Skeletal growth zones as age-markers in the sea urchinPsammechinus miliaris

Growth of the inshore sea urchinPsammechinus miliaris (Gmelin) was studied in Loch Creran, western Scotland, using the skeletal growth-marker tetracycline in order to test the validity of natural growth-banding in the coronal test plates as annual age-markers. In order to test whether tetracycline affected the growth ofP. miliaris, an injected and a control group of urchins were held in identical conditions in running sea water aquaria for 21 mo from 1989 to 1991 and measured periodically. A small but significant difference in mean size of injected compared to controls was recorded at 12 mo, but none during subsequent measurements. Size measurements during the trial were consistent with an annual growth cycle, with a maximum in spring and slowing or cessation of growth during autumn/winter. Tetracycline-labelled juveniles were recovered up to 18 mo after initial tagging in mark/recapture experiments undertaken from 1987 to 1989 at two intertidal marked quadrats in Loch Creran. Large numbers ofP. miliaris were also marked with tetracycline and held for 1 yr at 10 m depth in seabed cages in Loch Creran during 1988–1990. All of the intertidal recoveries, and about 69% of the caged specimens that had been successfully labelled, showed a consistent relationship between the position of the tetracycline tag and the pattern of natural growth zones. The remainder were mostly large, slow-growing urchins with the tag positioned near the plate margin. In these the outer growth bands were closely spaced and, particularly if major growth bands seemed to be broken up into double or multiple lines, the major bands were impossible to resolve at the margin. The results support the assumption that in wild populations the dark bands visible with reflected light (translucent in transmitted light) after charring the plate are formed when skeletal growth has stopped or slowed in winter. These lie between wider, lighter coloured (opaque in transmitted light) zones of active plate growth in spring/summer. The dark band formed beyond the tag usually was made up of several closely spaced fine lines, or sometimes of two closely spaced dark bands. The wide growth zones beyond the tag, like those formed previously, usually were broken by fine, dark lines that may represent brief discontinuities in growth. From tagging, the double dark bands can be related to growth over one year; but such anomalous bands, along with the general presence of fine, dark lines interrupting the growth zones, make it difficult reliably to estimate age from the closely spaced peripheral banding on older, slow-growing urchins.     

Growth pattern of the sea urchin, Loxechinus albus (Molina, 1782) in southern Chile: evaluation of growth models

The growth pattern of Loxechinus albus in southern Chile was studied using size-at-age data obtained by reading growth bands on the genital plates. The scatter plots of sizes-at-age for samples collected in three different locations indicated that growth is linear between ages 2 and 10. Five different growth models, including linear, asymptotic and non-asymptotic functions, were fitted to the data, and model selection was conducted based on the Akaike information criteria (AIC) and the Bayesian information criteria (BIC). The AIC identified the Tanaka model as the most suitable for two of the three sites. However, the BIC led to the selection of the linear model for all zones. Our results show that the growth pattern of L. albus is different from the predominantly asymptotic pattern that has been reported for other sea urchin species.     

Growth and mortality of subtidal red sea urchins (Strongylocentrotus franciscanus) at San Nicolas Island,California, USA: problems with models

Red sea urchins, Strongylocentrotus franciscanus, were tagged with tetracycline in 1990 at subtidal sites off San Nicolas Island, California, USA. After one year in the field, the sea urchins were collected and growth increments were measured based on tetracycline marks, which indicated initial slow growth, a maximum rate, and finally a prolonged period of very slow growth. Small red sea urchins (4 cm diam) were estimated to be 3 to 4 yr old, which is much older than has previously been reported. It is estimated that about 12 yr would be required to attain 10 cm diam. Survival has previously been modeled assuming a constant rate. If the population of red sea urchins is assumed to be stable and stationary, annual survival rate was between 71 and 77% yr^-1. Census data for the two years of study have permitted annual survival to be estimated without assuming stable and stationary population structure. Under these conditions, annual survival rate was between 79 and 86% yr^-1. Analysis of transitions in the size distributions from 1990 to 1991 suggested that annual survival may have been sizespecific: 91% yr^-1 for individuals 1.1 to 4.0 cm diam, 82% yr^-1 for individuals 4.1 to 7.0 cm diam, and 63% yr^-1 for those of 7.1 to 10.0 cm diam. An alternative explanation to size-specific survival in our study is sizespecific immigration.     

Resource allocation and growth rates in the sea urchin Evechinus chloroticus (Echinoidea: Echinometridae)

The morphometry of the sea urchin Evechinus chloroticus from habitats of contrasting algal abundance but of similar urchin density was examined at two localities in southern New Zealand during 1993. Populations from habitats of high algal abundance (Dusky Sound) had similar relationships of demipyramid (jaws) to test diameter, but individuals had significantly smaller jaws relative to their test diameter than those from a locality where algal abundance was low (Arapawa Island). The body wall mass (in relation to total wet weight) was similar for populations from both localities but, for Dusky Sound populations, individuals from exposed sites had greater relative body mass than those from sheltered sites. The ratios of gonad weight:total weight were similar between localities. However, E. chloroticus from Arapawa Island reached reproductive maturity at a smaller size than those from Dusky Sound. Growth rates of E. chloroticus varied among localities in Dusky Sound. Growth was modelled by the Tanaka function, which allows for rapid early growth until reproductive maturity is reached and declining growth rates thereafter. The results show that sea urchins respond to low resource availability by increasing the size of the food-gathering apparatus, maturing at a smaller size, and growing to a smaller size than individuals from food-rich habitats. Received: 3 December 1996 / Accepted: 29 January 1997     

Growth and reproduction of Loxechinus albus (Echinodermata: Echinoidea) at the southerly peripheries of their species range, Falkland Islands (South Atlantic)

Sea urchins Loxechinus albus were collected from an unfished population inhabiting inshore areas of the eastern part of the Falkland Islands (Southwest Atlantic) at bimonthly intervals between January 2005 and March 2006. The gonads of 491 specimens were sampled to ascertain GSI, and a subsample was examined microscopically in order to determine sex and maturity stage. Age was determined by ring counts on genital plates of 349 specimens with the annual periodicity of ring deposition validated by marginal increment analysis. This investigation suggests that the study population spawns at the warmest time of the year thus allowing for greater growth in their pelagic larvae and newly settled juveniles. Size at age data were found to be asymptotic and out of three growth functions tested the von Beralanffy growth model best described the data. The relatively short period of optimal water temperatures around the Falkland Islands does not enable L. albus to grow as fast as in other regions with higher seasonal temperatures (central Chilean coasts) resulting in relatively small adult sizes.     

Age studies based on daily growth increments in statoliths and growth lamellae in cuttlebone of cultured Sepia officinalis

One hundred and six individuals of Sepia officinalis were cultured throughout its life cycle in two different temperature regimes: 13-15°C and 18-20°C. The number of increments in the statoliths and the number of lamellae in the cuttlebone were read at known ages in different individuals. The formation of growth increments in the statoliths was linearly related with individual age, but it was independent of temperature. By comparison between the slope of these linear relationships and the bisecting line, the hypothesis "1 increment=1 day" was validated in individuals as old as 240 days. In specimens older than 240 days, the number of increments was underestimated due to the poor resolution of the later growth increments. The maximum number of days in captivity (420) was about 80% of the life span estimated for this species in the area studied. Preliminary validation was also obtained from statoliths marked with tetracycline. Increments between tetracycline marks were not visible. The mean distance between marks in ten statoliths was 44 µm (Lj). Considering the same distance in statoliths of wild individuals, the mean number of increments counted was 37 (Lj). This result is very close to the 40 days passed between both tetracycline marks. A straight line significantly different for each culture temperature defined the relationship between number of the cuttlebone lamellae and age. The number of lamellae in the cuttlebone does not correspond to the real age. The time necessary for the formation of one lamella was 8DŽ.3 days at 13-15°C, whereas the deposition of one lamella lasted 3.1ǃ.06 days at 18-20°C. In conclusion, the periodicity for lamellar deposition can be defined only if the temperature where the animal lived is considered.     

Moderate stoichiometric homeostasis in the sea urchin Lytechinus variegatus: effects of diet and growth on C:N:P ratios

The influence of dietary elemental contents on consumer stoichiometry was investigated in selected and combined soft tissues (as a proxy of the whole individual) of the omnivorous sea urchin, Lytechinus variegatus. We raised urchins for 4 months in controlled seawater tanks using three different diets with different nutritional contents (from lower to higher: seagrass, red macroalgae, and a formulated diet). Individuals fed the different diets varied an average of 19.7, 19.4, and 38 % in C:N, C:P, and N:P ratios, respectively, with stronger temporal variability for C:P and N:P ratios across tissues and whole individuals. This resulted in homeostasis parameters (1/H) of ?0.45, 0.09, and 0.38, respectively, for C:N, C:P, and N:P, indicative of homeostatic to weakly homeostatic organisms, at least for C:P and N:P ratios. Individuals fed the nutrient-rich formulated diet had higher growth rates (14 ± 0.83 g WW month^?1) than those fed macroalgae or seagrass (9.3 ± 0.57 and 3.4 ± 0.33 g WW month^?1, respectively). However, rapid body increments in more nutritional diets caused both a decrease in the %N and an increase in the %P of soft tissues, which resulted in significant but opposite effects of diet stoichiometry and growth in sea urchin C:N (R = ?0.74 and R = 0.93, for diet and growth effects, respectively) and N:P ratios (R = 0.60 and R = ?0.63, also, respectively, for diet and growth effects). Among potential compensatory mechanisms helping to preserve certain levels of homeostasis, ingestion rates (g WW diet per g WW of urchin) were higher for seagrass and macroalgae diets than for the nutrient-rich formulated diet. In contrast, absorption and growth efficiencies displayed significant negative associations with nutrient contents in diets and did not exhibit nutritional compensation. Overall, our results suggest that resource stoichiometry strongly determines the growth rate of individuals (R = 0.88, P < 0.01), and moderate variability in C:N:P ratios of sea urchins possibly arise from differences in the allocation of proteins and RNA to body components, similarly to what has been proposed by the growth rate hypothesis.     

Growth of the deep-sea irregular sea urchins Echinosigra phiale and Hemiaster expergitus in the Rockall Trough (N.E. Atlantic Ocean)

Growth in the deep-sea irregular sea urchins Echinosigra phiale (family Pourtalesiidae) and Hemiaster expergitus (family Hemiasteridae) was studied from deep-sea samples taken during the years 1973 to 1985 from two stations at 2900 and 2200 m depth in the Rockall Trough (N.E. Atlantic Ocean). Growth zones, similar to those described from sea urchins in shallow water, are present as a series of wide white bands separated by narrow, dark rings in the calcite stereom of the test plates after heating to 350°C. In shallow water, such growth zones seem to result from seasonally varying growth rates. In the supposedly constant conditions in the deep sea, a seasonal growth pattern is unexpected but may occur in response to recently discovered annual pulses in downward flux of detritus from the euphotic zone, providing a seasonally varying food supply for such deposit-feeding species living in the bottom sediment. On this assumption, growth curves were fitted to counts of growth zones (as representing age in years), in the larger lateral and ventral test plates of E. phiale and H. expergitus. The opportunity was also taken to fit growth curves derived from counts of growth zones in samples of the inshore spatangoids Spatangus purpureus and Echinocardium pennatifidum. Plots of counts against test length of Echinosigra phiale and H. expergitus, although scattered and not clearly asymptotic, indicate, growth to be slower than in the two inshore spatangoids, and than in the coastal species Echinocardium cordatum, for which there are good recent growth data, available.     

Effects of seasonality on the reproductive cycle of <Emphasis Type="Italic">Diadema</Emphasis> aff. <Emphasis Type="Italic">antillarum</Emphasis> in two contrasting habitats: implications for the establishment of a sea urchin fishery

Reproduction of Diadema aff. antillarum was examined between 2002 and 2005 at subtidal rocky bottoms around the Canary Islands. Two contrasting habitats (urchin barrens and grazing fronts) characterized by different levels of food availability were chosen, and factors thought to influence reproductive periodicity were monitored, including temperature, photoperiod, phytoplankton abundance and benthic food availability. Histological analyses showed that D. aff. antillarum had an annual reproductive cycle that was relatively synchronous across the studied sites and habitats. Photoperiod was the most significant factor that correlated with gonad periodicity; benthic food availability of 2 month lag was also correlated. However, some differences were detected between males and females in the timing of the onset of gametogenesis. Spawning was synchronized between both sexes from June to August. Results suggest that the optimum time of year to harvest urchin gonads would be between May and June when gonads were maximal in size but not full of gametes. This species may not provide optimal conditions for an industrial scale fishery, as sea urchins occurring in high density had small gonads and those producing larger volume or more marketable gonad tissue occurred in low densities where harvesting costs would exceed profit.     

Temporal and spatial variability in settlement of the sea urchin<Emphasis Type="Italic"> Paracentrotus lividus</Emphasis> in the NW Mediterranean

Settlement into the benthic habitat may be an important process in regulating sea urchin abundance, which potentially modifies the structure of benthic communities. Strong settlement events may increase sea urchin abundance beyond a certain threshold, leading to the formation of coralline barrens (overgrazed communities with a dominance of encrusting coralline algae). To understand the role of settlement in regulating sea urchin populations we first need to determine settlement variability. Temporal variation in settlement of the sea urchin Paracentrotus lividus was monitored at three sites in the Medes Islands, NW Mediterranean, during three settlement seasons (March 1998 through October 2000). Spatial variation in settlement was studied in 1999 at 50 sites along a gradient of exposures to waves and currents, inside and outside the archipelago, and separated by distances from tens to thousands of meters. Bathymetric distribution of settlement was also studied in 2000 at six sites at 5, 10, 15 and 20 m depths. Settlement of P. lividus occurred in a single annual peak within 3 weeks in May–June. Differences in settlement between years were more than two orders of magnitude. Spatial variability was found at all scales investigated, showing strong patchiness at the smallest spatial scales (tens of meters). Sea urchins settled preferentially at depths between 5 and 10 m. Substratum type, level of protection, and adult population densities were not significant in determining settlement. However, settlement was found to be related to the degree of exposure to waves and currents, indicating that physical processes are very important at the spatial scales investigated. This greatly variable settlement is a necessary, although not sufficient, condition to create gradients of adult P. lividus abundance. Further studies should be designed to investigate the interaction between settlement strength and post-settlement mortality.Communicated by O. Kinne, Oldendorf/Luhe     

Allocation of45calcium to body components of starved and fed purple sea urchins (Strongylocentrotus purpuratus)

Several lines of evidence in the literature indicate that environmental stress such as starvation may initiate reallocation of sea urchin endoskeletal tissue. For example, Aristotle's lantern enlarges under conditions of starvation, and sea urchins tagged with tetracycline and then fed develop a distinct growth line, while starved individuals develop a diffuse pattern. We designed anin vivo system to examine stress-related changes in calcification in the purple sea urchinStrongylocentrotus purpuratus. SmallS. purpuratus (ca. 2 cm test diam) were collected from the Mission Bay jetty or Imperial Beach (San Diego, California, USA) in 1987.⁴⁵Ca was incorporated from seawater into all body fractions including the organic tissue/coelomic fluid. In an initial experiment, sea urchins were fed or starved for 4 wk and then post-incubated in isotope. Overall, starved individuals deposited new calcite more slowly than did fed individuals; however, allocation was very different and calcification of teeth of starved sea urchins was nearly as great as in fed individuals. In a second experiment,S. purpuratus were first pre-labeled with isotope and then treated by feeding or starving. More of the labeled calcium was mobilized from the soft tissues and coelomic fluid into calcite in fed than in starved individuals. Growth of the teeth in starved sea urchins was significantly greater than in those fed. We conclude that starvation changes the metabolism of calcium in order to preferentially build teeth. However, we also found no evidence that calcium was resorbed from old skeletal calcite in order to build new skeleton.     

Effects of temperature and food ration on gonad growth and oogenesis of the green sea urchin, Strongylocentrotus droebachiensis

To assess the effects of both temperature and food ration on gonad growth and oogenesis of the green sea urchin, Strongylocentrotus droebachiensis (O.F. Müller), individuals collected December 1996 (winter experiment) and June 1997 (summer experiment) were maintained for 3 months in one of four experimental treatments: (1) 3 °C and fed ad libitum (high ration), (2) 3 °C and fed one-seventh of the maximum ration (low ration), and (3) 12 °C and fed the high ration; (4) 12 °C and fed the low ration. All individuals were fed an artificial diet and exposed to only 1 h of light every day. At the end of both experiments, mean gonad indices of sea urchins fed the high ration had increased significantly (11–24% and 6–19% in the winter and summer experiments, respectively), while the gonad indices of individuals fed the low ration did not change. At the high ration (both experiments), the increase in gonad index of sea urchins occurred primarily as the result of a significant increase in the mass of nutritive phagocytes, as revealed by histological analyses. Primary oocytes were significantly larger in individuals held at 3 °C than at 12 °C throughout the winter experiment, regardless of food ration; during the summer experiment, primary oocytes were significantly larger in individuals receiving the high ration, regardless of the temperature at which they were held. These results suggest that: (1) food availability is the most important factor regulating energy storage and the relative size of gonads throughout the year, (2) temperature affects the rate of growth and maturation of primary oocytes during the later stages of oogenesis, and (3) once gametogenesis has been initiated, mature ova will be produced, even under conditions of low food availability. Conditions of high food availability in summer and low temperature in winter would thus favor reproductive output in sea urchin populations. Received: 1 March 2000 / Accepted: 4 October 2000     

Growth and recruitment of the deep-sea urchin Echinus affinis

Large samples of the sea urchin Echinus affinis Mortensen were obtained from a time-series of Agassiz trawlings from a 2 200 m-deep permanent station (Station M), and at neighbouring positions, in the Rockall Trough (North-east Atlantic Ocean) over a period of 7 yr (1978 to 1985). Counts of growth zones visible in the skeletal elements of the test were used to age individuals. Various growth functions were fitted to counts from a full range of the sizes available. Functions giving a sigmoidal growth curve fit the early phase of growth better than the von Bertalanffy model, although the latter provided better fit amongst larger sizes. The fit of a robust and flexible model recently developed by Preece and Baines to describe the human growth curve overcame this limitation. Skeletal banding is thought to result from seasonally varying growth as a result of annually pulsed fallout of phyto-detrital food to the deep-sea floor. Early stages were found in only a few of a time series of samples obtained with a fine-meshed epibenthic sledge, suggesting that recruitment to the population from its annual breeding may only occasionally be successful. Postlarval growth was estimated from samples taken soon after presumed settlement and later in the year. The fitted growth curve showed good agreement to that obtained from annual banding, and corroborates an initially exponentially increasing growth rate. Postlarval survivorship was estimated, by means of computer simulation, from a sample that included postlarvae along with a range in juvenile size, to be about 10% amongst postlarvae after settlement and thereafter about 90% yr^-1. Adults are inferred to be up to about 28 yr old. A markedly uneven representation of ages in a large subsample of aged adults of even frequency in size is interpreted by means of simulations as probably reflecting multi-year cycles in recruitment success. The possible causes of a varying size structure amongst large samples of adults, which showed some spatial segregation in relation to the track of the trawl on the bottom at Station M, are discussed.     

Growth and production of<Emphasis Type="Italic"> Ophiocten gracilis</Emphasis> (Ophiuroidea: Echinodermata) on the Scottish continental slope

Growth and production of the bathyal ophiurid brittle star Ophiocten gracilis was studied from skeletal growth bands and disc size frequencies of specimens collected in sled and trawl samples taken on the continental slope off Scotland. Growth bands showed up in SEM examination as ring-like zones in surface relief and texture of the stereom microstructure of the intervertebral muscle insertions on the arm ossicles. Seasonal variability in somatic growth, presumed to underlie this growth pattern, may reflect reproduction and/or a possible non-feeding period during gonad maturation. Disc size-at-age was back-calculated from size-at-age interpreted from growth-band series on the vertebral ossicles from arms of O. gracilis. Pooled growth-band frequency data and normal-distribution mixtures based on size-at-age data were used to test for overgrowth of early growth bands on the ossicles from larger individuals. Von Bertalanffy and Gompertz growth models were fitted to the finalised back-calculated disc size-at-age data. These were used along with the modal structure of the observed disc size frequencies to develop a demographic model based on normal-distribution mixtures constrained by the growth model. These and other defining parameters were fitted by non-linear regression to size structure observed in a sample of the breeding population from 997 m depth on the Hebrides Terrace. Recruitment was estimated according to available data from sediment-trap time series. A ratio of somatic production/biomass, P_S/B, in the range of 0.43–0.54 was estimated using a fitted size/mass relationship and the increment summation method (ISM) applied to the fitted growth models. A narrower, but otherwise similar, range in estimated P_S/B ratios (0.48–0.49) was obtained in a parallel approach using the mass-specific growth rate method (MSGRM), whereby the same size/mass relationship was applied to the observed frequencies and growth parameters fitted to growth banding. Using previously obtained data on population density, a standing crop of 4.8 g wet weight (~0.58 mg AFDW) m^?2 would provide annual wet weight production in the range of 1.9–2.4 g (~0.23–0.29 mg AFDW) m^?2 in the population between ca. 700–1000 m depth. Somewhat greater production estimates (P_S/B=0.73–0.98) were obtained from MSGRM by pooling the sample with size frequencies from other large samples in which postlarval sizes were more numerous, but larger sizes less numerous. Similarly high production was estimated by MSGRM from a box corer sample from the Wyville-Thomson Ridge. Explanations for variability in size structure are discussed, but even the lower estimates are comparable to boreal shallow-water brittle stars. The high rate of growth and production by accepted deep-sea standards may be related to a capability for interface feeding.     

Feeding aggregations of sea stars (<Emphasis Type="Italic">Asterias</Emphasis> spp. and <Emphasis Type="Italic">Henricia sanguinolenta</Emphasis>) associated with sea urchin (<Emphasis Type="Italic">Strongylocentrotus droebachiensis</Emphasis>) grazing fronts in Nova Scotia

Migrating feeding aggregations (or fronts) of sea urchins can dramatically alter subtidal seascapes by destructively grazing macrophytes. While direct effects of urchin fronts on macrophytes (particularly kelps) are well documented, indirect effects on associated fauna are largely unknown. Secondary aggregations of predators and scavengers form around fronts of Strongylocentrotus droebachiensis in Nova Scotia. We recorded mean densities of the sea stars Asterias spp. (mainly A. rubens) and Henricia sanguinolenta of up to 11.6 and 1.7 individuals 0.25 m⁻² along an urchin front over 1 year. For Asterias, mean density at the front was 7 and 15 times greater than in the kelp bed and adjacent barrens, respectively. There was strong concordance between locations of peak density of urchins and sea stars (Asterias r = 0.98; H. sanguinolenta r = 0.97) along transects across the kelp–barrens interface, indicating that sea star aggregations migrated along with the urchin front at rates of up to 2.5 m per month. Size–frequency distributions suggest that Asterias at the front were drawn from both the barrens (smaller individuals) and the kelp bed (larger individuals). These sea stars fed intensively on mussels on kelp holdfasts and in adjacent patches. Urchin grazing may precipitate aggregations of sea stars and other predators or scavengers by incidentally consuming or damaging mussels and other small invertebrates, and thereby releasing a strong odor cue. Consumption of protective holdfasts and turf algae by urchins could facilitate feeding by these consumers, which may obtain a substantial energy subsidy during destructive grazing events.     

Tiger shark (Galeocerdo cuvier) abundance and growth in a subtropical embayment: evidence from 7 years of standardized fishing effort

The tiger shark (Galeocerdo cuvier Peron and Lesueur 1822) is a widely distributed predator with a broad diet and the potential to affect marine community structure, yet information on local patterns of abundance for this species is lacking. Tiger shark catch data were gathered over 7 years of tag and release research fishing (1991–2000, 2002–2004) in Shark Bay, Western Australia (25°45′S, 113°44′E). Sharks were caught using drumlines deployed in six permanent zones (~3 km² in area). Fishing effort was standardized across days and months, and catch rates on hooks were expressed as the number of sharks caught h⁻¹. A total of 449 individual tiger sharks was captured; 29 were recaptured. Tiger shark catch rate showed seasonal periodicity, being higher during the warm season (Sep–May) than during the cold season (Jun–Aug), and was marked by inter-annual variability. The most striking feature of the catch data was a consistent pattern of slow, continuous variation within each year from a peak during the height of the warm season (February) to a trough in the cold season (July). Annual growth rates of recaptured individuals were generally consistent with estimates from other regions, but exceeded those for populations elsewhere for sharks >275 cm fork length (FL), perhaps because mature sharks in the study area rely heavily on large prey. The data suggest that (1) the threat of predation faced by animals consumed by tiger sharks fluctuates dramatically within and between years, and (2) efforts to monitor large shark abundance should be extensive enough to detect inter-annual variation and sufficiently intensive to account for intra-annual trends.     

Validation of daily increment deposition in otoliths. Age and growth determination of Aphia minuta (Pisces: Gobiidae) from the northwest Mediterranean

The transparent goby Aphia minuta (Risso, 1810) is one of the main target species of the small-scale fishery off the Island of Majorca. Otolith microstructure and length-frequency analysis were used to study the age and growth of this species during the 1982/1983 and 1992/1993 fishing seasons. Daily periodicity of increment formation was determined by experiments with marked otoliths in individuals maintained in captivity. The length range of the catches during the 11 yr period was between 12 and 49 mm, with a main distribution (89%) between 24 and 40 mm. Otolith age-readings indicate that the population exploited in the commercial fishery consists of seven age-groups (2 to 8 mo old), with a very high proportion of individuals (95%) between 3 and 6 mo old. Population growth-curves revealed no differences between males and females. The growth parameters for the whole population are: asymptotic length, L _∞ = 53.69 mm; growth coefficient, K = 2.23 yr⁻¹; theoretical age at length zero, t ₀ = −0.005 yr. Those individuals of A. minuta caught in Majorca during the winter period reached a maximum age of 7 or 8 mo. Received: 30 December 1996 / Accepted: 16 April 1997     

Effects of seasonality and population density on the reproduction of the Indo-Pacific echinoid<Emphasis Type="Italic"> Echinometra mathaei</Emphasis> in Kenyan coral reef lagoons

Reproduction in the widely distributed tropical sea urchin Echinometra mathaei (de Blainville) was examined in three Kenyan reef lagoons that differed in substrate cover and E. mathaei population density. Histological examination of the gonads and gonad index measurements for 3 years showed a seasonal reproductive cycle with gametogenesis commencing in July, when temperature and light are at their lowest, and spawning commencing in December and peaking in February to May, when temperature and light reach their annual maxima. Monthly gonad indices correlated significantly with seawater temperature and light intensity. Male urchins had mature gametes for a longer period (8 months) than females (6 months), possibly an adaptive strategy that increases the probability of fertilization. Lunar periodicity was not observed, as male and female gonads were full of gametes on all days of the lunar cycle during the period of spawning. The peak in spawning activity coincides with the peak in phytoplankton abundance, which could ensure high food availability for the planktonic larvae. Gonad weights were significantly higher relative to urchin weight at the reef having the largest mean sizes and lowest population of urchins, indicating availability of food resources for growth and reproduction. E. mathaei at the reef with the highest density had the smallest urchins and high relative gonad sizes, indicative of a tradeoff between growth and reproduction when food is limited.Communicated by O. Kinne, Oldendorf/Luhe     

Heat waves,baby booms,and the destruction of kelp beds by sea urchins

Large populations of sea urchins, Strongylocentrotus droebachiensis (Müller), destroyed kelp beds along the Atlantic coast of Nova Scotia in the 1960's and 1970's. The origin of these large sea urchin populations is not understood. We have investigated the potential influence of variable growth and development of the planktonic larvae of sea urchins (in response to temperature and food abundance) on recruitment of benthic juveniles. The adult sea urchins were collected at Sandy Cove, Digby County, Nova Scotia, Canada, in December 1986. Temperature strongly affected larval size and the growth of the echinus rudiment within the range 3° to 9°C, and larvae grew most rapidly at 14°C. Food abundance had a smaller effect on larval growth, and these effects were apparent only at high temperature. Larvae fed the same concentration of two different algal food species grew and developed similarly. Correspondence between spring temperature variation and qualitative variation in sea urchin recruitment, as well as strong temperature effects on larval growth in culture, and the occurrence of a large, positive temperature anomaly in June 1960, all suggest that temperature effects on larval growth and development may have led to intense sea urchin recruitment in 1960 and the appearance of large adult populations 4 to 6 yr later. This result invites further research.     

Profitability and sustainability of edible sea urchin fishery in Sardinia (Italy)

Sea urchin (Paracentrotus lividus) fishery is intensively practiced in several areas of the Mediterranean basin. In Sardinia, as well as other Mediterranean countries, sea urchin is a basic ingredient for several dishes due to the delicacy of its gonads (roe), and demand is constantly increasing. Restrictions have been implemented in order to minimise the risk of overexploitation, however, these measures might jeopardize economic convenience in sea urchin harvesting. This paper estimates economic convenience within the edible sea urchin fishery in Sardinia. It aims to determine whether both profitability and sustainability, in terms of the preservation of sea urchin stock, can be guaranteed by actual policy regulation. We found high variability in terms of captures and profitability among firms, and a considerable degree of this variability is the result of technological differences between fishing methods. Analysis also suggests that a slight increase in allowed captures should generate a more than proportional increase in profits. This evidence gives some useful suggestions for improving the efficacy of policies in affecting the economic and environmental sustainability of the Mediterranean sea urchin fishery.