They were also detected
as early as 1985. The study informs for the first time that urban
sludges and composts can be a significant repository of zwitterionic
and cationic PFAS.
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