Predator-prey relationships between the rock lobster Jasus lalandii and the mussel Aulacomya ater at Robben Island on the Cape West Coast of Africa

The natural diet and mode of feeding of the rock lobster Jasus lalandii (H. Milne Edwards) was determined in a rock-lobster sanctuary near Cape Town, South Africa. Field observations were tested and confirmed by means of aquarium studies. Rock lobsters feed mainly upon ribbed mussels Aulacomya ater (Molina), which comprise the largest component of the sessile benthic fauna. Mussel remains were found as the major constituent in 97% of the rock-lobster stomachs examined. The density of rock lobsters averaged 8,100 per hectare (0.81 m^-2), while mussel biomass averaged more than 5 kg (wet whole weight) m^-2 within the same depth range (12 to 30 m). More than 80% of the mussel biomass comprised large individuals between 60 and 90 mm in length. Large rock lobsters (mainly males) were capable of feeding on all sizes of mussels, although many of these were inaccessible to predation. Smaller rock lobsters became progressively more limited in the size range of mussels which they could crack open and consume. Competition between rock lobsters for small mussels appeared to be intense, as mussels of suitable size for feeding were generally in short supply to most of the rock-lobster population. Hence, feeding and growth rates of rock lobsters are likely to be affected by the relative population densities of predator and prey. Growth rates of rock lobsters could be limited by food supplies even in areas where mussel biomass is comparatively large.     

Growth and mortality rates of the fan mussel <Emphasis Type="Italic">Pinna nobilis</Emphasis> in Lake Vouliagmeni (Korinthiakos Gulf,Greece): a generalized additive modelling approach

The temporal patterns and the effect of shell size and depth on growth and mortality rates of the endangered fan mussel Pinna nobilis were investigated in the marine Lake Vouliagmeni (Korinthiakos Gulf, Greece). A total of 160 individuals were tagged and monitored monthly for a period of 17 months. At each visit, the size of the tagged individuals (shell width, w) was measured in situ and recorded. Any mortality event was also recorded and attributed to natural causes or (illegal) fishing. Growth and mortality rates were modeled with generalized additive models, which are non-parametric flexible models that free the researcher from the limiting concept of a strict parametric shape. The use of GAMs allowed the exploration of shapes of growth and mortality response curves in relation to predictor variables and allowed the fitting of statistical models that better agree with ecological theory. Growth rates had a seasonal pattern, with an extended period of very slow growth between late autumn and early spring, i.e., during the cold season, another short period of slow growth during August (when water temperatures reached their maximum values exceeding 29°C), and a peak in growth rates during late spring–early summer, probably related to an optimum combination of temperature and food availability. Growth rates varied with shell size, with a peak at w ∼4.5 cm, followed by a sharp decline to an approximately constant level, with sizes ranging from 9 to 15 cm, and a further decline with larger sizes down to almost zero for w > 20 cm. Growth rates did not vary substantially with depth. Although P. nobilis is a protected species in the EU and its fishing is strictly prohibited, fishing mortality was very high in Lake Vouliagmeni (much greater than natural mortality), especially during the hot season when the lake was crowded by summer visitors. The fan mussels were poached exclusively by free-diving and due to the high turbidity of the lake’s water, fishing mortality was higher in shallow areas (and mostly for large individuals) and was practically zero at depths >9 m. Due to fishing mortality, a size segregation of P. nobilis was observed in the lake: large individuals were restricted to deeper areas, while young and small individuals were more abundant in shallow areas where there was preferential recruitment. Natural mortality was strikingly size dependent and P. nobilis suffered high natural mortality during the first year of life; the probability of death by natural causes quickly diminished as the fan mussels grew in size. No depth-related differences in natural mortality were found.     

Distribution and structure of heterotrophic protist communities in the northeast equatorial Pacific Ocean

The distribution and structure of heterotrophic protist communities and size-fractionated chlorophyll a were studied during the Korea Deep Ocean Study 98 (KODOS 98) research expedition (July 1998) in the northeast equatorial Pacific Ocean (5–11°N). Areas of convergence and divergence formed at the boundaries of the South Equatorial Current (SEC), North Equatorial Current (NEC), and North Equatorial Counter Current (NECC) during the expedition. Water column physicochemical characteristics significantly influenced the size structure of heterotrophic protist communities. Intense vertical mixing and high nutrient and chlorophyll a concentrations characterized SEC and NECC areas, which were affected by converging and diverging water masses, respectively. Nanophytoplankton dominated in SEC and NECC areas; both areas also had relatively high heterotrophic protist biomasses (average 743 µg C m^–2). NEC areas were characterized by a stratified vertical structure, low nutrient and chlorophyll a concentrations, and picophytoplankton dominance. The heterotrophic protist biomass in NEC areas averaged 414 µg C m^–2; nanoprotists (<20 µm) dominated the community. The nanoprotist biomass comprised 49–54% of the total heterotrophic protist biomass in SEC/NECC areas and 67–72% in NEC areas. The biomass of heterotrophic protists was higher in SEC/NECC areas than in NEC areas, but the relative importance of nanoprotists was greater in NEC areas than in SEC/NECC areas. Heterotrophic dinoflagellates were dominant components of the <20 µm and >20 µm size classes in both water columns. The biomass of heterotrophic protists significantly correlated with the net-, nano-, and picophytoplankton biomass in SEC/NECC areas and with the nano- and picophytoplankton biomass in NEC areas. Heterotrophic protists and phytoplankton also showed strong positive correlation in the study area. The size structure of the phytoplankton biomass coincided with that of heterotrophic protists; the heterotrophic protist biomass positively correlated with the protists prey source. These relationships suggest that the community structure of heterotrophic protists and the microbial food web depended on size classes within the phytoplankton biomass. Microzooplankton grazing and phytoplankton growth rates were higher in SEC/NECC areas than in NEC areas. In contrast, the potential primary production grazed by microzooplankton was relatively high in NEC areas (127.3%) compared with SEC/NECC areas (94.6%). Our results indicate that the relative importance and size structure of heterotrophic protists might vary according to two distinct water column structures.Communicated by T. Ikeda, Hakodate     

Population structure and energetics of the shallow-water antarctic sea star Odontaster validus in contrasting habitats

Individuals and populations of Odontaster validus Koehler differed markedly among different habitats, as revealed in a study from October 1984 through January 1986 in McMurdo Sound, Antarctica. At McMurdo Station, individual sizes (wet weight) and population biomass (g wet wt m^-2 and kJ m^-2) decreased significantly with increasing depth. Individuals from shallow (10 to 20 m) habitats were in superior nutritional condition to those from deeper water (30 and 165 m), as shown by higher gonad and pyloric cecum indexes, and by higher lipid and energetic levels in the pyloric ceca. Moreover, gonadal output (reproductive output) was higher in shallow-water individuals. Higher levels of chlorophyll in the pyloric ceca and richer yellow to red coloration of the body wall in the shallow-water individuals indicate that they utilize the higher levels of primary production at shallow depths. At East Cape Armitage, where nearly permanent, thick, snow-covered ice most of the year resulted in very low levels of benthic primary production, the lowdensity sea stars were all very small and nutritionally similar to the deep-water individuals at McMurdo Station. At Cape Evans, where the generally snow-free sea-ice that broke up in mid-summer resulted in a luxurient benthic cover of diatoms and macroalgae, the sea stars were smaller than at McMurdo Station at comparable depths, but population densities were higher, resulting in 4 to 9 times greater biomass. Growth rates of sea stars fed in the laboratory were very low, especially compared to laboratory-reared temperate and tropical species; well-fed individuals need about 9 yr to reach 30 g wet weight, near the mean size of shallowwater individuals at McMurdo Station. No growth was detected in individuals caged at McMurdo Station for one year, suggesting even lower growth rates in the field. The stable size-frequency distributions at the different sites and depths throughout the year-long study suggest highly stable populations with low temporal variability in recruitment, migration and mortality. These data indicate that individuals and populations of O. validus quantitatively and qualitatively reflect the general level of productivity of a habitat. Differences noted in size, coloration, nutrition, and reproductive effort may be the result of long-term integration of local levels of primary production. These ubiquitous sea stars may serve as a biotic indicator of productivity in localized habitats around the continental shelf of Antarctica.     

Direct estimation of natural mortality rates for littoral marine fishes using populational data from a marine reserve

 Visual censuses conducted in a marine reserve (Medas Islands) were used to estimate the natural mortality rates (M) for five common fish species in the NW Mediterranean Sea (Coris julis, Diplodus annularis, D. sargus, Serranus cabrilla and Symphodus roissali). Visual censuses of these same five species were also performed at three sites in unprotected areas of the coast where both commercial and sport fishing activity was normal. Censuses were conducted over a 3 year period. Estimates of M in the 3 years displayed scant seasonal or interannual variation, which may mean that the populations were in equilibrium during that period. The results of this study showed that the relationships between M and the growth parameters and maximum life span were unclear, and considerable caution is therefore recommended when using indirect methods of estimating M based on those parameters. For certain species the values of M were equal to or greater than the estimated total mortality in the exploited areas. The virtual absence of piscivorous predators in the unprotected area as a consequence of the high level of fishing in that area contrasts with the high abundance of such predators in the marine reserve. Since predation is the main contributor to M, estimated mortality in the unprotected areas is attributable nearly entirely to fishing. It is suggested that M may vary according to alterations taking place in conditions in the ecosystem inhabited by a species and thus that use of a value of M for a pristine population cannot be extrapolated to exploited areas. Received: 18 January 2000 / Accepted: 14 July 2000     

Comparison of Modern and Historical Fish Catches (AD 750–1400) to Inform Goals for Marine Protected Areas and Sustainable Fisheries

Abstract: We tested the unsustainable fishing hypothesis that species in assemblages of fish differ in relative abundance as a function of their size, growth rates, vagility, trophic level, and diet by comparing species composition in historical bone middens, modern fisheries, and areas closed to fishing. Historical data came from one of the earliest and most enduring Swahili coastal settlements (approximately AD 750–1400). Modern data came from fisheries near the archeological site and intensively harvested fishing grounds in southern Kenya. The areas we sampled that were closed to fishing (closures) were small (<28 km²) and permanent. The midden data indicated changes in the fish assemblage that are consistent with a weak expansion of fishing intensity and the unsustainable fishing hypothesis. Fishes represented in the early midden assemblages from AD 750 to 950 had longer life spans, older age at maturity, and longer generation times than fish assemblages after AD 950, when the abundance of species with longer maximum body lengths increased. Changes in fish life histories during the historical period were, however, one‐third smaller than differences between the historical and modern assemblages. Fishes in the modern assemblage had smaller mean body sizes, higher growth and mortality rates, a higher proportion of microinvertivores, omnivores, and herbivores, and higher rates of food consumption, whereas the historical assemblage had a greater proportion of piscivores and macroinvertivores. Differences in fish life histories between modern closures and modern fishing grounds were also small, but the life histories of fishes in modern closures were more similar to those in the midden before AD 950 because they had longer life spans, older age at maturity, and a higher proportion of piscivores and macroinvertivores than the modern fisheries. Modern closures and historical fish assemblages were considerably different, although both contained species with longer life spans.     

Protection from fishing alters the species composition of fish assemblages in a temperate-tropical transition zone

Closure of areas to fishing is expected to result in an increase in the abundance of targeted species; however, changes to populations of species not targeted by fishermen will depend upon their role in the ecosystem and their relationship with targeted species. The effects of protection on targeted and non-targeted reef fish species at the Houtman Abrolhos Islands, Western Australia were studied using baited remote underwater stereo–video cameras. Video images were collected from shallow (8–12 m) and deep (22–26 m) reef sites inside a Marine Protected Area (MPA) at each of three island groups and from three replicate fished locations at each of these groups that span a temperate-tropical transition area. The MPAs were established in 1994 and vary in size from 13.72 km² at the Pelsaert group in the south to 22.29 km² at the Easter group to 27.44 km² at the Wallabi group in the north. The relative abundances of 137 fish species from 42 families were recorded. Large differences in fish assemblage structure existed between MPA and fished locations, and also between shallow and deep regions. Targeted fish species Plectropomus leopardus, Lethrinus miniatus, Lethrinus nebulosus, Pagrus auratus and Glaucosoma hebraicum were more abundant inside MPAs than in areas open to fishing. Their abundance inside MPAs was between 1.13 and 8 times greater than their abundance at fished locations. For non-targeted fish species many were more abundant in areas open to fishing, e.g. Coris auricularis, Thalassoma lutescens, Thalassoma lunare, Dascyllus trimaculatus, however others were conversely more abundant inside MPAs, e.g. Gymnothorax spp, Kyphosus sydneyanus, Scarus microhinos, Chromis westaustralis, Chaetodon spp. This study demonstrates that the removal of abundant targeted species from an ecosystem by fishing can indirectly impact non-fished species and alter the trophic structure of fish assemblages. Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

Effect of feeding regime and irradiance on the photophysiology of the symbiotic sea anemone Aiptasia pulchella

To determine how the animal and algal components of the symbiotic sea anemone Aiptasia pulchella respond to changes in food availability and culture irradiance, sea anemones from a single clone were maintained at four irradiance levels (320, 185, 115, and 45 E m^-2 s^-1) and either starved or fed for 5 wk. Changes in protein biomass of sea anemones maintained under these conditions were not related to the productivity of zooxanthellae, since the protein biomass of fed A. pulchella decreased with increase in irradiance and there was no difference in protein biomass among starved sea anemones at the four irradiance levels. Except for the starved high-light sea anemones, the density of symbiotic zooxanthellae was independent of culture irradiance within both starved and fed. A. pulchella. Starved sea anemones contained over twice the density of zooxanthellae as fed sea anemones. Within both starved and fed individuals, chlorophyll per zooxanthella increased with decreasing culture irradiance while algal size remained constant (in fed sea anemones) at about 8.80 m diameter. Chlorophyll a: c ₂ ratios of zooxanthellae increased with decreasing culture irradiance in zooxanthellae from starved sea anemones but remained constant in zooxanthellae from fed sea anemones. As estimated from mitotic index data, the in situ growth rates of zooxanthellae averaged 0.007 d^-1 and did not vary with irradiance or feeding regime. Photosynthesis-irradiance (P-I) responses of fed A. pulchella indicated an increase in photosynthetic efficiency with decreasing culture irradiance. But there was no consistent pattern in photosynthetic capacity with culture irradiance. Respiration rates of fed sea anemones also did not vary in relation to culture irradiance. The parameter I _k , defined as the irradiance at which light-saturated rates of photosynthesis are first attained, was the only parameter from the P-I curves which increased linearly with increasing culture irradiance. The daily ratio of net photosynthesis to respiration for A. pulchella ranged from 1.6 to 2.8 for sea anemones maintained at the three higher irradiances, but was negative for those maintained at 45 E m^-2 s^-1. Since the final protein biomass was greatest for sea anemones maintained at the lowest irradiance, these results indicate that sea anemone growth cannot be directly related to productivity of zooxanthellae in this symbiotic association.     

Primary-Production measurements for the green seaweed Codium fragile in long island sound

Rates of primary production and compensation depths were determined for Codium fragile by 3 different measurements: (1) growth rate; (2) rate of ¹⁴C-fixation; (3) rate of O₂ evolution. The radiocarbon assay employed liquid scintillation counting of homogeneous suspensions of seaweed tissue in gelled fluor. Maximum rates of primary production ranged between 2.6 and 3.9 mg C-fixed/g dry weight/h. The compensation depth is regulated by local turbidity, as is vertical distribution. All 3 methods for the determination of compensation depth, when used simultaneously, gave the same value. Chlorophyll levels were found to vary inversely with available light, hence depth, whereas starch levels were found to vary directly with available light.     

Growth patterns of Amphiura filiformis support the hypothesis of organic enrichment in the Skagerrak-Kattegat area

Population size structure, abundance and biomass of the burrowing ophiuroid Amphiura filiformis were measured in the period 1970 to 1989 at three widely spaced sites at 55 to 100 m depth in the Skagerrak-Kattegat area. This species is a dominant component of the fauna in the area, and also one of the species accounting for a great part of a recent general increase in benthic biomass. Abundance at two of the sites and biomass at all three sites increased significantly with time from the 1970s onwards. Maximum individual size and growth of the cohort of adults showed a marked increase in the period 1980 to 1983 at the three sites. In the 1980s annual absolute growth increments of the recruits were clearly greater than in the 1970s, and size-specific growth rates were virtually unchanged. These results are consistent with the hypothesis that recent increases in benthic biomass in this area result from increased input of food to the benthos. A. filiformis has the potential for rapid growth; estimated maximum weight-specific growth rates were more than 1.5% d^-1 in the disc diameter interval 3 to 9 mm, which is comparable to rates found in shallow water filtering bivalves. The maximum disc diameter growth rate was ca. 0.4 mm mo^-1.     

Patterns of microzooplankton growth in dilution experiments across a trophic gradient: Implications for herbivory studies

To investigate the growth and grazing patterns of microzooplankton (MZP) in environments of differing productivity, dilution experiments measuring phytoplankton growth (μ) and grazing mortality (m) rates were performed using samples from contrasting locations along the Texas coast. Samples were collected from estuaries, coastal lagoons and offshore Gulf of Mexico locations in the spring and summer of 2001. MZP growth rates were determined in each dilution treatment. Although MZP biomass changed over time in most dilution treatments, adjusting μ and m for the actual grazer gradient (represented by geometric mean MZP biomass) did not cause a significant deviation from the nominal dilution gradient. Likewise, these adjustments did not yield significant regressions where none existed before adjustment. The dynamics of MZP taxonomic groups (ciliates, dinoflagellates) and size categories differed suggesting that in some cases internal predation may lead to trophic cascades. MZP biomass was higher in productive coastal waters and included a larger proportion of dinoflagellates than in the oligotrophic, ciliate-dominated waters of the Gulf of Mexico. The MZP biomass-to-chlorophyll a ratio was lowest in the hypereutrophic Nueces River, where MZP biomass significantly increased in all dilution treatments (net growth rates up to 2 day⁻¹) suggesting a strong top–down control. In the brown-tide dominated Upper Laguna Madre and the oligotrophic seagrass-dominated Lower Laguna Madre MZP growth was decoupled from that of phytoplankton. At these sites, MZP were likely fueled by bacterial carbon and mixotrophy, respectively. Observing the growth response of MZP in dilution experiments can provide insight into trophic structure and efficiency of the microbial food web.     

Population structure,mortality and growth of <Emphasis Type="Italic">Pinna nobilis</Emphasis> Linnaeus, 1758 (Mollusca,Bivalvia) at different depths in Moraira bay (Alicante,Western Mediterranean)

An investigation to characterize the causes of Pinna nobilis population structure in Moraira bay (Western Mediterranean) was developed. Individuals of two areas of the same Posidonia meadow, located at different depths (A1, −13 and A2, −6 m), were inventoried, tagged, their positions accurately recorded and monitored from July 1997 to July 2002. On each area, different aspects of population demography were studied (i.e. spatial distribution, size structure, displacement evidences, mortality, growth and shell orientation). A comparison between both groups of individuals was carried out, finding important differences between them. In A1, the individuals were more aggregated and mean and maximum size were higher (A1, 10.3 and A2, 6 individuals/100 m²; A1, x = 47.2 ± 9.9; A2, x = 29.8 ± 7.4 cm, P < 0.001, respectively). In A2, growth rate and mortality were higher, the latter concentrated on the largest individuals, in contrast to A1, where the smallest individuals had the higher mortality rate [A1, L = 56.03(1 − e^−0.17t ); A2, L = 37.59(1 − e^−0.40t ), P < 0.001; mean annual mortality A1: 32 dead individuals out of 135, 23.7% and A2: 16 dead individuals out of 36, 44.4%, and total mortality coefficients (z), z _A1(−30) = 0.28, z _A1(31–45) = 0.05, z _A1(46−) = 0.08; z _A2(−30) = 0.15, z _A2(31–45) = 0.25]. A common shell orientation N–S, coincident with the maximum shore exposure, was observed in A2. Spatial distribution in both areas showed not enough evidence to discard a random distribution of the individuals, despite the greater aggregation on the deeper area (A1) (A1, χ ² = 0.41, df = 3, P > 0.5, A2, χ ² = 0.98, df = 2 and 0.3 < P < 0.5). The obtained results have demonstrated that the depth-related size segregation usually shown by P. nobilis is mainly caused by differences in mortality and growth among individuals located at different depths, rather than by the active displacement of individuals previously reported in the literature. Furthermore, dwarf individuals are observed in shallower levels and as a consequence, the relationship between size and age are not comparable even among groups of individuals inhabiting the same meadow at different depths. The final causes of the differences on mortality and growth are also discussed.     

Limitation and failure of immunological technique (ELISA) in resolving the diet of the South African rock lobster Jasus Ialandii

 Declines in rock-lobster (Jasus lalandii) growth have prompted a re-assessment of their diet, for which we employed an immunological approach (enzyme-linked immunosorbent assay, ELISA). Antisera were raised against 26 prey species, and their specificity was determined using ELISA. Antibody-binding was compared using Western blots. The antisera showed high specificity to undigested prey with cross-reactions among antisera being reduced to <4%. However, cross-reactivity increased to 49% when tested against digested prey, with some antisera even failing to recognise homologous prey. Sodium dodecylsulphate (SDS) gel electrophoresis demonstrated that excess rock-lobster digestive enzymes prevented the identification of digested prey by ELISA. However, “inhibition ELISA” (modified ELISA) did demonstrate species-specific proteins in the digested extracts and could be used to identify digested prey accurately. Nevertheless, the problem of enzyme interference has to be solved before large-scale screening of rock-lobster diets by ELISA is feasible. Received: 6 October 1999 / Accepted: 6 June 2000     

Rates of primary productivity and growth in<Emphasis Type="Italic"> Ecklonia radiata</Emphasis> measured at different depths,over an annual cycle,at West Island,South Australia

The pattern of growth (biomass accumulation) in Ecklonia radiata throughout the year and across a depth profile was investigated using the traditional hole-punch method, and the information presented in context with concurrently measured in situ net productivity rates. The rate of net daily productivity showed a lack of consistent seasonal variability, remaining constant throughout the year at two of the four depths measured (3 m and 12 m), and becoming higher during winter at another (5 m). Throughout the year, rates of net daily productivity differed significantly across the depth profile. Net daily productivity rates averaged 0.017 g C g^–1 dwt day^–1 and 0.005 g C g^–1 dwt day^–1 at a depth of 3 m (1,394 mol O₂ g^–1 dwt day^–1) and 10 m (382 mol O₂ g^–1 dwt day^–1) respectively. In contrast, the biomass accumulation rate of E. radiata was highly seasonal, with low rates of growth occurring in autumn (0.002 g dwt g^–1 dwt day^–1 at both 3 and 10 m) and summer (0.007 and 0.004 g dwt g^–1 dwt day^–1 at 3 and 10 m respectively) and higher rates in spring (0.016 and 0.007 g dwt g^–1 dwt day^–1 at 3 and 10 m respectively) and winter (0.015 and 0.008 g dwt g^–1 dwt day^–1 at 3 and 10 m respectively). The proportion of assimilated carbon used for biomass accumulation varied throughout the year, between 5% and 41% at 3 m and between 28% and 128% at 10 m. The rates of biomass accumulation at all depths represented only a small proportion of the amount of carbon assimilated annually.Communicated by P.W. Sammarco, Chauvin     

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     

Redwood of the reef: growth and age of the giant barrel sponge Xestospongia muta in the Florida Keys

The growth of animals in most taxa has long been well described, but the phylum Porifera has remained a notable exception. The giant barrel sponge Xestospongia muta dominates Caribbean coral reef communities, where it is an important spatial competitor, increases habitat complexity, and filters seawater. It has been called the ‘redwood of the reef’ because of its size (often >1 m height and diameter) and presumed long life, but very little is known about its demography. Since 1997, we have established and monitored 12 permanent 16 m diameter circular transects on the reef slope off Key Largo, Florida, to study this important species. Over a 4.5-year interval, we measured the volume of 104 tagged sponges using digital images to determine growth rates of X. muta. Five models were fit to the cubed root of initial and final volume estimates to determine which best described growth. Additional measurements of 33 sponges were taken over 6-month intervals to examine the relationship between the spongocoel, or inner-osculum space, and sponge size, and to examine short-term growth dynamics. Sponge volumes ranged from 24.05 to 80,281.67 cm³. Growth was variable, and specific growth rates decreased with increasing sponge size. The mean specific growth rate was 0.52 ± 0.65 year⁻¹, but sponges grew as fast or slow as 404 or 2% year⁻¹. Negative growth rates occurred over short temporal scales and growth varied seasonally, significantly faster during the summer. No differences in specific growth rate were found between transects at three different depths (15, 20, 30 m) or at two different reef sites. Spongocoel volume was positively allometric with increasing sponge size and scaling between the vertical and horizontal dimensions of the sponge indicated that morphology changes from a frustum of a cone to cylindrical as volume increases. Growth of X. muta was best described by the general von Bertalanffy and Tanaka growth curves. The largest sponge within our transects (1.23 × 0.98 m height × diameter) was estimated to be 127 years old. Although age extrapolations for very large sponges are subject to more error, the largest sponges on Caribbean reefs may be in excess of 2,300 years, placing X. muta among the longest-lived animals on earth.     

Biomasses,catch rates and abundances of demersal fishes,particularly predators of prawns,in a tropical bay in the Gulf of Carpentaria,Australia

The demersal fish fauna of Albatross Bay, in the eastern Gulf of Carpentaria, northern Australia, was sampled on seven cruises from August 1986 to November 1988, using a random stratified trawl survey. Four depth zones between 7 and 45 m were sampled during both day and night. The mean biomass of fish from all seven cruises was 297 kg ha^–1 for days trawls and 128 kg ha^–1 for night trawls. The overall mean catch rates were 922 kg h^–1 for day trawls and 412 kg h^–1 for night trawls. There were marked differences between cruises in both the biomass and catch rate. Approx 890 000 fish of 237 species were collected. Of these, 25 species comprised 82% of the total biomass and 74% of the overall catch rate. The dominant families were Leiognathidae, Haemulidae and Clupeidae, with Sciaenidae and Dasyatidae important at night.Leiognathus bindus was the most abundant species. Twenty-five species occurred in more than 50% of trawls, withCaranx bucculentus the most frequently caught (96% of all trawls). Thirty four species were predators on prawns; their absolute mean biomass was 50 kg ha^–1 during the day and 39 kg ha^–1 at night. The corresponding catch rates were 171 and 125 kg h^–1. Multiple-regression analyses were used to discriminate the effects of diel, seasonal, depth and cruise patterns. Of the 31 most abundant species, 15 showed diel patterns of abundance; 11 species showed seasonal patterns of abundance; 23 species had differential depth distribution; and 13 species showed significant cruise-to-cruise variation in abundance. Cruise variations in abundance were tested against salinity, temperature, tidal exchange, plankton biomass and prawn abundances as well as periods (and lags) of total rainfall prior to sampling. Only total rainfall showed any significant correlation. Total rainfall over a period of 6 wk immediately prior to sampling showed significant positive correlations with the abundances of five species, with overall daytime catch rates, and with the suite of 34 prawn predators. Rainfall and river runoff into Albatross Bay were significantly correlated. In Albatross Bay, the complex of factors affecting fish abundances and the magnitude of between-cruise differences indicate that such tropical communities may be unpredictable and are not seasonally constant. The high catch rates in Albatross Bay relative to similar tropical areas elsewhere are discussed and attributed to the light exploitation of the Albatross Bay stocks. Other than a prawn fishery, there is no commercial trawling in Albatross Bay. Hence, the only fishing mortality is a result of by-catch from prawn trawling. The annual total of such fish by-catch is probably less than 10% of the estimated standing stock of 93 000 tonnes.     

Phytoplankton blooms are strongly impacted by microzooplankton grazing in coastal North Pacific waters

Phytoplankton growth and microzooplankton grazing were measured in two productive coastal regions of the North Pacific: northern Puget Sound and the coastal Gulf of Alaska. Rates of phytoplankton growth (range: 0.09–2.69 day⁻¹) and microzooplankton grazing (range: 0.00–2.10 day⁻¹) varied seasonally, with lowest values in late fall and winter, and highest values in spring and summer. Chlorophyll concentrations also varied widely (0.19–13.65 μg l⁻¹). Large (>8 μm) phytoplankton cells consistently dominated phytoplankton communities under bloom conditions, contributing on average 65% of total chlorophyll biomass when chlorophyll exceeded 2 μg l⁻¹. Microzooplankton grazing was an important loss process affecting phytoplankton, with grazing rates equivalent to nearly two-thirds (64%) of growth rates on average. Both small and large phytoplankton cells were consumed, with the ratio of grazing to growth (g:μ) for the two size classes averaging 0.80 and 0.42, respectively. Perhaps surprisingly, the coupling between microzooplankton grazing and phytoplankton growth was tighter during phytoplankton blooms than during low biomass periods, with g:μ averaging 0.78 during blooms and 0.49 at other times. This tight coupling may be a result of the high potential growth and ingestion rates of protist grazers, some of which feed on bloom-forming diatoms and other large phytoplankton. Large ciliates and Gyrodinium-like dinoflagellates contributed substantially to microzooplankton biomass at diatom bloom stations in the Gulf of Alaska, and microzooplankton biomass overall was strongly correlated with >8 μm chlorophyll concentrations. Because grazing tended to be proportionally greater when phytoplankton biomass was high, the absolute amount of chlorophyll consumed by microzooplankton was often substantial. In nearly two-thirds of the experiments (14/23), more chlorophyll was ingested by microzooplankton than was available for all other biological and physical loss processes combined. Microzooplankton were important intermediaries in the transfer of primary production to higher trophic levels in these coastal marine food webs. Received: 12 November 1999 / Accepted: 4 October 2000     

Relation of growth and condition with the <Emphasis Type="Italic">Pan</Emphasis> I locus in Atlantic cod (<Emphasis Type="Italic">Gadus morhua</Emphasis> L.) around Iceland

Growth and condition (both somatic and hepatosomatic index) of Atlantic cod spawning at different locations around Iceland was studied in relation to the Pan I locus. South of Iceland cod carrying the Pan I^AB and Pan I^BB genotypes were more frequent while cod carrying the Pan I^AA genotype was more frequent north of Iceland. Differences in growth were detected between cod spawning at different areas around Iceland. Cod spawning south of Iceland grew faster than cod spawning north of Iceland. Differences in growth rate were also observed among cod carrying different Pan I genotypes within a spawning area. The least frequent Pan I genotype expressed the highest growth in both south and north of Iceland. Cod carrying the Pan I^AA grew fastest at spawning locations south of Iceland, while cod carrying the Pan I^BB genotype grew fastest in north of Iceland. A consistent relationship between condition and the different Pan I genotypes was also observed in all the areas. Cod carrying the Pan I^AA expressed the highest somatic condition and the lowest hepatosomatic index. Together, these results indicate that the relation of growth and condition with the Pan I locus is more complicated than earlier thought and is likely to be influenced by other factors, like size-selective fishing and food supply.     

Population ecology of the green/black turtle (<Emphasis Type="Italic">Chelonia mydas</Emphasis>) in Bahía Magdalena,Mexico

The mangrove channels of Bahía Magdalena, Mexico, are important developmental areas for juvenile green, or black turtles (Chelonia mydas), but incidental bycatch and illegal hunting threaten population persistence. We studied size distribution, condition index (CI), growth rates, and mortality of black turtles in Estero Banderitas, the largest mangrove channel in Bahía Magdalena, to supply information for the development of effective conservation strategies. A total of 213 black turtles (including 88 recaptures) were caught in entanglement nets between July 2000 and July 2003. Average yearly catch per unit of effort (CPUE, 1 unit: 100 m of net fishing for 12 h) dropped during the study from 2.19 to 0.76. About 97% of all turtles were considered juveniles, average size was 54.6 ± 9.5 cm. Turtles were significantly smaller at the head of Estero Banderitas than in the central part of the Estero and in the open bay, indicating size-based habitat segregation. Average growth rate was 1.62 cm/year and declined with increasing size. Growth was seasonal and three times higher in summer (0.28 cm/month) than in winter (0.09 cm/month), body CI was also significantly higher during the summer months. A seasonalized von Bertalanffy growth function (VBGF) was used to model growth for the size range studied (43–73 cm SCL), with the parameters: L _∞ = 101 cm SCL; K = 0.04 year⁻¹; t ₀ = 0; C = 0.4 and t _s = 0.75. Growth data indicate that black turtles may spend up to 20 years in Bahía Magdalena before they reach maturity at about 77 cm SCL. The total mortality estimate (Z) from the length converted catch curve was 0.16, corresponding to a yearly survival probability of 0.85.