Modelling of microscale patch encounter by chemotactic protozoa

被引:20
作者
Blackburn, N [1 ]
Fenchel, T [1 ]
机构
[1] Univ Copenhagen, Marine Biol Lab, DK-3000 Helsingor, Denmark
关键词
D O I
10.1016/S1434-4610(99)70034-9
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
A model of protozoan chemotaxis, based on the rate of change of chemoreceptor occupancy, was used to analyse the efficiency of chemotaxis in a variety of situations. Simulated swimming behaviour replicated patterns observed experimentally. These were classified into three forms of chemosensory behaviour; run-tumble, steered turning, and helical klinotaxis, All three could be simulated from a basic model of chemotaxis by modifying memory times and rotational velocities. In order to steer during helical klinotaxis, the cell must have a short term memory for responding to a signal within a fraction of the time period of the helix. Steered turning was identified as a form where cells react to negative changes in concentration by steering around the turn to swim back up the gradient. All 3 forms were quite effective for encountering targets within the response radius, A response to negative changes in concentration, experienced when the cell is moving away from a target, was found to be important in the absence of periodic changes in swimming direction. The frequency of patch encounter at a fixed density was calculated to be roughly proportional to swimming speed. On the basis of the model, cells are only able to sense point sources within a radius of a few mm. However, even a response radius of 1 mm is enough to increase encounter probability of otherwise minute targets by 2 orders of magnitude. The mean time for patch encounter was calculated to be an exponential function of the mean distance between patches. This results in a very sharp threshold at approximately 6 cm, above which they are not encountered by protozoa within time periods of several days.
引用
收藏
页码:337 / 343
页数:7
相关论文
共 17 条
[1]   Robustness in bacterial chemotaxis [J].
Alon, U ;
Surette, MG ;
Barkai, N ;
Leibler, S .
NATURE, 1999, 397 (6715) :168-171
[2]   Formation of 30- to 40-micrometer-thick laminations by high-speed marine bacteria in microbial mats [J].
Barbara, GM ;
Mitchell, JG .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1996, 62 (11) :3985-3990
[3]   Spatially explicit simulations of a microbial food web [J].
Blackburn, N ;
Azam, F ;
Hagstrom, A .
LIMNOLOGY AND OCEANOGRAPHY, 1997, 42 (04) :613-622
[4]   Microscale nutrient patches in planktonic habitats shown by chemotactic bacteria [J].
Blackburn, N ;
Fenchel, T ;
Mitchell, J .
SCIENCE, 1998, 282 (5397) :2254-2256
[5]   SIMULATING BACTERIAL CLUSTERING AROUND PHYTOPLANKTON CELLS IN A TURBULENT OCEAN [J].
BOWEN, JD ;
STOLZENBACH, KD ;
CHISHOLM, SW .
LIMNOLOGY AND OCEANOGRAPHY, 1993, 38 (01) :36-51
[6]  
BROWN D A, 1974, Proceedings of the National Academy of Sciences of the United States of America, V71, P1388, DOI 10.1073/pnas.71.4.1388
[7]   Feeding in Peridiniopsis berolinensis (Dinophyceae):: new observations on tube feeding by an omnivorous, heterotrophic dinoflagellate [J].
Calado, A. J. ;
Moestrup, O. .
PHYCOLOGIA, 1997, 36 (01) :47-59
[9]  
CRENSHAW HC, 1993, B MATH BIOL, V55, P212
[10]   Motile chemosensory behaviour of phagotrophic protists: Mechanisms for and efficiency in congregating at food patches [J].
Fenchel, T ;
Blackburn, N .
PROTIST, 1999, 150 (03) :325-336