Attraction of Moths of Two Noctuidae Species to Field Traps Baited With a Mixture of two to three Homologous Acetates in Poland.

Field trials of a series of monounsaturated straight-chain acetates, including the (Z)-5-tetradecenyl acetate, (Z)-9-tetradecenyl acetate (pheromone blend A) and (Z)-5-decenyl acetate, (Z)-7-dodecenyl acetate, (Z)-9-tetradecenyl acetate (pheromone blend B), attracted the following species from the title family: Agrotis exclamationis (Linnaeus) and Agrotis segetum (Denis & Schiffermüller), respectively. Cutworms were monitored in the 2016-2017 season with the use of white Delta-type traps and different pheromone dispensers that contained above blends. The identified pheromone components at blend A elicited maximum trap captures when combined in a Z5-14:Ac/Z9-14:Ac-mixture ratio 100:16 at dose of 350 µg. The attractiveness of dispensers with pheromone blend B combined in a Z5-10:Ac/Z7-12:Ac/Z9-14:Ac-mixture ratio 1:1:1 at dose of 200 µg was the highest. Most kinds of the dispensers tested were similar or more active to the standard lures of the Csalomon company. Pheromone component of the A. exclamationis, (Z)-5-tetradecenyl acetate, was synthesized with a new, simple, and very efficient method in high summary yield and excellent isomeric purity.

Complete mitochondrial genome of wild aurochs (Bos primigenius) reconstructed from ancient DNA.

Extinct aurochs (Bos primigenius), accepted as the ancestor of domestic cattle, was one of the largest wild animals inhabiting Europe, Asia and North Africa. The gradual process of aurochs extinction finished in Poland in 1627, were the last recorded aurochs, a female, died. Some aspects of cattle domestication history and the distribution of aurochs genetic material among modern cattle breeds still remain unclear. Analyses of ancient DNA (aDNA) from bone sample deliver new genetic information about extinct wild aurochs as well as modern cattle phylogeny. DNA was extracted from a fragment of aurochs fossil bone found in the Pisz Forest, Poland. The sample was radiocarbon-dated to about 1500 yBP. The aDNA was used for Whole Genome Amplification in order to form a DNA bank. Auroch mitochondrial DNA sequences were amplified using sets of 41 primers overlapping the whole mtDNA, cloned and sequenced. The sequence of the whole mitochondrial genome was reconstructed and deposed in GenBank [GenBank:JQ437479]. Based on the phylogenetic analyses of the Bovine mitochondrial genomes, a phylogenetic tree was created. As expected, the tree clearly shows that the mtDNA sequence of the analyzed PWA (Polish Wild Aurochs) individual belongs to haplogroup P. In the course of the comparative mtDNA analysis we identified 30 nucleotide marker positions for haplogroup P and nine unique PWA differences compared to the two remaining haplotype P representatives. Our analysis provides the next step to the reconstruction of the demographic history of this extinct but still exciting species.

Testing uniformity of mutants of the Lathyrus sativus L. (grasspea) using Bennet's method.

In this paper interest is focused on uniformity of individual mutants. Because before the registration of a new variety the criteria for DUS (distinctness, uniformity and stability) are checked, so you should also check whether the mutant meets them. The aim of created mutants, in many genetic experiments, is to expand variation of the initial material. This is achieved through use of the mutagen or combination of mutagens on different stages of plants growth. The experimenter should choose some of obtained mutants (for example these which showed better property as regards the same trait). Calculations were done on the basis of results of test with variety Krab of the Lathyrus sativus L. (grasspea) species and 17 mutants getting from this variety. Uniformity was checked with the use of the Bennett's method which is based on testing of equality of coefficients of variation. After analysis the mutants with codes K3, K37, K63 and K64 were detected as uniform at the same level as variety Krab.

Formation of fumonisins and other secondary metabolites by Fusarium oxysporum and F. proliferatum: a comparative study.

The principal aim of this study was to estimate the formation of fumonisins (FB(1) and FB(2)), moniliformin (MON), and ergosterol (ERG) by Fusarium oxysporum and Fusarium proliferatum, while the formation of beauvericin (BEA) was estimated by the latter Fusarium species only. Moreover, the effect of temperature on the biosynthesis of mycotoxins was also evaluated. Fumonisins were formed by F. proliferatum, with the highest yield at 18 degrees C (720.0-1976.6 microg g(-1) for FB(1), 74.2-670.8 microg g(-1) for FB(2)) and only by three of four F. oxysporum strains at a very low level (0.02-4.77 microg g(-1) for FB(1), 0.02-2.15 microg g(-1) for FB(2)). The amount of MON formed by F. proliferatum was the highest (p < 0.001) at 32 degrees C (3056.87 microg g(-1)), while MON biosynthesis by F. oxysporum was lower 227.54 microg g(-1) (p < 0.001). BEA was produced by F. proliferatum with the highest level at 25 degrees C (p < 0.001). ERG-recognized as an indicator of fungal biomass development and as a consequence of mycotoxin formation-was found at the highest concentration at a biosynthesis temperature of 25 degrees C for F. proliferatum and F. oxysporum (p < 0.001).

Reaction of winter wheat (Triticum aestivum L.) cultivars to infection with Fusarium spp.: mycotoxin contamination in grain and chaff.

This study compares the susceptibility of winter wheat (Triticum aestivum L.) cultivars to Fusarium head blight (FHB) and accumulation of mycotoxins in kernels and chaff under different climatic conditions in two locations-Cerekwica near Poznan (Central West Poland) and Sitaniec, near Zamosc, Lublin region (South East Poland). Very high variations were found in the concentrations of mycotoxins (zearalenone, ZEA; nivalenol, NIV; deoxynivalenol, DON; moniliformin, MON) in examined fractions: Fusarium-damaged kernels (FDK) and healthy looking kernels (HLK) and in chaff for individual cultivars in both locations. In most cases, significantly higher concentrations of investigated toxins were recorded in wheat from the area of Lublin than from Poznan (p < 0.05). The highest Fusarium infection rates and mycotoxin biosynthesis levels were observed in the Lublin location, with the percentage of the FDK fraction ranging 8.1-81.6. In this region, ZEA concentration (microg g(-1)) after inoculation with F. culmorum and F. graminearum ranged from 0.02-0.48 and 0.32-1.04, respectively. In the Poznan area, the toxin concentrations were considerably lower, ranging 0.01-0.10 and 0.03-0.13 microg g(-1) for both isolates, respectively. The concentration of DON was significantly higher than ZEA or NIV levels. The levels of MON accumulation (microg g(-1)) in the FDK fraction were between 0.14 and 1.73 (Poznan area) and ND (not detected) to 2.51 (Lublin area). F. avenaceum infection rate ranged 7-35% in samples where the toxin was detected.