Light production by the arm tips of the deep-sea cephalopod Vampyroteuthis infernalis

The archaic, deep-sea cephalopod Vampyroteuthis infernalis occurs in dark, oxygen-poor waters below 600 m off Monterey Bay, California. Living specimens, collected gently with a remotely operated vehicle (ROV) and quickly transported to a laboratory ashore, have revealed two hitherto undescribed means of bioluminescent expression for the species. In the first, light is produced by a new type of organ located at the tips of all eight arms. In the second, a viscous fluid containing microscopic luminous particles is released from the arm tips to form a glowing cloud around the animal. Both modes of light production are apparently linked to anti-predation strategies. Use of the tip-lights is readily educed by contact stimuli, while fluid expulsion has a much higher triggering threshold. Coelenterazine and luciferase are the chemical precursors of light production. This paper presents observations on the structure and operation of the arm-tip light organs, the character of the luminous cloud, and how the light they produce is incorporated into behavioral patterns.     

The bioluminescent organs of the deep-sea cephalopod Vampyroteuthis infernalis (Cephalopoda: Vampyromorpha)

Vumpyroteuthis infernalis Chun is the sole member of the cephalopod subclass Vampyromorpha. The three putative types of photophore (fin base, dorsomedial or composite, and skin nodules) are described and it is concluded that the composite organ is not a light-emitting structure. It has structural similarities to an extra-ocular photoreceptor.
The fin-base photophore is capable of being everted from the pigmented pit in which it is seated. Its surface bears chromatophores which may modulate the emission and the photocytes contain an extensive network of microtubular elements and proteoglycan particles. The reflector is formed of a very thick layer of collagen fibrils in different orientations. The skin nodules are widely distributed over the animal. They have a collagenous reflector and core cells with structural similarities to those of the fin-base photocytes.
The photocytes have no morphological links with those of octopods or decapods. The thick collagen reflector, and absence of the iridosomal platelets present in the other subclasses, suggests an early separation of the Vampyromorpha from other coleoids.     

The statocyst of Vampyroteuthis infernalis (Mollusca: Cephalopoda)

The statocyst shows a remarkable combination of features of decapods and octopods confirming that Vampyroteuthis is a relic somewhere near the ancestor of both groups. The lining of the statocyst separates from the outer wall, forming an inner sac, filled with endolymph, surrounded by perilymph. This is the condition found in octopods, never in decapods. The macula is partly divided into a macula princeps and macula neglecta, as in decapods but never in octopods. There are numerous statoconia, but no large statolith has been seen. The crista has four parts as in decapods, but they are not sharply separated. There are numerous small anticristae, with the general form found in decapods, differentiated into pegs and hooks.
The wall of the inner sac contains numerous hair cells. These hairs protrude between the epithelial cells. The bases of the cells are drawn out into fine processes, presumably some dendritic and some axonal. There is thus a plexus of nerve fibres all over the wall, communicating with the crista nerve.
There is a very large posterior sac of unknown function, lying behind the crista. It contains only one large anticrista and the opening of Kölliker's canal, which is very large.     

Mitochondrial genome structure and evolution in the living fossil vampire squid, Vampyroteuthis infernalis, and extant cephalopods

Complete nucleotide sequences of mitochondrial (mt) genomes of the "living fossil" cephalopod Vampyroteuthis infernalis (Vampyromorpha) and the cuttlefish Sepia esculenta (Sepiida) were determined. The V. infernalis mt genome structure is identical to the incirrate octopod Octopus vulgaris mt genome structure, and is therefore more similar to that of the polyplacophoran Katharina tunicata, than to that of the other "living fossil" cephalopod Nautilus macromphalus. The mt genome structure of S. esculenta is identical to that of Sepia officinalis. Molecular phylogenetic analyses based on the mt protein genes from the completely sequenced cephalopod mt genomes suggested the monophyletic relationship of two myopsid squids Loligo bleekeri and Sepiotheuthis lessoniana, and the monophyletic relationship of two oegopsid squids Watasenia scintillans, and Todarodes pacificus. Sepiida appeared as the sister group of Teuthida (Myopsida + Oegopsida). The phylogenetic position of Vampyromorpha appeared as the sister group of Octopoda, although the monophyly of Vampyromorpha and Decapodiformes cannot be rejected outright by our phylogenetic analyses. The hypothesis that Vampyromorpha is basal among the coleoid cephalopods can be rejected because of low statistical support. Therefore, it is reasonable to recognize three major groups in Coleoidea--Vampyromorpha, Octopoda, and Decapodiformes.     

Spermatozoa ultrastructure of the pink shrimp Farfantepenaeus paulensis (Decapoda: Dendrobranchiata)

Braga, A.L., Nakayama, C.L., Suita de Castro, L.A. and Wasielesky, W. 2011. Spermatozoa ultrastructure of the pink shrimp Farfantepenaeus paulensis (Decapoda: Dendrobranchiata). —Acta Zoologica (Stockholm) 00 : 1–6. The spermatozoa ultrastructure of the pink shrimp Farfantepenaeus paulensis was investigated in this morphological study. Spermatophores and spermatozoa were analyzed by electron microscopy. The pink shrimp spermatophore is divided into two regions: the appendage and the spermatophore main body, where spermatozoa are grouped in a spermatic mass. Pink shrimp spermatozoa are unistellate and are composed of main body and single spike. The spermatozoa body comprises a perinuclear cytoplasmic band, nucleus, acrosomal cap, and subacrosomal region. The spermatozoa cell mean total length was 10.71 μm, the mean body diameter was 5.56 μm, and the mean spike length and diameter were 5.15 μm and 0.85 μm, respectively.     

Correlation between phylogenetic structure and function: examples from deep-sea Shewanella

The genus Shewanella is one of the typical deep-sea bacterial genera. Two isolated deep-sea Shewanella species, Shewanella benthica and Shewanella violacea, were found to be able to grow better under high hydrostatic pressure conditions than at atmospheric pressure. These species are not only piezophilic (barophilic), but also psychrophilic. Many psychrophilic and psychrotolerant Shewanella species have been isolated and characterized from cold environments, such as seawater in Antarctica or the North Sea. Some of these cold-adapted Shewanella were shown to be piezotolerant, meaning that growth occurs in a high-pressure habitat. In this review, we propose that two major sub-genus branches of the genus Shewanella should be recognized taxonomically, one group characterized as high-pressure cold-adapted species that produce substantial amounts of eicosapentaenoic acid, and the other group characterized as mesophilic pressure-sensitive species.     

Larval development of the tropical deep-sea echinoid Aspidodiadema jacobyi: phylogenetic implications

The complete larval development of an echinoid in the family Aspidodiadematidae is described for the first time from in vitro cultures of Aspidodiadema jacobyi, a bathyal species from the Bahamian Slope. Over a period of 5 months, embryos grew from small (98-micron) eggs to very large (3071-micron) and complex planktotrophic echinopluteus larvae. The fully developed larva has five pairs of red-pigmented arms (preoral, anterolateral, postoral, posterodorsal, and posterolateral); fenestrated triangular plates at the bases of fenestrated postoral and posterodorsal arms; a complex dorsal arch; posterodorsal vibratile lobes; a ring of cilia around the region of the preoral and anterolateral arms; and a long, unpaired posterior process containing a fenestrated rod. The presence of a posterior process and posterodorsal arms makes the larva of Aspidodiadema jacobyi much more similar to larvae of irregular urchins in the order Spatangoidea than to other families of the order Diadematoida, to which the family is normally assigned. This unexpected larval form lends support to a recommendation that the Aspidodiadematidae should be either elevated to ordinal status as a sister group of the order Diadematoida, or split off as a sister group of the other families within the order. In either case, if we accept the parsimonious hypothesis that the aboral process and posterodorsal arms were derived only once in the evolutionary history of euechinoids, then the larval data suggest that the Aspidodiadematidae may be very near the node where the irregular and regular euechinoids first diverged.     

Salivary glands in Cicadidae (Hemiptera: Cicadoidea): comparative morphology, ultrastructure, and their phylogenetic significance

The present investigation provides information on gross morphology and ultrastructure of salivary glands of species in Cicadidae in detail. The structure of the salivary glands of 11 representative species from 10 genera belonging to three subfamilies of Cicadidae was studied using light microscopy and transmission electron microscopy. In the examined species, the salivary glands are paired structures, and each of which is comprised of a principal gland (pg) and an accessory gland (ag). The pg is divided into anterior and posterior lobes, and both of which consist of numerous long digitate lobules. The lobules at the base of the long digitate lobules of posterior lobe are greatly short; here, we named as “short lobules.” All the lobules vary in size, disposition, length, and shape. The anterior lobe and posterior lobes are connected by an anterior–posterior duct (apd). Two efferent salivary ducts (esd), derived from corresponding posterior lobes, fuse to form a short common duct which enters into the saliva syringe. The ag is composed of a greatly tortuous and folded accessory salivary tube, a gular gland (gg) constituting of several acini, and an accessory salivary duct (asd). The asd joins the esd at the place where the latter emergences. Constituents and arrangement of the salivary glands, the number and shape of the long digitate lobules in the anterior and posterior lobes, and the visibility of the apd were promising characters for the taxonomic and phylogenetic analysis of Cicadoidea. The variations of secretory granules in size, shape, and electron density in lobule cells of pg of Platypleura kaempferi probably indicating different materials are synthesized. The absence of the infoldings of basal plasma membrane in the basal area of the cells and the presence of electron-lucent vesicles in the cytoplasm of the gg cells of P. kaempferi might suggest that the secretions of gg are more watery.     

Spermatozoa ultrastructure in Sciaenidae and Polynemidae (Teleostei:Perciformes) with some consideration on Percoidei spermatozoa ultrastructure

Spermatozoa ultrastructure was studied in five marines (Paralonchurus brasiliensis, Larimus breviceps, Cynoscion striatus, Micropogonias furnieri, Menticirrhus americanus, Umbrina coroides, Stellifer rastrifer), and one freshwater (Plagioscion squamosissimus) species of Sciaenidae and one species of Polynemidae (Polydactylus virginicus). The investigation revealed that, in all species, spermatozoa display a round head, a nucleus containing highly condensed, filamentous chromatin clusters, no acrosome, a short midpiece with a short cytoplasmic channel, and a flagellum showing the classic axoneme structure (9+2) and short irregular lateral fins. In Sciaenidae, the spermatozoa are type II, the flagellar axis is parallel to the nucleus, the lateral nuclear fossa is double arched, the centriolar complex is outside the nuclear fossa, the proximal centriole is anterior and perpendicular to the distal centriole, and no more than ten spherical (marine species) or elongate (freshwater species) mitochondria are observed. Polynemidae spermatozoa are of the intermediate type with the flagellar axis eccentric to the hemi-arc-shaped nucleus, and exhibit no nuclear fossa, the centriolar complex close to the upper nuclear end, the proximal centriole lateral and oblique to the distal centriole, and one large ring-shaped mitocondrion. The data available show that no characteristic is exclusively found in the spermatozoa of members of the Sciaenidae family when compared to other Percoidei with type II spermatozoa. However, three characteristics were exclusively found in Polynemidae: (1) the hemi-arched nucleus; the positioning of the centrioles; and (2) the ring-shaped mitocondrion. The interrelationships between Sciaenidae and Polynemidae as well as between these two families and other Percoidei are herein discussed.     

The ultrastructure of the lens of the cephalopod Sepiola: A scanning electron microscopic study

The ultrastructure of the eye lens of Sepiola atlantica was investigated using scanning electron microscopy. The main lens elements in both the anterior and posterior half of the Sepiola lens are plate-like configurations with fiber-like extensions at their margins. Anteriorly the plates are plano-convex, posteriorly subspherical. The central, primordial, posterior plates are spherical with no marginal extensions. The plates are mutually anchored by protrusions and invaginations and by push-button attachments. The posterior and anterior halves are separated by a septum which consists of concentric zones of radially orientated elongated cells. The marginal extensions of the plates and the septal elements are closely associated. The unique structure of the septum makes it a good candidate for the high resistance barrier between the posterior and anterior halves of the Sepiola lens (Jacob and Duncan, 1981).     

Comparative body wall musculature and muscle fibre ultrastructure in branchiobdellidans (Annelida: Clitellata), and their phylogenetic significance

The body wall muscles in five species of branchiobdellidans are all arranged in the oligochaete pattern and the muscle fibres are obliquely striated. The structure of the circular muscle fibres do vary to some degree. The longitudinal muscle fibres in Ankyrodrilus legaeus, Branchiobdella kozarovi, and Xironogiton instabilis all are round circomyarian and thus double-obliquely striated. These species represent three of the four genera composing the family Branchiobdellidae. Although Bdellodrilus illuminatus and Cambarincola fallax, from the families Bdellodrilidae and Cambarincolidae, respectively, also possess a few round circomyarian fibres, most are polyplatymyarian comparable to single-obliquely striated fibres. A similar division of branchiobdellidan families is obtained based on the number of anterior nephridial pores. The muscular structure in the branchiobdellidans shows both similarities and differences with the leeches and the lumbriculid oligochaetes. One phylogenetic explanation for this is that the branchiobdellidans separated from the common clitellate ancestor before the oligochaetes and leeches became recognizable taxa.     

Adaptation of a deep-sea cephalopod to the photic environment. Evidence for three visual pigments

Watasenia scintillans, a bioluminescent deep-sea squid, has a specially developed eye with a large open pupil and three visual pigments. Photoreceptor cells (outer segment: 476 micron; inner segment: 99 micron) were long in the small area of the ventral retina receiving downwelling light, whereas they were short (outer segment: 207 micron; inner segment: 44 micron) in the other regions of the retina. The short photoreceptor cells contained the visual pigment with retinal (lambda max approximately 484 nm), probably for the purpose of adapting to their environmental light. The outer segment of the long photoreceptor cells consisted of two strata, a pinkish proximal area and a yellow distal area. The visual pigment with 3-dehydroretinal (lambda max approximately 500 nm) was located in the pinkish proximal area, giving high sensitivity at longer wavelengths. A newly found pigment (lambda max approximately 471 nm) was in the yellow distal area. The small area of the ventral retina containing two visual pigments is thought to have a high and broad spectral sensitivity, which is useful for distinguishing the bioluminescence of squids of the same species in their environmental downwelling light. These findings were obtained by partial bleaching of the extracted pigment from various areas of the retina and by high-performance liquid chromatographic analysis of the chromophore, complemented by microscopic observations.     

The ultrastructure of the spermatozoon of Haplotaxis ornamentus (Annelida,Oligochaeta, Haplotaxidae) and its phylogenetic significance

Summary The spermatozoon of Haplotaxis ornamentus has characteristics common to all oligochaete sperm: filiform; primary acrosome vesicle carried on an acrosome tube and containing an axial rod (perforatorium) in an invagination (subvesicular space or secondary acrosomal invagination); an elongate, highly condensed cylindrical nucleus followed by a cylindrical midpiece of radially adpressed mitochondria not penetrated by the axoneme; a single (distal) centriole persistent, though modified, at maturity; axoneme with 9 doublets, each with two outer glycogen granules, and centrally two singlets accompanied by two solid fibres. A peculiar haplotaxid combination of characters (none unique) is slight withdrawal of the primary vesicle into the acrosome tube with a strongly emergent capitulate axial rod and moderately short midpiece. This ultrastructure is consistent with location of the Haplotaxidae at the base of the Haplotaxida (Haplotaxina — Alluroidina — Moniligastrina — Lumbricina). Tubificida sperm, although also plesiomorph for the Oligochaeta, have the autapomorphy elongate periaxial sheath (secondary tube), excepting the Phreodrilidae whose sperm show convergent resemblances to the Lumbricina. The term annuloid has been introduced for annulus-like structures of varied origins.     

Stable isotopes document the trophic structure of a deep-sea cephalopod assemblage including giant octopod and giant squid

Although deep-sea cephalopods are key marine organims, their feeding ecology remains essentially unknown. Here, we report for the first time the trophic structure of an assemblage of these animals (19 species) by measuring the isotopic signature of wings of their lower beaks, which accumulated in stomachs of stranded sperm whales. Overall, the species encompassed a narrow range in δ¹³C values (1.7‰), indicating that they lived in closely related and overlapping habitats. δ¹³C values can be interpreted in terms of distribution with the more ¹³C-depleted species (e.g. Stigmatoteuthis arcturi, Vampyroteuthis infernalis) having a more pelagic habitat than the more ¹³C-enriched, bathyal species (e.g. Todarodes sagittatus and the giant squid Architeuthis dux). The cephalopods sampled had δ¹⁵N values ranging 4.6‰, which is consistent with the species spanning approximately 1.5 trophic levels. Neither the giant octopod (Haliphron atlanticus) nor the giant squid reached the highest trophic position. Species δ¹⁵N was independent of body size, with large squids having both the highest (Taningia danae) and lowest (Lepidoteuthis grimaldii) δ¹⁵N values. Their trophic position indicates that some species share the top of the food web, together with other megacarnivores such as the sperm whale.     

Spermatozoa of tapeworms (Platyhelminthes,Eucestoda): advances in ultrastructural and phylogenetic studies

New data on spermiogenesis and the ultrastructure of spermatozoa of ‘true’ tapeworms (Eucestoda) are summarized. Since 2001, more than 50 species belonging to most orders of the Eucestoda have been studied or reinvestigated, particularly members of the Caryophyllidea, Spathebothriidea, Diphyllobothriidea, Bothriocephalidea, Trypanorhyncha, Tetraphyllidea, Proteocephalidea, and Cyclophyllidea. A new classification of spermatozoa of eucestodes into seven basic types is proposed and a key to their identification is given. For the first time, a phylogenetic tree inferred from spermatological characters is provided. New information obtained in the last decade has made it possible to fill numerous gaps in the character data matrix, enabling us to carry out a more reliable analysis of the evolution of ultrastructural characters of sperm and spermiogenesis in eucestodes. The tree is broadly congruent with those based on morphological and molecular data, indicating that convergent evolution of sperm characters in cestodes may not be as common as in other invertebrate taxa. The main gaps in the current knowledge of spermatological characters are mapped and topics for future research are outlined, with special emphasis on those characters that might provide additional information about the evolution of tapeworms and their spermatozoa. Future studies should be focused on representatives of those major groups (families and orders) in which molecular data indicate paraphyly or polyphyly (e.g. ‘Tetraphyllidea’ and Trypanorhyncha) and on those that have a key phylogenetic position among eucestodes (e.g. Diphyllidea, ‘Tetraphyllidea’, Lecanicephalidea, Nippotaeniidea).     

Alarm pheromones of the Attini: Their phylogenetic significance

The volatile components present in the mandibular glands of a number of species of the attine genera Cyphomyrmex (1 species), Trachymyrmex (3 species), and Acromyrmex (2 species) were investigated and compared with those present in Atta. The extracts were found to consist of mixtures of a number of compounds. All but one of these mixtures contained some or all of the following compounds: 3-octanone, 4-methyl-3-heptanone, 3-octanol, and 4-methyl-3-heptanol. The behavioural responses of Trachymyrmex and Cyphomyrmex workers to these compounds were tested. A common chemical heritage based on 3-ketones and 3-alcohols appeared to exist among the genera studied. The chemical data were compared with an accepted phylogeny of these genera to see whether it supported the phylogeny.     

黄胫小车蝗室内种群的建立及亚洲小车蝗痘病毒的增殖

1966年美国人最早从草地血黑蝗Ｍｅｌａｎｏｐｌｕｓｓａｎｇｕｉｎｉｐｅｓ上分离到病毒[1] ,1969年确认为是一种痘病毒(ｅｎｔｏｍｏｐｏｘｖｉｒｕｓ ,ＥＰＶ) [2 ] ,其后他们用这种草地蝗虫大量增殖痘病毒 ,现已进入了田间试验阶段[3] 。 1981年我国也从草地蝗虫中分离到痘病毒[4 ] ,但我国没有人研究过草地蝗虫的大量饲养问题 ,草地蝗虫的大量饲养与鳞翅目昆虫不同 ,即使在当地条件下饲养也很困难 ,这使得我国利用痘病毒防治草地蝗虫的研究一直停滞不前。2 0世纪 80年代末 ,我们从新疆和内蒙古的其它重要草地蝗虫中分离到痘病毒[5] ,能…     

Fast and flexible: the cephalopod repertoire

The cephalopods differ remarkably from their molluscan cousins such as snails and bivalves. Fast moving, active predators, they have behavioural and physiological capabilities that stimulate and fascinate marine zoologists. Research on their methods of prey capture and handling, in particular, demonstrates the adaptability of the cephalopod format.     

Molecular phylogenetic perspective on the evolution of the deep-sea fish genusCyclothone (Stomiiformes: Gonostomatidae)

A portion of mitochondrially encoded 12S and 16S ribosomal RNA genes were sequenced from 13 currently recognized species of the midwater deep-sea fish genusCyclothone (Stomiiformes: Gonostomatidae) and three gonostomatid outgroup taxa. Phylogenetic analyses using maximum parsimony and maximum likelihood methods were performed on unambiguously aligned, combined sequences (803 bp) of the two genes. The resultant tree topologies from the two methods were congruent, being robust and supported by various tree statistics, enabling the evolutionary history ofCyclothone to be described in detail. The molecular phylogeny demonstrated striking inconsistencies with previously proposed “natural groups”, although the latter could be confidently refuted by the molecular data. The most significant characteristic of the evolutionary history ofCyclothone was the independent acquisition of an apomorphic depth habitat from the relatively ancestral, lower mesopelagic habitat, by each of three major distinct lineages that had diverged earlier in their evolution. Moreover, such macroevolutionary habitat shifts had been necessarily accompanied by morphological and ecological novelties, presumably originating from paedomorphosis. Repeated evolution of such changes strongly suggests ontogenetic plasticity inCyclothone which could enable these fishes to acquire larval-like, simple organization of body structure. Such a body plan could help them subsist in food-poor surroundings and regulate reproductive variables that take advantage of increasing larval survival toward shallower depths. Recent speciation events, on the contrary, have produced contemporary sister species of allopatric (or microallopatric) distributions, but few morphological and ecological differences. Even if remarkable miniaturization has occurred, such as in the Mediterranean endemicC. pygmaea, it had to have been a simple truncation of ancestral species' ontogeny without attendance of any discernible paedomorphic features. On the basis of the fossil record, geological history of the Mediterranean region, and ectotherm molecular divergence rate, it was estimated thatCyclothone radiation had already started in the early-middle Miocene (17–20 million years ago).