首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献,搜索用时 250 毫秒
1.
Managing fisheries using length‐based harvest regulations is common, but such policies often create trade‐offs among conservation (e.g. maintaining natural age‐structure or spawning stock biomass) and fishery objectives (e.g. maximizing yield or harvest numbers). By focusing harvest on the larger (older) fish, minimum‐length limits are thought to maximize biomass yield, but at the potential cost of severe age and size truncation at high fishing mortality. Harvest‐slot‐length limits (harvest slots) restrict harvest to intermediate lengths (ages), which may contribute to maintaining high harvest numbers and a more natural age‐structure. However, an evaluation of minimum‐length limits vs. harvest slots for jointly meeting fisheries and conservation objectives across a range of fish life‐history strategies is currently lacking. We present a general age‐ and size‐structured population model calibrated to several recreationally important fish species. Harvest slots and minimum‐length limits were both effective at compromising between yield, numbers harvested and catch of trophy fish while conserving reproductive biomass. However, harvest slots consistently produced greater numbers of fish harvested and greater catches of trophy fish while conserving reproductive biomass and a more natural population age‐structure. Additionally, harvest slots resulted in less waste in the presence of hooking mortality. Our results held across a range of exploitation rates, life‐history strategies and fisheries objectives. Overall, we found harvest slots to represent a valuable option to meet both conservation and recreational fisheries objectives. Given the ubiquitous benefits of harvest slots across all life histories modelled, rethinking the widespread use of minimum‐length limits is warranted.  相似文献   

2.
In Mediterranean European countries, 85% of the assessed stocks are currently overfished compared to a maximum sustainable yield reference value (MSY) while populations of many commercial species are characterized by truncated size‐ and age‐structures. Rebuilding the size‐ and age‐structure of exploited populations is a management objective that combines single species targets such as MSY with specific goals of the ecosystem approach to fisheries management (EAF), preserving community size‐structure and the ecological role of different species. Here, we show that under the current fishing regime, stock productivity and fleet profitability are generally impaired by a combination of high fishing mortality and inadequate selectivity patterns. For most of the stocks analysed, a simple reduction in the current fishing mortality (Fcur) towards an MSY reference value (FMSY), without any change in the fishing selectivity, will allow neither stock biomass nor fisheries yield and revenue to be maximized. On the contrary, management targets can be achieved only through a radical change in fisheries selectivity. Shifting the size of first capture towards the size at which fish cohorts achieve their maximum biomass, the so‐called optimal length, would produce on average between two and three times higher economic yields and much higher biomass at sea for the exploited stocks. Moreover, it would contribute to restore marine ecosystem structure and resilience to enhance ecosystem services such as reservoirs of biodiversity and functioning food webs.  相似文献   

3.
We address the problem of optimal size‐selective exploitation in an age‐structured fish population model by systematically examining how density and size dependency in growth, mortality and fecundity affect optimal harvesting patterns when judged against a set of fisheries objectives. The study offers five key insights. First, while minimum‐length limits often maximize the biomass yield, exploitation using harvest slots (i.e. regulations that protect both immature and very large individuals) can generate within 95% of maximum yield; harvest slots also generally maximize the number of fish that are harvested. Second, density dependence in growth and size‐dependent mortality predict more liberal optimal size limits than those derived under assumptions of no density and size dependence. Third, strong density dependence in growth maximizes the catch of trophy fish only when modest harvest is introduced; the same holds for numbers harvested, when the stock–recruitment function follows the Ricker type. Fourth, the inclusion of size‐dependent maternal effects on fecundity or egg viability has only limited effects on optimal size limits, unless the increase in fecundity with mass (“hyperallometry”) is very large. However, large hyperallometry in fecundity shifts the optimal size limit for biomass yield from the traditional minimum‐length limit to a harvest slot. Fifth, harvest slots generally provide the best compromises among multiple objectives. We conclude that harvest slots, or more generally dome‐shaped selectivity to harvest, can outperform the standard minimum‐length selectivity. The exact configuration of optimal size limits crucially depends on objectives, local fishing pressure, the stock–recruitment function, and the density and size dependency of growth, mortality and fecundity.  相似文献   

4.
5.
6.
Ecosystem‐based fishery management requires considering the effects of actions on social, natural and economic systems. These considerations are important for forage fish fisheries, because these species provide ecosystem services as a key prey in food webs and support valuable commercial fisheries. Forage fish stocks fluctuate naturally, and fishing may make these fluctuations more pronounced, yet harvest strategies intended to ameliorate these effects might adversely affect fisheries and communities. Here, we evaluate trade‐offs among a diverse suite of management objectives by simulating outcomes from several harvest strategies on forage fish species. We demonstrate that some trade‐offs (like those between catches and minimizing collapse length) were universal among forage species and could not be eliminated by the use of different control rules. We also demonstrate that trade‐offs vary among forage fish species, with strong trade‐offs between stable, high catches and high‐biomass periods (“bonanzas”) for menhaden‐ and anchovy‐like fish, and counterintuitive trade‐offs for sardine‐like fish between shorter collapses and longer bonanzas. We find that harvest strategies designed to maintain stability in catches will result in more severe collapses. Finally, we show that the ability of assessments to detect rapid changes in population status greatly affects control rule performance and the degree and type of trade‐offs, increasing the risk and severity of collapses and reducing catches. Together, these results demonstrate that while default harvest strategies are useful in data‐poor situations, management strategy evaluations that are tailored to specific forage fish may better balance trade‐offs.  相似文献   

7.
Abstract Length, life history and ecological characteristics of landed fish communities were studied over a 10‐year period to test theories of fishing disturbance during a time of increased gear and closure management in heavily utilised fisheries. It was predicted that with greater management restrictions: (1) the earliest and fastest responses in the fishery will be seen in those species with faster turnovers, or relatively lower vulnerabilities to fishing; (2) the fishery would transition to a landed catch with higher mean trophic levels, and greater mean body lengths. In addition, the removal of a non‐selective, small‐mesh seine nets should benefit the catch of gears that previously had the greatest species selectivity overlap with the seine net. Many predictions were supported, although maximum lengths and lengths at maturity responded more rapidly than anticipated. The response to eliminating the non‐selective seine net was a more rapid increase in sizes caught by gears with a larger overlap in size (hook and lines) than species selectivity (gill nets). The simultaneous comparison of management systems over time indicates that open‐access fishing grounds can benefit from restrictions imposed in adjacent fishing grounds. The study indicated that multi‐species coral reef fisheries management objectives of maximising yields, as well as maintaining the fish community’s life‐history diversity, require management trade‐offs that balance local socio‐economic and biodiversity needs.  相似文献   

8.
This paper examines some effects of exploitation on a simple ecosystem containing two interacting fish species, with life histories similar to mackerel (Scomber scombrus) and cod (Gadus morhua), using a dynamic, size‐spectrum model. Such models internalize body growth and mortality from predation, allowing bookkeeping of biomass at a detailed level of individual predation and growth and enabling scaling up to the mass balance of the ecosystem. Exploitation set independently for each species with knife‐edge, size‐at‐entry fishing can lead to collapse of cod. Exploitation to achieve a fixed ratio of yield to productivity across species can also lead to collapse of cod. However, harvesting balanced to the overall productivity of species in the exploited ecosystem exerts a strong force countering such collapse. If balancing across species is applied to a fishery with knife‐edge selection, size distributions are truncated, changing the structure of the system and reducing its resilience to perturbations. If balancing is applied on the basis of productivity at each body size as well as across species, there is less disruption to size‐structure, resilience is increased, and substantially greater biomass yields are possible. We note an identity between the body size at which productivity is maximized and the age at which cohort biomass is maximized. In our numerical results based on detailed bookkeeping of biomass, cohort biomass reaches its maximum at body masses <1 g, unlike standard yield‐per‐recruit models, where body growth and mortality are independent externalities, and cohort biomass is maximized at larger body sizes.  相似文献   

9.
Minimizing the impact of fishing is an explicit goal in international agreements as well as in regional directives and national laws. To assist in practical implementation, three simple rules for fisheries management are proposed in this study: 1) take less than nature by ensuring that mortality caused by fishing is less than the natural rate of mortality; 2) maintain population sizes above half of natural abundance, at levels where populations are still likely to be able to fulfil their ecosystem functions as prey or predator; and 3) let fish grow and reproduce, by adjusting the size at first capture such that the mean length in the catch equals the length where the biomass of an unexploited cohort would be maximum (Lopt). For rule 3), the basic equations describing growth in age‐structured populations are re‐examined and a new optimum length for first capture (Lc_opt) is established. For a given rate of fishing mortality, Lc_opt keeps catch and profit near their theoretical optima while maintaining large population sizes. Application of the three rules would not only minimize the impact of fishing on commercial species, it may also achieve several goals of ecosystem‐based fisheries management, such as rebuilding the biomass of prey and predator species in the system and reducing collateral impact of fishing, because with more fish in the water, shorter duration of gear deployment is needed for a given catch. The study also addresses typical criticisms of these common sense rules for fisheries management.  相似文献   

10.
11.
12.
Recruitment overfishing occurs when stocks are fished to a level where recruitment declines proportionally with adult abundance. Although typically considered a commercial fishery problem, recruitment overfishing can also occur in freshwater recreational fisheries. This study developed an age‐structured model to determine if minimum‐length limits can prevent recruitment overfishing in black crappie, Pomoxis nigromaculatus (LeSueur), and walleye, Sander vitreus (Mitchill) fisheries considering angling effort response to changes in fish abundance. Simulations showed that minimum‐length limits prevented recruitment overfishing of black crappie and walleye, but larger minimum‐length limits were required if angler effort showed only weak responses to changes in fish abundance. Low angler‐effort responsiveness caused fishing mortality rates to remain high when stock abundance declined. By contrast, at high effort responsiveness, anglers left the fishery in response to stock declines and allowed stocks to recover. Angler effort for black crappie and walleye fisheries suggested that angler effort could be highly responsive for some fisheries and relatively stable for others, thereby increasing the risk of recruitment overfishing in real fisheries. Recruitment overfishing should be considered seriously in freshwater recreational fisheries, and more studies are needed to evaluate the responsiveness of angler effort to changes in fish abundance.  相似文献   

13.
Analysing how fish populations and their ecological communities respond to perturbations such as fishing and environmental variation is crucial to fisheries science. Researchers often predict fish population dynamics using species‐level life‐history parameters that are treated as fixed over time, while ignoring the impact of intraspecific variation on ecosystem dynamics. However, there is increasing recognition of the need to include processes operating at ecosystem levels (changes in drivers of productivity) while also accounting for variation over space, time and among individuals. To address similar challenges, community ecologists studying plants, insects and other taxa increasingly measure phenotypic characteristics of individual animals that affect fitness or ecological function (termed “functional traits”). Here, we review the history of trait‐based methods in fish and other taxa, and argue that fisheries science could see benefits by integrating trait‐based approaches within existing fisheries analyses. We argue that measuring and modelling functional traits can improve estimates of population and community dynamics, and rapidly detect responses to fishing and environmental drivers. We support this claim using three concrete examples: how trait‐based approaches could account for time‐varying parameters in population models; improve fisheries management and harvest control rules; and inform size‐based models of marine communities. We then present a step‐by‐step primer for how trait‐based methods could be adapted to complement existing models and analyses in fisheries science. Finally, we call for the creation and expansion of publicly available trait databases to facilitate adapting trait‐based methods in fisheries science, to complement existing public databases of life‐history parameters for marine organisms.  相似文献   

14.
Hydropower‐related damage to fish remains a great challenge, making objective monitoring of turbine‐related fish injury a necessity. The catch of fish at turbine outlets is currently realised by net fishing, but potential catch‐related injuries are largely unknown. Catch efficiency and fish‐friendliness in relation to fish handling, exposure time, floating debris and fish biomass of four fish recovery installations were assessed using seven species. Highly species‐specific lethal and sublethal effects were observed. Exposure time had the strongest effects on catch‐related damage, being up to 150‐fold increase after 12 hr compared to 1 hr. Up to 84% mortality occurred in the most sensitive species Thymallus thymallus L. Besides exposure time, higher current speed and biomass within the net resulted in greater fish damage. To minimise catch‐related effects, keeping emptying periods <1–2 hr and considering the effects of current speed, fish and debris biomass are crucial to increase data comparability among studies.  相似文献   

15.
Gravel pit lakes are increasingly common, and there is an urgent need to better understand the functioning of these artificial and disconnected ecosystems. However, our knowledge of the environmental determinants of fish community structure within these types of lakes remains poor. In this study, we quantified the taxonomic diversity, fish species and life‐stage composition in 17 gravel pit lakes sampled in 2012 and 2013 located in south‐west France to determine the potential role of environmental variables (i.e. lake morphology, productivity, water quality and human‐use intensity) as drivers of fish community structure and composition. Our results demonstrated that fish community structure significantly differed between gravel pit lakes, and we notably found that lakes managed for angling hosted higher levels of taxonomic diversity. We also found that young and large lakes supported higher native species biomass and were dominated by native European perch (Perca fluviatilis). Older, smaller and more productive lakes, located closer to the main urban area, supported a higher biomass of non‐native species such as largemouth bass (Micropterus salmoides). Native and non‐native sport fishing species such as northern pike (Esox lucius), pikeperch (Sander lucioperca), common carp (Cyprinus carpio) and cyprinid prey species were positively associated with fishery management effort, suggesting that management practices play also a critical role in shaping fish species composition. Overall, our study demonstrated that fish community composition followed a predictable shift along environmental gradients associated with the maturation of gravel pit lakes and the associated human practices.  相似文献   

16.
The natural mortality (M) and purse‐seine catchability and selectivity were estimated for yellowtail scad, Trachurus novaezelandiae, Richardson, a small inshore pelagic species harvested off south‐eastern Australia. Hazard functions were applied to two decades of data describing catches (mostly stable at a mean ± SE of 315 ± 14 t p.a.) and effort (declining from a maximum of 2,289 to 642 boat days between 1999/2000 and 2015/2016) and interdispersed (over 9 years) annual estimates of size at age (0+ to 18 years) to enable survival analysis. The data were best described by a model with eight parameters, including catchability (estimated at <0.1 × 10?7 boat/day), M (0.22/year) and variable age‐specific selection up to 6 years with a 50% retention among 5‐year‐olds (larger than the estimated age at maturation). The low catchability implied very low fishing mortality by the purse‐seine fleet. Ongoing monitoring and applied gear‐based studies are required to validate purse‐seine catchability and selectivity, but the data nevertheless imply T. novaezelandiae could incur additional fishing effort and, in doing so, alleviate pressure on other regional small pelagics.  相似文献   

17.
Marine fisheries target and catch fish both for direct human consumption (DHC) as well as for fishmeal and fish oil, and other products. We derived the fractions used for each for 1950–2010 by fishing country, and thus provide a factual foundation for discussions of the optimal use of fisheries resources. From 1950 to 2010, 27% (~20 million tonnes annually) of globally reconstructed marine fisheries landings were destined for uses other than DHC. Importantly, 90% of fish destined for uses other than DHC are food‐grade or prime food‐grade fish, while fish without a ready market for DHC make up a much smaller proportion. These findings have implications for how we are using fish to feed ourselves or, more appropriately, how we are not using fish to feed ourselves.  相似文献   

18.
19.
Coral reefs support numerous ornamental fisheries, but there are concerns about stock sustainability due to the volume of animals caught. Such impacts are difficult to quantify and manage because fishery data are often lacking. Here, we suggest a framework that integrates several data‐poor assessment and management methods in order to provide management guidance for fisheries that differ widely in the kinds and amounts of data available. First, a resource manager could assess the status of the ecosystem (using quantitative metrics where data are available and semi‐quantitative risk assessment where they are not) and determine whether overall fishing mortality should be reduced. Next, productivity susceptibility analysis can be used to estimate vulnerability to fishing using basic information on life history and the nature of the fishery. Information on the relative degree of exploitation (e.g. export data or ratios of fish density inside and outside no‐take marine reserves) is then combined with the vulnerability ranks to prioritize species for precautionary management and further analysis. For example, species that are both highly exploited and vulnerable are good candidates for precautionary reductions in allowable capture. Species that appear to be less vulnerable could be managed on a stock‐specific basis to prevent over‐exploitation of some species resulting from the use of aggregate catch limits. The framework could be applied to coral reef ornamental fisheries which typically lack landings, catch‐per‐unit‐effort and age‐size data to generate management guidance to reduce overfishing risk. We illustrate the application of this framework to an ornamental fishery in Indonesia.  相似文献   

20.
Fishing operations on any given stock rarely generate fishing mortality that is uniform across all ages and sizes. Population‐selectivity refers to a scaled version of the age‐ or size‐specific fishing mortality experienced by a fish population. Although it is common to apply a sigmoid logistic curve for the selectivity produced by many kinds of fishing gear, the general characteristics of population–selection curves have not been well examined. In this study, generalized additive models were fit to sets of selection coefficients taken from 15 recent stock assessments conducted using the virtual population analysis approach. The selection coefficients predicted by the models provided smoothed representations of the shapes and temporal dynamics of selectivity. Four broad types of selectivity were found: increasing, asymptotic, domed, and having a saddle. Four specific cases, each dominated by one type of selection curve, were examined in detail. For all 15 stocks, the population–selection curves were not stable through time but underwent changes in shape, which in some cases were quite radical. Temporal variation in population‐selectivity has important implications for the conduct of fisheries modelling activities such as evaluating management strategies and forecasting catch and stock size.  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号