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1.
利用联合国粮农组织(FAO)1950-2011年渔获物捕捞量资料, 分析了我国海域(包括大陆海域、台湾海域、香港海域和澳门海域)129种渔获物的营养级指数变化特征。研究表明, 1950-1974年我国海洋营养级指数在3.45左右波动, 1975-1978年下降至3.35左右, 1982-1987年急剧下降到3.25并维持到1996年, 1997-2011年平稳回升至3.34。与全球海洋营养级指数相比, 1984年之前我国高于全球水平, 而1984年之后则低于全球水平。就生物类群而言, 鱼类对我国海洋营养级指数的贡献最大, 达73.1-85.8%; 甲壳动物次之, 为9.2-15.5%; 软体动物较小, 为3.3-11.6%; 其他无脊椎动物的贡献最小, 不超过1.8%。过度捕捞使我国部分渔获物由原来的长寿命、高营养级的底层鱼类变为现在的短寿命、低营养级的无脊椎动物和中上层鱼类。渔业捕捞许可管理制度、禁渔期和禁渔区制度、海洋捕捞产量“零增长”和“负增长”计划、增殖放流、扩大海洋保护区面积等措施的实施可能是我国海洋营养级指数回升的主要原因。  相似文献   

2.
Trophic indicators were used to compare two Malian freshwater reservoirs whose main differences are based on their different fishing pressures. Data were collected from a scientific survey of small-scale fishery landings conducted in 2002/2003. The trophic levels of fish species caught by artisanal fisheries are estimated from observations of scientific fishing or from the metabase Fishbase. Important differences exist in the trophic structure of both reservoirs. In Selingue (with high fishing pressure), very few top predators are found in the catches while the low trophic level fishes increase in total catches. In Manantali (with low fishing pressure), the top predators contribute twice as much to catches compared to Selingue. Hence, the mean trophic level of catches in Selingue (2.80) is lower than in Manantali (2.97). When comparing these results with those of study made in 1994/1995, it clearly appears that the effects of the fishing pressure in Selingue are obvious through a decrease of 0.12 in the mean trophic level while in Manantali this mean level has increased by 0.33 due to a recent strategic targeting of top predators. Trophic spectra seem to be relevant tools to characterize exploited fish communities from multi-specific and multi-gear small-scale fisheries catch data.  相似文献   

3.
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.  相似文献   

4.
The study aimed to describe and assess indicators that can potentially contribute to the development of Ecosystem-based Approach to Fisheries Management (EAFM) of prawn stocks in the Malindi-Ungwana Bay, the most productive coastal ecosystem in Kenya. A comprehensive EAFM is required to holistically manage fisheries resources and their associated habitats. The study assessed ecological indicators based on objectives of harvest sustainability and biodiversity conservation. Analyses were performed on data sourced from the State Department of Fisheries, and research databases. Trends in historical landings (1985–2010) of penaeid shrimps from the Malindi-Ungwana Bay were analyzed using LOWESS. Number-size spectra analysis was used to assess the exploitation status of the shrimps, while biomass-trophic level spectra (BTLS) analysis was applied as a potential tool for analyzing multifactor effects on the bay. IndiSeas-based ecosystem indicators were used to assess impact of the prawn trawl fishery on biodiversity of the bay. Results indicate long-term series with two peaks (1997 and 2000) in historical landings of penaeid shrimps and a monotonous decline in catches during 2002–2010. Slopes of number-size spectra suggested increased fishing mortality with time (2008–2012), while patterns of intercepts indicated a general increase in fisheries productivity of the bay. BTLS analysis using demersal fish survey and fish by-catch data suggested reduced levels of biomass across trophic levels and a temporal decline in trophic levels of fish species caught, however, the short time span constrains robust conclusions from the BTLS analysis. Biodiversity and conservation based indicators (e.g. fish sizes, trophic levels and proportion of predators in catches) adopted from the IndiSeas program showed the Malindi-Ungwana Bay to be ecologically degraded. There is need to initiate long-term monitoring programs to strengthen temporal scale of analysis of the datasets and to support use of ecological indicators for resource management and development of an EAFM in data-poor WIO countries.  相似文献   

5.
IndiSeas (“Indicators for the Seas”) is a collaborative international working group that was established in 2005 to evaluate the status of exploited marine ecosystems using a suite of indicators in a comparative framework. An initial shortlist of seven ecological indicators was selected to quantify the effects of fishing on the broader ecosystem using several criteria (i.e., ecological meaning, sensitivity to fishing, data availability, management objectives and public awareness). The suite comprised: (i) the inverse coefficient of variation of total biomass of surveyed species, (ii) mean fish length in the surveyed community, (iii) mean maximum life span of surveyed fish species, (iv) proportion of predatory fish in the surveyed community, (v) proportion of under and moderately exploited stocks, (vi) total biomass of surveyed species, and (vii) mean trophic level of the landed catch. In line with the Nagoya Strategic Plan of the Convention on Biological Diversity (2011–2020), we extended this suite to emphasize the broader biodiversity and conservation risks in exploited marine ecosystems. We selected a subset of indicators from a list of empirically based candidate biodiversity indicators initially established based on ecological significance to complement the original IndiSeas indicators. The additional selected indicators were: (viii) mean intrinsic vulnerability index of the fish landed catch, (ix) proportion of non-declining exploited species in the surveyed community, (x) catch-based marine trophic index, and (xi) mean trophic level of the surveyed community. Despite the lack of data in some ecosystems, we also selected (xii) mean trophic level of the modelled community, and (xiii) proportion of discards in the fishery as extra indicators. These additional indicators were examined, along with the initial set of IndiSeas ecological indicators, to evaluate whether adding new biodiversity indicators provided useful additional information to refine our understanding of the status evaluation of 29 exploited marine ecosystems. We used state and trend analyses, and we performed correlation, redundancy and multivariate tests. Existing developments in ecosystem-based fisheries management have largely focused on exploited species. Our study, using mostly fisheries independent survey-based indicators, highlights that biodiversity and conservation-based indicators are complementary to ecological indicators of fishing pressure. Thus, they should be used to provide additional information to evaluate the overall impact of fishing on exploited marine ecosystems.  相似文献   

6.
Marine fisheries as ecological experiments   总被引:1,自引:0,他引:1  
There are many examples of ecological theory informing fishery management. Yet fisheries also provide tremendous opportunities to test ecological theory through large-scale, repeated, and well-documented perturbations of natural systems. Although treating fisheries as experiments presents several challenges, few comparable tests exist at the ecosystem scale. Experimental manipulations of fish populations in lakes have been widely used to develop and test ecological theory. Controlled manipulation of fish populations in open marine systems is rarely possible, but fisheries data provide a valuable substitute for such manipulations. To highlight the value of marine fisheries data, we review leading ecological theories that have been empirically tested using such data. For example, density dependence has been examined through meta-analysis of spawning stock and recruitment data to show that compensation (higher population growth) occurs commonly when populations are reduced to low levels, while depensation (the Allee effect) is rare. As populations decline, spatial changes typically involve populations contracting into high-density core habitats while abandoning less productive habitats. Fishing down predators may result in trophic cascades, possibly shifting entire ecosystems into alternate stable states, although alternate states can be maintained by both ecological processes and continued fishing pressure. Conversely, depleting low trophic level groups may affect central-place foragers, although these bottom–up effects rarely appear to impact fish—perhaps because many fish populations have been reduced to the point that they are no longer prey limited. Fisheries provide empirical tests for diversity–stability relations: catch data suggest that more diverse systems recover faster and provide more stable returns than less diverse systems. Fisheries have also provided examples of the tragedy of the commons, as well as counter-examples where common property resources have been managed successfully. We also address two barriers to use of fisheries data to answer ecological questions: differences in terminology for similar concepts and misuse of records of fishery landings (catch data) as a proxy for biomass trends.  相似文献   

7.
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.  相似文献   

8.
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.  相似文献   

9.
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.  相似文献   

10.
Fisheries statistics are known to be underestimated, since they are mainly based on information about commercial fisheries. However, various types of fishing activities exist and evaluating them is necessary for implementing effective management plans. This paper assesses the characteristics and catches of the French European sea bass recreational fishery along the Atlantic coasts, through the combination of large-scale telephone surveys and fishing diaries study. Our results demonstrated that half of the total catches (mainly small fish) were released at sea and that the mean length of a kept sea bass was 46.6 cm. We highlighted different patterns of fishing methods and type of gear used. Catches from boats were greater than from the shore, both in abundance and biomass, considering mean values per fishing trip as well as CPUE. Spearfishers caught the highest biomass of sea bass per fishing trip, but the fishing rod with lure was the most effective type of gear in terms of CPUE. Longlines had the highest CPUE value in abundance but not in biomass: they caught numerous but small sea bass. Handlines were less effective, catching few sea bass in both abundance and biomass. We estimated that the annual total recreational sea bass catches was 3,173 tonnes of which 2,345 tonnes were kept. Since the annual commercial catches landings were evaluated at 5,160 tonnes, recreational landings represent 30% of the total fishing catches on the Atlantic coasts of France. Using fishers'' self-reports was a valuable way to obtain new information on data-poor fisheries. Our results underline the importance of evaluating recreational fishing as a part of the total amount of fisheries catches. More studies are critically needed to assess overall fish resources caught in order to develop effective fishery management tools.  相似文献   

11.
As China’s second-largest large marine ecosystem, the East China Sea Shelf has suffered from overfishing, eutrophication, and physical disturbance over the last several decades. A trophic mass-balance model of this ecosystem was developed in order to characterize the structure and functioning of its food web, to identify its keystone species, and to quantify the ecological impacts of fishing that it sustained during the early 2000s. Using a multivariate statistical analysis, we identified 38 functional groups for the trophic model, including fish and invertebrate groups targeted and not targeted by fisheries. Pelagic sharks and rays were identified as the keystone species in the ecosystem. Strong benthic–pelagic coupling was indicated in this ecosystem. In particular, this study highlighted the interdependent relationships that exist among plankton, benthic invertebrates, and detritus. Recent fishing activities were characterized by high exploitation rates for various commercially targeted and non-targeted species, leading to the removal of much of the ecosystem’s fishable production. Overall, our findings give a preliminary explanation of the current problems of eutrophication and fishery depletion and other changes in the East China Sea Shelf, and highlight the need for developing ecosystem-based fisheries management.  相似文献   

12.
Competition between marine mammals and fisheries for marine resources-whether real or perceived-has become a major issue for several countries and in international fora. We examined trophic interactions between marine mammals and fisheries based on a resource overlap index, using seven Ecopath models including marine mammal groups. On a global scale, most food consumed by marine mammals consisted of prey types that were not the main target of fisheries. For each ecosystem, the primary production required (PPR) to sustain marine mammals was less than half the PPR to sustain fisheries catches. We also developed an index representing the mean trophic level of marine mammal's consumption (TL(Q)) and compared it with the mean trophic level of fisheries' catches (TL(C)). Our results showed that overall TL(Q) was lower than TL(C) (2.88 versus 3.42). As fisheries increasingly exploit lower-trophic level species, the competition with marine mammals may become more important. We used mixed trophic impact analysis to evaluate indirect trophic effects of marine mammals, and in some cases found beneficial effects on some prey. Finally, we assessed the change in the trophic structure of an ecosystem after a simulated extirpation of marine mammal populations. We found that this lead to alterations in the structure of the ecosystems, and that there was no clear and direct relationship between marine mammals' predation and the potential catch by fisheries. Indeed, total biomass, with no marine mammals in the ecosystem, generally remained surprisingly similar, or even decreased for some species.  相似文献   

13.
The largest perturbation on upper trophic levels of many marine ecosystems stems from fishing. The reaction of the ecosystem goes beyond the trophic levels directly targeted by the fishery. This reaction has been described either as a change in slope of the overall size spectrum or as a trophic cascade triggered by the removal of top predators. Here we use a novel size- and trait-based model to explore how marine ecosystems might react to perturbations from different types of fishing pressure. The model explicitly resolves the whole life history of fish, from larvae to adults. The results show that fishing does not change the overall slope of the size spectrum, but depletes the largest individuals and induces trophic cascades. A trophic cascade can propagate both up and down in trophic levels driven by a combination of changes in predation mortality and food limitation. The cascade is damped as it comes further away from the perturbed trophic level. Fishing on several trophic levels leads to a disappearance of the signature of the trophic cascade. Differences in fishing patterns among ecosystems might influence whether a trophic cascade is observed.  相似文献   

14.

Implementing new and effective control strategies to reduce populations of invasive species is needed to offset their negative impacts worldwide. The spread of Indo-Pacific lionfish (Pterois sp.) through much of the western Atlantic has been one of the most publicized marine invasions globally, and is considered a major biodiversity threat whose longer-term impacts are still uncertain. Marine managers have explored several strategies to control lionfish, such as fishing tournaments (derbies) and commercial fisheries. Commercial fisheries for invasive species are controversial because they could create perverse incentives to maintain these populations, and they have never been demonstrated to successfully control target populations. We analyzed the development and impacts of an opportunistic fishing operation aimed at commercializing invasive lionfish in the Mexican Caribbean. We examined official lionfish landings and compared them to catches from lionfish derbies and lionfish densities from locations in the state of Quintana Roo, Mexico. We found that commercial fishers, particularly from one fishing cooperative on Cozumel Island, were effective at catching lionfish, with landings peaking at 20,000 individuals in 2014. This number is comparable to the number of lionfish caught in derbies across the entire Caribbean in the same year. Ecological survey data suggest a?~?60% reduction in lionfish density on Cozumel reefs over two years (2013–2015), matching the peak landings in the lionfish fishing operation. However, the fishery’s apparent success as a control tool during the time window analyzed seemed to trigger its own demise: a decline in landings was followed by evaporating market interest and loss of economic viability. If fisheries are to be established and used as management strategies to control future invasions, managers must develop strategic collaboration plans with commercial fishing partners.

  相似文献   

15.
Two mass-balance trophic models are constructed to describe the Gulf of Thailand ecosystem (10–50 m depth): one model pertains to the initial phase of fisheries development, and the other to when the resources were severely depleted. The two phases are compared, and changes brought about by fishing discussed. A dynamic simulation model, Ecosim, is then used successfully to reproduce the 1980 state of the fishery based on the 1963 model and the development in catches. In addition the 1980 model is used to predict how the ecosystem groups may bounce back following marked reduction in fishing pressure. Finally, the 1963 model is used to study alternative scenarios for how the fisheries development could take place, notably the effect of exploiting only the resources of larger species. The study validates that the Ecosim model can be used to predict ecosystem level changes following changes in fishing pressure, therefore fishing induced changes can to a large extent explain the changes in ecosystem pools and fluxes observed over time.  相似文献   

16.
捕捞对北部湾海洋生态系统的影响   总被引:12,自引:0,他引:12  
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.  相似文献   

17.
Sharks are highly vulnerable to intense and prolonged fishery extraction. This article analyzes the data on shark landings from the artisan fishing fleet on Costa Rica's Pacific coast between 1988 and 1997. The data come from an invoicing system administered by the Costa Rican Fisheries Institute (Instituto Costarricense de la Pesca y Acuacultura, INCOPESCA). Pacific coast shark fishing during the period under study represented approximately 20% of the total national fisheries volume. According to data from the invoicing system, the Northern Pacific region was the most productive, reporting 58% of the shark catch nationwide. Within this region, shark fishing in Papagayo Gulf represented 91% and 53% of the landings by fishery region and nationwide, respectively. The mid-sized and advanced (length of boat > 10 meters) artisan fishing fleets reported 96% of the shark catches in the zone. The study of shark fisheries in the Papagayo Gulf zone is crucial for an understanding of fishery dynamics for this resource at the national level. A monthly chronological series was constructed with the landings in the Papagayo Gulf zone, and a Univariate Box-Jenkins (UBJ) Model was estimated for first-order moving averages MA(1) with a seasonal component of the Yt = lamda(t-1) + gammaS12 + a(t) type.  相似文献   

18.
Detailed information of fish diets is required if we are to understand complex interactions between species and successfully manage resources at an ecosystem level. We compiled diet information from 76 species of fish targeted by recreational and commercial fishers in North West Australia. Based on 81 independent studies we demonstrate that species targeted by the fishery are all carnivores, however the type of prey they consume and their trophic level is variable (3.31–4.49) and trophic range of some species spans different trophic levels (e.g. Lethrinus nebulosus, 3.46–4.35). These findings infer that in highly diverse systems, such as coral reefs, trophic cascades instigated by fishing must be investigated at the species, rather than functional or trophic level. Moreover, as prey availability is likely to vary spatially and temporally, diet must be quantified locally to assess ecosystem level impacts of fishing.  相似文献   

19.
In the present study, we tested five trophic indicators and we demonstrated their usefulness to assess the environmental status of marine ecosystems and to implement an ecosystem approach to fisheries management (EAFM). The tested indicators include the slope of the biomass spectrum, the mean trophic level (MTL), the marine trophic index (MTI) and two newly developed indicators, the high trophic level indicator (HTI) and the apex predator indicator (API). Indicators are compared between current state and potential reference situations, using as case studies: the Celtic Sea/Bay of Biscay, North Sea and English Channel ecosystems. Trophic spectra are obtained from Ecopath models while reference situations are estimated, simulating with EcoTroph and Ecosim different fishing pressures including three candidate scenarios for an EAFM. Inter-ecosystems assessments are done using Ecopath models, simulations outputs and scientific surveys data to assess the current states of the studied ecosystems, contrast the reference situations and analyze the responses of all indicators. Sensitivity analyses are also conducted on the main simulation parameters to test the robustness of the chosen indicators. Ecosystems specific targets for EAFM are proposed for the five trophic indicators estimated from whole-ecosystem models, while in the Celtic Sea/Bay of Biscay ecosystem targets are proposed for the MTL (=3.85) and HTI (48%) estimated from standard bottom-trawl surveys. The HTI is proposed to be relevant for survey data and the API is recommended using whole-ecosystem models. We conclude that HTI and API show trends in ecosystems health better than MTI.  相似文献   

20.
Several management strategies for ecosystems with biological interaction are discussed, including predator removal, predator-prey coexistence, prey exploitation, overexploitation, and introduction of sanctuaries. Some case studies related to ecosystem management are briefly presented; these describe Lakes Victoria and Tanganyika, discarding from shrimp trawl fisheries and the development in the North Sea that led to introduction of multispecies analysis. The concept of fishing down the food web is discussed and the average trophic levels at which the fisheries operate in different ecosystem types are estimated based on quantified trophic flow models. On a global level, while on average fisheries operate around two trophic levels above the primary producers, still one third of the catch of the 70 major fish species caught in the world is of piscivorous fish. Using exploitation-predation rate indices for different ecosystem types, the amount of finfish consumed globally by finfish is roughly estimated to be three times the catches of finfish. Finally some implications for the management of ecosystems are drawn up. It makes little difference if short-term prognoses are based on single-species or multispecies considerations. Multispecies models may, however, give the better long-term advice, and adaptive management may facilitate the move towards such long-term goals.  相似文献   

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