A list of the genera of living organisms known or believed to contain luminous species is provided in the Appendix, in a systematic context. The constraints on the accuracy of such a list and some aspects of the apparent distribution of bioluminescence are discussed.
This study evaluates the role of protozoa in larval fish feeding by describing protozoa in larval fish diets and testing the hypothesis that, in the Irish Sea, larval fish feed on protozoan prey at rates that potentially sustain their food requirements. Gut contents of 11 taxonomic groups of larval fish were examined, and protist prey occurred in the diet of all of them. Protozoan prey were identified, which provided an insight into their trophic role. Most of the protozoan prey were autotrophic or mixotrophic. In general, larval fish diets were constant over the spring/summer period, regardless of prey availability in the field and the composition of larval fish assemblage (taxonomy and size). A laboratory experiment on ingestion rates of flounder larvae as a function of ciliates concentration was conducted. Combined laboratory and field data showed that, in the Irish Sea, it is unlikely that ciliates are often the primary food source of flounder larvae, and, by implication, other larval fish as well. However, ciliates and other protozoa could be a substantial component of the larval fish diet, and they may potentially prevent food limitation.
The aim of this work was to establish the role of imidazolopyrazines in the bioluminescence of copepods and other marine organisms. A highly sensitive assay (down to 10-17 mol) for coelenterazine was established using reactivation of the CaZ+-activated photoprotein obelin, and for vargulin using Vargula hilgendorfi luciferase. Coelenterazine and its luciferase was found in all (8 species) the luminous copepods examined. In Euaugaptilus species more than 90% of the luciferase was found in the legs, with the luminous cells, but over 40% of the coelenterazine was found in the bodies. Coelenterazine was found in luminous organisms from six phyla: Sarcomastigophora (Radiolaria), Cnidaria, Ctenophora, Arthropoda, Mollusca. Chordata (Pisces). Only in the first three of these were Ca 2 +-activated photoproteins present.
The problems faced by deep-sea animals in achieving sexual and other encounters require sensory and effector systems the synergy of which can span the often very substantial distances that separate individuals. Bioluminescent systems provide one of the links between individuals, and the sexual dimorphism of some photophores suggests that they are employed to attract a mate. However, nearest-neighbour values for many deep-sea animals put them beyond the effective range of bioluminescent signals and it is therefore likely that these signals are employed at intermediate ranges, once an initial contact (perhaps olfactory) has been made.
The luminescent material emitted from the post-cleithral organ of searsid fishes is in the form of granule-packed cells. From this material a partially purified extract may be prepared which shows some of the properties to be expected from a photoprotein. The purified material luminesces on treatment with hydrogen peroxide and, specifically, ferrous iron. The properties of the luminescent system appear similar to those of material isolated from the luminous polychaeteChaetopterus.
Spectral measurements of red bioluminescence were obtained from the deep-sea stomiatoid fishes Aristostomias scintillans (Gilbert) and Malacosteus niger (Ayres). Red luminescence from suborbital light organs extends to the near infrared, with peak emission at approximately 705 nanometers in the far red. These fishes also have postorbital light organs that emit blue luminescence with maxima between 470 and 480 nanometers. The red bioluminescence may be due to an energy transfer system and wavelength-selective filtering.
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