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首页> 外文期刊>The Journal of Experimental Biology >Hydrodynamic stimulation of dinoflagellate bioluminescence: a computational and experimental study
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Hydrodynamic stimulation of dinoflagellate bioluminescence: a computational and experimental study

机译:鞭毛生物发光的流体动力刺激:计算和实验研究

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摘要

Dinoflagellate bioluminescence provides a near-instantaneous reporter of cell response to flow. Although both fluid shear stress and acceleration are thought to be stimulatory, previous studies have used flow fields dominated by shear. In the present study, computational and experimental approaches were used to assess the relative contributions to bioluminescence stimulation of shear stress and acceleration in a laminar converging nozzle. This flow field is characterized by separate regions of pronounced acceleration away from the walls, and shear along the wall. Bioluminescence of the dinoflagellates Lingulodinium polyedrum and Ceratocorys horrida, chosen because of their previously characterized different flow sensitivities, was imaged with a low-light video system. Numerical simulations were used to calculate the position of stimulated cells and the levels of acceleration and shear stress at these positions. Cells were stimulated at the nozzle throat within the wall boundary layer where, for that downstream position, shear stress was relatively high and acceleration relatively low. Cells of C. horrida were always stimulated significantly higher in the flow field than cells of L. polyedrum and at lower flow rates, consistent with their greater flow sensitivity. For both species, shear stress levels at the position of stimulated cells were similar to but slightly greater than previously determined response thresholds using independent flow fields. L polyedrum did not respond in conditions where acceleration was as high as 20 g. These results indicate that shear stress, rather than acceleration, was the stimulatory component of flow. Thus, even in conditions of high acceleration, dinoflagellate bioluminescence is an effective marker of shear stress.
机译:鞭毛生物发光提供了细胞对血流反应的近乎瞬时的报告。尽管流体剪切应力和加速度都被认为是刺激性的,但先前的研究已经使用了以剪切为主的流场。在本研究中,使用计算和实验方法来评估层流收敛喷嘴中剪切应力和加速度对生物发光刺激的相对贡献。该流场的特征在于远离壁的明显加速的分离区域,并且沿着壁剪切。用弱光视频系统成像了由于鞭毛的先前具有不同的流动敏感性而选择的鞭毛的多鞭毛藻和大角藻的生物发光。使用数值模拟来计算受激细胞的位置以及这些位置的加速度和切应力水平。在壁边界层内的喷嘴喉处刺激细胞,对于下游位置,剪应力相对较高,而加速度相对较低。在流场中,比起多角锥虫细胞,在更低的流速下,总会刺激霍氏梭菌细胞显着更高,这与其更高的流动敏感性相符。对于这两个物种,在受激细胞位置处的剪切应力水平与使用独立流场确定的响应阈值相似,但略大于先前确定的响应阈值。在加速高达20 g的条件下,多唾液不适。这些结果表明,剪切应力而不是加速度是流动的刺激成分。因此,即使在高加速度的条件下,鞭毛生物发光也是剪切应力的有效标志。

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