Alum reduced phosphorus release from flooded soils under cold spring weather conditions.

The effectiveness of amendments such as alum [Al2 (SO4 )3 ·18H2 O] in reducing phosphorus (P) loss to floodwater has been reported under summer conditions and laboratory-controlled environments, but not under actual spring weather conditions in cold climate regions with high diurnal temperature variations when potential for P losses is high. The effectiveness of alum in reducing P release under Manitoba spring weather conditions was evaluated in a 42-day experiment using 15-cm soil monoliths from eight agricultural soils, which were unamended or alum-amended (5 Mg ha-1 ) and flooded to a 10-cm head. Dissolved reactive P (DRP) concentrations and pH of porewater and floodwater were determined on flooding day and every 7 days after flooding (DAF). Porewater and floodwater DRP concentrations in unamended soils increased 1.4- to 4.5-fold, and 1.8- to 15.3-fold, respectively, from 7 to 42 DAF. In alum-amended soils, DRP concentrations averaged across soils was 43%-73% (1.0-2.0 mg L-1 ) lower in porewater, and 27%-64% (0.1-1.2 mg L-1 ) lower in floodwater than unamended soils during the flooding period. The reduction of DRP by alum was more pronounced under high fluctuating diurnal spring air temperature than with controlled air temperature (4°C) in a previous similar study. Acidic pH in porewater and floodwater due to alum did not persist over 7 days. This study showed that alum application is a viable option in reducing P released to floodwater in agricultural soils of cold regions where flooding-induced P loss is prevalent in the spring.

Phosphorus speciation of sequential extracts of organic amendments using nuclear magnetic resonance and X-ray absorption near-edge structure spectroscopies.

The chemical forms of phosphorus in organic amendments are essential variables for proper management of these amendments for agro-environmental purposes. This study was performed to elucidate the forms of phosphorus in various organic amendments using state-of-the-art spectroscopic techniques. Anaerobically digested biosolids (BIO), hog (HOG), dairy (DAIRY), beef (BEEF), and poultry (POULTRY) manures were subjected to sequential extraction. The extracts and residues after extraction were analyzed by solution (31)P nuclear magnetic resonance (NMR) and synchrotron-based P 1s X-ray absorption near-edge structure (XANES) spectroscopies, respectively. Most of the total P analyzed by inductively coupled plasma- optical emission spectroscopy in the sequential extracts of organic amendments was orthophosphate, except POULTRY, which was dominated by organic P. The labile P fraction in all the organic amendments, excluding POULTRY, was mainly orthophosphate from readily soluble calcium and some aluminum phosphates. In the poultry litter, Ca phytate was the main P species controlling P solubility. The recalcitrant fraction of BIO was mainly associated with Al and Fe. Those of HOG, DAIRY, and POULTRY were calcium phytate, which were identified only as organic species in the XANES spectra. The combination of the three techniques-sequential chemical extraction, solution (31)P NMR spectroscopy, and P 1s XANES-provided molecular characterization of P in organic amendments that would not have been possible with just one or a combination of any two of these techniques. Therefore, P speciation of organic amendments should use solid-phase and aqueous speciation techniques as deemed feasible.

Predicting phosphorus availability from soil-applied composted and non-composted cattle feedlot manure.

Prediction of phosphorus (P) availability from soil-applied composts and manure is important for agronomic and environmental reasons. This study utilized chemical properties of eight composted and two non-composted beef cattle (Bos taurus) manures to predict cumulative phosphorus uptake (CPU) during a 363-d controlled environment chamber bioassay. Ten growth cycles of canola (Brassica napus L.) were raised in pots containing 2 kg of a Dark Brown Chernozemic clay loam soil (fine-loamy, mixed, Typic Haploboroll) mixed with 0.04 kg of the amendments. Inorganic P fertilizer (KH2PO4) and an unamended control were included for comparison. All treatments received a nutrient solution containing an adequate supply of all essential nutrients, except P, which was supplied by the amendments. Cumulative P uptake was similar for composted (74 mg kg-1 soil) and non-composted manures (60 mg kg-1 soil) and for the latter and the fertilizer (40 mg kg-1 soil). However, the CPU was significantly higher for organic amendments than the control (24 mg kg-1 soil) and for composted manure than the fertilizer. Apparent phosphorus recovery (APR) from composted manure (24%) was significantly lower than that from non-composted manure (33%), but there was no significant difference in APR between the organic amendments and the fertilizer (27%). Partial least squares (PLS) regression indicated that only two parameters [total water-extractable phosphorus (TPH2O) and total phosphorus (TP) concentration of amendments] were adequate to model amendment-derived cumulative phosphorus uptake (ACPU), explaining 81% of the variation in ACPU. These results suggest that P availability from soil-applied composted and non-composted manures can be adequately predicted from a few simple amendment chemical measurements. Accurate prediction of P availability and plant P recovery may help tailor manure and compost applications to plant needs and minimize the buildup of bioavailable P, which can contribute to eutrophication of sensitive aquatic systems.