858 research outputs found

    Central Arctic Caribou and Petroleum Development: Distributional, Nutritional, and Reproductive Implications

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    We synthesize findings from cooperative research on effects of petroleum development on caribou (Rangifer tarandus granti) of the Central Arctic Herd (CAH). The CAH increased from about 6000 animals in 1978 to 23000 in 1992, declined to 18 000 by 1995, and again increased to 27 000 by 2000. Net calf production was consistent with changes in herd size. In the Kuparuk Development Area (KDA), west of Prudhoe Bay, abundance of calving caribou was less than expected within 4 km of roads and declined exponentially with road density. With increasing infrastructure, high-density calving shifted from the KDA to inland areas with lower forage biomass. During July and early August, caribou were relatively unsuccessful in crossing road/pipeline corridors in the KDA, particularly when in large, insect-harassed aggregations; and both abundance and movements of females were lower in the oil field complex at Prudhoe Bay than in other areas along the Arctic coast. Female caribou exposed to petroleum development west of the Sagavanirktok River may have consumed less forage during the calving period and experienced lower energy balance during the midsummer insect season than those under disturbance-free conditions east of the river. The probable consequences were poorer body condition at breeding and lower parturition rates for western females than for eastern females (e.g., 1988–94: 64% vs. 83% parturient, respectively; p = 0.003), which depressed the productivity of the herd. Assessments of cumulative effects of petroleum development on caribou must incorporate the complex interactions with a variable natural environment.On a procédé à une synthèse des résultats de travaux de recherche coopérative concernant les effets de l’exploitation pétrolière sur le caribou (Rangifer tarandus granti) formant la harde du centre de l’Arctique (HCA). La population de celle-ci est passée de 6000 têtes en 1978 à 23 000 en 1992, puis a diminué à 18 000 en 1995 pour augmenter de nouveau à 27 000 en 2000. La production nette des veaux allait de pair avec les changements dans la taille de la harde. Dans la zone de développement de Kuparuk (KDA), située à l’ouest de Prudhoe Bay, l’abondance des caribous qui mettaient bas était inférieure à celle prévue dans une bande de 4 km de part et d’autre des routes, et elle déclinait de façon exponentielle avec la densité routière. Avec une augmentation des infrastructures, on assistait à un déplacement du vêlage à forte densité de la KDA vers des zones de l’intérieur ayant une biomasse de fourrage moins importante. Durant juillet et au début d’août, il était assez rare que les caribous réussissent à traverser les corridors routiers/pipeliniers dans la KDA, surtout lorsqu’ils formaient de vastes agrégations harcelées par les insectes; l’abondance de même que les déplacements des femelles étaient en outre moindres au sein du complexe pétrolier de Prudhoe Bay qu’à d’autres endroits situés le long du rivage arctique. Il est possible que les femelles qui étaient exposées à l’exploitation pétrolière à l’ouest de la rivière Sagavanirktok aient consommé moins de fourrage au cours de la période de vêlage et que, durant la saison des insectes au milieu de l’été, elles aient connu une balance énergétique inférieure à celle des femelles vivant sans perturbations à l’est de la rivière. Les conséquences probables étaient un état corporel de qualité inférieure au moment de l’accouplement, et des taux de parturition plus faibles pour les femelles situées à l’ouest que pour celles situées à l’est (p. ex., de 1988 à 1994: 64 % c. 83 % de parturientes respectivement: p = 0,003), faisant ainsi baisser la productivité de la harde. Les évaluations des effets cumulatifs de l’exploitation pétrolière sur le caribou doivent intégrer les interactions complexes avec un environnement naturel variable

    SciClone: Inferring clonal architecture and tracking the spatial and temporal patterns of tumor evolution

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    The sensitivity of massively-parallel sequencing has confirmed that most cancers are oligoclonal, with subpopulations of neoplastic cells harboring distinct mutations. A fine resolution view of this clonal architecture provides insight into tumor heterogeneity, evolution, and treatment response, all of which may have clinical implications. Single tumor analysis already contributes to understanding these phenomena. However, cryptic subclones are frequently revealed by additional patient samples (e.g., collected at relapse or following treatment), indicating that accurately characterizing a tumor requires analyzing multiple samples from the same patient. To address this need, we present SciClone, a computational method that identifies the number and genetic composition of subclones by analyzing the variant allele frequencies of somatic mutations. We use it to detect subclones in acute myeloid leukemia and breast cancer samples that, though present at disease onset, are not evident from a single primary tumor sample. By doing so, we can track tumor evolution and identify the spatial origins of cells resisting therapy

    Shedding light on the elusive role of endothelial cells in cytomegalovirus dissemination.

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    Cytomegalovirus (CMV) is frequently transmitted by solid organ transplantation and is associated with graft failure. By forming the boundary between circulation and organ parenchyma, endothelial cells (EC) are suited for bidirectional virus spread from and to the transplant. We applied Cre/loxP-mediated green-fluorescence-tagging of EC-derived murine CMV (MCMV) to quantify the role of infected EC in transplantation-associated CMV dissemination in the mouse model. Both EC- and non-EC-derived virus originating from infected Tie2-cre(+) heart and kidney transplants were readily transmitted to MCMV-naĂŻve recipients by primary viremia. In contrast, when a Tie2-cre(+) transplant was infected by primary viremia in an infected recipient, the recombined EC-derived virus poorly spread to recipient tissues. Similarly, in reverse direction, EC-derived virus from infected Tie2-cre(+) recipient tissues poorly spread to the transplant. These data contradict any privileged role of EC in CMV dissemination and challenge an indiscriminate applicability of the primary and secondary viremia concept of virus dissemination

    A targeted decision aid for the elderly to decide whether to undergo colorectal cancer screening: development and results of an uncontrolled trial

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    Abstract: Background: Competing causes of mortality in the elderly decrease the potential net benefit from colorectal cancer screening and increase the likelihood of potential harms. Individualized decision making has been recommended, so that the elderly can decide whether or not to undergo colorectal cancer (CRC) screening. The objective is to develop and test a decision aid designed to promote individualized colorectal cancer screening decision making for adults age 75 and over. Methods: We used formative research and cognitive testing to develop and refine the decision aid. We then tested the decision aid in an uncontrolled trial. The primary outcome was the proportion of patients who were prepared to make an individualized decision, defined a priori as having adequate knowledge (10/15 questions correct) and clear values (25 or less on values clarity subscale of decisional conflict scale). Secondary outcomes included overall score on the decisional conflict scale, and preferences for undergoing screening. Results: We enrolled 46 adults in the trial. The decision aid increased the proportion of participants with adequate knowledge from 4% to 52% (p < 0.01) and the proportion prepared to make an individualized decision from 4% to 41% (p < 0.01). The proportion that preferred to undergo CRC screening decreased from 67% to 61% (p = 0. 76); 7 participants (15%) changed screening preference (5 against screening, 2 in favor of screening) Conclusion: In an uncontrolled trial, the elderly participants appeared better prepared to make an individualized decision about whether or not to undergo CRC screening after using the decision aid
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