3,460 research outputs found

    Pollination patterns in safflower (Carthamus tinctorius L.) : a thesis presented in partial fulfilment of the requirements for the degree of Master of Agricultural Science in Plant Science at Massey University

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    The influence of environmental conditions on safflower (Carthamus tinctorius L.) floret characters and insects were studied in relation to pollination in this species. Insect activity was studied in a field experiment using part of the world germplasm collection of safflower. Honey bees were the most likely cross-pollinators. Activity of honey bees did not vary between genotypes studied. Correlations between insect and weather data were mainly non-significant. A sample of 12 genotypes from the world collection were intensively studied in controlled environment rooms. Single plants were used as plots in a randomised complete block design, in each of four environments (day/night temperature treatments of 28/22°c and 24/l8°c in combination with vapour pressure deficit treatments of -1.0 and -0.4 kPa). Environments reflected New Zealand summer conditions. Coefficients of variation were acceptable for most characters. Considerable genotypic, environmental and genotype-environment interaction variances were observed for most characters. Standardised partial regression coefficients (path coefficients) and principal factors were utilized to determine the characters most important in self-pollination of safflower. These characters were: the length of the style-stigma; the rate of style-stigma growth; the rate of corolla tube growth and amounts of viable pollen present during floret expansion. Pollen viabilities remained high for the longest time in higher humidity environments. Large amounts of pollen were produced at the lower humidity. Floral parts were largest in the cool dry environment, however rates of style-stigma and corolla expansion were greater at lower temperatures. It was concluded that synchronization of the rates of style-stigma and corolla tube growth were important in maintaining the stigma in close proximity to viable pollen, and thus promoting the possibility of self-pollination. Self-pollination was greatest at the lower temperature and lower humidity. The basic self-pollination mechanism observed was in agreement with previous authors. A number of improvements for future controlled environment experiments involving safflower were suggested. The implications of pollination of safflower on germplasm collection and maintenance, artificial crossing and breeding plans were discussed

    The Effects of Burst Activity on Soft Gamma Repeater Pulse Properties and Persistent Emission

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    Soft Gamma Repeaters (SGRs) undergo changes in their pulse properties and persistent emission during episodes of intense burst activity. SGR 1900+14 has undergone large flux increases following recent burst activity. Both SGR 1900+14 and SGR 1806-20 have shown significant changes in their pulse profile and spin-down rates during the last several years. The pulse profile changes are linked with the burst activity whereas the torque variations are not directly correlated with the bursts. Here, we review the observed dynamics of the pulsed and persistent emission of SGR 1900+14 and SGR 1806-20 during burst active episodes and discuss what implications these results have for the burst emission mechanism, the magnetic field dynamics of magnetars, the nature of the torque variability, and SGRs in general.Comment: 9 pages, Woods Hole 2001 GRB and SGR Conferenc

    Aprofundir en la vida de les coses: l'etnografis a la investigació educativa

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    The Happiest Days?

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    First published in 1990. Routledge is an imprint of Taylor & Francis, an informa company

    The Dynamic Behavior of Soft Gamma Repeaters

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    Soft Gamma Repeaters (SGRs) undergo changes in their pulse properties and persistent emission during episodes of intense burst activity. Both SGR 1900+14 and SGR 1806-20 have shown significant changes in their spin-down rates during the last several years, yet the bulk of this variability is not correlated with burst activity. SGR 1900+14 has undergone large changes in flux and a dramatic pulse profile change following burst activity in 1998. The flux level of SGR 1627-41 has been decreasing since its only recorded burst activity. Here, we review the global properties of SGRs as well as the observed dynamics of the pulsed and persistent emission properties of SGR 1900+14, SGR 1806-20 and SGR 1627-41 during and following burst active episodes and discuss what implications these results have for the burst emission mechanism, the magnetic field dynamics of magnetars, the nature of the torque variability, and SGRs in general.Comment: Invited review to appear in "High Energy Studies of Supernova Remnants and Neutron Stars" (COSPAR 2002). 12 pages, 7 figure

    Control of erythroid differentiation: asynchronous expression of the anion transporter and the peripheral components of the membrane skeleton in AEV- and S13-transformed cells

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    Chicken erythroblasts transformed with avian erythroblastosis virus or S13 virus provide suitable model systems with which to analyze the maturation of immature erythroblasts into erythrocytes. The transformed cells are blocked in differentiation at around the colony-forming unit- erythroid stage of development but can be induced to differentiate in vitro. Analysis of the expression and assembly of components of the membrane skeleton indicates that these cells simultaneously synthesize alpha-spectrin, beta-spectrin, ankyrin, and protein 4.1 at levels that are comparable to those of mature erythroblasts. However, they do not express any detectable amounts of anion transporter. The peripheral membrane skeleton components assemble transiently and are subsequently rapidly catabolized, resulting in 20-40-fold lower steady-state levels than are found in maturing erythrocytes. Upon spontaneous or chemically induced terminal differentiation of these cells expression of the anion transporter is initiated with a concommitant increase in the steady- state levels of the peripheral membrane-skeletal components. These results suggest that during erythropoiesis, expression of the peripheral components of the membrane skeleton is initiated earlier than that of the anion transporter. Furthermore, they point a key role for the anion transporter in conferring long-term stability to the assembled erythroid membrane skeleton during terminal differentiation

    Parametric Alignment of Drosophila Genomes

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    The classic algorithms of Needleman--Wunsch and Smith--Waterman find a maximum a posteriori probability alignment for a pair hidden Markov model (PHMM). In order to process large genomes that have undergone complex genome rearrangements, almost all existing whole genome alignment methods apply fast heuristics to divide genomes into small pieces which are suitable for Needleman--Wunsch alignment. In these alignment methods, it is standard practice to fix the parameters and to produce a single alignment for subsequent analysis by biologists. Our main result is the construction of a whole genome parametric alignment of Drosophila melanogaster and Drosophila pseudoobscura. Parametric alignment resolves the issue of robustness to changes in parameters by finding all optimal alignments for all possible parameters in a PHMM. Our alignment draws on existing heuristics for dividing whole genomes into small pieces for alignment, and it relies on advances we have made in computing convex polytopes that allow us to parametrically align non-coding regions using biologically realistic models. We demonstrate the utility of our parametric alignment for biological inference by showing that cis-regulatory elements are more conserved between Drosophila melanogaster and Drosophila pseudoobscura than previously thought. We also show how whole genome parametric alignment can be used to quantitatively assess the dependence of branch length estimates on alignment parameters. The alignment polytopes, software, and supplementary material can be downloaded at http://bio.math.berkeley.edu/parametric/.Comment: 19 pages, 3 figure
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