Kidder George W, Petersen Christopher W, Preston Robert L
Mt. Desert Island Biological Laboratory, Salisbury Cove, Maine 04672, USA.
J Exp Zool A Comp Exp Biol. 2006 Apr 1;305(4):318-27. doi: 10.1002/jez.a.252.
Teleost fish experience passive osmotic water influx in fresh water (FW) and water outflux in salt water, which is normally compensated by water flow driven by active ion transport mechanisms. Euryhaline fish may also minimize osmotic energy demand by "behavioral osmoregulation", seeking a medium isotonic with their body fluids. Our goal was to evaluate the energy requirement for osmoregulation by the euryhaline fish Fundulus heteroclitus, to determine whether it is of sufficient magnitude to favor behavioral osmoregulation. We have developed a method of weighing small fish repetitively for long periods without apparent damage, which was used to assess changes in water content following changes in external salinity. We found that cold (4 degrees C) inhibits osmoregulatory active transport mechanisms in fish acclimated to warmer temperatures, leading to a net passive water flux which is reversed by rewarming the fish. A sudden change of salinity at room temperature triggers a transient change in water content and the initial slope can be used to measure the minimum passive flux at that temperature. With some reasonable assumptions as to the stoichiometry of the ion transport and ATP-generating processes, we can calculate the amount of respiration required for ion transport and compare it to the oxygen uptake measured previously under the same conditions. We conclude that osmoregulation in sea water requires from 6% to 10% of the total energy budget in sea water, with smaller percentages in FW, and that this fraction is probably sufficient to be a significant selective driving force favoring behavioral osmoregulation under some circumstances.
硬骨鱼在淡水中会被动地发生渗透水流入,而在盐水中则会发生水流出,这通常由主动离子转运机制驱动的水流来补偿。广盐性鱼类也可能通过“行为渗透调节”来最小化渗透能需求,即寻找与它们体液等渗的介质。我们的目标是评估广盐性鱼类——异齿底鳉的渗透调节能量需求,以确定其大小是否足以支持行为渗透调节。我们开发了一种长时间重复称量小鱼且无明显损伤的方法,用于评估外部盐度变化后鱼体含水量的变化。我们发现,低温(4摄氏度)会抑制适应较高温度的鱼类的渗透调节主动转运机制,导致净被动水通量,而将鱼重新升温可使其逆转。室温下盐度的突然变化会引发含水量的短暂变化,其初始斜率可用于测量该温度下的最小被动通量。基于离子转运和ATP生成过程的化学计量关系做出一些合理假设后,我们可以计算出离子转运所需的呼吸量,并将其与之前在相同条件下测得的氧气摄取量进行比较。我们得出结论,在海水中渗透调节需要消耗海水总能量预算的6%至10%,在淡水中消耗的比例较小,并且在某些情况下,这一比例可能足以成为支持行为渗透调节的重要选择驱动力。