1,255 research outputs found

    TELLUS: A combined surface temperature, soil moisture and evaporation mapping approach

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    There are no author-identified significant results in this report

    How to calculate the dose of chemotherapy

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    Body surface area-dosing does not account for the complex processes of cytotoxic drug elimination. This leads to an unpredictable variation in effect. Overdosing is easily recognised but it is possible that unrecognised underdosing is more common and may occur in 30% or more of patients receiving standard regimen. Those patients who are inadvertently underdosed are at risk of a significantly reduced anticancer effect. Using published data, it can be calculated that there is an almost 20% relative reduction in survival for women receiving adjuvant chemotherapy for breast cancer as a result of unrecognised underdosing. Similarly, the cure rate of cisplatin-based chemotherapy for advanced testicular cancer may be reduced by as much as 10%. The inaccuracy of body surface area-dosing is more than an inconvenience and it is important that methods for more accurate dose calculation are determined, based on the known drug elimination processes for cytotoxic chemotherapy. Twelve rules for dose calculation of chemotherapy are given that can be used as a guideline until better dose-calculation methods become available. Consideration should be given to using fixed dose guidelines independent of body surface area and based on drug elimination capability, both as a starting dose and for dose adjustment, which may have accuracy, safety and financial advantages

    Fracture initiation and crack propagation of acrylonitrile-butadiene-styrene (ABS) in organic solvents

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    The effects of organic liquid environments on the fracture behaviour of acrylonitrile-butadiene-styrene (ABS) have been investigated. Fracture initiation experiments showed that K i 2 , ( K i being the stress intensity factor at crack/craze initiation), could be meaningfully correlated with the solvent solubility parameter ( Ī“ s ) of the different liquid environments and had a minimum value at Ī“ s = Ī“ p , where Ī“ p was the solubility parameter of ABS. For the range of organic liquids used, hydrogen bonding did not have any significant effects on the correlations. It was demonstrated that the K i 2 āˆ’ Ī“ s correlations could also be usefully extended to other materials such as plain and glass-filled polystyrenes. At a common crack speed ( Ć„ ), the fracture toughness ( R ) values in ā€œcrazingā€ liquids (i.e. alcohols) were greater than those in ā€œcrackingā€ solvents (i.e. acetone, benzene, toluene, etc.) which usually caused a ā€œdissolutionā€ effect on the plastic. From crack propagation experiments, and using fracture mechanics analyses, definite R ( Ć„ ) and K c ( Ć„ ) relationships for ABS immersed in toluene, carbon tetrachloride and methanol were determined. These experimental results showed that crack propagation was relaxation controlled and agreed well with a recent theoretical analysis due to Williams and Marshall for environmental crack and craze growth in polymers. Finally, SEM pictures were presented to show the remarkable differences in the fracture morphologies of ABS in both ā€œcrazingā€ and ā€œcrackingā€ liquid environments.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/44670/1/10853_2004_Article_BF00551442.pd

    Pulmonary vasoconstrictor action of KCNQ potassium channel blockers

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    KCNQ channels have been widely studied in the nervous system, heart and inner ear, where they have important physiological functions. Recent reports indicate that KCNQ channels may also be expressed in portal vein where they are suggested to influence spontaneous contractile activity. The biophysical properties of K+ currents mediated by KCNQ channels resemble a current underlying the resting K+ conductance and resting potential of pulmonary artery smooth muscle cells. We therefore investigated a possible role of KCNQ channels in regulating the function of pulmonary arteries by determining the ability of the selective KCNQ channel blockers, linopirdine and XE991, to promote pulmonary vasoconstriction. Linopirdine and XE991 both contracted rat and mouse pulmonary arteries but had little effect on mesenteric arteries. In each case the maximum contraction was almost as large as the response to 50 mM K+. Linopirdine had an EC50 of around 1 Ī¼M and XE991 was almost 10-fold more potent. Neither removal of the endothelium nor exposure to phentolamine or Ī±,Ī²-methylene ATP, to block Ī±1-adrenoceptors or P2X receptors, respectively, affected the contraction. Contraction was abolished in Ca2+-free solution and in the presence of 1 Ī¼M nifedipine or 10 Ī¼M levcromakalim

    Understanding species distribution in dynamic populations : a new approach using spatioā€temporal point process models

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    Funding: EU consolidatorā€™s grant STATEMIG 310820 (SB).Understanding and predicting a speciesā€™ distribution across a landscape is of central importance in ecology, biogeography and conservation biology. However, it presents daunting challenges when populations are highly dynamic (i.e. increasing or decreasing their ranges), particularly for small populations where information about ecology and life history traits is lacking. Currently, many modelling approaches fail to distinguish whether a site is unoccupied because the available habitat is unsuitable or because a species expanding its range has not arrived at the site yet. As a result, habitat that is indeed suitable may appear unsuitable. To overcome some of these limitations, we use a statistical modelling approach based on spatioā€temporal logā€Gaussian Cox processes. These model the spatial distribution of the species across available habitat and how this distribution changes over time, relative to covariates. In addition, the model explicitly accounts for spatioā€temporal dynamics that are unaccounted for by covariates through a spatioā€temporal stochastic process. We illustrate the approach by predicting the distribution of a recently established population of Eurasian cranes Grus grus in England, UK, and estimate the effect of a reintroduction in the range expansion of the population. Our models show that wetland extent and perimeterā€toā€area ratio have a positive and negative effect, respectively, in crane colonisation probability. Moreover, we find that cranes are more likely to colonise areas near already occupied wetlands and that the colonisation process is progressing at a low rate. Finally, the reintroduction of cranes in SW England can be considered a humanā€assisted longā€distance dispersal event that has increased the dispersal potential of the species along a longitudinal axis in S England. Spatioā€temporal logā€Gaussian Cox process models offer an excellent opportunity for the study of species where information on life history traits is lacking, since these are represented through the spatioā€temporal dynamics reflected in the model.PostprintPeer reviewe
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