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Risk is by no means a simple concept. Natural variability and definitional problems with the concept of probability complicate the measurement and use of risk as an analytical tool. Variability requires that risk assessment methods separate natural from total risk when attempting to estimate anthropogenic risk. Failure to do so results in the over estimation of anthropogenic risk and the eventual loss of credibility for risk assessment methodologies. The common frequentist approach to probability is not consistent with anything but a modelling approach to risk assessment. When combined with its ability to account for natural variability, incorporate laboratory-assay data and offer complete statistical and experimental control, modelling is a promising approach to risk assessment. Modelling, however, is not without its drawbacks. Initialization bias can result in the over, or under, estimation of both natural and anthropogenic risk. Furthermore, model estimates are time dependent. The convergence of natural and anthropogenic risk poses problems for modelling-based risk assessment and requires clear statements as to the importance of the time dimension in risk assessment. When combined, the drawbacks to modelling-based risk assessment argue that risk should never be stated as a scalar quantity. Instead, modelling-based risk assessment should provide estimates of the complete range of risk measures (total, natural, and anthropogenic) as well as indications of convergence time. Only then can the modelling-based approach be viewed as the most appropriate means of carrying out scientifically credible risk assessment.  相似文献   
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Rat prosomatostatin was isolated from a somatostatin-producing cell line and was partially microsequenced. This indicated the amino terminal structure of cellular prosomatostatin and implied a 92-amino acid sequence for the somatostatin precursor. Based on the structure for cellular prosomatostatin, a peptide was synthesized and used to develop a radioimmunoassay directed toward the amino terminal portion of prosomatostatin. This assay has revealed two peptides containing the amino-terminal portion of prosomatostatin in a somatostatin-secreting CA-77 rat medullary thyroid carcinoma cell line. These two peptides - MW 4000 and 8000 daltons - lack somatostatin immunoreactivity. Thus, processing of prosomatostatin occurs both at the amino and carboxyl regions. These results open the way for elucidation of the structure, function and metabolism of non-somatostatin peptides derived from the amino terminus of prosomatostatin.  相似文献   
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Aphid size, although generally a good indicator of fecundity is not a good indicator of aphid performance over a wide range of conditions. In general, the greater the mean relative growth rate (MRGR) of apterous morphs of Rhopalosiphum padi (L.), the greater their fecundity. Intrinsic rate of increase (rm) is even more closely correlated with mean relative growth rate than fecundity.Once these criteria are quantified for a morph of a particular species of aphid over a range of conditions the morphs intrinsic rate of increase on a particular host can be estimated by a quick measure of its mean relative growth rate.
Résumé La taille des pucerons, bien que considérée généralement comme un bon indice de la fécondité, n'est pas un bon indice pour leurs performances dans une grande gamme de conditions. En général, plus le taux moyen de croissance relative est élevé chez les types aptères de Rhopalosiphum padi, plus leur fécondité est importante. Le taux intrinsèque de croissance (rm) est encore plus étroitement lié au taux moyen de croissance relative que la fécondité.Une fois que ces critères ont été quantifiés pour un type d'une espèce donnée de puceron dans une gamme de conditions, les taux intrinsèques de croissance des différents types sur un hôte particulier peuvent être estimés par une mesure rapide de leur taux moyen de croissance relative.
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During the final stages of spermatogenesis in rainbow trout a dramatic increase in the level of histone H4 hyperacetylation is observed which is closely correlated with the replacement of histones by protamines. In order to understand further how H4 hyperacetylation might assist in protamine replacement of the histones, we have investigated the effect of H4 hyperacetylation on chromatin structure in trout testes actively undergoing the replacement process. Long chromatin fragments enriched in hyperacetylated H4 have been isolated and characterized. Evidence is presented that hyperacetylated H4 is clustered in certain regions (domains) of late stage testis chromatin and within these domains the chromatin exhibits an altered, highly relaxed structure which is believed to be the result of the extensive hyperacetylation. These domains, which are nearly devoid of protamine, are postulated to represent an initial structural transition which is necessary for the proper histone removal and protamine replacement process to take place.  相似文献   
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