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1.
Pyroteuthis margaritifera has morphologically distinctive photophores on the tentacles, eyeball and in the mantle cavity. The photogenic tissue in each photophore is identical, has a blue-green fluorescence and luminesces on treatment with dilute hydrogen peroxide. The photocytes frequently contain organized fibrillar material akin to that in the photocytes of certain other cephalopods. Several different types of blood vessel are present among the photocytes, including some, apparently restricted to the photophores, with a microvillous endothelium. Haemocyanin is present not only within identifiable blood vessels but also in some intercellular spaces.
On the basis of their characteristic optical systems the photophores can be separated into three types: (1) tentacular; (2) ocular and anal; (3) branchial and median abdominal. The tentacular photophores have collagenous reflector and light guide systems and the median ones are double organs. The ocular and anal organs do not have collagenous optical structures but an elaborate variety of reflective iridosomes. Those in the aperture of the photophores appear to act as interference filters. The branchial and abdominal organs have iridosomes as the major reflective tissue but collagenous fibrils function as light guides in the aperture of these organs and their emission is diffuse rather than collimated.  相似文献   

2.
Photogenic organs (photophores) of the velvet belly lantern shark (Etmopterus spinax) are under hormonal control, since melatonin (MT) and prolactin (PRL) trigger luminescence while α-melanocyte-stimulating hormone (α-MSH) prevents this light to be emitted. A recent study supported, however, the presence of numerous nerve fibres in the photogenic tissue of this shark. Immunohistochemical and pharmacological results collected in this work support these nerve fibres to be inhibitory GABAergic nerves since (i) GABA immunoreactivity was detected inside the photogenic tissue, where previous labelling detected the nerve fibre structures and (ii) GABA was able to inhibit MT and PRL-induced luminescence, which was on the other hand increased by the GABA(A) antagonist bicuculline (BICU). In addition, we also demonstrated that BICU can induce light per se by provoking pigment retraction in the pigmented cells composing the iris-like structure of the photophore, attaining, however, only about 10% of hormonally induced luminescence intensity at 10(-3)mol L(-1). This strongly supports that a GABA inhibitory tonus controls photophore "aperture" in the photogenic tissue of E. spinax but also that MT and PRL have more than one target cell type in the photophores.  相似文献   

3.
P. J. Herring    P. N. Dilly    Celia  Cope 《Journal of Zoology》1985,206(4):567-589
Females and juveniles of Selenoteuthis scintillans have photophores of several structural types, distributed on the tentacles and eyeballs, and within the mantle cavity and tail. Three distinct photophore types can be recognized on the basis of their accessory structures, though their photocytes are identical. The tail and some tentacular photophores (Type 1) lack any accessory optical structures; other tentacular and abdominal photophores (Type 2) have collagenous diffusing fibres; the anal and ocular photophores (Type 3) have a variety of iridosomes but no collagen. The distal tentacular organ is a double structure composed of a unit each of Type 1 and Type 2. Ocular photophores 1 and 5 are also double structures, composed of two Type 3 units. The photophores closely resemble in structure those of Lycoteuthis diadema. The photocytes have a marked fluorescence and luminesce on treatment with dilute hydrogen peroxide. The bio-luminescence intensity of the tail organ may be modified by chromatophore movements and has a blue-green spectral emission.
The photophores of juvenile Lampadioteuthis megaleia are similar in structure to those of Selenoteuthis but somewhat less complex. A comparison between the morphology of the photophores of lycoteuthid and enoploteuthid squids emphasizes the close similarity between the two families. At the ultrastructural level, certain photophores of both families have very characteristic microvillous blood vessels associated with the photocytes.  相似文献   

4.
External and histological examination of the photophores of the linebelly swallower Pseudoscopelus sagamianus reveal three epidermal layers of cells that form the light-producing and light-transmitting components of the photophores. Photophores among the examined photophore tracts are not significantly different in structure but the presence of mucous cells in the superficial layers of the photophore suggest continued function of the epidermal photophore in contributing to the mucous coat. This is the first evidence of intrinsic bioluminescence in primarily epidermal photophores reported in ray-finned fishes.  相似文献   

5.
P. J. Herring    P. N. Dilly    Celia  Cope 《Journal of Zoology》1992,227(3):479-491
The oceanic squid Octopoteuthis danue Joubin has one type of photophore on the head, body and arms, but another type on the eight arm tips. The first type has acomplexcapillary network, with elastic walls and a thick reflector. The arm tip organs have no such capillary core but a dense matrix containing paracrystalline assemblies.
Taningia danae Joubin (the only other genus in the family Octopoteuthidae) has only two large arm tip photophores. These are similar in their general organization to the arm tip photophores of Octopoteuthis , but their detailed structure is quite different.
There has evidently been independent evolution of photophores in this family of squids.  相似文献   

6.
1. Isolated photophores from the luminous fish Porichthys produce light in response to adrenaline and the metabolic inhibitors iodoacetic acid (IAA) or potassium cyanide (KCN).2. We attempted to analyse the interactions of cellular metabolism and adrenergic stimulation of the photogenic cells.3. Photophores were treated with IAA in the presence of pyruvate. In these conditions, IAA does inhibit glycolysis without inducing any luminescent activity of the cells.4. Similarly, other photophores were incubated with KCN in the presence of glucose, in order to inhibit cellular respiration while keeping the luminous system inactive.5. We observed that adrenergic stimulation of these photophores remained effective and induced a light emission, demonstrating that glycolytic and oxidative metabolism are not absolutely essential to the mechanism underlying adrenergic activation of the luminous system.6. The comparison of these luminescences with adrenergic responses of control photophores showed that the light emission to adrenaline was markedly inhibited by glycolysis blockade but potentiated by an inhibition of cellular respiration.7. As the inhibitory effect of IAA does not result from a direct action of IAA on the luminous system, these results suggest that adrenaline activation of adrenergic receptors might interact with glycolysis in photogenic cells.8. Glyceraldehyde 3-phosphate, or some derivatives, could be implicated in the glycolytic control of luminescence in the photophores.  相似文献   

7.
Spatial and temporal aspects of luminous responses in several common species of Southern California lanternfish (Myctophidae) were analyzed using T.V. image intensifier and photomultiplier techniques.The two principal types of luminous tissue, photophores and luminous tissue patches, responded in strikingly and consistently different ways to both mechanical and electrical stimulation. While typically producing a variable intensity glow spontaneously, the entire photophore array proved capable of coordinated, simultaneous activation by electrical stimulation. Although never active in undisturbed shipboard animals, luminous tissue patches, primarily, supra- and infracaudal organs, produced brilliant, rapid, transient displays to both mechanical and electrical stimulation. Light from the supra- and infracaudal organs is produced by 3–9 visually distinct subunits capable of both simultaneous and temporally variable activation.Electrical excitation gave maximum response rates of up to 30 flashes/sec in the luminous patches of all the species tested, whether tissue was from caudal organs or ventral or supraorbital patches. Chemical stimulation never triggered luminous responses from luminous tissue patches, and gave only ambiguous results with photophores.The results are discussed in terms of effector control and functional potential of the various luminous displays.  相似文献   

8.
The photophores of Meganyctiphanes were investigated with regard to the control of light production and with respect to their role in a hitherto unknown communication system using light flashes which became evident from observation of specialised signalling behaviour. To that purpose the light production was recorded during presentation of a range of stimuli delivered to the intact, tethered shrimp. Stimuli used were changes in ambient light, water turbulence, simulated predator approach and light flashes, as well as electric shocks and serotonin injections. Strong negative light gradients, exaggerating the natural sunset signal, reliably elicited light production, the peak of which lasted on average 2 min. In the late phase of this light production, low frequency water oscillations and turbulent flow (assumed intraspecific communication signals at close range) elicited transient increases in light production. Artificial light flashes presented to a group of shrimp evoked a signalling behaviour in which the animal points the light of its photophore beamers (positioned at the ventral side and normally directed downwards) for a fraction of a second at observers within the same depth level. The responses produced by the signalling behaviour indicate a fixed delay with respect to the triggering flash. Electric stimulation of the ventral nerve cord via implanted electrodes resulted in a strong light production with a latency of 160 ms. Injection of serotonin, resulting in haemolymph concentrations of 10–5 M and higher, initiated increasingly strong and increasingly long-lasting continuous light production. Implications for the control of the photophores are discussed. Electronic Publication  相似文献   

9.
10.
The development of luminous structures and the acquisition of luminescence competence during the ontogeny of the velvet belly lantern shark Etmopterus spinax, a deep‐sea squalid species, were investigated. The sequential appearance of nine different luminous zones during shark embryogenesis were established, and a new terminology for them given. These zones form the complex luminous pattern observed in free‐swimming animals. The organogenesis of photophores (photogenic organs) from the different luminous zones was followed, and photophore maturation was marked by the appearance of green fluorescent vesicles inside the photocytes (photogenic cells). Peroxide‐induced light emissions as well as spontaneous luminescence analysis indicated that the ability of E. spinax to produce light was linked to the presence of these fluorescent vesicles and occured prior to birth. The size of photogenic organs, as well as the percentage of ventral body surface area occupied by the luminous pattern and covered by photophores increased sharply during embryogenesis but remained relatively stable in free‐swimming animals. All these results strongly suggest camouflage by counter‐illumination in juvenile E. spinax.  相似文献   

11.
The swallowerfishes previously identified as Pseudoscopelus altipinnis and P. cf. altipinnis (Prokofiev, Kukuev, 2005) are described as a complex of two new, closely-related, allopatric species having antitropical distribution. P. astronesthidens—superspecies is most closely related to P. altipinnis due to its dark orobranchial cavity and the details of its photophore arrangement, but is unique within the genus in the disconnection between the mxf and apf series of photophores and in the details of jaws dentition. P. astronesthidens sp. n. (North Atlantic) differs from P. australis sp. n. (Southern Hemisphere) mainly in the long upper jaw and pectoral fins and in the presence of the ppf series of photophores. P. altipinnis Parr, 1933 is considered as a senior synonym of P. microps Fowler, 1934. A revised key for identification of the linebellies of the genus Pseudoscopelus is given.  相似文献   

12.
The general morphology and ultrastructure of the epidermal and arm tip photophores of H. macrohista have been compared. Both types of photophore have similar structures
and the photocytes of each are characterized by dense aggregations of endoplasmic reticulum. The filter region of the epidermal photophores contains protoporphyrin.  相似文献   

13.
The trigeminofacial innervation of the cephalic photophores and lateral line organs of Tarletonbeania crenularis has been studied from gross dissections. The facial and trigeminal roots leave the brainstem separately, but later intermingle forming a trigemino‐facial complex. The seventh nerve gives rise to the hyomandibular trunk and sends a branch rostrad to join the trigeminal forming the supra‐ and infraorbital trunks. The supraorbital trunk innervates the Dn photophore, the snout, the iris, the supraorbital lateral line organs and part of the olfactory sacs. The infraorbital trunk supplies the infraorbital lateral line organs, the Vn photophore and the tissues surrounding the premaxillaries. The hyomandibular trunk passes to the opercular photophores and lateral line organs, and together with a branch from the infraorbital trunk supplies the branchiostegal photophores and lateral line organs of the mandible.  相似文献   

14.
Krönström, J. and Mallefet, J. 2009. Evidence for a widespread involvement of NO in control of photogenesis in bioluminescent fish. —Acta Zoologica (Stockholm) 91 : 474–483. The presence of nitric oxide synthase (NOS) and nerve fibres in the photophores of seven bioluminescent fish species (Hygophum benoiti, Myctophum punctatum, Electrona risso, Cyclothone braueri, Vinciguerria attenuata, Maurolicus muelleri and Porichthys notatus) with endogenous photocytes, were investigated. Antibodies directed against neuronal and inducible NOS (n and iNOS respectively) and NADPH‐diaphorase activity were used to reveal the locations of NOS, while antibodies directed against acetylated tubulin were used to visualize nerve fibres. The nNOS antibody labelled structures in all investigated photophores except in the organs from P. notatus. The photocytes of P. notatus showed NADPH‐diaphorase activity. In the myctophid species, NOS‐like immunoreactivity was found in small intracellular structures of the photocytes and in nerve fibres reaching the photocytes. nNOS‐positive fibres were also found among lens/filter cells in V. attenuata, and in M. muelleri the cytoplasm of lens/filter cells contained NOS‐like material. In C. braueri, a cell type located at a collecting chamber for luminous products in the photophore contained NOS‐like material. All photophores received an innervation reaching the photocytes, as well as other components including lens/filter areas. The results of this study comply with an involvement of nitric oxide in the control of bioluminescence in several fish species.  相似文献   

15.
The effects of 6-hydroxydopamine (6-OHDA) on the bioluminescent response of Porichthys photophores were investigated as part of a pharmacological study of the neural control of luminescence in this fish. Subcutaneous injections of 6-OHDA induce a luminescent response similar to that of norepinephrine (NE), suggesting a sympathomimetic action. The luminescent response to electrical stimulation is almost completely and irreversibly abolished within 24 hours following low-dose treatment of the photophores with 6-OHDA, while the sensitivity of these organs to exogenous NE is increased significantly over the few days post-treatment. During this period the photophores continuously emitted a steady low-level glow. Electronmicroscopic studies of such photophores revealed progressive destruction of the nerve endings. Photophore luminescent sensitivity to NE subsequently became sub-normal, and at this stage electron microscopy revealed an increasingly larger number of damaged photocytes, supportive cells and, in one case, lens cells. From these results it is suggested that 6-OHDA initially impairs neuro-photocyte transmission by destroying catecholaminergic nerve endings. In turn, the transmitter reuptake mechanism is also impaired, thus accounting for development of supersensitive responses to exogenous NE. Subnormal luminescent responses to NE appear as a result of loss of photocyte competence due to structural deterioration. The latter are interpreted as the consequence of removal of trophic factors supplied by the photophore adrenergic innervation.Suppression of luminescent response to both electrical stimulation and exogenous NE in photophores treated with higher doses of 6-OHDA, may be due to a direct effect of this drug on the receptor sites of the photocytes.  相似文献   

16.
Four genera of the teleost family Stomiidae, the loosejaw dragonfishes, possess accessory cephalic photophores (AOs). Species of three genera, Aristostomias, Malacosteus, and Pachystomias, are capable of producing far‐red, long‐wave emissions (>650nm) from their AOs, a character unique among vertebrates. Aristostomias and Malacosteus posses a single far‐red AO, while Pachystomias possesses anterior and posterior far‐red AOs, each with smaller separate photophores positioned in their ventral margins. The purpose of this study was to establish the primary homology of the loosejaw AOs based on topological similarity of cranial nerve innervation, and subject these homology conjectures to tests of congruence under a phylogenetic hypothesis for the loosejaw dragonfishes. On the basis of whole‐mount, triple‐stained specimens, innervation of the loosejaw AOs is described. The AO of Aristostomias and the anterior AO of Pachystomias are innervated by the profundal ramus of the trigeminal (Tpr), while the far‐red AO of Malacosteus and a small ventral AO of Pachystomias are innervated by the maxillary ramus of the trigeminal (Tmx). The largest far‐red AO of Pachystomias, positioned directly below the orbit, and the short‐wave AO of Photostomias are innervated by a branch of the mandibular ramus of the trigeminal nerve. Conjectures of primary homology drawn from these neuroanatomical similarities were subjected to tests of congruence on a phylogeny of the loosejaws inferred from a reanalysis of a previously published morphological dataset. Optimized for accelerated transformation, the AO innervated by the Tpr appears as a single transformation on the new topology, thereby establishing secondary homology. The AOs innervated by the Tmd found in Pachystomias and Photostomias appear as two transformations in a reconstruction on the new topology, a result that rejects secondary homology of this structure. The secondary homology of AOs innervated by the Tmx found in Malacosteus and Pachystomias is rejected on the same grounds. Two short‐wave cephalic photophores present in all four genera, the suborbital (SO) and the postorbital (PO), positioned in the posteroventral margin of the orbit and directly posterior to the orbit, respectively, are innervated by separate divisions of the Tmd. The primary homologies of the loosejaw PO and SO across loosejaw taxa are proposed on the basis of similar innervation patterns. Because of dissimilar innervation of the loosejaw SO and SO of basal stomiiforms, primary homology of these photophores cannot be established. Because of similar function and position, the PO of all other stomiid taxa is likely homologous with the loosejaw PO. Nonhomology of loosejaw long‐wave photophores is corroborated by previously published histological evidence. The totality of evidence suggests that the only known far‐red bioluminescent system in vertebrates has evolved as many as three times in a closely related group of deep‐sea fishes. J. Morphol., 2010. © 2009 Wiley‐Liss, Inc.  相似文献   

17.
A contribution to the knowledge of the photophore structure of the mesopelagic fish Cyclothone braueri (Gonostomatidae) from the central Mediterranean Sea (Strait of Messina) is given by means of a structural and ultrastructural study, to better identify and classify the real anatomical structures costituing these luminous organs. The photocytes exhibit numerous secretory granules, of different electron density, embedded in an extremely developed rough endoplasmic reticulum. The lens appear to be composed of tightly contiguous polyhedral cells. The reflector is made up of cells rich in guanine crystals, embedded in an amorphous matrix and is surrounded by a layer of connective tissue containing melanocytes. Unlike the present knowledge, it is shown that the bioluminescence emitted from C. braueri light organs has glandular nature, with photophores similar to type α from Bassot classification. The phenomenon of adaptive convergence, documenting how the morphology and physiology of the light organs of teleosts is similar in different species despite their taxonomic distance, is confirmed also for C. braueri.  相似文献   

18.
Lanternfish, a family Myctophidae, use ventro-lateral body photophores for camouflage of the ventral silhouette, a strategy called counterillumination. While other deep-sea fishes possess pigmented filters and silver reflectors to match sunlight filtering down through the depths, myctophids developed a blue-green reflector for this purpose. In this study, we showed in a lanternfish Diaphus watasei that the reflector comprised monolayered iridophores containing multilayered guanine crystals which enable high reflection with light interference colouration. Platelets shape in body photophores is an unique near-regular hexagonal, probably to allow the homogeneity of reflection angle of the luminescence from photocytes. Focus point of the parabola-like reflector is positioned on the photocytes that ensures the light produced from the photocytes is redirected to the ventral direction. In vitro luminescence reaction using purified luciferase and the substrate coelenterazine showed the light emission at λmax 454 nm, while reflection spectra of the iridophores exhibit peaks at longer wavelength, which accomplish to alter the luminescence emitted from photocytes to longer wavelength to fit the mesopelagic light environment. Taken together, we revealed multiple mechanistic elaborations in myctophid body photophores to achieve effective control of biochemical luminescence for counterillumination.  相似文献   

19.
The putatively luminous villous tissue in an abdominal pouch of a male specimen of the oceanic midwater shark Euprotomicroides zantedeschia is described. The epithelium within the pouch is probably stratified. The most conspicuous cell type is tall columnar cells, typically containing small cytoplasmic granules and a large inclusion. Cells with similar cytoplasmic characteristics, thought to be photogenic cells, are present in the epidermal skin photophores in other selachians which are known to be luminous.  相似文献   

20.
A new myctophid species, Diaphus pallidus sp.n., was captured in the Gulf of Aden. The species can be distinguished from most of its congeners by the high number of dorsal fin rays and low number of gill rakers. It can be distinguished from D. lucidus (Goode & Bean) by the form of the operculum and by the situation of some of the body photophores.  相似文献   

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