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The combined effects of temperatures of 14, 17, 20, 22, and 25°C and salinities of 36–12‰ on embryos and larvae of the sand dollar Scaphechinus mirabilis was studied. Embryonic development is the most sensitive stage in the early ontogenesis of S. mirabilis. It is completed at a temperature of 14–20°C in a salinity range of 36–24‰ and at temperature of 22°C to 26‰. The fertilization proceeds in wider ranges of temperature and salinity. Among the swimming larvae, blastulae showed the greatest resistance to variations of these environmental factors. All the larvae survived at a temperature of 14–22°C and a salinity of 36–20‰, and more than 70% of them at 18‰. The pluteus I is the most vulnerable stage; probably this is related to the formation of the larval skeleton and transition to phytoplankton feeding. The survival of larvae at the age of 20 days was 100% at 14–22° C and a salinity of 36–24‰, most of them survived at 14–20°C and a salinity 18‰. The temperature 25 ° C is the most damaging for early development of S. mirabilis. The duration of development of that species lasts 28.5–29 days at 20°C and a salinity of 32.2–32.6‰. At 20 and 22°C, the larvae settled and completed metamorphosis more quickly if sand from the parental habitat was present. The larvae did not settle during the experiment (14 days) at 14 ° C and in the absence of sand.

Under laboratory conditions, the development of larvae of the sand dollar Scaphechinus mirabilis (Agassiz) took 28.5–29 days from fertilization to settling and the end of metamorphosis at a temperature 20°C and salinity 32.2–32.6‰ The cleavage divisions were completed in 12 hours after fertilization (AF) by the release of free swimming ciliary blastula from the egg membrane. The larvae attained pluteus I stage with one pair of arms at an age of 40 hours. In 4.5–5 days the pluteus II stage with three pairs of arms, and in 9 days the pluteus III stage with four pairs of arms were formed. On the 20–21st day AF the larvae developed a vestibule, in which the adult skeleton rudiments, spicules, plates and pedicellariae were formed on the 26–27th day AF. The size of the larvae at an age of 22.5 days was 1064.3 ± 44.7 μm. The settling of larvae was recorded on the 28–29th day of development. Most of the larvae completed their metamorphosis in 4.5–5 hours after settling.

The survival ability of the adult sand dollar Scaphechinus mirabilis (Agassiz) in varying environments was studied. In an experiment on a hard substrate, 88% of the animals survived for 40 days (August–September) during variation of sea water temperature from 21.0 to 16.5°C and variation of salinity from 33.3 to 31.5‰. At 17°C, the salinity tolerance range was 34–24‰. At the same temperature. 100% of the animals remained alive for 14 days within a salinity range from 34 to 18‰; at 16 and 14‰ the ratio of surviving sea urchins was 30 and 20% respectively. Thus, S. mirabilis has considerable adaptive capabilities and is able to survive for a long time under extreme environmental changes.

The larval development of three crabs of the Varunidae family, (Hemigrapsus sanguineus, H. penicillatus, and H. longitarsis), widely spread in Russian waters of the Sea of Japan, were studied under laboratory conditions. At a temperature of 20–22°C and a salinity of 32‰ about 30% of larvae a complete developmental cycle, including five zoeal stages and megalopa, took from 22 to 30 days. All larval stages are illustrated and described in detail. Zoea I and zoea II of the studied crabs are not distinguishable. Zoea III–V of these species differ in the number of dorsomedial setae on the abdominal somite I and in the number of setae on the posterodorsal arch. The megalopae of three Hemigrapsus species possess a different number of segments, aesthetascs and setae on the antennular exopod. In spite of the great similarity of larvae of genera Hemigrapsus and Eriocheir, the latter possesses a number of distinctive features in all developmental stages, supporting the separation of these genera.

The combined effects of temperature (8, 12, 14, 17, 20, 22 and 25°C) and a salinity decrease from 36 to 12‰ on the development of the sea urchin Echinocardium cordatum (Pennant) were studied. Embryonic development proved to be the process most vulnerable to a salinity decrease. It was completed successfully at 8–20°C within a narrow salinity range of 36–28‰ Larvae at the most resistant stage, the blastula, survived at 12–22°C and a salinity of 36–18‰. Larvae at the most sensitive stage, pluteus I with the first pair of arms, died even in a favorable environment, a temperature of 17–20°C and a salinity of 34–28‰. That may be related to qualitative alterations during skeleton formation and to transition to phytoplankton feeding. The resistance of larvae to variations in environmental factors gradually increased in the pluteus II and III stages; however, it significantly decreased before the settling of the larvae. Larvae that were 37 days old survived at a temperature of 14–20°C within a salinity range of 36–22‰ and at 22 and 25°C, they survived at a salinity of 36–24‰; however, all the larvae became abnormal at 25°C. The larvae settled earlier on sand inhabited by adult individuals of E. cordatum than on sand from other locations, and they settled faster at 20–25°C, than at 14 and 17°C. The juveniles, if lacking an opportunity to burrow in the sand, died within 14 days after settling.

The occurrence of the solitary ascidian Ciona savignyi Herdman, 1882 in Vostok Bay (Peter the Great Bay, Sea of Japan) was first documented in 2004. Adult specimens occurred in fouling communities of floating docks in Gaidamak Bay and on different anthropogenic substrates. The introduction of this ascidian into Vostok Bay is attributable to fishing ships which regularly frequent ports of Japan and to favorable environmental conditions (temperature and salinity of seawater).

The effect of various combinations of temperature, which increases from 14°C up to 25°C in the summer season, and salinity, which varies from 34 to 12‰ in the early stages of development of the sea star Asterina (= Patiria) pectinifera (Muller et Troschel) from Vostok Bay, Sea of Japan, was studied. The most vulnerable process in the early ontogenesis of A. pectinifera is its embryonal development, which is completed successfully within narrow ranges of temperature (20–22°C) and salinity (34–26‰). The ability of gametes to fertilize was retained in wider ranges of temperature and salinity. The dipleurula was the most responsive of the larval stages; the resistance of blastula, bipinnaria, and brachiolaria at ages of 12.5 and 15.5 days was almost the same for fluctuations of temperature from 14 up to 25°C and salinity from 34 to 18 and 16‰ Settling of the brachiolaria and completion of metamorphosis were also responsive to variations in the environmental factors. Settling of the larvae was faster at 17°C without illumination (on the 22nd–24th days of development) than at 22°C with the day-night mode (27th–28th day of development). The lack of light apparently had a positive effect on the settling of the brachiolaria.

We studied the effects of different combinations of temperature (5, 10, 14, 17, 20, and 22°C) and salinity (from 32 to 8‰) on the development of the starfish Asterias amurensis Lutken from Vostok Bay, Sea of Japan. Embryonic development is the most vulnerable stage; it passes successfully at 10–17°C and the salinity range of 32 to 26‰. Blastulae are the most tolerant of changing environmental factors. They survive and develop at the temperatures of 5–17°C and in the salinity range of 32–18‰. Gastrulae and bipinnariae survive under higher temperature values and salinity from 32 to 20‰. The tolerance for decreased salinity during the process of fertilization and in the latest stage of development, the brachiolaria with the developing juvenile starfish, was confined to the salinity range of 32–22‰, which agrees with the tolerance of adult starfish Asterias amurensis. Thus, for normal development of the Amur starfish in the early stages, some particular conditions of temperature and salinity are required. This is, probably, due to adaptive capabilities of each developmental stage and the peculiarities of the ecological conditions at particular depths.

The development of the starfish Asterina (= Patiria) pectinifera (Muller et Troschel) from fertilization to metamorphosis took 27–28 days at 22°C and a salinity of 33–33.4‰. The embryonic development was completed by the release of swimming ciliary blastula from egg envelopes 13 h after fertilization. The larvae passed into the stage of gastrula and reached the stage of dipleurula in 35 h and the stage of bipinnaria in 3.5 days. At the stage of brachiolaria, by the 12th day of development, two lateral brachioles and one medioventral brachiole with papillae developed in the larvae. The attachment disk and the primordia of five radial canals of the juvenile starfish became visible by the 15th and 18th days, respectively. By the 24th–25th day, a differentiated primordium of a juvenile starfish had developed in the brachiolaria. The size of the larvae prior to settlement was 1765.4 ± 51.5 µm. Metamorphosis was completed one day after settlement.

Under laboratory conditions the development of the starfish Asterias amurensis Lutken from Vostok Bay (Sea of Japan) was studied at 14 and 17°C. At 14°C and a salinity of 31.6–32.6‰, ciliated coeloblastulae hatched from egg envelopes 19 h after fertilization. At this temperature the development proceeded slowly and stopped at the stage of bipinnaria. At 17°C and normal salinity of seawater, the development of A. amurensis was successful. The swimming blastula appeared in 14 h. It took 30.5 h for the embryos to reach the gastrula stage. The larvae began swimming in a horizontal position with the apical tip ahead. The dipleurula appeared at 60 h. These larvae began feeding. At 71 h after the beginning of development, the early bipinnaria has developed. In the larva, the edged ciliated band, the preoral plate, and the anal plate were already formed. At the age of 4.2 days, the larvae reached the stage of bipinnaria and the brachiolaria stage developed by 26–28 days after fertilization. The larvae had three identical brachiolar arms with attachment papillae on their tips and an attachment disk. In 37–44 days (at 17°C) the pelagic phase of A. amurensis development was completed by the attachment of larvae to the bottom plates and termination of metamorphosis. Most likely, the specificity to a substrate is not expressed in the brachiolaria of A. amurensis. They can settle on almost any hard substrate which is coated with a bacterial film. The newly settled juvenile starfish had five well-developed arms and moved using their ambulacral podia.

The reactions of the starfish Asterias amurensis and Patiria pectinifera that live in Vostok Bay at the salinity of 32–33‰ to a salinity decrease were studied under laboratory conditions. The lower limits of the desalination tolerance range of A. amurensis and P. pectinifera were, respectively, 24 and 20‰. A. amurensis proved to be less resistant to desalination. Under experimental conditions, all specimens of this species survived the salinity of 22‰, while those of P. pectinifera tolerated 18‰. At the same time, A. amurensis responded more actively than P. pectinifera to unfavorable changes in the environment. Turned to their dorsal side and exposed to a salinity of 16 to 32‰, the former reverted to the normal position within a shorter time than the latter. Being a more euryhaline species, P. pectinifera endured a salinity decrease to 6 or 8‰ over, respectively, 21 or 28 h. However, only 30–40% of all specimens could recover locomotory activity 12 or 8.5 h after being placed into water of normal salinity.

The effects of seawater temperature (12, 16, 20, 22, and 25°C) and salinity (of 8 to 34‰) in different combinations on the larvae of the rhizocephalan Peltogaster reticulatus (Crustacea: Cirripedia), a parasite of the hermit crab Pagurus proximus, were examined. The development of P. reticulatus is comprised of five naupliar stages and one cypris stage. Nauplii have a specific structure, the flotation collar encircling the dorsal side of the larval body. Larvae lack the pigmented nauplius eye, and they show no positive phototaxis. Successful naupliar development occurred in temperature and salinity ranges of 16–25°C and 20 to 34‰, respectively; but all nauplii died at 12°C and 16‰. The duration of each naupliar stage increased under lowering of the seawater temperature. At 22–25°C and 26–28‰, the entire development cycle was completed in 72–80 h; and at 16°C and 20‰ it lasted 153 h. The cypris larvae showed a greater resistance to decreased salinity in comparison with the nauplii. At temperatures of 16–25°C and salinities of 14 to 34‰, the lifespan of cyprids was 6 to 12 days, and it decreased at increasing temperature.

Summary Responses of larvae of two rhizocephalan species to changes in seawater temperature and salinity were studied under laboratory conditions. Peltogasterella gracilis parasitizes the hermit crab Pagurus pectinatus, which occurs at stable salinity and gradually changing temperature in summer. Sacculina polygenea is a parasite of the crab Hemigrapsus sanguineus, which lives in the intertidal zone in summer where salinity and temperature can fluctuate during the day. The development of both species is comprised of five naupliar stages and the cyprid stage, and it was considered successful if more than 50% of the nauplii attained the cyprid stage. P. gracilis nauplii successfully developed at 12–20°C and 30–34‰, but at 22°C successful development occurred in a narrower salinity range (32–34‰). All nauplii died both at 25°C and in 26‰. S. polygenea nauplii successfully reached the cyprid stage at higher temperatures (18–25°C) and a wider salinity range (18–34‰) than P. gracilis nauplii, but at 12°C and 16...

The vertical distribution of larvae of the sea urchin Strongylocentrotus intermedius in conditions of superficial desalination was studied under laboratory conditions. In the earlier stages of development, the larvae accumulated in the water column zone with a salinity below the optimal level. The long-term observations of the larval accumulations revealed the deceleration of, and abnormalities in, the development and death of the larvae. The larvae at the pre-settling stages changed their behavior: when they reached layers of a salinity unfavorable for their survival or development, the larvae did not enter them and instead moved down instead. Obviously, S. intermedius larvae are only capable of actively choosing their position within the water column with the salinity gradient at the later stages of development.

The responses of the larvae of the cirripede barnacle Peltogasterella gracilis (Crustacea: Cirripedia: Rhizocephala) that parasitizes the hermit crab Pagurus pectinatus to different combinations of seawater temperature (25, 22, 20, 16, and 12°C) and salinity (from 34 to 8‰) were studied in a laboratory. The nauplii of P. gracilis completed the entire cycle of development at 22 to 12°C in a narrow range of salinity (from 34 to 28‰), which agrees well with the environmental conditions of the crab hosts' habitat. At favorable temperatures (22–20°C) and salinity (34–28‰), the nauplii reached the cypris stage in 88 ± 2 h, while at 12°C and 34–30‰, the naupliar development took 156 ± 5 h. The cypris larvae appeared more resistant compared with the nauplii, in terms of changes in both the temperature and salinity of seawater. They actively swam at all experimental temperatures and in the salinity range of 34–18‰. At temperatures (22–16°C) and salinities (34–24‰) favorable for the cyprids, their longevity in plankton equaled 6–10 days. Thus, the nauplii of P. gracilis is the more vulnerable stage of development in the life cycle of this parasitic barnacle. The tolerance against changes in environmental factors is due to the adaptive capabilities of parasitic larvae and the environmental conditions in the habitats of its host, a typical marine crustacean. The insignificant parasitization rate of the hermit crab by its rhizocephalan parasite may be explained by the death of the nauplii of P. gracilis, which occurs when they enter to the surface water layer.

Our studies show that seawater from different sites in Nakhodka Bay has a deleterious effect on the development of the sea urchinStrongylocentrotus intermedius. As development proceeded to the pluteus I stage, the percentage of abnormal larvae maintained in water from Nakhodka, Novitskogo, and Vrangelya Bights increased markedly (66.7±2.2, 67.1±2.6, and 54.6±1.8%, respectively). These larvae developed more slowly, were smaller, and differed from those in the control in the intensity of color of their echinochrome granules. In water from Nakhodka and Novitskogo bights, larval survival rates were lower than in the control. This suggests that the water of Nakhodka Bay is heavily polluted, especially in its harbor areas.

Larval development of the rhizocephalanSacculina polygenea (Crustacea: Cirripedia: Rhizocephala) parasitizing the coastal crabHemigrapsus sanguineus was studied in Vostok Bay, the Sea of Japan. At 22–23°C, the entire cycle of larval development takes 2.5 days and includes five naupliar stages and one cypris stage. Like other rhizocephalans, the larvae ofS. polygenea are lecithotrophic and only grow slightly in size in the course of development, and like all sacculinids, they have no flotation collar. The naupliar stages IV and V have a tubercle between the furcal rami; this tubercle is absent in the larvae of the genusPeltogasterella, but it has been described inS. carcini. The first seta of the antennule only disappears completely at the fourth stage, although it is markedly reduced at the third stage. No morphological differences, except differences in size, are found between male and female nauplii.

Temperature (25, 22, 16, and 12°C) and salinity (32–14‰) effects on the development of the low-boreal holothurianEupentacta fraudatrix were investigated. By studying the desalination resistance of adult holothurians,E. fraudatrix was shown to be a stenohaline species. The lower salinity limit at which both the larvae and adults survived was 22‰. Fertilization and development to the stage of free-swimming blastula occurred at the bottom. Embryogenesis, a critical stage of development, was successfully completed at a salinity of 32–26‰ and temperature of 22–16°C. The fertilization and development of a free-swimming blastula proved to be most resistant to temperature changes. The blastulae that developed at lowered temperatures (16–12°C) were capable of further development and settling at the same temperatures, which is likely associated with the peculiarities of the species range. If the early development proceeded at a higher temperature (22°C), the larvae failed to adapt to and perished from sharp temperature decreases at later stages of development. Thus, the lecithotrophic larva and a short period of larval development in the pelagial larvae (3–3.5 days from fertilization to settlement) ofE. fraudatrix are caused by the stenohalinity and environmental conditions of the species and, in turn, contribute to the fact that the young animals settle in the vicinity of their parents.

Apostichopus (= Stichopus) japonicus blastulae and gastrulae were acclimated for 18 h to salinities of 32‰ (control), 24 and 22‰ (the lower limit of the range of tolerance), and 20‰ (below the range of tolerance). Acclimation to 20‰ resulted in the appearance of teratic larvae, most of which subsequently died. Acclimation to 24, 22, and 20‰ led to a shift in the range of tolerance of the larvae at further stages of development. With a decrease in salinity, acclimated larvae developed more successfully than unacclimated larvae. Acclimated larvae attained the pentactula stage and settled at a salinity range of 32–20‰; unacclimated larvae, at 32–22‰. At different stages of development, acclimated larvae survived greater decreases in salinity than unacclimated larvae. The acclimation effects could be traced up to metamorphosis and settling, i.e., two weeks after the end of the acclimation process.

The ability to survive under extreme environmental conditions was studied in the adults of the heart sea urchin Echinocardium cordatum (Pennant). At seawater temperatures of 13.3 to 14.8°C and salinity of 33.2–33.4‰, being devoid of the possibility to burrow into the sand or eat, some sea urchins died on day 5 and all individuals had perished by the end of day 8. At a temperature of 19°C, the salinity tolerance range of adults was limited to 33–28‰. Only 30 to 20% of sea urchins transferred to a solid substrate survived for 7 days at a salinity of 33 to 24‰, but all of them perished toward the end of day 8.

Summary The hyaline spheres (HS) in auricularia of Stichopus japonicus consist of extracellular material in which solitary cells are present. This extracellular material can be stained by dyes for lipids. There are no membranes or other structural elements in HS. The cells within HS are most probably responsible for secreting the extracellular material. HS are not embryonic inductors of the ciliary rings which appear during metamorphosis. They probably store nutrients which permit larvae to complete metamorphosis successfully, but this remains to be established.