Counterillumination in the Hawaiian bobtail squid,<Emphasis Type="Italic"> Euprymna scolopes</Emphasis> Berry (Mollusca: Cephalopoda)

The mutualism between the Hawaiian bobtail squid Euprymna scolopes and the luminescent symbiont Vibrio fischeri has been used extensively as a model system for studies ranging from co-speciation and biogeography to gene regulation and the evolution of pathogenesis. In this association, the luminescent bacterium V. fischeri is housed in a complex light organ within the mantle cavity of E. scolopes. Prior hypotheses have assumed that sepiolid squids in general utilize the bioluminescence produced by their V. fischeri symbionts for counterillumination, a behavior that helps squid camouflage themselves by matching down-welling moonlight via silhouette reduction. This assumption, based solely on the morphology of the squid light organ, has never been empirically tested for Euprymna in the laboratory. Here, we present data demonstrating that E. scolopes can modify the intensity of light produced by V. fischeri in the light organ as down-welling light intensity changes. Bacterial bioluminescence from the light organ is directly correlated with down-welling light intensity, suggesting that E. scolopes individuals utilize and control V. fischeri luminescence for counterillumination.Communicated by P.W. Sammarco, Chauvin     

Disruptive counterillumination and its anti-predatory value in the plainfish midshipman Porichthys notatus

The plainfin midshipman Porichthys notatus Girard occurs in nearshore waters off the western coast of North America. We found that the ventrally directed photophores of juvenile laboratory-grown P. notatus function in counterillumination. Their bioluminescence matched downwelling light to obscure the silhouette as viewed from below. P. notatus did not obligatorily counterilluminate at all times in appropriate light. A hydrodynamic stimulus, in addition to appropriate downwelling light, was required to induce counterillumination. This is perhaps an adaptation to conserve its Vargula-type luciferin, which is obtained from its diet. The angular distribution of light produced by P. notatus approximated that typical of downwelling light in the ocean. There was a direct relationship between downwelling irradiance and the maximum intensity of P. notatus luminescence. Insufficient light was produced to replace the light blocked by the fish under lighting conditions typical of the natural environment. The luminescence was, however, effective in eliminating the silhouette of P. notatus as observed with an image-intensifying camera and by dark-adapted human observers. Consequently, the effectiveness of counterillumination probably originates in part from the disruptive pattern of the luminous photophores. P. notatus from the Puget Sound population, which lacks a luciferin source and is non-luminous, displayed counterillumination behavior when its luminescent system was activated by force-feeding the fish with dried Vargula hilgendorfi. Experiments using adult P. notatus as predators on a mixed population of non-luminous (Puget Sound) and luminous (Santa Barbara Channel) juvenile P. notatus revealed that under conditions of dim overhead illumination non-luminous P. notatus were preyed upon at twice the rate of luminous individuals. This is the first experimental evidence suggesting that counterillumination is effective as an anti-predatory strategy. Received: 25 August 1998 / Accepted: 25 March 1999     

Luminescent flashing in the midwater squids Pterygioteuthis microlampas and P. giardi

The luminescent flashing capabilities and swimming behavior were examined for two species of small midwater squids (Pterygioteuthis microlampas and P. giardi). Recently captured squid were placed in a small aquarium, where their movements and luminescent flashes could be recorded with an image intensifier, a photomultiplier tube and associated equipment. Flashing behavior was initiated by disturbing the squid with an eletrical shock. The following 4 behaviors were observed: (1) a short flash and a rapid departure from the electrode; (2) a short flash and a delayed, slow departure from the electrode; (3) a longer flash persisting after a rapid departure from the electrode; (4) a longer flash when departure was prevented by continuing the shock. Luminescent flashes probably have a general defensive function, discouraging or disrupting an attack by potential predators, and within this context there may exist numerous strategies involving flashes.     

Inception of formation and early morphogenesis of the bacterial light organ of the sea urchin cardinalfish, <Emphasis Type="Italic">Siphamia versicolor</Emphasis>

The cardinalfish Siphamia versicolor (Perciformes: Apogonidae) forms a bioluminescent symbiosis with the marine luminous bacterium Photobacterium mandapamensis, harboring the bacteria in a ventral, disc-shaped light organ and using the bacterial light apparently for counterillumination and attracting prey. Little definitive information has been available on the developmental and microbiological events surrounding the initiation of symbiosis, a critical stage in the life history of the fish, in S. versicolor or any of the many other species of bacterially luminous fish. To identify the stage at which light organ formation begins, to determine the origin of cells forming the light organ, and to characterize its bacterial colonization status during development, early developmental stages of S. versicolor obtained and reared from wild-caught mouth-brooding males were examined with histological and microbiological methods. A light organ primordium was not evident in embryos, post-embryos, or pre-release larvae, whereas the light organ began to form within 1 day of release of full-term pre-flexion larvae from the mouths of male fish. Analysis of post-release larvae revealed that the light organ arises from a proliferation and differentiation of intestinal epithelial cells, and that it quickly develops structural complexity, including the formation of chambers and gaps contiguous with the intestinal epithelium. However, the nascent light organ remained uncolonized by the symbiotic bacteria through several days of post-release development, even in the presence of high numbers of the symbiotic bacteria. These results demonstrate that the inception of light organ formation in S. versicolor occurs independently of its symbiotic bacteria and that receptivity to bacterial colonization apparently requires substantial post-release development of the light organ. Larvae therefore most likely acquire their symbiotic bacteria from seawater, during or shortly after the transition from the pre-flexion to the flexion developmental stage.     

Vision in the lanternfish Stenobrachius leucopsarus (Myctophidae)

The visual system of the midwater fish Stenobrachius leucopsarus (Myctophidae) has been studied by biochemical, anatomical, and electrophysiological methods. Partial bleaching analysis in the presence of hydroxylamine showed that the eye contains a single extractable photopigment, based on retinal and absorbing maximally at 492 nm. The photoreceptor population consists entirely of rods, approximately 5.0×10⁵ rods per mm² and 1.8×10⁷ per retina. Visual sensitivity is enhanced by the lack of pigment granules in the pigment epithelium and the presence of a choroidal tapetum lucidum. Influenced by the high concentration of visual pigment, the spectral sensitivity has a broad plateau between 460 and 540 nm, which suggests that the eye retains high sensitivity to a diversity of bioluminescent stimuli and depth-attenuated solar light.     

Bioluminescence in the Monterey Submarine Canyon: image analysis of video recordings from a midwater submersible

Video images of bioluminescence were recorded in situ during a 1985 study of the midwater environment of the Monterey Canyon, using a single-person, untethered submersible. Gelatinous organisms were responsible for the most brilliant bioluminescent displays, often exhibiting elaborate kinetics in response to mechanical stimulation. Images of bioluminescent displays recorded from identified organisms are shown and display patterns are described. All bioluminescence emission spectra from captured specimens were blue, with peak emissions between 460 and 494 nm. Image-analysis of recordings of mechanically stimulated bioluminescence revealed source densities between 43 and 175 m^-3 and intensities between 2.5 and 37.3 W sr^-1 m^-3. The predominant display type at all depths studied (between 100 and 560 m) was luminous secretions. Despite high intensities of mechanically stimulated bioluminescence, no spontaneous light production was recorded in the absence of mechanical stimulation.     

Vertical distributions of euphausiids and fish in relation to light intensity in the Northeastern Atlantic

The relationship between the vertical distributions of euphausiids and fish and light intensity has been studied directly by using a photometer in conjunction with an acoustically controlled rectangular midwater trawl. Samples were taken at a position centered on 47°N; 17°W on 15 and 16 May 1978. Five species of euphausiid and six species of fish have been analysed, both groups contained migrant and non-migrant species. The population of each of these species occurred throughout a light regime spanning at least three orders of magnitude of intensity; none of them was restricted to, or followed, and isolume. There were no sexual or size differences in the distributions of the euphausiids, but the population of Argyropelecus hemigymnus was probably stratified during the day, with smaller individuals occurring shallower than large ones. The results are discussed in relation to previous observations and to the theories of photic regulation of distributions and migrations.     

Life history of Gonatus onyx (Cephalopoda: Teuthoidea): deep-sea spawning and post-spawning egg care

 A reproductive strategy consisting of deep- water spawning and egg-care was inferred for the midwater squid Gonatus onyx Young, 1972. Brooding females and associated eggs and hatchlings, captured between 1250 and 1750 m depth off southern California, are described. Brooding females appear to be senescent and lack tentacles. Large eggs of this species (3 mm) at cold temperatures (3 °C at capture depth) may require as long as 9 mo to develop. The high lipid content of the digestive gland in adult females of this species may provide fuel to support such an extended “brooding” period. Received: 22 February 1999 / Accepted: 25 May 2000     

Diel patterns of planktonic bioluminescence in the northern Sargasso Sea

Day-night changes in the vertical distribution, intensity, and size of bioluminescence flashes were investigated during a series of cruises to the northern Sargasso Sea in 1987 and 1988. Overall, depth integrated bioluminescence potential and flash density estimated from in situ measurements with a pumping bathyphotometer were 2 to 5 x higher at midnight than at midday. Depths from 50 to 100 m exhibited the most substantial day to night increases in bioluminescence potential and flash density. When classified by flash size (photon output per flash event), the increase from day to night was significant for all flash sizes, but was most dramatic for small flashes producing <7 x 10⁸ photons flash^-1. Bioluminescence potential and flash density increased 2 to 3 x during bathyphotometer measurements made at dusk. Bioluminescent light budgets estimated from day and night net collections in May and August 1987 also predicted 2.5 x higher nighttime than daytime mesoplankton bioluminescence. However, large bioluminescent taxa (mesoplankton) capable of significant vertical migrations only contributed on the order of 15% of the total bioluminescence in surface waters. Our results do not support the idea that most of the nightly increase in bioluminescence potential and flash density are due to vertical migration of bioluminescent organisms; rather they are consistent with an alternate view that photoinhibition of bioluminescent flashing by dinoflagellates may be primarily responsible for the diel patterns.     

Red bioluminescence in fishes: on the suborbital photophores of Malacosteus,Pachystomias and Aristostomias

Many deep-sea animals produce blue bioluminescence, but species of three genera of midwater dragonfishes also produce red light. In addition to numerous small body photophores, species of these genera (Malacosteus, Pachystomias and Aristostomias) have large suborbital photophores that emit red light and postorbital ones that emit blue light. Pachystomias microdon additionally has a red-emitting preorbital photophore. Fluorescence measurements from the intact suborbital photophores, and from their exposed cores, confirm the previous hypothesis that the red light emitted by Malacosteus is spectrally altered by a superficial shortwave cutoff brown filter. No such filter is present in the other two genera. Studies of the anatomy of the photophores show that the suborbital photophore of Malacosteus is similar in general organisation to other photophores, including the postorbital photophore. The red-emitting photophores of Pachystomias and Aristostomias, however, have a unique organisation, in which the bulk of the photophore comprises a gland that lies outside the thick reflector. Strands of tissue run from the gland into the photogenic core of the photophore through numerous pores in the reflector. The production and use of red light by these fishes is discussed in the context of these results.Electronic Supplementary Material Supplementary material is available for this article at     

Sinking rates and dissolution of midwater fish fecal matter

The sinking rates of fecal matter from 7 southern California midwater fish species were investigated. Feces were obtained from 162 specimens of Stenobrachius leucopsarus, Triphoturus mexicanus, Leuroglossus stilbius, Lampanyctus ritteri, Argyropelecus affinis and Parvilux ingens, which were collected in the Santa Barbara and San Clemente Basins between 1977 and 1979. In addition, feces obtained from 6 laboratory-maintained specimens of the midwater zoarcid Melanostigma pammelas were used for repeated sinking-rate measurements. The mean of the measured sinking rates for all species was 1.19 cm s^-1 (1 028 m d^-1), which is much higher than the known descent rates of euphausiid and copepod fecal pellets and of most other particulate organic detritus. Dissolution characteristics were also investigated for fecal matter from 4 species collected by the same series of net hauls: S. leucopsarus, T. mexicanus, A. affinis, and Sternoptyx obscura. The release of dissolved organic compounds from this material is low and does not represent a significant output during the relatively short time required to sink through the water column. These findings suggest that midwater fish fecal matter may represent a major source of organic transfer between the pelagic community and the benthos.     

Planktonic bioluminescence in the pack ice and the marginal ice zone of the Beaufort Sea

An icebreaker cruise into the Beaufort Sea in the fall of 1986 provided a unique opportunity for studying planktonic bioluminescence in ice fields and in the marginal ice zone. Bathyphotometer casts (bioluminescence intensity, seawater temperature, beam attenuation coefficient, and salinity) and biological collections were made to a depth of 100 m. A light budget, which describes the planktonic species responsible for the measured bioluminescence, and a dinoflagellate species budget were constructed from the mean light output from luminescent plankton and plankton counts. The vertical distribution of bioluminescence among the ice stations was similar. The maximum intensities were 2 to 8×10⁶ photons s^-1 cm^-3 in the upper 50 m of the sea-ice interface. The marginal ice zone station (MIZ) exhibited a maximum intensity of 2 to 3×10⁸ photons s^-1 cm^-3 between 5 and 30 m depth. At Ice Station 2, Metridia longa and their nauplii contributed approximately 80% of stimulable bioluminescence in the upper 10 m but, overall, Protoperidinium spp. dinoflagellates contributed most of the light to a depth of 100 m. In the MIZ, Protoperidinium spp. dinoflagellates contributed 90% of the light within the upper 10 m, decreasing to 43% of the contributed light at a depth of 40 m. Below 40 m, dinoflagellate bioluminescence decreased to a few percent of the total to a depth of 90 m. Metridia spp. copepods contributed more than 50% of the light at depths from 40 to 90 m. Ostracods, larvaceans, and euphausiid furcilia contributed <1% of all bioluminescence at all depths sampled. Correlation analyses between measured bioluminescence (photons s^-1 cm^-3), the number of bioluminescent dinoflagellates and the light budget for the MIZ indicated highly significant associations: r=0.919, p=0.001, and r=0.912, p<0.001, respectively (Student's two-tailed t-tests). Bioluminescence was negatively correlated with seawater salinity at all stations (p=0.001). Maximum bioluminescence was measured in the less saline surface waters at all stations.     

Localization of bioluminescence in the siphonophore Nanomia cara

The base of the tentacle of the developing physonect larva (Nanomia cara) has a bioluminescent region. The ability to produce light in the larva is transitory; this ability first appears at about two days of development and is disappearing by eight days, as the larva begins to feed. Subsequently paired bilaterally symmetrical bioluminescent organs are found on the nectophores and the bracts of the adult colony. In both the larva and the adult, bioluminescence is mediated by a calcium specific photoprotein. In all cases the photocytes lack a green fluorescent protein.     

Geographic variation in Loligo forbesi in the Northeast Atlantic Ocean: analysis of morphometric data and tests of causal hypotheses

Geographic variation in the squid Loligo forbesi was investigated using multivariate analysis of morphometric and meristic characters in samples of squid taken from 13 localities in the Northeast Atlantic Ocean. Two character sets, body morphometrics and beak morphometrics, indicated similar patterns of variation, with squid from the Azores differing markedly from those on the continental shelf. No consistent pattern was apparent in meristic data. Partial Mantel tests indicated that similarity matrices for morphological data were significantly correlated with distance matrices for (a) geographic proximity, (b) whether the capture site was on the continental shelf or the Azorean bank, and (c) (beak data only) average seasurface temperature at site of capture. Partial Mantel tests on allozyme data for the same individuals support hypothesis (b). The results suggest that L. forbesi in the Azores may reasonably be regarded as a distinct stock, differing significantly from L. forbesi on the continental shelf.     

Three new modes of luminescence in the leiognathid fish Gazza minuta: Discrete projected luminescence,ventral body flash,and buccal luminescence

Three new modes of luminescence are described for Gazza minuta (Bloch) (Perciformes: Leiognathidae) as observed in specimens collected in the Philippines in April and May, 1982: discrete projected luminescence (DPL), ventral body flash, and buccal luminescence. DPL sharply contrasts with previously reported modes of diffuse luminescence in leiognathids (counterillumination and opercular flash) in being a pair of bright collimated beams of light emanating from the fish in an anteroventral direction. The brightness, coherence, directionality, and control of DPL suggest striking similarities to luminescence in anomalopid (flashlight) and monocentrid (pinecone) fishes and perhaps in certain apogonids (cardinalfishes). The structural correlate for DPL is a small clear patch of skin lying at the posterior margin of each opercular cavity. Luminescence from the internally located light organ traverses transparent bone and translucent muscle before passing through the clear skin of the patch area. Behavioral and anatomical observations of ventral body flash and buccal luminescence are also presented. These new modes of luminescence indicate a much greater than expected diversity of luminescent behaviors in leiognathids, perhaps greater than that of any other organism yet studied. The internal location of the light organ is recognised as providing the potential for this diversity.     

Luminescence from non-bioluminescent tissues in oceanic cephalopods

Several tissues (e.g. kidney, blood, digestive gland) in oceanic cephalopods which do not exhibit in vivo bioluminescence, luminesce when homogenized in the presence of air or when simply exposed to air in a vial (blood). The source of the luminescence appears to be a luciferin: treatment of kidney homogenates and blood with a photophore extract presumably containing luciferase resulted in a 20-fold increase in light production. Luminescence was also found in the renal fluid, which may be the source of luminescent clouds produced by squids. The variability in luminescence found in some tissues of cephalopods appeared to be related to feeding. Luminescence was also detected in the digestive glands of midwater octopods.     

Sperm storage and mating in the deep-sea squid Taningia danae Joubin, 1931 (Oegopsida: Octopoteuthidae)

Spermatangium implantation is reported in the large oceanic squid Taningia danae, based on ten mated females from the stomachs of sperm whales. Implanted spermatangia were located in the mantle, head and neck (on both sides) or above the nuchal cartilage, under the neck collar and were often associated with incisions. These cuts ranged from 30 to 65 mm in length and were probably made by males, using the beak or arm hooks. This is the first time wounds facilitating spermatangium storage have been observed in the internal muscle layers (rather than external, as observed in some other species of squid). The implications of these observations for the mating behavior of the rarely encountered squid T. danae are discussed.     

Light quality in relation to growth,photosynthetic rates and carbon metabolism in two species of marine plankton algae

The effect of light quality on growth, photosynthesis and carbon metabolism in two species of marine algae,Cyclotella nana (Hustedt) andDunaliella tertiolecta (Butcher), was examined. Relative growth constants forC. nana were 0.37, 0.29 and 0.25 in blue, white and green light, respectively. Corresponding constants were 0.41, 0.31 and 0.29 forD. tertiolecta. Photosynthetic rates in both species were higher in blue light and lower in green light compared with white light of the same intensity. More than 60% of¹⁴C assimilated byC. nana orD. tertiolecta grown in blue or green light was incorporated into the ethanol-insoluble fraction, compared with 10 to 30% in this fraction in white light. The relative importance of the various components within this fraction was independent of light quality. Although less¹⁴C was assimilated into the ethanol-soluble fraction in blue or green light, there was a relative increase in some amino acids and organic acids in this fraction and a decrease in sugars and sugar phosphates relative to white light of the same intensity. These differences were independent of light intensity, photosynthetic rate and cell density in the cultures.     

The trophic link between squid and the emperor penguin <Emphasis Type="Italic">Aptenodytes forsteri</Emphasis> at Pointe Géologie,Antarctica

Cephalopod beaks retrieved from stomachs of dead emperor penguin chicks at Pointe Géologie, Terre Adélie, provide information on taxonomic and size composition of the penguin’s squid diet, on the trophic range of the squid species preyed upon and on the fractional trophic impact of the penguin on the whole food web. Emperor penguins prey upon four squid species (Psychroteuthis glacialis, Kondakovia longimana, Gonatus antarcticus, Alluroteuthis antarcticus) and do not take squid larger than 480 mm mantle length. Larger squid live either below the penguin’s diving range or are beyond its handling capacity. Nitrogen stable isotope ratios indicate that squids cover a range of about two trophic levels (2.5–8‰ δ¹⁵N). The impact of the emperor penguin, however, concentrates on the upper part of this range, about 68% of its squid prey being >6‰ δ¹⁵N. The principal components of the emperor’s diet, fish, krill and squid, differ distinctly in average trophic level. Consequently the trophic position of the emperor penguin changes accordingly with diet composition and may differ by almost one trophic level between different emperor penguin colonies.     

Bioluminescence of deep-sea coronate medusae (Cnidaria: Scyphozoa)

Bioluminescence is the production of visible light by a living organism. The light commonly appears as flashes from point sources (involving one or more cells, usually described as photocytes) or as a glandular secretion. A visible flash usually involves synchronous light emission from a group of cells or, if from a single-celled organism such as a dinoflagellate, from a group of organelles. The number of cells (or organelles) responding synchronously is the main determinant of the flash intensity. Bioluminescence is a common phenomenon in many deep-sea animals and is widespread among the Cnidaria. In this paper, we compare and contrast in situ and laboratory recordings of the bioluminescent responses of specimens of the deep-sea scyphozoans Atolla wyvillei, Atolla vanhoffeni, Atolla parva, Nausithoe rubra, Paraphyllina intermedia, Periphyllopsis braueri and Periphylla periphylla. Displays in all seven species consist of localised flashes and propagated waves of light in the surface epithelium. The first few single waves propagate at rates of up to 60 cm s^-1 but subsequent ones in any sequence of stimuli gradually decrease in speed. After several single wave responses, a subsequent stimulus may elicit multiple waves that persist for several seconds. Following such a frenzy, the specimen becomes temporarily refractory to further stimuli, but if rested will recover its normal responses and may produce further frenzies. The dome area, situated above the coronal groove, of the genera Paraphyllina, Periphylla, and Nausithoe is covered with luminescent point sources. Such point sources are generally absent from the dome of species of Atolla. Captured specimens of A. parva also produce secretory bioluminescence, corroborating prior in situ observations of this ability. Secretory bioluminescence in P. periphylla takes the form of scintillating particles released from the lappet margins. We did not observe secretory displays in specimens of any other species in the laboratory, but one instance of apparent secretory luminescence was recorded in situ in a specimen of A. wyvillei.Communicated by J. P. Thorpe, Port Erin