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R W McDowell

Publications and source records attributed to R W McDowell.

16 recordsLinked to original sources

Phosphorus movement and speciation in a sandy soil profile after long-term animal manure applications.

Long-term application of phosphorus (P) with animal manure in amounts exceeding removal with crops leads to buildup of P in soil and to increasing risk of P loss to surface water and eutrophication. In most manures, the majority of P is held within inorganic forms, but in soil leachates organic P forms often dominate. We investigated the mobility of both inorganic and organic P in profile samples from a noncalcareous sandy soil treated for 11 yr with excessive amounts of pig slurry, poultry manure, or poultry manure mixed with litter. Solution 31P nuclear magnetic resonance spectroscopy was used to characterize NaOH-EDTA-extractable forms of P, corresponding to 64 to 93% of the total P concentration in soil. Orthophosphate and orthophosphate monoesters were the main P forms detected in the NaOH-EDTA extracts. A strong accumulation of orthophosphate monoesters was found in the upper layers of the manure-treated soils. For orthophosphate, however, increased concentrations were found down to the 40- to 50-cm soil layers, indicating a strong downward movement of this P form. This was ascribed to the strong retention of orthophosphate monoesters by the solid phase of the soil, preventing orthophosphate sorption and facilitating downward movement of orthophosphate. Alternatively, mineralization of organic P in the upper layers of the manure-treated soils may have generated orthophosphate, which could have contributed to the downward movement of the latter. Leaching of inorganic P should thus be considered for the assessment and the future management of the long-term risk of P loss from soils receiving large amounts of manure.

Animals↗

Phosphorus and sediment loss in a catchment with winter forage grazing of cropland by dairy cattle.

The loss of phosphorus and sediment to surface waters can impair their quality. It was hypothesized that the practice of winter grazing dairy cattle on cropland of moderate slope (5-20%) would exacerbate the loss of P and suspended sediment (SS) from land to water. In a small (4.3 ha) catchment two flumes were installed, upstream and downstream of one field (about 2 ha) that had been cropped for 2 yr and grazed in winter (June-July) by dairy cattle. Flow proportional samples were taken and measured for dissolved reactive phosphorus (DRP), particulate phosphorus (PP), total phosphorus (TP), and SS. During the 2002 hydrologic year (March-February) loads of SS increased per hectare downstream (1449 kg ha(-1)) compared to upstream (880 kg ha(-1)). The same increase from upstream (873 kg ha(-1)) to downstream (969 kg ha(-1)) happened in 2003. However, while in 2003 TP increased downstream by 1.64 kg ha(-1) compared to upstream (0.24 kg ha(-1)), in 2002 an increase of only 0.006 kg ha(-1) at the downstream flume occurred compared to upstream (0.98 kg ha(-1)). Investigation of P transport pathways suggested that overland flow contributed <0.1 kg P ha(-1) to stream flow, 10 and 5% of TP load in 2002 and 2003, with the greater load in 2002 reflecting more rainfall in that year. The contribution to stream flow by subsurface flow was estimated at 0.3 kg P ha(-1). Stream bed sediments showed an increase in total P concentration in summer when no flow occurred due to the admission by the farmer of 10 cattle upstream of the cropped paddock in summer 2001-2002 and 20 cattle between the two flumes in 2003 to graze stream banks. This action was calculated to contribute via dung at least, the remaining P lost: about 0.5 kg P in 2002 and 1.0 kg P in 2003. Clearly, not allowing animals to "clear-up" stream banks is a priority if good surface water quality is to be achieved. Furthermore, compared to stock access the impact of winter grazing cropland on P losses was minimal, but SS load was increased by an average of 75%.

Animal Husbandry↗

An examination of spin-lattice relaxation times for analysis of soil and manure extracts by liquid state phosphorus-31 nuclear magnetic resonance spectroscopy.

Phosphorous (P)-31 nuclear magnetic resonance (NMR) spectroscopy is used in the analysis of P forms in extracts of soils and manures for environmental and agronomic purposes. Quantitative spectra require knowledge about spin-lattice relaxation times (T1) to ensure adequate delays between pulses. This paper determined T1 values of P forms in reconstituted (0.2 g in 0.7 mL(-1)) samples of freeze-dried 0.25 M NaOH plus 50 mM EDTA extracts of eight diverse soils (Aquept, Dystrochrept x 2, Hapludand, Rendoll, Udand, Haplostoll, and Orthod), three different manures (dairy cattle, deer, and sheep), and one epiphyte moss. Total concentrations in the reconstituted samples ranged from 5 to 175 mg Fe mL(-1), 2 to 62 mg Mn mL(-1), and 72 to 837 mg P mL(-1). Values of T1 for orthophosphate monoesters, orthophosphate diesters, and pyrophosphate varied from 0.42 to 1.69 s in soils and from 0.89 to 2.59 s in manures and the epiphyte. In contrast, T(1) for orthophosphate varied from 0.78 to 1.94 s in soils and 1.45 to 5.82 s in manures and the epiphyte. For quantitative 31P NMR, delay times should be three to five times the T1 value, translating to delays of 3 to 5 s for soils and up to 25 s for manures. If the required delay is too long then strategies such as adding paramagnetics could shorten T1, provided this does not increase line-broadening too much. A regression relationship was obtained between orthophosphate T1 values and the ratio of P concentration to Fe and Mn concentration on a w/v basis (r2= 0.97, P < 0.001), and between the T1 for all other compound classes and the ratio of P to Fe and Mn (r2= 0.70, P < 0.01). By combining measurement of Fe, Mn, and P in the reconstituted extract and these relationships, T1 can be estimated and the appropriate delay time used. If T1 is not considered and the delay time is too short, some peaks will be under- or over-represented and the relative distribution of P forms not quantitative.

Animals↗

Mechanisms of phosphorus solubilisation in a limed soil as a function of pH.

Phosphorus (P) quantity-intensity relationships are central to the solubility and release of P from soil to water. Relationships between P extractable by 0.5 M NaHCO extractable P (Olsen P; quantity, Q) and P extractable by 0.01 M CaCl(2) (CaCl(2)-P; possible predictor of soil solution or drainage water P; intensity, I) are curvilinear: above a certain Olsen P concentration, CaCl(2)-P becomes much more soluble than when below it. Aluminium-, Fe- and Ca-P forms (extractable by Olsen's reagent) are thought to control P solubility. Thus, our objectives were to identify P forms in equilibrium with CaCl(2)-P via solubility equilibrium experiments, and the behaviour of CaCl(2)-P in relation to Al, Fe and Ca associated P, determined with 31P high power decoupling magic angle spinning nuclear magnetic resonance spectroscopy (31P HPDec/MAS NMR). Results indicated that two Q-I relationships occurred, one for soils above pH 5.8, and the other for soils below pH 5.8. Above pH 5.8, soils were saturated with respect to hydroxyapatite (Ca(5)(PO(4))(3)OH) and undersaturated with respect to beta-tricalcium phosphate (beta-Ca(3)(PO(4))(2)), while log ion-activity products showed that all soils and pHs were either saturated or in equilibrium with variscite (AlPO(4).2H(2)O) or its amorphous analogue. Using 31P HPDec/MAS NMR, Ca-P was best correlated with CaCl(2)-P in soils above pH 5.8, and with Al-P in soils below this pH. This study demonstrates the value of solid-state NMR in conjunction with wet chemical techniques for the study of labile P and P loss from pasture soils with a wide range of managements.

Calcium Compounds↗

Soil phosphorus quantity-intensity relationships to predict increased soil phosphorus loss to overland and subsurface flow.

Soil phosphorus (P) quantity-intensity (q-i) relationships, based on common extraction methods, may potentially be used to estimate the risk of P loss in overland flow and subsurface drainage water. Some workers have used nonlinear q-i relationships to derive thresholds in soil test P (STP; a quantity factor) above which the risk of P loss increases, while others find linear relationships and no threshold. We present here a simple modelling exercise (based on Langmuir adsorption theory) along with data from literature to explain the behaviour of q-i relationships, and to give an explanation for this apparent discrepancy. The data indicate that q-i relationships are dependent upon the soil to solution ratio of the P intensity parameter, adsorption capacity (Qmax) and strength (K) of the soil, and the total range in STP. In turn, this affects the calculation of a threshold in STP. The q-i relationship tends towards linearity under conditions of a narrow total range of STP and/or when using a wide soil to solution ratio for estimating the P intensity parameter. Under such conditions, a threshold is difficult to detect, and uncertain. We conclude that the sensitivity of thresholds to experimental conditions and soils needs to be considered if thresholds are to be successful in environmental management to decrease P loss to surface waters.

Phosphorus↗

Phosphorus losses in subsurface flow before and after manure application to intensively farmed land.

A study was conducted to examine the loss of P in subsurface flow from three cultivated soils of varying soil P concentrations. Measurements were made in flow waters from the soils before applying manure and then 3 weeks after sowing the soils to grass. An additional measurement of P in flow waters was made 1 year later. Dissolved reactive P (DRP) concentrations measured in flow water before (0.15-0.20 mg l(-1)) and after (0.39-0.51 mg l(-1)) manure application exceed current estimates of those required to promote surface water eutrophication (0.05 mg l(-1)). Concentrations of DRP1 year after manurial application increased compared to 3 weeks after application and was attributed to the slow movement of P down the cultivated soil. Concentrations of soil P were significantly increased down the soil profile and attributed to the P saturation of soils before manurial application. The results suggest that despite the establishment of fast growing grass, P concentrations would not be mitigated in the short-term (= 1 year), due to the large contribution of P in subsurface pathways.

Agriculture↗

Soil phosphorus fractions in solution: influence of fertiliser and manure, filtration and method of determination.

This study investigated the forms of soil P released to solution, accuracy of their determination, and influence of colloids on P sorption/desorption dynamics. A Hagerstown silt loam, amended with dairy and poultry manure or superphosphate at five rates (0, 25, 50, 100, and 200 kg P ha(-1)), was extracted at two soil:solution ratios (1:5 and 1:100) and filtered at three pore sizes (0.8, 0.45, and 0.22 microm). Results showed that relative to the proportion of dissolved organic P (DOP, determined as the difference between total dissolved P [TDP] and P detected by ion chromatography), DRP increased with amendment rate. Relative to Mehlich-3 extractable P, DRP exhibited a power relationship with a much greater potential for soil P release at concentrations in excess of ca. 50 mg Mehlich-3 P kg(-1). Concentrations of DRP, determined by the acid molybdate method, were on average 12.5% greater than P detected by ion chromatography indicating P was solubilised during colorimetric determination. A linear relationship was found between total Al and DRP, which could indicate acid mediated hydrolysis of A1-humic-P substances, although acid mediated desorption of P from colloids cannot be discounted. No difference in solubilised P was found between solutions filtered at 0.22 and 0.45 microm, but was found between 0.8 microm and smaller filter sizes. Organic P extracted from manured soils was more recalcitrant than that extracted from soils amended with superphosphate, the later attributed to its accumulation in more labile pools. The sorption/desorption of P by colloids in solution were greatly affected by the rate of amendment and the soil:solution extraction ratio. More P was sorbed by superphosphate solutions compared to dairy manure amended soil solutions and was attributed to the saturation of colloidal P sorption sites by organic matter. In order to minimise the effects of colloids on P dynamics and the potential for hydrolysis in solution, filtration to at least 0.45 microm is required. However, soils with a lesser aggregate stability may require additional filtration.

Absorption↗

Fatal hemorrhage caused by varicose veins.

Varicose veins are a common, worldwide medical problem, but are generally considered non-life-threatening. We report three cases of fatal hemorrhage resulting from varicose veins and review the literature. The pathology of acute perforations onto the skin surface in varicose venous disease is described.

Aged↗

Assessing site vulnerability to phosphorus loss in an agricultural watershed.

A P index was developed as a tool to rank agricultural fields on the basis of P loss vulnerability, helping to target remedial P management options within watersheds. We evaluated two approaches, a soil P threshold and components of a P index, by comparing site vulnerability estimates derived from these two approaches with measured runoff P losses in an agricultural watershed in Pennsylvania. Rainfall-surface runoff simulations (70 mm h(-1) for 30 min) were conducted on 57 sites representing the full range of soil P concentrations and management conditions found in the watershed. Each site was comprised of two, abutting 2-m2 runoff plots, serving as duplicate observations. For sites that had not received P additions for at least six months prior to the study, Mehlich-3 P concentration was strongly associated with dissolved P concentrations (r2 = 0.86) and losses (r2 = 0.83) in surface runoff, as well as with total P concentration (r2 = 0.80) and loss (r2 = 0.74). However, Mehlich-3 P alone was poorly correlated with runoff P from sites receiving manure within three weeks prior to rainfall. The P index effectively described 88 and 83% of the variability in dissolved P concentrations and losses from all sites in the watershed, and P index ratings exhibited strong associations with total P concentrations (r2 = 0.81) and losses (r2 = 0.79). When site-specific observations were extrapolated to all fields in the watershed, management recommendations derived from a P index approach were less restrictive than those derived from the soil P threshold approach, better reflecting the low P loads exported from the watershed.

Agriculture↗

Approximating phosphorus release from soils to surface runoff and subsurface drainage.

Phosphorus application in excess of crop needs has increased the concentration of P in surface soil and runoff and led many states to develop P-based nutrient management strategies. However, insufficient data are available relating P in surface soil, surface runoff, and subsurface drainage to develop sound guidelines. Thus, we investigated P release from the surface (0-5 cm depth) of a Denbigh silt loam from Devon, U.K. (30-160 mg kg-1 Olsen P) and Alvin, Berks, Calvin, and Watson soils from Pennsylvania (10-763 mg kg-1 Mehlich-3 P) in relation to the concentration of P in surface runoff and subsurface drainage. A change point, where the slopes of two linear relationships between water- or CaCl2-extractable soil P and soil test phosphorus (STP) (Olsen or Mehlich-3) meet, was evident for the Denbigh at 33 to 36 mg kg-1 Olsen P, and the Alvin and Berks soils at 185 to 190 mg Mehlich-3 P kg-1. Similar change points were also observed when STP was related to the P concentration of surface runoff (185 mg kg-1) and subsurface drainage (193 mg kg-1). The use of water and CaCl2 extraction of surface soil is suggested to estimate surface runoff P (r2 of 0.92 for UK and 0.86 for PA soils) and subsurface drainage P (r2 of 0.82 for UK and 0.88 for PA soils), and to determine a change point in STP, which may be used in support of agricultural and environmental P management.

Forecasting↗

The effects of soil carbon on phosphorus and sediment loss from soil trays by overland flow.

Soil chemical constituents influence soil structure and erosion potential. We investigated manure and inorganic fertilizer applications on soil chemistry (carbon [C] quality and exchangeable cations), aggregation, and phosphorus (P) loss in overland flow. Surface samples (0-5 cm) of a Hagerstown (fine, mixed, semiactive, mesic Typic Hapludalf) soil, to which either dairy or poultry manure or triple superphosphate had been applied (0-200 kg P ha(-1) yr(-1) for 5 yr), were packed in boxes (1 m long, 0.15 m wide, and 0.10 m deep) to field bulk density (1.2 g cm(-3)). Rainfall was applied (65 mm h(-1)), overland flow collected, and sediment and P loss determined. All amendments increased Mehlich 3-extractable P (19-177 mg kg(-1)) and exchangeable Ca (4.2-11.5 cmol kg(-1)) compared with untreated soil. For all treatments, sediment transport was inversely related to the degree of soil aggregation (determined as ratio of dispersed and undispersed clay; r = 0.51), exchangeable Ca (r = 0.59), and hydrolyzable carbohydrate (r = 0.62). The loss of particulate P and total P in overland flow from soil treated with up to 50 kg P ha(-1) dairy manure (9.9 mg particulate phosphorus [PPI, 15.1 mg total phosphorus [TP]) was lower than untreated soil (13.3 mg PP, 18.1 mg TP), due to increased aggregation and decreased surface soil slaking attributed to added C in manure. Manure application at low rates (<50 kg P ha(-1)) imparts physical benefits to surface soil, which decrease P loss potential. However, at greater application rates, P transport is appreciably greater (26.9 mg PP, 29.5 mg TP) than from untreated soil (13.3 mg PP, 18.1 mg TP).

Carbon↗

Uptake and release of phosphorus from overland flow in a stream environment.

Phosphorus runoff from agricultural fields has been linked to fresh-water eutrophication. However, edge-of-field P losses can be modified by benthic sediments during stream flow by physiochemical processes associated with Al, Fe, and Ca, and by biological assimilation. We investigated fluvial P when exposed to stream-bed sediments (top 3 cm) collected from seven sites representing forested and agricultural areas (pasture and cultivated), in a mixed-land-use watershed. Sediment was placed in a 10-m-long, 0.2-m-wide fluvarium to a 3-cm depth and water was recirculated over the sediment at 2 L s(-1) and 5% slope. When overland flow (4 mg dissolved reactive phosphorus [DRP] and 9 mg total phosphorus [TP] L(-1)) from manured soils was first recirculated, P uptake was associated with Al and Fe hydrous oxides for sediments from forested areas (pH 5.2-5.4) and by Ca for sediments from agricultural areas (pH 6.5-7.2). A large increase (up to 200%) in readily available P NH4Cl fraction was noted. After 24 h, DRP concentration in channel flow was related to sediment solution P concentration at which no net sorption or desorption of P occurs (EPC0) (r2 = 0.77), indicating quasi-equilibrium. When fresh water (approximately 0.005 mg P L(-1) mean base flow DRP at seven sites) was recirculated over the sediments for 24 h, P release kinetics followed an exponential function. Microbial biomass P accounted for 34 to 43% of sediment P uptake from manure-rich overland flow. Although abiotic sediment processes played a dominant role in determining P uptake, biotic process are clearly important and both should be considered along with the location and management of landscape inputs for remedial strategies to be effective.

Agriculture↗

Particulate phosphorus transport within stream flow of an agricultural catchment.

There is interest in quantifying phosphorus (P) loss from intensively grazed dairy landscapes to identify key pathways and target remediation methods. The Bog Burn drains a dairying catchment in Southland, New Zealand, and has been monitored at fortnightly intervals over a 12-mo period at four sites for suspended sediment (SS), dissolved reactive phosphorus (DRP), and total phosphorus (TP). Time-integrated samplers, deployed at 0.6 median water depth at each site (calculated from previous year's flow data), collected sediment samples, which were analyzed for SS, bioavailable phosphorus (BAP), and TP. Mean concentrations of DRP and TP in stream flow and BAP and TP in sediment were generally highest in summer or autumn (0.043 mg DRP L(-1), 0.160 mg TP L(-1), 173 mg BAP kg(-1), 2228 mg TP kg(-1)) and lowest in winter or spring (0.012 mg DRP L(-1), 0.034 mg TP L(-1), 6 mg BAP kg(-1), 711 mg TP kg(-1)), while loads were highest in winter. Analysis of (137)Cs concentrations in trapped sediment, topsoil, subsoil, and stream bed and bank sediment indicated that trapped sediment was derived from topsoil and entered the stream either through tile drainage or, to a lesser extent, overland flow. Because concentrations of DRP and TP in stream flow are in excess of recommended limits for good water quality (>0.01 mg DRP L(-1), 0.033 mg TP L(-1)), management should focus on the topsoil and specifically on decreasing P loss via tile drainage. This is best achieved by decreasing soil Olsen P concentrations, especially because, on average, Olsen P concentrations in the catchment were above the agronomic optimum.

Agriculture↗

Phosphorus in fresh and dry dung of grazing dairy cattle, deer, and sheep: sequential fraction and phosphorus-31 nuclear magnetic resonance analyses.

Knowledge of phosphorus (P) fractions in dung of animals (dairy cattle, deer, sheep) grazing pasture is important for soil fertility and the potential for P transport in runoff and subsequent surface water quality deterioration. We used sequential fractionation and 31P nuclear magnetic resonance (NMR) spectroscopy to determine P forms in fresh and air-dried (to simulate field conditions during grazing) dung. Sheep dung was richest in P (8 g kg(-1)), and cattle dung poorest (5.5 g kg(-1)). Data for sequential fractionation indicated that most P was extractable by water (15-36%) and bicarbonate (36-45%) in fresh dung, and shifted toward recalcitrant, HCl (12-28%), and residual P forms (15-31%) with drying. Organic P concentration in dung was poor (maximum of 15% of total P), probably due to the poor concentration of phytate in pasture. The 31P NMR spectra of NaOH-EDTA extracts supported this by detecting a low concentration of monoesters (9-19% of total P in extracts), of which phytate is a major component. The 31P NMR data also showed that changes in organic P concentration with drying could be due to the degradation of diesters. Data indicate the decreasing bioavailability of dairy cattle, deer, and sheep dung with drying and the need to consider this effect with respect to P returns for soil fertility and the potential for runoff.

Animals↗

Analysis of potentially mobile phosphorus in arable soils using solid state nuclear magnetic resonance.

In many intensive agroecosystems continued inputs of phosphorus (P) over many years can significantly increase soil P concentrations and the risk of P loss to surface waters. For this study we used solid-state 31P nuclear magnetic resonance (NMR) spectroscopy, high-power decoupling with magic angle spinning (HPDec-MAS) NMR, and cross polarization with magic angle spinning (CP-MAS) NMR to determine the chemical nature of potentially mobile P associated with aluminum (Al) and calcium (Ca) in selected arable soils. Three soils with a range of bicarbonate-extractable Olsen P concentrations (40-102 mg P kg(-1)) were obtained from a long-term field experiment on continuous root crops at Rothamsted, UK, established in 1843 (sampled 1958). This soil has a threshold or change point at 59 mg Olsen P kg(-1), above which potentially mobile P (as determined by extraction with water or 0.01 M CaCl2) increases much more per unit increase in Olsen P than below this point. Results showed that CaCl2 and water preferentially extracted Al-P and Ca-P forms, respectively, from the soils. Comparison among the different soils also indicated that potentially mobile P above the threshold was largely present as a combination of soluble and loosely adsorbed (protonated-cross polarized) P forms largely associated with Ca, such as monetite (CaHPO4) and dicalcium phosphate dihydrate (CaHPO4-2H2O), and some Al-associated P as wavellite. The findings of this study demonstrate that solid-state NMR has the potential to provide accurate information on the chemical nature of soil P species and their potential mobility.

Agriculture↗