Influence of kinetic sorption and diffusion on pesticide movement through aggregated soils

Laboratory studies were carried out to investigate solute leaching at different times from application in relation to temperature and initial soil moisture. Aggregates of a heavy clay soil were treated with a non-interactive solute (bromide) and the herbicides chlorotoluron, isoproturon and triasulfuron. The soil was incubated at 90% field capacity and either 5 or 15 degrees C. The influence of application to initially dry and initially wet aggregates on the behaviour of isoproturon was also investigated. At intervals, samples were either leached in small columns, centrifuged to characterise the fraction of chemical available in pore water under natural moisture conditions or extracted with organic solvents to assess total residues in soil. Bromide concentrations in leachate and in pore water extracted by centrifugation were constant with time. In contrast, availability for leaching and concentration in pore water of the herbicides decreased with increasing time from application in soil incubated at 15 degrees C. The effect of residence time was much smaller at 5 than at 15 degrees C. At the higher temperature, pesticide concentrations in leachate and pore water declined faster than would be expected from degradation alone, probably due to slow diffusion of the pesticides into soil aggregates where they are less available for leaching and/or slow sorption-desorption. The faster decline in availability for leaching at 15 than at 5 degrees C was attributed to faster degradation of the readily available fraction. There was no significant influence of initial soil moisture on either the leaching behaviour of isoproturon or its availability in soil water.     

Metal biomonitoring with mosses: procedures for correcting for soil contamination

Highly variable total concentrations of 15 elements have been found in five species of epigeic mosses growing in remote areas of Italy and in northern Victoria Land (continental Antarctica). It is very likely that soil particles entrapped in the mosses cause these high element concentration differences, thereby leading to inexact interpretations of baseline concentrations and of element distribution in different parts of mosses. A simple procedure for estimating more plausible background values that consists of subtracting the substratum contribution from raw concentrations of elements in mosses is reported. The normalization of total concentrations to the regional soil composition is also emphasized, in order to point out other possible metal sources.     

A lysimeter experiment to investigate temporal changes in the availability of pesticide residues for leaching

Leaching of three pesticides (isoproturon, chlorotoluron and triasulfuron) and a tracer (bromide) were determined in four contrasting soils ranging in texture from sandy loam to clay. The compounds were applied to undisturbed columns of soil and four columns for each soil were randomly selected and leached with 24-mm equivalent of water at prescribed time intervals (3, 9, 24, 37 and 57 d after application). A rapid decline in leached loads of isoproturon and chlorotoluron as time from application to irrigation increased was observed in all soils. In contrast, triasulfuron and bromide loads only decreased rapidly in the clay soil. Bromide losses decreased with decreasing clay contents of the soil and therefore with a decrease in structural development. Magnitudes of pesticide losses varied from soil to soil, depending on structural development and the organic carbon content. Pesticide degradation experiments on disturbed and undisturbed soil samples showed that the rapid decline of leached loads with time was faster than could be explained by degradation alone. Five physico-chemical processes are put forward to explain the different patterns of pesticide leached loads observed in the soils: (1) relative extent of preferential flow, (2) sorption capacity of the compounds to the different soils, (3) extent of degradation of the compounds in the soil, (4) variation in sorption kinetics between compounds associated with pesticide diffusion into soil aggregates, and (5) protection of the compounds by a combination of intra-aggregate diffusion and the presence of preferential flow pathways.     

Humic acid enhanced remediation of an emplaced diesel source in groundwater. 1. Laboratory-based pilot scale test

The enhanced solubility of petroleum-derived compounds in humic acid solutions is the basis for a new groundwater remediation technology. In this unique pilot-scale test, a stationary contaminant source consisting of diesel fuel was placed below the water table in a model sand aquifer (1.2 x 5.5 x 1.8-m deep) and flushed with water at a flow rate of 2 cm/h over 5 years. At 51 days, laboratory grade humic acid was added to the water and maintained at a level of approximately 0.8 g/l. The addition of humic acid had only a small impact on the aqueous transport of the BTEX components, which were rapidly dissolved from the diesel, but had a large effect on the flushing of PAHs, including methylated naphthalenes (MNs). Binding to aqueous humic acid enhanced the solubilization of MNs two- to tenfold. During aqueous transport, biodegradation of the BTEX and PAHs occurred, limiting the lateral and longitudinal extent of the diesel contaminant plume in the model aquifer. It appears that through enhanced solubilization, the overall biodegradation rate of the MNs was increased. As the various MNs were depleted from the diesel source, the MN plume shrank and then disappeared.     

Preliminary Measurements of Turbulence and Environmental Parameters in a Sub-Tropical Estuary of Eastern Australia

In natural systems, mixing is driven by turbulence, but current knowledge is limited in estuarine zones where predictions of contaminant dispersion are often inaccurate. A series of detailed field studies was conducted in a small sub-tropical creek in eastern Australia. Hydrodynamic, physio-chemical and ecological measurements were conducted simultaneously to assess the complexity of the estuarine zone, notably the interactions between turbulence and environment. The measurements were typically performed at high frequency over a tidal cycle. The results provide an original data set to complement long-term monitoring and a basis for a more detailed study of mixing in sub-tropical systems. Unlike many long-term observations, velocity and water quality scalars were measured herein with sufficient spatial and temporal resolutions to determine quantities of interest in the study of turbulence, while ecological indicators were sampled systematically and simultaneously. In particular the results yielded contrasted outcomes, and the finding impacts on the selection process for key water quality indicators.     

Some biologically important low molecular weight organic acids in the sediments of Loch Eil

The isolation of biologically important low molecular weight organic acids from organically enriched sediments in Loch Eil, Scotland, was carried out by extraction of pore water with acidified ethyl acetate. High concentrations of acetic acid, up to 1.8 mg g^-1 dry weight of sediment were found at Station E-24. Propionate, butyrate, valerate, lactate and traces of succinate were also found. Succinate was present in significant amounts, 42.2 g g^-1 dry weight of sediment at Station E-70, which received a higher input of organic matter than E-24. Both propionate and succinate were absent from a control station in the Lynn of Lorne where the sediment was low in carbon compared with Loch Eil. In experimental tanks, acetate levels increased as the input of organic carbon (as cellulose) was increased up to a load level of 1.5 g m^-2 day^-1. Above this, acetate decreased and succinate appeared. Succinate was not detected in low-loaded tanks. Experiments with sieved mud showed a vertical distribution of the different acids with depth. Lactate and succinate reached highest concentration in the 0 to 3 cm layer, acetate at 3 to 6 cm and propionate at 6 to 9 cm. The results are discussed in relation to the role of these acids as food sources and as indicators of biochemical pathways taking place in sediments with different carbon input levels.     

Crop substitution in the estimation of economic benefits due to ozone reduction

Prior estimates of economic loss from ozone damage to food crops have not allowed for farmer substitution in inputs—and particularly have not allowed for acreage shifts between crops—in response to yield changes. This is a potentially serious problem since benefits from air pollution control legislation may also be estimated without allowing for this direct substitution. This study explores how much acreage shifting might occur between corn, soybeans, and wheat if ozone were reduced to background levels, and how such substitution might affect the estimation of benefits from ozone reduction.     

The application of adaptive cluster sampling for rare subtidal macroalgae

Adaptive cluster sampling (ACS) is a targeting sampling method that provides unbiased abundance estimators for populations of rare species that may be inadequately sampled with simple random sampling (SRS). ACS has been used successfully to estimate abundances of rockfish and sardine larvae from shipboard surveys. In this study, we describe the application of ACS for subtidal macroalgae. Using SCUBA, we measured abundances of Codium mamillosum, C. pomoides, and Halimeda cuneata at three islands and two levels of wave exposure. The three species were relatively patchy and could be sampled with ACS at one site per dive. Their distributions differed among islands and with exposure to wave energy, with H. cuneata found at only one island. ACS is a useful tool for understanding the spatial distribution and abundance of populations of rare benthic species, but, as was the case in this study, may not be as efficient as sampling with SRS with comparable replication.     

The paradox of risk assessment: comparing responses of fathead minnows to capture-released and diet-released alarm cues from two different predators

Summary. Many aquatic prey are known to use chemical alarm cues to assess their risk of predation. In fishes, such alarm cues can be released either through damage of the epidermis during a predatory attack (capture-released) or through release from the predator feces (diet-released). In our study, we compared the importance of capture- versus diet-released alarm cues in risk assessment by fathead minnows (Pimephales promelas) that were na?ve to fish predators. We utilized two different fish predators: a specialized piscivore, the northern pike (Esox lucius) and a generalist predator, the brook trout (Salvelinus fontinalis). Handling time of pike consuming minnows was much shorter than for trout consuming minnows, likely resulting in less epidermal damage to the minnows during attacks by pike. In accordance with this, minnows showed a less intense antipredator response to capture-released cues from pike than capture-released cues from trout. This represents a paradox in risk assessment for the minnows as they respond to the specialized piscivore, the more dangerous predator, with a less intense antipredator response. In contrast, the minnows showed a stronger antipredator response to the specialized piscivore than to the generalist when given diet cues. This work highlights the need for researchers to carefully consider the nature of the information available to prey in risk assessment.