7,675 research outputs found

    The avifauna of Hazen Camp, Ellesmere Island, N.W.T.

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    Large scale flow around turbulent spots

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    Numerical simulations of a model of plane Couette flow focusing on its in-plane spatio-temporal properties are used to study the dynamics of turbulent spots.Comment: 16 pages, 6 figure

    Literary Evidence for Roman Arithmetic with Fractions

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    Isolated familial pheochromocytoma as a variant of von Hippel-Lindau disease.

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    Inherited pheochromocytomas are often part of familial syndromes, especially multiple endocrine neoplasia type 2 (MEN 2), retinal cerebellar hemangioblastomatosis [von Hippel-Lindau (vHL) disease] or neurofibromatosis type 1. It is not clear whether isolated familial pheochromocytoma exists as a separate clinical entity. In a family with pheochromocytomas in three generations and with at least seven affected members, we investigated by clinical and genetic analyses the presence or absence of associated conditions. The clinical investigations included ophthalmological and radiological studies for von Hippel-Lindau disease (magnetic resonance imaging of the brain, computed tomography of the abdomen, and direct ophthalmoscopy after mydriasis) and annual calcitonin stimulation tests for C cell disease in five members who agreed to regular follow-up. Besides the pheochromocytomas (so far, these have been multiple in five of seven individuals) no definite second associated condition was found. Genetic analysis did not identify any MEN 2-specific RET protooncogene point mutations (which are present in 97% of MEN 2a families). However, despite the complete absence of other clinical manifestations of the vHL disease (besides pheochromocytomas), a previously undescribed germline missense mutation in the vHL tumor suppressor gene was found (C775G transversion with a predicted substitution of a leucine by a valine at codon 259 in the putative vHL protein). We conclude that in this family the sole occurrence of pheochromocytoma is a variant of vHL disease

    Ocean stratification under oscillatory surface buoyancy forcing

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    Laboratory experiments with overturning circulation driven by oscillatory heat fluxes at one boundary are used to explore implications, for the ocean stratification, of a cyclic fluctuation in sea-surface buoyancy forcing. Fluctuations having a range of periods spanning the timescale for global recycling of the ocean volume through the thermocline are considered, with emphasis on inter-hemispheric \u27see-saw\u27 oscillations. Episodic sinking of dense water in the oceans is represented by convection in a channel with a base that is cooled over a central region and subjected to oscillatory heating near both ends, while providing a constant total heat input. For this simplified system the time-average interior temperature is found to be insensitive to the forcing period, but does vary with oscillation amplitude, whereas the interior fluctuations increase with forcing period. The circulation and density field are significantly different from those given by a steady forcing equal to the time-average of the actual oscillatory forcing, even for high-frequency oscillations. The results indicate that the overall stratification lies between that expected from the strongest phase of deep sinking and that given by symmetric sinking in both hemispheres. Glacial cycles are predicted to involve significant temperature fluctuations in the abyssal ocean. However, they are too short for the ocean to remain in quasi-equilibrium with the changing boundary conditions
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