Phosphorus uptake of maize as affected by ammonium and nitrate nitrogen - Measurements and model calculations -

Phosphorus uptake is often enhanced by ammonium compared to nitrate nitrogen nutrition of plants. A decrease of pH at the soil-root interface is generally assumed as the cause. However, an alteration of root growth and the mobilization of P by processes other than net release of protons induced by the source of nitrogen may also be considered. To study these alternatives a pot experiment was conducted with maize using a fossil Oxisol high in Fe/Al-P with low soil solution P concentration. Three levels of phosphate (0, 50, 200 mg P kg^?1) in combination with either ammonium or nitrate nitrogen (100 mg N kg^?1) were applied. Plants were harvested 7 and 21 d after sowing, P uptake measured and root and shoot growth determined. To assess the importance of factors involved in the P transfer from soil into plants, calculations were made using a model of Barber and Claassen. In the treatments with no and low P supply NH₄-N compared to NO₃-N nutrition increased the growth of the plants by 25 % and their shoot P content by 38 % while their root growth increased by 6 % only. The rhizosphere pH decreased in the NH₄-N treatments by 0.1 to 0.6 units as compared to the bulk soil while in the NO₃-N treatments it increased by 0.1 to 0.5 units. These pH changes had a minor influence on P uptake only, as was demonstrated by artificially altering the soil pH to 4.7 and 6.3 respectively. At the same rhizosphere pH, however, P influx was doubled by the application of NH₄-compared to NO₃-N. It is concluded that in this soil the enhancement of P uptake of maize plants after ammonium application cannot be attributed to the acidification of the rhizosphere but to effects mobilizing soil phosphate or increasing P uptake efficiency of roots. Model calculation showed that these effects accounted for 53 % of the P influx per unit root length in the NO₃-N and 72 % in the NH₄-N supplied plants if no P was applied. With high P application the respective figures were only 18 and 19%.     

Prediction of deoxynivalenol and zearalenone concentrations in Fusarium graminearum inoculated backcross populations of maize by symptom rating and near‐infrared spectroscopy

Gibberella ear rot (GER) caused by Fusarium graminearum is a destructive disease in maize of temperate regions resulting in yield reduction and contamination by the mycotoxins deoxynivalenol (DON) and zearalenone (ZON). We wanted to analyse whether prediction of DON and ZON concentrations is feasible either by GER severity ratings or by near‐infrared spectroscopy (NIRS). We analysed 80 and 102 lines developed by backcrossing doubled‐haploid lines from segregating populations to the resistant and susceptible parent, respectively, by artificial infection at three locations in Germany and France. Both backcross (BC) populations differed substantially in their means for all traits with significant (P < 0.01) genotypic variances. DON and ZON concentrations measured by immunotests were significantly (P < 0.01) correlated with each other and with GER severity within each BC population (0.6 ≤ r ≤ 0.9, P < 0.01). DON concentration measured by immunotest and NIRS significantly correlated (r ≈ 0.9, P < 0.01). In conclusion, DON and ZON concentrations could be reliably predicted by GER severity. Additional NIRS analysis of DON concentration might be useful for the positively selected fraction.     

Diagnostic value of molecular markers for <Emphasis Type="Italic">Lr</Emphasis> genes and characterization of leaf rust resistance of German winter wheat cultivars with regard to the stability of vertical resistance

Breeding for resistance is an efficient strategy to manage wheat leaf rust caused by Puccinia triticina f. sp. tritici. However, a prerequisite for the directed use of Lr genes in breeding and the detection of new races virulent to these Lr genes is a detailed knowledge on Lr genes present in wheat cultivars. Therefore, respective molecular markers for 18 Lr genes were tested for specificity and used to determine Lr genes in 115 wheat cultivars. Results obtained were compared to available pedigree data. Using respective molecular markers, genes Lr1, Lr10, Lr26, Lr34 and Lr37 were detected, but data were not always in accordance with pedigree data. However, leaf rust scoring data of field trials confirmed the reliability of DNA markers. These reliable marker data facilitated the analyses of the development of virulent leaf rust races from 2002 to 2009 based on released cultivars. A sudden change from low infection rates to susceptibility was observed for Lr1, Lr3, Lr10, Lr13, Lr14, Lr16, Lr26 and Lr37 since 2006. Cultivars carrying several leaf rust resistance genes showed no significant shift to susceptibility except one cultivar which revealed an increasing infection rate at a low level. In summary, it turned out that pedigree data are often not reliable and a detection of Lr genes by diagnostic markers is fundamental to combine Lr genes in cultivars for a durable resistance against leaf rust, and to conduct reliable surveys based on released cultivars, instead of ‘Thatcher’ NILs.     

Degradation of Cry1Ab protein from genetically modified maize in the bovine gastrointestinal tract

Immunoblotting assays using commercial antibodies were established to investigate the unexpected persistence of the immunoactive Cry1Ab protein in the bovine gastrointestinal tract (GIT) previously suggested by enzyme-linked immunosorbent assay (ELISA). Samples of two different feeding experiments in cattle were analyzed with both ELISA and immunoblotting methods. Whereas results obtained by ELISA suggested that the concentration of the Cry1Ab protein increased during the GIT passage, the immunoblotting assays revealed a significant degradation of the protein in the bovine GIT. Samples showing a positive signal in the ELISA consisted of fragmented Cry1Ab protein of approximately 17 and 34 kDa size. Two independent sets of gastrointestinal samples revealed the apparent discrepancy between the results obtained by ELISA and immunoblotting, suggesting that the antibody used in the ELISA reacts with fragmented yet immunoactive epitopes of the Cry1Ab protein. It was concluded that Cry1Ab protein is degraded during digestion in cattle. To avoid misinterpretation, samples tested positive for Cry1Ab protein by ELISA should be reassessed by another technique.     

Pflanzenverfügbarkeit der Phosphatvorräte ackerbaulich genutzter Böden. -Langfristige Feldversuche zur Nutzbarkeit des Bodenphosphors und zur Bewertung der Bodenuntersuchung -

Availability of Phosphate Reserves in Arable Soils - Long Term Field Experiments for Assessing Soil P Reserves and Critical Soil Test Values - The objective of this work is to quantify the plant availability of soil P reserves accumulated by former fertilizer applications, the possibility of utilizing them by arable field crops and to determine critical soil test values. For this purpose several long term field experiments with large plots without replicates were initiated in 1977 on luvisols from loess (pH 6.8 – 7.4) in Lower Saxony with a sugar beet - winter wheat - winter barley/winter wheat crop rotation. Annual P applications were 0, 45, 90, 135 and 180 kg P₂O₅/ha as triple phosphate. Application of other fertilizers and plot management were according to farmer's practice. Despite of high yield levels phosphate response of plants was only 2 % at its maximum in the average of all crops in 15 years. This was confirmed by small plot experiments with four replicates placed into the large plots after 9 years, when soil P levels had been differentiated under the influence of plant P removal and P application. Herewith in agreement, shoot P concentration was found within the range generally regarded sufficient. It is therefore concluded that plant P demand has been fully satisfied by soil P reserves. Soil P test values, monitored by the P(H₂O) method of Sissingh, decreased markedly in 15 years, when no P was applied, they remained approximately constant when P application was equal to P removal and they increased when P addition was higher than P removal. Plants on a site with 4 mg P(H₂O)/L initially had severe P deficiency. Maximum yield was obtained when the soil P level was raised to 11 mg P(H₂O)/L. It is concluded that P reserves, which are often high in German arable soils, can be utilized by field crops and thus be lowered to about 10 mg P(H₂O)/L by reducing or omitting P dressings. For practical purposes it is suggested to restrict P application, if necessary at all, to the sugar beet crop in the rotation because they often respond more than small grain.     

Prediction of carbon mineralization rates from different soil physical fractions using diffuse reflectance spectroscopy

Soil carbon (C) mineralization rate is a key indicator of soil functional capacity but it is time consuming to measure using conventional laboratory incubation methods. Recent studies have demonstrated the ability of visible-near infrared spectroscopy (NIRS) for rapid non-destructive determination of soil organic carbon (SOC) and nitrogen (N) concentration. We investigated whether NIRS (350-2500 nm) can predict C mineralization rates in physically fractionated soil aggregates (bulk soil and 6 size fractions, n=108) and free organic matter (2 size fractions, n=27) in aerobically incubated samples from a clayey soil (Ferralsol) and a sandy soil (Arenosol). Incubation reference values were calibrated to first derivative reflectance spectra using partial least-squares regression. Prediction accuracy was assessed by comparing laboratory reference values with NIRS values predicted using full hold-out-one cross-validation. Cross-validated prediction for C respired (500 days) in soil aggregate fractions had an R² of 0.82 while that of C mineralized (300 days) in organic matter fractions was 0.71. Major soil aggregate fractions could be perfectly spectrally discriminated using a 50% random holdout validation sample. NIRS is a promising technique for rapid characterization of potential C mineralization in soils and aggregate fractions. Further work should test the robustness of NIRS prediction of mineralization rates of aggregate fractions across a wide range of soils and spectral mixture models for predicting mass fractions of aggregate size classes.     

A follow up study on antibodies against Lawsonia intracellularis in mares and foals from two breeding farms in Germany

Equine proliferative enteropathy (EPE) caused by Lawsonia (L.) intracellularis is an emerging disease in foals, particularly in North America. Since a case report in Germany exists, the objective of this study was to examine the incidence of L. intracellularis-antibodies in healthy horses from two German breeding farms. In group 1, serum samples from 24 (year 1) and 16 (year 2) Haflinger mares and their foals were taken. In group 2, over a period of five months, serum samples of six warmblood mares and foals were collected monthly from birth until the foals became seronegative. Serum samples were tested using an ELISA system. Results are expressed as Percentage of Inhibiton (PI). All adult mares (100%) of both groups were seropositive at each point in time (PI-value > 30). In group 1,7/24 foals (29.2%) in year 1 and 4/16 foals (25%) in year 2 had antibodies.The seropositive foals from year 2 had the same dams as the seropositive foals from year 1. In group 2 five of six foals were seropositive after birth. Antibodies decreased from March to July in mares and foals. In July, all five foals tested negative for the first time between the ages of 82 and 141 days (median 115 days). PI-values of mares were significantly correlated with PI-values of their foals. Higher PI-values were seen in younger foals and early in spring. Loss of antibodies in foals at the age of three to five months could be a risk factor for infection and appearance of EPE.     

Differentiation of viable, apoptotic and necrotic cells in bronchoalveolar lavage fluid of normal horses and horses with recurrent airway obstruction

Proinflammatoric cytokines are released extracellularly during necrosis. These lead to inflammation and destruction of surrounding tissues. The aim of this study was to compare the number of viable, apoptotic and necrotic cells in the bronchoalveolar lavage fluid (BALF) of normal horses and horses with recurrent airway obstruction (RAO) and to determine if fluorescence microscopy is a reliable method for this examination. A group of six normal horses and a group of ten horses with RAO were examined. Samples were assessed using annexin-V and propidium iodide immunofluorescence assay and examined by fluorescence microscopy (16 horses) and flow cytometry (nine of 16 horses). We found no significant differences in percentages of apoptotic and viable cells between both groups. The number of necrotic cells was significantly increased in horses with RAO counted by fluorescence microscopy. Cells with high granularity and macrophages had a significantly higher percentage of necrotic cells than lymphocytes. There was a good agreement between both methods. No significant differences were detected. The correlation between both methods is significant. Higher amounts of necrotic cells in the bronchial lumina of horses with RAO could be a reason for tissue damage and continuous lung tissue inflammation. Fluorescence microscopy was applicable for examination of BALF. Therapy should be aimed at the reduction of necrotic cells in the bronchial lumina. Further studies are required to find ways to reduce inflammatory cell infiltration and necrosis in bronchial lumina.