BURROW VENTILATION IN THE TUBE-DWELLING SHRIMP CALLIANASSA-SUBTERRANEA (DECAPODA, THALASSINIDEA) - I - MORPHOLOGY AND MOTION OF THE PLEOPODS, UROPODS AND TELSON
Ej. Stamhuis et Jj. Videler, BURROW VENTILATION IN THE TUBE-DWELLING SHRIMP CALLIANASSA-SUBTERRANEA (DECAPODA, THALASSINIDEA) - I - MORPHOLOGY AND MOTION OF THE PLEOPODS, UROPODS AND TELSON, Journal of Experimental Biology, 201(14), 1998, pp. 2151-2158
The morphology of the pleopods, uropods and telson of the tube-dwellin
g shrimp Callianassa subterranea have been studied using dissection mi
croscopy and scanning electron microscopy. The kinematics of these app
endages were examined by motion analysis of macro-video recordings of
ventilating shrimps in transparent artificial burrows. The pleopods sh
ow the usual crustacean biramous anatomy, but all segments are rostro-
caudally flattened. The protopodite bears a triangular medially orient
ed endopodite and a scoop-shaped exopodite, The contralateral endopodi
tes are linked by the appendix interna, ensuring a perfect phase relat
ionship between contralateral pleopods, The outer rims of the exopodit
es are fringed with long fern-leaf-like plumose setae bearing flattene
d setules, These setae have very mobile joints and can be turned cauda
lly, The slits between contralateral endopodites have rims of leaf-lik
e setae as well. Setae of the same leaf-like type fringe the uropods,
but these are nonmotile. The telson has a narrow fringe of leaf-like s
etae, locally interrupted by long mechanoreceptory setae. A shrimp, wa
ndering through the burrow or resting, holds its pleopods against the
abdomen with the exopodites and their setal fringes retracted medially
. The uropods are folded medially as well, probably to reduce the shri
mp's drag. During ventilation, the uropods are extended against the tu
be wall, leaving only a small opening for flow ventral from the telson
, and the pleopods beat at a frequency of approximately 1 Hz (0.9+/-0.
2 Hz). Fourier analysis of pleopod kinematics showed that the motion p
attern of the first flow-generating pleopod pair (PP1) consisted mainl
y of the first harmonic (75%) and to a lesser extent of the third harm
onic (20%), resulting in almost perfect sinusoidal motion. The motion
patterns of PP2 and PP3 could be modelled by assigning pure sinusoids
with a 120 degrees phase shift and a rostro-caudal ranking to the thre
e pairs of pleopods.