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Catch Data (catch + data)
Selected AbstractsFactors influencing fish catch levels on Kenya's coral reefsFISHERIES MANAGEMENT & ECOLOGY, Issue 4 2007S. C. Mangi Abstract, The factors influencing fish catches on Kenya's coral reefs were studied. Catch data were collected at the species level by counting the number of fish landed at each landing site of each fishing ground. Live coral cover, topographic complexity, fish and sea urchin density, and the number of fishers and gear units used in each fishing ground were compared with catch data. Fishing grounds included one location where only basket traps were allowed, six locations where all gear types were used except beach seines, and three locations where all types of gear, including beach seines, were used. Catch and effort variables were similar across the fishing grounds whereas live coral cover and sea urchin density differed (P < 0.01). The sites fished by all types of gear including beach seines had the lowest coral cover (8.4 ± 0.9%) and topographic complexity (1.12 ± 0.01). Catch levels were positively correlated with the number of fishers and fish density but not with the number of gear units deployed or sea urchin density. The number of fishers and live coral cover were the strongest factors determining total catch levels. The results suggest that high levels of fishing effort coupled with the use of destructive gear types, exacerbate the effects of overfishing on Kenya's reefs. [source] Ecological relevance of temporal stability in regional fish catchesJOURNAL OF FISH BIOLOGY, Issue 5 2003H. Hinz The concept of habitat selection based on ,Ideal Free Distribution' theory suggests that areas of high suitability may attract larger quantities of fishes than less suitable or unsuitable areas. Catch data were used from groundfish surveys to identify areas of consistently high densities of whiting Merlangius merlangus, cod Gadus morhua and haddock Melanogrammus aeglefinus in the Irish Sea and plaice Pleuronectes platessa, sole Solea solea, lemon sole Microstomus kitt in the English Channel over a period of 10 and 9 years respectively. A method was introduced to delineate areas of the seabed that held consistently high numbers of fishes objectively from large datasets. These areas may constitute important habitat characteristics which may merit further scientific investigations in respect to ,Essential Fish Habitats'(EFH). In addition, the number of stations with consistently high abundances of fishes and the number of stations where no fishes were caught gave an indication of the site specificity of the fish species analysed. For the gadoids, whiting was found to be less site specific than cod and haddock, while for the flatfishes, plaice and sole were less site specific than lemon sole. The findings are discussed in the context of previously published studies on dietary specializm. The site specificity of demersal fishes has implications for the siting process for marine protected areas as fish species with a strong habitat affinity can be expected to benefit more from such management schemes. [source] From small-scale habitat loopholes to decadal cycles: a habitat-based hypothesis explaining fluctuation in pelagic fish populations off PeruFISH AND FISHERIES, Issue 4 2004Arnaud Bertrand Abstract The Peru-Humboldt Current system (HCS) supports the world's largest pelagic fisheries. Among the world's eastern boundary current systems, it is the most exposed to high climatic stress and is directly affected by El Niño and La Niña events. In this volatile ecosystem, fish have been led to develop adaptive strategies in space and time. In this paper, we attempt to understand the mechanisms underlying such strategies, focusing on the El Niño 1997,98 in Peru from which an extensive set of hydrographic, capture and acoustic survey data are available. An integrated analysis of the data is crucial, as each has substantial shortcomings individually; for example, both catch data and acoustic surveys may easily lead to wrong conclusions. Existing hypotheses on anchovy and sardine alternations lead us to a ,habitat-based' synthetic hypothesis. Using our data, an integrated approach evaluated how fish responded to habitat variation, and determined the consequences in terms of fish-population variability. Various factors occurring at a range of different spatio-temporal scales were considered: interdecadal regime (warm ,El Viejo'/cool ,La Vieja' decadal scale); strength and the duration of the El Niño Southern Oscillation event (interannual scale); population condition before the event (interannual scale); fishing pressure and other predation (annual scale); changes in reproductive behaviour (intra-annual scale); presence of local upwelling (local scale). During El Niño 1997,98, anchovy was able to exploit a small-scale temporal and spatial ,loophole' inside the general unfavourable conditions. Moreover, sardine did not do better than anchovy during this El Niño and was not able to take advantage of the ,loophole' opened by this short-term event. Our results question the traditional view that El Niño is bad for anchovy and good for sardine. [source] Managing non-target, data-poor species using catch limits: lessons from the Alaskan groundfish fisheryFISHERIES MANAGEMENT & ECOLOGY, Issue 4 2010R. F. REUTER Abstract, The 2006 reauthorisation of the Magnuson-Stevens Fishery Conservation and Management Act requires annual catch limits for all target and non-target species within federally managed fisheries in the United States. In Alaska, both target and non-target species in the Alaska groundfish fisheries have been managed using catch limits since the early 1990s. Non-target species that are caught incidentally in a fishery require monitoring to ensure that the population is not negatively impacted by commercial fishing. Resource assessment scientists have been challenged with obtaining sufficient data to recommend an acceptable catch level for management of these species. This paper reviews three case studies where a catch limit is determined for non-target species when certain data are limited: (1) varying levels of biomass and catch data for all species within a species group or complex; (2) adequate catch data but no biomass data; (3) emerging target fishery of data-poor species, plus an example of how a complex of ecosystem component species is managed. [source] Factors influencing fish catch levels on Kenya's coral reefsFISHERIES MANAGEMENT & ECOLOGY, Issue 4 2007S. C. Mangi Abstract, The factors influencing fish catches on Kenya's coral reefs were studied. Catch data were collected at the species level by counting the number of fish landed at each landing site of each fishing ground. Live coral cover, topographic complexity, fish and sea urchin density, and the number of fishers and gear units used in each fishing ground were compared with catch data. Fishing grounds included one location where only basket traps were allowed, six locations where all gear types were used except beach seines, and three locations where all types of gear, including beach seines, were used. Catch and effort variables were similar across the fishing grounds whereas live coral cover and sea urchin density differed (P < 0.01). The sites fished by all types of gear including beach seines had the lowest coral cover (8.4 ± 0.9%) and topographic complexity (1.12 ± 0.01). Catch levels were positively correlated with the number of fishers and fish density but not with the number of gear units deployed or sea urchin density. The number of fishers and live coral cover were the strongest factors determining total catch levels. The results suggest that high levels of fishing effort coupled with the use of destructive gear types, exacerbate the effects of overfishing on Kenya's reefs. [source] Linking spatial pattern of bottom fish assemblages with water masses in the North SeaFISHERIES OCEANOGRAPHY, Issue 1 2009SIEGFRIED EHRICH Abstract Understanding the links between large scale spatial structuring of fish assemblages and shaping factors is essential to develop comprehensive ecosystem-based fisheries management. In this study, we investigated spatial patterns of bottom fish assemblages in the North Sea in relation to prevailing water masses in the region. We based our analysis on catch data from the German Small-Scale Bottom Trawl Survey conducted between 1987 and 2005 and used both ordination techniques and Mantel tests. Spatial variability of bottom fish assemblages was larger than inter-annual variability. Five significantly different bottom fish assemblages were associated with the following prevailing hydrographical regimes: i) the English Channel, ii) Continental Coastal, iii) central North Sea, iv) northern North Sea, and v) northern Atlantic water masses. Associations were generated by gradients in relative proportions of abundant species such as grey gurnard (Eutrigla gurnardus), dab (Limanda limanda), whiting (Merlangius merlangus), haddock (Melanogrammus aeglefinus) and Norway pout (Trisopterus esmarki). Taking into account large scale spatial structuring of catch data Mantel tests confirmed significant correlation between the fish assemblages and hydrographical variables. In summary, our results strongly support the hypotheses that hydrographical features such as water masses, fronts, and residual currents could shape bottom fish associations in the North Sea. Spatial demarcations of bottom fish assemblages indicated by this study can be used to support ecosystem-based fisheries management strategies. [source] Environmental effects on recruitment and productivity of Japanese sardine Sardinops melanostictus and chub mackerel Scomber japonicus with recommendations for managementFISHERIES OCEANOGRAPHY, Issue 4 2005AKIHIKO YATSU Abstract We compared a wide range of environmental data with measures of recruitment and stock production for Japanese sardine Sardinops melanostictus and chub mackerel Scomber japonicus to examine factors potentially responsible for fishery regimes (periods of high or low recruitment and productivity). Environmental factors fall into two groups based on principal component analyses. The first principal component group was determined by the Pacific Decadal Oscillation Index and was dominated by variables associated with the Southern Oscillation Index and Kuroshio Sverdrup transport. The second was led by the Arctic Oscillation and dominated by variables associated with Kuroshio geostrophic transport. Instantaneous surplus production rates (ISPR) and log recruitment residuals (LNRR) changed within several years of environmental regime shifts and then stabilized due, we hypothesize, to rapid changes in carrying capacity and relaxation of density dependent effects. Like ISPR, LNRR appears more useful than fluctuation in commercial catch data for identifying the onset of fishery regime shifts. The extended Ricker models indicate spawning stock biomass and sea surface temperatures (SST) affect recruitment of sardine while spawning stock biomass, SST and sardine biomass affect recruitment of chub mackerel. Environmental conditions were favorable for sardine during 1969,87 and unfavorable during 1951,67 and after 1988. There were apparent shifts from favorable to unfavorable conditions for chub mackerel during 1976,77 and 1985,88, and from unfavorable to favorable during 1969,70 and 1988,92. Environmental effects on recruitment and surplus production are important but fishing effects are also influential. For example, chub mackerel may have shifted into a new favorable fishery regime in 1992 if fishing mortality had been lower. We suggest that managers consider to shift fishing effort in response to the changing stock productivity, and protect strong year classes by which we may detect new favorable regimes. [source] An evaluation of the potential influence of SST and currents on the oceanic migration of juvenile and immature chum salmon (Oncorhynchus keta) by a simulation modelFISHERIES OCEANOGRAPHY, Issue 1 2004Tomonori Azumaya Abstract Using a salmon migration model based on the assumption that swimming orientation is temperature dependent, we investigated the determining factors of the migration of juvenile and immature chum salmon (Oncorhynchus keta) in the North Pacific. We compared the predictions of the model with catch data of immature and juvenile chum salmon collected by Japanese research vessels from 1972 to 1999. The salmon migration model reproduced the observed distributions of immature chum salmon and indicates that passive transport by wind-driven and geostrophic currents plays an important role in the eastward migration of Asian salmon. These factors result in a non-symmetric distribution of Asian and North American chum salmon in the open ocean. The directional swimming component contributes to the northward migration in summer. The model results indicate that during the first winter Asian chum salmon swim northward against the southward wind-driven currents to stay in the western North Pacific. This suggests that Asian chum salmon require more energy to migrate than other stocks during the first winter of their ocean life. [source] APPLIED ISSUES: Size-dependent mortality of migratory silver eels at a hydropower plant, and implications for escapement to the seaFRESHWATER BIOLOGY, Issue 10 2010O. CALLES Summary 1.,The European eel population has decreased drastically during recent decades, and new EU-legislation calls for measures to change this negative trend. This decline has been attributed to a number of factors, including habitat fragmentation by structural barriers that prevent eels moving between freshwater and the sea. The success of downstream migrating adult silver eels migrating past a hydroelectric plant (HEP) in Sweden was examined by radio-telemetry, and the results were considered in a historical context by analysing catch data from the river for 1957,2006. 2.,The choice of routes and passage success were quantified for three treatment groups and one control group of silver eels. The first treatment, the reservoir group (n = 50), was released into the reservoir upstream of the HEP, and these fish could proceed downstream by passing through the HEP (20 mm rack and turbines) or by entering the spill gates into the former channel, bypassing the HEP. The second treatment group (inside rack, n = 15) was released downstream of the 20-mm rack and had to pass through the turbines to continue migration to the sea. The third treatment group consisted of dead radio-tagged eels (n = 6) that were released into the turbines to study the extent of drifting by dead individuals. Finally, the control group (n = 50) was released downstream of the HEP to test for effects of confounding factors. 3.,Most live individuals displayed migratory behaviour and continued to proceed downstream after release. Only 8% of the fish released in the reservoir or downstream of the HEP (control) did not migrate. The probability of reaching the next HEP, 24 km further downstream, was high for the control group (96%) and the reservoir-released individuals that passed the HEP via the spill gates and the former channel (83%). Survival was low and size-dependent for the individuals that passed the turbines (40%) and even lower for the individuals that had to pass through the rack and the turbines (26%). The overall passage success for eels released in the reservoir was 30%, including both routes. 4.,Annual catch data from 1957 to 2006 showed that the number of eels in the River Ätran has decreased. Despite this decrease, escapement biomass has remained unchanged, because of the fact that the mean size of eels has doubled. Passage data from 2007 show that changes in size and abundance have resulted in a reduction of relative escapement to the sea to values that are 21,24% of what they were in 1957,66. However, this low level of escapement could potentially be rectified if appropriate measures facilitating HEP passage are successfully implemented, since the potential escapement biomass in the river, owing to the large size of the eels, has changed little since the 1950s. [source] Consequences of climatic change for water temperature and brown trout populations in Alpine rivers and streamsGLOBAL CHANGE BIOLOGY, Issue 1 2006RENATA E. HARI Abstract Twenty-five years of extensive water temperature data show regionally coherent warming to have occurred in Alpine rivers and streams at all altitudes, reflecting changes in regional air temperature. Much of this warming occurred abruptly in 1987/1988. For brown trout populations, the warming resulted in an upward shift in thermal habitat that was accelerated by an increase in the incidence of temperature-dependent Proliferative Kidney Disease at the habitat's lower boundary. Because physical barriers restrict longitudinal migration in mountain regions, an upward habitat shift in effect implies habitat reduction, suggesting the likelihood of an overall population decrease. Extensive brown trout catch data documenting an altitudinally dependent decline indicate that such a climate-related population decrease has in fact occurred. Our analysis employs a quantitatively defined reference optimum temperature range for brown trout, based on the sinusoidal regression of seasonally varying field data. [source] Recruitment of Anguilla spp. glass eels in the Waikato River, New Zealand.JOURNAL OF FISH BIOLOGY, Issue 9 2009Evidence of declining migrations? The timing of Anguilla spp. glass eel recruitment into the Waikato River, North Island, New Zealand, was studied over a 2 year period (2004,2005). While glass eels of both the shortfin eel Anguilla australis and the endemic longfin eel Anguilla dieffenbachii were caught, the former comprised >97% of the species composition. There was a positive correlation of glass eel migrations with spring tides, with peak migration periods typically occurring within a few hours of the peak of high tide, and between 2 and 4 days after the day of spring tide. Both water temperature and discharge had significant inverse relationships with glass eel catches, with temperature explaining >30% of the variance in catch periodicity. Comparison of catch data 30 years apart showed that main migration periods appear to occur several weeks earlier today than previously. Reduced catch per unit effort and duration of runs from recent years' sampling (compared with the 1970s) indicate that a reduction in recruitment may also have occurred during this period, something recorded in other temperate species of Anguilla. [source] Long distance migration and marine habitation in the tropical Asian catfish, Pangasius krempfiJOURNAL OF FISH BIOLOGY, Issue 3 2007Z. Hogan A synthesis of catch data from southern Laos and life-history information indicate that adult Pangasius krempfi, an important Asian catfish, migrates up the Mekong River from the South China Sea in Vietnam past Cambodia, arriving in southern Laos each year in May. Strontium concentrations in the otoliths of river-caught P. krempfi are, on average, three to four times higher than the levels of strontium in the otoliths of related freshwater species, indicating marine and estuary habitation for fish caught in southern Laos. Pangasius krempfi muscle tissue samples from the same fish also exhibit stable isotope (,15N and ,13C) values characteristic of marine environments. The results of this investigation support the conclusion that P. krempfi is anadromous, spending a part of its life at sea and in the brackish water of the Mekong Delta before returning to spawn in fresh water. The fish travels at least 720 km to the Khone Falls in southern Laos, and possibly further. Spawning probably occurs in fresh water from June to August at which time young fish move down the Mekong River to the Mekong Delta. The data answer a previously unresolved question (the long-distance migratory behaviour of P. krempfi) and have important implications for the management and conservation of Mekong River fishes. [source] Rapid invasion of a subtropical lake fishery in central Mozambique by Nile tilapia, Oreochromis niloticus (Pisces: Cichlidae)AQUATIC CONSERVATION: MARINE AND FRESHWATER ECOSYSTEMS, Issue 6 2008Olaf L.F. Weyl Abstract 1.Lake Chicamba, Mozambique (19°08,S; 33°08,E) is a large (116 km2) impoundment in the headwaters of the Buzi River system, which was invaded by Oreochromis niloticus in 1996 from a small (<0.3 km2) upstream reservoir. 2.Experimental and artisanal catch data showed no O. niloticus until January 1996; after this O. niloticus was recorded in up to 83% of experimental seine net catches, 33% of experimental gill net catches, 43% of boat angling and 23% of shore angling catches, and in 48% of artisanal gill net catches. 3.During the period January to March 1997, O. niloticus mean (upper, lower 95% confidence interval) yields in the artisanal fishery were 5.2 (3.6, 7.0) t month,1. 4.The rapid invasion of this lake illustrates the significant invasion threat that small point-sources of this species pose to southern African freshwater systems. 5.The study recommends: (1) that this species should not be used for aquaculture or fisheries enhancement in catchments that have not been invaded, and (2) that the eradication of potential point sources of O. niloticus in non-invaded catchment systems should be considered. Copyright © 2007 John Wiley & Sons, Ltd. [source] | |||||||||||||