Wöhl Saskia, Schuster Stefan
Universität Erlangen-Nürnberg, Institut für Zoologie II, Staudtstrasse 5, D-91058 Erlangen, Germany.
J Exp Biol. 2007 Jan;210(Pt 2):311-24. doi: 10.1242/jeb.02646.
Once their shots have successfully dislodged aerial prey, hunting archer fish monitor the initial values of their prey's ballistic motion and elicit an adapted rapid turning maneuver. This allows these fish to head straight towards the later point of catch with a speed matched to the distance to be covered. To make the catch despite severe competition the fish must quickly and yet precisely match their turn and take-off speed to the initial values of prey motion. However, the initial variables vary over broad ranges and can be determined only after prey is dislodged. Therefore, the underlying neuronal circuitry must be able to drive a maneuver that combines a high degree of precision and flexibility at top speed. To narrow down which neuronal substrate underlies the performance we characterized the kinematics of archer fish predictive starts using digital high-speed video. Strikingly, the predictive starts show all hallmarks of Mauthner-driven teleost C-type fast-starts, which have previously not been noted in feeding strikes and were not expected to provide the high angular accuracy required. The high demands on flexibility and precision of the predictive starts do not compromise their performance. On the contrary, archer fish predictive starts are among the fastest C-starts known so far among teleost fish, with peak linear speed beyond 20 body lengths s(-1), angular speed over 4500 deg. s(-1), maximum linear acceleration of up to 12 times gravitational acceleration and peak angular acceleration of more than 450 000 deg. s(-2). Moreover, they were not slower than archer fish escape C-starts, elicited in the same individuals. Rather, both escapes and predictive starts follow an identical temporal pattern and all kinematic variables of the two patterns overlap. This kinematic equivalence strongly suggests that archer fish recruit their C-start escape network of identified reticulospinal neurons, or elements of it, to drive their predictive starts. How the network drives such a rather complex behavior without compromising speed is a wide open question.
一旦它们的喷射成功击落空中猎物,射水鱼在捕食时会监测猎物弹道运动的初始值,并引发适应性快速转向动作。这使这些鱼能够以与待游动距离相匹配的速度径直游向猎物稍后的被捕点。为了在激烈竞争中成功捕获猎物,鱼必须迅速且精确地使它们的转向和起飞速度与猎物运动的初始值相匹配。然而,初始变量在很宽的范围内变化,并且只有在猎物被击落之后才能确定。因此,潜在的神经回路必须能够在最高速度下驱动一种兼具高度精确性和灵活性的动作。为了缩小哪种神经基质是这种行为的基础,我们使用数字高速视频对射水鱼预测性起跳的运动学特征进行了描述。令人惊讶的是,预测性起跳显示出所有由莫氏神经元驱动的硬骨鱼C型快速启动的特征,而此前在捕食攻击中并未注意到这些特征,并且预计它们无法提供所需的高角度精度。对预测性起跳的灵活性和精确性的高要求并没有影响其表现。相反,射水鱼的预测性起跳是迄今为止已知的硬骨鱼中最快的C型启动之一,峰值线速度超过20体长/秒,角速度超过4500度/秒,最大线加速度高达重力加速度的12倍,峰值角加速度超过450,000度/秒²。此外,它们并不比在同一批个体中引发的射水鱼逃避C型启动慢。相反,逃避和预测性启动都遵循相同的时间模式,并且两种模式的所有运动学变量都重叠。这种运动学上的等效性强烈表明,射水鱼利用其已识别的网状脊髓神经元的C型启动逃避网络或其中的元件来驱动它们的预测性启动。该网络如何在不影响速度的情况下驱动这种相当复杂的行为,这是一个亟待解决的问题。