Colloidal phosphorus in surface runoff and water extracts from semiarid soils of the western United States

Colloidal particles in runoff may have an important role in P transfer from soils to waterbodies, but remain poorly understood. We investigated colloidal molybdate-reactive phosphorus (MRP) in surface runoff and water extracts of calcareous arable soils from the semiarid western United States. Colloidal MRP was determined by ultrafiltration and operationally defined as MRP associated with particles between 1 microm and 1 nm diameter, although a smaller pore-size filter (0.3 nm) was used to define the lower size limit of colloids in water extracts. In surface runoff from three calcareous soils generated by simulated sprinkler irrigation, colloidal MRP concentrations ranged between 0.16 and 3.07 microM, constituting between 11 and 56% of the MRP in the <1-microm fraction. Concentrations were strongly correlated with agronomic and environmental soil-test P concentrations for individual soils. Water extracts of a range of similar soils contained two size fractions of colloidal MRP: a larger fraction (1.0-0.2 microm) probably associated with fine clays, and a smaller fraction (3-0.3 nm) probably associated with Ca-phosphate minerals. Colloidal MRP was solubilized in the acidic medium of the colorimetric detection procedure, suggesting that a fraction of the filterable MRP in runoff from calcareous soils may not be as readily bioavailable as free phosphate in waterbodies. Our results suggest that colloidal MRP is an important but poorly understood component of P transfer in runoff from calcareous western U.S. soils and should be given greater consideration in mechanistic studies of the P transfer process.     

Phosphorus in surface runoff from calcareous arable soils of the semiarid Western United States

Management strategies that minimize P transfer from agricultural land to water bodies are based on relationships between P concentrations in soil and runoff. This study evaluated such relationships for surface runoff generated by simulated sprinkler irrigation onto calcareous arable soils of the semiarid western United States. Irrigation was applied at 70 mm h(-1) to plots on four soils containing a wide range of extractable P concentrations. Two irrigation events were conducted on each plot, first onto dry soil and then after 24 h onto wet soil. Particulate P (>0.45 microm) was the dominant fraction in surface runoff from all soils and was strongly correlated with suspended sediment concentration. For individual soil types, filterable reactive P (<0.45 microm) concentrations were strongly correlated with all soil-test P methods, including environmental tests involving extraction with water (1:10 and 1:200 soil to solution ratio), 0.01 M CaCl(2), and iron strips. However, only the Olsen-P agronomic soil-test procedure gave models that were not significantly different among soils. Soil chemical differences, including lower CaCO(3) and water-extractable Ca, higher water-extractable Fe, and higher pH, appeared to account for differences in filterable reactive P concentrations in runoff from soils with similar extractable P concentrations. It may therefore be possible to use a single agronomic test to predict filterable reactive P concentrations in surface runoff from calcareous soils, but inherent dangers exist in assuming a consistent response, even for one soil within a single field.     

The Role of Soil Surface Crusting in Desertification and Strategies to Reduce Crusting

Soil crusting decreases infiltration, increases erosion, and impedes vegetation establishment, so reducing the impact of crusting is of major importance in combating desertification. Although surface crusting has been the subject of considerable research over the past 50 years or more, the practical management of soil crusts remains a challenge for many dryland communities. Crusting occurs in two steps, an initial aggregate breakdown period that occurs under rainfall and a subsequent hardening phase during drying. Several factors influence crust development, but the single most important one is soil aggregate stability. Strategies to reduce crusting can be based either on protecting the surface from raindrop impact or improving aggregate stability, or a combination of both. However, crust control is labor and/or capital intensive and must be thought out clearly in terms of the benefits to be achieved.     

Transport of veterinary antibiotics in overland flow following the application of slurry to arable land

The environment may be exposed to veterinary medicines administered to livestock due to the application of organic fertilisers to land. Slurry is often spread on to fields following the harvest of the previous crop. Despite recommendations to do so, the slurry may not be ploughed into the soil for some time. If precipitation occurs before incorporation then it is likely that the slurry and any antibiotic residues in the slurry will be transported towards surface waters in overland flow. This phenomenon has been investigated in a plot study and transport via 'tramlines' has been compared to that through crop stubble. Three veterinary antibiotics, from the tetracycline, sulphonamide and macrolide groups, were applied to the plots in pig slurry. Twenty four hours after the application the plots were irrigated. Following this the plots received natural rainfall. Sulphachloropyridazine was detected in runoff from the tramline plot at a peak concentration of 703.2 microgl(-1) and oxytetracycline at 71.7 microgl(-1). Peak concentrations from the plot that did not contain a tramline were lower at 415.5 and 32 microgl(-1), respectively. In contrast, tylosin was not detected at all. Mass losses of the compounds were also greater from the tramline plot due to greater runoff generation. These did not exceed 0.42% for sulphachloropyridazine and 0.07% for oxytetracycline however.     

Leachate chemistry of field-weathered spent mushroom substrate

Passive leaching by rainfall and snowmelt is a popular method to treat piles of spent mushroom substrate (SMS) before its reuse. During this field weathering process, leachate percolates into the underlying soils. A field study was conducted to examine the chemistry of SMS leachate and effects of infiltration. Two SMS piles were deposited (90 and 150 cm in height) over a Typic Hapludult and weathered for 24 mo. Leachate was collected biweekly using passive capillary samplers. The SMS leachate contained high concentrations of dissolved organic carbon (DOC; 0.8-11.0 g L(-1)), dissolved organic nitrogen (DON; 0.1-2 g L(-1)), and inorganic salts. The pH, electrical conductivity, and acid neutralizing capacity were 6.6 to 9.0, 21 to 66 ds m(-1), and 10 to 75 mmolc L(-1), respectively. Inorganic chemistry of the leachate was dominated by K+, Cl-, and SO24-. Leachate DOC was predominantly low molecular weight (<1000 Da) organic acids. During 2 yr of weathering, the 90-cm SMS pile released (per cubic meter of SMS) 3.0 kg of DOC, 1.6 kg of dissolved N, and 26.6 kg of inorganic salts. The 150-cm pile released (per cubic meter of SMS) 2.8 kg of DOC, 0.7 kg of dissolved N, and 13.6 kg of inorganic salts. The 150 cm pile retained more water and exhibited lower net nitrification compared with the 90-cm pile. The top 90 cm of soil retained 20 to 89% of the leachate solutes. Weathering of SMS in piles of 90 cm depth or greater may adversely affect ground water quality.