Frantsevich Leonid, Gorb Stanislav
Department of Insect Ethology and Sociobiology, Schmalhausen-Institute of Zoology, B.Chmielnicki str. 15, 01601 Kiev, Ukraine.
Arthropod Struct Dev. 2004 Jan;33(1):77-89. doi: 10.1016/j.asd.2003.10.003.
Two combined mechanisms on the hornet tarsus are adapted to attachment to the substrate: a friction-based (claws and spines) and an adhesion-based one (arolium). There are two ranges of substrate roughness optimal for attachment, either very smooth or very rough. There is an intermediate range of substrate grains of small but non-zero size, where both of these mechanisms fail. The optimal size of substrate grains for hornet grasping was 50-100 microm. Maximal hold to the substrate was achieved when surface irregularities were clamped between the claws of opposite legs. In such a position, the insect could withstand an external force which was almost 25 times larger than its own weight. The tarsal chain is an important part of the entire attachment mechanism. The articulations in the kinematic chain of tibia-tarsus-pretarsus are monocondylar. Three tarsal muscles and one head of the claw retractor muscle originate in the tibia. On pull to the retractor tendon, the tarsus bends in a plane. All elements of the tarsal kinematic chain have one active degree of freedom. The distance between the intertarsomeric articulation point and the tendon of the claw retractor (75-194 microm) corresponds to an efficiency of 1 degrees per 1-3 mircom of pulling distance travelled by the tendon. The claw turns about 1 degrees per 4.3-5.0 microm of pulling distance travelled by the unguitractor. The arolium turns forward and downward simultaneously with flexion of the claws. The kinematic chain of the arolium lacks real condylar joints except the joint at the base of the manubrium. Other components are tied by flexible transmissions of the membranous cuticle. The walking hornet rests on distal tarsomeres of extended tarsi. If the retractor tendon inside the tarsus is fixed, passive extension of the tarsomeres might be replaced by claw flexion. Tarsal chain rigidity, measured with the force tester, increased when the retractor tendon was tightened. Probably, pull to the tendon compresses the tarsomeres, increasing friction within contacting areas of rippled surfaces surrounding condyles within articulations.
一种基于摩擦(爪子和刺),另一种基于粘附(爪垫)。存在两个最适合附着的基质粗糙度范围,要么非常光滑,要么非常粗糙。存在一个中等范围的小但非零尺寸的基质颗粒,在这个范围内这两种机制都会失效。黄蜂抓握的最佳基质颗粒尺寸为50 - 100微米。当表面不规则处被相对腿的爪子夹住时,可实现对基质的最大抓力。在这样的位置,昆虫能够承受几乎比其自身重量大25倍的外力。跗节链是整个附着机制的重要组成部分。胫节 - 跗节 - 前跗节运动链中的关节是单髁的。三条跗节肌和一条爪收缩肌的头部起源于胫节。当拉动收缩肌腱时,跗节在一个平面内弯曲。跗节运动链的所有元件都有一个主动自由度。跗节间关节点与爪收缩肌腱之间的距离(75 - 194微米)对应于肌腱每移动1 - 3微米产生1度的效率。爪每移动4.3 - 5.0微米转动约1度。随着爪子的弯曲,爪垫同时向前和向下转动。除了柄基部的关节外,爪垫的运动链缺乏真正的髁状关节。其他部分通过膜质表皮的柔性传动相连。行走的黄蜂依靠伸展的跗节的远端跗分节休息。如果跗节内的收缩肌腱固定,跗分节的被动伸展可能会被爪的弯曲所取代。用测力计测量时,当收缩肌腱收紧时,跗节链的刚性增加。可能是对肌腱的拉动压缩了跗分节,增加了关节内围绕髁的波纹表面接触区域内的摩擦力。