Pelagic eggs and larvae of Coelorinchus kishinouyei (Gadiformes: Macrouridae) collected from Suruga Bay, Japan

Pelagic eggs and larvae of the macrourid fish Coelorinchus kishinouyei, collected from Suruga Bay, southern Japan and subsequently identified by 16S rRNA gene nucleotide sequences, are described. The spherical eggs, 1.18–1.31 mm in diameter, contained a single oil globule, 0.28–0.33 mm in diameter, and had hexagonally patterned ornamentation on the chorion, 0.017–0.022 mm in width. Melanophores were present on the embryo, yolk and oil globule after the blastopore had closed. Within 1 day after hatching, the body axis of the yolk-sac larvae was bent slightly at the anterior trunk region. During this stage many melanophores formed on the head, trunk, tail, yolk and oil globule, along with small irregular wrinkles on the dorsal and ventral finfolds. Pelagic eggs (after the caudal end of the embryo had detached from the yolk) and yolk-sac larvae also developed xanthophores on the embryo and yolk, and head, trunk, dorsal and ventral finfolds just before tail tip, and yolk, respectively. The pelagic larvae had a short tail, stalked pectoral-fin base and no elongate first dorsal and pelvic-fin rays. Three clusters of melanophores were present on the tail (anterior two embedded to muscle and one just before tail tip subsequently lost with development) and a cluster around the anus (beyond 3.9 mm head length). Nucleotide sequence analyses of comparative adult specimens appeared to confirm a previous proposal that C. productus is a junior synonym of C. anatirostris.     

Evolution of pelagic direct development in the starfish Pteraster tesselatus (Asteroidea: Velatida)

Despite a diversity of larval forms, remarkably conservative features of asteroid development define a larval body plan that occurs throughout the class. However, recent work on the starfish Pteraster tesselatus has documented a highly derived pattern of development. Several features, including radial symmetry, parallel embryonic and adult axes of symmetry, absence of a preoral lobe, and formation of coeloms in the adult orientation from seven separate enterocoels, have not been reported in asteroids before. The complete absence of the larval body plan features that are found in other asteroids, indicates that P. tesselatus develops directly from the embryo to the juvenile and has a pelagic, nonfeeding (lecithotrophic), but nonlarval mode of development. I postulate that direct development evolved over an extended period in a lineage of brooding, deep-sea velatid (probably pterastcrid) ancestors of P. tesselatus. Selection for increased developmental efficiency (loss of nonfunctional larval features) in the brooded offspring, could explain the lack of larval settlement structures, the nonlarval arrangement of coeloms, the lack of a preoral lobe, the transverse orientation of the juvenile disc, and the lack of bilateral symmetry. The pattern of coclomogenesis could have been derived from that of other velatids (e.g. solasterids) by relatively simple changes in timing and orientation of entcroeoel formation. Rotation and posterior translation of the coelomic fate map of the archenteron prior to enlerocoel formation would produce the coelomic compartments in the adult orientation that characterizes direct development in P. tesselatus. These unusual developmental features lead to a radically different interpretation for the evolution of the pelagic ‘larva’ of P. tesselatus: (1) evolution of benthie brooding, (2) extreme simplification of development involving the loss of all larval features from the life cycle, and (3) subsequent re-evolution of pelagic development. In the case of P. tesselatus, where all larval structures were lost, there do not seem to be functional constraints preventing the re-evolution of pelagic development. Analysis of pelagic and benthie larvae, in other asteroids, suggests that major ecological transitions in life histories need not be associated with substantia] changes in morphology. The loss of pelagic development should have occurred repeatedly and should be readily reversible. These findings have interesting implications for the loss and evolution of pelagic dispersal in the life histories of marine benthie invertebrates.     

Observations et discussions sur le développement embryonnaire des Phoronida

Resume La fécondation est généralement interne chez les phoronidiens. La segmentation des ceufs est totale, egale (parfois légèrement inégale) et de type radiaire (avec quelquefois une apparence fortuite de segmentation spirale). La gastrula est formée par embolie. La bouehe derive de la zone blastoporale sans formation d'un vrai stomodeum. L'anus est mis en place par perforation de l'ectodersme et représente une néo-formation indépendante du blastopore. Le mesoderme est issu par proliferation cellulaire des regions antérieure et laterales de l'archentéron. Le protoccele est forme par des cellules mésodermiques se disposant le long de la paroi du lobe préoral. Le métaccele est issu probablement suivant les espèces d'une ou deux masses. La formation du mesoderme correspond á une variation de la méthode entéroccelique typique. Les phoronidiens doivent être considérés comme des deutérostomiens, d'après l'ensemble de nos résultats (voir aussi Emig, 1973).

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Observations and discussions on the embryonic Development in Phoronida

Summary Internal fertilization (in metaccelom) generally occurs in Phoronida. The eggs are extruded to the exterior through the nephridia, shed freely into the sea-water or retained in the lophophoral concavity. The cleavage of phoronid eggs is total, equal (or subequal) and radial (with sometimes fortuitous appearance of spiral cleavage patterns). The gastrula is formed by emboly. The mouth is derived from the anterior remnant of the blastopore without a true stomodeum. The anus arises by perforation, as an independent structure of the blastopore. The mesoderm formed by budding originates as isolated cells proliferated from the anterior and lateral surfaces of the archenteron. In the preoral hood appears a protoccel by mesodermal cells lining the walls of the blastoccel. The trunk clom (or metaccel) of Actinotrocha originates from one or two posterior masses of mesodermal cells. It is possible that the mode of formation of this coelom varies in respect to the different species. The mesoderm elaboration is considered as a modified enteroccelous method.The acceptance of Phoronida as deuterostomes is regarded as the logical consequence of the present considerations (see also Emig, 1973): radial cleavage, origin of mesoderm by a derived enteroccelous method, trimetamerous actinotrocha.

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Abbréviations des figures a anus - lp lobe préoral - ar archentéron - b blastoccele - ma mésoderme de la région anterieure de l'archentéron - ml mésoderme des régions latérales de l'archentéron - bl blastopore - mes cellule mésodermique - bo bouche - n ebauche des - n éphridiesect mesderme - s sophage - end endoderme - p protocle - est estomac - t ebauche des tentacules - g ebauche du ganglion nerveux - te tentacule - gn glandes nidamentaire - v vestibule - i intestin     

The eggs and larvae of the giant mudskipper, <Emphasis Type="Italic">Periophthalmodon schlosseri</Emphasis>, collected from a mudflat in Penang,Malaysia

 Eggs of the giant mudskipper, Periophthalmodon schlosseri were collected from a burrow in Penang, Malaysia, in November 1998, and hatched larvae were reared in the laboratory. The eggs were demersal with adhesive filaments and elliptical in shape (0.83–1.43 mm in long-axis diameter). Newly hatched larvae (2.1–2.6 mm in notochord length) possessed a yolk sac. The number of myomeres was 10 + 17 = 27. The mouth and anus were already opened. The larvae started feeding one day after hatching and completely absorbed the yolk by the third day at a water temperature of 24.5–28.0°C. Received: April 9, 2002 / Revised: October 25, 2002 / Accepted: December 10, 2002     

Local shifts in position and polarized motility drive cell rearrangement during sea urchin gastrulation

This study examines the mechanisms of epithelial cell rearrangement during archenteron elongation in the sea urchin embryo using scanning electron microscopy, differential interference contrast videomicroscopy, cell marking, and fluorescently labeled chimaeric clones. Archenteron elongation involves two major processes: local shifts in position of cells in the archenteron wall and polarized motility of the cells as they rearrange. Fluorescently labeled chimaeric clones introduced into the archenteron of Lytechinus pictus are initially 4-5 cells wide; by the end of gastrulation the clones elongate and narrow, so that they are one cell wide in the narrowest region of the archenteron. The extent of clonal mixing indicates that cells in the archenteron change their relative positions by only 1-2 cell diameters during cell rearrangement. Cells at the blastopore rearrange concomitantly with cells in the archenteron, resulting in a 35% decrease in blastopore diameter. Endoderm cells undergo polarized, stage-specific changes in shape and motility as they rearrange; (1) they flatten markedly along their apical-basal axis throughout archenteron elongation; (2) just prior to the onset of cell rearrangement, basal surfaces of all cells in the archenteron extend long, polarized lamellipodial protrusions along the axis of extension of the archenteron; (3) as cell rearrangement begins, basal surfaces round up and the cells become isodiametric; (4) by the 3/4 gastrula stage the cells become stretched along the animal-vegetal axis, apparently due to filopodial traction, and finally (5) they continue to rearrange, returning to a less elongated shape by the end of gastrulation. Direct observation of gastrulation in the cidaroid Eucidaris tribuloides indicates that in this species cell rearrangement is accomplished by progressive circumferential intercalation of cells without upwardly directed filopodia. This intercalation is accompanied by explosive, apparently stochastic, cortical blebbing activity at the boundaries between cells, suggesting that in addition to whatever cell rearrangement may be generated by filopodial tension, such activity is an important component of the active rearrangement process.     

Larval development,growth and age determination in the sharpnose pufferfishCanthigaster valentini (Teleostei: Tetraodontidae)

The eggs, early larvae and juveniles of the sharpnose pufferfishCanthigaster valentini are described, based on material collected in Great Barrier Reef waters. Eggs were obtained in the field by divers and reared in the laboratory. The eggs are spherical, strongly adhesive, 0.68–0.72 mm in diameter, possess a dense cluster of small oil droplets, and hatch around sunset 3 to 5 days after fertilization. Newly hatched larvae have a small yolk sac, pectoral fin folds, 17 myomeres (6 pre-anal, 11 post-anal) and measure 1.30–1.40 mm in notochord (standard) length. The eggs ofC. valentini differ from those of other tetraodontids in being much smaller and having a longer incubation time. The larvae can be distinguished from other tetraodontid larvae by pigmentation, myomere count and size at hatching. Growth is most rapid during the first day of larval life. Age determinations (based on otolith microstructure) of field collected juveniles, both pelagic and newly settled, indicate a pelagic phase of between 64 and 113 days for this species. This estimate appears consistent with the extended pelagic juvenile stages observed in other tetraodontiform fishes and could indicate thatC. valentini can delay settlement for some time after becoming competent to settle at a minimum age of 64 days.     

Evolution of deuterostomy – and origin of the chordates

The chordates are usually characterized as bilaterians showing deuterostomy, i.e. the mouth developing as a new opening between the archenteron and the ectoderm, serial gill pores/slits, and the complex of chorda and neural tube. Both numerous molecular studies and studies of morphology and embryology demonstrate that the neural tube must be considered homologous to the ventral nerve cord(s) of the protostomes, but the origin of the ‘new’ mouth of the deuterostomes has remained enigmatic. However, deuterostomy is known to occur in several protostomian groups, such as the chaetognaths and representatives of annelids, molluscs, arthropods and priapulans. This raises the question whether the deuterostomian mouth is in fact homologous with that of the protostomes, viz. the anterior opening of the ancestral blastopore divided through lateral blastopore fusion, i.e. amphistomy. A few studies of gene expression show identical expression patterns around mouth and anus in protostomes and deuterostomes. Closer studies of the embryology of ascidians and vertebrates show that the mouth/stomodaeum differentiates from the anterior edge of the neural plate. Together this indicates that the chordate mouth has moved to the anterior edge of the blastopore, so that the anterior loop of the ancestral circumblastoporal nerve cord, which is narrow in the protostomes, has become indistinguishable. In the vertebrates, the mouth has moved further around the anterior pole to the ‘ventral’ side. The conclusion must be that the chordate mouth (and that of the deuterostomes in general) is homologous to the protostomian mouth and that the latest common ancestor of protostomes and deuterostomes developed through amphistomy, as suggested by the trochaea theory.     

Regional requirements for Dishevelled signaling during Xenopus gastrulation: separable effects on blastopore closure, mesendoderm internalization and archenteron formation

During amphibian gastrulation, the embryo is transformed by the combined actions of several different tissues. Paradoxically, many of these morphogenetic processes can occur autonomously in tissue explants, yet the tissues in intact embryos must interact and be coordinated with one another in order to accomplish the major goals of gastrulation: closure of the blastopore to bring the endoderm and mesoderm fully inside the ectoderm, and generation of the archenteron. Here, we present high-resolution 3D digital datasets of frog gastrulae, and morphometrics that allow simultaneous assessment of the progress of convergent extension, blastopore closure and archenteron formation in a single embryo. To examine how the diverse morphogenetic engines work together to accomplish gastrulation, we combined these tools with time-lapse analysis of gastrulation, and examined both wild-type embryos and embryos in which gastrulation was disrupted by the manipulation of Dishevelled (Xdsh) signaling. Remarkably, although inhibition of Xdsh signaling disrupted both convergent extension and blastopore closure, mesendoderm internalization proceeded very effectively in these embryos. In addition, much of archenteron elongation was found to be independent of Xdsh signaling, especially during the second half of gastrulation. Finally, even in normal embryos, we found a surprising degree of dissociability between the various morphogenetic processes that occur during gastrulation. Together, these data highlight the central role of PCP signaling in governing distinct events of Xenopus gastrulation, and suggest that the loose relationship between morphogenetic processes may have facilitated the evolution of the wide variety of gastrulation mechanisms seen in different amphibian species.     

Phylogenèse des Phoronida

Phylogenese of Phoronida. Lophophorata and the Archimerata concept The main phylogenetic characteristics of Phoronida and other Lophophorates are discussed: 1. Archimeric segmentation of the body; 2. Egg cleavage of radial (or biradial) type, coeloblastula and gastrulation by invagination (emboly); 3. Mesoderm formation by a derived enteroccelous method (primitive stage of enteroc? ly); 4. Bringing of the anus anteriorly to lie rocoelous method (primitive stage of enterocoely); 4. Bringing of the anus anteriorly to lie sence of a true lophophore; 6. Larva not of trochophoral type, but actinotroch related to Tornaria-Dipleurula; 7. Nervous system basi-epithelial with primitive neurulation in Phoronopsis, without any orthogons; 8. Adult nervous ganglion neo-formed, not issuing from the apicale plate; in Phoronida this ganglion is located in the prosome and not in the mesosome; 9. Lack of cephalization. All these characteristics are closely related to that of the primitive phyla of the Chordata assemblage. The only exception is the presence of protonephridia with solenocytes in actinotroch, but such organs are also described in Cephalochordata. The Lophophorata (Phoronida, Brachiopoda, Bryozoa) are undoubtedly a primitive group on the Chordata trend and the Phoronida appear to be the most phylogenetically evolved phylum of this group with predominating position. The validity of placing the Lophophorata within the Echinoderm-Hemichordata assemblage is demonstrated. The term Archic?lomata appears not suitable and its substitution by Archimerata, assemblage at the base of the Chordata, is here proposed. The Archimerata concept brings together the Lophophorata, Echinodermata and Hemidiordata and is considered as a phylogenetic stage and a natural systematic unit.     

Vital dye mapping of the gastrula and neurula of Xenopus laevis. I. Prospective areas and morphogenetic movements of the superficial layer.

The disposition of prospective areas and the course of morphogenetic movements during gastrulation and neurulation were investigated by vital staining. The prospective lining of the archenteron, the prospective neural area, and the prospective epidermal area are represented on the surface of the early gastrula. The prospective lining of the archenteron occupies the area within 65–70° of the vegetal pole and is divided into prospective archenteron roof and prospective archenteron floor by the blastopore pigment line which functions as the locus of invagination. A crescent-shaped neural area lies immediately above the prospective archenteron roof, rising from it at 125° lateral to the dorsal midline to a point 130° above the vegetal pole in the dorsal midline. In the early gastrula, most, if not all, mesoderm is deep to the surface layer and is mapped by the insertion of dyed agar spikes. Results thus far indicate that the prospective notochord lies in the dorsal deep marginal zone, followed laterally by the medial region of the somites, the lateral region of the somites, and the lateral plate.The morphogenetic significance of the comparative disposition of the anlagen in Xenopus is discussed.     

Cleavage and gastrulation in the shrimp Sicyonia ingentis: invagination is accompanied by oriented cell division.

Embryos of the penaeoidean shrimp Sicyonia ingentis were examined at intervals during cleavage and gastrulation using antibodies to beta-tubulin and DNA and laser scanning confocal microscopy. Cleavage occurred in a regular pattern within four domains corresponding to the 4-cell-stage blastomeres and resulted in two interlocking bands of cells, each with similar spindle orientations, around a central blastocoel. Right-left asymmetry was evident at the 32-cell-stage, and mirror-image embryos occurred in a 50:50 ratio. Gastrulation was initiated by invagination into the blastocoel at the 62-cell-stage of two mesendoderm cells, which arrested at the 32-cell-stage. Further invagination and expansion of the archenteron during gastrulation was accompanied by rapid and oriented cell division. The archenteron was composed of presumptive naupliar mesoderm and the blastopore was located at the site of the future anus of the nauplius larva. In order to trace cell lineages and determine axial relationships, single 2- and 4-cell-stage blastomeres were microinjected with rhodamine-dextran. The results showed that the mesendoderm cells which initiated gastrulation were derived from the vegetal 2-cell-stage blastomere, which could be distinguished by its slightly larger size and the location of the polar bodies. The mesendoderm cells descended from a single vegetal blastomere of the 4-cell-stage. This investigation provides the first evidence for oriented cell division during gastrulation in a simple invertebrate system. Oriented cell division has previously been discounted as a potential morphogenetic force, and may be a common mechanism of invagination in embryos that begin gastrulation with a relatively small number of cells.     

Comparison of laboratory-reared eggs, embryos and larvae of five labrid fishes

Eggs, embryos and larvae of five labrid fishes, Thalassoma cupido, Pteragogus flagellifer, Pseudolabrus japonicus, Halichoeres tenuispinnis, and H. poecilopterus, reared in the laboratory are described and compared. The eggs were buoyant and spherical, with a single, spherical oil globule. P. japonicus eggs were unique in lacking melanophores on the oil globule. Eggs of the remaining species closely resembled each other, except in diameter. Incubation periods were short, ranging from ca. 19 h in H. poecilopterus to ca. 31 h in P. japonicus. The newly-hatched embryos also resembled each other, having a short tail and large oval or pear-shaped yolksac, the anterior tip of which extended beyond the snout. The single oil globule was located at the anterior tip of the yolk. As the yolksac diminished with growth, its anterior tip moved posteriorly. The yolk and oil globule were completely absorbed 3 or 4 days after hatching. In all free embryos and larvae except for Pteragogus flagellifer, needle-like projections appeared on both the dorsal and anal finfold margins 12 h to 1 day after hatching. Although morphology of free embryos and larvae of all five species was very similar, differences in pigmentation, location of the anus, and the needle-like projections were apparent. Artificial keys to the newly-hatched embryos and larvae are given.     

Ventral nerve cord in Phoronopsis harmeri larvae

The nervous system organization is considered a phylogenetically important character among metazoans. The phylum Phoronida is included in a supraphyletic taxon known as Lophotrochozoa. Many lophotrochozoans possess a metameric ventral nerve cord as adults or larvae. Phoronids do not exhibit external metamery either as larvae or as adults. The current study describes the ventral nerve cord in the young larva of Phoronopsis harmeri. This structure is apparent both in the serotonergic and FMRF-amidergic nervous system in young larvae. The ventral nerve cord extends from the mouth to the tentacular ridge. Both serotonergic and FMRF-amidergic components consist of two ventrolateral nerves, each with several unipolar neurons. The ventrolateral nerves connect to each other by means of thin repetitive transversal nerves ("commissures"). The abundance of neurons and nerves in the epidermis of the oral field of actinotrocha larva likely reflects the importance of this area in collection of food particles. The ventral nerve cords of the actinotrocha and the metatrochophore differ in their positions with respect to ciliated bands: the cord is located between the preoral and postoral ciliated bands in the actinotrocha but between the postoral ciliated band and telotroch in the metatrochophore. The presence of the ventral nerve cord, which contains repetitive elements (neurons and "commissures"), in the early development of P. harmeri may recapitulate some stages of nervous system development during phoronid phylogeny. The larval nervous system does not contain nervous centers under the tentacular ridge that can correlate with the catastrophic metamorphosis and unique body plan of phoronids.     

Development of the dendrobatid frog Colostethus machalilla

To provide a developmental correlate with other frogs, we prepared a normal table of development for the dendrobatid, Colostethus machalilla and analyzed the morphology of its early development. This frog reproduces in captivity and deposits moderately sized eggs (1.6 mm in diameter) in terrestrial nests. The father guards the embryos until tadpole hatching. We divided development until hatching into 25 stages and implemented methods for in vitro culture of the embryos. The external and internal morphology of embryos were evaluated by observations in whole mount and in sections. Neural, notochord and somite specific antibodies were used to analyze gene expression patterns by immunostaining of embryos. Embryonic development of C. machalilla is slow and deviates from Xenopus laevis. In C. machalilla the elongation of the notochord, neural plate and somite formation occur after blastopore closure, possibly due to a delay in the dorsal convergence and extension movements. The gastrula of C. machalilla also deviates from X. laevis. The archenteron remains small until blastopore closure, where small cells accumulate at the blastopore lips. Simultaneously, the blastocoel roof thins until it becomes a monolayer of cells. Although C. machalilla does not form an embryonic disk, its thick blastopore lips resemble the embryonic disk of the marsupial frog Gastrotheca riobambae and represent an interesting deviation from the gastrulation pattern observed in X. laevis.     

Animal phylogeny in the light of the trochaea theory

Ultrastructural similarities unite Choanoflagellata and Metazoa as the Kingdom Animalia. Mctazoa (Porifera + Placozoa + Gastraeozoa) are characterized by the presence of collagen, septate/tight junctions and spermatozoa. Porifera and Placozoa lack basal lamina, nerve cells and synapses, which characterize Gastraeozoa (Cnidaria + Trochaeozoa). Gnidaria have cnidoblasts and lack the multiciliate cells found in almost all Trochaeozoa (Gastroneuralia + Protornaeozoa). Gastroneuralia (Spiralia + Aschelminthes) have an apical brain and a pair of ventral nerves, a blastopore which becomes mouth and anus, a mouth surrounded by a downstream collecting system of compound cilia, and a mesoderm formed from the blastopore lips. Spiralia (Articulata + Parenchymia + Bryozoa) have spiral cleavage and 4d-cell mesoderm, whereas these characters are lacking in Aschelminthes, which all lack primary larvae. Protornaeozoa (Ctenophora + Notoneuralia) have mesoderm from vegetal cells. Ctenophores have colloblasts. Notoneuralia have a dorsal nervous system behind the apical area and form a new mouth surrounded by an upstream collecting system of single cilia on monociliate cells; the blastopore becomes the anus surrounded by a ring of compound cilia.
These features fit the trochaea theory, which proposes that Gastroneuralia and Notoneuralia evolved independently from the trochaea, a blastaea with the blastopore surrounded by a ring of compound cilia, which were both locomotory and particle collecting.     

A Paedomorphic Origin of the Oligomerous Animals?

Anatomical, developmental, and functional studies have demonstrated that the protostone Phoronida (Tentaculata/Lophophorata) share several characters in common with more primitive deuterostomes, thus belonging to the Oligomera and suggesting a level of direct connection between higher (coelomate) Gastroneuralia and lower Deuterostomia. In reevaluation of the characters of the cleavage, the tentacle apparatus, the mesoderm-coelom organization, the nervous system, and also the fate of the blastopore, there is essential support for an evolutionary differentiation of bilaterian animals along a monolinear sequence of recent megagroups (in contrast to other theories): As still reflected by the Phoronida, such monolinear pathway from mesenchymatous to coelomate Gastroneuralia (Spiralia) to Heteroneuralia (Oligomera) to Notoneuralia (Chordata) was made possible predominantly by decisive paedomorphic processes for the tentacles and the nervous system in gastroneuralian pre-Heteroneuralia.     

TEMPORAL RELATIONS BETWEEN EXTENSION OF ARCHENTERON ROOF AND REALIZATION OF NEURAL INDUCTION DURING GASTRULATION OF NEWT EMBRYO

This investigation was performed in order to analyze the basic relationships between the archenteron roof and the overlying ectoderm in primary induction in the Cynopus (Triturus) pyrrhogaster embryo.
The part of the archenteron roof that is active in inducing capacity extends linearly after invagination at the speed of 0.15 mm per hr at 23°C until stage 13b. The period of contact at each position of the presumptive neuro-ectoderm with the active archenteron roof could be estimated by the formula described in the Discussion.
Pieces of the presumptive neuro-ectoderm were isolated from gastrulae at three developmental stages and cultured separately in Holtfreter solution after being divided caudo-cranially into 4 parts. The result showed that some of them were able to differentiate into neural tissues even in the mid-gastrula stage and that the presumptive neuro-ectoderm acquired the capacity to differentiate into neural tissue along a caudocranial axis from the part adjacent to the blastopore during gastrulation.
It could be estimated that 3 hr of contact with the active archenteron roof is sufficient for the presumptive neuro-ectoderm to differentiate into neural tissue.
The present study also showed that the neuralizing capacity of the whole prospective neuro-ectodermal area has already been determined before the end of stage 13, i.e., within less than 14 hr after first contact of the ectoderm with the active archenteron roof at 23°C.     

Reconstruction of Starfish Eggs by Electric Cell Fusion: A New Method of Detect the Cytoplasmic Determinant for Archenteron Formation

A method of detecting cytoplasm carrying the determinant for archenteron formation in starfish was established. Animal egg fragments (AEFs) which had been severed from the vegetal halves were fused electrically into pairs with fragments prepared from various regions of immature oocytes. It has been previously shown that the vegetal halves are exclusively endowed with the ability to form the archenteron; AEFs alone develop into so-called permanent blastulae. Eggs thus reconstructed were allowed to develop in order to assess the presence of the determinant in the added fragments. Only AEFs fused with fragments from near the vegetal pole of the oocytes formed the archenteron and developed into bipinnariae and juveniles.
Comparison between the inner and outer (including cortex) cytoplasm of small vegetal fragment showed that the outer cytoplasm gave the reconstructed egg a greater ability to form an archenteron than the inner cytoplasm.     

RAPID EVOLUTION OF GASTRULATION MECHANISMS IN A SEA URCHIN WITH LECITHOTROPHIC LARVAE

This study documents evolutionary modifications in mechanisms of gastrulation in Heliocidaris erythrogramma, an echinoid with lecithotrophic larvae. Radially symmetrical cell rearrangements and changes in cell shape drive elongation of the archenteron in the ancestral mode of echinoid gastrulation. Cell marking experiments indicate that in H. erythrogramma, however, prolonged movement of cells over the ventral lip of the blastopore accompanies extension of the archenteron. Evolutionary modifications to archenteron extension in H. erythrogramma thus include utilization of a different type of cellular movement as well as the imposition of dorsoventral asymmetry in cellular movements. The conservation of gastrulation mechanisms among phylogenetically divergent echinoids with planktotrophic development suggests that the plesiomorphic condition has persisted at least 250 million years and perhaps much longer. Yet H. erythrogramma diverged from an ancestor with planktotrophic development only about 10 mya, indicating that morphogenetic mechanisms of early development can undergo substantial evolutionary changes, even after long periods of stasis.     

SEM observation of the External Yolk Syncytial Layer in Blastopore Closure of the Medaka, Oryzias latipes

The embryonic surface of the teleost, Oryzias latipes , was observed by scanning electron microscopy (SEM) to examine the last phase of epiboly or blastopore closure. The surface of the external yolk syncytial layer (E–YSL), a surface cytoplasmic layer encompassing the yolk sphere situated beyond the blastoderm, was highly undulated with surface folds of random orientation throughout most of epiboly (st. 14–20). Scattered microvilli were observed on the surface of the margin of the yolk plug in st. 18–20. The microvilli, 1 to 6 μm in length, were projected in a bunch at the end of blastopore closure (st. 20–21). The appearance of these microvilli in the last phase of epiboly is discussed with respect to the mechanism of epiboly.