Head waving in Aplysia californica. II. Functional anatomy and muscular activity during behaviour.

1994 ◽  
Vol 195 (1) ◽  
pp. 53-74
Author(s):  
F M Kuenzi ◽  
T J Carew
Keyword(s):  
Muscle Activity ◽  
Body Wall ◽  
Longitudinal Muscle ◽  
Aplysia Californica ◽  
The Body ◽  
Vertical Posture ◽  
Muscle Fibres ◽  
Spatial And Temporal Patterns ◽  
Head Region ◽  
Muscle Fascicles

Bending and twisting movements of the body during head-waving behaviour of the sea hare Aplysia californica are produced by the concerted action of the muscles of the body wall on the hydrostatic skeleton formed by the haemocoel and internal organs. In this study, we describe the orientations and possible mechanical actions of muscles in the body wall. We also describe the spatial and temporal patterns of longitudinal muscle activity during different head-waving movements in a freely moving animal. The body-wall muscles are arranged as a network of longitudinal, circular and left- and right-handed helical muscle fascicles. Each fascicle consists of a few to several hundred muscle fibres enclosed in a connective tissue sheath. The sheath also connects muscle fascicles of different orientations at the points where they cross, forming a tightly connected network. In addition, a series of large longitudinal muscle fascicles, including the lateral columellar muscles, lies against the inside wall of the dorsal hemicylinder of the animal. In animals with hydrostatic skeletons, longitudinal and circular muscles are necessary for producing all basic elongation, shortening and bending movements, and in Aplysia, the extensive distribution of helical muscles provides the animal with the ability to twist its body about the longitudinal axis, as is observed during horizontal head-waving movements. Muscle activity in the lateral muscles is antiphasically coordinated during horizontal bends, and when the animal is bent to one side, movement towards the centre is accompanied by muscle activity on the side of shortening, i.e. there is no passive return to centre. The muscles near the holdfast are the most active during head-waving movements, with relatively little activity in the head region. The activity of dorsal muscles corresponds to both the existing vertical posture of the body and to discrete dorsal bending movements. In most cases, depression of the head is passive, i.e. both dorsal and ventral longitudinal muscles relax, although foot muscles may also be involved. These observations, together with the constancy of the hydrostatic pressure in the haemocoel during all movements in animals attached to the substratum, suggest specific patterns of motor neurone coordination during different movements.

scholarly journals THE STRUCTURE OF THE SMOOTH MUSCLE FIBRES IN THE BODY WALL OF THE EARTHWORM

1957 ◽  
Vol 3 (1) ◽  
pp. 111-122 ◽  
Author(s):  
Jean Hanson
Keyword(s):  
Smooth Muscle ◽  
Phase Contrast ◽  
Body Wall ◽  
Longitudinal Muscle ◽  
Lumbricus Terrestris ◽  
Mirror Image ◽  
The Body ◽  
The Other ◽  
Muscle Fibres ◽  
Muscle Coat

1. The structure of the smooth muscle fibres in the longitudinal muscle coat of the body wall of Lumbricus terrestris has been investigated by phase contrast light microscopy and electron microscopy. 2. The muscle fibre is ribbon-shaped, and attached to each of its two surfaces is a set of myofibrils. These are also ribbon-shaped, and they lie with their surfaces perpendicular to the surfaces of the fibre, and their inner edges nearly meeting in the middle of the fibre. These fibrils are oriented at an angle to the fibre axis, and diminish greatly in width as they approach the edge of the fibre. The orientation of the set of fibrils belonging to one surface of the fibre is the mirror image of that of the set belonging to the other surface; thus, when both sets are in view in a fibre lying flat on one face, the fibre exhibits double oblique striation. A comparison of extended and contracted fibres indicates that as the fibre contracts, the angle made between fibre and fibril axes increases (e.g. from 5 to 30°) and so does the angle made between the two sets of fibrils (e.g. from 10 to 60°). 3. The myofibril, throughout its length, contains irregularly packed filaments, commonly 250 A in diameter, which are parallel to its long axis and remain straight in contracted muscles. Between them is material which probably consists of much finer filaments. Thus A and I bands are absent. 4. Bound to one face of each fibril, but not penetrating inside it, is a regularly spaced series of transverse stripes. They are of two kinds, alternating along the length of the fibril, and it is suggested that they are comparable to the Z and M lines of a cross-striated fibril. The spacing of these stripes is about 0.5 µ ("Z" to "Z") in extended muscles, and 0.25 µ in contracted muscles. A bridge extends from each stripe across to the stripeless surface of the next fibril.

The Cuticle of Peripatopsis Moseleyi

1964 ◽  
Vol s3-105 (71) ◽  
pp. 281-299
Author(s):  
ELAINE A. ROBSON
Keyword(s):  
Body Wall ◽  
Light And Electron Microscopy ◽  
Thick Layer ◽  
The Body ◽  
Muscle Fibres ◽  
Terrestrial Arthropods ◽  
Dermal Glands ◽  
Arthropod Cuticle ◽  
Primitive Condition ◽  
Pore Canals

The integument of Peripatopsis moseleyi has been examined by light and electron microscopy with particular reference to the structure and formation of the cuticle. The evidence supports the idea that Peripatus is a true arthropod but not that it has direct affinities with the annelids. The characteristics of arthropod cuticle are present in their simplest form and pore canals and dermal glands are lacking. The cuticle is 1 or 2 µ, thick except in the hardened claws and spines. Above the procuticle (chitinprotein) is a thin 4-layered epicuticle. It is possible that the innermost of the 4 layers (prosclerotin) may correspond to cuticulin of other arthropods. In the claws and spines tanning in this layer extends to the procuticle. Hydrofuge properties of the cuticle probably depend on the outer layers of epicuticle, and it is suggested that the lamina concerned might consist of oriented lipid associated with lipoprotein (Dr. J. W. L. Beament). Wax and cement are absent. Non-wettability of the cuticle is probably ensured by the contours of micropapillae which cover the surface. Similar structures arise in Collembola and other terrestrial arthropods by convergence. The formation of new cuticle before ecdysis is described. After the epicuticular layers are complete, the bulk of the procuticle is laid down in a manner probably common to all arthropods. Secreted materials originate in small vesicles derived from rough endoplasmic reticulum and from scattered Golgi regions. The latter contribute to larger vacuoles which rise to the surface of the cell and liberate material in a fluid state. This later consolidates to form procuticle. Vesicles may also open to the surface directly, and ribosomes probably occur free in the cytoplasm. At this stage the cell surface is reticulate, especially under micropapillae. The ordinary epidermis has only one kind of cell, attached to the cuticle by tonofibrils disposed like the ribs of a shuttlecock, and to the fibrous sheaths of underlying muscle-fibres by special fibres of connective tissue. These features and the presence of numerous sensory papillae are associated with the characteristic mobility of the body wall. The appearance of epidermal pigment granules, mitochondria, the nuclear membrane, and a centriole are noted. No other cells immediately concerned in the formation of cuticle have been found. By contrast myriapods, which do not have wax either, possess dermal glands secreting far more lipid than is found in the Onychophora. The wax layer found in insects and some arachnids constitutes an advance of high selective value which emphasizes the primitive condition of the Onychophora. It is noted that the thick layer of collagen separating the haemocoel from the epidermis probably restricts the transfer of materials. It is suggested that since some features of cuticular structure and formation appear to be common to all arthropods, it is possible that some of the endocrine mechanisms associated with ecdysis may also be similar throughout the phylum.

Head waving in Aplysia californica. I. Behavioural characterization of searching movements.

1994 ◽  
Vol 195 (1) ◽  
pp. 35-51
Author(s):  
F M Kuenzi ◽  
T J Carew
Keyword(s):  
Body Movement ◽  
Aplysia Californica ◽  
The Body ◽  
Head Region ◽  
Discrete Movements ◽  
Vertical Movements ◽  
Searching Behaviour ◽  
Neural Organization ◽  
Discrete Movement ◽  
The Individual

Searching is an important component of several types of goal-directed behaviour. In soft-bodied animals, searching behaviour can appear quite complex because the range of body movement is not constrained by joints, limbs or muscles with discrete areas of origin and insertion. In addition, animals exhibiting this type of behaviour utilize their maximum freedom of movement. In this paper, we describe the head-waving searching behaviour of the sea hare Aplysia californica by characterizing patterns of movements and the changes in body shape that underlie these movements. A bout of head waving consists of a series of discrete movements separated by pauses. Each discrete movement lasts 4-10s and is directed either horizontally or vertically with respect to stationary part of the animal. Large movements, such as bending from the extreme right to the extreme left, consist of a series of these shorter movements separated by pauses lasting 1-2s. In all head-waving movements, the transverse axis of the head is kept relatively parallel with the substratum. Thus, vertical movements require only bending of the body, whereas horizontal movements require twisting of the body, particularly when the posture is more erect. During head waving, the anterior two-thirds of the body is free to move, but most of the bending occurs immediately posterior to the head region. There is no periodicity of movements within a bout of head waving, although isolated instances of repeated movements are sometimes observed. Therefore, although the individual movements during head waving are relatively simple, the absence of a patterned sequence accounts for the complexity of the overall behaviour. These observations both constrain models of the neural organization of head waving and provide criteria for categorizing head-waving movements in further behavioural and physiological studies.

Gross anatomy of the muscle systems and associated innervation of Apatemon cobitidis proterorhini metacercaria (Trematoda: Strigeidea), as visualized by confocal microscopy

Parasitology ◽  
2003 ◽  
Vol 126 (3) ◽  
pp. 273-282 ◽  
Author(s):  
M. T. STEWART ◽  
A. MOUSLEY ◽  
B. KOUBKOVÁ ◽  
š. šEBELOVÁ ◽  
N. J. MARKS ◽  
...  
Keyword(s):  
Nervous System ◽  
Oral Sucker ◽  
Body Wall ◽  
Circular Muscle ◽  
Gross Anatomy ◽  
The Body ◽  
Muscle Fibres ◽  
Filamentous Actin ◽  
Attachment Structures ◽  
A Site

The major muscle systems of the metacercaria of the strigeid trematode, Apatemon cobitidis proterorhini have been examined using phalloidin as a site-specific probe for filamentous actin. Regional differences were evident in the organization of the body wall musculature of the forebody and hindbody, the former comprising outer circular, intermediate longitudinal and inner diagonal fibres, the latter having the inner diagonal fibres replaced with an extra layer of more widely spaced circular muscle. Three orientations of muscle fibres (equatorial, meridional, radial) were discernible in the oral sucker, acetabulum and paired lappets. Large longitudinal extensor and flexor muscles project into the hindbody where they connect to the body wall or end blindly. Innervation to the muscle systems of Apatemon was examined by immunocytochemistry, using antibodies to known myoactive substances: the flatworm FMRFamide-related neuropeptide (FaRP), GYIRFamide, and the biogenic amine, 5-hydroxytryptamine (5-HT). Strong immunostaining for both peptidergic and serotoninergic components was found in the central nervous system and confocal microscopic mapping of the distribution of these neuroactive substances revealed they occupied separate neuronal pathways. In the peripheral nervous system, GYIRFamide-immunoreactivity was extensive and, in particular, associated with the innervation of all attachment structures; serotoninergic fibres, on the other hand, were localized to the oral sucker and pharynx and to regions along the anterior margins of the forebody.

scholarly journals Serotonin modulates muscle function in the medicinal leech Hirudo verbana

2011 ◽  
Vol 7 (6) ◽  
pp. 885-888 ◽  
Author(s):  
Shannon P. Gerry ◽  
David J. Ellerby
Keyword(s):  
Body Wall ◽  
Longitudinal Muscle ◽  
Force Production ◽  
Physiological Saline ◽  
The Body ◽  
Hirudo Verbana ◽  
Work Production ◽  
Large Length ◽  
Body Wall Muscles

The body wall muscles of sanguivorous leeches power mechanically diverse behaviours: suction feeding, crawling and swimming. These require longitudinal muscle to exert force over an extremely large length range, from 145 to 46 per cent of the mean segmental swimming length. Previous data, however, suggest that leech body wall muscle has limited capacity for force production when elongated. Serotonin (5-HT) alters the passive properties of the body wall and stimulates feeding. We hypothesized that 5-HT may also have a role in allowing force production in elongated muscle by changing the shape of the length–tension relationship (LTR). LTRs were measured from longitudinal muscle strips in vitro in physiological saline with and without the presence of 10 µM 5-HT. The LTR was much broader than previously measured for leech muscle. Rather than shifting the LTR, 5-HT reduced passive muscle tonus and increased active stress at all lengths. In addition to modulating leech behaviour and passive mechanical properties, 5-HT probably enhances muscle force and work production during locomotion and feeding.

scholarly journals Muscle fibre recruitment can respond to the mechanics of the muscle contraction

2006 ◽  
Vol 3 (9) ◽  
pp. 533-544 ◽  
Author(s):  
James M Wakeling ◽  
Katrin Uehli ◽  
Antra I Rozitis
Keyword(s):  
Motor Unit ◽  
Muscle Activity ◽  
The Body ◽  
Motor Unit Recruitment ◽  
Triceps Surae ◽  
Medial Gastrocnemius ◽  
Muscle Fibres ◽  
Strain Rates ◽  
Lower Velocity ◽  
Muscle Fascicle

This study investigates the motor unit recruitment patterns between and within muscles of the triceps surae during cycling on a stationary ergometer at a range of pedal speeds and resistances. Muscle activity was measured from the soleus (SOL), medial gastrocnemius (MG) and lateral gastrocnemius (LG) using surface electromyography (EMG) and quantified using wavelet and principal component analysis. Muscle fascicle strain rates were quantified using ultrasonography, and the muscle–tendon unit lengths were calculated from the segmental kinematics. The EMG intensities showed that the body uses the SOL relatively more for the higher-force, lower-velocity contractions than the MG and LG. The EMG spectra showed a shift to higher frequencies at faster muscle fascicle strain rates for MG: these shifts were independent of the level of muscle activity, the locomotor load and the muscle fascicle strain. These results indicated that a selective recruitment of the faster motor units occurred within the MG muscle in response to the increasing muscle fascicle strain rates. This preferential recruitment of the faster fibres for the faster tasks indicates that in some circumstances motor unit recruitment during locomotion can match the contractile properties of the muscle fibres to the mechanical demands of the contraction.

The ultrastructure of the cuticle of the nematode Syphacia obvelata (Rudolphi, 1802). II. Modifications of the cuticle in the head end

1973 ◽  
Vol 51 (2) ◽  
pp. 197-202 ◽  
Author(s):  
T. A. Dick ◽  
K. A. Wright
Keyword(s):  
Body Wall ◽  
Buccal Capsule ◽  
The Body ◽  
Head Region ◽  
Limited Region ◽  
Structural Role ◽  
Mouth Cavity ◽  
Median Zone ◽  
Syphacia Obvelata ◽  
Somatic Muscles

The head region of the pinworm Syphacia obvelata (Rudolphi, 1802) has been examined to determine the nature of modification of the cuticle responsible for, or associated with, lips and buccal capsule, cephalic papillae and amphids, cephalic inflations, and cervical alae. The median zone of the cuticle was found to be the most modified and variation in the extent and distribution of striated material is compatible with its proposed structural role. The variations found are probably related to compensation for stresses that may develop in the cuticle during the complex movements of the head end. Lips are only inconspicuous expansions of the body wall cuticle, while esophageal cuticle is strikingly different in appearance. It is proposed to refer to all regions of the mouth cavity bounded by both the lips and esophagus as the buccal capsule while only the limited region bounded by body wall cuticle may be referred to as stoma. A mechanism involving three groups of intrahypodermal cytoskeletal filaments attached to the tips of somatic muscles, esophagus, and cuticle is proposed to move the lips.

A new species of Chiridota (Echinodermata: Holothuroidea: Apodida: Chiridotidae) from Japan, and First record of C. rigida from Japan

Zootaxa ◽  
2017 ◽  
Vol 4341 (2) ◽  
pp. 243
Author(s):  
YUSUKE YAMANA ◽  
HAYATO TANAKA
Keyword(s):  
Intertidal Zone ◽  
Sea Cucumber ◽  
Body Wall ◽  
Longitudinal Muscle ◽  
First Record ◽  
The Body ◽  
New To Japan ◽  
Spinous Processes ◽  
Curved Rod ◽  
A New Species

A new apodid sea cucumber, Chiridota impatiens sp. nov., is described from the intertidal zone of Okinawa, Japan, and C. rigida Semper, 1867 is also described from the intertidal zone of Wakayama, as new to Japan. C. impatiens sp. nov. is approximately 60–70 mm, with 12 tentacles and 4–7 pairs of digits per tentacle, red or reddish brown in living specimens. The tentacles contain curved rod ossicles, with spinous processes and many branches in C. rigida, however, in C. impatiens sp. nov., the curved rod ossicles are crescent-shaped, sometimes distally, with spinous processes and rarely a few branches on the circumference. In both species, the body wall contains flattened rod ossicles, mostly present along the longitudinal muscle and mesentery, curved rod ossicles primarily in the body wall, and wheel ossicles only in the wheel-papillae. In C. rigida, the contents of the wheel-papillae form a hemispherical sack-shaped structures, in which the teeth-side of the wheel ossicles mostly faces towards the outside of the body. In C. impatiens sp. nov., the contents of the wheel-papillae form a cord-shaped structure (present in both preserved and living specimens), in which the teeth-side of the wheel ossicles faces various directions, and that can be induced to break through the skin of the papillae if stimulated in living specimens. 

Differentiation of Ectoderm Implanted into the Primordium of the Limb Bud in the Amphibian Embryo and its Influence upon the Limb

1946 ◽  
Vol 22 (3-4) ◽  
pp. 101-106
Author(s):  
WALTER BRANDT
Keyword(s):  
Body Wall ◽  
Distal Part ◽  
The Body ◽  
Limb Bud ◽  
Muscle Fibres ◽  
Tail Bud ◽  
Amphibian Embryo ◽  
Microscopical Analysis ◽  
Proximal Half ◽  
Host Embryo

1. A microscopical analysis was made concerning the differentiation of ectoderm cut from the tip of the tail-bud of an amphibian embryo (Amblystoma mexicanum, stages 35-37, Harrison) after its implantation into the primordium of the limb-bud of a host embryo 3-5 weeks after operation. 2. The ectoderm which lay deep in the tissues of the limb differentiated either into solid epithelial cords or into cysts. 3. The ectoderm which was attached outside the limb differentiated into notched ectodermal elevations which included a mesenchymal core. 4. A microscopical analysis was made concerning the development of deformities of limbs as the result of the operation. 5. The scapula may be divided into isolated pieces, bundles of muscle fibres separating the pieces from each other. 6. A supernumerary piece of cartilage can develop close to the cartilage of the scapula. 7. The suprascapula may be absent and its place taken by a mass of muscle fibres. 8. A phocomelias may be produced when the whole length of the humerus and the elbow-joint lies inside the body wall. In this case the implanted ectoderm covers the area where the limb would normally develop. 9. The humerus may be reduplicated. 10. The humerus may be too short. 11. The proximal half of the humerus may possess a diameter different from that of the distal half. 12. One skeletal element only of the forearm (radius or ulna) may be present when the place which would normally be occupied by one of these elements was taken by implanted ectoderm. 13. The elements of the carpus and of the hand may appear irregularly scattered throughout the tissues of the distal part of the limb. In these cases the implanted ectoderm was attached to the surface of the distal end of the limb. 14. The fingers can show: (a) abnormal positions, (b) abnormal numbers, (c) syndactylias, (d) one finger too long, others too short.

The musculature of Peripatus and its innervation

1980 ◽  
Vol 288 (1031) ◽  
pp. 481-510 ◽  
Keyword(s):  
Body Wall ◽  
Fibre Length ◽  
Gross Anatomy ◽  
Small Degree ◽  
The Body ◽  
Muscle Fibres ◽  
Neuromuscular Synapses ◽  
Thick Filaments ◽  
Small Muscle ◽  
Tubule Diameter

The musculature of the Onychophoran Peripatus dominicae , its ultrastructure and details of innervation are described. Significant differences were noted between its gross anatomy and that reported in previous accounts, notably in the presence of inner circular body wall muscle and a prominent, functionally significant, levator of the leg. The former is important in regard to the evolutionary position of the Onychophora while the latter helps us to understand the control of walking in a lobopodial leg, and therefore the evolution of arthropod locomotion, which was the focus of our interest. Individual muscle fibres are either directly or indirectly attached to the body wall by collagen. There is a small degree of branching of fibres, with or without anastomosis, near their insertions, but most are as long as the muscle of which they are part, and are unbranched except for an occasional thin arm, emerging at an angle, that becomes invaded by collagen fibres and inserts in the skin. Diameters of muscle fibres vary from 1 to 45 pm. They are invaginated by two separate systems of unique wide (0.3 pm) tubules, longitudinal and radial. These are lined with similar material to that forming the basement material of the sarcolemma, and also contain fine strands with collagen-type cross-banding that connect to collagen bundles outside the fibres. In addition there are narrow tubules of ordinary T-tubule diameter. Both wide and narrow tubules make contacts with sarcoplasmic reticulum cysternae. Dense Z bodies are attached to both kinds of wide tubule, to the inside of the sarcolemma, and are scattered, without any obvious array, in the sarcoplasm. Thin myofilaments emerge from the Z bodies parallel to the fibre axis. Thick filaments occur in clusters with a loosely hexagonal array, but without any regular relation to thin ones: relatively few orbits of thin around thick filaments were seen in many muscle fibres regardless of fibre length and conditions during fixation. A unique innervation pattern was found, consisting of a combination of muscle arm to nerve contacts, which appear to be the commonest, and nerve on muscle fibre synapses. At least 13 motor axons were found to supply each small muscle or cluster of muscle fibres in a large muscle. Each muscle arm simultaneously makes synaptic contact with 3 to 7 axons. Nerve on muscle junctions contain from 1 to 8 axons, each making synaptic contacts. The details of the postsynaptic endplate-specializations resemble those seen in mammalian endplates and are markedly different from both arthropod and annelidan neuromuscular synapses.

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