Transport quantities of the classical spin chain with the quenched disorder in the antiferromagnetic coupling Ji are evaluated using the dynamical simulation at finite temperatures T > 0 . Since the classical model is nonintegrable, spin and thermal conductivities remain finite even in the pure case. On the other hand, the role of disorder becomes crucial at low T leading to a vanishing transport due to the Anderson localization within the linearized regime. The crossover from the insulator to the conductor appears both for the spin and thermal transport at quite low T * J. Still the many-body localization regime at T > 0 evidenced by extremely short mean free paths can be strongly enhanced by introducing into the model an additional staggered field.
Cadmium (Cd) was shown to co-localise with calcium (Ca) in oxalate crystals in the stems and leaves of Cd tolerant Gomphrena claussenii, but Cd binding remained unresolved. Using synchrotron radiation X-ray absorption near edge spectroscopy we demonstrate that in oxalate crystals of hydroponically grown G. claussenii the vast majority of Cd is bound to oxygen ligands in oxalate crystals (>88%; Cd-O-C coordination) and the remaining Cd is bound to sulphur ligands (Cd-S-C coordination). Cadmium binding to oxalate does not depend on the amount of Ca supplied or from which organs the crystals originate (stems and mature leaves). By contrast, roots contain no oxalate crystals and therein Cd is bound predominantly by S ligands. The potential to remove Cd by extraction of Cd-rich oxalate crystals from plant material should be tested in phytoextraction or phytomining strategies.
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