Age and growth in <Emphasis Type="Italic">Odontocymbiola magellanica</Emphasis> (Gastropoda: Volutidae) from Golfo Nuevo,Patagonia, Argentina

Growth, age and somatic production of the benthic predator Odontocymbiola magellanica were studied in Golfo Nuevo (42°S 65°W), on the South American Atlantic shelf. Stable oxygen isotope ratios confirmed semiannual formation of internal and external shell growth marks. Mean shell length (SL) of females was 115 and 112 mm for males, while population modal shell-free wet mass (SFWM) was 62.8 g. A Gompertz growth function (SL_∞ = 200 mm, K = 0.197, t ₀ = 5.486) fitted 113 pairs of size-at-age data (12 shells) best. O. magellanica is a long-lived species, reaching up to 20 years of age. The maximum individual somatic production of 29.3 g SFWM per year is attained at 145 mm SL, which corresponds to about 12 years of age. The life span of this volutid seems to be twice compared with other large gastropods. O. magellanica is a valuable and exploitable resource regarding its large size and somatic production, but on the other hand, its slow growth, late maturity and direct development makes it extremely vulnerable to overexploitation.     

Age,growth, and mortality of the prosobranch<Emphasis Type="Italic"> Zidona dufresnei</Emphasis> (Donovan, 1823) in the Mar del Plata area,south-western Atlantic Ocean

The volutid snail Zidona dufresnei is a benthic top predator in the Mar del Plata (Argentina) shelf area where it was subjected to unregulated commercial exploitation for more than 20 years. So far there is no stock management, and hitherto even the most basic information on population dynamics of this species is missing. Annual formation of internal shell growth bands visible by x-ray was confirmed by the stable oxygen isotope record in the shell carbonate that reflects seasonal oscillations in water temperature. A Gompertz growth function ( , K=0.211 year^–1, t₀=5.496) fitted 142 pairs of size-at-age data (30 shells) best. Maximum individual production amounted to 26.8 g shell-free wet mass (SFWM) at 115 mm shell length. Based on a size-frequency distribution derived from commercial catches, annual mortality rate of Z. dufresnei was estimated to be 0.61 (±0.21) year^–1.Communicated by O. Kinne, Oldendorf/Luhe     

Gonadal cycle in an<Emphasis Type="Italic"> Adelomelon brasiliana</Emphasis> (Neogastropoda: Volutidae) population of Buenos Aires province,Argentina

The reproductive season of the Adelomelon brasiliana population of Mar del Plata extends from September to April (austral spring and summer), showing synchronisation with water temperature. Adult gonad state is related to shell-free wet mass. Oocytes reach 200 m in diameter before spawning. In autumn, a resting phase begins, when no new oocytes develop and the non-spawned ones undergo reabsorption. Gonadic development begins during the early winter, when new previtellogenic oocytes can be observed through histology. The long reproductive season would increase the ability of the species to recover from harvesting.Communicated by O. Kinne, Oldendorf/Luhe     

Respiration rates of<Emphasis Type="Italic"> Beroe ovata</Emphasis> in the Black Sea

Metabolic rates of the ctenophore Beroe ovata within the length range from 0.4 mm (newly hatched larvae) to 60 mm were investigated. At 20° the respiration rates (Q, µg O₂ ind.^–1 h^–1) of individuals with wet weights (W, mg) less than or greater than 100 mg changed according to the equations Q=0.093W^0.62 and Q=0.016W^0.99, respectively. The weight-specific respiration rate of the juvenile ctenophores with wet body weights of 0.021–100 mg diminished approximately 20-fold (from 0.35 to 0.017 µg O₂ mg^–1 h^–1, respectively), but did not change within the range from 100 to 30,000 mg. The difference in the slope of the regression lines seems to be attributable to the ontogenetic changes in B. ovata metabolism. For the tested temperature range of 10–28°, the mean Q₁₀ coefficient was equal to 2.17±0.5. The basal metabolism of B. ovata narcotised by chloral hydrate was 4.5±0.9 times lower than total metabolism. Such a metabolic range is considered to be characteristic of aquatic invertebrates with high levels of locomotory activity.Communicated by O. Kinne, Oldendorf/Luhe     

Growth,production and ecological significance of Ophiura albida and O. ophiura (Echinodermata: Ophiuroidea) in the German Bight

Growth and production of the shallow-water ophiuroids Ophiura albida and O. ophiura were investigated at two stations in the German Bight from 1988 to 1991. Growth rings visible on the vertebral ossicles of the ophiuroid arms were interpreted as annual age markers. A correction for overgrown first rings allows for more exact estimations of growth and age. In both species growth could be described by Von Bertalanffy growth functions with the asymptotic disc diameter D =10.1 mm, K=0.229 and t _o=-0.192 in O. albida and D =27.7 mm, K=0.084 and t _o=0.042 in O. ophiura. Somatic production was calculated from mass specific growth rates. Annual production:biomass (P:B) ratios were estimated at 0.32 for O. albida and 0.43 for O. ophiura.AWI Publication Number: 618     

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.     

Growth,mortality and yield-per-recruit of deep-water royal red prawns (Haliporoides sibogae) off eastern Australia,using the length-based MULTIFAN method

The MULTIFAN method of Fournier et al. was used to analyse a series of monthly length-frequency distributions of deep-water royal red prawns (Haliporoides sibogae de Man, 1907, Solenoceridae) for the estimation of growth, mortality and yield-per-recruit. Length data were collected from commercial catches made between Latitude 33° and 35°S from November 1988 to May 1990. MULTIFAN distinguished six cohorts in the royal red prawn population, aged at 6 mo intervals from about 1.5 to 4 yr. Most prawns were between 2 and 3 yr of age. Females and males were fully recruited at 23.1 and 21.5 mm carapace length (CL) respectively, when about 2 yr old. Females grew faster and reached larger sizes at age than males (growth coefficient, K=0.37 yr^-1 and asymptotic length, L =48.3 mm CL for females, and K=0.49 yr^-1 and L =33.5 mm CL for males). Total mortality (Z) was estimated at 1.6 and 1.2 yr^-1 for females and males, respectively. Approximate values for natural mortality (M) ranged from 0.6 to 0.7 yr^-1 for females, and from 0.4 to 0.8 yr^-1 for males. Analysis of yield-per-recruit suggested that while the current yield could possibly be increased by decreasing the length at first capture (L _c ), there seems to be little potential for an increase in yield from increased fishing effort in the area currently fished.     

Moderate seawater acidification does not elicit long-term metabolic depression in the blue mussel Mytilus edulis

Marine organisms are exposed to increasingly acidic oceans, as a result of equilibration of surface ocean water with rising atmospheric CO₂ concentrations. In this study, we examined the physiological response of Mytilus edulis from the Baltic Sea, grown for 2 months at 4 seawater pCO₂ levels (39, 113, 243 and 405 Pa/385, 1,120, 2,400 and 4,000 μatm). Shell and somatic growth, calcification, oxygen consumption and \textNH₄ ⁺ {\text{NH}}_{4}^{ + } excretion rates were measured in order to test the hypothesis whether exposure to elevated seawater pCO₂ is causally related to metabolic depression. During the experimental period, mussel shell mass and shell-free dry mass (SFDM) increased at least by a factor of two and three, respectively. However, shell length and shell mass growth decreased linearly with increasing pCO₂ by 6–20 and 10–34%, while SFDM growth was not significantly affected by hypercapnia. We observed a parabolic change in routine metabolic rates with increasing pCO₂ and the highest rates (+60%) at 243 Pa. \textNH₄ ⁺ {\text{NH}}_{4}^{ + } excretion rose linearly with increasing pCO₂. Decreased O:N ratios at the highest seawater pCO₂ indicate enhanced protein metabolism which may contribute to intracellular pH regulation. We suggest that reduced shell growth under severe acidification is not caused by (global) metabolic depression but is potentially due to synergistic effects of increased cellular energy demand and nitrogen loss.     

Juvenile length-at-age data reveal that spanner crabs (<Emphasis Type="Italic">Ranina ranina</Emphasis>) grow slowly

The spanner crab (Ranina ranina) is a widespread and abundant brachyuran in offshore sand substrata of the Indo-Pacific region. Little is known of this species biology, population dynamics and ecology, despite it being the target of commercial fishing operations in many areas. Previous studies of R. ranina growth using length-frequency analysis of samples collected with commercial fishing gear have derived widely divergent estimates of growth parameters. The estimated time taken to reach 100 mm rostral carapace length (minimum legally exploited size in Queensland, Australia) in those studies has ranged from 1.75 to 8.83 years for females and from 1.08 to 3.58 years for males. Our data show that the commercial fishing apparatus used in those studies is size selective and catches only adult crabs. The resulting size bias in samples collected using that apparatus precludes the application of length-frequency-based techniques to estimate growth parameters from those samples. We devised a new dredge to collect samples of juvenile R. ranina and to calculate juvenile growth rates from modal progression in those samples. We combined those data with estimated mean maximum lengths (L) of 121.7 mm for females and 155.9 mm for males from commercial catch data to model other von Bertalanffy growth parameters using bootstrap methods. Those modelled parameters (K=0.29, T₀=–0.24 for females; K=0.23, T₀=–0.25 for males) indicate that R. ranina grows more slowly than most previous estimates suggest, with females requiring an average of 6.35 years and males 4.31 years to reach 100 mm rostral carapace length. This slow growth is consistent with the slow metabolism of R. ranina, and indicates that this species would be likely to recover slowly from overexploitation.Communicated by G.F. Humphrey, Sydney     

Growth in the bivalve Yoldia eightsi at Signy Island,Antarctica, determined from internal shell increments and calcium-45 incorporation

The growth rate of the infaunal nuculanid bivalve Yoldia eightsi at Factory Cove, Signy Island, South Orkney Islands (maritime Antarctica), was estimated from internal shell increments and ⁴⁵Ca incorporation of individuals collected monthly from December 1987 to April 1989. Acetate peels of etched shells revealed clear first-order increments, with less well defined, narrower, second-and third-order increments. The first-order increments were assumed to be annual, although there is no independent confirmation of this assumption. Unfortunately abrasion of the umbo region and the small thin shells of Y. eightsi meant that in no case could a complete sequence of increments be measured realiably on any individual shell. Measurements of 1043 first-order increments from 130 shells where a minimum of two consecutive increments could be detected were therefore pooled, and a population growth curve constructed from a Ford-Walford plot. This indicated a slow growth rate, with a maximum shell height of 22.3 mm (equivalent to a shell length of 35.6 mm) being reached at an age >60 yr. The size-frequency distribution of 1521 individuals pooled from winter (July to October) samples revealed a distinct lack of smaller (younger) individuals, possibly reflecting poor recruitment in areas of dense adult populations. The largest shell recovered in the samples was 33.5 mm in length, with an estimated age of 52 yr. Short-term ⁴⁵Ca-incorporation experiments indicated a mean daily rate of growth increment of 3.8 m for individuals of 12 mm shell height, which matches the proposed annual growth rate if growth is assumed to occur for about 150 d each year and the first-order increments are assumed to be annual.     

Age,growth and population structure of <Emphasis Type="Italic">Modiolus barbatus</Emphasis> from the Adriatic

Age, growth and population structure of Modiolus barbatus from Mali Ston Bay, Croatia were determined using modal size (age) classes in length frequency distributions, annual pallial line scars on the inner shell surface, internal annual growth lines in shell sections of the middle nacreous layer and Calcein marked and transplanted mussels. The length frequency distributions indicated that M. barbatus attain a length of ∼40 mm in 5–6 years indicating that a large proportion of the population in Mali Ston Bay is <5 years old. Some mussels of ∼60 mm were predicted to be 14 years old using the Von Bertalanffy growth (VBG) equation. Up to the first 6 pallial line scars were visible in young (<6 years) mussels but in older shells the first scars became obscured by nacre deposition as the mussel increased in length and age. The age of the older shells (>6 years) was determined from the middle nacreous lines in shell section, which formed annually in winter between February and March; the wider dark increments forming during summer (June to September). The oldest mussel, determined from the middle nacreous lines, was >12 years, with the majority of mussels aged between 3 and 6 years of age. The ages of mussels ascertained using the growth lines were not dissimilar to the ages predicted from the length frequency distributions. Age at length curves produced using modal size class data were not different from the data obtained using the pallial scar rings and internal growth lines. Taken together these data suggest that M. barbatus attains a length of 40 and 50 mm within 5 and 8 years, respectively. Eighty one percent of individual M. barbatus injected with a Calcein seawater solution (300 mg Calcein l⁻¹), into their mantle cavity successfully deposited a fluorescent line, which was visible in suitably prepared shell sections under ultra violet light. Incorporation of Calcein into the mussel shells was seasonally variable with the lowest frequency of incorporation in mussels marked in February and recovered in May. Seasonal shell growth was observed with significantly higher growth rates in mussels marked in May and removed in August (ANCOVA, F _3,149 = 23.11, P < 0.001). Mussels (∼18 to 22 mm) marked in May and recovered in August displayed maximal growth rates of >2.5 mm month⁻¹ compared with a mean mussel growth rate of 1.2 ± 0.6 mm month⁻¹. At other times of the year mussel shell growth ranged from immeasurable to 1.48 mm month⁻¹.     

Growth and size structure in a baltic Mytilus edulis population

Since Mytilus edulis L. has very few predators and competitors for space, it has become a biomass dominant in the Baltic proper covering hard substrates from the water surface to more than 30 m depth. In order to investigate the factors controlling size and production in a Baltic M. edulis population, growth was studied by the analysis of annual growth rings, measurements of caged individuals and the analysis of size classes in the population, and on settlement ropes. The total number of mussels in a representative mussel bed at 4 m depth varied between 36 000 and 158 000 ind · m^-2 during the year, mainly due to variations in very small mussels (<2 mm), whereas the abundance of mussels 2mm was rather constant between about 17 000 and 28 000 ind · m^-2. Maximum numbes of mussels < 2 mm, amounting to 132 000 ind · m^-2, were found after settlement in summer, but still half a year later in spring, 65 000 ind · m^-2 < 2 mm were registered, due to very strong intraspecific competition for food and space leading to the competitive suppression of small individuals and large variations in growth rates. Due to the special size-structure of the population only the analysis of annual growth rings could be used to estimate natural shell growth. From being very low in the smallest mussels, growth was linear between about 2–10 yr of age, corresponding to about 3–20 mm length, after which it decreased with a L=32 mm. Over the linear interval, growth in the populations from 3–6 m and 10–15m depth was 3.1 and 2.2 mm · yr^-1, respectively. Meat growth showed strong annual variations mainly due to gonad production. Starving mussels could, however, while utilizing energy reserves, survive losses of up to 78% of their meat biomass. This ability of M. edulis to respire away its own biomass and its apparent tolerance of weight loss has important implication. It will drastically reduce the energy flow to destruents from mussels dying naturally, which is of special significance in the Baltic, where predators and scavengers are scarce. It enables the mussels to endure bad food conditions and buffer strong seasonal variations in food abundance, maintaining the strongly food-and space-limited Baltic M. edulis population at the carrying capacity of the area.     

Stable isotopic investigation of physiological and environmental changes recorded in shell carbonate from the giant clam Tridacna maxima

The aragonitic shell of the photosymbiont-bearing bivalve Tridacna maxima contains a record of the physiological and environmental changes the organism has experienced during its lifetime. This record is preserved as chemical and microstructural variations throughout the shell. Stable isotopic analyses of oxygen (¹⁸O/¹⁶O) and carbon (¹³C/¹²C) in shell carbonate were combined with growth increment studies to interpret the shell record of specimens collected from the Rose Atoll (Lat. 14°31S; Long. 168°10W) in April 1982. The seasonal water temperature cycle is recorded in the oxygen isotopic signature of the clams, permitting the recognition of annual cycles in the ¹⁸O profile. The total number of these cycles corresponds to the age of a specimen, while the cycle length is a measure of the yearly growth rate. Large-amplitude cycles, reflecting year-round calcification, characterize the early portion of the growth record. With the onset of sexual maturity and slower growth at an age of approximately ten years, the cycles decrease in amplitude and become more erratic. During this later growth phase calcification is limited to the cooler months of the year, perhaps in response to a re-ordering of energy priorities between growth and gametogenesis. A growth curve developed from the ¹⁸O profile indicates rapid juvenile shell growth followed by slower growth thereafter producing a lifespan of several decades. Carbon isotopic analyses of T. maxima were compared to analyses of the symbiont-barren gastropod Terebra areolata collected from the same locality in April 1984. A 2 depletion in the ¹³C composition of T. maxima shell carbonate is attributed to a symbiontenhanced metabolic rate and an increased flow of isotopically light, respired CO₂ into the carbon pool used in calcification. Such a depletion may prove useful in identifying the presence of photosymbionts in extinct species of fossil mollusks.     

Otolith age validation and growth-rate variation in flyingfish (Hirundichthys affinis) from the eastern Caribbean

A study of otolith aging and growth-rate variation in the flyingfish Hirundichthys affinis (Günther) was conducted in the eastern Caribbean (10–16°N; 58–62°W) in 1987–1989. Daily otolith-increment formation was validated in laboratory-reared larvae, confirming the usefulness of otolith-increment counts for age determination of H. affinis juveniles (<150 mm fork length, FL). A mark-recapture programme to validate increment formation in wild adults was unsuccessful due to tetracycline-linked mortality and insufficient tetracycline uptake in slow-growing adult otoliths. A von Bertalanffy growth curve fitted to juvenile size-at-age data gave preliminary growth-curve parameters of t ₀=2.85 d and k=0.00854 on a daily basis, with an asymptotic length, L, of 245 mm FL, for eastern Caribbean flyingfish. Juvenile growth rate in H. affinis is sensitive to spatial and temporal variation in temperature. Growth rates were higher where sea-surface temperatures were higher, and were higher for juveniles hatched in warmer months (April–July) than in colder months (November–March). Growth rates were also higher near islands than at more oceanic locations. Variation in juvenile growth rates may influence the spatial and temporal variation in spawning frequency observed in H. affinis.     

Effect of growth factors and light quality on the growth,pigmentation and photosynthesis of two diatoms,Thalassiosira gravida and Phaeodactylum tricornutum

Recruitment, life span and growth rate were investigated in field and experimental populations of Abra alba (Wood) in Kiel Bay, FRG (55°N) from 1975 to 1978 to determine production to biomass (P:B) ratios and to assess the importance of A. alba to production by commercial fish. Life span and growth rates were determined from changes in length frequency modes at each site and from winter rings on the shell. A peak of recruitment usually occurred in August, sometimes followed by a second peak between December and February. Life span was between a little more than one year and two and a half years. Growth rates were highest at the two sites in offshore fishing grounds, where bivalves reached a mean length of 13 to 16 mm at the end of two years. At the inshore control site and in the nearby experimental containers, individuals reached a mean length of 7 mm at the end of two years. Production estimates ranged from 110 to 3.000 mg C m^-2 year^-1, differing markedly among sites and among years. Production was highest during the first year after recruitment, occurring mainly between July and December. Mortality occurred mainly between January and June, and was in approximate balance with production over a three-year period. Annual P:B ratios were from 1.3 to 3.4; a long-term mean P:B ratio of 2.2 is suggested for Kiel Bay populations of A. alba. Annual production by A. alba appears to exceed considerably consumption by fish of commercial size. The significance of A. alba in the food web of Kiel Bay may thus be as food for juvenile fish or for intermediate-level predators that are themselves prey for larger fish.Publication No. 431 of the Sonderforschungsbereich 95 Meer-MeeresbodenPublication No. 1031 of the CSIRO Marine Laboratories     

Daily energy requirements and trophic positioning of the sand shrimp<Emphasis Type="Italic"> Crangon septemspinosa</Emphasis>

Sand shrimp, Crangon septemspinosa Say, are important to the trophic dynamics of coastal systems in the northwestern Atlantic. To evaluate predatory impacts of sand shrimp, daily energy requirements (J ind.^–1 day^–1) were calculated for this species from laboratory estimates of energy losses due to routine (R_R), active (R_A), and feeding (R_SDA) oxygen consumption rates (J ind.^–1 h^–1), coupled with measurements of diel motile activity. Shrimp used in this study were collected biweekly from the Niantic River, Connecticut (41°33N; 72°19W) during late spring and summer of 2000 and 2001. The rates of shrimp energy loss due to R_R and R_A increased exponentially with increasing temperature, with the magnitude of increase greater between 6°C and 10°C (Q₁₀=3.01) than between 10°C and 14°C (Q₁₀=2.85). Rates of R_R doubled with a twofold increase in shrimp mass, and R_SDA was 0.130 J h^–1+R_R, irrespective of shrimp body size. Shrimp motile activity was significantly greater during dark periods relative to light periods, indicating nocturnal behavior. Nocturnal activity also increased significantly at higher temperatures, and at 20°C shifted from a unimodal to a bimodal pattern. Laboratory estimates of daily metabolic expenditures (1.7–307.4 J ind.^–1 day^–1 for 0.05 and 1.5 g wet weight shrimp, respectively, between 0°C and 20°C) were combined with results from previous investigations to construct a bioenergetic model and make inferences regarding the trophic positioning of C. septemspinosa. Bioenergetic model estimates indicated that juvenile and adult shrimp could meet daily energy demands via opportunistic omnivory, selectively preying upon items of high energy content (e.g. invertebrate and fish tissue) and compensating for limited prey availability by ingesting readily accessible lower energy food (e.g. detritus and plant material).Electronic Supplementary Material Supplementary material is available in the online version of this article at Communicated by J.P. Grassle, New Brunswick     

Energy expended on growth and gonad output in the ribbed musselAulacomya ater

Length/weight relationships have been computed for shell, flesh and byssus ofAulacomya ater (Molina) and energy values used to convert the weights to energy equivalents. Shell accounts for some 26% of total body energy, while the contribution of the byssus declines from 15 to 8% during growth. Observations of juvenile growth rates have been used to generate a Gompertz growth equation which predicts attainment of maximum length (90 mm) after 11 years. Reproductive condition has been assessed by monitoring seasonal fluctuations in the flesh weight of standard-sized individuals, calculated from monthly length/weight regressions. There appear to be three spawnings, of variable date and intensity, each year. From the above data, annual energy expenditure on growth and gonad output has been calculated for individuals of various sizes. The ratio of total production to biomass is a declining clining function of shell length, dropping from 29.5 at 5 mm to 0.8 at 85 mm. The proportion of total production expended on gamete output increases steadily from 25% at attainment of maturity (15 mm) to 81% at 85 mm length. The considerable effects of changing size composition on the amount and type of production in natural populations are discussed.     

Life history of the red mullet Mullus surmuletus from the bottom-trawl fishery off the Island of Majorca (north-west Mediterranean)

The red mullet Mullus surmuletus is one of the main target species of the trawling fishery along the continental shelf off the Island of Majorca. The size distribution of the catches, and the reproduction, age and growth of this species have been studied based on sampling carried out from 1990 to 1992. The length range of the catches was between 10 and 32 cm, with a main distribution between 15 and 20 cm, but this included small specimens (recruits of 10 to 11 cm) from August. In the >19 cm length-class, females clearly dominated. Monthly variations in the gonadosomatic index (GSI) and in the percentage of mature specimens showed that males spawn from December to June, whereas the reproductive activity of the females centres around spring. Fifty percent of males and females mature at 15 and 16.8 cm, respectively, corresponding to 1 yr of age. Otolith age-readings indicate that the population exploited in the trawl fishery consists of six age-groups, including a very high proportion of individuals between 0 and 4 yr old. Population growth curves revealed that females grow comparatively slowly over a longer period of time and attain greater asymptotic sizes than males. The growth parameters for the whole population are: asymptotic length, L =31.28 cm; growth coefficient, K=0.211 yr^-1; theoretical age when length is zero, t ₀=-2.348 yr.     

Observations on some population parameters of exploited stocks of Senilia senilis (=Arca senilis) in Sierra Leone

The West African cockle Senilia senilis (L.) (=Arca senilis L., 1758) from some estuaries and muddy shores of Sierra Leone was studied from September, 1973 to February, 1975. Quantitative samples were obtained along transects using quadrats and sieves; some random hand-picked collections were also made. The length, number of rings and the maximum width of the inter-ring bands along the outer convex surface of the right valve were recorded from samples of 25 specimens. All the cockle beds examined were exploited and had stocks with a mean density of 9 large (>10 mm) cockles/m², and at River No. 2 estuary at peak spatfall, of 130 seed cockles/m². Spat settlement began in November-December after the rainy season, reached a peak in January-February and continued to the early part of the following rainy season (May-June). Seed cockles were absent from August to October. In the length-frequency distributions, modes were clear and associated with certain shell-ring numbers. Rings on shells were formed once a year, during July to September, the period of maximum rainfall, and they were successfully used in ageing the cockles. The first ring was formed at a mean age of 7 months and the subsequent ones annually. The growth period of the inter-ring bands, considered to extend from August to the following July (s. senilis growth year), may actually be of only 10 months duration. Sublittoral cockles from No. 2 estuary showed a higher growth rate than those from the levels exposed at low tide and subjected to greater exploitation. Cockles from the Sierra Leone River Estuary showed even greater growth. s. senilis grows slowly and lives long (up to 8 to 9 years), and its von Bertalanffy parameters are: River No. 2 estuary cockles k=0.27 to 0.31 and L =99 mm; Sierra Leone River Estuary cockles k=0.22 and L =145 mm. At No. 2 estuary, cockles enter the fishery at 22 to 25 mm (14 to 15 months old) and exploitation is heavy, resulting in the stocks being dominated by a few young year-classes.