捕捞对北部湾海洋生态系统的影响

利用Ecopath with Ecosim (EwE) 5.1软件构建了北部湾海洋生态系统1959—1960年的Ecosim模型,包含渔业、海洋哺乳动物、海鸟、中上层鱼类、底层鱼类、底栖无脊椎动物等20个功能组,通过与1997—1999年调查数据对比,分析了捕捞活动对北部湾生态系统的结构和功能的影响.结果表明：近40年来在捕捞强度不断增加的压力下,生态系统的结构和功能发生显著变化,长寿命、高营养级的肉食性鱼类生物量下降明显,系统以短寿命、小型鱼类和无脊椎动物占优势.1999年的大中型鱼类的生物量仅为1960年的6%,而小型鱼类和无脊椎动物则明显上升,尤其是头足类生物量上升了2.7倍,渔获物的营养级则从1960年的3.2降低到1999年的298,体现了“捕捞降低海洋食物网”的特点,目前的开发模式是不可持续的.利用20世纪90年代数据预测了降低捕捞压力后生态系统的变化.本研究证实了可以使用Ecosim模型预测捕捞压力对生态系统的影响.     

Trophic interactions and community structure in the upwelling system off Central Chile (33-39°S)

Trophic interactions and community structure in the upwelling system off Central Chile (USCCh) (33-39°S) are analyzed using biological and ecological data concerning the main trophic groups and the Ecopath with Ecosim software version 5.0 (EwE). The model encompasses the fisheries, cetaceans, sea lion, marine birds, cephalopods, large-sized pelagic fish (sword fish), medium-sized pelagic fish (horse mackerel, hoki), small-sized pelagic fish (anchovy, common sardine), demersal fish (e.g. Chilean hake, black conger-eel), benthic invertebrates (red squat lobster, yellow squat lobster) and other groups such as zooplankton, phytoplankton and detritus. Input data was gathered from published and unpublished reports and our own estimates. Trophic interactions, system indicators and food web attributes are calculated using network analysis routines included in EwE. Results indicate that trophic groups are aligned around four trophic levels (TL) with phytoplankton and detritus at the TL=1, while large-sized pelagic fish and cetaceans are top predators (TL>4.0). The fishery is located at an intermediate to low trophic level (TL=2.97), removing about 15% of the calculated system primary production. The pelagic realm dominates the system, with medium-sized pelagic fish as the main fish component in biomass, while small-sized pelagic fish dominate total landings. Chilean hake is by far the main demersal fish component in both, biomass and yield. Predators consume the greater part of the production of the most important fishery resources, particularly juvenile stages of Chilean hake. Consequently, mortality by predation is an important component of total mortality. However, fishery also removes a large fraction of common sardine, anchovy, horse mackerel, and Chilean hake. The analysis of direct and indirect trophic impacts reveals that Chilean hake is a highly cannibalistic species. Chilean hake is also an important predator on anchovy, common sardine, benthic invertebrates, and demersal fish. The fisheries heavily impact on Chilean hake, common sardine, anchovy, and horse mackerel. Total system biomass (B=476 t km⁻² year⁻¹) and throughput (T=89454 t km⁻² year⁻¹) estimated in the USCCh model are in accordance with models of comparable systems. Considering system attributes derived from network analysis, the USCCh can be characterized as an immature system, with short trophic chains and low trophic transfer efficiency. Finally, we suggest that trophic interactions should be considered in stock assessment and management programs in USCCh. In addition, future research programs should be carried out in order to understand the ecosystem effects of fishing and trophic control in this highly productive food web.     

Combined Fishing and Climate Forcing in the Southern Benguela Upwelling Ecosystem: An End-to-End Modelling Approach Reveals Dampened Effects

The effects of climate and fishing on marine ecosystems have usually been studied separately, but their interactions make ecosystem dynamics difficult to understand and predict. Of particular interest to management, the potential synergism or antagonism between fishing pressure and climate forcing is analysed in this paper, using an end-to-end ecosystem model of the southern Benguela ecosystem, built from coupling hydrodynamic, biogeochemical and multispecies fish models (ROMS-N₂P₂Z₂D₂-OSMOSE). Scenarios of different intensities of upwelling-favourable wind stress combined with scenarios of fishing top-predator fish were tested. Analyses of isolated drivers show that the bottom-up effect of the climate forcing propagates up the food chain whereas the top-down effect of fishing cascades down to zooplankton in unfavourable environmental conditions but dampens before it reaches phytoplankton. When considering both climate and fishing drivers together, it appears that top-down control dominates the link between top-predator fish and forage fish, whereas interactions between the lower trophic levels are dominated by bottom-up control. The forage fish functional group appears to be a central component of this ecosystem, being the meeting point of two opposite trophic controls. The set of combined scenarios shows that fishing pressure and upwelling-favourable wind stress have mostly dampened effects on fish populations, compared to predictions from the separate effects of the stressors. Dampened effects result in biomass accumulation at the top predator fish level but a depletion of biomass at the forage fish level. This should draw our attention to the evolution of this functional group, which appears as both structurally important in the trophic functioning of the ecosystem, and very sensitive to climate and fishing pressures. In particular, diagnoses considering fishing pressure only might be more optimistic than those that consider combined effects of fishing and environmental variability.     

Ecological role and historical trends of large pelagic predators in a subtropical marine ecosystem of the South Atlantic

Large pelagic predators occupy high positions in food webs and could control lower trophic level species by direct and indirect ecological interactions. In this study we aimed to test the hypotheses: (1) pelagic predators are keystone species, and their removals could trigger impacts on the food chain; (2) higher landings of pelagic predators could trigger fishing impacts with time leading to a drop in the mean trophic level of catches; and (3) recovery in the pelagic predators populations, especially for sharks, could be achieved with fishing effort reduction. We performed a food web approach using an Ecopath with Ecosim model to represent the Southeastern and Southern Brazil, a subtropical marine ecosystem, in 2001. We then calibrated the baseline model using catch and fishing effort time series from 2001 to 2012. Afterwards, we simulated the impact of fishing effort changes on species and assessed the ecological impacts on the pelagic community from 2012 to 2025. Results showed that the model was well fitted to landing data for the majority of groups. The pelagic predators species were classified as keystone species impacting mainly on pelagic community. The ecosystem was resilient and fisheries seem sustainable at that time. However, the temporal simulation, from 2001 to 2012, revealed declines in the biomass of three sharks, tuna and billfish groups. It was possible observe declines in the mean trophic level of the catch and in the mean total length of landings. Longline fisheries particularly affected the sharks, billfish and swordfish, while hammerhead sharks were mostly impacted by gillnet fishery. Model simulations showed that large sharks’ biomasses could be recovered or maintained only after strong fishing effort reduction.     

Ecological effects of longline fishing and climate change on the pelagic ecosystem off eastern Australia

Pelagic longline fisheries target (or catch incidently) large apex predators in the open ocean (e.g. tunas, billfish and sharks) and have the potential to disrupt the ecosystem functionality if these predators exert strong top–down control. In contrast, warming of oceans from climate change may increase bottom–up effects from increases in primary productivity. An ecosystem model of a large pelagic ecosystem off eastern Australia was constructed to explore the potential ecological effects of climate change and longlining by Australia’s Eastern Tuna and Billfish Fishery. The model reproduced historic biomass and fishery catch trends from 1952 to 2006 for seven functional groups. Simulated changes in fishing effort and fishing mortality rate on individual target species from 2008 to 2018 resulted in only modest (<20%) changes in the biomass of target species and their direct predators or competitors. A simulated increase in phytoplankton biomass due to climate change resulted in only small increases (<11%) in the biomass of all groups. However, climate-related changes to the biomass of micronekton fish (−20%) and cephalopods (+50%) resulted in trophic cascades. Our results suggest there may be ecological redundancy among high trophic level predators since they share a diverse suite of prey and collectively only represent <1% of the total system biomass. In contrast, micronekton fishes and cephalopods have high biomasses and high production and consumption rates and are important as both prey and predators. They appear to exert ‘wasp–waist’ control of the ecosystem rather than top–down or bottom–up processes reported to drive other pelagic systems.     

北部湾生态通道模型的构建

根据1997年～1999年在北部湾进行的渔业资源和生态环境调查数据,利用EwE软件构建北部湾生态系统的营养通道模型,模型由16个功能组构成,包括了哺乳动物和海鸟,每一组都代表在生态系统中具有相似地位的有机体,基本覆盖了北部湾生态系统能量流动的主要过程.模型分析表明,北部湾生态系统的能量流动主要以捕食食物链途径为主,其中无脊椎动物在能量从低级向高层次转换中起关键作用.各功能组的营养级范围为1.00～4.04,哺乳动物占据了最高营养层.生态网络分析表明,系统的能量流动主要有6级,来自初级生产者的能流效率为12.2%,来自碎屑的转换效率为12.3%,平均能量转换效率为12.2%.模型估算的可利用的生物量密度为8.7 t·km^-2,生态系统的生物生产量只占系统净初级生产力的1.81%.当前北部湾海洋生态系统处于不稳定状态.     

Exploring the dynamics of ecological indicators using food web models fitted to time series of abundance and catch data

Previously, standardized snap-shot models of the Southern Benguela (1980–1989), Southern Humboldt (1992) and Southern Catalan Sea (1994) ecosystems were examined and found to facilitate assessment of ecosystem characteristics related to the gradient in exploitation status of the ecosystems; highest level of exploitation in the South Catalan Sea (North-western Mediterranean), high in the Southern Humboldt and lower in the Southern Benguela. Subsequently, these models were calibrated and fitted using available catch, fishing effort/mortality and abundance data series and incorporated environmental and internal drivers. This study furthers the previous comparative analyses by comparing changes in ecosystem structure using a selection of ecosystem indicators from the calibrated models and assessing how these indicators change over time in these three contrasting ecosystems. Indicators examined include community turnover rates (production/biomass), trophic level of landings and the community, biodiversity indicators, ratios of predatory/forage fish and pelagic/demersal fish biomass, catch ratios, and network analysis indicators. Using the set of model-derived indicators, the three ecosystems were ranked in terms of exploitation level. This ranking was performed using the values of these indicators in recent years (ecosystem state) as well as their trends over time (ecosystem trend). The non-parametric Kruskal–Wallis and Median tests were used to test for significance of the difference between indicators from the three ecosystems in the last 5 years of the simulation to compare present ecosystem states. We compared the slope of the lineal trend and its significance between ecosystems using the generalized least-squares regression taking auto-correlation into consideration to analyse ecosystem trends. The indicators that capture better the high impacts of fishing prevalent in the Mediterranean and Humboldt ecosystems, and the more conservative exploitation of the Southern Benguela, are the fish/invertebrates biomass and catch ratio, the demersal/pelagic fish biomass and catch ratio (depending on the ecosystem and the fishery being developed), flows to detritus, and the mean trophic level of the community (when large, poorly quantified groups such as zooplankton and detritus are excluded). This study suggests that the best option for classifying ecosystems according to the impact of fishing is to consider a broad range of indicators to understand how and why an ecosystem is responding to particular environmental or fishing drivers (or more likely a combination of these). Our results highlight the importance of including indicators capturing trends over time as well as recent ecosystem states. We also identified 23 pairs of indicators that correlated similarly in the three ecosystems (they showed a significant correlation with same sign). Further comparisons may contribute towards generalization of this list, progressing towards a better understanding of the behaviour of ecological indicators.     

Trophic levels of teleost and elasmobranch species in the Persian Gulf and Oman Sea

Knowing the trophic level of marine organisms is essential to understanding their ecological role in the ecosystem and for quantifying the ecosystem effects of fishing to establish effective management of fishing resources. In comparison to other systems, information about the trophic level of marine organisms in the Persian Gulf and Oman Sea is very scarce. Here, the main aim was to estimate trophic level in these areas using all available diet information from different marine species using TrophLab software. The trophic level of 32 fish species was estimated with the available diet data. The trophic level ranged from 2.28 to 4.50. High trophic levels were found for Chorocentrus nudus (TL = 4.7), Saurida tumbil (TL = 4.6), Rhizoprionodon acutus (TL = 4.5), Torpedo sinuspersici (TL=4.5), Gymnura poecilura (TL = 4.5), Sphyraena putnamae (TL = 4.5) and Euthynnus affinis (TL = 4.5). In contrast, lower trophic levels were estimated for Tenualosa ilisha (TL = 2.28) and Sardinella sindensis (TL = 2.92). As expected, a positive correlation was found between the trophic level and body size, indicating changes in the diet due to variations in predatory capacities. The results of this study may be useful in the formulation of trophic indicators and modelling of the ecosystems.     

Reef Fishes at All Trophic Levels Respond Positively to Effective Marine Protected Areas

Marine Protected Areas (MPAs) offer a unique opportunity to test the assumption that fishing pressure affects some trophic groups more than others. Removal of larger predators through fishing is often suggested to have positive flow-on effects for some lower trophic groups, in which case protection from fishing should result in suppression of lower trophic groups as predator populations recover. We tested this by assessing differences in the trophic structure of reef fish communities associated with 79 MPAs and open-access sites worldwide, using a standardised quantitative dataset on reef fish community structure. The biomass of all major trophic groups (higher carnivores, benthic carnivores, planktivores and herbivores) was significantly greater (by 40% - 200%) in effective no-take MPAs relative to fished open-access areas. This effect was most pronounced for individuals in large size classes, but with no size class of any trophic group showing signs of depressed biomass in MPAs, as predicted from higher predator abundance. Thus, greater biomass in effective MPAs implies that exploitation on shallow rocky and coral reefs negatively affects biomass of all fish trophic groups and size classes. These direct effects of fishing on trophic structure appear stronger than any top down effects on lower trophic levels that would be imposed by intact predator populations. We propose that exploitation affects fish assemblages at all trophic levels, and that local ecosystem function is generally modified by fishing.     

An ecological model of the artificial ecosystem (northern Hangzhou Bay,China): analysis of ecosystem structure and fishing impacts

The artificial ecosystem is a large-scale enclosure in northern Hangzhou Bay, China. Using the Ecopath with Ecosim software, a trophic structure model is constructed for 2006–2007 to characterize the food web structure, functioning, and describing the ecosystem impacts of fishing. Input information for the model were gathered from published and unpublished reports and from our own estimates during the period 2006–2007. Pedigree work and simple sensitivity analysis were carried out to evaluate the quality and the uncertainty of the model. Results show that the food web in the enclosed sea area was dominated by a detritus pathway. The trophic levels of the groups varied from 1.00 for primary producers and detritus to 3.90 for piscivorous fish in the artificial system. Using network analysis, the system network was mapped into a linear food chain, and five discrete trophic levels were found with a mean transfer efficiency of 9.8% from detritus, 9.4% from primary producer within the ecosystem. The geometric mean of the trophic transfer efficiencies was 9.5%. Detritus contributed 57% of the total energy flux, and the other 43% came from primary producers. The ecosystem maturity indices-TPP/TR (total primary production/total respiration), FCI (Finn cycling index), A (ascendancy) and TB/TDET were 2.672, 25%, 31.5%, and 0.013, respectively, showing that the artificial system is at developmental stage according to Odum’s theory of ecosystem development. The ‘Keystoneness’ result indicates that herbivorous zooplankton was identified as keystone species in this system. Furthermore, a simple dynamical simulation was preformed for varying fishing mortality over 10 years. The biomass of most fish groups has a small increase when the fishing mortality at current level. Increasing fishing mortality by twofold resulted in a marked decrease in biomass of piscivorous fish accompanied by an increase in that of other fish groups, notable zooplanktivorous fish. Generally, this study represents the first attempt to evaluate the food web structure and the potential effects of fisheries in the artificial coastal ecosystem. It is concluded that this model is a potential tool for use in the management of the artificial ecosystem in northern Hangzhou Bay.     

北部湾秋季底层鱼类多样性和优势种数量的变动趋势

根据1992年、2001年和2006年秋季在北部湾进行的底拖网调查数据,对该海域鱼类的种类组成、物种多样性、优势种及其数量的变动趋势进行分析。1992年共记录鱼类171种,隶属17目77科;2001年记录鱼类156种,隶属18目71科;2006年记录157种,隶属17目67科。3个年代记录的鱼类均以鲈形目的种类数最多,其中1992年为96种(占56.14%)、2001年90种(占57.69%)和2006年89种(占56.69%)。鱼类的Pielou均匀度指数(J')和Shannon-Wiener多样性指数(H')的变化趋势一致:以2001年最高,为0.72和3.64;其次为1992年,为0.64和3.27;2006年最低,分别为0.52和2.64。丰富度指数(D)呈逐年下降的趋势:为1992年的21.03,2001年的20.74和2006年的19.61。建立非线性回归模型对北部湾3个年代出现的6种共有优势种(发光鲷Acropoma japonicum、带鱼Trichiurus haumela、二长棘鲷Parargyrops edita、黄斑鲾Leiognathus bindus、竹荚鱼Trachurus japonicus和黄带绯鲤Upeneus sulphureus)的数量变化趋势进行分析。结果表明:北部湾鱼类中的经济价值较高的优势种逐渐被低值和小型的鱼类所替代,但繁殖力较强和寿命较短的鱼类变动较小。在6种共同优势种中,黄斑鲾和发光鲷的渔获率呈上升趋势;带鱼和黄带绯鲤的渔获率呈下降趋势;而二长棘鲷和竹荚鱼的渔获率基本保持不变。研究结果表明,北部湾鱼类的优势种更替明显,总体变化趋势是k选择种类(以红笛鲷和黑印真鲨等为代表)逐渐被r选择种类(发光鲷、鲾科和天竺鱼科等为代表)所替代,即寿命长、个体大和营养级高的鱼类数量减少,寿命短、个体小和营养级较低的种类增多。     

Overfishing and the Replacement of Demersal Finfish by Shellfish: An Example from the English Channel

The worldwide depletion of major fish stocks through intensive industrial fishing is thought to have profoundly altered the trophic structure of marine ecosystems. Here we assess changes in the trophic structure of the English Channel marine ecosystem using a 90-year time-series (1920–2010) of commercial fishery landings. Our analysis was based on estimates of the mean trophic level (mTL) of annual landings and the Fishing-in-Balance index (FiB). Food webs of the Channel ecosystem have been altered, as shown by a significant decline in the mTL of fishery landings whilst increases in the FiB index suggest increased fishing effort and fishery expansion. Large, high trophic level species (e.g. spurdog, cod, ling) have been increasingly replaced by smaller, low trophic level fish (e.g. small spotted catsharks) and invertebrates (e.g. scallops, crabs and lobster). Declining trophic levels in fisheries catches have occurred worldwide, with fish catches progressively being replaced by invertebrates. We argue that a network of fisheries closures would help rebalance the trophic status of the Channel and allow regeneration of marine ecosystems.     

Modelling marine ecosystem response to climate change and trawling in the North Sea

The marine ecosystem response to climate change and demersal trawling was investigated using the coupled hydrodynamic-biogeochemical water column model GOTM-ERSEM-BFM for three contrasting sites in the North Sea. Climate change forcing was derived from the HadRM3-PPE-UK regional climate model for the UK for the period 1950–2100 using historical emissions and a medium emissions scenario (SRESA1B). Effects of demersal trawling were implemented as an additional mortality on benthic fauna, and changes in the benthic–pelagic nutrient and carbon fluxes. The main impacts of climate change were (i) a temperature-driven increase in pelagic metabolic rates and nutrient cycling, (ii) an increase in primary production fuelled by recycled nutrients, (iii) a decrease in benthic biomass due to increased benthic metabolic rates and decreased food supply as a result of the increased pelagic cycling, and (iv) a decrease in near-bed oxygen concentrations. The main impacts of trawling were (i) reduced benthic biomass due to the increased mortality, and (ii) the increased benthic–pelagic nutrient fluxes, with these effects counteracting each other, and relatively small changes in other variables. One important consequence was a large decrease in the de-nitrification flux predicted at the two summer-stratified sites because less benthic nitrate was available. The effects of trawling scaled linearly with fishing effort, with greatest sensitivity to fishing in summer compared to fishing in winter. The impacts of climate change and trawling were additive, suggesting little or no non-linear interactions between these disturbances.     

Ecosystem Overfishing in the Ocean

Fisheries catches represent a net export of mass and energy that can no longer be used by trophic levels higher than those fished. Thus, exploitation implies a depletion of secondary production of higher trophic levels (here the production of mass and energy by herbivores and carnivores in the ecosystem) due to the removal of prey. The depletion of secondary production due to the export of biomass and energy through catches was recently formulated as a proxy for evaluating the ecosystem impacts of fishing–i.e., the level of ecosystem overfishing. Here we evaluate the historical and current risk of ecosystem overfishing at a global scale by quantifying the depletion of secondary production using the best available fisheries and ecological data (i.e., catch and primary production). Our results highlight an increasing trend in the number of unsustainable fisheries (i.e., an increase in the risk of ecosystem overfishing) from the 1950s to the 2000s, and illustrate the worldwide geographic expansion of overfishing. These results enable to assess when and where fishing became unsustainable at the ecosystem level. At present, total catch per capita from Large Marine Ecosystems is at least twice the value estimated to ensure fishing at moderate sustainable levels.     

Long-term changes in Krill biomass and distribution in the Barents Sea: are the changes mainly related to capelin stock size and temperature conditions?

Krill plays a significant role in the Barents Sea ecosystem, providing energy transport between different trophic levels. The current paper presents the results of a long-term study (1980–2009) based on pelagic trawl catches from August to September. Our investigations show that the krill species were distributed widely in the Barents Sea and that the largest krill concentrations were restricted to the west-central and eastern parts of the Barents Sea. The current paper presents the relative biomass indices, and the estimates must be interpreted as minimum biomass. The mean annual krill biomass was estimated to be 22 million tonnes in wet weight, with the highest values being as much as 48 million tonnes. Capelin is the largest pelagic stock, and in some years, their biomass can amount to 4–7 million tonnes, which can impose high predation pressure on krill. When their biomass is high, capelin may consume close to 26 million tonnes annually. The predation from pelagic (herring and blue whiting) and bottom (cod and haddock) fish species was much lower, being 9 and 1 million tonnes, respectively. A negative relationship between krill biomass and capelin stock size above 74°N was observed during the study period. However, during the last decade, the krill biomass has increased despite heavy predation from capelin in some years. A positive significant linear relationship between the mean annual Kola temperature and the krill biomass seems to indicate that the recent warming conditions have favourable impacts on the krill populations in the Barents Sea.     

Human activities as a driver of spatial variation in the trophic structure of fish communities on Pacific coral reefs

Anthropogenic activities such as land‐use change, pollution and fishing impact the trophic structure of coral reef fishes, which can influence ecosystem health and function. Although these impacts may be ubiquitous, they are not consistent across the tropical Pacific Ocean. Using an extensive database of fish biomass sampled using underwater visual transects on coral reefs, we modelled the impact of human activities on food webs at Pacific‐wide and regional (1,000s–10,000s km) scales. We found significantly lower biomass of sharks and carnivores, where there were higher densities of human populations (hereafter referred to as human activity); however, these patterns were not spatially consistent as there were significant differences in the trophic structures of fishes among biogeographic regions. Additionally, we found significant changes in the benthic structure of reef environments, notably a decline in coral cover where there was more human activity. Direct human impacts were the strongest in the upper part of the food web, where we found that in a majority of the Pacific, the biomass of reef sharks and carnivores were significantly and negatively associated with human activity. Finally, although human‐induced stressors varied in strength and significance throughout the coral reef food web across the Pacific, socioeconomic variables explained more variation in reef fish trophic structure than habitat variables in a majority of the biogeographic regions. Notably, economic development (measured as GDP per capita) did not guarantee healthy reef ecosystems (high coral cover and greater fish biomass). Our results indicate that human activities are significantly shaping patterns of trophic structure of reef fishes in a spatially nonuniform manner across the Pacific Ocean, by altering processes that organize communities in both “top‐down” (fishing of predators) and “bottom‐up” (degradation of benthic communities) contexts.     

A framework to assess the health of rocky reefs linking geomorphology,community assemblage,and fish biomass

The recovery of historic community assemblages on reefs is a primary objective for the management of marine ecosystems. Working under the overall hypothesis that, as fishing pressure increases, the abundance in upper trophic levels decreases followed by intermediate levels, we develop an index that characterizes the comparative health of rocky reefs. Using underwater visual transects to sample rocky reefs in the Gulf of California, Mexico, we sampled 147 reefs across 1200 km to test this reef health index (IRH). Five-indicators described 88% of the variation among the reefs along this fishing-intensity gradient: the biomass of piscivores and carnivores were positively associated with reef health; while the relative abundances of zooplanktivores, sea stars, and sea urchins, were negatively correlated with degraded reefs health. The average size of commercial macro-invertebrates and the absolute fish biomass increased significantly with increasing values of the IRH. Higher total fish biomass was found on reefs with complex geomorphology compared to reefs with simple geomorphology (r² = 0.14, F = 44.05, P < 0.0001) and the trophic biomass pyramid also changed, which supports the evidence of the inversion of biomass pyramids along the gradient of reefs’ health. Our findings introduce a novel approach to classify the health of rocky reefs under different fishing regimes and therefore resultant community structures. Additionally, our IRH provides insight regarding the potential gains in total fish biomass that may result from the conservation and protection of reefs with more complex geomorphology.     

Environmental perturbation and the structure and functioning of a tropical aquatic ecosystem

In Tissawewa, a shallow, eutrophic reservoir in southeastern Sri Lanka, the effect of a major drought on the ecosystem was studied by monitoring the size-structured fish community and its resource base. Primary production was determined as well as the production and diets of ten taxa belonging to four trophic guilds (i.e. herbivorous/detritivorous, benthivorous, zooplanktivorous/insectivorous, piscivorous) that made up more than 98% of the total fish biomass. Two extreme states of the ecosystem were distinguished. Before the drought most primary production was generated byphytoplankton, suspended fine particulate detritus was an important food source and total fish density was high. After the drought the ecosystem was characterised by high macrophyte density, low concentration of suspended detritus and low total fish density. The availability and origin of detritus appeared to be the major factor influencing fish production in Tissawewa. The small pelagic herbivore/detritivore A. melettinus contributed the most biomass and production to the fish community before the drought. After the drought, however, biomass and production dropped considerably. In contrast, the production of the most important species in terms of fisheries yield, the exotic herbivorous/detritivorous tilapias, was hardly affected. Although the composition of their food, benthic detritus, had markedly changed. In Sri Lankan reservoirs a subsidiary fishery for pelagic minor cyprinids was suggested to increase the current yield which is based almost entirely on the exotic tilapia species. The perturbation observed in this study, however, showed that the production of pelagic species was affected particularly by the environmental changes. Exploitation of these species can, therefore, only be considered in combination with hydrological and other management measures that control the environmental conditions of the reservoirs. This revised version was published online in July 2006 with corrections to the Cover Date.     

Lake size and fish diversity determine resource use and trophic position of a top predator in high‐latitude lakes

Prey preference of top predators and energy flow across habitat boundaries are of fundamental importance for structure and function of aquatic and terrestrial ecosystems, as they may have strong effects on production, species diversity, and food‐web stability. In lakes, littoral and pelagic food‐web compartments are typically coupled and controlled by generalist fish top predators. However, the extent and determinants of such coupling remains a topical area of ecological research and is largely unknown in oligotrophic high‐latitude lakes. We analyzed food‐web structure and resource use by a generalist top predator, the Arctic charr Salvelinus alpinus (L.), in 17 oligotrophic subarctic lakes covering a marked gradient in size (0.5–1084 km²) and fish species richness (2–13 species). We expected top predators to shift from littoral to pelagic energy sources with increasing lake size, as the availability of pelagic prey resources and the competition for littoral prey are both likely to be higher in large lakes with multispecies fish communities. We also expected top predators to occupy a higher trophic position in lakes with greater fish species richness due to potential substitution of intermediate consumers (prey fish) and increased piscivory by top predators. Based on stable carbon and nitrogen isotope analyses, the mean reliance of Arctic charr on littoral energy sources showed a significant negative relationship with lake surface area, whereas the mean trophic position of Arctic charr, reflecting the lake food‐chain length, increased with fish species richness. These results were supported by stomach contents data demonstrating a shift of Arctic charr from an invertebrate‐dominated diet to piscivory on pelagic fish. Our study highlights that, because they determine the main energy source (littoral vs. pelagic) and the trophic position of generalist top predators, ecosystem size and fish diversity are particularly important factors influencing function and structure of food webs in high‐latitude lakes.     

Fisheries impact on the East China Sea Shelf ecosystem for 1969–2000

An ecosystem model representing the continental shelf of the East China Sea was fitted to a time series of data available from 1969 to 2000 using Ecopath with Ecosim. We used a process-oriented model to explore the extent to which changes in marine resources and the ecosystem were driven by trophic interactions and fishing activities. Fishing effort was used to drive the model, and observed catches were compared with the predicted catches in modeling. A reduction in the sum of the squared deviations of the observed and predicted catches was used as a metric for calibrating and assessing the goodness-of-fit of the model. Trophodynamic indicators were used to explore the ecosystem’s structural and functional changes from 1969 to 2000. The model’s predictions were consistent with observed catches for most functional groups. Trophodynamic indicators suggest a degradation pattern over time: both the mean trophic level of community and a modified version of Kempton’s index of biodiversity decreased over the time, while the total flow to detritus and the loss of production due to fishing increased from 1969 to 2000. Additionally, the ratio of demersal/pelagic abundances decreased as a result of an overall decrease in the abundance of demersal species and increase in pelagic fish in the ecosystem.