ABSTRACT
Effects of chemical uptake onto polar organic chemical integrative samplers (POCIS) exposed to total suspended solid (TSS) sediment concentrations of 0 and 3600â¯ppm were investigated for 12 pesticides at constant concentration, temperature, and flow velocity. The effects of sediment exposure on POCIS uptake were negligible for compounds with polyethersulfone-water partition coefficients greater than three (i.e., log KPESWâ¯>â¯3). However, significant effects were observed for 3 of 12 compounds tested, and the maximum effect was an approximate 4-fold increase in sampling rate for the sediment experiment relative to the control. Effects of sediment on the pesticide distribution between polyethersulfone (PES) membranes and Oasis HLB sorbent were also investigated. The fraction of pesticide accumulated on PES membranes was relatively low for most compounds and ranged from 0 to 33%. In contrast, four compounds with higher affinity for PES accumulated preferentially on the membranes (fraction ranging from 64 to 96%), suggesting that a sampling rate derived from the additive contribution of membrane extraction and the more typical extraction of analytes from HLB sorbent would improve the sensitivity of sampling rate estimations for these compounds. However, for these same compounds, the combined sampling rate, Rs (HLB + PES), was considerably more susceptible to a sediment effect than the traditional sampling rate determination, relying solely on extraction from HLB sorbent.
Subject(s)
Environmental Monitoring/methods , Organic Chemicals/analysis , Water Pollutants, Chemical/analysis , Geologic Sediments/chemistry , Membranes, Artificial , Organic Chemicals/chemistry , Pesticides/analysis , Polymers , Sulfones , Water/chemistryABSTRACT
The effects of changing hydrodynamic conditions and changing temperatures on polar organic chemical integrative sampler (POCIS) sampling rates (Rs ) were investigated for 12 crop protection chemicals. Exposure concentration was held constant in each laboratory experiment, and flow velocities were calculated from measured mass transfer coefficients of the water boundary layer near the surface of POCIS devices. At a given temperature Rs generally increased by a factor of 2 to 5 between a stagnant condition and higher flow velocities (6-21 cm/s), but Rs for most compounds was essentially constant between the higher flow velocities. When temperature was varied between 8 and 39 °C for a given flow condition, Rs increased linearly. In general, Rs increased by a factor of 2 to 4 and 2 to 8 over this temperature range under flow and stagnant conditions, respectively. An Arrhenius model was used to describe the dependence of POCIS sampling rates on temperature. Adjustments of Rs for temperature did not fully explain observed differences between time-weighted average concentrations of atrazine determined from POCIS and from composite water sampling in a field setting, suggesting that the effects of other competing factors still need to be evaluated. Environ Toxicol Chem 2018;37:2331-2339. © 2018 SETAC.
Subject(s)
Environmental Monitoring/methods , Hydrodynamics , Organic Chemicals/analysis , Temperature , Water/chemistry , Atrazine/analysis , Rheology , Water Pollutants, Chemical/analysisABSTRACT
The authors performed a multiple-pulsed atrazine experiment to measure responses of autotrophic endpoints in outdoor stream mesocosms. The experiment was designed to synthetically simulate worst-case atrazine chemographs from streams in agricultural catchments to achieve 60-d mean concentrations of 0 µg/L (control), 10 µg/L, 20 µg/L, and 30 µg/L. The authors dosed triplicate streams with pulses of 0 µg/L, 50 µg/L, 100 µg/L, and 150 µg/L atrazine for 4 d, followed by 7 d without dosing. This 11-d cycle occurred 3 times, followed by a recovery (untreated) period from day 34 to day 60. Mean ± standard error 60-d atrazine concentrations were 0.07 ± 0.03 µg/L, 10.7 ± 0.05 µg/L, 20.9 ± 0.24 µg/L, and 31.0 ± 0.17 µg/L for the control, 10-µg/L, 20-µg/L, and 30-µg/L treatments, respectively. Multivariate analyses revealed that periphyton and phytoplankton community structure did not differ among treatments on any day of the experiment, including during the atrazine pulses. Control periphyton biomass in riffles was higher immediately following the peak of the first atrazine pulse and remained slightly higher than some of the atrazine treatments on most days through the peak of the last pulse. However, periphyton biomass was not different among treatments at the end of the present study. Phytoplankton biomass was not affected by atrazine. Metaphyton biomass in pools was higher in the controls near the midpoint of the present study and remained higher on most days for the remainder of the study. Ceratophyllum demersum, a submersed macrophyte, biomass was higher in controls than in 20-µg/L and 30-µg/L treatments before pulse 3 but was not different subsequent to pulse 3 through the end of the present study. Maximum daily dissolved oxygen (DO, percentage of saturation) declined during each pulse in approximate proportion to magnitude of dose but rapidly converged among treatments after the third pulse. However, DO increased in controls relative to all atrazine treatments during the last 17 d of the experiment, likely a result of metaphyton cover in the pools. Finally, atrazine significantly limited uptake of PO4(3-) and uptake and/or denitrification of NO3(-) but only during pulses; percentage of dose removed from the water column was >85% for P and >95% for N after pulse 3 through the end of the present study. Collectively, only DO and metaphyton biomass differed at the end of the present study and only slightly. Some other endpoints were affected but only during pulses, if at all. The high levels of primary production and accumulation of algal biomass in all streams suggest that effects of pulses of atrazine at the concentrations used in the present study appear transient and likely do not represent ecologically significant adverse outcomes to periphyton, phytoplankton, and aquatic macrophytes, particularly in agricultural streams subjected to high nutrient loads.