Spatial and temporal trends in the fate of silver nanoparticles in a whole-lake addition study.

Abstract

Studies of the fate and toxicity of nanoparticles, including nanosilver (AgNPs), have been primarily conducted using bench scale studies over relatively short periods of time. To better understand the fate of AgNPs in natural aquatic ecosystems over longer time scales and ecological settings, we released suspensions of AgNPs (30-50 nm, capped with polyvinylpyrrolidone) into a boreal lake at the Experimental Lakes Area in Canada. Approximately 9 kg of silver was added from a shoreline point source from June to October 2014, which resulted in total Ag (TAg) concentrations of about 10 μg L-1 or less. In addition, dissolved Ag concentrations (DAg) were typically very low. Using single particle inductively coupled plasma mass spectrometry (sp-ICP-MS) analysis of grab samples, we found that the nanoparticles typically ranged in the 40-60 nm size class and were widely distributed throughout the lake, while larger aggregates (i.e. >100 nm) were infrequently detected. The highest occurrence of aggregates was found near the addition site; however, size distributions did not vary significantly among spatial locations or time suggesting rapid dispersal upon entry into the lake. Lake stratification at the thermocline was not a barrier to mobility of the AgNPs, as the particles were also detected in the hypolimnion. Environmental factors influenced Ag size distributions over sampling locations and time. Total dissolved phosphorus, bacterioplankton chlorophyll-a, and sampling time strongly correlated with aggregation and dissolution dynamics. AgNPs thus appear to be relatively mobile and persistent over the growing season in lake ecosystems.