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THESIS APPROVAL

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undulatory swimming. Also, the peristaltic crawling was present when worm had a<br />

movement by getting extra traction from bristles that can be projected from the side of<br />

its body. The explanation of such phenomena in most oligochaetes is there are<br />

muscles arranged into two distinct layers in the body wall - the circular and<br />

longitudinal muscle layers. A nerve cord below the intestine along the entire length<br />

of the body worm has a major role of controlling these muscles that cause it to move.<br />

Because of no hard skeletal elements to which these muscles attach, the forces were<br />

produced since worms contract simply act upon the inner fluid-filled body<br />

compartments (Jamieson, 1981). This design is referred to as a hydrostatic skeleton,<br />

a typical manner of many burrowing invertebrates which lack appendages (Barnes,<br />

1974). When the worm crawls, chaeta are protruded in those segments that are<br />

undergoing shortening and thickening due to longitudinal muscle contraction. This<br />

helps to anchor these segments to the substrate. In contrast, chaetae are retracted in<br />

segments that are undergoing elongation and thinning due to circular muscle<br />

contraction (Jamieson, 1981).<br />

Clump living of L. hoffmeisteri population found in this observation<br />

indicates an orientation behavior which is referred to as thigmotaxis (Drewes and<br />

Fourtner, 1989). In nature, suitably cramped microhabitats may be established<br />

including tight spaces between submerged, decaying leaves or crevices in submerged<br />

(Stephenson, 1930). These preferred habitats offer worm protection from predators as<br />

well as access them to food (Brinkhurst and Gelder, 1991). Additionally, these<br />

organisms seemed to be vigilant in the environmental surroundings. Worms showed<br />

rapidly pulled back their tail if they were touched by using glass rod. This reflex<br />

response in L. hoffmeisteri is as possible as other oligochaetes since there are<br />

mechanosensory neurons present in these animals to detect touch, vibration and<br />

pressure. Drewes and Cain (1999) described this mechanism in which when a tail<br />

segments of oligochaete worm was touched, it responded reflexively by waving of<br />

muscle contraction that move in a direction opposite to the actual direction of body<br />

propulsion in the term retrograde. Furthermore, those tails holding up to the water<br />

surface were quickly withdrawn when they felt threatened. Since these worms have<br />

tiny photoreceptor cells scattered along their tail segments (Drewes and Fourtner,<br />

89

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