A general bioeconomic simulation model for annual-crop marine fisheries

A generalized bioeconomic simulation model of annual-crop marine fisheries is described and its use in marine fisheries management is demonstrated. The biological submodel represents the recruitment of new organisms into the fishery, the movement of organisms from one fishing area to another and from one depth to another, the growth of organisms and the mortality of organisms resulting both from natural causes and from fishing. The economic submodel represents the fishing effort exerted on each resource species, the monetary costs of fishing, the value of the harvest and the rent (or excess profits) to the fishery.Basic dynamics of the model results from changes in the number of organisms in the fishery over time, which can be summarized as a set of difference equations of the general form ΔN/Δt = R + I ? E ? M ? F where ΔN/Δt is the net change in number of organisms in the fishery over time, R is recruitment, I is immigration, E is emigration, M is natural mortality and F is fishing mortality. R is a driving variable, whereas I, E, M and F are functions of the state of the system at any given point in time. The model can be run in a deterministic or stochastic mode. Values for parameters affecting rates of recruitment, movement, growth, natural mortality and fishing mortality can be selected from uniform, triangular or normal distributions.Use of the model within a fisheries-management framework is demonstrated by evaluating several management alternatives for the pink shrimp (Penaeus duorarum) fishery on the Tortugas grounds in the Gulf of Mexico. Steps involved in use of the model, including parameterization, validation, sensitivity analysis and stochastic simulations of management policies, are explained.     

A simulation model to explore the relative value of stock enhancement versus harvest regulations for fishery sustainability

Harvest restrictions and stock enhancement are commonly proposed management responses for sustaining degraded fisheries, but comparisons of their relative effectiveness have seldom been considered prior to making policy choices. We built a population model that incorporated both size-dependent harvest restrictions and stock enhancement contributions to explore trade-offs between minimum length limits and stock enhancement for improving population sustainability and fishery metrics (e.g., catch). We used a Murray cod Maccullochella peelii peelii population as a test case, and the model incorporated density-dependent recruitment processes for both hatchery and wild fish. We estimated the spawning potential ratio (SPR) and fishery metrics (e.g., angler catch) across a range of minimum length limits and stocking rates. Model estimates showed that increased minimum length limits were much more effective than stock enhancement for increasing SPR and angler catches in exploited populations, but length limits resulted in reduced harvest. Stocking was predicted to significantly increase total recruitment, population sustainability, and fishery metrics only in systems where natural reproduction had been greatly reduced via habitat loss, fishing mortality was high, or both. If angler fishing effort increased with increased fish abundance from stocking efforts, fishing mortality was predicted to increase and reduce the benefits realized from stocking. The model also indicated that benefits from stock enhancement would be reduced if reproductive efficiency of hatchery-origin fish was compromised. The simulations indicated that stock enhancement was a less effective method to improve fishery sustainability than measures designed to reduce fishing mortality (e.g., length limits).     

Life History and Conservation of Totoaba macdonaldi

We conducted a literature review on the biology, ecology, fishery, and protection of totoaba ( Totoaba macdonaldi ), an endemic, threatened fish of the Gulf of Calfornia, Mexico. Reinterpretation and integration of published and unpublished information enabled us to confirm and estimate specific biological parameters of the totooba, make hypothetical constructs of its life history, and to propose ideas for its preservation. In specific, we found (1) that the mean age of first reproduction of male and female totoaba are 6 and 7 years, respectively; (2) that the intrinsic rate of natural mortality was estimated as 0.268 per year and (3) that in the mid 1980s an estimated 120,300 juveniles died each year in the shrimp fishery by-catch and 6200 adults (26 kg average weight) died due to poaching. The parameters of an individual growth model for juveniles and adults were also estimated. Decreased spring water input from the Colorado River into the Gulf of California may have caused a contraction of the spawning season and a reduction of the carrying capacity of juvenile totoaba. An increase in annual survival during recent years indicates recovery of the stock that might be related to protection of adults. We argue that habitat restoration, which includes the elimination of growth and recruitment over-fishing, is critical to increasing numbers of totoaba, and thereby lifting the fishing ban, and to the delisting of totoaba.     

Lower thermal capacity limits of the common brown shrimp (Crangon crangon,L.)

Brown shrimp (Crangon crangon, L.) are subjected to a huge annual temperature range, and certain thermal conditions during winter have been identified to affect the brown shrimp population. Despite that, little is known about its thermal biology with regard to critically low temperatures. In the present study, we determined the critical thermal minima (CT_min) and the critical lethal minima (CL_min) of male and female brown shrimp of different body sizes in laboratory-based experiments. For the CT_min trials, shrimp were acclimated to 4.0, 9.0, and 14.0 °C and exposed to a cooling rate of ?0.2 °C min^?1. In the CL_min trials, brown shrimp were exposed to a cooling rate of ?1.0 °C day^?1 without prior thermal acclimation. Acclimation temperature significantly affected the temperature tolerance of brown shrimp (p < 0.001). CT_min among the experimental groups just varied slightly, and no clear effect of gender or body size was observed. In the CL_min trials, brown shrimp even tolerated the coldest temperature of ?1.7 °C that could be established in the experimental setup. However, we observed a negative relationship between temperature and reactivity within the range of 7.0 and 1.0 °C that was determined by means of the flicking response. This relationship suddenly broke between 1.0 and 0.0 °C where an abrupt drop in the reactivity of the shrimp became apparent. The results of this study revealed that brown shrimp hold a wider thermal range as originally reported and that it can cope with subzero temperatures. Implications of low-temperature tolerance are discussed in the context of the brown shrimp’s ecology as well as stock assessment.     

Size-selective harvesting alters life histories of a temperate sex-changing fish.

Selective mortality, whether caused naturally by predation or through the influence of harvest practices, initiates changes within populations when individuals possessing certain heritable traits have increased fitness. Theory predicts that increased mortality rates will select for changes in a number of different life history characteristics. For example, fishing often targets larger individuals and has been shown repeatedly to alter population size structure and growth rates, and the timing of maturation. For sex-changing species, selective fishing practices can affect additional traits such as the mature population sex ratio and the timing of sexual transformation. Using historical comparisons, we examined the effects of exploitation on life history characteristics of California sheephead, Semicossyphus pulcher, a temperate protogynous (female-male sex changer) labrid that inhabits nearshore rocky environments from central California, USA, to southern Baja California, Mexico. Recreational fishing intensified and an unregulated commercial live-fish fishery developed rapidly in southern California between the historical and current studies. Collections of S. pulcher from three locations (Bahia Tortugas, Catalina Island, and San Nicolas Island) in 1998 were compared with data collected 20-30 years previously to ascertain fishery-induced changes in life history traits. At Bahia Tortugas, where fishing by the artisanal community remained light and annual survivorship stayed high, we observed no changes in size structure or shifts in the timing of maturation or the timing of sex change. In contrast, where recreational (Catalina) and commercial (San Nicolas) fishing intensified and annual survivorship correspondingly declined, males and females shifted significantly to smaller body sizes, females matured earlier and changed sex into males at both smaller sizes and younger ages and appeared to have a reduced maximum lifespan. Mature sex ratios (female:male) increased at San Nicolas, despite a twofold reduction in the mean time spent as a mature female. Proper fisheries management requires measures to prevent sex ratio skew, sperm limitation, and reproductive failure because populations of sequential hermaphrodites are more sensitive to size-selective harvest than separate-sex species. This is especially true for S. pulcher, where different segments of the fishery (commercial vs. recreational) selectively target distinct sizes and therefore sexes in different locations.     

Slow Growth and Lack of Recovery in Overfished Holothurians on the Great Barrier Reef: Evidence from DNA Fingerprints and Repeated Large-Scale Surveys

Abstract:  Commercially fished holothurians have important functions in nutrient recycling, which increases the benthic productivity of coral reef ecosystems. Thus, removal of these animals through fishing may reduce the overall productivity of affected coral reefs. To investigate the potential for recovery of overfished holothurian (  Holothuria nobilis ) stocks on the Great Barrier Reef (GBR), we (1) conducted field surveys on 23 reefs after fishery closure, (2) modeled total virgin biomass and compared it with the total amount fished, and (3) estimated individual growth rates with a DNA fingerprinting technique. Two years after fishery closure, no recovery of H. nobilis stocks on reefs previously open to fishing was observed. Densities on reefs protected from fishing since the onset of the fishery in the mid 1980s remained about four times higher than on fished reefs. Based on density estimates and geographic information system data on the habitat area of each reef, we calculated that the virgin biomass (in the main fished area between 12° and 19°S) was about 5500 t and is now about 2500 t. The reduction is on the same order of magnitude as the total amount fished until 1999 (approximately 2500 t). The DNA analysis of repeated samples on three locations indicated high recapture rates of fingerprinted and released individuals of H. nobilis . Fitting growth curves with Francis's growth function indicated that medium-sized individuals (1 kg) grew 35–533 g /year, whereas large animals (2.5 kg) consistently shrank. Small animals (<500 g) were rarely observed. In combination, these data indicate that production of H. nobilis stocks is very low, presumably with low mortality, low recruitment, and slow individual growth rates. Consistent with anecdotal evidence, recovery of H. nobilis stocks on the GBR may take several decades, and we suggest a highly conservative management plan to protect both the stocks and the ecosystem.     

Marine reserves,fisheries ban,and 20 years of positive change in a coral reef ecosystem

By 2004, Belize was exhibiting classic fishing down of the food web. Groupers (Serranidae) and snappers (Lutjanidae) were scarce and fisheries turned to parrotfishes (Scarinae), leading to a 41% decline in their biomass. Several policies were enacted in 2009–2010, including a moratorium on fishing parrotfish and a new marine park with no-take areas. Using a 20-year time series on reef fish and benthos, we evaluated the impact of these policies approximately 10 years after their implementation. Establishment of the Southwater Caye Marine Reserve led to a recovery of snapper at 2 out of 3 sites, but there was no evidence of recovery outside the reserve. Snapper populations in an older reserve continued to increase, implying that at least 9 years is required for their recovery. Despite concerns over the feasibility of banning parrotfish harvest once it has become a dominant fin fishery, parrotfishes returned and exceeded biomass levels prior to the fishery. The majority of these changes involved an increase in parrotfish density; species composition and adult body size generally exhibited little change. Recovery occurred equally well in reserves and areas open to other forms of fishing, implying strong compliance. Temporal trends in parrotfish grazing intensity were strongly negatively associated with the cover of macroalgae, which by 2018 had fallen to the lowest levels observed since measurements began in 1998. Coral populations remained resilient and continued to exhibit periods of net recovery after disturbance. We found that a moratorium on parrotfish harvesting is feasible and appears to help constrain macroalgae, which can otherwise impede coral resilience.     

Population dynamics of naturalised Manila clams <Emphasis Type="Italic">Ruditapes philippinarum</Emphasis> in British coastal waters

The Manila clam Ruditapes philippinarum was introduced to Poole Harbour (lat 50°N) on the south coast of England in 1988 as a novel species for aquaculture. Contrary to expectations, this species naturalised. We report on individual growth patterns, recruitment, mortality and production within this population. On the intertidal mudflats the abundance of clams (>5 mm in length) varied seasonally between 18 and 56 individuals m⁻². There appear to be two recruitment events per year and there were 6 year classes in the population. A mid-summer decline in abundance was partly due to increased mortality but probably also a result of down-shore migration in response to high water temperatures and the development of anoxic conditions. A winter fishery removes c 75% of clams of fishable size (maximum shell length ≥40 mm) and c 20% of the annual production. The fishery depresses the maximum age and size attained by the clams but appears to be sustainable. Clam mortality due to factors other than fishing is highest in late-winter to early spring. The growth of the clams is intermediate in comparison with many published studies but remarkably good given their intertidal position. As on the coasts of the Adriatic Sea, where the clam is also non-native, the Manila clam has thrived in a shallow, eutrophic, lagoon-like system on the English coast. While the Poole Harbour population is currently Europe’s most northerly reported self-sustaining, naturalised population, given forecasts of increasing air and sea temperatures it might be expected that this species will eventually spread to more sites around the coasts of Northern Europe with associated economic and ecological consequences.     

Management and exploitation dynamics of small-scale fisheries in the Bay of Biafra: An integrative analysis of purse seine fishing activity

For many decades, fisheries research has focused on stock assessment and the impact of the fishery effort on resources. Although this knowledge remains necessary, a more integrated analysis of the joint dynamics of resource and operational activities is needed to provide more useful advice for the management of fishery systems. Since 1994 a new approach to fishery science has been carried out for Cameroonian small-scale fisheries, the aim being the incorporation into fishery science of research on fishery management, fishing processes and fishermen's behaviour. This paper presents a more systemic data approach which combines biological parameters and operational factor analyses with the goal of sustainable development. From two years of data collected on the purse seine fishing units operating in the Bay of Biafra (2002 and 2003), a set of three correspondence analyses is applied: (1) to the length frequency distribution of Ethmalosa fimbriata, (2) to the number of visits per fishing ground, and (3) to the species appearance frequency in the landings. These three analyses were plotted per month-year period. The results are presented in the form of an annual exploitation cycle, linking fishing grounds, the main species caught, and corresponding fishing period.     

A bioeconomic model of an international fishery

The conventional analyses of exploited fisheries is extended to situations where several national fleets harvest the resource. Using a simple biological model, the dynamics of such a fishery are explored and the open-access equilibria described. The model highlights the mutual interdependencies of the several fishing fleets, which are of importance when considering management policies in a regime of extended national jurisdiction. Several alternatives for managing such fisheries are also discussed.     

Modeling spawning dates of Hucho taimen in Mongolia to establish fishery management zones.

The ecological impacts of recreational fisheries are of growing concern and pose a number of unique management challenges. Here we report on our efforts to provide guidance for managing a recreational fishery for taimen, the giant Eurasian trout (Hucho taimen) in Mongolia. This species has declined dramatically across its range of Siberia and Central Asia, and is currently listed as endangered in Mongolia. Strong populations persist in remote regions of Mongolia because of limited anthropogenic impacts and harvest, though interest in the fishery is expanding rapidly. Current fishing regulations list the spring "opening date" for taimen fishing as 15 June, although regulations have not been consistently enforced, partially because taimen spawn much earlier than 15 June in much of the country. Through a combination of statistical models, climate data, knowledge of taimen biology, and geographic information systems (GIS), we model taimen spawning dates for potential habitat in Mongolia. A parametric bootstrap procedure was used to simulate variability in spawning date derived from inter-annual climate variability and model error, from which we estimated the date in which taimen spawning is predicted to occur with 90% confidence. We recommend the designation of three fisheries management zones, with corresponding opening dates of 20 May, 1 June, and 15 June. Our fishery opening date recommendations are less restrictive than existing regulations. Provided there is little or no catch-and-release fishing mortality, this approach serves both environmental and human needs by protecting taimen during the reproductive period, while still allowing a post-spawning catch-and-release fishery that benefits local economies and generates revenue (through fishing concession fees) for local conservation efforts.     

Defining trade-offs among conservation, profitability, and food security in the California current bottom-trawl fishery

Although it is recognized that marine wild-capture fisheries are an important source of food for much of the world, the cost of sustainable capture fisheries to species diversity is uncertain, and it is often questioned whether industrial fisheries can be managed sustainably. We evaluated the trade-off among sustainable food production, profitability, and conservation objectives in the groundfish bottom-trawl fishery off the U.S. West Coast, where depletion (i.e., reduction in abundance) of six rockfish species (Sebastes) is of particular concern. Trade-offs are inherent in this multispecies fishery because there is limited capacity to target species individually. From population models and catch of 34 stocks of bottom fish, we calculated the relation between harvest rate, long-term yield (i.e., total weight of fish caught), profit, and depletion of each species. In our models, annual ecosystem-wide yield from all 34 stocks was maximized with an overall 5.4% harvest rate, but profit was maximized at a 2.8% harvest rate. When we reduced harvest rates to the level (2.2% harvest rate) at which no stocks collapsed (<10% of unfished levels), biomass harvested was 76% of the maximum sustainable yield and profit 89% of maximum. A harvest rate under which no stocks fell below the biomass that produced maximum sustainable yield (1% harvest rate), resulted in 45% of potential yield and 67% of potential profit. Major reductions in catch in the late 1990s led to increase in the biomass of the most depleted stocks, but this rebuilding resulted in the loss of >30% of total sustainable yield, whereas yield lost from stock depletion was 3% of total sustainable yield. There are clear conservation benefits to lower harvest rates, but avoiding overfishing of all stocks in a multispecies fishery carries a substantial cost in terms of lost yield and profit.     

Effects of Illegal Harvest of Eggs on the Population Decline of Leatherback Turtles in Las Baulas Marine National Park,Costa Rica

Abstract: Within 19 years the nesting population of leatherback turtles (Dermochelys coriacea) at Parque Nacional Marino Las Baulas declined from 1500 turtles nesting per year to about 100. We analyzed the effects of fishery bycatch and illegal harvesting (poaching) of eggs on this population. We modeled the population response to different levels of egg harvest (90, 75, 50, and 25%) and the effect of eradicating poaching at different times during the population decline. We compared effects of 90% poaching with those of 20% adult mortality because both of these processes were present in the population at Las Baulas. There was a stepwise decline in number of nesting turtles at all levels of egg harvest. Extirpation times for different levels of poaching ranged from 45 to 282 years. The nesting population declined more slowly and survived longer with 20% adult mortality (146 years) than it did with 90% poaching (45 years). Time that elapsed until poaching stopped determined the average population size at which the population stabilized, ranging from 90 to 420 nesting turtles. Our model predicted that saving clutches lost naturally would restore the population when adult mortality rates were low and would contribute more to population recovery when there were short remigration intervals between nesting seasons and a large proportion of natural loss of clutches. Because the model indicated that poaching was the most important cause of the leatherback decline at Las Baulas, protecting nests on the beach and protecting the beach from development are critical for survival of this population. Nevertheless, the model predicted that current high mortality rates of adults will prevent population recovery. Therefore, protection of the beach habitat and nests must be continued and fishery bycatch must be reduced to save this population.     

Complementarity of No‐Take Marine Reserves and Individual Transferable Catch Quotas for Managing the Line Fishery of the Great Barrier Reef

Abstract: Changes in the management of the fin fish fishery of the Great Barrier Reef motivated us to investigate the combined effects on economic returns and fish biomass of no‐take areas and regulated total allowable catch allocated in the form of individual transferable quotas (such quotas apportion the total allowable catch as fishing rights and permits the buying and selling of these rights among fishers). We built a spatially explicit biological and economic model of the fishery to analyze the trade‐offs between maintaining given levels of fish biomass and the net financial returns from fishing under different management regimes. Results of the scenarios we modeled suggested that a decrease in total allowable catch at high levels of harvest either increased net returns or lowered them only slightly, but increased biomass by up to 10% for a wide range of reserve sizes and an increase in the reserve area from none to 16% did not greatly change net returns at any catch level. Thus, catch shares and no‐take reserves can be complementary and when these methods are used jointly they promote lower total allowable catches when harvest is relatively high and encourage larger no‐take areas when they are small.     

Ecological and economic considerations on fishing and rearing of Tapes phillipinarum in the lagoon of Venice

A population dynamic model for Tapes philippinarum has been developed, using experimental data for the estimation of mortality, and literature information for recruitment. The population dynamic model has been coupled to a eco-physiological model of T. philippinarum previously developed, in order to simulate the evolution of individual size and number of individuals in each age class.The resulting age-size class model has been used to analyse the implication of different scenarios of fishing/harvesting of the bivalve in the lagoons of the Northern Adriatic Sea, where fishery and aquaculture represent important economic activities.Ten years long simulations have been performed, in which initial density, harvesting efficiency, minimum harvested size, were varied. Comparisons between the different strategies are made in term of total yields and bio-economic income. The model gives suggestions on the optimal fishing effort, in case of fishery, and on optimal seeding size and seeding moment, in case of aquaculture.A discussion of model results provides indications on harvesting policies which are appropriate from ecological-economical point of view. The final result is that economically more profitable strategies coincide with ecologically more conservative policies.     

Invasion dynamics of the varnish clam (Nuttallia obscurata): a matrix demographic modeling approach

Marine invaders have become a significant threat to native biodiversity and ecosystem function. In this study, the invasion of the varnish clam (Nuttallia obscurata) in British Columbia, Canada, is investigated using a matrix modeling approach to identify the life history characteristics most crucial for population growth and to investigate population differences. Mark-recapture analyses and field collections from 2003 to 2004 were used to determine individual growth, survival rates, and fecundity for two sites. A multi-state matrix model was used to determine population growth rates and to conduct sensitivity and elasticity analyses. A life table response experiment was also used to determine what life history stage contributed most to observed differences in population growth rates. Population survey data were used in conjunction with the matrix model to determine plausible recruitment levels and to investigate recruitment scenarios. Both populations are currently declining but are likely sustainable because of the pulsed nature of large recruitment events. Survival of larger clams (>40 mm) is the most important for population growth based on elasticity and sensitivity analyses. Adult survival also had the largest influence on observed differences between site-specific population growth rates. The two populations studied differed in recruitment dynamics; one experiencing annual recruitment with higher post-settlement mortality and the other, episodic recruitment and lower post-settlement mortality. The most influential factor for the successful invasion of the varnish clam appears to be survival of the larger size classes. Therefore, any process that decreases adult survival (e.g., predation, commercial harvest) will have the greatest impact on population growth.     

Optimal fishery policy with artificial enhancement through stocking: California's white sturgeon as an example

Although optimal fishery policy has been derived from different kinds of economic and biological models, the interaction of fishing policy with artificial stocking policy has not been explicitly considered. We here determine optimal size limits, fishing effort, and stocking rate for three cases of interest: (1) recruitment-limited population, pre-recruitment stocking; (2) adult biomass-limited population, post-recruitment stocking; and (3) adult biomass-limited and recruitment-limited population, post-recruitment stocking. Results show that lower size limits should be set at the size at which the current market value exceeds the total future value of an individual, both to the fishery and to reproduction. Imposition of upper size limits is rarely optimal. Stocking is advisable when the hatchery cost times the relative contribution of stocking to recruitment is less than the contribution to the value of the catch. Optimal policy ranges from infinite effort at a specific size limit with maximum stocking when the cost of stocking is zero, to lower values of size limit and effort as stocking costs increase, the amount of stocking decreases, and more natural reproduction is optimal. Thus, as hatchery costs decline (or value of captured fish increases), optimal stocking/fishery policy varies from an unstocked fishery to a “put and take” fishery. The results are applied to the sturgeon fishery in the San Francisco Bay Estuary as an example. They imply that a reduced lower size limit and greater fishing mortality together with stocking would be optimal, but that current levels are conservative. The stocking decision depends critically on the values of parameters that are currently poorly known, such as: hatchery costs, survival to the fishery and the mechanisms controlling the sturgeon population.     

Population dynamics of the endangered fan mussel <Emphasis Type="Italic">Pinna nobilis</Emphasis> in a marine lake: a metapopulation matrix modeling approach

A metapopulation, time-invariant, stage-classified matrix model was developed to assess the dynamics of an important Pinna nobilis population in the marine Lake Vouliagmeni (Korinthiakos Gulf, Greece). The main aim of the study was to provide insight on the life cycle of the fan mussel and reveal influential factors for its population dynamics, with a special focus on the effect of poaching. The size of the fan mussel shell was selected as a state variable, and the model consisted of five size classes. The lake was divided in two regions, a shallow region of high (illegal) fishing mortality and high recruitment (region 1) and a deeper region of low mortality and low recruitment (region 2). The estimation of the transition matrix (stage-specific growth and mortality probabilities) was based on a tagging survey between 2005 and 2006, while independent annual surveys for abundance estimation using distance sampling techniques were utilized for the estimation of recruitment and stage-specific fertilities. The population was found to be increasing with an intrinsic rate of increase r = 0.038; however, r was not statistically different from zero. The life expectancy and expected lifetime offspring production of individuals in region 1 was markedly lower than that of individuals in region 2. Due to poaching, the life expectancy of a yearling fan mussel was less than 2.5 years in region 1, while it was almost 12 years in region 2. The highest expected annual natural mortality of fan mussels occurred on their first year of life after settlement (~43%) and greatly declined at greater sizes. Perturbation analysis revealed that the population growth rate was most sensitive to the vital rates of the larger size classes in region 2 and to fertilities corresponding to offspring that settled in the same region. The spatial distribution and abundance of the species was greatly dependent on the extent of poaching, which caused a size segregation of individuals, with small and young individuals being abundant in region 1, and larger and older individuals being restricted in region 2. If poaching ceased, the fan mussel population would be increasing with a significantly higher intrinsic rate of increase (r = 0.186), while if region 2 was also illegally exploited at the same intensity as region 1, the fan mussel population would be decreasing with r = −0.364 and would eventually collapse. The existence of refuge areas, where fan mussels may grow and reproduce, providing adjacent areas with offspring, seems crucial for the viability of local populations. Transplantation of fan mussels from high mortality areas to low mortality refuges might prove to be an effective measure to protect local populations of the species.     

Life history strategy of a southern European population of brown shrimp (Crangon crangon L.): evidence for latitudinal changes in growth phenology and population dynamics

This study provides a comprehensive examination of the life cycle dynamics of the brown shrimp (Crangon crangon L.) in the Mondego estuary, Portugal, a habitat located near the southern edge of the range of this species in European waters. The phenology of all life stages was documented (from the occurrence of ovigerous females, developing embryos, planktonic larvae and benthic post-larvae), and migration patterns of larvae into and out of the estuary were examined. Temperature-dependent functions of egg and larval development were combined with data on field abundance to predict the timing and magnitude of occurrence of larvae and recruits. Compared to brown shrimp at higher latitudes, southern conspecifics grow slower, mature earlier and have smaller brood sizes, and larvae have a more protracted settlement period. The Mondego estuary, besides acting as nursery area, is a dynamic platform for C. crangon to use in different stages, sizes and seasons.     

Effects of density and simulated recruitment and mortality on sex change in a protandric simultaneous hermaphroditic shrimp, Lysmata wurdemanni

Sex change in many hermaphrodite animals has been suggested to be environmentally determined, especially socially. To investigate whether sex change in the protandric simultaneous hermaphrodite shrimp Lysmata wurdemanni (Gibbes 1850) is socially mediated, two experiments were conducted in the laboratory between September 2002 and April 2004 using laboratory-cultured shrimp that originated from Port Aransas, Texas, USA. The size at sex change (from male to simultaneous hermaphrodite) in this shrimp is variable, with the minimum around 2.4 cm in total length (TL). Large shrimp (2.4–4.5 cm TL) still in the male-phase (MP) have been found in the wild and laboratory environments. This study tested the hypothesis that large MP shrimp delay changing to the euhermaphrodite-phase (EP) due to social control. In the first experiment, ten shrimp were raised in large (110-l) and small (20-l) containers to test the effect of habitat size/density on sex change. The percentage of shrimp changing to EP was significantly higher in the large container (low density) than in the small container after 60 and 120 days. But after 570 days sex ratios were the same, 2 MP:8 EP. In the second experiment, group composition was changed over time to simulate population recruitment and mortality. MP shrimp delayed sex change when EP shrimp were present. However, if group structure is stable, some MP shrimp may not change sex during their lifetime. Under certain demographic conditions, such as when postlarvae (PL) were added to (simulating recruitment) or EP shrimp were removed from (simulating mortality) a group, all old MP (from original PL) shrimp changed to EP. The response of old MP shrimp to simulated recruitment is faster than to simulated mortality. The present study confirms that social control affects the size and timing of sex change in L. wurdemanni. However, some MP shrimp never change sex suggesting that genetics might also play a role in the sex ratios of L. wurdemanni populations.