Discharge of treated wastewater from municipalities into streams has been a standard practice for decades. Such wastewater is treated primarily for the purpose of reducing the potential for biological oxygen consumption by microorganisms in the receiving waters, as a result of the discharged wastewater effluent. Oxygen consumption by microorganisms degrades organic materials in the wastewater reducing the oxygen levels in the water body into which the effluent is discharged and thereby harm aquatic organisms, including fish.
In recent decades concerns have developed related to inorganic nutrients, some metals, and other chemicals within wastewater which create harm. Due to a study published by Kolpin et al.1, a greater focus on a range of chemicals not previously considered has evolved. This study, published by the United States Geological Society, raised awareness regarding the wide range of personal care products and other chemicals in rivers and streams across the US due to discharge from wastewater treatment facilities.
Since the early 1960s, researchers at Penn State University have investigated and developed an alternative wastewater discharge practice somewhat unique in a humid region. Rather than discharging treated wastewater to a stream, and thereby directly impacting the stream quality, the effluent is applied to the forested and the cropped land managed by the University. This application area, nicknamed "The Living Filter", presently accepts all wastewater effluent generated from the campus plus some from the municipality. This reduces the likelihood for excess nutrients to enter streams which deliver water to the Chesapeake Bay, protects the local cold-water fishery from discharges of warm wastewater which is harmful to the fish, and prevents the delivery of other chemicals contained in the wastewater from directly contacting aquatic ecosystems.
However, there are always consequences of behavior changes, and this alternative use facility is not immune to such. Questions have arisen regarding whether the application of the wastewater effluent has negatively impacted the soil's ability to allow water to infiltrate the soil surface2,3,4,5 and caused greater runoff, whether there is a possible contamination of the local wells with chemicals (nutrients, antibiotics or other pharmaceutical compounds, personal care products) contained in the wastewater effluent, and whether those chemicals are creating negative environmental impacts, such as through the uptake of chemicals into plants6 grown on the site, or the development of antibiotic resistance in soil organisms7 at the site.
As a result of some of these concerns, this study is conducted to determine the impacts of the irrigation of wastewater effluent on soil hydraulic conductivity at saturation. The approach used involves collecting soils from selected sites either within or outside the irrigated area and matching the soil sample container size with the laboratory setup. It is important for the soil sample container to fit into the laboratory apparatus and for the water that moves downward through the soil matrix in the sample to be separated from the water that moves downward between the soil and the soil sample container. The protocol describes how the laboratory apparatus is constructed to ensure this occurred.
Soil samples are collected using a hydraulic core sampler attached to a tractor. Soil cores are collected from selected areas in the undulating landscape and retained in a plastic sleeve fitted into the soil core sampler. These cores are collected from a Hagerstown silt loam, located either in a summit landscape position or in a depressional area. Six representative summits and six depressional sites are sampled from the irrigated area (a total of 12 irrigated area sampling sites). In addition, three summits and three depressional sites are sampled from an adjacent, non-irrigated area (a total of six non-irrigated sites). A maximum of six cores is collected at each site to a maximum depth of approximately 1,200 mm, with each core sample being approximately 150 mm long (100 mm of the sample being contained in the plastic sleeve and 50 mm being contained in the cutting head of the metal sampler). After removal from the metal sampler, the plastic sleeves containing the collected soil cores are fitted with end caps, transported upright to the laboratory, and stored upright until they are used to determine the saturated hydraulic conductivity. Concurrently, soil samples are collected at each depth for the determination of soil and soil solution concentrations of Calcium (Ca), Magnesium (Mg), and Sodium (Na) using a Mehlich 3 extraction for estimates of soil concentrations8 and deionized water extracts at a 1:2 ratio of soil mass:water mass. The chemical analyses of the water extracts were obtained from Inductively Coupled Plasma Atomic Emission Spectroscopy (ICP-AES) and were used to calculate the Sodium Adsorption Ratio (SAR).
The determination of the saturated hydraulic conductivity is carried out primarily using a constant head method9. A solution containing Ca and Na salts to mimic the effluent electrical conductivity (EC) and SAR of the effluent is created so the soil will be exposed to water quality variables similar to the wastewater applied in the field. In this case, the EC is 1.3 dS/m and the SAR is 3, reflecting the EC and SAR of the effluent in recent years prior to the sample period. [Technically, the units for SAR are (milliequivalents/liter)½ and are not usually identified in the literature.]
The modification to the constant head method of Klute and Dirksen9 is the development of a flow separator by Walker8 to prevent flow through the column which occurred outside the soil matrix from being included in the estimate of the soil hydraulic conductivity. The flow separator is built using polyvinyl chloride (PVC) tubing selected and machined to match the soil sample size. A screen supports the soil sample and allows the water that has moved through the soil matrix to flow out the bottom of the sample. A second outlet emits the water that has flowed down the inside of the plastic sleeve, thereby eliminating so-called "wall flow" from being incorrectly included in the estimate of the amount of water that moves through the soil matrix.