Phosphorus runoff from incorporated and surface-applied liquid swine manure and phosphorus fertilizer.

Excessive fertilization with organic and/or inorganic P amendments to cropland increases the potential risk of P loss to surface waters. The objective of this study was to evaluate the effects of soil test P level, source, and application method of P amendments on P in runoff following soybean [Glycine max (L.) Merr.]. The treatments consisted of two rates of swine (Sus scrofa domestica) liquid manure surface-applied and injected, 54 kg P ha(-1) triple superphosphate (TSP) surface-applied and incorporated, and a control with and without chisel-plowing. Rainfall simulations were conducted one month (1MO) and six months (6MO) after P amendment application for 2 yr. Soil injection of swine manure compared with surface application resulted in runoff P concentration decreases of 93, 82, and 94%, and P load decreases of 99, 94, and 99% for dissolved reactive phosphorus (DRP), total phosphorus (TP), and algal-available phosphorus (AAP), respectively. Incorporation of TSP also reduced P concentration in runoff significantly. Runoff P concentration and load from incorporated amendments did not differ from the control. Factors most strongly related to P in runoff from the incorporated treatments included Bray P1 soil extraction value for DRP concentration, and Bray P1 and sediment content in runoff for AAP and TP concentration and load. Injecting manure and chisel-plowing inorganic fertilizer reduced runoff P losses, decreased runoff volumes, and increased the time to runoff, thus minimizing the potential risk of surface water contamination. After incorporating the P amendments, controlling erosion is the main target to minimize TP losses from agricultural soils.

Phosphorus runoff: effect of tillage and soil phosphorus levels.

Continued inputs of fertilizer and manure in excess of crop requirements have led to a build-up of soil phosphorus (P) levels and increased P runoff from agricultural soils. The objectives of this study were to determine the effects of two tillage practices (no-till and chisel plow) and a range of soil P levels on the concentration and loads of dissolved reactive phosphorus (DRP), algal-available phosphorus (AAP), and total phosphorus (TP) losses in runoff, and to evaluate the P loss immediately following tillage in the fall, and after six months, in the spring. Rain simulations were conducted on a Typic Argiudoll under a corn (Zea mays L.)-soybean [Glycine max (L.) Merr.] rotation. Elapsed time after tillage (fall vs. spring) was not related to any form of P in runoff. No-till runoff averaged 0.40 mg L(-1) and 0.05 kg ha(-1) DRP and chisel-plow plots averaged 0.24 mg L(-1) and 0.02 kg ha(-1) DRP concentration and loads, respectively. The relationship between DRP and Bray P1 extraction values was approximated by a logistic function (S-shaped curve) for no-till plots and by a linear function for tilled plots. No significant differences were observed between tillage systems for TP and AAP in runoff. Bray P1 soil extraction values and sediment concentration in runoff were significantly related to the concentrations and amounts of AAP and TP in runoff. These results suggest that soil Bray P1 extraction values and runoff sediment concentration are two easily measured variables for adequate prediction of P runoff from agricultural fields.

Selection and characterization of a carrot cell line tolerant to glyphosate.

Cultured carrot (Daucus carota L.) cells were adapted to growing in 25 millimolar glyphosate by transfer into progressively higher concentrations of the herbicide. Tolerance was increased 52-fold, and the adaptation was stable in the absence of glyphosate. The uptake of glyphosate was similar for adapted and nonadapted cells. Activity of the enzyme 5-enolpyruvylshikimic acid-3-phosphate synthase was 12-fold higher in the adapted line compared to nonadapted cells, while activities of shikimate dehydrogenase and anthranilate synthase were similar in the two cell types. The adapted cells had higher levels of free amino acids-especially threonine, methionine, tyrosine, phenylalanine, tryptophan, histidine, and arginine-than did nonadapted cells. Glyphosate treatment caused decreases of 50 to 65% in the levels of serine, glycine, methionine, tyrosine, phenylalanine, and tryptophan in nonadapted cells, but caused little change in free amino acid levels in adapted cells.The adaptation reported here supports the growing body of evidence linking tolerance to glyphosate with increased levels of the enzyme 5-enolpyruvylshikimic acid-3-phosphate synthase. The elevated levels of aromatic amino acids, which may confer resistance in adapted cells, suggest that control of the shikimate pathway may be altered in these cells.

Effects of aspartate and other compounds on glyphosate uptake and growth inhibition in cultured carrot cells.

The strong correlation between glyphosate uptake and growth inhibition of cultured carrot (Daucus carota L. cv Danvers) cells incubated in the presence of aspartate suggests that aspartate reverses glyphosate inhibition of growth primarily by reducing intracellular glyphosate concentration. Other compounds which reverse glyphosate inhibition of cell growth gave a range of effects on glyphosate uptake: succinate, alpha-ketoglutarate, glutamate, pyruvate, and malate at 10 millimolar and phenylalanine at 2 millimolar reduced uptake by 0, 8, 11, 16, 27, and 34%, respectively. These results suggest that more than one mechanism of reversal may operate in these cells.Glyphosate and aspartate produced only minor effects on intracellular ammonia, media pH, and cell viability. This suggests that ammonia toxicity may not be an important mechanism of action of glyphosate in this system.

Influence of Leaf Starch Concentration on CO(2) Assimilation in Soybean.

Net photosynthetic rate, CO(2) compensation concentration, and starch and soluble sugar concentrations were measured in soybean (Glycine max [L.] Merrill) leaves in an attempt to evaluate the effect of carbohydrate concentration on rate of CO(2) assimilation.Plants were grown in a controlled environment room at 23.5 C, 50% relative humidity, 16-hour photoperiod, and quantum flux (400-700 nm) of 510 mueinsteins/m(2).sec (30,090 lux) at plant level. On the 21st day after seeding, plants were subjected for 12.5 hours to one of three CO(2) concentrations (50, 300, or 2000 mul/l) in an attempt to alter leaf carbohydrate levels. Following the CO(2) treatment, gas exchange measurements were made at a CO(2) concentration of 300 mul/l on the lowermost trifoliolate leaf. Immediately after measurement, the leaf was removed and stored at -20 C until carbohydrate analyses were performed.Increasing the CO(2) concentration for 12.5 hours significantly increased leaf starch concentration but not soluble sugar concentration. There was a strong negative correlation between net photosynthetic rate and starch concentration. Net photosynthetic rate declined from approximately 38 to 22 mg CO(2)/dm(2) leaf area.hr as starch concentration increased from 0.5 to 3 mg/cm(2) leaf area. Carbohydrate concentrations had no effect on compensation concentration.The decrease in net photosynthetic rate as starch concentration increased resulted from an increase in mesophyll (liquid phase) CO(2) diffusion resistance. This suggests that starch accumulation may reduce net photosynthetic rate by impeding intracellular CO(2) transport.