Growth and population dynamic model for the non-zooxanthellate temperate solitary coral Leptopsammia pruvoti (Scleractinia, Dendrophylliidae)

In corals where complex life history processes decoupling age from size (e.g., fragmentation, fusion, partial colony mortality) are rare or clearly detectable, individual age may be determined from size, and age-based growth and population dynamic models may be applied. One example is the solitary Mediterranean coral Leptopsammia pruvoti Lacaze-Duthiers 1897, whose population size and structure, and growth rates were determined at Calafuria (43°28′N and 10°20′E), Ligurian Sea, from December 2007 to June 2009. Growth rate decreased with increasing size. The growth curve derived from field measurements confirmed the one obtained by growth band analysis. The frequency of individuals decreased exponentially with age, indicating a steady state population. Turnover time was 2.3 years. Maximum life span was 13 years. Most reproductive output was from intermediate age classes (6 years), while older individuals (>7 years), although having higher fecundity, were rare and accounted for a minority of population reproductive output. In comparison with other solitary dendrophylliids, L. pruvoti life strategy was characterized by a reproduction with r-strategy correlates (high fecundity, short embryo incubation, small planula size, fast achievement of sexual maturity), and a rate of demographic renewal occurring halfway along the r–K continuum (intermediate turnover time and maximum longevity).     

The role of life histories and trophic interactions in population recovery

Factors affecting population recovery from depletion are at the focus of wildlife management. Particularly, it has been debated how life‐history characteristics might affect population recovery ability and productivity. Many exploited fish stocks have shown temporal changes towards earlier maturation and reduced adult body size, potentially owing to evolutionary responses to fishing. Whereas such life‐history changes have been widely documented, their potential role on stock's ability to recover from exploitation often remains ignored by traditional fisheries management. We used a marine ecosystem model parameterized for Southeastern Australian ecosystem to explore how changes towards “faster” life histories might affect population per capita growth rate r. We show that for most species changes towards earlier maturation during fishing have a negative effect (3–40% decrease) on r during the recovery phase. Faster juvenile growth and earlier maturation were beneficial early in life, but smaller adult body sizes reduced the lifetime reproductive output and increased adult natural mortality. However, both at intra‐ and inter‐specific level natural mortality and trophic position of the species were as important in determining r as species longevity and age of maturation, suggesting that r cannot be predicted from life‐history traits alone. Our study highlights that factors affecting population recovery ability and productivity should be explored in a multi‐species context, where both age‐specific fecundity and survival schedules are addressed simultaneously. It also suggests that contemporary life‐history changes in harvested species are unlikely to increase their resilience and recovery ability.     

Disease progression and mortality in neoplasticMya arenaria in the field

Four 6-mo mark-and-recapture experiments conducted in Long Island Sound, USA, from 1988 to 1990, involving approximately 2250 individual observations, demonstrated that under natural conditions significantly higher mortality (p0.001, chi-square test) occurred amongMya arenaria (L.) with hematopoietic neoplasia than those diagnosed as non-neoplastic. Using a blood-screening technique, the clams were diagnosed and placed in one of three diagnostic groups based on the severity of the disease (the percentage neoplastic cells per total number of blood cells): non-neoplastic (NN), 0%; low-severity neoplastic (LSN), < 50%; high-severity neoplastic (HSN), > 50%. Mortality of those clams initially diagnosed as HSN ranged from 48% to 78%, depending on the test period, as compared to 3% to 21% for the non-neoplastic. Mortality in the LSN treatment varied from 8% to 34%. Both progression and remission were evident in clams at all stages of the disease. Mortality and rates of progression and remission in individuals appeared to be linked to water temperatures. Differential mortality may be responsible for the apparent seasonal cycle of prevalence in populations.     

Demography of the intertidal brown alga Pelvetia fastigiata in Southern California,USA

The demography of Pelvetia fastigiata was studied from 1973 through 1977 in the intertidal zone near La Jolla, California, USA. Populations were usually small and relatively stable as new recruits replaced older individuals that were lost; however, in 1977 high recruitment substantially increased total abundances. The survivorship of recruits was similar regardless of the season or year of recruitment. Mortality rates decreased with age, and the mean life expectancy continued to increase for at least 1 yr. Losses of juveniles were high; 50% lived 80 d and only 9% survived to the age of first reproduction (about 1.5 yr). Plants present at the start of the study had higher survivorship rates than new recruits, 19 and 7%, respectively, living more than 3 yr. Individuals within aggregations of large plants lived longer than most dispersed individuals, and aggregations remained intact throughout the study in spite of low recruitment. Established individuals had low mortality rates and populations probably relied on these persistent individuals for reproduction.     

The capacity of the filter-feeding bivalve Mya arenaria L. to affect water transport in sandy beds

Benthic filter feeding macrofauna organisms may be an important factor linking sediment and water column. Transport of water and concomitantly of suspended matter is directly related to the size of the benthic filter feeding population. This paper aims to determine the potential for water transport by the bivalve Mya arenaria along a coastal stretch of roughly 100 km length in the southern Baltic Sea. Quantification of population filtration rates specific to the area is based on distribution, abundance and biomass of M. arenaria and calculated according to previously published filtration rate–biomass relations. Calculated rates range up to >8 m³ m^–2 day^–1 (at 5–20 m water depth in sandy sediment) with the potential to locally process a volume of water equivalent to the water column within <1 day. Data from 1991–2002 at one site suggest that the area-specific potential population filtration rate remains remarkably constant in time despite changes in population structure of M. arenaria. The related impact on pore water exchange within the permeable sediment associated with the leakage of water from the gape of M. arenaria valves is discussed.Communicated by L. Hagerman, Helsingør     

Gastropod predation on egg cases of skates (Chondrichthyes,Rajidae) in the southwestern Atlantic: quantification and life history implications

Mean predation rates (± SD) on egg cases of the skates Bathyraja macloviana, B. albomaculata, Amblyraja doellojuradoi, and Psammobatis spp. from the southwestern Atlantic were estimated to be 0.151 (±0.230), 0.423 (±0.344), 0.254 (±0.390), and 0.150 (±0.288), respectively. These estimates are within the ranges reported earlier (14–40%). Egg cases of B. albomaculata were preyed on in higher proportion than expected from their abundance and suffered a heavier predation rate where the snail Trophon acanthodes was present. Predation rates were not correlated with the thickness of the egg case wall, which indicates that other factors (ecological or chemical) could explain this pattern. Five types of boreholes were found in the egg cases: one was attributable to muricid gastropods, one to naticid gastropods, and a third type to an unknown gastropod (probably Fusitriton magellanicus); the remaining were of unknown origin. Cladistic analyses showed that skates are secondarily oviparous and have maximized adaptations for living in deep water. We suggest that oviparity in skates appeared as an adaptation to maximize fecundity (40–160 eggs per year, as compared to 2–18 pups annually or biannually in viviparous guitarfishes, the plesiomorphic sister clade of skates). If a predation rate of 24% (the mean of predation rates of all skate species studied to date) is applied to the range of fecundities reported for skates, the result is that 18–114 viable pups are produced annually per female skate. Even with a high mortality rate of 64% (the only direct estimate of natural mortality for any elasmobranch), each female skate produces 17–54 eggs annually. These values are higher than most elasmobranch fecundities. This maximization of fecundity is possible mainly because the fecundity of oviparous species is not limited by body size, as in viviparity. The protracted egg-laying season (4–12 months) of most skates (as in many other deep-sea fishes) maximizes the number of eggs laid.Communicated by P.W. Sammarco, Chauvin     

Analysis of growth rate in Mya arenaria using the Von Bertalanffy equation

Field studies were conducted in Gloucester, Massachusetts, USA, to determine linear shell growth rates for Mya arenaria. These rates were then compared with those reported for the same species from other locations. Most shell deposition occurred from March through November of each year. Winter interruptions in growth were not as marked in the small clams as in the larger ones (>60.0 mm). Annual variations in growth were slight during the period 1973–1974. Growth of mature clams (>35.0 mm) slowed during the spawning season. No significant sexual dimorphism in mean annual growth rates was detected. Winter rings were shown to be a reliable method for determining age in clams from Gloucester. Age-size relationships, based on two independent measures of annual growth, winter rings and tagging experiments, were computed using the Von Bertalanffy growth equation. No well-defined latitudinal patcerns in growth could be established for M. arenaria.     

Effects of Lunatia heros predation on the population dynamics of Mya arenaria and Macoma balthica in Maine,USA

The interaction between the naticid snail predator Lunatia heros and 2 iteroparous, infaunal, intertidal bivalves was investigated in Lubec, Maine, USA. The Mya arenaria population consists primarily of young, small individuals. M. arenaria survivorship is low when young (3.5% yr^-1 for the first 5 yr), then increases. M. arenaria can attain a length of 60 mm, but it is susceptible to L. heros attack only until it is 30 mm long. It delays reproduction until it is 20 mm long (3.8 yr) and diverts its resources instead into rapid early growth (4.9 mm yr^-1 for the first 5 yr). The Macoma balthica population has a larger proportion of older individuals than does that of M. arenaria. Survivorship is higher for M. balthica than for M. arenaria (76.3% yr^-1 for the first 5 yr). Unlike M. arenaria, M. balthica attains a final length of only 25 mm and all sizes are susceptible to L. heros attack. M. balthica grows slowly (2.7 mm yr^-1 for the first 5 yr) and diverts its resources into earlier reproduction at a length of 10 mm (2.9 yr). These contrasting life-history patterns and the possible relationship between bivalve resource allocation and refuges from predation are discussed.     

Plasticity in size and age at maturity in a monogamous fish: effect of host coral size and frequency dependence

The number and maximum body size of the gobioid fish, Paragobiodon echinocephalus, increase with the size of its obligate host coral, Stylophora. Only the largest two individuals breed monogamously in each coral head, and the reproductive success of each spawning is positively correlated with body size. In this study, the plasticity in size and age at maturity in P. echinocephalus was examined. We analyzed life history data from gobies 15–20 mm TL (total length) at their initial marking. Gobies found in larger corals were of lower rank in size order and began to breed later at a larger size, usually upon moving to other corals. The size at maturity ranged widely from 17.2 to 36.0 mm TL. After maturation, growth rates decreased. Mortality, however, was not affected by the timing of maturation. The host coral size did not affect the growth and mortality of marked fish, but the mortality rate of juveniles prior to marking appeared to be higher in smaller corals. The estimated lifetime reproductive success did not differ between the gobies inhabiting corals of different size. Thus the plasticity in size and age at maturity in this species may be maintained by frequency-dependent selection in choosing a host coral size that affects an individual’s social status. Received: 5 April 1995/Accepted after revision: 18 February 1996     

A simulation model for the management of vicuña populations

The population dynamics of the vicuña was modelled based on field data from the Central Galeras Sector, Perú. Rains were simulated in order to obtain net primary productivity and grass availability which act upon density-dependent fecundity and mortality. The model produces a population growth curve that tends to stabilize at densities around 100 vicuñas per km². Harvest and shearing processes were simulated as part of the vicuña population management model. Harvest was based upon a fixed threshold density D_e below which no harvest occurs; for densities above D_e harvesting is applied at a rate proportional to the difference between D_e and the current population density (fixed escapement or ‘bang-bang’ harvest rule). Management optimization was analyzed by determining the optimal escapement density D_e, which maximized either net profits or the number of animals harvested. Analyzing the results as cumulative totals over 20 years of simulation, an optimum harvest production was obtained for a D_e of about 40 vicuñas per km², and maximum profit was obtained for a D_e around 70 vicuñas per km². Analyzing the results of 20 years of simulation as annual averages with an original population density of 40 vicuñas per km², the harvest production and profits were maximized for a D_e of 40 and 60 vicuñas per km², respectively.The model was validated using data from the Reserva Nacional San Guillermo, Argentina, where vicuña and guanaco populations coexist (although their interaction was not modelled). The sensitivity analysis was performed with three different techniques: (a) stepwise multiple linear regression, (b) visual graphic analysis based on a polar coordinates system, and (c) direct evaluation of the effect on management decisions. The curve shape parameters of the fecundity and mortality functions proved to be the most important ones in determining the outcome of the model.     

Gill pump characteristics of the soft clamMya arenaria

Pumping rates in the soft clamMya arenaria, collected in June 1987 in the Great Belt, Denmark, were determined as rates at which clams cleared suspensions of algae,Dunaliella marina. The frictional resistance of the siphons to water flow was estimated by studying the effect of excision of the siphons at the base on the rate of water pumping. The frictional resistance was also calculated from the Poiseuille equation. Excision of the siphons had no measurable effect on the pumping rate, and calculations indicated pressure losses ranging between 0.3 to 1.2 mm H₂O. This is consistent with the conception that the capacity of filter feeding bivalves to process large amounts of water depends upon a low resistance to water flow in the siphons.     

Effects of constant and cyclic temperatures on the salinity tolerance of the estuarine sandhopper Orchestia chiliensis

The survival of Orchestia chiliensis (Milne Edwards, 1840) was investigated at salinities between 0.3 and 68 and constant or 10 C° cyclic temperatures between 5° and 25° C. Mortality increased with age, temperature and at salinity extremes. Small individuals show little seasonal acclimatisation apart from increased thermal tolerance at the highest exposure temperature. Larger individuals show a lateral shift in the mortality curve to the right in summer, giving increased survival at most salinities. Salinity had less effect on amphipods in cyclic regimes and survival was similar in 5° to 15° C and 10° to 20° C cycles. Mortality of larger individuals was higher in the 15° to 25° C cycle, but seasonal acclimatisation gave increased resistance at all fluctuating temperatures during the summer. Mortality in cyclic temperatures was higher than at similar constant temperatures. O. chiliensis does not actively evade immersion and diel temperature changes of 10 C° represent an important stress factor. This would affect all life stages and influence field populations both in the winter and the summer.     

Mechanisms of habitat segregation between an invasive (Mytilus galloprovincialis) and an indigenous (Perna perna) mussel: adult growth and mortality

The invasive mussel Mytilus galloprovincialis and the indigenous mussel Perna perna coexist intertidally on the south coast of South Africa through partial vertical habitat segregation: M. galloprovincialis dominates the upper shore and P. perna the lower shore. Recruitment patterns can explain the zonation of P. perna, but not the invasive species. We examined the role of post-recruitment interactions by measuring spatial and temporal differences in adult growth and mortality rates of the two species. Specifically, we tested the hypothesis that interspecific differences in growth and mortality reflect adult distribution patterns. The two study locations, Plettenberg Bay and Tsitsikamma, are 70 km apart with two sites (separated by 300–400 m) per location, each divided into three vertical zones. Growth was measured seasonally using different marking methods in 2001 and 2003. Cumulative adult mortality was measured through summer in 2003/2004. Both species generally grew more slowly upshore, but they showed different effects of season. For P. perna, growth was significantly reduced in winter in the low zone, but unaffected by season in the high zone. For M. galloprovincialis, growth was either unaffected by season or increased in winter, even in the high zone. Thus, growth of P. perna and M. galloprovincialis was reduced under cool winter and warm summer temperatures, respectively; and while growth was more similar between species in summer, M. galloprovincialis grew much faster than P. perna in winter. Mortality of P. perna increased upshore. For M. galloprovincialis, mortality was not zone-dependent and was significantly greater than for P. perna on the low-shore and (generally) across the shore in Tsitsikamma. Both species had higher growth and mortality rates in Plettenberg Bay than in Tsitsikamma. Thus, P. perna seems able to maintain spatial dominance on the low-shore and at certain sites because of higher mortality of M. galloprovincialis. We conclude that seasonality in growth of the two species reflects their biogeographic affinities and that coexistence is possible through pre-recruitment effects that limit the vertical distribution of P. perna and post-recruitment effects that limit M. galloprovincialis.     

Population dynamics of the temperate Australian soft coral Capnella gaboensis

Populations of over 100 colonies of Capnella gaboensis Verseveldt, 1977 at each of four study sites in Sydney Harbour were monitored for recruitment, survival, and mortality from October 1982 to November 1984. Larval settlement and survival were observed in the laboratory. Successful in situ larval settlement of C. gaboensis was estimated to be in the order of 0.26%. The predominant mode of recruitment was from larvae. Asexual recruitment resulted only from the fission of large colonies, and not by fragmentation or by stolon development. Mortality of newly settled C. gaboensis in situ during their first year was estimated to be around 99.75%. For colonies more than 1 yr old, mortality was highest amongst juveniles. After colonies reach about 3 yr of age, they have a high expectation of further life, until they reach about 15 yr of age; life expectancy declines each year thereafter. These estimates of life expectancy are based upon the conservative assumption that the largest colonies are about 20 yr old. The likely causes of mortality for colonies in the field are: predation by urchins, ovulids and nudibranchs; abrasion by kelp; and overgrowth by algae and sponges. The causes of mortality for larvae and recruits in the field, however, can be predicted only on the basis of laboratory studies and observations of field conditions.     

Photosynthate partitioning by phytoplankton in a New Zealand coastal upwelling system

A stimulation model of copepod population dynamics (development rate, fecundity, and mortality) was used to compute the predatory consumption necessary to control population growth in three dominant copepod species (Pseudocalanus sp., Paracalanus parvus, and Calanus finmarchicus) on Georges Bank, given observed seasonal cycles of copepod and predator populations. The model also calculated secondary production of each species. Copepod development rate and fecundity were functions of temperature while mortality was a function of predator abundance and consumption rate. Daily inputs of temperature and predator abundance (chaetognaths, ctenophores, and Centropages spp.) were derived from equations fit to field data. Model runs were made with various consumption rates until the model output matched observed copepod seasonal cycles. Computed consumption rates were low compared with published values from field and laboratory studies indicating that, even at conservative estimates of consumption, predators are able to control these copepod populations. Combined annual secondary production by the small copepod species, Pseudocalanus sp. and P. parvus, was nearly twice that of the larger C. finmarchicus with P. parvus having the highest total annual production.     

Chronic parasitic infection alters reproductive output in deer mice

Parasitized animals may alter their life histories to minimize the costs of parasitism. Organisms are predicted to decrease investment in current reproduction when parasitism has the greatest impact on current reproductive ability. In contrast, if parasitism decreases residual reproductive value, hosts should increase current reproductive investment, referred to as fecundity compensation or terminal investment. In mammalian hosts, parasitic infection most often leads to reductions in current host reproduction, perhaps attributable to the emphasis on parasites that are unlikely to impact the host’s residual reproductive value. In this study, the life history response of a rodent, Peromyscus maniculatus, to infection with a parasite that should strongly impact the residual reproductive value of its host (Schistosomatium douthitti, Trematoda) was examined. Infection decreased survival for hosts exposed to a high dose of parasites and was chronic in survivors, confirming that infection had strong impacts for the residual reproductive value of the host. As predicted, infected mice increased their reproductive output, producing litters of greater mass due to heavier offspring. However, this increased output was observed after a greater delay to begin breeding in infected mice and was not observed in animals that suffered early mortality. The deer mouse S. douthitti system may provide a rare example of fecundity compensation in mammals.     

Diet and food preferences of the adult horseshoe crab Limulus polyphemus in Delaware Bay,New Jersey,USA

Adult horseshoe crabs Limulus polyphemus (L.) feed on a wide variety of infaunal and epifaunal invertebrates during their spring spawning migration in Delaware Bay, New Jersey, USA. Comparison of the gut contents with estimates of available prey showed that the most abundant potential prey item, the bivalve Gemma gemma, was avoided. The thinner shelled but comparatively scarce clam Mulinia lateralis was a preferred prey item. In the laboratory, crabs fed on G. gemma when it was the only available item but not when M. lateralis or soft-shell clams, Mya arenaria, were offered in conjunction. Large M. lateralis (>10mm) were preferred to small M. lateralis; there was no discrimination between M. lateralis and M. arenaria of the same size. Male and female horseshoe crabs had similar gut contents and laboratory feeding preferences, despite the fact that females are larger than males. Crabs spawning later in the summer contained more food than did crabs collected at the peak of spawning activity.     

Interactive effects of pH,temperature and light during ammonia toxicity events in Elodea canadensis

Increased nutrient loading threatens many freshwater ecosystems. Elevated temperatures may increase the sensitivity to eutrophication in these ecosystems. Higher concentrations of possibly toxic reduced nitrogen (NH _x ) in the water layer may be expected as production and anaerobic breakdown rates will increase. Apart from temperature, NH _x and its effect on aquatic macrophytes will also depend on pH and light. We examined the interactive effects of NH _x , temperature, pH and light on Elodea canadensis in a full factorial laboratory experiment. Results demonstrate that high NH _x and high temperature together with low pH and low light causes the strongest toxic effects regarding relative growth rate and leaf tissue mortality. The adverse effects of high temperature and low light are most likely caused by increased metabolic activity and reduced photosynthesis, respectively. Severe toxicity at low pH compared to high pH can be ascribed to the ability of E. canadensis to induce a specialised bicarbonate-concentrating pathway at high pH, resulting in much higher carbon availability, needed for detoxification of NH _x . We conclude that NH _x toxicity will become more pronounced under higher temperatures, but that effects on aquatic macrophytes will strongly depend on pH of the water layer and specific metabolic adaptations of different species.     

Induced triploidy in the soft-shelled clam Mya arenaria: energetic implications

Given that triploid adult bivalves reportedly grow larger and faster than their diploid siblings, such differences should be traceable to variation in energy allocation. In one proposed mechanism, retarded gametogenesis found in triploid adults may allow them more energy for somatic growth. Another hypothesis states that triploids are more heterozygous; increased heterozygosity has been positively correlated with enhanced growth. Juvenile soft-shelled clams, Mya arenaria, were treated with cytochalasin B to induce triploidy and examined with respect to components of a balanced energy equation (C=P+R+E). The variables measured were oxygen uptake (V _{o 2}), filtration rate (FR), dry tissue weight, shell length, shell height and shell inflation. Energy budgets were constructed and diploid and triploid groups compared. Few significant differences were found between diploid and triploid juvenile clams with respect to energy budget components. However, at seven loci assayed electrophoretically the triploid individuals were nearly twice as heterozygous as their diploid siblings. Moreover, tripoloid variances were less than diploid variances for every variable measured. Increased heterozygosity has been correlated with the decreased variance of morphological parameters. This study is believed to be the first to show decreased variance of physiological properties as well as morphological characters. Overall the data clearly indicate that energy allocation in juvenile M. arenaria is not related to ploidy.     

A Contemporary,Sex‐Limited Change in Body Size of an Estuarine Turtle in Response to Commercial Fishing

Abstract: Juvenile growth rate and adult body size are important components of life‐history strategies because of their direct impact on fitness. The diamondback terrapin (Malaclemys terrapin) is a sexually dimorphic, long‐lived turtle inhabiting brackish waters throughout the Atlantic and Gulf coasts of the United States. In parts of its range, terrapins face anthropogenically imposed mortality: juveniles of both sexes inadvertently enter commercial crab traps and drown. For adult females, the carapace eventually grows large enough that they cannot enter traps, whereas males almost never reach that critical size. We compared age structure, carapace dimensions, growth curves, and indices of sexual dimorphism for a Chesapeake Bay population of terrapins (where mortality of turtles is high due to crab traps) with contemporary terrapins from Long Island Sound and museum specimens from Chesapeake Bay (neither group subject to commercial crab traps). We also calculated the allochronic and synchronic rates of evolutionary change (haldanes) for males and females to measure the rate of trait change in a population or between populations, respectively. We found a dramatic shift to a younger male age structure, a decrease in the length of time to terminal female carapace size, a 15% increase in female carapace width, and an increase in sexual dimorphism in Chesapeake Bay. In a new twist, our results implicate a fishery in the selective increase in size of a reptilian bycatch species. These sex‐specific changes in life history and demography have implications for population viability that need to be considered when addressing conservation of this threatened turtle.