Different recombination frequencies in wheat doubled haploid populations obtained through maize pollination and anther culture

This study compared the meiotic recombination frequency between wheat doubled haploid (DH) populations obtained through two different methods, maize pollination (MP♀) and anther culture (AC♂). The comparison was based on a genetic linkage analysis, performed with DNA markers. Thirty-five polymorphic markers (15 SSR, 15 AFLP, 5 RAPD) were screened in MP♀ and AC♂ doubled haploids populations, derived from the same hybrid genotype (F₁ of ‘Eta’ × ‘Darkhan 15’). Nine linkage groups, comprising 35 loci (the MP♀ lines) and 31 loci (the AC♂ lines), were constructed. The linkage groups in both DH populations showed identical orders of markers, except for one group mapping to chromosome 6B. The MP♀ and AC♂ linkage maps differed significantly in recombination frequencies for corresponding intervals. In total, the AC♂ linkage map (495.5 cM) was 40.5% longer than the MP♀ map (352.8 cM), indicating a significantly higher meiotic recombination rate in pollen mother cells. The enhancement in recombination was visible in five of nine linkage groups, and in 7 intervals between individual loci out of 19 compared. Moreover, for 6 other intervals a lack of linkage was observed in the AC♂ population, as compared to the MP♀ map.     

Surface and subsurface microbial biomass, community structure and metabolic activity as a function of soil depth and season

Microbial biomass, size and community structure along with an estimate of microbial activity and soil chemical parameters were determined at three depths in two soils (e.g. sandy loam Ultic Hapludalf and silt loam Mollic Hapludalf) replicated three times under one winter and summer season. Microbial biomass and community structure were estimated from phospholipid-PO₄ content and fatty acid methyl ester (FAME) measurements. Microbial activity and assimilative capacity were estimated using a ³H-acetate incorporation into phospholipids and by incubating the soil samples at the average winter and summer temperatures, 3 and 20 °C, respectively. We found that the size of the microbial biomass in both the surface and the subsurface soils was not significantly affected by the seasonal variation but activity increased by as much as 83% at the summer temperatures in the surface soil. We demonstrated using FAME analysis that for both soils seasonal changes in the subsurface microbial community occurred. These findings suggest that winter conditions will shift the population activity level in both the surface and subsurface systems and the biochemical structure of the community in the subsurface. In all cases, the inorganic chemical properties of the soil, as a function of season, remained constant. The greatly increased activity of microbial population at the higher temperature will favor the capacity of the system to utilize nutrients or organic materials that may enter soil. During low temperature seasons the capacity of either surface or subsurface soils to assimilate materials is generally diminished but the reduction reflects changes in metabolism and not a reduced biomass size.     

Evaluation of Naturally-Occurring Organisms as Food for Juvenile Crayfish Procambarus clarkii1

Nutritionally important food items for crayfish have been difficult to identify and little information exists for third instar (first-feeding) crayfish. In this study, three major groups of potentially-important foods were fed to communally-reared third instar crayfish (Procambarus clarkii) and weight gain and survival were measured over a 30 day period. Mean weight gain (% increase) of crayfish fed the zooplankton Daphnia magna alone or in combination with other food items, ranged 2, 277–3, 239%, while mean weight gain of crayfish fed unidentified aquatic bacteria, the aquatic macrophyte Myriophyllum spicatus, combinations of bacteria and plant, or a negative control ranged 254–767%. No significant interaction of food items was detected. Bacteria appear to be a utilizable nutritional source for juvenile crayfish, but, using the methods employed in this study, do not support maximum rates of weight gain. Thus, pond management strategies that maximize zooplankton populations at the time of crayfish hatching might be beneficial.     

Identification of synthetic regioisomeric lutein esters and their quantification in a commercial lutein supplement

Synthetic mixtures of 24 mono- and diesters of the asymmetric hydroxylated carotenoid lutein with lauric, myristic, palmitic, and stearic acids were analyzed by liquid chromatography-ultraviolet/visible spectroscopy (LC-UV-vis) and characterized by LC-mass spectrometry (MS) and nuclear magnetic resonance spectroscopy (NMR). These compounds were then used for identifying the composition of a commercial lutein supplement. This is the first report of chromatographic separation of mixed fatty acid lutein diesters. Preferential MS loss of fatty acids or water occurred initially at the 3'-hydroxy position in the epsilon-ionone ring and subsequently at the 3-hydroxy position in the beta-ionone ring. This selective fragmentation leads to facile assignment of the specific fatty acids to the appropriate regioisomeric ionone ring. A commercial lutein supplement contained low levels of two pairs of regioisomeric monoesters and nearly equal levels of three homogeneous diesters and five pairs of mixed diesters. Palmitic acid was the predominant fatty acid, with lower amounts of myristic, stearic, and lauric acids.     

Phosphonic analogues of morphactins. Part V: Peptides containing 9-aminofluoren-9-ylphosphine oxides

Di- and tripeptides containing P-terminal 9-aminofluoren-9-ylphosphine oxides were synthesised and evaluated for herbicidal activity using Spirodela oligorriza (Kurz.) Hegelm. The glycylglycyl and threonyl peptides showed high activity as measured by the reduction of dry matter.     

An automated,cost-effective and scalable,flood-and-drain based root phenotyping system for cereals

Background

Genetic studies on the molecular mechanisms of the regulation of root growth require the characterisation of a specific root phenotype to be linked with a certain genotype. Such studies using classical labour-intensive methods are severely hindered due to the technical limitations that are associated with the impeded observation of the root system of a plant during its growth. The aim of the research presented here was to develop a reliable, cost-effective method for the analysis of a plant root phenotype that would enable the precise characterisation of the root system architecture of cereals.

Results

The presented method describes a complete system for automatic supplementation and continuous sensing of culture solution supplied to plants that are grown in transparent tubes containing a solid substrate. The presented system comprises the comprehensive pipeline consisting of a modular-based and remotely-controlled plant growth system and customized imaging setup for root and shoot phenotyping. The system enables an easy extension of the experimental capacity in order to form a combined platform that is comprised of parallel modules, each holding up to 48 plants. The conducted experiments focused on the selection of the most suitable conditions for phenotyping studies in barley: an optimal size of the glass beads, diameters of the acrylic tubes, composition of a medium, and a rate of the medium flow.

Conclusions

The developed system enables an efficient, accurate and highly repeatable analysis of the morphological features of the root system of cereals. Because a simple and fully-automated control system is used, the experimental conditions can easily be normalised for different species of cereals. The scalability of the module-based system allows its capacity to be adjusted in order to meet the requirements of a particular experiment.

     

Effect of visible implant elastomers on the growth,survival and tag retention in juvenile Atlantic sturgeon (Acipenser oxyrinchus) in laboratory conditions

This study identifies the possibility of using visible implant elastomers (VIE) to tag juvenile Atlantic sturgeon (Acipenser oxyrinchus). The mean body weight was 2.4 ± 0.4 g, and mean body length 5.5 ± 0.5 cm. Markers in three colours were used: blue, orange and green. Implant elastomers were injected in the rostrum and in the tail shaft. The experiment was conducted over a period of 10 weeks and included also a control group, that is, no tagging. No significant effect of tagging on the specific growth rate, feed conversion ratio and condition factor of juvenile Atlantic sturgeon was observed. The fish in all groups increased their body weight more than 10 times, reaching body weight of 25–28 g. The final survival in all of the groups was approximately 40%. The final tag retention varied depending on the implant colour. The highest retention of 100% was obtained with orange VIE and was significantly different from blue and green. Tag retention was dependent on the place of marking (P > 0.05). A correlation was observed between the applied dye and the place of marking (P = 0.0166). The best results were obtained when marking with orange VIE in the rostrum as all markers were visible after 70 days even without the use of UV light. According to our research, marking with VIE does not negatively affect growth and survival of juvenile Atlantic sturgeon and can be recommended for fish with an initial body weight of approximately 2.5 g in the case of short‐term research.     

Identification of proteins related to microspore embryogenesis responsiveness in anther cultures of winter triticale (×<Emphasis Type="Italic">Triticosecale</Emphasis> Wittm.)

For a better understanding of the physiological background of microspore embryogenesis (ME), the protein profile was analyzed in four winter triticale DH lines, which show extremely different embryogenic potential. The analysis were conducted with anthers at the phase of development optimal for ME induction and then after low temperature (LT, 3 weeks at 4 °C) ME-inducing tillers treatment. The sub-proteome of anthers was mapped by two-dimensional gel electrophoresis (2-DE). The protein species significantly more abundant (at least 2-fold) in responsive DH lines after LT treatment were chosen for identification by MALDI-TOF/TOF analysis. In total, 31 protein species were successfully identified as involved in the determination of microspore competence, stress response and in the regulation of ME induction. Microspore competence required sufficient energy supply and efficient system of cell protection that determine survival under prolonged LT stress treatment. LT stress was associated with increased accumulation of proteins typical for cell defence against oxidative stress (e.g., l-ascorbate peroxidase), chaperons (e.g., HSP70) and other enzymes/factors ensuring protein biosynthesis, stability and active cell divisions. Also here, effective cell defence required undisturbed energy supply. Among proteins that accumulated differentially in accordance with microspore embryogenic potential again the most important role seems to be played by the enzymes ensuring energy production and determining ability of plant stress adaptation. Two protein species (enolase, 12S storage protein), proposed earlier as candidates for markers of embryogenesis in other in vitro plant culture systems confirmed their utility for triticale anther cultures.