Catch equations: restoring the missing terms in the nominally generalized Baranov catch equation

Observational models for the catch of fish at age a (or size) at time t are fundamental equations in fisheries science, linking a population model with data. The well known Baranov catch equation (which assumes that fishing and natural mortalities are constant over both age and time) is a nominal basis of those most commonly used in fish stock assessment and fish population models (which assume that fishing and natural mortalities vary with both age and time). But, what should a catch equation look like, if the instantaneous rates of fishing and natural mortalities of fish of age a at time t vary with age a and time t? Without answering this question, use of those catch equations in fish stock assessment and population models renders their results uncertain. In this paper, I derive a general catch in number or in biomass equation as observational models of an age- and time-dependent model for a fish population by Taylor series expansion of, and by directly manipulating, a general catch integral, reduce it to commonly used catch equations, and compare the performance of 11 of them using data on the western king prawn Penaeus latisulcatus. I show that the nominal generalization of the Baranov catch equation misses several terms. In so doing, I derive the catch equations more accurately and restore these missing terms. Although almost all approximations overestimate the catch per recruit for older prawns, all commonly used catch equations and their extensions perform worse than theoretically sound representations of the general catch equation and their approximations. The age-specific bias of all models is <2.5, <18 and <90% for a time interval of sampling of 1, 7 and 30 days, respectively. Such large biases even for moderate values of the length of the time interval of sampling highlight a need for assessing the utility of commonly used catch equations for individual species.     

Neutral theory and the evolution of ecological equivalence

Since the publication of the unified neutral theory in 2001, there has been much discussion of the theory, pro and con. The hypothesis of ecological equivalence is the fundamental yet controversial idea behind neutral theory. Assuming trophically similar species are demographically alike (symmetric) on a per capita basis is only an approximation, but it is equivalent to asking: How many of the patterns of ecological communities are the result of species similarities, rather than of species differences? The strategy behind neutral theory is to see how far one can get with the simplification of assuming ecological equivalence before introducing more complexity. In another paper, I review the empirical evidence that led me to hypothesize ecological equivalence among many of the tree species in the species-rich tropical forest on Barro Colorado Island (BCI). In this paper, I develop a simple model for the evolution of ecological equivalence or niche convergence, using as an example evolution of the suite of life history traits characteristic of shade tolerant tropical tree species. Although the model is simple, the conclusions from it seem likely to be robust. I conclude that ecological equivalence for resource use are likely to evolve easily and often, especially in species-rich communities that are dispersal and recruitment limited. In the case of the BCI forest, tree species are strongly dispersal- and recruitment-limited, not only because of restricted seed dispersal, but also because of low recruitment success due to heavy losses of the seedling stages to predators and pathogens and other abiotic stresses such as drought. These factors and the high species richness of the community strongly reduce the potential for competitive exclusion of functionally equivalent or nearly equivalent species.     

Klimawandel und Bachforellenrückgang – gibt es einen Zusammenhang? Resultate aus der Schweiz

Background, aim, and scope In response to a 60?% decrease in brown trout catch between 1980 and 2000, a Swiss-wide search was initiated to investigate possible causes. The project, named ‘Fischnetz’ (fishing net), investigated 12 hypotheses. One of those suggested a detrimental effect of global climate change. I report here which parameters changed and what the possible consequences for native brown trout are. Materials and methods The literature is critically analysed and results are synthesised to show the interactions between different climatic factors and their effects on fish. Results In the last 25 years, an increase in temperature by approximately 1?°C was indicated in the rivers of Switzerland. This is associated with an earlier emergence of trout from the gravel. Warming results in an upward shift of the preferred thermal habitats. Furthermore, an increase in the clinical outbreak of the Proliferative Kidney Disease PKD (for which a temperature of 15?°C for more than 2–4 weeks is necessary) can be recorded. The precipitation pattern changed and an intensification of high floods in winter results in higher erosion. This can in turn lead to an increased level of fine sediments which may affect health of juvenile brown trout and is assumed to reduce reproduction success. Discussion The consequences of climate change are discussed in concert with other anthropogenic factors. Storage reservoirs, as well as water withdrawal (and return of heated water, respectively) affect temperature profiles and sediment load. Fragmentation, channelization and straightening of rivers accelerate clogging and restrain fish from upward migration and evacuation to more suitable habitats. Conclusions With increasing temperatures a downsizing of habitats of cold-water fish species, as well as an increase of diseases which are temperature sensitive, is assumed. Recommendations and perspectives Mitigation measures which lead to a morphological improvement of river systems, such as river widening and improvement of the connectivity between river stretches and their tributaries, as well as improving river bank vegetation, are recommended.     

Economic Growth and Marine Biodiversity: Influence of Human Social Structure on Decline of Marine Trophic Levels

Abstract:  We assessed the effects of economic growth, urbanization, and human population size on marine biodiversity. We used the mean trophic level (MTL) of marine catch as an indicator of marine biodiversity and conducted cross-national time-series analyses (1960–2003) of 102 nations to investigate human social influences on fish catch and trends in MTL. We constructed path models to examine direct and indirect effects relating to marine catch and MTL. Nations' MTLs declined with increased economic growth, increased urbanization, and increased population size, in part because of associated increased catch. These findings contradict the environmental Kuznets curve hypothesis, which claims that economic modernization will reduce human impact on the environment. To make informed decisions on issues of marine resource management, policy makers, nonprofit entities, and professional societies must recognize the need to include social analyses in overall conservation-research strategies. The challenge is to utilize the socioeconomic and ecological research in the service of a comprehensive marine-conservation movement.     

Redistribution of benefits but not detection in a fisheries bycatch‐reduction management initiative

Reducing the capture of small fish, discarded fish, and bycatch is a primary concern of fisheries managers who propose to maintain high yields, species diversity, and ecosystem functions. Modified fishing gear is one of the primary ways to reduce by‐catch and capture of small fish. The outcomes of gear modification may depend on c ompetition among fishers using other similar resources and other gears in the same fishing grounds and the subsequent adoption or abandonment of modified gears by fishers. We evaluated adoption of modified gear, catch size, catch per unit effort (CPUE), yield, and fisher incomes in a coral reef fishery in which a 3‐cm escape gap was introduced into traditional traps. There were 26.1 (SD 4.9) fishers who used the experimental landing sites and 228(SD 15.7) fishers who used the control landing sites annually over 7 years. The size of fish increased by 10.6% in the modified traps, but the catch of smaller fish increased by 11.2% among the other gears. There was no change in the overall CPUE, yields, or per area incomes; rather, yield benefits were redistributed in favor of the unmodified gears. For example, estimated incomes of fishers who adopted the modified traps remained unchanged but increased for net and spear fishers. Fishers using escape‐gap traps had a high proportion of income from larger fish, which may have led to a perception of benefits, high status, and no abandonment of the modified traps. The commensal rather than competitive outcome may explain the continued use of escape‐gap traps 3 years after their introduction. Trap fishers showed an interest in negotiating other management improvements, such as increased mesh sizes for nets, which could ultimately catalyze community‐level decisions and restrictions that could increase their profits.     

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.     

‘Coastal squeeze’— an historical perspective

The use of salt marsh for agricultural use has probably been going on for thousands of years. This paper will look at the situation in southeast England, particularly the Wash. Here enclosure for extended grazing and over the last several hundred years, for arable cultivation, may have taken place since Roman Times. An enclosure of Freiston Shore salt marsh (1979) and a proposed further enclosure at Gedney Drove End at about the same time raised concerns about the cumulative effect of these developments on nature conservation interests. These concerns prompted the nature conservation agencies to oppose the Gedney Drove End enclosure. Though the conservation argument did not persuade the Government that no further enclosure should take place, economic circumstances changed such that the pressure for the creation of new agricultural land diminished. This marked the end of ‘reclamation’ in the Wash. Since then, in the UK at least, there have been no further enclosures of salt marsh for agriculture. What were the arguments that lead to this change? Up to this point the perceived wisdom, in the Wash at least, was that as enclosure took place new inter-tidal land was created to seaward— with no net loss of inter-tidal land. Today we accept that this is not the case and a policy of managed re-alignment has increasingly been adopted in England, at sites ranging from the Porlock shingle ridge in north Devon to the salt marshes of Freiston in the Wash. It is argued that recognition of ‘coastal squeeze’ probably began in the Wash some 20 years ago. It would appear that we are now witnessing a reversal of this trend. How far will it take us? Will we see a return of the large expanses of tidal swamp around the Wash and elsewhere along the southern North Sea coast? Is this an inevitable consequence of global warming? This paper provides an historical perspective of the issues and arguments that have led us to recognize ‘coastal squeeze’ and the importance of dynamic coast, including the European Commission’s ‘EURosion Project’, which reported in 2004 (Salman et al. 2004).     

Strategic directions for agent-based modeling: avoiding the YAAWN syndrome

In this short communication, we examine how agent-based modeling has become common in land change science and is increasingly used to develop case studies for particular times and places. There is a danger that the research community is missing a prime opportunity to learn broader lessons from the use of agent-based modeling (ABM), or at the very least not sharing these lessons more widely. How do we find an appropriate balance between empirically rich, realistic models and simpler theoretically grounded models? What are appropriate and effective approaches to model evaluation in light of uncertainties not only in model parameters but also in model structure? How can we best explore hybrid model structures that enable us to better understand the dynamics of the systems under study, recognizing that no single approach is best suited to this task? Under what circumstances – in terms of model complexity, model evaluation, and model structure – can ABMs be used most effectively to lead to new insight for stakeholders? We explore these questions in the hope of helping the growing community of land change scientists using models in their research to move from ‘yet another model’ to doing better science with models.     

How well do sunken vessels approximate fish assemblages on coral reefs? Conservation implications of vessel-reef deployments

The amount of artificial habitat (termed ??artificial reef??, AR) in marine systems is rapidly increasing, yet the effect of most types of AR on reef communities remains unknown. We examined the role of well-established vessel-reefs in structuring coral reef fish assemblages by comparing assemblages on 7 World War II wrecks (>65?years old) to those on interspersed coral patch reefs of comparable size in a tropical lagoon. Fish abundance, species richness, diversity and feeding guild structure on wrecks were similar to natural reefs; however, species composition differed between the two reef types (R?=?0.189?C0.341, average dissimilarity: 67.3?C68.8?%). Despite being more species-rich and diverse, fish assemblages on larger wrecks were less similar to assemblages on their adjacent natural reefs than smaller wrecks. Wrecks may also have affected fish abundance on adjacent natural reefs, with reefs adjacent to larger wrecks supporting higher abundances than reefs adjacent to smaller wrecks. Our results indicate that increases in vessel-reef habitat may not greatly affect reef fish assemblage parameters, but may affect the relative abundances of particular species.     

Spatio-temporal patterns in the diversity of demersal fish communities off the south coast of South Africa

The diversity of ecological communities has been the focus of many studies. Because biodiversity provides several indicators used in an Ecosystem Approach to Fisheries (EAF) to track changes in fish communities, we investigated the spatial and temporal patterns in the diversity of some demersal fish communities subjected to varying fishing pressure. Depth and catch rate were the most important predictors in explaining changes in diversity followed by longitude and survey year. Diversity, as measured by the various indices except for taxonomic distinctness (∆*), initially declined with increasing depth to about a depth of 80 m, then increased to about 150 m after which it declined. Taxonomic distinctness index (∆*) showed an increase in the taxonomic heterogeneity of the demersal community below the 300-m isobath. Diversity remained relatively constant with increase in longitude to around 24°E (which has the lowest diversity) after which it increased. The assessment of the temporal trend in diversity indicates that survey year has a significant effect on all diversity indices except for ∆*. Diversity increased and dominance declined with time. This may be result of a decline in the abundance of dominant species or an increase in the abundance less dominant species, or a combination of both effects. Multivariate analysis of the set of diversity indices showed three groups of indices: those reflecting species richness (S, Margalef’s d), those measuring mainly taxonomic relatedness (∆*), and those balancing the richness and evenness components of diversity (J′, H′, λ, ∆, Hill’s N1, and Hill’s N2). The relationship between evenness, catch rate, and size was also investigated. Size classes with highest evenness were found to have lowest catch rate and vice versa. This highlights the need to consider the size and trophic level of species when linking diversity to the functioning of ecosystems.     

Fishing the line near marine reserves in single and multispecies fisheries.

Throughout the world "fishing the line" is a frequent harvesting tactic in communities where no-take marine reserves are designated. This practice of concentrating fishing effort at the boundary of a marine reserve is predicated upon the principle of spillover, the net export of stock from the marine reserve to the surrounding unprotected waters. We explore the consequences and optimality of fishing the line using a spatially explicit theoretical model. We show that fishing the line: (1) is part of the optimal effort distribution near no-take marine reserves with mobile species regardless of the cooperation level among harvesters; (2) has a significant impact on the spatial patterns of catch per unit effort (CPUE) and fish density both within and outside of the reserve; and (3) can enhance total population size and catch simultaneously under a limited set of conditions for overexploited populations. Additionally, we explore the consequences of basing the spatial distribution of fishing effort for a multispecies fishery upon the optimality of the most mobile species that exhibits the greatest spillover. Our results show that the intensity of effort allocated to fishing the line should instead be based upon more intermediate rates of mobility within the targeted community. We conclude with a comparison between model predictions and empirical findings from a density gradient study of two important game fish in the vicinity of a no-take marine-life refuge on Santa Catalina Island, California (USA). These results reveal the need for empirical studies to account for harvester behavior and suggest that the implications of spatial discontinuities such as fishing the line should be incorporated into marine-reserve design.     

Shifts in a Pacific Ocean Fish Assemblage: the Potential Influence of Exploitation

Abstract:  As in many regions of the world, marine fishes and invertebrates along the Pacific coast of the United States have long been subjected to overexploitation. Despite this history, however, we lack basic information on the current status of many fishes along this coastline. We used data from a quarter century of fishery-independent, coast-wide trawl surveys to study systematically the demersal fish assemblages along the U.S. Pacific coast. We documented fundamental shifts in this fish assemblage. Average fish size, across a diversity of species, has declined 45% in 21 years. There have been major shifts in the constituent species of the assemblage, with some species achieving annual population growth rates of >10% and others declining in excess of 10% per year. Annual rate of change in population size appeared to be a function of life history interacting with fishing pressure. Negative trends in population size were particularly apparent in rockfish ( Sebastes spp.). However, across all taxa examined, trends in population size were associated with size of maturity, maximum size, and growth rate. Trends in population size were associated inversely with harvest levels, but stocks that mature late tended to decline faster than would be predicted by catch rates alone. Our results are disquieting because they raise the possibility that fishing-induced phase shifts in fish communities may affect the recovery of fishes, even after the implementation of severe fishing restrictions.     

Zooplankton proportion estimates from non-uniform sample volumes

The relative abundance of organisms from different taxa provides information about ecosystem health and diversity. When the numbers of sampled organisms are modelled as Poisson counts, and the sample volumes are not uniform, variance for the proportion attributable to each taxon is difficult to compute. We present a method for computing approximate variances for this situation. The point estimates and their standard errors reduce to the standard multinomial maximum likelihood results when sample volumes are uniform. Further, given initial estimates of population densities for the taxa of interest, optimal sample volumes can be computed. The methods are illustrated for zooplankton counts from Andrus Lake, Michigan.     

Site fidelity and homing behaviour in intertidal fishes

The theory of ecological cognition poses that the brains and behaviour of animals are shaped by the environmental challenges they face in their everyday lives. Site fidelity and homing ability was tested for five species of intertidal rock pool fish by tagging and displacing them to new rock pools at various distances from their ‘home’ rock pools. Three of the species were rock pool specialists whilst the remaining two spend a small proportion of their life in rock pools during early ontogeny. The three specialists showed strong site fidelity with >50 % of individuals found in the same pool 42 days after tagging. In contrast, the non-specialist species showed low fidelity and poor homing abilities. Homing success in the rock pool specialists remained relatively stable as displacement distance increased. The effect of body size on homing ability was species dependent, with only one species showing a significantly greater tendency to home with increasing size.     

Simulation model of universal law of school size distribution applied to southern bluefin tuna (Thunnus maccoyii) in the Great Australian Bight

A universal law of animal group size distribution correlates well to observed fish school size distribution from fisheries catch data. I applied the law to fisheries independent aerial survey data of southern bluefin tuna (Thunnus maccoyii) collected over a 10-year period in the Great Australian Bight. The law does not correlate to the observed school size distribution. A computer model originally demonstrated the formation of the universal law from simple rules. I redesigned this model as an individual-based simulation model calibrated from acoustic tag observations and state a mathematical formula for a resultant new family of transient group size distributions. The new formula correlates accurately to the simulation and to the aerial survey data. I use the mathematical model to estimate area of aggregation and total abundance. This approach is new as it does not seek stationary states of group size distribution and because it demonstrates a quantitative relationship between individual behaviour and group size distribution. This work elevates the pattern of group size distribution from a curiosity to a useful tool, and introduces a new family of transient distributions that may have a general application to other grouping phenomena.     

Multiscale advanced raster map analysis system: Definition, design and development

This paper brings together a multidisciplinary initiative to develop advanced statistical and computational techniques for analyzing, assessing, and extracting information from raster maps. This information will provide a rigorous foundation to address a wide range of applications including disease mapping, emerging infectious diseases, landscape ecological assessment, land cover trends and change detection, watershed assessment, and map accuracy assessment. It will develop an advanced map analysis system that integrates these techniques with an advanced visualization toolbox, and use the system to conduct large case studies using rich sets of raster data, primarily from remotely sensed imagery. As a result, it will be possible to study and evaluate raster maps of societal, ecological, and environmental variables to facilitate quantitative characterization and comparative analysis of geospatial trends, patterns, and phenomena. In addition to environmental and ecological studies, these techniques and tools can be used for policy decisions at national, state, and local levels, crisis management, and protection of infrastructure. Geospatial data form the foundation of an information-based society. Remote sensing has been a vastly under-utilized resource involving a multi-million dollar investment at the national levels. Even when utilized, the credibility has been at stake, largely because of lack of tools that can assess, visualize, and communicate accuracy and reliability in timely manner and at desired confidence levels. Consider an imminent 21st century scenario: What message does a multi-categorical map have about the large landscape it represents? And at what scale, and at what level of detail? Does the spatial pattern of the map reveal any societal, ecological, environmental condition of the landscape? And therefore can it be an indicator of change? How do you automate the assessment of the spatial structure and behavior of change to discover critical areas, hot spots, and their corridors? Is the map accurate? How accurate is it? How do you assess the accuracy of the map? How do we evaluate a temporal change map for change detection? What are the implications of the kind and amount of change and accuracy on what matters, whether climate change, carbon emission, water resources, urban sprawl, biodiversity, indicator species, human health, or early warning? And with what confidence? The proposed research initiative is expected to find answers to these questions and a few more that involve multi-categorical raster maps based on remote sensing and other geospatial data. It includes the development of techniques for map modeling and analysis using Markov Random Fields, geospatial statistics, accuracy assessment and change detection, upper echelons of surfaces, advanced computational techniques for geospatial data mining, and advanced visualization techniques.     

Synergistic interactions between chemical alarm cues and the presence of conspecific and heterospecific fish shoals

Chemical and visual sources of information are used by aquatic prey during risk assessment. Here, we test the behavioral response of littoral prey fish to combinations of chemical alarm cues (skin extract) and the visual presence of a fish shoal. We scented minnow traps with either alarm cues or water (control) placed inside the trap, a jar that contained either a fish shoal or nothing (control), and recorded the number and species of fish captured. We predicted that chemical alarm cues would reduce the number of fish captured and that a fish shoal would increase the number of fish captured. The predicted effect of chemical and visual cues combined depended on the nature of the interaction. We found that the lowest catch rate was for the combination of alarm cue + no shoal, but the highest catch rate occurred for the combination of alarm cue + shoal. Fish shoal + water had the second highest catch rate and no shoal + water had the second lowest catch rate. We conclude that chemical alarm cues induce area avoidance in the absence of a shoal, but a strong behavioral proclivity to increase shoal cohesion in the presence of a shoal. The presence of a shoal in the traps induced alarmed fish to shoal with them and thus, enter the traps. This occurred even though traps were the source of the alarm cue.Communicated by A. Mathis     

Conditions for coexistence of freshwater mussel species via partitioning of fish host resources

Riverine freshwater mussel species can be found in highly diverse communities where many similar species coexist. Mussel species potentially compete for food and space as adults, and for fish host resources during the larval (glochidial) stage. Resource partitioning at the larval stage may promote coexistence. A model of resource utilization was developed for two mussel species and analyzed to determine conditions for coexistence. Mussel species were predicted to coexist when they differed in terms of their success in contacting different fish host species; very similar strategies offered limited possibilities for coexistence. Differences in the mussel species’ maximum infestation loads on the fish hosts that coincided with differences in their fish host contact success promoted coexistence. Mussel species with a given set of trade-offs in fish host use were predicted to coexist only for a subset of relative fish host abundances, so a shift in relative fish host abundances could result in the loss of a mussel species. An understanding of the conditions for freshwater mussel species coexistence can help explain high mussel diversity in rivers and guide ongoing conservation activities.     

Measuring the impact of dynamic antipredator traits on predator-prey-resource interactions

This article analyzes the limitations of the most widely used method for quantifying the impact of dynamic antipredator traits on food chain dynamics and discusses alternative approaches. The standard method for a predator-prey-resource chain estimates the effects of the prey's defensive behavior by comparing population densities or fitness measures in a "predator cue" treatment to those in a no-predator treatment. This design has been interpreted as providing a measure of the "nonconsumptive effect" of the predator on the prey and the "trait-mediated indirect effect" of the predator on the resource. Other approaches involve measurements of the impact of the behavior in the presence of functional predators. The questions addressed here are: (1) How consistent are the results of different approaches? (2) How time-dependent are their results? (3) How well do they correspond to theoretical measures of effect size? (4) How useful are the measurements in understanding system dynamics? A model of a tritrophic system in which the prey species adjusts a defensive trait adaptively is used to evaluate the experimental designs. Measures of changes in prey fitness or population density in a cue treatment generally include offsetting effects of the cost of the behavior and the benefit of more resources. This means that the sign of the effect, as well as its magnitude, may change depending on when the experiment is terminated. Because predation is not present in the cue treatment, few conclusions can be drawn about the impact of the behavior on population densities or fitness of the prey in a natural setting with predators. Cue experiments often do not accurately separate trait-mediated from density-mediated effects on the resource. Most scalar measures of effects are sensitive to experimental duration and initial densities. Use of a wider range of experimental designs to measure trait-related effects is called for.     

Structure,composition and seasonal dynamics of the larval and juvenile fish community in the mangrove estuary of Tanshui River,Taiwan

The temporal and spatial patterns of species composition and abundance of fish larvae and juveniles in the Tanshui River mangrove estuary (Taiwan) were studied monthly using a drift bag-net in daylight. A total of 44591 individuals representing 55 families and 105 species were collected over 12 mo (August 1989 to July 1990). The community was dominated numerically by a few species. Sardinella melanura was most numerous, making up 70.15% of the total catch, followed by Stolephorus buccaneeri (19.59%), Thryssa kammalensis (2.96%), and Gerres abbreviatus (2.61%). These four species constituted ca. 95% of the total catch, the remaining 5% consisted of another 101 species. This estuary functions as a nursery and feeding area in the early life history of these fish. There was a separation in peak-immigration and seasonal utilization of the estuary by the dominant species. The abundance of fish larvae and juveniles decreased in an upstream direction.