Hydrodynamic interaction leads to the accumulation of Chlamydomonas reinhardtii near a solid-liquid interface.

IF 2.4 3区 物理与天体物理 Q2 PHYSICS, FLUIDS & PLASMAS
Chunhe Li, Hongyi Bian, Yateng Qiao, Jin Zhu, Zijie Qu
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引用次数: 0

Abstract

The physical mechanism of microbial motion near solid-liquid interfaces is crucial for understanding various biological phenomena and developing ecological applications. However, limited works have been conducted on the swimming behavior of C.reinhardtii, a typical "puller" type cell, near solid surfaces, particularly with varying and conflicting experimental observations. Here, we investigate the swimming behavior of C.reinhardtii using a three-dimensional real-time tracking microscopy system both near a solid-liquid interface and in the fluid bulk region. We explore the relationships between the cell density, swimming speed and orientation with respect to the distance from the solid-liquid interface, confirming the phenomenon of C.reinhardtii accumulation near the solid-liquid interface. Based on the traditional definitions of "pusher" and "puller" cells, we propose a simplified model consisting of a pair of mutually perpendicular force dipoles for C.reinhardtii. This model is employed to analyze the complex hydrodynamic interactions between C.reinhardtii and the solid surface, providing a potential theoretical explanation for the observed accumulation phenomenon at the solid-liquid interface.

水动力相互作用导致莱茵衣藻在固液界面附近聚集。
微生物在固液界面附近运动的物理机制对于理解各种生物现象和开发生态应用至关重要。然而,关于c.r ainhardtii(一种典型的“拉”型细胞)在固体表面附近的游动行为的研究有限,特别是实验观察结果不同且相互矛盾。在这里,我们使用三维实时跟踪显微镜系统研究了莱茵哈蒂虫在固液界面附近和流体体积区域的游动行为。我们探索了细胞密度、游动速度和方向与离固液界面距离的关系,证实了赖因哈蒂弧菌在固液界面附近聚集的现象。基于传统的“推”和“拉”细胞的定义,我们提出了一个由一对相互垂直的力偶极子组成的简化模型。该模型用于分析c.r inhardtii与固体表面之间复杂的水动力相互作用,为观察到的固液界面堆积现象提供了潜在的理论解释。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Physical Review E
Physical Review E PHYSICS, FLUIDS & PLASMASPHYSICS, MATHEMAT-PHYSICS, MATHEMATICAL
CiteScore
4.50
自引率
16.70%
发文量
2110
期刊介绍: Physical Review E (PRE), broad and interdisciplinary in scope, focuses on collective phenomena of many-body systems, with statistical physics and nonlinear dynamics as the central themes of the journal. Physical Review E publishes recent developments in biological and soft matter physics including granular materials, colloids, complex fluids, liquid crystals, and polymers. The journal covers fluid dynamics and plasma physics and includes sections on computational and interdisciplinary physics, for example, complex networks.
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