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Assessing mitigation of phosphorus (P) leaching from subsurface drainage systems is challenging due to high spatial and temporal variation in leaching. Mean measured total P leaching from a clayey soil in an eight-year study period (four replicates per treatment) was (kg ha -1  year -1 ): 1.21 from shallow autumn tillage (ShT), 0.84 from unfertilised fallow (UF), 0.81 from conventional autumn ploughing (CT) and 0.57 from structure liming (SL-CT). Treatment was not significant using Richards-Baker flow index or a distance factor as covariate (p = 0.084 and 0.057). A tendency for lower leaching was obtained comparing SL-CT with ShT (p adjusted  = 0.060 and 0.009 respectively). A combination of measures adapted to drainage conditions and clay content in different parts of the field is proposed since P leaching was approximately halved from an adjacent field (4.3 ha) in a three-year post-period compared with a three-year pre-period for structure liming the entire field and drainage system renovation plus structure lime drain backfilling.

To improve understanding of phosphorus (P) retention processes in small constructed wetlands (CWs), we analysed variations in sediment deposition and accumulation in four CWs on clay soils in east-central Sweden. Sediment deposition (in traps) generally exceeded the total suspended solids (TSS) load suggesting that resuspension and wetland base erosion were important. This was confirmed by quantification of particle accumulation (on plates) (1-23 kg m -2  year -1 ), which amounted to only 13-23% of trap deposition. Spatial mean P concentrations in accumulated sediment on plates (0.09-0.15%) were generally similar to temporal mean P concentrations of particles in water (0.11-0.15%). Deposition/accumulation was minor in one wetland with high hydraulic load (400 m year -1 ), suggesting that such small wetlands are not efficient as particle sinks. Economic support for CWs are given, but design and landscape position are here demonstrated to be important for effective P retention.

Horse paddocks have been identified as a significant contributor of animal waste nutrients to natural waters; thus, modified paddock management is needed. Because chemical amendments pose a health risk to horses, an alternative for reducing nutrient translocation from manure is to add available organic residues to the soil. To examine the feasibility of outdoor use of organic materials to reduce nutrient losses from paddock soils, three commonly available organic materials (peat, wheat straw, and wood chips) were tested for their nutrient retention capacities in batch experiments followed by leaching experiments in an in-house lysimeter station using artificial rainfall. Results showed that the grounded peat and wood chips retained some phosphorus (P), whereas grounded wheat straw released P to the solution. In leaching experiments, peat reduced nitrogen (N) losses by 40% but increased P and carbon (C) losses severalfold. Wheat straw was ineffective in reducing P, N, or C losses and in some cases increased the losses. Wood chips effectively reduced P and C losses, by 70 and 40%, respectively, but not N losses. It was concluded that, among the three organic materials, only the wood chips can be used outdoors to reduce nutrient losses from paddock soils., (Copyright © by the American Society of Agronomy, Crop Science Society of America, and Soil Science Society of America, Inc.)

The series of papers in this issue of AMBIO represent technical presentations made at the 7th International Phosphorus Workshop (IPW7), held in September, 2013 in Uppsala, Sweden. At that meeting, the 150 delegates were involved in round table discussions on major, predetermined themes facing the management of agricultural phosphorus (P) for optimum production goals with minimal water quality impairment. The six themes were (1) P management in a changing world; (2) transport pathways of P from soil to water; (3) monitoring, modeling, and communication; (4) importance of manure and agricultural production systems for P management; (5) identification of appropriate mitigation measures for reduction of P loss; and (6) implementation of mitigation strategies to reduce P loss. This paper details the major challenges and research needs that were identified for each theme and identifies a future roadmap for catchment management that cost-effectively minimizes P loss from agricultural activities.

Poland has the largest agricultural area within the Baltic Sea drainage basin and reducing the risk of phosphorus (P) and nitrogen (N) leaching from Polish soils to water is therefore essential. Increased acidity is known to reduce soil fertility and may trigger P leaching from non-calcareous soils. As part of advisor training, 25 farms each in Pomerania and north-western Mazovia were visited and 1500 ha arable soil, including 180 ha grassland soil, were monitored in 2013–2014. The soil was mainly coarse textured, but 25% of the Pomeranian farms were dominated by silty or clayey soils. More or less regular drainage systems were found on 20% of the farms, while 50% had simpler, older (>30 years) systems with a few single pipes. The farmers often used only ammonium sulphate or other acidifying N mineral fertiliser. Median pH on the Pomeranian farms, analysed in potassium chloride solution [pH(KCl)], was 5.2 and liming was advised for fields on most (72%) of these farms. Soil P content, measured by double-lactate extraction (PDL), was positively and significantly correlated (Pearson coefficient 0.57;p < .001) with soil pH and was generally higher for pig farms. Mean PDL(P given in elemental form) tended to be lower on dairy farms and arable farms and was significantly lower (mean 51 mg PDL kg−1soil) on mixed farms (with just a few cows and poultry) than on pig farms (mean 122 mg PDL kg−1soil). Farm-gate balances indicated deficits of P and potassium (K) on many of the small mixed farms in Pomerania and the soil can be expected to be nutrient depleted. In contrast, the pig farms demonstrated surplus farm-gate P balances (mean 27 kg ha−1). The P leaching risk is discussed relative to soil threshold values and to results from Swedish long-term field experiments. [ABSTRACT FROM PUBLISHER]

Lag times in reduced nutrient leaching after improved agricultural practices must be assessed to inform management decisions and evaluate their cost-effectiveness. This study estimated the leaching of phosphorus (P) and nitrogen (N) at two scales, a 33.8-ha nested field (data from 1973 to 2011) and an 820-ha agricultural catchment (data from 1992 to 2010). Field management was evaluated along with long-term nutrient trends. Estimates including and excluding nutrient concentrations in the stream under dry catchment conditions (mean 2.5 months year−1) revealed that wastewater contributed 10% of the total P (TP) catchment leaching, mostly in dissolved reactive (DRP) form. More recent flow-proportional sampling at the two scales demonstrated 45% higher particulate P leaching from the field than with discrete water sampling, whereas a past discrete sampling strategy may have overestimated DRP contributions to the stream. The accumulated field P balance was increasingly negative after 1987, whereas crop yields increased. From 1998, the measured accumulated TP leaching from the field was lower than the mean accumulated leaching, considering the estimated downward trend (−10%) over the 38-year study period ( p < 0.05). The average total N (TN) field leaching of 28 kg ha−1 year−1 (1973-2011) was 10% higher than the catchment leaching (1992-2010). The rates and timing of fields N and P fertilization became better adapted to crop requirements over time, and thereafter, a 14% reduction in TN leaching was estimated. No significant trends were estimated for catchment leaching for either TP or TN over the 18-year period, demonstrating an extended lag period for reduced nutrient leaching and the need for long-term monitoring of the effects of pollution mitigation. Copyright © 2014 John Wiley & Sons, Ltd. Highlights Time lag in P and N leaching responses to reduce nutrient surpluses, Close relationship with N export at nested scale, Scale effects in Q indices and PP transport, Point sources of pollution prolonging the time lag for DRP leaching mitigation [ABSTRACT FROM AUTHOR]

Catch crops are a potential option to reduce phosphorus (P) losses, but little is known about their establishment success and capacity to retain P on clayey soils in regions with short autumns, e.g. Sweden. This study screened biomass production and P retention by eight catch crop species: the perennials chicory ( Cichorium intybus L.), cocksfoot ( Dactylis glomerata L.), perennial ryegrass ( Lolium perenne L.) and red clover ( Trifolium pratense L.) and the annuals phacelia ( Phacelia tanacetifolia L.), white mustard ( Sinapis alba L.), oilseed radish ( Raphanus sativus L. oleiformis ) and white radish ( R. longipinnatus ). The catch crops were grown at six field sites, where the perennial species were under-sown with barley and the annual species were after-sown following barley harvest. Biomass production, P content in above-ground and below-ground plant parts and content of available P in the soil were determined in autumn and survival rate of the catch crops in the following spring. Biomass production and P retention in autumn both differed significantly between species ( p < 0.0001), and were greatly affected by site-specific conditions and time of sowing, which differed between experiments. Growth of catch crops can also be suppressed by low precipitation. Content of P in roots varied substantially between species, a factor which must be considered in species comparisons. The under-sown species produced more or equivalent amounts of biomass, retained more or equivalent amounts of P in autumn and survived better over winter than the after-sown species. Thus under-sown catch crops generally seem more suitable as catch crops for P. [ABSTRACT FROM AUTHOR]

Abstract Efficient phosphorus (P) fertilization strategies are essential for intensive crop production with minimal negative environmental impacts. A key factor in sustainable P use is assessment of the plant available soil P pool using soil P tests. This study determined isotopically exchangeable P after six days of reaction with 33PO 4 (P- E (6 d)) to determine how accurately two commonly used P tests, Olsen and AL (acid ammonium acetate lactate) can quantify the amount of labile P. Soil samples were taken from both highly P-amended and unamended plots at six sites within the Swedish long-term soil fertility experiments. According to P K-edge XANES spectroscopy, the P speciation was dominated by Al-bound P and organic P, with additional contributions from Fe-bound P and Ca phosphates in most soils. The results showed that the AL test overestimated P- E (6 d) by a factor of 1.70 on average. In contrast, the Olsen test underestimated P- E (6 d), with the mean ratios of P-Olsen to P- E (6 d) being 0.52 for high-P and 0.19 for low-P soils. The 33P/31P ratio in the Olsen extract of a 33PO 4 spiked soil was closer to that of a 0.005 mol L−1 CaCl 2 soil extract than the corresponding ratio in the AL extract, suggesting that AL extraction solubilized more non-labile P. In conclusion, the AL and Olsen methods are not suitable for direct quantification of the isotopically exchangeable soil P pool after 6 days of equilibration. However, based on the results, Olsen may be superior to AL for classification of soil P status, due to its even performance for calcareous and non-calcareous soils and lower extraction of non-labile P. Highlights • Extraction with sodium bicarbonate (Olsen) underestimated isotopically exchangeable P. • P fertilization increased the ratio of Olsen-P to isotopically exchangeable P. • AL extraction solubilized a large fraction of non-isotopically exchangeable P. • For classification purposes, the Olsen test is probably superior to AL. [ABSTRACT FROM AUTHOR]

With time, different soil-forming processes such as weathering, plant growth, accumulation of organic matter, and cultivation are likely to affect phosphorus (P) speciation. In this study, the depth distribution of P species was investigated for an agricultural clay soil, Lanna, Sweden. Small amounts of apatite-P was demonstrated in the topsoil whereas the speciation of P at 70–100 cm depth consisted of approximately 86% apatite according to P K-edge XANES (X-ray absorption near-edge structure) spectroscopy. Because there were only minor differences in bulk mineralogy and texture, these variations in P speciation were interpreted as the result of apatite weathering of the topsoil. Speciation modeling on soil extracts supported this idea: hydroxyapatite was not thermodynamically stable in the top 50 cm of the soil. Apatite was enriched in the bulk soil relative to the clay fraction, as expected during apatite dissolution. Combined results from batch experiments, XANES spectroscopy and X-ray diffraction suggested chemical transformations of the topsoil as a result from accumulation of organic matter and airing from tillage followed by enhanced weathering of apatite, amphiboles, clay minerals, and iron oxides. This caused the formation of poorly crystalline secondary iron and aluminum (hydr)oxides in the topsoil, which retained part of the released P from apatite. Other P was incorporated into organic forms. Furthermore, the results also showed that short-term acidification below the current pH value (below 5.5 in the topsoil and 7.2 in the deeper subsoil) caused significant solubilization of P. This is attributed to two different mechanisms: the instability of Al-containing sorbents (e.g. Al hydroxides) at low pH (in the topsoil), and the acid-mediated dissolution of apatite (the subsoil). [ABSTRACT FROM AUTHOR]