The water used by 85% of the Asian population originates in Tibetan Plateau. During April and May of 2006, water samples were collected from four major Asian rivers in the Plateau (i.e. the Salween, Mekong, Yangtze River and Yarlung Tsangpo) and analyzed for Cu, Pb, Zn, Ag, Mo, Cd, Co, Cr, Ni, Li, Mn, Al, Fe, Mg and Hg. The results showed that elements such as Mg were rather high in Tibetan rivers, giving a mean electrical conductance of 36 mS/m. In a few locations, the results also showed relatively high concentrations of Al and Fe (>1 mg/L). However, the concentrations of Cu, Zn, Ag, Cd, and Cr were generally low. Contamination with Pb was identified at a few locations in the Salween and Ni at a few sites in the Yangtze River. For the first time, total dissolved metal contents in source water of four major Asian rivers were evaluated at the same time.

Acid mine drainage (AMD), a legacy of coal and mineral extraction, contaminates streams with complex mixtures of acid and heavy metals that are usually partitioned between the water column and substrate. Understanding the conditions under which sediments retain toxicity after the water column is cleared is important for predicting the long term success of remediation efforts. We conducted laboratory and field experiments to evaluate the relative contribution of acidity versus metals to the toxicity of AMD contaminated sediment towards aquatic macroinvertebrates. Laboratory bioassays showed that precipitate-coated substrate from AMD-impacted sites were toxic to Ctenodaphnia magna and reduced growth of mayflies (Ephemeroptera: Heptageniidae). Toxicity correlated more with acidity released from the sediment than with metals. After transplantation to a clean stream, the same Al- and Fe-contaminated substrate were not toxic to daphnia and was readily colonized by benthic macroinvertebrates within 5 weeks.

To investigate the consequences of acidification and metal accumulation on the biology of aquatic bryophytes, the acid-tolerant liverwort Scapania undulata (L.) Dum. and the acid-sensitive moss Rhynchostegium riparioides (Hedw.) Cardot were transplanted from one stream to two other streams of differing acidity (pH 5.20 and 6.38). The bryophytes were collected in a circumneutral (pH 6.57) stream in the Vosges Mountains. Metal accumulation was semi-quantitatively measured in shoots by energy dispersive TEM X-ray spectroscopy (EDXS). After 1 month, the two species remained green without alteration signs. Although no marked ultrastructural damage was observed in either species, some cells seemed to be necrotic, with flattened chloroplasts, in R. riparioides. Lipid droplet accumulation was observed in some leaf cells of S.undulata when transplanted to the most acidic stream. Metal was mostly localised in the cell wall, and was only sometimes detected in small vacuoles. Under acidic conditions, R. riparioides showed the highest relative amount of Al and the lowest amount of Fe, whereas the acid-tolerant bryophyte species S. undulata contained more Fe and less Al. The capability to limit the uptake of metals into the cytoplasm varies according to the bryophyte species. This could be an explanation of the tolerance of S. undulata to acidification.

Aluminium is a non-essential element for biological systems and is used in water and wastewater processes that rely on (micro)biological purification processes. The effect of Al doses ranging from 100 to 2,000 μg/l on the microbial dissolved oxygen uptake (respiration) over a 24-h period was assessed. Results indicated that Al can reduce the 24-h respiration, but the effects of pH depression due to Al dosing during testing should be taken into account.

The competing ligand exchange method was used to investigate the competitive binding of Ni(II) by Al(III) and Fe(III) in model aqueous solutions and freshwaters. Graphite furnace atomic absorption spectrometry and adsorptive cathodic stripping voltammetry were used to monitor the rate of uptake of the Ni by Chelex 100 chelating resin and dimethylglyoxime as the competing ligands, respectively. The results have revealed that Ni(II)-humate complexes were more labile in presence of the mixture of Al(III) and Fe(III), compared to the lability of the Ni(II)-humate complexes when only one of the two, Al(III) or Fe(III), was present. The environmental significance of this work is that in model solutions simulating freshwater containing humic substances and the target trace metal Ni(II) and cations, Al(III) and Fe(III), the competitive binding of Ni(II), Al(III) and Fe(III) by humic substances makes Ni(II)-humate complexes labile, releasing free Ni²⁺-aqua complex, which reported to be toxic.