Evidence for the involvement of calcium in the hatching of Globodera rostochiensis

Low concentrations of ruthenium red and lanthanum chloride inhibited hatching of juveniles from eggs in cysts of Globodera rostochiensis in potato root diffusate. Pro-bit analysis for 31 cysts at seven concentrations of ruthenium red showed that 50% inhibition with 95% fiducial limits occured at 47 ± 23 μm; a similar value of 59 ± 14 μm was obtained using eggs removed from cysts. Results for 10 to 20 cysts at six concentrations of lanthanum chloride suggested a somewhat higher value for 50% inhibition of 110 ± 83 μM. In contrast hatching of eggs in cysts of Heterodera schachtii in water was unaffected by 5 ITIM lanthanum chloride and 625 μM ruthenium red, concentrations which cause over 90% inhibition of hatch in G. rostochiensis.
Two calcium ionophores synergised hatching of a 1971 population of G. rostochiensis in dilute diffusate. Optimal concentrations of 2 μM for A23187 and 10 μM for BrX537A increased the hatch from 17 ± 3–6 juveniles/cyst to 114 ± 44 juveniles/cyst and 138 ± 40 juveniles/cyst respectively. Ionophores in the absence of diffusate hatched very few eggs of this population but caused a greater hatch in a second (1975) population which gave a high hatch in water of 43 ± 10 juveniles/cyst. This was increased by A23187 to 181 ± 41 juveniles/cyst. The results with both the inhibitors and the ionophores suggest that hatching in G. rostochiensis might be a calcium-mediated process.     

Microinjected Polystyrene Beads Move Along Astral Rays in Sand Dollar Eggs

Movements of polystyrene beads along astral rays of the sperm aster and the mitotic aster were investigated in eggs of the sand dollars, Clypeaster japonicus and Scaphechinus mirabilis . Polystyrene beads injected into the unfertilized egg were at a standstill in the protoplasm. After fertilization, these beads exhibited movements toward the center of the sperm aster along the rays, and finally gathered around the astral center. They were distributed in blastomeres together with the mitotic centers during successive cleavages. When injected into eggs during mitosis, beads moved to the centers of the mitotic asters along astral rays. The injected beads did not move when the aster was disorganized by treatment with Colcemid, and moved when it formed after UV-irradiation. These results indicate that microtubules of astral rays are essential to the movement of polystyrene beads. The movement of small polystyrene beads (0.2–0.3 μm in diameter) resembled the saltatory movement of endogenous cytoplasmic granules, and the movement of large beads (ca. 1 μm in diameter) resembled the female pronuclear migration. All of these movements observed in fertilized eggs were demonstrated to be microtubule-dependent, perhaps sharing the same basic mechanisms.     

Direct development of the brittle star Amphiodia occidentalis (Ophiuroidea, Amphiuridae) from the northeastern Pacific Ocean

Abstract. The highly modified development of the brittle star Amphiodia occidentalis is described from post-fertilization to the juvenile stage. Fertilized eggs are negatively buoyant, ∼190 μm in diameter, surrounded by a thick hyaline layer and a tough fertilization envelope. After gastrulation, embryos flatten into a bilaterally symmetrical disk with a U-shaped ridge surrounding an indented stomodeum on the oral surface. Internally, a ring of ∼22 calcitic ossicles grows at the edge of the disk. Vestigial ophiopluteal structures such as a ciliated band, paired larval spicules, or larval arms are not expressed during development. Although the fertilization envelope disintegrates on day 3, developmental stages remain immotile for five more days until they move with podia. At hatching, five hydrocoelic lobes are evident on the left side of the post-gastrula, and these migrate clockwise around the stomodeum, establishing pentamerous radial symmetry. Central and radial plates originate on the right side and migrate to a dorsocentral location as pentamerous symmetry is established. Development of the juvenile oral skeletal frame follows closely that described by Hendler (1978) for Amphioplus abditus except that A. occidentalis did not form buccal scales. The juvenile mouth opened by day 12. Fifty-five days after fertilization, juveniles had not added their first arm segments, although the first lateral arm plates had appeared. Developmental stages identical to those described here have been found in plankton tows taken in Oregon usually after storms that bring high waves. The unusual development of this species probably occurs in both benthic and pelagic environments.     

Reproduction, spawning, and development of 5 ophiuroids from Australia and New Zealand

Abstract. Reproduction and development in 5 brittle stars: Ophiactis resiliens, Ophionereis fasciata, Ophiothrix caespitosa, Ophiothrix spongicola , and Ophionereis schayeri were investigated in a series of laboratory spawning and fertilization trials. Ophiactis resiliens spawned in 90% of trials, both spontaneously (in response to disturbance) and after temperature and light shock. Ophiothrix caespitosa and Ophiothrix spongicola spawned in 100% of trials, largely due to spontaneous gamete release. In contrast, Ophionereis fasciata and Ophionereis schayeri spawned in only 32% and 50% of trials respectively, and only in response to temperature and light shock. All 5 species required an aggregation of males and females for spawning and fertilization. The breeding periods of each species, estimated from the spawning trials, are reported. Eggs of Ophiactis resiliens, Ophionereis fasciata, Ophiothrix caespitosa , and Ophiothrix spongicola were 83 μm, 99 μm, 105 μm, and 128 μm in diameter, respectively, and all underwent planktotrophic development through an ophiopluteus. Eggs of Ophionereis schayeri were 241 μm in diameter and underwent lecithotrophic development through an armless bilateral larva that secondarily transformed into a radial vitellaria. The two Ophionereis species, with differing modes of development, provide an ideal opportunity to examine life-history evolution within a clade; however, these species were the most difficult to spawn. Ophiactis resiliens and the two Ophiothrix species spawned readily when they were visually mature at collection, and are thus useful species for developmental studies.     

Significance of an Increase of Intracellular Adenosine Concentration for Dormancy in Starfish Blastulae

Adenosine at concentrations greater than 6 μg/ml halted embryonic development of the starfish Asterina pectinifera specifically at the 256-cell stage which corresponds to the onset of blastulation. When a fertilized egg was cultured continuously in sea water containing adenosine from fertilization, a gradual increase in intracellular concentrations of free adenosine was observed before a cessation of development took place. On the other hand, intracellular concentrations of ATP, ADP and AMP in the embryo cultured in sea water containing adenosine were nearly the same as those of an embryo cultured in sea water without adenosine. By returning the development-arrested embryo to normal sea water the embyro developed normally to the bipinnaria stage accompanied by a gradual decrease in the intracellular cencentration of adenosine.
Treatment of fertilized eggs with 9-β-d-arabinofuranosyl-9H-purine-6-amine (25 μg/ml) or 2'-deoxyadenosine (10 μg/ml) halted development specifically before the onset of blastulation in an irreversible manner. Embryos treated with 3'-deoxyadenosine (50 μg/ml) shortly after fertilization developed to healthy blastulae but hatching never occurred. These results exclude the possibilities that the action of adenosine is mediated by the inhibition of DNA synthesis or RNA polyadenylylation.     

Reproduction and larval development of the gastropod molluskTegula rustica in Peter the Great Bay, Sea of Japan

The reproduction and larval development of the prosobranch gastropod molluskTegula rustica were studied under laboratory conditions. In Vostok Bay (Peter the Great Bay), the reproduction of theTegula takes place in August, when the water temperature is 19–20°C. Under laboratory conditions, the spawning of females was stimulated by adding a sperm emulsion to a vessel containing adult females. We observed asynchronous and intermittent release of gametes. The egg cell is 190 μm in diameter. Fertilization is external, and the course of development includes a lecithotrophic pelagic larva. Complete development, from fertilization to metamorphosis, takes 7 days in a laboratory culture. The larvae settle when the shell size across the first whorl is 220–230 μm and the total shell whorl is about 90°. The shape of the veliger shell is elongated mitriform and the velum is rounded, made up of a single lobe. The sculpture of the protoconch is irregularly ribbed.     

Fertilization Cone of Carp Eggs as Revealed by Scanning Electron Microscopy

The process of formation of the fertilization cone in carp eggs was examined by scanning electron microscopy. The fertilized eggs responded to penetration of one sperm by primary and secondary steps of formation of a fertilization cone of unique morphology. In the primary step, the earliest fertilization cone was seen at the superior or anterosuperior part of a fused sperm head in inseminated eggs fixed 20 sec after immersion in fresh water. The cone reached a maximum of more than 10 μm in length and 3–4 μm in thickness by 40 sec, resulting in a transient plugging of the micropylar canal. In the secondary step, usually seen at 105–120 sec, a conformation reminiscent of a very small caldera volcano was formed, with the shortened earlier cone and part of the sperm tail at its top. By 2.5 min, the fertilization cone had become conical, and the sperm tail still extended from its top. At 3 min, the sperm tail was often not detectable, but a cytoplasmic eminence was still seen as a trace of the fertilization cone. The role of the earlier fertilization cone in blocking polyspermy is discussed.     

Fine Structure of the Envelope and Micropyles in the Eggs of the White Sturgeon, Acipenser transmontanus Richardson

The structure of the egg envelope and micropyles of the white sturgeon was examined with light and electron microscopy. The mature ovum is 3.5–4.0 mm in diameter and is covered by a thick envelope (50 μm) that consists of four distinct layers. The outermost layer, L4, is electron dense and amorphous. Interior to this is layer three (L3), containing numerous pores, or ductules. Layer two (L2) contains screwlike projections that anchor L3 and L4 to the egg. The innermost layer, L1, is closely apposed to the oolemma. Numerous micropyles (average 7) are restricted to a 100–200 μm region at the animal pole and penetrate the egg envelope. The outer opening of these rnicropyles measures 15 μm in diameter. The micropylar canal tapers twice, eventually terminating at the oolemma with an inner opening diameter of 1.2 μm. The micropyles of the white sturgeon egg appear more complex than micropyles in other fish eggs.     

Changes in the second stage juveniles of Globodeva rostochiensis prior to hatching in response to potato root diffusate

cAMP levels in eggs of G. rostochiensis and the diameter of the nucleolus of the nucleus within the dorsal pharyngeal gland cell of the second stage juvenile have been measured as indicators of the response of the nematode to the hatching stimulus in potato root diffusate. The nucleolus increased from 2.72 ± 0.103 μm for unhatched individuals to 3.28 ± 0.14 μm and 3.88 ± 0.15 μm after soaking eggs in potato root diffusate for 3 and 4 days respectively. Juveniles expressed from unstimulated eggs in water to potato root diffusate for 4–5 days showed a similar increase in size of the nucleolus to 3.94 ±0.15 μm but those released into water for this time had smaller nucleoli of 3.20 ± 0.98 μm. The change in diameter of the nucleolus is probably related to the accumulation of secretions in this gland cell before hatching. Preliminary results with dibutyryl analogues of CAMP and cGMP showed some inhibition of hatch in 10% potato root diffusate. Theophylline had a similar effect but NaF was dissimilar in that the effect of this inhibitor was not reversible. A standard radioimmunoassay showed that significant changes in cAMP levels occurred in the unhatched juveniles within cysts after treatment with potato root diffusate for 2.5 or 8 h compared with values for cysts kept in water. This change occurs before other known responses of the juveniles to potato root diffusate and it defines the period of interest for future work on the initial action of hatching factor.     

Reproduction and development of the conspicuously dimorphic brittle star Ophiodaphne formata (Ophiuroidea)

Ophiodaphne formata is a conspicuously dimorphic ophiuroid; the disk diameters are approximately 1 mm for males and 5 mm for females. The dwarf male clings to the larger female, with the oral surfaces and bursae of the paired ophiuroids closely appressed. Moreover, the female of each pair adheres aborally to the oral surface of a host sand dollar, Astriclypeus manni. Spawning and external fertilization occur in August, at Tsuruga Bay, Sea of Japan. Development of the dimorphic brittle star O. formata is described for the first time, from spawning through metamorphosis, with special attention to the formation of the skeletal system and the external morphology of early juveniles. Fertilized eggs are about 90 microm in diameter, pale pink, and negatively buoyant. The embryos undergo equal, total, and radial cleavage, and the larval skeleton first forms as a pair of tetraradiate spicules. Larval development proceeds to an 8-armed planktotrophic ophiopluteus, with skeletal elements that consist of a body rod and two recurrent rods. Three weeks after fertilization, all the pluteal arms, except for the postero-lateral arms, are absorbed, and the metamorphosing larvae sink to the bottom. Metamorphosis is completed 21.5 days after fertilization, and the resulting juvenile is pentagonal and approximately 270 microm in diameter. The smallest specimen (480 microm in disk diameter) collected by field sampling exhibited male features on the skeletal plates of the jaw and disk. Sexual dimorphism, the peculiar pairing behavior, and the close relationship with the host sand dollar may have evolved as distinct reproductive characteristics in this ophiuroid with its typical ophiopluteus larvae.     

CHANGES IN ACTIVITIES OF THYMIDYLATE SYNTHASE AND DIHYDROFOLATE REDUCTASE IN SEA URCHIN EGGS AFTER FERTILIZATION

Thymidylate synthase activity in sea urchin eggs increases just after fertilization and decreases 30 min later. Then, cyclic variation in the activity occurs in association with the cleavage cycle. Dihydrofolate reductase activity in fertilized eggs is almost the same as in unfertilized eggs and shows no marked change within 3 hr after fertilization. Aminopterin, an analogue of dihydrofolate, inhibits dihydrofolate reductase, and arrests cleavage. On incubation in sea water containing aminopterin (20-100μM) from the time of fertilization, the development of Clypeaster and Pseudocentrotus eggs was arrested at the 32–64 cell stage, and that of Anthocidaris eggs was arrested at the morula stage. Dihydrofolate (100μM) counteracts the inhibitory effect of aminopterin on egg cleavage. Thymidine at concentrations above 10μM also prevents inhibition by aminopterin. Other deoxyribonucleosides at concentrations of 10μM to 100μM do not affect inhibition of egg cleavage by aminopterin. Deoxyadenosine at concentrations above 5 mM inhibits egg cleavage, but other deoxyribonucleosides have no effect.     

Time Sequence of Early Events in Fertilization in the Medaka Egg

The time sequence of early events in fertilization was examined in eggs of the medaka Oryzias latipes . The mean time after insemination required for sperm attachment to the egg surface through the micropyle depended on sperm concentrations. It was 3 ± 1 sec with a range from 1 to 6 sec after insemination when concentration of spermatozoa was high (about 2 × 10⁸/ml at 23°–25°C). The mean time from sperm attachment until cessation of its movement on the egg surface was 4 ± 1 sec with a range from 1 to 9 sec. Small cortical alveoli at the animal pole region within 15 μm of the sperm attachment point began to undergo exocytosis 9 ± 0.3 sec (range 5–16 sec) after sperm attachment. The velocity at which the exocytosis wave propagated increased from the earliest initiation point of exocytosis up to the 100 μm area, and became constant at about 12 μm/sec from 100 μm to 500 μm from the sperm attachment point. The present results suggest that at the time of fertilization in the fish egg, exocytosis of small cortical alveoli in the area about 15 μm away from the sperm attachment point occurs simultaneously.     

Achromosomal Division of Early Starfish Embryos Cultured in the Presence of Actinomycin D

Embryos of the starfish Asterina pectinifera were examined for their ability to undergo the early events of embryonic development in the presence of actinomycin D, a most widely used inhibitor of RNA synthesis. Fertilized eggs continued to divide eight or nine times in the presence of 25 μg ml⁻¹actinomycin D, although delay of development was observed. Chromatin disintegrated in the blastomeres of actinomycin D-treated embryos specifically at the 32-cell stage and the nucleus was undetectable at later stages. Before the 32-cell stage, RNA synthesis was not affected by the presence of actinomycin D whereas DNA synthesis was severely inhibited. The stage when achromosomal divisions cease and embryos begin to die corresponds to the period just before onset of blastulation, suggesting that the presence of the nucleus and chromosomes is a prerequisite for blastula formation and development beyond the 512-cell stage in this species.     

The fecundity of the walleye pollock, Theragra chalcogramma (Pallas), spawning in Canadian waters

The ovaries of 113 walleye pollock from a resident stock in the Strait of Georgia, British Columbia were examined for determination of fecundity. Oocytes were sized and counted in 20 μm intervals of diameter. Without exception, ovaries contained a pronounced bimodal distribution of oocyte diameters with peaks at 100 and 400–600 μm. Oocytes ≥ 180 μm diameter were undergoing trophoplasmic growth leading to hydration. 'Apparent' fecundity is defined as the estimated number of yolked oocytes ≥ 180 μm diameter, regardless of potential resorbtion. Previous workers have not shown that significant resorbtion takes place in the post-spawned ovary. Total oocyte complement (≥40μm diameter) was best expressed by a linear model where F_t = 33004 f.l. – 869627, where f.l. = fork length in cm and r = 0.86. Estimates of F_t , ranged from 117700 to 1394 100 oocytes ≥40μm. Age was weakly related to fecundity, reflecting large individual differences in annual growth after age 4 years. Apparent fecundity best suited a linear model where F_a = 23522 f.l. – 599713 and r = 0.91. Estimates of F_a fell within the range 58 379–1 151 527. Relative fecundity (eggs g⁻¹) decreased over most of the length range encountered in the sample. The average-sized female in Georgia Strait is twice as fecund as her counterparts in the north-western Pacific Ocean, containing some 390 000 to 420 000 oocytes 7ge;180 μm diameter compared to about 200 000 oocytes in a north-western female of comparable length.     

A gastric-brooding asteroid, Smilasterias multipara

The gastric-brooding asterinid sea star, Smilasterias multipara, broods from late August to early November in the shallow sublittoral zone of southeastern Australia. We observed males and females spawning in the laboratory. They shed gametes through gonopores on the sides of the arms. The eggs were orange, about 1.0 mm in diameter, and heavier than seawater. They were externally fertilized by sperm, and placed into the stomach of the female by the tube feet. Twenty-four hours after fertilization, the first cleavage occurred. Cleavage was equal, total, and radial. Development via a non-feeding lecithotrophic brachiolaria was direct, there being no planktrotrophic bipinnaria or brachiolaria larva. Embryos developed, through wrinkled blastula and gastrula stages, into brachiolariae with arms. All of the surfaces of the brachiolaria were covered by cilia. At metamorphosis, a starfish rudiment appeared on the posterior portion of the larval body, while the anterior portion of the larval body was absorbed. Two months after fertilization, metamorphosis was complete. After metamorphosis, juveniles in the stomach grew six pairs of tube feet in each arm. Juveniles, 3 mm in diameter, emerged from the mouth of the mother in early November. Developmental evidence suggests that this asteroid has evolved mechanisms for the protection of larvae and juveniles from gastric digestion.     

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.     

Development of eggs and larvae of the flounders Rhombosolea tapirina and Ammotretis rostratus (Pisces: Pleuronectidae)

The stages of development of laboratory-reared eggs and larvae of Rhombosolea tapirina and Ammotrelis rostratus are described. They both exhibited á typical pleuronectid pattern of development. At ambient seawater temperature of 11.1–13.8° C R. tapirina eggs hatched 83–93 h after fertilization and larvae metamorphosed c. 65 days later at mean length of 8.83 mm. Hatching of A. rostratus eggs occurred 93–105 h after fertilization and larvae metamorphosed after c. 69 days (mean length 11.21 mm) at 12.7–16.5° C. The two species can be readily separated by their morphology, meristics and pigmentation. In particular, the eggs differ in diameter, only R. tapirina larvae possess a pair of spines in the otic region, and juvenile A. rostratus have only a left pelvic fin.     

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

The pelagic eggs, yolk-sac and pelagic larvae of the macrourid fish, Coryphaenoides marginatus, from Suruga Bay in southern Japan, are described. The identification of the pelagic eggs based on 16S rRNA gene nucleotide sequences agreed with that obtained from morphological analyses. The spherical eggs, 1.14–1.30 mm in diameter, contained a single oil globule 0.30–0.38 mm in diameter, and had hexagonally patterned ornamentation on the chorion, 0.025–0.033 mm in width. Many melanophores were present on the anterodorsal region of the embryo after the caudal end had detached from the yolk. Within a day after hatching, each of the yolk-sac larvae had a body axis that was bent slightly at the anterior trunk region, many dorsal and lateral melanophores on the trunk plus several on the gut, and small irregular wrinkles on the dorsal and anal fin membranes. The pelagic larvae had a short caudal region in comparison to other known congeners (length 2.0–3.2+ times head length vs. 4–7, respectively), a short stalked pectoral fin base, and no elongate first dorsal and pelvic fin rays. They were further characterized by the presence of numerous very dense melanophores from just behind the eye to the anterior part of the caudal region at 5.1 mm head length (25.8+ mm total length). The significant difference in vertical distribution between the pelagic eggs and larvae (dominant depths ca. 200–350 m vs. ca. 10–100 m, respectively), with no subsequent collection of pelagic larvae with greater than 6 mm head length, indicate two stages (rising and falling) of ontogenic vertical migration.