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The upside-down jellyfish Cassiopea xamachana (Scyphozoa: Rhizostomeae) has been predominantly studied to understand its interaction with the endosymbiotic dinoflagellate algae Symbiodinium. As an easily culturable and tractable cnidarian model, it is an attractive alternative to stony corals to understanding the mechanisms driving establishment and maintenance of symbiosis. Cassiopea is also unique in requiring the symbiont in order to complete its transition to the adult stage, thereby providing an excellent model to understand symbiosis-driven development and evolution. Recently, the Cassiopea research system has gained interest beyond symbiosis in fields related to embryology, climate ecology, behavior, and more. With these developments, resources Ohdera et al. Cassiopea xamachana System Review including genomes, transcriptomes, and laboratory protocols are steadily increasing. This review provides an overview of the broad range of interdisciplinary research that has utilized the Cassiopea model and highlights the advantages of using the model for future research.

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1. In the polychaetePlatynereis dumerilii, the hormone-elaborating portion of the prostomium was determined by means of prostomium transection and implantation experiments. The area in question lies between the two pairs of eyes, extending longitudinally from the posterior border of the anterior eyes to about the posterior border of the posterior eyes. This corresponds approximately with the brain area delimited by the anterior and posterior dorsoventral connective tissue tubes and which is covered ventrally by the infracerebral gland epithelium. 2. The infracerebral gland-complex and neurosecretory neurons within the brain were envisaged as possible sites of hormone synthesis. 3. The infracerebral gland-complex inPl. dumerilii was investigated with light-and electron-microscopical techniques. A leaf-shaped area (measuring 120 by 95 μm at the most) of the pericapsular epithelium at the ventral side of the brain, adjacent to the main blood vessel and to its efferent branches, consists of specialized columnar epithelial cells. Numerousa-cells and scarceb-cells can be distinguished. Fibre tracts with glia fibres and axons (some being neurosecretory axons) descend from the neuropile and in part terminate with prominent end-structures at the inner face of the brain capsule in the gland region. Probably some axons penetrate the capsule and make contact with the gland cells. Neither structural nor experimental findings prove that the infracerebral gland synthesizes the brain hormone. Accessory functions are discussed. 4. Investigations in secretory brain cells ofPl. dumerilii are reported. In agreement with Müller (1973), a lack of correlation between the number of stainable neurosecretory neurons and the hormonal activity of the brain was found: in immature worms (to which high hormonal titers are ascribed) only few or even no neurosecretory brain cells at all were detectable. Prostomium transection and implantation experiments show further that not all regions of the brain which enclose neurosecretory neurons produce brain hormone. The results are discussed with reference to the hypotheses of Müller (1973) which suggest that the appearance of stainable neurosecretory brain cells indicates inactivation of neurons possibly previously involved with hormone synthesis.

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