Ecology of a corallivorous gastropod,<Emphasis Type="Italic"> Coralliophila abbreviata</Emphasis>, on two scleractinian hosts. II. Feeding,respiration and growth

Coralliophila abbreviata is a corallivorous gastropod that has been observed to cause large feeding scars on reef-building corals on Floridian and Caribbean reefs. We detected differences in the population structure (length-frequency distribution and sex ratios) of C. abbreviata populations living on two coral host taxa, Acropora palmata and Montastraea spp., in the Florida Keys in a previous study. We hypothesize that diet (host) has a major influence on snail population structure and, thus, we characterize metabolism, feeding and growth for snails residing on these coral taxa. Here, we present results of a reciprocal transplant experiment demonstrating that the taxon of the host influences snail growth rates, as indicated by changes in shell and body tissue weight. Regardless of the host from which they were drawn, snails resident on A. palmata grew faster than those resident on Montastraea spp. Thus, diet influences snail population structure. However, the tissue of Montastraea spp. provides more N and C per area of tissue than that of A. palmata. Respiration rates and tissue composition of snails collected from the two host taxa did not differ. Therefore, snails feeding on Montastraea spp. should have to consume less tissue per day to satisfy their metabolic requirements compared to snails feeding on A. palmata. Feeding rates for snails on A. palmata were measured in the laboratory over 48 h (1–9 cm² coral tissue snail⁻¹ day⁻¹) and estimated from feeding scars observed in the field (weekly mean rate of 1.07 cm² coral tissue snail⁻¹ day⁻¹). The lack of definition of snail feeding scars on Montastraea spp. required the calculation of coral tissue consumption rates based on estimated minimum carbon requirements. Calculated feeding rates for C. abbreviata were 0.13–0.88 cm² coral tissue day⁻¹ snail⁻¹, when feeding on Montastraea spp., and 0.44–3.28 cm² coral tissue day⁻¹ snail⁻¹, when feeding on A. palmata. The calculated range for the latter is consistent with measured rates. Thus, C. abbreviata exhibits high variation in growth parameters in response to environmental variability and/or food source. At mean levels of snail density on reefs off Key Largo, Fla., 20% of A. palmata colonies lose between 1.32 and 9.84 cm² tissue day⁻¹, while 50% of Montastraea spp. colonies lose between 1.04 and 7.04 cm² tissue day⁻¹. Together with published coral tissue regeneration rates, these results suggest that if sustained, such rates of predation could have a serious effect on the viability of these coral populations on Florida's reefs.     

Change in the uptake and cellular Si:N ratio in diatoms responding to the ambient Si:N ratio and growth phase

A change in the Si:N ratio of diatom cells during growth was examined for Chaetoceros socialis and Thalassiosira sp., with different initial silicate to nitrate (Si:N) ratios in the media. During exponential growth, C. socialis assimilated silicate and nitrate with a molar ratio of 0.5, independent of the ratio in the media, but after the depletion of nitrate, silicate continued to be taken up, and the Si:N ratio in the stationary phase increased to 2 as a function of the Si:N ratios in the media. In contrast, the ratio of silicate to nitrate taken up by Thalassiosira sp. increased with an increase in the Si:N ratio in the media. The Si:N ratio in the cells during the stationary phase increased in response to an increase in this ratio in the media. The Si:chl  a ratio also increased with the increase in the initial Si:N ratio in the media, while the N:chl  a ratio did not change to a great extent, indicating the changes in the cellular Si:N ratio was derived from changes in the Si content of the cells. These results indicated that the cellular Si:N ratio changed with the Si:N ratio in the medium, and the Si:N uptake ratio during the growth phase was different depending on diatom species. Thus, the dominance of different diatom species may affect nutrient composition and dynamics in the ocean.     

Temperature and development in larvae of the turbot Scophthalmus maximus

Turbot (Scophthalmus maximus L.) were reared at 12 and 16°C until 26 d after hatching. At both temperatures, starting at the neural plate stage, somites were initially formed every 75 min. Expressed as a percentage of development time (DT, fertilisation to 90% larvae hatching) somite formation occurred relatively earlier during embryogenesis at 12°C (45% DT) than at 16°C (55% DT). At 12°C, after the 32-somite stage the rate of somite formation decreased to one every 300 min. The larvae hatched after 6 d at 12°C and 3 d at 16°C at a relatively primitive stage of development, prior to the opening of the mouth and anus, with unpigmented eyes, and a straight gut. Temperature altered the relative timing of organogenesis in the larval stages. At 12°C, the following characters appeared (in this order): swimbladder>loop in the gut (at the time of yolk exhaustion)>caudal fin. In contrast, at 16°C, the caudal fin appeared at the same time as the loop in the gut. At 16°C, spines formed on the head in the region of the otic capsule at the time the swimbladder formed and the yolk was exhausted, but were absent in 12°C larvae. At both temperatures, in 1 d-old larvae the myotomes just behind the yolk-sac contained 200 inner muscle fibres (presumptive white muscle). The initial growth of inner muscle was largely due to hypertrophy, but by 26 d at 12°C and 11 d at 16°C hyperplastic growth became important, as evidenced by a significant increase in the number of small fibres (<10 m²). By 26 d the average number of inner muscle fibres had increased to 341 at 12°C and 988 at 16°C. New muscle fibres were added in distinct germinal zones at the dorsal and ventral apices of the myotomes. Metamorphosis was associated with a thickening of the superficial (presumptive red) muscle layer and the appearance of tonic muscle fibres.     

Ichthyofaunas of a temperate estuary and adjacent marine embayment. Implications regarding choice of nursery area and influence of environmental changes

A fine-mesh seine net was used at regular intervals to collect fishes from the entrance channel and basin of the Blackwood River Estuary (south-western Australia), from Deadwater Lagoon, which is joined to the entrance channel by a narrow and shallow water-course and thus constitutes part of this estuary, and from Flinders Bay into which the estuary discharges. Sampling was at six-weekly intervals between February and December 1994. The juveniles of some marine species, such as Pelates sexlineatus, Rhabdosargus sarba and Aldrichetta forsteri, were either found only in the estuary or were in far higher densities in the estuary than in Flinders Bay. In contrast, the juveniles of some other marine species, such as Sillago schomburgkii, were relatively abundant in both environments, while others such as S. bassensis, Pelsartia humeralis, Lesueurina platycephala and Spratelloides robustus were either far more abundant in Flinders Bay or entirely restricted to this marine embayment. The various marine species found in inshore waters thus apparently vary considerably in their “preference” for estuaries as nursery areas. Although some marine species were abundant in the shallows of the estuary, the fish fauna of these waters was dominated by the estuarine-spawning species Leptatherina wallacei, Favonigobius lateralis, L. presbyteroides and Atherinosoma elongata. The above regional differences help account␣for the very marked difference that was found between the compositions of the shallow-water␣ichthyofaunas of Flinders Bay and each of the three estuarine regions. The ichthyofaunal compositions of the basin and channel underwent pronounced changes during winter, when freshwater discharge increased markedly and salinities in the estuary thus declined precipitously. This faunal change was mainly attributable to the emigration of marine stragglers, a reduction in the densities of marine estuarine-opportunist species such as Pelates sexlineatus and R. sarba, and the immigration of large numbers of both young 0+ Aldrichetti forsteri from the sea and of L. wallacei from the river. Although most of the above species were also abundant in Deadwater Lagoon, the ichthyofaunal composition of this region did not undergo the same seasonal changes, presumably due to the lack of riverine input and thus the maintenance of relatively high salinities throughout the year. The number of marine straggler species was much lower in Deadwater Lagoon than in the estuary basin, reflecting a far more restricted tidal exchange with the entrance channel. However, the overall density of fishes was far higher in Deadwater Lagoon than in the estuary basin or entrance channel, due mainly to the far higher densities of the estuarine species Atherinosoma elongata and L. wallacei and of the 0+ age class of the marine species R. sarba. The high densities of certain species in Deadwater Lagoon are assumed to be related, at least in part, to the high level of productivity and protection that is provided by the presence of patches of Ruppia megacarpa, an aquatic angiosperm that was not present in the estuary basin or entrance channel. Received: 3 December 1996 / Accepted: 19 December 1996     

Reproductive biology of the red alga Polysiphonia lanosa (Ceramiales) in the Bay of Fundy, Canada

The purpose of this investigation was to establish reproductive phenology of the dioecious marine floridean red alga Polysiphonia lanosa (L.) Tandy. Specifically, the distribution and frequencies of male and female plants, timing of their sexual maturity, fecundity and success of fertilization were investigated. The presence of cystocarps was taken as an indication of syngamy. Populations of P. lanosa in the Bay of Fundy reproduce in spring, summer and autumn. Both male and female filaments were present in equal abundance at all sampling locations, grew in close proximity, and occurred with equal abundance at all elevations above chart datum. During the growing season most of the mature plants contained reproductive organs with apparently functional gametangia containing gametes the structure and behavior of which conformed to those reported in the literature for other species of the genus. Male and female plants of P. lanosa matured synchronously during late May to early July at all collecting sites. The ratio of spermatia to carpogonia calculated for the sampled population was high, 3000–4800 spermatia:1 carpogonium. At the end of the growing season (late October) the fertilization success was at its maximum of 50 to 90% and at its minimum in July at 24%. The three free-living life-history phases (females, males and tetrasporophytes) were abundant and occurred with equal frequency, indicating that a complete life cycle was common at the studied location. Received: 10 December 1996 / Accepted: 16 January 1997     

Do protandric pandalid shrimp have environmental sex determination?

Based on demographic analysis of four different temporally enclosed demes of Pandalus borealis in Gullmarsfjorden on the Swedish west coast and published information, I discuss the notion of environmental sex determination in protandric pandalid shrimps as suggested by sex allocation theory. Demographic results showed that age structure and mortality rates varied substantially between four studied periods without noticeable effects on the age of sex change in the fjord populations. The majority of shrimps changed sex at an approximate age of 3 years and became females at an age of 3 to 4 years, however, low proportions (4 to 7%) of 2nd year females (transitional at ca. 1 year) and 3rd year females (5 to 12%) (transitional at ca. 2 years) were present each year. Low proportions of primary females were also found in two of the temporally enclosed demes, in 1985 (9%) and in 1987 (5%). These results do not indicate that yearly variations in age structure, mortality, or frequency of older breeders in the breeding population affect the age of sex change in temporally enclosed fjord demes of this protandric species. An alternative to assuming that the protandric mode of reproduction in pandalid shrimp is combined with environmental sex determination is suggested. Received: 24 September 1996 / Accepted: 6 November 1996