The corallimorpharian Rhodactis rhodostoma appears to be an opportunistic species capable of rapidly monopolizing patches of unoccupied shallow substrate on tropical reefs. On a fringing coral reef at Eilat, Israel, northern Red Sea, we examined patterns of abundance and clonal replication in R. rhodostoma in order to understand the modes and rates of spread of polyps across the reef flat. Polyps were abundant on the inner reef flat (maximum 1510 polyps m^-2 and 69% cover), rare on the outer reef flat, and completely absent on the outer reef slope at >3 m depth. Individuals cloned throughout the year via 3 distinct modes: longitudinal fission, inverse budding, and marginal budding. Marginal budding is a replicative mode not previously described. Cloning mode varied significantly with polyp size. Approximately 9% of polyps cloned each month, leading to a clonal doubling time of about 1 year. The rate of cloning varied seasonally and depended on day length and seawater temperature, except for a brief reduction in cloning during midsummer when polyps spawned gametes. Polyps of R. rhodostoma appear to have replicated extensively following a catastrophic low-tide disturbance in 1970, and have become an alternate dominant to stony corals on parts of the reef flat.

Polyps of the tropical corallimorpharian Rhodactis rhodostoma segregate sexes between center and edge positions within aggregations produced by clonal replication. On a reef flat at Eilat, northern Red Sea, infertile polyps and males occur mainly along the edges of clonal aggregations, while females mostly occupy central positions within each aggregation. In addition, on the inner to middle reef flat where polyps of this species are abundant, aggregations consist mostly of females. On the outer reef flat, where polyps are rare, a sampled aggregation consisted mostly of males and infertile polyps. Male polyps are significantly smaller than females, and the smallest polyps are infertile. Fecundity increases significantly with polyp size in females, but testis size and number do not vary with body size in males. Oocytes are present in polyps during most of the year and gradually increase in size until annual spawning in June-July during the period of maximum day length. Testes do not vary significantly in size during the year and remain a small proportion of body mass (<8%). In contrast, females invest up to 30% of their body mass into gonads during the months immediately before spawning. The annual spawning of gametes coincides with a temporary drop in the frequency of clonal replication by polyps. We estimate that each female polyp of R. rhodostoma may release up to 3000 large eggs (500 p,m in maximum diameter) each summer. The high investment of this corallimorpharian in sexual production of planktonic propagules may allow rapid dispersal to reef habitats distant from parent populations.

Evidence for classical neurotransmitters in sea anemones remains controversial. We used high performance liquid chromatography with electrochemical detection (HPLC-EC) and electron microscopical imunocytochemistry to determine the presence of serotonin and precursor synthetic enzymes of other biogenic amines in tentacles of the sea anemone Aiptasia pallida. Using HPLC-EC we found dopamine and serotonin (5-hydroxytryptamine, 5-HT) in both tentacles and whole animal homogenates. Antibodies to tyrosine hydroxylase, dopamine β-hydroxylase, phenylethanolamine N-methyltransferase, and 5-HT were used with the peroxidase-antiperoxidase method to reveal positive immunoreactivity to these substances in neurons of tentacles. Immunogold labeling of serial thin sections with the anti-5-HT antibody revealed reactive products in synaptic vesicles at interneuronal, neuromuscular, and neuro-spirocyte synapses. These results suggest that both catecholamine and indolamine neurotransmitters occur in sea anemones in addition to the neuropeptide Antho-RFamide, indicating the presence of multiple types of transmitter substances in an early nervous system.

The effects of temperature on the development of marine invertebrates have been studied primarily in benthic species. For this study, gametes were collected from Nanomia bijuga, a mesopelagic siphonophore, and were self-crossed. Fertilized eggs kept at 8 and 12°C developed more slowly at the lower temperature. Developing stages were preserved after 2, 4, 6, and 9 days of development for comparative analysis with SEM. Concurrent experiments compared survival. Eggs collected from two additional colonies were placed in four temperature treatments: 4, 8, 12, and 18°C. The young developed normally in all treatments, but survived longer at lower temperatures. Young of N. bijuga will develop to siphonulae possessing tentacles, nematocysts, and a functional gastrozooid without being fed. Nonetheless, it is likely that food constraints, rather than temperature, limited survival in this study.

Predation on kamptozoans (phylum Kamptozoa = Entoprocta) is not mentioned in any literature on the phylum. We have found a plagiostomid turbellarian flatworm (Plagiostomum sp.) preying upon Barentsia benedeni in an estuarine sublittoral fouling community in Long Island Sound, USA. Previous records of predation on kamptozoans by nudibranch opisthobranchs (sea slugs) are reviewed. Predation on kamptozoans by some members of two phyla, Mollusca and Platyhelminthes, is thus now known.

A mermithid, a parasite of a spider (Araneae: Thomisidae) in Baltic amber (40 mya), is described as Heydenius araneus n.sp. (Nematoda: Mermithidae) and represents the first fossil record of a nematode parasite of an arachnid. After a critical examination of reports of naturally occurring helminths of extant spiders, I conclude that although mermithid parasitism is well established in this host group, previous reports of hairworm parasites of spiders are “nomina dubia,” putative records, or refer to mermithid nematodes.

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.

Settlement timing and differential settlement for the larval stage of the green sea urchin, Strongylocentrotus droebachiensis, in the southern Gulf of Maine was studied during the summer of 1996. Settlement densities on astroturf panels were highest in June and early July (13 to 37 m^-2 d^-1), and peaked in mid-June (199 m^-2 d^-1). Settlement was low to nonexistent from mid-July through August (0 to 2 m^-2 d^-1). During the peak in settlement, no selection for substrate type was observed. In the remainder of the settlement period, differential settlement occurred, with a preference for substrate covered with live coralline algae. Test diameter of newly settled urchins varied among the substrates, with urchins settling on live coralline algae having the largest test diameter (0.43 ± 0.01 mm). There were no differences in test diameter among the different weeks in which sampling was done. Sustained onshore winds occurred only during peak settlement, suggesting that wind drift currents may concentrate larvae and influence patterns of larval settlement.

Natural growth lines in the ossicles of echinoids have been used to estimate age, calculate growth curves, and infer population age-structure. However, few studies evaluate whether these bands are added annually-a critical assumption of the aging technique. We tested whether the banding pattern is annual in Strongylocentrotus droebachiensis. Sea urchins were tagged with a fluorescent marker, released into tidepools, and collected 1 year later. We quantified the position of the fluorescent mark relative to subsequent growth bands. In 30 individuals ranging in test diameter from 14 to 77 mm, and in a series of ∼2 mm size intervals, we examined 3 interambulacral plates (aboral, ambital, and oral) and a rotula from Aristotle's lantern. Overall, only 7 sea urchins (23%) added a complete band to all 4 ossicles. In 6 sea urchins (20%) at least 1 ossicle added more than 1 complete band. In many sea urchins, especially those >55 mm in diameter, most ossicles added less than 1 band. The banding pattern in ossicles seriously underestimates age in S. droebachiensis and population parameters inferred from these growth lines are biased. Before using the growth-band aging method in other echinoids, it must be demonstrated that 1 band is added annually for all sizes in a population under field conditions.

The fragmentation and rearrangement of the ciliary bands that occurs during the auricularia-to-doliolaria transformation is described for the non-feeding auricularia larva of Holothuria mexicana and the more typical planktotrophic auricularia of Stichopus californicus. The ciliary band of the auricularia larva runs along a series of ridges that project from the sides of the body. Fragmentation results from a loss of ciliary band cells from the zones between the ridges. The remaining fragments then reorient, elongate, and fuse to form the 5 circumferential bands of the doliolaria. The fate of the band cells lost during this process could not be determined with certainty, but they disappear after being sequestered beneath the epithelium for a time, probably through histolysis. Cell counts indicate that significant numbers of cells are also lost from the ridges. Normal swimming ceases just before transformation begins, probably because the nerve supply to all or parts of the band is disrupted, and this may play a role in initiating morphogenesis.

We studied the effects of brackish water on larval attachment, events of metamorphosis, and juvenile mortality in three colonial ascidian species that live in a Florida coastal lagoon. Eudistoma olivaceum and Eudistoma hepaticum are restricted in their adult distribution to areas of relatively high and constant salinity near inlets, whereas Ecteinascidia turbinata extends more than 20 km into the Indian River, where salinity can be much more variable. In all three species, metamorphosis proceeded more quickly at 33 ppt than at lower salinities. The thresholds for successful metamorphosis differed among species in a manner that corresponded to the adult distributions, with E. turbinata being capable of completing metamorphosis at salinities as low as 22 ppt, E. hepaticum as low as 24 ppt, and E. olivaceum as low as 26 ppt. Larvae of both Eudistoma species delayed settlement in very low salinity water, whereas those of E. turbinata settled very quickly, then failed to complete metamorphosis. Juvenile mortality at salinities lower than 22 ppt was 100% for all three species. Survival in salinities higher than 22 ppt was strongly correlated with salinity in E. olivaceum and E. hepaticum, but not E. turbinata.