58 research outputs found

    Cooperative Second-Generation Breeding and Testing of Coastal Douglas-fir in the US Pacific Northwest

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    Forest tree improvement got underway in the Pacific Northwest of the USA in the 1950s. Graft incompatibility became evident by the early 1960s and dampened enthusiasm for grafted clonal orchards for this species A different approach, the IFA-PNW �Progressive Tree Improvement System� was launched in 1966. The emphasis here was on forming local cooperatives to share costs, and on progeny testing large numbers of trees using wind-pollinated seed in small testing zones. This phase ran from 1967 till 1993, during which over 26,000 first-generation parents were tested in 109 breeding units (between local cooperatives, the USDI Bureau of Land Management, the USDA Forest Service and WA Department of Natural Resources), with over 3 million progeny test trees planted. A second-generation breeding and testing strategy was developed between 1996 and 1997: Adjacent first-generation testing programs could merge to share genetic material for breeding and testing. Breeding population size for any merged programs should be at least 300 selections. Within a breeding population, breeding groups of 20-30 selections each would be used to manage inbreeding and create multiple populations. The top 10-20 percent of selections within a breeding population could also be assigned an elite population. A minimum of nine breeding groups would be needed within a given testing zone. Each new testing zone was to use all of the families from "local" breeding groups and only the most elite selections from breeding groups originating further away from the testing zone. Each selection would be used in at least two crosses. The committee proposed using three types of tests, each with a specific purpose and design: family-ranking/selection tests; longterm stability tests; and adaptability-screening tests. Breeding and testing is in various stages of completion for seven different programs, which would lead to nine or 10 testing zones. The rule of thumb in choosing selections (first-generation parents, forward selections from open-pollinated progeny tests and from full-sib orchards) crossed to form the second-generation populations has been a 1 in 10 between-family selection intensity. Most selections were based on age-15 height. Where available information on stem sinuosity, forking, ramicorn branches and wood specific gravity were also considered. Between five and six tests have been established per testing zone, with 20 trees planted per family per site in single-tree plots. Trials established to date have contained from 143 to 283 full-sib crosses. All tests are fenced to protect the seedlings from browse. Tests will probably be measured twice, around seven and 12 years from seed (or when the trees are 15 and 30 feet tall respectively).Papers and abstracts from the 27th Southern Forest Tree Improvement Conference held at Oklahoma State University in Stillwater, Oklahoma on June 24-27, 2003

    GPs' decision-making when prescribing medicines for breastfeeding women: Content analysis of a survey

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    <p>Abstract</p> <p>Background</p> <p>Many breastfeeding women seek medical care from general practitioners (GPs) for various health problems and GPs may consider prescribing medicines in these consultations. Prescribing medicines to a breastfeeding mother may lead to untimely cessation of breastfeeding or a breastfeeding mother may be denied medicines due to the possible risk to her infant, both of which may lead to unwanted consequences. Information on factors governing GPs' decision-making and their views in such situations is limited.</p> <p>Methods</p> <p>GPs providing shared maternity care at the Royal Women's Hospital, Melbourne were surveyed using an anonymous postal survey to determine their knowledge, attitudes and practices on medicines and breastfeeding, in 2007/2008 (n = 640). Content analysis of their response to a question concerning decision-making about the use of medicine for a breastfeeding woman was conducted. A thematic network was constructed with basic, organising and global themes.</p> <p>Results</p> <p>335 (52%) GPs responded to the survey, and 253 (76%) provided information on the last time they had to decide about the use of medicine for a breastfeeding woman. Conditions reported were mastitis (24%), other infections (24%) and depressive disorders (21%). The global theme that emerged was "<it>complexity of managing risk in prescribing for breastfeeding women"</it>. The organising themes were: <it>certainty around decision-making; uncertainty around decision-making; need for drug information to be available, consistent and reliable; joint decision-making; the vulnerable "third party" </it>and <it>infant feeding decision</it>. Decision-making is a spectrum from a straight forward decision, such as treatment of mastitis, to a complicated one requiring multiple inputs and consideration. GPs use more information seeking and collaboration in decision-making when they perceive the problem to be more complex, for example, in postnatal depression.</p> <p>Conclusion</p> <p>GPs feel that prescribing medicines for breastfeeding women is a contentious issue. They manage the risk of prescribing by gathering information and assessing the possible effects on the breastfed infant. Without evidence-based information, they sometimes recommend cessation of breastfeeding unnecessarily.</p

    NMR methods to monitor the enzymatic depolymerization of heparin

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    Heparin and the related glycosaminoglycan, heparan sulfate, are polydisperse linear polysaccharides that mediate numerous biological processes due to their interaction with proteins. Because of the structural complexity and heterogeneity of heparin and heparan sulfate, digestion to produce smaller oligosaccharides is commonly performed prior to separation and analysis. Current techniques used to monitor the extent of heparin depolymerization include UV absorption to follow product formation and size exclusion or strong anion exchange chromatography to monitor the size distribution of the components in the digest solution. In this study, we used 1H nuclear magnetic resonance (NMR) survey spectra and NMR diffusion experiments in conjunction with UV absorption measurements to monitor heparin depolymerization using the enzyme heparinase I. Diffusion NMR does not require the physical separation of the components in the reaction mixture and instead can be used to monitor the reaction solution directly in the NMR tube. Using diffusion NMR, the enzymatic reaction can be stopped at the desired time point, maximizing the abundance of larger oligosaccharides for protein-binding studies or completion of the reaction if the goal of the study is exhaustive digestion for characterization of the disaccharide composition. In this study, porcine intestinal mucosa heparin was depolymerized using the enzyme heparinase I. The unsaturated bond formed by enzymatic cleavage serves as a UV chromophore that can be used to monitor the progress of the depolymerization and for the detection and quantification of oligosaccharides in subsequent separations. The double bond also introduces a unique multiplet with peaks at 5.973, 5.981, 5.990, and 5.998 ppm in the 1H-NMR spectrum downfield of the anomeric region. This multiplet is produced by the proton of the C-4 double bond of the non-reducing end uronic acid at the cleavage site. Changes in this resonance were used to monitor the progression of the enzymatic digestion and compared to the profile obtained from UV absorbance measurements. In addition, in situ NMR diffusion measurements were explored for their ability to profile the different-sized components generated over the course of the digestion

    Analysis and characterization of heparin impurities

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    This review discusses recent developments in analytical methods available for the sensitive separation, detection and structural characterization of heparin contaminants. The adulteration of raw heparin with oversulfated chondroitin sulfate (OSCS) in 2007–2008 spawned a global crisis resulting in extensive revisions to the pharmacopeia monographs on heparin and prompting the FDA to recommend the development of additional physicochemical methods for the analysis of heparin purity. The analytical chemistry community quickly responded to this challenge, developing a wide variety of innovative approaches, several of which are reported in this special issue. This review provides an overview of methods of heparin isolation and digestion, discusses known heparin contaminants, including OSCS, and summarizes recent publications on heparin impurity analysis using sensors, near-IR, Raman, and NMR spectroscopy, as well as electrophoretic and chromatographic separations
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