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1.
Abstract:  Marine protected areas, and other fishery management systems that impart partial or total protection from fishing, are increasingly advocated as an essential management tool to ensure the sustainable use of marine resources. Beneficial effects for fish species are well documented for tropical and reef systems, but the effects of marine protected areas remain largely untested in temperate waters. We compared trends in sport-fishing catches of nine fish species in an area influenced by a large (500-km2) towed-fishing-gear restriction zone and in adjacent areas under conventional fishery management controls. Over the period 1973–2002 the mean reported weight of above-average-sized (trophy) fish of species with early age at maturity and limited home range was greatest within the area influenced by the fishing-gear restriction zone. The reported weight of trophy fish of species that mature early also declined less and more slowly over time within the area influenced by the fishing-gear restriction zone. Importantly, the mean reported weight of trophy fish of species that mature late and those that undertake extensive spatial movements declined at the same rate in all areas. Hence these species are likely to require protected areas >500 km2 for effective protection. Our results also indicated that fish species with a localized distribution or high site fidelity may require additional protection from sport fishing to prevent declines in the number or size of fish within the local population.  相似文献   

2.
Abstract: The adoption of fisheries closures and gear restrictions in the conservation of coral reefs may be limited by poor understanding of the economic profitability of competing economic uses of marine resources. Over the past 12 years, I evaluated the effects of gear regulation and fisheries closures on per person and per area incomes from fishing in coral reefs of Kenya. In two of my study areas, the use of small‐meshed beach seines was stopped after 6 years; one of these areas was next to a fishery closure. In my third study area, fishing was unregulated. Fishing yields on per capita daily wet weight basis were 20% higher after seine‐net fishing was stopped. The per person daily fishing income adjacent to the closed areas was 14 and 22% higher than the fishing income at areas with only gear restrictions before and after the seine‐net restriction, respectively. Incomes differed because larger fish were captured next to the closed area and the price per weight (kilograms) increased as fish size increased and because catches adjacent to the closure contained fish species of higher market value. Per capita incomes were 41 and 135% higher for those who fished in gear‐restricted areas and near‐closed areas, respectively, compared with those who fished areas with no restrictions. On a per unit area basis (square kilometers), differences in fishing income among the three areas were not large because fishing effort increased as the number of restrictions decreased. Changes in catch were, however, larger and often in the opposite direction expected from changes in effort alone. For example, effort declined 21% but nominal profits per square kilometer (not accounting for inflation) increased 29% near the area with gear restrictions. Gear restrictions also reduced the cost of fishing and increased the proportion of self‐employed fishers.  相似文献   

3.
Abstract: Freshwater biodiversity conservation is generally perceived to conflict with human use and extraction (e.g., fisheries). Overexploited fisheries upset the balance between local economic needs and endangered species’ conservation. We investigated resource competition between fisheries and Ganges river dolphins (Platanista gangetica gangetica) in a human‐dominated river system in India to assess the potential for their coexistence. We surveyed a 65‐km stretch of the lower Ganga River to assess habitat use by dolphins (encounter rates) and fishing activity (habitat preferences of fishers, intensity of net and boat use). Dolphin abundance in the main channel increased from 179 (SE 7) (mid dry season) to 270 (SE 8) (peak dry season), probably as a result of immigration from upstream tributaries. Dolphins preferred river channels with muddy, rocky substrates, and deep midchannel waters. These areas overlapped considerably with fishing areas. Sites with 2–6 boats/km (moderately fished) were more preferred by dolphins than sites with 8–55 boats/km (heavily fished). Estimated spatial (85%) and prey–resource overlap (75%) between fisheries and dolphins (chiefly predators of small fish) suggests a high level of competition between the two groups. A decrease in abundance of larger fish, indicated by the fact that small fish comprised 74% of the total caught, may have intensified the present competition. Dolphins seem resilient to changes in fish community structure and may persist in overfished rivers. Regulated fishing in dolphin hotspots and maintenance of adequate dry season flows can sustain dolphins in tributaries and reduce competition in the main river. Fish‐stock restoration and management, effective monitoring, curbing destructive fishing practices, secure tenure rights, and provision of alternative livelihoods for fishers may help reconcile conservation and local needs in overexploited river systems.  相似文献   

4.
The changes in a tropical demersal fish community in the southeast Gulf of Carpentaria, Australia, were examined by comparing the results of a survey undertaken in 1964 before the area was fished, with two surveys in 1985 and 1986 after 20 yr of commercial trawl fishing. The numerical abundance of 52 of the 82 fish taxa had not changed significantly, but that of 18 had decreased while 12 had increased. One taxon (Paramonacanthus spp.) had decreased by more than 500 times and another (Saurida micropectoralis) had increased substantially in abundance. The changes occurred throughout the area surveyed, but the largest changes were offshore. In the pre-trawling community most taxa were caught mainly during the night, while in the post-trawling community most were caught in the same numbers during day and night. In 10 of the 30 taxa that changed in abundance, changes were within a family and could not be explained. For the remaining 20, the changes could be related to their position in the water column: benthic taxa decreased and bentho-pelagic taxa increased. The changes were assessed in relation to fishing effort, and changes in the mud content of the substrate in the study area. Although the changes did not correlate with the fishing effort among three zones in the study area, it is suggested that fishing effort and discarding of the by-catch caused the change in 18 taxa. The magnitude of the decreases of some species might be related to changes in the sediment or possibly other long-term environmental change. There was also a change in the diel behaviour in the fish community that perhaps may be related to the effects of fishing on a tropical multispecies fish community.  相似文献   

5.
Abstract:  The application of no-take areas in fisheries remains controversial. Critics argue that many targeted species are too mobile to benefit from area protection and that no-take areas are only appropriate for resident species. The degree of protection does not depend on the size of the no-take area but rather on the time fish reside inside its boundaries during key life-history events (i.e., spawning) and during periods of peak fishing activity. We evaluated the potential of a small no-take marine protected area (MPA) inside a coastal embayment as a harvest refuge for a mobile, possibly migratory, long-lived fish species. We used acoustic telemetry to track movements of 30 transmitter-tagged white stumpnose (Rhabdosargus globiceps) across and on both sides of the boundary of a small (34 km2) no-take area over a full year. Being landlocked on 3 sides, the location of the MPA inside the lagoon made it practical to detect all boundary crossings and to calculate the time individual fish used the MPA. We detected frequent movements across the boundary, with strong seasonal and individual variations. There were significant differences in MPA use patterns between fish from different release areas. The time spent in the MPA by individual fish during summer (mean 50%; max 98%) was out of proportion with the size of that area (4% of total habitat). Summer coincided with peak recreational fishing activity and with the spawning season of this species. The small MPA provided a refuge for a part of the spawning stock of white stumpnose. Our findings suggest that if strategically placed, a small no-take area can be effective in protecting mobile species and that models of spillover from no-take areas should account for seasonal and individual variation in area use and the spatiotemporal distribution of fish and fishers.  相似文献   

6.
Despite the rapid rate of human-induced species losses, the relative influence of natural and anthropogenic factors on the functional diversity of species assemblages remains unknown for most ecosystems. A model was previously developed to predict the diversity structure of coral reef fish assemblages in 10 atolls of low human pressure and contrasting morphology of the Tuamotu Archipelago (French Polynesia). This existing model predicted smoothed histograms (spectra) of species richness according to size classes, diet classes and life-history classes of fish assemblages using a combination of environmental characteristics at different spatial scales. The present study applied the model to Tikehau, another atoll of the same archipelago where commercial fishing is practiced and where the same sampling strategy was reproduced. Significant differences appeared between predicted and observed species richness in several size, diet and life-history classes of fish assemblages in Tikehau. Two parameters which were not accounted for in the initial model, i.e. fishing pressure and atoll position within the archipelago, explained together 63% of variance in model residuals, >60% being explained by fishing pressure only. The respective effects of fishing and atoll position on the diversity of coral reef fish assemblages are discussed, with the potential of such modelling approach to assess the relative importance of factors affecting functional diversity within communities.  相似文献   

7.
Fisheries bycatch of marine megafauna is a worldwide conservation issue. In this study, we propose a method for generating reliable maps of sea turtle bycatch hotspots. Based on a well-defined area of fishing effort determined from the longline sets monitored in 2007 and 2010, we calculated the fishing area with the highest turtle bycatch density for both years. Our results show that it is important to consider all the components of fishing effort (area, number of hooks and soak time) in order to standardize the bycatch events, and thus the spatial density of the captures can be considered an index of abundance and aggregation of the species. Moreover, the high-resolution level of the analyses was useful for investigating the cumulative effect of the longline sets, which often overlap, and made it possible to correctly map the capture density and the intensity of the fishing effort at any given location.  相似文献   

8.
The largest African Great Lakes, Tanganyika, Malawi, and Victoria, which have the richest lacustrine fish faunas of any of the world's lakes, provide a unique comparative series for studies of evolutionary mechanisms, community ecology, and fish behavior. Their colorful littoral fishes are also known to aquarists worldwide. This paper examines the origins of their fish diversity, looking at the history of the lakes, colonization from river systems, and evolution of endemic faunas within each lake. All three lakes support fisheries of great socioeconomic importance for the rapidly rising human populations. The paper also examines the vulnerability of the faunas to fishing pressures and introductions of exotic species. In Malawi and Victoria, bottom-trawling has altered the cichlid species composition. The loss of an estimated 200 taxa of endemic cichlid species from Lake Victoria's fauna, following introductions of exotic fishes (tilapias and predatory centropomid Lates ) 40 years ago, stresses the need to protect the unique fish faunas in Lakes Tanganyika and Malawi.  相似文献   

9.
The multiple-recapture technique can be used to study some aspects of the dynamics of large fish populations, if a part of the fishing fleet is considered as experimental fishing boats by appointing obserers to release tagged fish which are captured, while untagged fish captured are retained. The tagged and untagged populations are assumed to have different properties such as catchability and survival rates. The fish are sampled during a number of sampling surveys with equal duration and no intervening time intervals between them. It is assumed that fish suffer from mortalities during sampling surveys. The parameters of untagged populations can be estimated with the help of the readily estimated parameters of tagged fish (Rafail, 1972), the relationship between the parameters of tagged and untagged populations, and the numbers of untagged fish captured during the sampling surveys. The estimates are free from Types A and B tagging errors.  相似文献   

10.
This paper used the case study of the Wakatobi Marine National Park, Indonesia to examine changes in the diversity, density and maturity of grouper species over a 5-year period following the establishment of a small-scale no-take area (NTA). This work was carried out to investigate whether “small” NTAs could be effective management strategies over a time scale that is relevant to local fishery communities and their perception of management success. Our research also documents the ecology of these species, information essential if we are to understand how management practises are to affect coral reef fish species. Designation of this “small NTA” increased the density of groupers by 30% over a 5-year period of protected status. After 5 years of protection, grouper populations within this NTA were more mature and double the density of those within the adjacent lightly fished sites and nearly five times those of a heavily fished site. During this time all other nearby fished sites underwent large declines in grouper density. The nearby lightly fished Kaledupa site decreased by up to 50% year−1. Such drastic declines are considered the impact of the exponential development of ever efficient and unsustainable methods of fishing within the study region. This NTA was not of benefit to all grouper species; the reasons for which are not clear. Such questions require further detailed research about the life history, population and behavioural ecology of Indo-Pacific grouper species. Such information is critical for urgently needed fisheries management. The present study found that a small scale NTA of 500 m length was large enough to increase the population of top predatory fish. In conjunction with other socially acceptable small scale NTAs it could help maintain and increase important fish stocks over a larger area. The use of “small” NTAs within networks of reserves should become a useful tool in the management of the locally exploited coral reefs.  相似文献   

11.
Abstract: Customary management systems (i.e., management systems that limit the use of marine resources), such as rotational fisheries closures, can limit harvest of resources. Nevertheless, the explicit goals of customary management are often to influence fish behavior (in particular flight distance, i.e., distance at which an organism begins to flee an approaching threat), rather than fish abundance. We explored whether the flight distance of reef fishes targeted by local artisanal fishers differed between a customary closure and fished reefs. We also examined whether flight distance of these species affected fishing success and accuracy of underwater visual census (UVC) between customary closed areas and areas open to fishing. Several species demonstrated significant differences in flight distance between areas, indicating that fishing activity may increase flight distance. These relatively long flight distances mean that in fished areas most target species may stay out of the range of spear fishers. In addition, mean flight distances for all species both inside and outside the customary‐closure area were substantially smaller than the observation distance of an observer conducting a belt‐transect UVC (mean [SE]= 8.8 m [0.48]). For targeted species that showed little ability to evade spear fishers, customary closures may be a vital management technique. Our results show that customary closures can have a substantial, positive effect on resource availability and that conventional UVC techniques may be insensitive to changes in flight behavior of fishes associated with fishing. We argue that short, periodic openings of customary closures may allow the health of the fish community to be maintained and local fishers to effectively harvest fishes.  相似文献   

12.

Background and Scope

There is a multitude of uses in the seas worldwide: fishing, shipping, tourism, exploitation of oil and gas, sea-bed mining, waste disposal, etc. They all compete for space and resources. Each of them has its specific impact on marine ecosystems. Furthermore, they interact with each other and with the marine environment. Fisheries are the most deleterious interactions of man with marine ecosystems by withdrawing a major part of the annual production of large fish, molluscs and crustacea. Many marine habitats are destroyed by fishing, particularly by heavy bottom trawling.

Basics of Fisheries

The production of a fish stock can be increased by removing the old fish. Fishing is sustainable as long as it is restricted to the removal of the surplus production. Subventions and market forces are opposed the rational way of effort reduction aiming at the recovery of overexploited stocks. Fishing has collateral effects on target species. Heavy selective fishing of large, slow-growing predatory fish will favour small, fast-growing species of a lower level in the trophic pyramid. Fishing in marine ecosystems is a complex process in which biological and economic factors interact. At different scales of space and time they are superimposed by changes in the oceanic environment. Climatic variations and global warming of the Ocean differ in their effects from region to region, and they affect distribution, composition and fishing yield of the various exploited fish stocks. Politics has a major impact on the development of fisheries; historical examples are the collapse of the Eastern Bloc with its big distant water fishing fleets, or the introduction of the 200 nm Economic Zones, putting most fish stocks under national jurisdiction.

Discussion

Fishery science is still striving to understand the variability of year-class strength in fish stocks. In the foreground of modern research, however, are the interactions in multi-species communities in relation to changes in the abiotic and biotic environment and to different kinds of management. We have no possibility to study the complex interactions in marine fish communities by controlled experiments. The only information we have are records on landings and fishing efforts. They provide the basis for sophisticated mathematical models. Ecosystem modelling is a relatively young field in marine ecology. In Europe and North America fishery science is more than hundred years old. It is not possible, however, to apply the methods and models of, e.g., North Sea research to low latitude ecosystems and fisheries.

Conclusions

The sustainable use and protection of the marine living resources and biodiversity are global challenges. Each Large Marine Ecosystem calls for specific solutions in terms of research and management. Problems have to be tackled not only by computer models and remote sensing, but also by field research in all parts of the world. The further development of marine and fisheries research in developing countries is a matter of north-south-partnerships with high win-win spin-offs. Over the past decades some excellent groups of marine scientists from several tropical countries have been established who are very open for partnership projects in the true sense. They offer great opportunities to jointly study the richness of marine fauna, flora, and ecosystems in tropical and subtropical shelf seas and up-welling regions.  相似文献   

13.
Closure of areas to fishing is expected to result in an increase in the abundance of targeted species; however, changes to populations of species not targeted by fishermen will depend upon their role in the ecosystem and their relationship with targeted species. The effects of protection on targeted and non-targeted reef fish species at the Houtman Abrolhos Islands, Western Australia were studied using baited remote underwater stereo–video cameras. Video images were collected from shallow (8–12 m) and deep (22–26 m) reef sites inside a Marine Protected Area (MPA) at each of three island groups and from three replicate fished locations at each of these groups that span a temperate-tropical transition area. The MPAs were established in 1994 and vary in size from 13.72 km2 at the Pelsaert group in the south to 22.29 km2 at the Easter group to 27.44 km2 at the Wallabi group in the north. The relative abundances of 137 fish species from 42 families were recorded. Large differences in fish assemblage structure existed between MPA and fished locations, and also between shallow and deep regions. Targeted fish species Plectropomus leopardus, Lethrinus miniatus, Lethrinus nebulosus, Pagrus auratus and Glaucosoma hebraicum were more abundant inside MPAs than in areas open to fishing. Their abundance inside MPAs was between 1.13 and 8 times greater than their abundance at fished locations. For non-targeted fish species many were more abundant in areas open to fishing, e.g. Coris auricularis, Thalassoma lutescens, Thalassoma lunare, Dascyllus trimaculatus, however others were conversely more abundant inside MPAs, e.g. Gymnothorax spp, Kyphosus sydneyanus, Scarus microhinos, Chromis westaustralis, Chaetodon spp. This study demonstrates that the removal of abundant targeted species from an ecosystem by fishing can indirectly impact non-fished species and alter the trophic structure of fish assemblages. Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users.  相似文献   

14.
Abstract:  A loss of large vertebrates has occurred in aquatic and terrestrial ecosystems, but data to measure long-term population changes are sparse. Historical photographs provide visual and quantitative evidence of changes in mean individual size and species composition for groups of marine fish that have been targeted by sport fishing. I measured such trends for 13 groups of recreationally caught "trophy" reef fish with photographs taken in Key West, Florida, from 1956 to 2007. The mean fish size declined from an estimated 19.9 kg (SE 1.5) to 2.3 kg (SE 0.3), and there was a major shift in species composition. Landings from 1956 to 1960 were dominated by large groupers ( Epinephelus spp.), and other large predatory fish were commonly caught, including sharks with an average length of just <2 m. In contrast, landings in 2007 were composed of small snappers ( Lutjanus spp. and Ocyurus chrysurus ) with an average length of 34.4 cm (SE 0.62), and the average length of sharks declined by more than 50% over 50 years. Major declines in the size of fish caught were not reflected in the price of fishing trips, so customers paid the same amount for a less-valuable product. Historical photographs provide a window into a more pristine coral reef ecosystem that existed a half a century ago and lend support to current observations that unfished reef communities are able to support large numbers of large-bodied fish.  相似文献   

15.
Effects of Artisanal Fishing on Caribbean Coral Reefs   总被引:6,自引:0,他引:6  
Abstract:  Although the impacts of industrial fishing are widely recognized, marine ecosystems are generally considered less threatened by artisanal fisheries. To determine how coral reef fish assemblages and benthic communities are affected by artisanal fishing, we studied six Caribbean islands on which fishing pressure ranged from virtually none in Bonaire, increasing through Saba, Puerto Rico, St Lucia, and Dominica, and reaching very high intensities in Jamaica. Using stationary-point fish counts at 5 m and 15 m depth, we counted and estimated the lengths of all noncryptic, diurnal fish species within replicate 10-m-diameter areas. We estimated percent cover of coral and algae and determined reef structural complexity. From fish numbers and lengths we calculated mean fish biomass per count for the five most commercially important families. Groupers (Serranidae), snappers (Lutjanidae), parrotfish (Scaridae), and surgeonfish (Acanthuridae) showed order-of-magnitude differences in biomass among islands. Biomass fell as fishing pressure increased. Only grunts (Haemulidae) did not follow this pattern. Within families, larger-bodied species decreased as fishing intensified. Coral cover and structural complexity were highest on little-fished islands and lowest on those most fished. By contrast, algal cover was an order of magnitude higher in Jamaica than in Bonaire. These results suggest that following the Caribbean-wide mass mortality of herbivorous sea urchins in 1983–1984 and consequent declines in grazing pressure on reefs, herbivorous fishes have not controlled algae overgrowing corals in heavily fished areas but have restricted growth in lightly fished areas. In summary, differences among islands in the structure of fish and benthic assemblages suggest that intensive artisanal fishing has transformed Caribbean reefs.  相似文献   

16.
 Visual censuses conducted in a marine reserve (Medas Islands) were used to estimate the natural mortality rates (M) for five common fish species in the NW Mediterranean Sea (Coris julis, Diplodus annularis, D. sargus, Serranus cabrilla and Symphodus roissali). Visual censuses of these same five species were also performed at three sites in unprotected areas of the coast where both commercial and sport fishing activity was normal. Censuses were conducted over a 3 year period. Estimates of M in the 3 years displayed scant seasonal or interannual variation, which may mean that the populations were in equilibrium during that period. The results of this study showed that the relationships between M and the growth parameters and maximum life span were unclear, and considerable caution is therefore recommended when using indirect methods of estimating M based on those parameters. For certain species the values of M were equal to or greater than the estimated total mortality in the exploited areas. The virtual absence of piscivorous predators in the unprotected area as a consequence of the high level of fishing in that area contrasts with the high abundance of such predators in the marine reserve. Since predation is the main contributor to M, estimated mortality in the unprotected areas is attributable nearly entirely to fishing. It is suggested that M may vary according to alterations taking place in conditions in the ecosystem inhabited by a species and thus that use of a value of M for a pristine population cannot be extrapolated to exploited areas. Received: 18 January 2000 / Accepted: 14 July 2000  相似文献   

17.
Fishing has wide-ranging impacts on marine ecosystems. One of the most pervasive signs of intensive fishing is "fishing down the food web", with landings increasingly dominated by smaller species from lower trophic levels. Decreases in the trophic level of landings are assumed to reflect those in fish communities, because size-selective mortality causes decreases in the relative abundance of larger species and in mean body size within species. However, existing analyses of fishing impacts on the trophic level of fish communities have focused on the role of changes in species composition rather than size composition. This will provide a biased assessment of the magnitude of fishing impacts, because fishes feed at different trophic levels as they grow. Here, we combine body size versus trophic level relationships for North Sea fishes (trophic level assessed using nitrogen stable-isotope analysis) with species-size-abundance data from two time-series of trawl-survey data (whole North Sea 1982-2000, central and northern North Sea 1925-1996) to predict long-term trends in the trophic structure of the North Sea fish community. Analyses of the 1982-2000 time-series showed that there was a slow but progressive decline in the trophic level of the demersal community, while there was no trend in the trophic level of the combined pelagic and demersal community. Analyses of the longer time-series suggested that there was no trend in the trophic level of the demersal community. We related temporal changes in trophic level to temporal changes in the slopes of normalised biomass size-spectra (which theoretically represent the trophic structure of the community), mean log2 body mass and mean log2 maximum body mass. While the size-based metrics of community structure showed long-term trends that were consistent with the effects of increased fishery exploitation, these trends were only correlated with trophic level for the demersal community. Our analysis suggests that the effects of fishing on the trophic structure of fish communities can be much more complex than previously assumed. This is a consequence of sampled communities not reflecting all the pathways of energy transfer in a marine ecosystem and of the absence of historical data on temporal and spatial changes in the trophic level of individuals. For the North Sea fish community, changes in size structure due to the differential effects of fishing on species and populations with different life histories are a stronger and more universal indicator of fishing effects than changes in mean trophic level.  相似文献   

18.
An agent-based model was used to evaluate the response of a two-species fish community to fishing boat exploration strategies, namely: boats following high-yield boats (Cartesian); boats fishing at random sites (stochast-random); and boats fishing at least exploited sites (stochast-pressure). At low fishing pressure, the stochast-random mode yielded a high average catch per boat while sustaining fish biomass. At high fishing pressure, the Cartesian mode was more effective. For the Cartesian strategy, fish biomass exhibited four distinct behaviors with increasing number of boats. In the first phase, the fish biomass dropped with increasing number of boats due to a corresponding rise in biomass extraction. Rapid exploitation occurred in the second phase, when two or more boats occupied the same initial area, that led to the faster abandonment of those sites which then underwent biomass recovery. In the third phase, adding more boats resulted in a fluctuating stock biomass, where the combined effects of initial spatial distribution of boats and rapid localization led to either full stock recovery when boats were eventually confined to a single location due to spillovers, or stock extirpation when the entire area became fully occupied. Beyond the third phase, stock extirpation was assured. In order to break the pattern of localization (bandwagon effect), we introduced stochast-random intruders in a Cartesian-dominated fishery. Adding a single intruder changed the patchy-structured stock biomass pattern of a purely Cartesian fishery to a uniformly explored stock biomass pattern because of the additional spatial information provided by the intruder. Consequently, the average catch per boat increased but at the expense of a disproportionate decline in equilibrium biomass.  相似文献   

19.
Fishing the line near marine reserves in single and multispecies fisheries.   总被引:3,自引:0,他引:3  
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.  相似文献   

20.
A dynamic simulation model was constructed using outputs from a balanced Gulf of Maine (GOM) energy budget model as the initial parameter set. The model was structured to provide a recipient control set of dynamics, largely based off of flows to and from different biological groups. The model was used to produce Monte Carlo simulations that were compared (percent change in biomass) with basecase simulations for a variety of scenarios. Changes in primary production, large increases in pelagic and demersal fish biomass, increases in fishing mortality, and large increases in top predators such as baleen whales and pinnepids were simulated. These scenarios roughly simulated the potential impacts of climate change, altered fishing pressure, additional protected species mitigations, and combinations thereof. Results suggest that the GOM system is primarily influenced by bottom-up processes involving phytoplankton, zooplankton, and bacterial biomass. Pelagic and demersal fish were important in determining trends in some of the scenarios. Marine mammals, large pelagic fish, and seabirds have a minor role in the GOM system in terms of biomass flows among the ecosystem components. The system is resilient to large-scale change due, in part to many predator–prey linkages. However, major alterations could occur from sustained climate change, high fishing rates, and by combinations of these types of external forcing mechanisms.  相似文献   

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