Swimming, feeding, circulation and vision in the Australian box jellyfish, Chironex fleckeri (Cnidaria:Cubozoa)

1995 ◽  
Vol 46 (7) ◽  
pp. 985 ◽  
Author(s):  
WM Hamner ◽  
MS Jones ◽  
PP Hamner

Juvenile Chironex fleckeri medusae were maintained in aquaria for several months. One individual was raised over a nine-month period to subadult condition for the first time. The medusae did not feed naturally in most aquaria but they accepted and digested prey items placed by hand onto the manubrium. Medusae maintained in planktonkreisels, however, extended tentacles and captured and ingested live Acetes, large prawns and fish by subumbrellar flexing of the pedalia. Digestion of prey was rapid and food particles were circulated directionally through functional canals and lacunae primarily by contractions of the bell but also by peristaltic contractions of interradial gastrovascular tissues. In the laboratory, medusae visually reacted to dark objects by swimming away from them. Swimming behaviour of medusae in the sea and natural predation by green turtles (Chelonia rnydas) on C. fleckeri are described.

1992 ◽  
Vol 156 (9) ◽  
pp. 655-658 ◽  
Author(s):  
Christopher E Beadnell ◽  
Timothy A Rider ◽  
John A Williamson ◽  
Peter J Fenner

Toxicon ◽  
1990 ◽  
Vol 28 (7) ◽  
pp. 821-835 ◽  
Author(s):  
Iekhsan Othman ◽  
Joseph W. Burnett

2005 ◽  
Vol 155 (2) ◽  
pp. 219-226 ◽  
Author(s):  
Sharmaine Ramasamy ◽  
Geoffrey K. Isbister ◽  
Jamie E. Seymour ◽  
Wayne C. Hodgson

2015 ◽  
Vol 8 ◽  
Author(s):  
Lisa-Ann Gershwin ◽  
Merrick Ekins

Tropical box jellyfish include some of the world's most venomous animals, leading researchers and the media to wonder whether changes in climate may drive these species into sub-tropical waters. The discovery, therefore, of small box jellyfish in the waterways of the Gold Coast and Sunshine Coast of south-east Queensland raised concern. This pygmy species proved to be new to science, separated from other species in the genusChiropsellaby its very small size; its semi-circular phacellae; very shallow, coalesced gastric saccules; its peculiar, long pedalia where the ‘palm’ is greatly reduced and the non-opposing ‘fingers’ branch off together at the same level; and a knee-like bend of the pedalial canal. The residential canal/river habitat of this species of chirodropid raises the question of whether this area is also suitable for habitation by the larger, more virulent chirodropids such as the so-called ‘deadly box jellyfish’,Chironex fleckeri. This new species,Chiropsella saxonisp. nov., brings the total number of chirodropid species described from Australian waters to five.


Toxicon ◽  
1999 ◽  
Vol 37 (11) ◽  
pp. 1621-1626 ◽  
Author(s):  
David A Bloom ◽  
Jose Burnett

1999 ◽  
Vol 354 (1380) ◽  
pp. 161-182 ◽  
Author(s):  
J. B. Messenger ◽  
J. Z. Young

This paper describes the ontogeny, breakdown and absorption of the radular teeth of cephalopods and, for the first time, considers the function of the ‘bolsters’ or radular support muscles. The radular ribbon, which bears many regularly arranged transverse rows of teeth one behind the other, lies in a radular canal that emerges from the radular sac. Here the radular teeth are formed by a set of elongate cells with microvilli, the odontoblasts. These are organized into two layers, the outer producing the radular membrane and the bases of the teeth, the inner producing the cusps. The odontoblasts also secrete the hyaline shield and the teeth on the lateral buccal palps, when these are present. At the front end of the radular ribbon the teeth become worn in feeding and are replaced from behind by new ones formed continuously in the radular sac, so that the whole ribbon moves forward during ontogeny. Removal of the old teeth is achieved by cells in the radular organs; these cells, which are formed from modified odontoblasts (‘odontoclasts’), dissolve the teeth and membranes and absorb them. There is a subradular organ in all cephalopods. In Octopus vulgaris , which bores into mollusc shells and crustacean carapaces, it is especially well–developed and there is also a supraradular organ. A characteristic feature of the cephalopod radular apparatus is the pair of large radular support muscles or ‘bolsters’. Their function seems never to have been investigated, but experiments reported here show that when they elongate, the radular teeth become erect at the bending plane and splayed, presumably enhancing their ability to rake food particles into the pharynx. The bolsters of Octopus function as muscular hydrostats: because their volume is fixed, contraction of their powerful transverse muscles causes them to elongate. In decapods and in nautiloids each bolster contains a ‘support rod’ of semi–fluid material, as well as massive transverse musculature. This rod may elongate to erect the radular teeth. At the extreme front end of the bolsters in Octopus there are many nerve fibres that may constitute a receptor organ signalling the movements of the radula against hard material. Such nerves are absent from decapods and from octopods that do not bore holes. The buccal mass of Nautilus is massive, with heavily calcified tips to the beaks and a wide radular ribbon, with 13 rather than nine elements in each row. Nevertheless all the usual coleoid features are present in the radular apparatus and the teeth are formed and broken down in the same way. However, Nautilus has a unique structure, the radular appendage. This comprises a papillate mass extending over the palate in the mid–line and forming paired lateral masses that are in part secretory. The organ is attached to the front of the radula by muscles and connective tissue. Its function is unknown.


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