Seasonal Biomass Accumulation and Nutrient Uptake of Canola,Mustard, and Flax on a Black Chernozem Soil in Saskatchewan

ABSTRACT

Seed yield and nutrient use efficiency are related to biomass accumulation and nutrient uptake in the growing season. Biomass accumulation and nutrient uptake of canola (Brassica napus L. and Brassica rapa L.), mustard (Brassica juncea L.) and flax (Linum usitatissimum L.) and the relationship to days after emergence (DAE) or growing degree days (GDD) were determined during the 1998 and 1999 growing seasons in field experiments at Melfort, Saskatchewan, Canada. In general, biomass accumulation and nutrient uptake increased with time at early growth stages and reached a maximum at late growth stages. Significant R² values for both biomass accumulation and nutrient uptake indicated that a cubic polynomial type equation was suitable to represent these parameters as a function of DAE. All oilseed crops maximized biomass at mid way to the end of pod forming stages (74–84 DAE or 750–973 GDD). Maximum biomass accumulation rate occurred at the early to late bud forming stage (42–49 DAE or 390–498 GDD), and it was 146–190 kg ha^?1d^?1 for canola, 158–182 kg ha^?1d^?1 for mustard, and 174–189 kg ha^?1d^?1 for flax. Maximum nutrient uptake occurred during flowering to early ripening (59–82 DAE or 597–945 GDD). Maximum nutrient uptake rate normally occurred at branching to early bud formation (21–42 DAE or 142–399 GDD). There was a close correlation between biomass accumulation and nutrient uptake, and among nutrients, suggesting interrelated absorption. For nitrogen (N), phosphorus (P), potassium (K), sulfur (S), and boron (B), respectively, maximum nutrient uptake rate was 2.3–4.5, 0.3–0.5, 2.5–5.7, 0.7–1.1, and 0.005–0.008 kg ha^?1d^?1 for canola; 2.3–3.9, 0.4–0.5, 2.6–4.9, 1.2–1.4, and 0.006–0.008 kg ha^?1d^?1 for mustard; and 3.2–4.0, 0.3–0.4, 2.9–4.1, 0.3–0.5, and 0.004–0.009 kg ha^?1d^?1 for flax. In general, maximum nutrient uptake rate and amount occurred earlier than maximum biomass accumulation rate and amount, and maximum rates of both nutrient uptake and biomass accumulation occurred earlier than their maximum amounts. The findings suggest that for high seed yields, there should be adequate supply of nutrients for plants, particularly to sustain high nutrient uptake rate at branching to bud forming stage and high biomass accumulation rate at early to late bud forming stage.     

Effect of zinc‐biofortified seeds on grain yield of wheat,rice, and common bean grown in six countries

Seeds enriched with zinc (Zn) are ususally associated with better germination, more vigorous seedlings and higher yields. However, agronomic benefits of high‐Zn seeds were not studied under diverse agro‐climatic field conditions. This study investigated effects of low‐Zn and high‐Zn seeds (biofortified by foliar Zn fertilization of maternal plants under field conditions) of wheat (Tritcum aestivum L.), rice (Oryza sativa L.), and common bean (Phaseolus vulgaris L.) on seedling density, grain yield and grain Zn concentration in 31 field locations over two years in six countries. Experimental treatments were: (1) low‐Zn seeds and no soil Zn fertilization (control treatment), (2) low‐Zn seeds + soil Zn fertilization, and (3) Zn‐biofortified seeds and no soil Zn fertilization. The wheat experiments were established in China, India, Pakistan, and Zambia, the rice experiments in China, India and Thailand, and the common bean experiment in Brazil. When compared to the control treatment, soil Zn fertilization increased wheat grain yield in all six locations in India, two locations in Pakistan and one location in China. Zinc‐biofortified seeds also increased wheat grain yield in all four locations in Pakistan and four locations in India compared to the control treatment. Across all countries over 2 years, Zn‐biofortified wheat seeds increased plant population by 26.8% and grain yield by 5.37%. In rice, soil Zn fertilization increased paddy yield in all four locations in India and one location in Thailand. Across all countries, paddy yield increase was 8.2% by soil Zn fertilization and 5.3% by Zn‐biofortified seeds when compared to the control treatment. In common bean, soil Zn application as well as Zn‐biofortified seed increased grain yield in one location in Brazil. Effects of soil Zn fertilization and high‐Zn seed on grain Zn density were generally low. This study, at 31 field locations in six countries over two years, revealed that the seeds biofortfied with Zn enhanced crop productivity at many locations with different soil and environmental conditions. As high‐Zn grains are a by‐product of Zn biofortification, use of Zn‐enriched grains as seed in the next cropping season can contribute to enhance crop productivity in a cost‐effective manner.     

Effect of ethanol and red wine on ochratoxin a-induced experimental acute nephrotoxicity

Ochratoxin A (OTA), is a nephrotoxic mycotoxin present in wine, which is nephrotoxic in humans. Our working hypothesis is that natural substances in wine may counteract OTA toxicity. Thirty-six rats were randomized to OTA dissolved in saline, red wine, or 13.5% ethanol or to OTA-free wine, ethanol, or saline. OTA (289 microg/kg of body weight/48 h) was administered by gastric gavage for 2 weeks. Serum creatinine, tubular enzymuria, renal lipohydroperoxides (LOOH), reduced (GSH) and oxidized (GSSG) glutathione, and renal superoxide dismutase activity (SOD) were determined in renal tissue. OTA alone produced significant increases in renal lipoperoxides and significant decreases in SOD and GSH/GSSG ratio. In red wine or ethanol, OTA was less nephrotoxic, reducing oxidative damage as revealed by LOOH. In OTA-wine and OTA-ethanol groups, SOD activity was higher than in the OTA-treated one, suggesting that both ethanol and nonalcoholic fractions may preserve antioxidant reserve. GSH/GSSG ratio was significantly preserved only in the OTA-wine group and not in OTA-ethanol. Red wine may exert a protective effect against OTA nephrotoxicity by limiting oxidative damage. The ostensible protection afforded by ethanol deserves further investigation.     

Hairpin RNAs and retrotransposon LTRs effect RNAi and chromatin-based gene silencing

The expression of short hairpin RNAs in several organisms silences gene expression by targeted mRNA degradation. This RNA interference (RNAi) pathway can also affect the genome, as DNA methylation arises at loci homologous to the target RNA in plants. We demonstrate in fission yeast that expression of a synthetic hairpin RNA is sufficient to silence the homologous locus in trans and causes the assembly of a patch of silent Swi6 chromatin with cohesin. This requires components of the RNAi machinery and Clr4 histone methyltransferase for small interfering RNA generation. A similar process represses several meiotic genes through nearby retrotransposon long terminal repeats (LTRs). These analyses directly implicate interspersed LTRs in regulating gene expression during cellular differentiation.     

New data on three molecular markers from different cellular genomes in Mediterranean accessions reveal new insights into phylogeography of <Emphasis Type="Italic">Pisum sativum</Emphasis> L. subsp. <Emphasis Type="Italic">elatius</Emphasis> (Bieb.) Schmalh.

Twelve accessions classified as Pisum sativum subsp. elatius, mostly from West and Central Mediterranean, were analysed for three markers from different cellular genomes: rbcL (plastid genome), coxI (mitochondrial genome) and SCA (nuclear genome). Based on geographical distribution of their allele combinations analysed in this and the earlier study, we suggest a putative history of wild representatives of P. sativum. The ancestor of this species belonged to lineage A (coxI+, rbcL+, SCA ^f ); it appeared in East Mediterranean, then spread westward most probably during one of the Pleistocene coolings when the sea was smaller, so that representatives of lineage A remained in the Eastern Mediterranean and on the islands of Sicily and Menorca. Mutation leading to the loss of the restriction site for PsiI in coxI−, gave rise to lineage C (coxI−, rbcL+, SCA ^f ) which spread widely in the Mediterranean and is now found in France, Greece and Ethiopia. Mutation leading to rbcL− gave rise to lineage D (coxI−, rbcL−, SCA ^f ), now found in Egypt (P. sativum subsp. jomardii) and Spain. Mutational transition of SCA ^f to SCA ^s most probably took place in North-Eastern Mediterranean since the resulting lineage B (coxI−, rbcL−, SCA ^s ) now occupies the Tauro-Caucasian area. In Asia Minor and North Israel, line B met the ancestral line A so that both lines coexist there presently. The lineage B gave rise to the cultivated P. sativum subsp. sativum.     

Preparation of stable isotope-labeled 2-nitrobenzaldehyde derivatives of four metabolites of nitrofuran antibiotics and their comprehensive characterization by UV, MS, and NMR techniques

A convenient method is presented for the preparation of the carbon-13-labeled 2-nitrobenzaldehyde derivatives of the nitrofuran metabolites 3-amino-2-oxazolidinone (AOZ), semicarbazide (SC), 1-aminohydantoin (AH), and 3-amino-5-morpholinomethyl-2-oxazolidinone (AMOZ), with the purpose of using them as internal standards for the quantification of trace levels of nitrofuran residues by liquid chromatography-tandem mass spectrometry in foods of animal origin. The synthesis encompasses the nitration of [1,2,3,4,5,6-(13)C(6)]toluene prior to chromyl compound-mediated oxidation of the methyl group into the corresponding aldehyde. The four metabolites of nitrofuran antibiotics were derivatized independently with the resulting ring-labeled 2-nitrobenzaldehyde (NBA) to obtain the target compounds. Both the isotopically enriched and native substances were used to perform a comprehensive fragmentation study by electrospray ionization (ESI) collision-induced dissociation (CID) mass spectrometry (MS). Full characterization of the nitrofuran derivatives was accomplished with ultraviolet (UV) and exhaustive nuclear magnetic resonance (NMR) analysis. A major advantage of the described procedure is that it can be extended to the preparation of other carbon-13-labeled derivatives of metabolites of nitrofuran antibiotics.     

Geographic Classification of Heavy Metal Concentrations in Mosses and Stream Sediments in the Federal Republic of Germany

The results of the first German moss monitoring programme to estimate heavy metal pollution in the Federal Republic of Germany were combined with other large-scale investigations carried out in Germany and then classified geographically in a new form. Using Monte Carlo assisted factor analysis, six factors indicating sources of pollution were identified from the sets of element data from the moss monitoring project (As, Cd, Cr, Cu, Fe, Ni, Pb, Ti, V, Zn) and the data sets for SO₂ and particulate. The geographic distribution patterns of the factor values showed the regions in which the various sources are to be found. By combining the data the primarily anthropogenic chromium concentrations of the mosses were compared with the mainly geogenic chromium concentrations of the stream sediments in the form of examples. After normalization, the transformed chromium concentrations were transferred to a map of the entire area using inverse distance weighting. Anthropogenic and geogenic influences are being discussed on the basis of the results.     

Tetraploid and hexaploid wheats express identical isoforms of nsLTP1

Nonspecific lipid-transfer proteins (nsLTPs) have been recognized as allergens in several plant species among which are cereals important in human nutrition. In this report, we purified a 9600 +/- 1 Da protein from both soft wheat and farro bran. Mass spectrometric analyses revealed that these proteins are identical, belong to the nsLTP1 class, and have high sequence homology with nsLTP1 isolated from other cereal species. Their identification was further supported by the ability of the soft wheat nsLTP1 to transfer pyrene-labeled lipids between donor and acceptor membranes. The results are discussed in view of the increasing diffusion on the markets of bran-rich products.     

Development of an enzyme-linked immunosorbent assay for bisphenol a using chicken immunoglobulins

Bisphenol A was coupled, after derivatization into a suitable hapten, to bovine serum albumin and ovalbumin in order to produce immunizing and coating antigens. The immunizing antigens were injected into chickens, which allowed the isolation of specific bisphenol A immunoglobulins from the egg yolk. These antibodies were used in an indirect competitive enzyme-linked immunosorbent assay for the determination of bisphenol A in aqueous solutions. Various parameters, influencing the assay sensitivity, were evaluated. The applicability of the assay for the determination of bisphenol A in milk was also studied. The assay was not as sensitive as other analytical techniques used in bisphenol A analysis, since typical I(50) levels of 2.5 microM were reached in aqueous solutions. This study nevertheless illustrates the usefulness and the potency of chicken antibodies in the analysis of migration residues from packaging materials using immunochemical techniques. In addition, the assay showed to be quite specific for bisphenol A as well. Only for bisphenol A analogues, cross reactivities of about 40% were reached, enabling the use of the antibodies for the screening of bisphenol A and alike compounds.