The Action of Drugs, Especially Acetylcholine, on the Annelid Body Wall (Lumbricus, Arenicola)

1939 ◽  
Vol 16 (3) ◽  
pp. 251-257
Author(s):  
K. S. WU
Keyword(s):  
Skeletal Muscle ◽  
Spontaneous Activity ◽  
Body Wall ◽  
Lumbricus Terrestris ◽  
The Body ◽  
Arenicola Marina ◽  
Earthworm Gut ◽  
Mammalian Intestine ◽  
Earthworm Lumbricus ◽  
Vertebrate Skeletal Muscle

1. The actions of certain drugs (acetylcholine, eserine, atropine, nicotine, adrenaline) on strips of the body wall of the earthworm (Lumbricus terrestris) and lugworm (Arenicola marina) are described. 2. The body wall of the earthworm and lugworm resembles the dorsum of the leech, and also vertebrate skeletal muscle, in the following points: relatively insensitive to acetylcholine alone, sensitivity to acetylcholine greatly increased by eserine, response to acetylcholine abolished by nicotine. In these points, the muscles mentioned contrast with the earthworm gut and the mammalian intestine, which are: very sensitive to acetylcholine alone, sensitivity not greatly increased by eserine, response to acetylcholine abolished by atropine. 3. The various types of body wall strip differ among themselves as regards spontaneous activity, response to eserine alone, and response to adrenaline.

Memoirs: On the Reproductive Processes of the Earthworm, Lumbricus Terrestris

1925 ◽  
Vol s2-69 (274) ◽  
pp. 245-290
Author(s):  
A. J. GROVE
Keyword(s):  
Body Wall ◽  
Seminal Fluid ◽  
Lumbricus Terrestris ◽  
The Body ◽  
The Other ◽  
Reproductive Processes ◽  
Longitudinal Muscles ◽  
Earthworm Lumbricus

During the sexual congress of L.terrestris, the co-operating worms become attached to one another in a head-to-tail position in such a way that segments 9-11 of one are opposed to the clitellum of the other, and vice versa. At these points the attachment between the worms is an intimate one, assisted by the secretion of the glands associated with the diverticula of the setal pores found in certain segments, and is reinforced by the mutual penetration of the setae into the opposed body-surfaces. There is also a slighter attachment between segment 26 of one and 15 of the other. Each worm is enclosed in a slime-tube composed of mucus secreted from the epidermis. The exchange of seminal fluid is a mutual one. The fluid issues from the apertures of the vasa deferentia in segment 15, and is conducted beneath the slime-tube in pit-like depressions in the seminal grooves, which extend from segment 15 to the clitellum on each side of the body, to the clitellum, where it accumulates in the space between the lateral surfaces of segments 9-11 of one worm and the clitellum of the other. Eventually it becomes aggregated into masses in the groove between segments 9 and 10, and 10 and 11, and passes thence into the spermathecae. The seminal groove and its pit-like depressions are brought into existence by special muscles lying in the lateral blocks of longitudinal muscles of the body-wall.

Kinematic scaling of locomotion by hydrostatic animals: ontogeny of peristaltic crawling by the earthworm lumbricus terrestris

1999 ◽  
Vol 202 (6) ◽  
pp. 661-674 ◽  
Author(s):  
K.J. Quillin
Keyword(s):  
Body Mass ◽  
Body Wall ◽  
Deformable Body ◽  
Lumbricus Terrestris ◽  
The Body ◽  
Duty Factor ◽  
Body Segments ◽  
The Relationship ◽  
Dynamic Shape ◽  
Earthworm Lumbricus

This study examined the relationship between ontogenetic increase in body size and the kinematics of peristaltic locomotion by the earthworm Lumbricus terrestris, a soft-bodied organism supported by a hydrostatic skeleton. Whereas the motions of most vertebrates and arthropods are based primarily on the changes in the joint angles between rigid body segments, the motions of soft-bodied organisms with hydrostatic skeletons are based primarily on the changes in dimensions of the deformable body segments themselves. The overall kinematics of peristaltic crawling and the dynamic shape changes of individual earthworm segments were measured for individuals ranging in body mass (mb) by almost three orders of magnitude (0.012-8.5 g). Preferred crawling speed varied both within and among individuals: earthworms crawled faster primarily by taking longer strides, but also by taking more strides per unit time and by decreasing duty factor. On average, larger worms crawled at a greater absolute speed than smaller worms (U p2finity mb0.33) and did so by taking slightly longer strides (l p2finity mb0.41, where l is stride length) than expected by geometric similarity, using slightly lower stride frequencies (f p2finity mb-0.07) and the same duty factor (df p2finity mb-0.03). Circumferential and longitudinal body wall strains were generally independent of body mass, while strain rates changed little as a function of body mass. Given the extent of kinematic variation within and among earthworms, the crawling of earthworms of different sizes can be considered to show kinematic similarity when the kinematic variables are normalized by body length. Since the motions of peristaltic organisms are based primarily on changes in the dimensions of the deformable body wall, the scaling of the material properties of the body wall is probably an especially important determinant of the scaling of the kinematics of locomotion.

Stretch-sensitive neural units in the body wall of the earthworm, Lumbricus terrestris L

1976 ◽  
Vol 65 (1) ◽  
pp. 39-50
Author(s):  
C. D. Drewes ◽  
C. R. Fourtner
Keyword(s):  
Body Wall ◽  
Lumbricus Terrestris ◽  
Spike Frequency ◽  
The Body ◽  
Frequency Sensitivity ◽  
Segmental Nerve ◽  
Longitudinal Stretch ◽  
Sensory Neural ◽  
Earthworm Lumbricus

1. Sensory neural units responding to sinusoidal stretching of the body wall were studied in the earthworm, Lumbricus terrestris L. 2. A phasic stretch-sensitive unit found in segmental nerve I responded optimally to stretching at frequencies of 4-6/min. 3. The number of spikes per stretch and the spike frequency in the unit were directly related to the amplitude of the applied stretch within a range of 0-2-0-7 mm stretch/segment. 4. The ranges of amplitude and frequency sensitivity for the unit in isolated preparations corresponded closely to stretch parameters seen during peristaltic locomotion in intact animals. 5. Stretch-sensitive responses in segmental nerve II-III were more variable; some units responded to longitudinal stretch while others responded to relaxation.

The Mechanism of Proboscis Movement in Arenicola

1954 ◽  
Vol s3-95 (30) ◽  
pp. 251-270
Author(s):  
G. P. WELLS
Keyword(s):  
Body Fluid ◽  
Body Wall ◽  
The Body ◽  
Stage I ◽  
Stage Iii ◽  
Forward Movement ◽  
Arenicola Marina ◽  
Buccal Mass ◽  
The Difference ◽  
Longitudinal Muscles

The mechanism of proboscis movement is analysed in detail in Arenicola marina L. and A. ecaudata Johnston, and discussed in relation to the properties of the hydrostatic skeleton. Proboscis activity is based on the following cycle of movements in both species. Stage I. The circular muscles of the body-wall and buccal mass contract; the head narrows and lengthens. Stage IIa. The circular muscles of the mouth and buccal mass relax; the gular membrane (or ‘first diaphragm’ of previous authors) contracts; the mouth opens and the buccal mass emerges. Stage IIb. The longitudinal muscles of the buccal mass and body-wall contract; the head shortens and widens and the pharynx emerges. Stage III. As Stage I. The two species differ anatomically and in their hydrostatic relationships. In ecaudata, the forward movement of body-fluid which extrudes and distends the proboscis is largely due to the contraction of the gular membrane and septal pouches. In marina, the essential mechanism is the relaxation of the oral region which allows the general coelomic pressure to extrude the proboscis. The gular membrane of marina contracts as that of ecaudata does, but its anatomy is different and it appears to be a degenerating structure as far as proboscis extrusion is concerned. Withdrawal of the proboscis may occur while the head is still shortening and widening in Stage IIb, or while it is lengthening and narrowing in Stage III. The proboscis is used both in feeding and in burrowing; in the latter case nothing enters through the mouth; the difference is largely caused by variation in the timing of withdrawal relative to the 3-stage cycle.

scholarly journals The Arginase Activity of the Tissues of the Earthworms Lumbricus Terrestris L., and Eisenia Foetida (Savigny)

1960 ◽  
Vol 37 (4) ◽  
pp. 775-782
Author(s):  
A. E. NEEDHAM
Keyword(s):  
Body Wall ◽  
Lumbricus Terrestris ◽  
Total Activity ◽  
The Body ◽  
Arginase Activity ◽  
Unit Weight ◽  
Eisenia Foetida ◽  
Previous Evidence ◽  
Urea Production ◽  
The Difference

1. The difference in arginase activity between the tissues of Eisenia and those of Lumbricus shows a relationship to the difference in urea output by living worms of the two species under the same dietary régime. 2. In Eisenia the difference in activity between the tissues of fasting and feeding worms is much smaller than in Lumbricus. The specific outputs of urea by living, fasting and feeding worms likewise differ less than in Lumbricus. 3. These facts strengthen previous evidence in favour of a Krebs-Henseleit type of mechanism for urea production in earthworms. 4. In Eisenia the difference in arginase activity between gut and body wall is similar to, but smaller than, that in Lumbricus, and the body wall makes a major contribution to the total activity. 5. The combined concentrations of ammonia-, amino-, and urea-nitrogen initially present in homogenates of the tissues of these worms are proportional to the combined amounts of the three components excreted per unit weight by living worms of the same species and régime. 6. The two species differ in a number of other properties investigated.

scholarly journals The Movements of the Proboscis in Glycera Dibranchiata Ehlers

1937 ◽  
Vol 14 (3) ◽  
pp. 290-301
Author(s):  
G. P. WELLS
Keyword(s):  
Central Nervous System ◽  
Nervous System ◽  
Body Wall ◽  
The Body ◽  
Inhibitory Influence ◽  
Spontaneous Movement ◽  
Arenicola Marina ◽  
Glycera Dibranchiata ◽  
The Central Nervous System ◽  
Nervous Conduction

1. The gut of Glycera consists of (a) the buccal tube, (b) the pharynx, containing the jaws with their associated muscles and glands and the principal stomatogastric ganglia, (c) the oesophagus, leading from the pharynx to (d) the intestine, in which digestion occurs. 2. An "isolated extrovert" preparation is described, consisting of the buccal tube, pharynx and oesophagus. The movements of the buccal tube and oesophagus are recorded separately. The preparation has the following properties: (a) The buccal tube shows vigorous, rapid contractions with a somewhat irregular rhythm. These contractions are due to impulses coming forwards from the pharynx, the buccal tube itself having little power of spontaneous movement. (b) The oesophagus shows tone-waves, on which more rapid contractions of small amplitude may be superposed. These contractions and tone-waves are due to impulses originating in the wall of the oesophagus itself. (c) In a few preparations only, synchronous movements of buccal tube and oesophagus were seen. The site of origin of this synchronous activity was not determined. 3. An "extrovert-body wall" preparation is described, in which the movements of the body wall and buccal tube are separately recorded while the normal nervous conduction paths between them remain intact. The preparation has the following properties: (a) In most cases the body wall shows slight movements only, and the buccal tube moves little or not at all. If, however, the buccal tube be cut across close to the mouth, it begins an irregular rhythm of vigorous contractions, due to impulses originating in the pharynx, which usually continues without diminution for hours. The quiescence of the buccal tube before this cut is made indicates that the central nervous system normally exerts an inhibitory influence on the pharynx. (b) In a few preparations, correlated outbursts of contraction in the body wall and buccal tube were seen. These outbursts, which possibly correspond to extrusion movements of the intact worm, are due to impulses originating in the central nervous system. 4. The results are compared with those previously obtained on Arenicola marina, and reported in an earlier paper.

Excretion of thiosulphate, the main detoxification product of sulphide, by the lugworm arenicola marina L

1999 ◽  
Vol 202 (7) ◽  
pp. 855-866 ◽  
Author(s):  
K. Hauschild ◽  
W.M. Weber ◽  
W. Clauss ◽  
M.K. Grieshaber
Keyword(s):  
Body Wall ◽  
Sea Water ◽  
The Body ◽  
Cell Junctions ◽  
Metabolic Inhibitors ◽  
Coelomic Fluid ◽  
Arenicola Marina ◽  
Double Exponential ◽  
Electrophysiological Measurements ◽  
Double Exponential Function

Thiosulphate, the main sulphide detoxification product, is accumulated in the body fluids of the lugworm Arenicola marina. The aim of this study was to elucidate the fate of thiosulphate. Electrophysiological measurements revealed that the transepithelial resistance of body wall sections was 76+/−34 capomega cm2 (mean +/− s.d., N=14), indicating that the body wall of the lugworm is a leaky tissue in which mainly paracellular transport along cell junctions takes place. The body wall was equally permeable from both sides to thiosulphate, the permeability coefficient of which was 1. 31×10(−)3+/−0.37×10(−)3 cm h-1 (mean +/− s.d., N=30). No evidence was found for a significant contribution of the gills or the nephridia to thiosulphate permeation. Thiosulphate flux followed the concentration gradient, showing a linear correlation (r=0.997) between permeated and supplied (10–100 mmol l-1) thiosulphate. The permeability of thiosulphate was not sensitive to the presence of various metabolic inhibitors, implicating a permeation process independent of membrane proteins and showing that the lugworm does not need to use energy to dispose of the sulphide detoxification product. The present data suggest a passive permeation of thiosulphate across the body wall of A. marina. In live lugworms, thiosulphate levels in the coelomic fluid and body wall tissue decreased slowly and at similar rates during recovery from sulphide exposure. The decline in thiosulphate levels followed a decreasing double-exponential function. Thiosulphate was not further oxidized to sulphite or sulphate but was excreted into the sea water.

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