Floodplain ecosystem response to climate variability and land-cover and land-use change in Lower Missouri River basin

This contribution aims at characterizing the extreme responses of Lower Missouri River basin ecosystems to land use modification and climate change over a 30-year temporal extent, using long term Landsat data archives spanning from 1975 to 2010. The inter-annual coefficient of variation (CoV) of normalized difference vegetation index was used as a measure of vegetation dynamics to address ecological consequences associated with climate change and the impact of land-cover/land-use change. The slope of a linear regression of inter-annual CoV over the entire time span was used as a sustainability indicator to assess the trend of vegetation dynamics from 1975 to 2010. Deduced vegetation dynamics were then associated with precipitation patterns, land surface temperature, and the impact of levees on alluvial hydrologic partitioning and river channelization reflecting the links between society and natural systems. The results show, a higher inter-annual accumulated vegetation index, and lower inter-annual CoV distributed over the uplands remaining virtually stable over the time frame investigated; relatively low vegetation index with larger CoV was observed over lowlands, indicating that climate change was not the only factor affecting ecosystem alterations in the Missouri River floodplain. We cautiously conclude that river channelization, suburbanization and agricultural activities were the possible potential driving forces behind vegetation cover alteration and habitat fragmentation on the Lower Missouri River floodplain.     

Sample size for diversity studies in tetraploid alfalfa (<Emphasis Type="Italic">Medicago sativa</Emphasis>) based on codominantly coded SSR markers

The number of genotypes investigated per population is important for the reliability of diversity studies. The objective of this study was to determine the sample size for the identification of differences among populations of an outcrossing autotetraploid species, alfalfa (Medicago sativa), using codominantly coded SSR markers. One hundred and twenty genotypes from each of two closely related populations were analysed with two markers. Twenty random subsamples for each of three sample sizes (10, 20 and 40 genotypes) were built. Compared to the populations with 120 genotypes, alleles that were no longer present in subsamples with 40 genotypes were mainly rare, whereas abundant alleles were also excluded in subsamples with 10 genotypes. F _ST values for pairs of subsamples between the two populations were always significantly different based on 40 genotypes, whereas for 10 genotypes more than half of the pairs were not significantly different. We concluded that 40 genotypes are a reasonable sample size for diversity studies with closely related populations of tetraploid alfalfa investigated with SSR markers. Twenty genotypes may be an economical alternative for large scale studies, but 10 genotypes were a too low number for reliable results.     

Temperature signals contribute to the timing of photoperiodic growth cessation and bud set in poplar

Bud set, the cornerstone delimiting the seasonal growth period in trees, is the dynamic net result of the often photoperiod-controlled growth cessation and the subsequent bud formation. Here, we show that in hybrid poplar, the critical day length for growth cessation and the duration of bud formation each vary with local climatic conditions in identical genotypes. The detailed dissection of bud set suggests temperature as one additional environmental factor that modifies the sensitivity to day-length signals at growth cessation and influences the duration of bud formation in poplar. The ability of perennial plants to integrate additional environmental signals with photoperiod signaling may add to short-term acclimatization to the predicted longer growing seasons in future climates.     

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Cleavage products of lycopene produced by in vitro oxidations: characterization and mechanisms of formation

The aim of this study was to produce in vitro oxidation products of lycopene, which could be possible in vivo metabolites. An oxidation of lycopene with potassium permanganate gave a range of lycopene degradation compounds resulting from the oxidative cleavage of one or two carbon-carbon double bonds. Eleven apo-lycopenals/ones and six apo-carotendials were obtained and tentatively characterized by HPLC-DAD-MS. Apo-11-lycopenal and apo-8,6'-carotendial were isolated and characterized by (1)H NMR for the first time. Lycopene was submitted to an oxidation by atmospheric oxygen catalyzed by a metalloporphyrin, a model system of the active center of cytochrome P450 enzymes. (Z)-Isomers, monoxides, and cleavage compounds of (E)-lycopene were formed. We propose a mechanism of oxidation of lycopene by this system.     

Production of Haploid Sugar Beet (Beta vulgaris L.) by Culturing Unpollinated Ovules

The culture of unpollinated ovules is shown to be a suitable system for the production of haploid sugar beet (Beta vulgaris L.). The yield of haploids depended upon the genotype and varied between 0 and 13 % with a mean of 1.0 %. Haploid plants could be produced from approximately 50 % of all genotypes examined. The majority of the haploids isolated (about 90%) maintained the haploid genome level during the in vitro culture and propagation; 10% of the haploid clones showed a spontaneous doubling to the diploid genome level.