Summary
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1.
The swimmerets ofJasus lalandii, in contrast to those well known in the nephropid lobsters (e.g.Homarus) and astacurans (crayfish), do not display spontaneous antero-posterior beating, but are either apposed actively to the ventral surface of the abdomen, or rotated outward (Fig. 2). These movements are imposed by the geometrical arrangement of the bicondylar joints at the base of the swimmeret (Fig. 3), and involve contraction of either the remotor muscle, or the promotor-rotator muscles (Figs. 2, 3). Each swimmeret includes a short, thick blade-like exopodite that contains two antagonistic muscles, a large curler and a small adductor muscle (Fig. 3). Each swimmeret is innervated by 80 motor neurons (MNs) which are disposed in two clusters in the ganglion.
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2.
The modulation of the tonic discharge of the muscles which maintain the swimmeret position at rest (remotor and curler) has been studied in two situations: body rolling (Fig. 4) and walking activity (Fig. 5). In the female, in which the most anterior pair of swimmerets are biramous, both endopodite and exopodite curler muscles display the same responses to body rolling (Fig. 4). In all these situations no overt swimmeret movement occurs.
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3.
Nevertheless, rhythmicity exists inJasus, but it is limited to the gravid female when the swimmerets bear the eggs (Fig. 6). In contrast to other decapod Crustacea, this swimmeret beating is not metachronous (Fig. 6).
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4.
Movement monitoring (Fig. 7) and EMG recordings (Figs. 9, 10) have demonstrated the involvement of the swimmerets in the three phases of the tail flick response (preparation, flexion, extension). During the preparatory phase, in response to mechanical stimulation of the legs, the swimmerets open on the stimulated side (on both sides in the case of a symmetrical stimulation) (Fig. 7). During the rapid abdominal flexion of the tail flick all swimmerets open fully regardless of the stimulus (Figs. 7, 8). Two different units in the rotator muscle EMG are responsible for swimmeret opening during the preparatory and the flexion phases of the tail flick (Figs. 9, 10).
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5.
The curler muscle of the endopodite in the female displays antagonistic activities to that of the exopodite during tail flicks (Fig. 10).
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6.
Selective swimmeret blockage demonstrates that they contribute to the thrust efficacy in tail flicks. In particular they are responsible for the variation of the maximal force produced at its onset. This effect could be interpreted as a consequence of force redistribution by the swimmerets acting on water flow (produced by the tail fan). This mechanism implies a functional role for the swimmerets in righting and steering responses (Fig. 11).
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Abbreviations
- EMG :
-
electromyogram
- imp/s :
-
impulse per second
- MN :
-
motor neuron
- SW :
-
swimmeret
References
Bent SA, Chapple WJ (1977) Peripheral and central asymmetry in the swimmeret system of the hermit crab,Pagurus pollicarus. J Comp Physiol 118:75–92
Cattaert D (1984) Polymorphisme d'expression d'un système locomoteur vestigial chez le homardHomarus gammarus. Thèse 3ème cycle, Université de Bordeaux I, p 74
Cattaert D, Clarac F (1983) Influence of walking on swimmeret beating in the lobsterHomarus gamarus. J Neurobiol 14:421–439
Cattaert D, Clarac F (1987) Rami motor neurons and motor control of the swimmeret system ofHomarus gammarus. J Comp Physiol A 160:55–68
Clarac F (1985) Stepping reflexes and the sensory control of walking in Crustacea. In: Barnes WJP, Gladden MH (eds) Feedback and motor control in invertebrates and vertebrates. Croom Helm, London, pp 379–400
Clarac F, Chasserat C (1986) Basic processes of locomotor coordination in the rock lobster. I Statistical analysis of walking parameters. Biol Cybern 55:159–170
Cruse H, Müller U (1984) A new method measuring leg position of walking crustaceans shows that motor output during return stroke depends upon load. J Exp Biol 110:319–322
Davis WJ (1968a) The neuromuscular basis of lobster swimmeret beating. J Exp Zool 168:363–378
Davis WJ (1968b) Quantitative analysis of swimmeret beating in the lobster. J Exp Biol 48:643–662
Davis WJ (1968c) Lobster righting responses and their neural control. Proc R Soc Lond B 144:480–495
Davis WJ (1971) Functional significance of motoneuron size and soma position in swimmeret system of the lobster. J Neurophysiol 34:274–288
Heitler WJ (1983) The control of rhythmic limb movements in Crustacea. In: Roberts A, Roberts BL (eds) Neural origin of rhythmic movements. Symp Soc Exp Biol 37:351–382
Kotak VC, Page CH (1986) Tactile stimulation of the swimmeret alters motor programs for abdominal posture in the lobsterHomarus americanus. J Comp Physiol A 158:225–235
Lang F, Govind CK, Costello WJ, Greene SI (1977) Developmental neuroethology: Changes in escape and defensive behavior during growth of the lobster. Science 197:682–685
Laverack MS, MacMillan DL, Neil DM (1976) A comparison of beating parameters in larval and post larval locomotor systems of the lobsterHomarus gammarus (L). Phil Trans R Soc Lond B 274:87–99
Lindberg RG (1955) Growth, population, dynamics and field behavior in the spiny lobsterPalunirus interruptus. Univ Calif Berkeley Publ Zool 59:157–248
Marrelli JD, Hsiao HS (1976) Miniature angle transducer for marine arthropods. Comp Biochem Physiol 54A:121–123
Miyan JA (1982) The neuronal basis of the swimmeret equilibrium reaction in the lobsterNephrops norvegicus (L). PhD thesis, University of Glasgow
Neil DM (1985) Multisensory interactions in the crustacean equilibrium system. In: Barnes WJP, Gladden MH (eds) Feedback and motor control in invertebrates and vertebrates. Croom Helm, London, pp 277–298
Neil DM, Miyan JA (1986) Phase dependant modulation of auxiliary swimmeret muscle activity in the equilibrium reactions of the Norway lobster,Nephrops norvegicus (L). J Exp Biol 126:157–179
Paterson NF (1968) The anatomy of the cap rock lobsterJasus lalandii. Ann South African Mus 51:1–232
Takahata M, Hisada M (1985) Interactions between the motor systems controlling uropod steering and abdominal posture in crayfish. J Comp Physiol A 157:547–554
Tatsumi H, Haragashira M, Suzuki R (1985) Interrelations between posture and locomotion in response to body rotation in crayfish. J Comp Physiol A 157:509–517
Yoshino M, Takahata M, Hisada M (1980) Statocyst control of the uropod movement in response to body rolling in crayfish. J Comp Physiol 139:243–250
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Cattaert, D., Clarac, F. & Neil, D.M. Anatomical and physiological organization of the swimmeret system of the spiny lobsterJasus lalandii as adaptive components of the tail flick. J. Comp. Physiol. 162, 187–200 (1988). https://doi.org/10.1007/BF00606084
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DOI: https://doi.org/10.1007/BF00606084