Response of maize (Zea mays) to the application of foliar fertilizers in the Sudan and Guinea savanna zone of Nigeria

Soil fertility problems resulting in low maize yields in smallholder farms are common in the West African moist savanna. The effectiveness of commercial foliar fertilizers in improving maize growth and yield was evaluated in three savanna agro‐ecological zones of Nigeria in two steps. In step one, eight commercial foliar fertilizers were assessed in a greenhouse study with two soil types using maize (Zea mays L. cv. 2004 TZE‐Y POPDT STR C4). The treatments included a control and a reference that received the optimum concentrations of nutrients. In step 2, three promising products from the greenhouse study (Turbotop, Agroleaf General, and Agroleaf high‐P) were evaluated under field conditions to validate the efficacy of products to enhance crop growth and yield. The foliar products were applied at the rate of 5 kg ha^?1. The treatments also included three rates of P application (0, 30, and 60 kg P ha^?1) as triple super phosphate (TSP) with or without foliar fertilizers. In the greenhouse study, differences in maize shoot dry matter yield and N and P concentrations, attributable to the spraying of the commercial foliar fertilizers, were observed for both soils. Spraying Turbotop, Agroleaf General, and Agroleaf high‐P gave the highest shoot dry biomass and N and P uptake compared to other products. Under field conditions, foliar spraying of Agroleaf high‐P significantly increased the shoot dry biomass of maize compared with the 0 P treatment in all locations. The grain yield of maize ranged from 1 to 4 t ha^?1 with significant differences across sites. Products with high concentrations of P and N in their formulation improved maize yield suggesting that appropriate management of P and N resources is a prerequisite for a sustainable maize intensification in the savanna agro‐ecologies.     

Contribution of nitrification and denitrification to the emission of N2O in a freeze‐thaw event in an agricultural soil

The amounts of N₂O released in freeze‐thaw events depend on site and freezing conditions and contribute considerably to the annual N₂O emissions. However, quantitative information on the N transformation rates in freeze‐thaw events is scarce. Our objectives were (1) to quantify gross nitrification in a Luvisol during a freeze‐thaw event, (2) to analyze the dynamics of the emissions of N₂O and N₂, (3) to quantify the contribution of nitrification and denitrification to the emission of N₂O, and (4) to determine whether the length of freezing and of thawing affects the C availability for the denitrification. ¹⁵NO was added to undisturbed soil columns, and the columns were subjected to 7 d of freezing and 5 d of thawing. N₂O emissions were determined in 3 h intervals, and the concentrations of ¹⁵N₂O and ¹⁵N₂ were determined at different times during thawing. During the 12 d experiment, 5.67 mg NO ‐N (kg soil)^–1 was produced, and 2.67 mg NO ‐N (kg soil)^–1 was lost. By assuming as a first approximation that production and loss occurred exclusively during thawing, the average nitrate‐production rate, denitrification rate, and immobilization rate were 1.13, 0.05, and 0.48 mg NO ‐N (kg soil)^–1 d^–1, respectively. Immediately after the beginning of the thawing, denitrification contributed by 83% to the N₂O production. The ratios of ¹⁵N₂ to ¹⁵N₂O during thawing were narrow and ranged from 1.5 to 0.6. For objective (4), homogenized soil samples were incubated under anaerobic conditions after different periods of freezing and thawing. The different periods did not affect the amounts of N₂ and N₂O produced in the incubation experiments. Further, addition of labile substrates gave either increases in the amounts of N₂O and N₂ produced or no changes which suggested that changes in nutrient availability due to freezing and thawing are only small.     

Ray tracheids in Pinus radiata are more highly resistant to soft rot as compared to axial tracheids: relationship to lignin concentration

A visual decay assessment of Pinus radiata wood, which was part of a framing timber in a house in the North Island of New Zealand, indicated the presence of surface decay. Microscopic observations, employing confocal laser scanning microscopy (CLSM), scanning electron microscopy (SEM) and transmission electron microscopy (TEM), provided evidence of decay by cavity-forming soft rot (SR) fungi. A comparison of ray tracheids (RT) with axial tracheids (AT) indicated that RT were considerably more resistant to SR than AT. In the heavily degraded regions of wood, where axial tracheid walls contained abundant SR cavities, the walls of RT contained only a few or no cavities. An assessment of lignin concentration in the cell walls by a combination of TEM, confocal fluorescence and UV microscopy provided evidence of greater lignin concentration in the secondary wall of RT as compared to AT, which may explain the observed greater resistance of RT to soft rot. Dedicated to Professor Dr. Dr. h.c. mult. Walter Liese on the occasion of his 80th birthday.     

Molecular characterization of dimeric alpha-amylase inhibitor genes in wheat and development of genome allele-specific primers for the genes located on chromosome 3BS and 3DS

Alpha-amylase inhibitors are attractive candidates for the control of seed weevils as these insects are highly dependent on starch as an energy source. For weevil control, alpha-amylase inhibitors and their genes could be used to genetically engineer weevil resistant seeds. Thirty genes encoding dimeric alpha-amylase inhibitors were isolated from Triticum aestivum L. ‘Chinese Spring’ and characterized by nucleotide and amino acid sequence analysis. Eleven representative alpha-amylase inhibitor genes were identified, and the deduced amino acid sequences of these genes were of high coherence (95.1%). These inhibitors and others obtained from the wheat EST database were clustered into three groups, the genes from ‘Chinese Spring’ were present in each group. Specific primer sets were designed for each group, based on the SNPs of these genes, and the chromosome locations of each group of inhibitor genes investigated by amplification of the ‘Chinese Spring’ ditelosomic lines. There were two and one groups of inhibitor genes on chromosomes 3BS and 3DS, respectively, whereas no group of inhibitor genes was found on chromosome 3AS. Thus, the primer set for each group of inhibitor genes was genome allele-specific. The two known inhibitors, 0.53 and 0.19, were located on chromosomes 3BS and 3DS, respectively. The validity of the three genome allele-specific primer sets was confirmed by amplifications in 15 accessions of Triticum urartu, Triticum monococcum, Aegilops tauschii and Triticum dicoccoides. These results gave further support at the molecular level, that the 24 kDa dimeric alpha-amylase inhibitors in cultivated wheat are encoded by a multigene family.     

Effect of litter quality and soil fungi on macroaggregate dynamics and associated partitioning of litter carbon and nitrogen

We investigated the effect of plant residue decomposability and fungal biomass on the dynamics of macroaggregate (250–2000 μm) formation in a three months' incubation experiment and determined the distribution of residue-derived C and N in the microbial biomass and in aggregate size fractions (250–2000 μm, 53–250 μm and <53 μm) using ¹³C and ¹⁵N data. A silty loam soil (sieved <250 μm) was incubated with and without addition of ¹⁵N labelled maize leaves (C/N = 27.4) and roots (C/N = 86.4). Each treatment was carried out with and without fungicide application. The addition of maize residues enhanced soil respiration and microbial biomass C and N and resulted in increased macroaggregate formation with a higher and more rapid maximum macroaggregation in the soil amended with maize leaves than in that with addition of roots. Fungicide application led to a significant decline of microbial biomass C and mineralization of the added residues compared to untreated soils, which demonstrates a successful suppression of part of the active microbial biomass by the fungicide. However, this was not confirmed by a generally lower ergosterol concentration. Consequently, ergosterol was no reliable fungal biomarker in periods of rapid decline of the fungal biomass. A single addition of fungicide was insufficient for continued inhibition of the fungal biomass. Yet, a significant delay (28–42 days) in macroaggregation in fungicide treated compared to untreated samples highlighted the importance of the fungal biomass in macroaggregate formation. Macroaggregates were enriched in maize-derived ¹³C and ¹⁵N compared to microaggregates or the fraction < 53 μm. They turned over rapidly with decreasing substrate availability, which entailed a transfer of maize-derived C and N stored within macroaggregates during the first weeks of incubation to microaggregates with proceeding incubation time. Our results indicate that this transfer happened within macroaggregates, because no considerable amount of free particulate organic matter (POM) was released upon macroaggregate breakdown. We conclude that substrate decomposability and fungal activity are key factors determining extent and dynamics of macroaggregation during decomposition processes. Macroaggregate formation implied rapid incorporation and thereby short-term protection of maize-derived C and N. Moreover, macroaggregates allowed a transfer of maize-derived organic matter into microaggregates within macroaggregates, which prevented the release of significant amounts of free POM upon macroaggregate breakdown. Consequently, macroaggregates constitute to the transfer of recently added C into more stable soil organic matter fractions.     

Whole-genome shotgun sequencing of mitochondria from ancient hair shafts

Although the application of sequencing-by-synthesis techniques to DNA extracted from bones has revolutionized the study of ancient DNA, it has been plagued by large fractions of contaminating environmental DNA. The genetic analyses of hair shafts could be a solution: We present 10 previously unexamined Siberian mammoth (Mammuthus primigenius) mitochondrial genomes, sequenced with up to 48-fold coverage. The observed levels of damage-derived sequencing errors were lower than those observed in previously published frozen bone samples, even though one of the specimens was >50,000 14C years old and another had been stored for 200 years at room temperature. The method therefore sets the stage for molecular-genetic analysis of museum collections.     

Transfer of insecticide residues to food stored on or near plywood impregnated with organochlorine insecticides

Formulations of aldrin and dieldrin have been used for a number of years to treat exposed timber components used in the construction of freight containers. The extent to which these insecticides migrate to foodstuffs stored on or near treated plywood has been examined under laboratory conditions and is reported here. A limited survey of organochlorine insecticide residues in samples of foodstuffs, taken from commercial loads carried in freight containers, indicated that residue levels are unlikely to present a health hazard.