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1.
Abstract  Lough Neagh produces over 500 t of grown eel annually and employs 300 people fishing yellow and silver eel. Glass eel are transported upstream and stocked into the Lough. Since glass eel returns crashed in the 1980s, additional glass eel seed has been purchased from other fisheries. The fishery now faces ecological, social and economic pressures. Prices for the product have fallen; recruitment to the fishery has declined, and seed has decreased in availability and increased in price. Fishers are less inclined to take up the hard work required to make a living fishing eel and the fisher population is ageing. The European Commission has recognised the decline of eel and proposed emergency measures, which may further affect the viability of the fishery. The sustainability of the fishery is examined, based on the relationship between glass eel input and grown eel outputs over a period of 45 years, set against increasing environmental, socio-economic, and natural resource pressures. Spawning escapement of silver eel is estimated by mark–recapture experiments.  相似文献   

2.
Monitoring of yellow‐phase and silver‐phase Anguilla anguilla during their continental life history is necessary for evaluation of stock recovery measures. Eel population data for an Irish lake (Lough Sheelin) were compiled for the period 1993–2014. Catch data from 2009 to 2014 provided minimum estimates of recent silver eel production ranging annually from 0.79 to 1.84 kg/ha. Long‐term changes in yellow eel abundance and silver eel size structure were assessed as part of a fishery monitoring programme. Yellow eel catch per unit effort (CPUE) in the lake (from longline surveys) was considerably higher in the 1990s (52.2–62.1 eels/100 hooks) than 2002–2008 (1.9–15.8 eels/100 hooks). Conversely, during 1993–2014, the mean size of silver eels migrating from the lake increased significantly (p < .001), from 659 mm to 838 mm. The results suggest that in the absence of direct yellow eel abundance data, interannual variation in silver eel size structure may be a useful monitoring tool for local eel stocks as part of Eel Management Plans (EMP's).  相似文献   

3.
One of the actions that has been implemented to support the recovery of the panmictic population of European eel is stocking of waterbodies where natural recruitment is low or null. However, growth conditions of the stocked eels can vary greatly. This circumstance emphasises the importance to determine ideal habitat conditions to contribute to the success of stocking actions and, consequently, to increase the production of silver eels. This study aims to evaluate the early settlement and growth of stocked glass eels in the upper reaches of a fragmented river. Stocking was carried out, in 2014, at three sites of an inland tributary of the Mondego river basin (Central Portugal), and its monitoring was conducted during the following two years, until 2016, along with the collection of environmental and hydromorphological parameters. The results showed a successful dispersion throughout the study area. Growth varied spatially, although environmental parameters have not clearly explained this variation, but overall with high growth rates and a positive allometric growth in this early stage of stocking, suggesting a good condition of the stocked individuals. This study showed that these upper reaches of fragmented watercourses, a shared feature amongst most European rivers that are currently inaccessible for natural recruitment, may be suitable habitats for eel stocking.  相似文献   

4.
Abstract– Two almost eel-free lakes (339 and 299 ha respectively) in southeastern Sweden were stocked with French elvers in the autumn of 1980. The introduced eel stocks were monitored from the time of stocking and onwards using outlet traps equipped with fine-meshed screens and subsequently by test-fishing with long-lines and fyke-nets. Up to and including the spring run of 1994, more than 5,900 eels or about 2,600 kg were recaptured from one of the lakes, mostly as migrating silver eels. This means a recapture rate of about 11%. In the other lake most recaptures came from fyke-netting of the yellow eel stock. In this lake only 1.7% have been recaptured up to this point. These differences in yield and recapture rates from the two lakes are discussed in the context of lake productivity, growth rates, sex ratios, sizes of stocked elvers and size at silvering. In cconomic terms, the results from the higher-yielding lake indicate an excellent rate of profit. After approximately 10 years, the investment (cost of the introduced elvers) was paid back at a lending interest rate of 10%.  相似文献   

5.
Abstract –  Since the 1980s, the European eel Anguilla anguilla stock is in steep decline. Lipid reserves are essential to cover energetic requirements for silver eel migration and reproduction. Two large and independent data sets from Belgium and The Netherlands show an average one-third decrease in fat contents of yellow eels over the past 15 years. Also Le Cren's relative condition factor decreased. On the basis of the somatic energy reserves, reproductive potential of eels from various latitudes over Europe was estimated, assuming fat levels in yellow eel are indicative of those in silver eels. Only large individuals, females as well as males, with high lipid content seem to be able to contribute to the spawning stock. The decrease in fat content in yellow eels may be a key element in the stock decline and raises serious concerns about the chances of the stock to recover.  相似文献   

6.
The sex ratio of wild Japanese eels in the Kaoping River of southwestern Taiwan has been extremely skewed towards females in the recent years. However, the sex ratio skewed towards males after Typhoon Mindulle, July 2, 2004 then recovered to the previous female-dominated status in the following year. To determine why the sex ratio drastically changed, eels captured in the river were examined by both morphologic characteristics and otolith elemental signatures by solution-based inductively coupled plasma mass spectrometry (SB-ICPMS) and laser-ablation ICPMS (LA-ICPMS). Most of the eels collected in the river after the typhoon had a blue-gray colored back, with morphology and sex ratio similar to that of cultured eels, which differed from wild yellow eels which had a green colored back. The chemical signature in otoliths of eels with a blue-gray colored back was similar to that of cultured eels, with significantly lower Sr/Ca ratios but slightly higher Mn/Ca ratios than for wild eels. This confirmed that the reversal in eel sex ratio in the Kaoping River estuary resulted from cultured eels that had escaped from eel farms. Eel farmers estimated that about 30,000 eels escaped during the typhoon, sufficient to reverse the sex ratio of the eels in the river. Furthermore, silver eels caught in the estuary in the winter 2004 were also mostly males. The chemical signature in otoliths of these silver eels was similar to that of escaped cultured eels. Their morphology and mean GSIs, however, were comparable to wild silver eels. Thus, cultured eels that have escaped from eel farms can silver normally in the wild. Consequently, cultured eels may help to balance the sex ratio of the wild eel population and may contribute to the spawning stock of Japanese eel.  相似文献   

7.
There is expanding interest in the culture of the Australian shortfin eel Anguilla australis Richardson; however, there is a lack of fundamental biology and husbandry information necessary to further develop an industry within Australia. The present study was undertaken to gain a preliminary understanding of basic husbandry requirements for rearing of juvenile A. australis (glass eels and elvers) in tanks and earthen ponds. Newly caught glass eels were successfully acclimated to culture conditions. During tank culture trials, specific growth rates (SGR) and survival rates ranged from ?2.1 to 2.8% day?1 and 52% to 100% respectively. Glass eels weaned onto a commercial eel diet exhibited a significantly greater SGR and survival rate than those weaned onto a commercial trout diet. Glass eels weaned onto an eel diet over a 15‐day period grew slightly faster than eels weaned over a 5‐day period, but survival rates were not significantly different for each treatment. SGRs (up to 2.8% day?1) were significantly higher for glass eels fed at 9 and 12% day?1 than at 6% day?1. Stocking densities between 2.5 kg m?3 and 30 kg m?3 did not influence either SGR or survival rates. SGRs were significantly higher for glass eels cultured at 25 °C than at lower temperatures. During pond culture trials, SGRs and survival rates ranged from 1.36 to 1.65% day?1 and 39% to 77% respectively. The SGR and survival rates of juvenile eels stocked into ponds receiving supplementary feeding with a commercial eel diet were not significantly different to those of eels stocked into ponds that did not receive supplementary feeding.  相似文献   

8.
Over a period of 34 years (1954–1987), a total of 11.9 million glass eels were stocked all over Austria to improve the yields of commercial fishermen and to make the lakes more attractive for anglers. Nearly half (48%) of the imported glass eels were introduced into natural, previously eel‐free Alpine lakes until stocking ceased in 1988. Twenty‐five years later, their occurrence could be verified in 56% (N = 22) of the Austrian Alpine lakes larger than 50 ha and mean body length had increased to 66 cm. Eels from seven selected Austrian Alpine lakes exhibited a yearly mean increase in length between 0.6 and 1.5 cm, indicating a comparatively poor growth compared with the majority of eel populations from within their natural distribution range. At the same time, high expectations in developing a flourishing eel fishery were not met. In all but one lake, the harvest remained below 3% of the total yearly catch and salmonids remained the dominant target species. During peak harvest in the 1980s, it exceeded 8% in mesotrophic Wallersee (2600 kg). Simulations of stock development indicated that the yield could have been improved, but contrary to earlier expectations eels never became important for local cuisine and catches remained too low for the development of a profitable export business. On the other hand, eels may have contributed to the loss of small‐bodied fish taxa.  相似文献   

9.
Viral infections have been suggested to play a role in the decline of the panmictic population of the European eel (Anguilla anguilla). However, despite the importance of knowledge about pathogenic eel viruses, little is known about their spread in the wild European eel population and only a few eel pathogenic viruses have been described so far. In this study, we aimed to investigate the health status of the A. anguilla stock in North Rhine Westphalia (NRW) State of Germany. For this purpose, we examined tissue samples of 16 elvers, 100 yellow eels and 6 silver eels, sampled from the rivers Rhine, Lippe and Ems. Virus detection was performed via a combination of cell culture and PCR. Next to the detection of frequently encountered pathogenic eel viruses (anguillid herpesvirus 1 and eel virus European X (EVEX)), we isolated the eel picornavirus 1 (EPV-1) from tissue of yellow eels and elvers and demonstrate the distribution of EPV-1 in wild eel population in NRW.  相似文献   

10.
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11.
Abstract– Studies were performed with both a mechanical and a photosensory arrangement of the experimental tanks. Silver (migratory) eels were more active than yellow (stationary) eels. Comparison of pooled data on yellow eels tested under natural geomagnetic field conditions with those on eel tested under unnatural ones prcded no evidence of difference in activity. Silver and yellow eels showed stronger activity during the 6 days around new moon compared with the phase around full moon as well as a peak before new moon and a smaller peak before full moon. Under each kind of unnatural field condition, the activity relationships reversed or were cancelled. The directional choice of eels under natural conditions (controls) pointed to magnetic NW and mostly also in the opposite direction. When the magnetic north was changed by 90°, the tested yellow eels followed this change to about the same degree. The additional change of both the inclination (from 68° or 45° or 30°) and total intensity (by a reduction to 31% of the natural field) resulted in a change of the preferences of about 90° relative to magnetic north. Reversal of magnetic north by 180°, which is identical to a change of the inclination from 68° to 112°, also resulted in a change of the preferences by about 90°. Three experiments using compensation of both the horizontal and the vertical geomagnetic field led to circular directional preferences at random in two cases and in one case to about NW of the residual field magnetic north. The navigational abilities of the eel, on the basis of its magnetic sensitivity, are discussed.  相似文献   

12.
A size‐age modelling technique is presented for assessing the vital rates, stock and recruitment of eel populations in semi‐closed lagoons with fully monitored migration of silver eels. Data for yellow and silver European eels (Anguilla anguilla L.) were obtained in 2011 from the Comacchio lagoon (Italy). The analysis was performed in three steps: (i) correction of yellow eel data, which are affected by the fyke nets selectivity during samplings, (ii) estimation of survival curve, stock, recruitment and metamorphosis rates of the population (calibration using data from 2011) and (iii) validation of the model using the observed amount of silver eel migrating population of the next year. A bootstrap procedure was used to assess the level of uncertainty for each parameter using the 95% intervals of the highest posterior density distribution HPDD (Bayesian approach). The measured abundance of silver eels was 0.56 ind·ha?1, while the yellow eel abundance and recruitment were estimated by the model for 2011 at 8.77 ind·ha?1 and 5.99 ind. ha?1 respectively. The model performance during validation was satisfactory as the observed total mass of migrating population of 2012 (3777 kg) was inside the 95% HPDD intervals (3197–3839 kg) of model's predictions. The estimated stocks and recruitment were at least ten times lower from the respective estimations of previous studies of 1989 highlighting the crucial conditions of the population. The proposed modelling approach can provide significant information about eel population conditions, facilitating the evaluation of a range of management options in the context of eel conservation plans.  相似文献   

13.
The population dynamics and exploitation of the yellow eel (Anguilla anguilla (L.)) stock on the Swedish west coast were studied. In contrast to a generally observed reduction in the recruitment of glass eels in Europe, including in Swedish waters, there was no indication of a decline in the total eel fishery yields along the Swedish west coast. Long-term records of daily catches as well as by test fishing results also shown that this stability in eel fishery yields has not been maintained by an increase in fishery effort, as the catch-per-unit-efforts in the past 20 years have been more or less unchanged. These findings implied that the number of recruits to the fishery has been rather stable, possibly indicating that density-dependent factors at the elver and yellow eel stages may moderate variations in glass eel recruitment. Total instantaneous rate of mortality was estimated from records on eel length distribution in the professional fyke-net fishery. The estimated total mortality rate in an isolated archipelago population on the west coast was chosen as an approximation of the instantaneous rate of natural mortality and net emigration in the west coast eel stock. The differences between these two estimates could, thus be regarded as the mortality that occurred due to fishing. It was found that the eel fishery was very intense and most fish were caught in small sizes, resulting in a low escapement rate of maturing fish.  相似文献   

14.
Overwintering dormancy behaviour was studied in female silver eels in Lake Mälaren in Sweden between 2008 and 2010. Depth choices and movements in relation to temperature were analysed from pressure and temperature records for 13 eels with implanted data storage tags, covering 17 overwintering periods and three intervening summer periods. Dormancy commenced in October–November as temperatures fell below 4–12 °C. Eels tended to remain motionless throughout the winter, with some short periods of activity signalled by small changes in depth distributions. During dormancy, the eel shows a clear avoidance of shallow areas <5 m in favour of the 10–25‐m‐depth interval. Activity tended to resume 4–6 months later in April–May as temperatures rose above 3–7 °C and ice cover broke, and eels spent more time at shallower depths of <5–10 m. The majority of the eels were assessed as being in the silver eel stage at the time of tagging. During the autumn months, the diving behaviour, with frequent and large vertical excursions and periods at the surface, was similar to that seen in migrating eels in the Baltic and Atlantic Ocean. In spring and summer, the behaviour differed, being dominated by more gradual depth variations, implying that the eels reverted from silver eel migration behaviour to yellow eel foraging behaviour. Body weight declined during dormancy, but other studies of starvation over comparable time periods showed significantly higher average specific weight losses, implying that the Mälaren silver eels must have fed between the end of dormancy and recapture.  相似文献   

15.
Abstract – For decades, the European eel Anguilla anguilla (L.) population has been declining strongly despite several management attempts, so additional experiments need to be conducted on management measures. The use of freshwater protected areas has been advocated but their efficiency has never been assessed. In this study, we investigated whether the population structure and the silver eel (mature migrating stage) production differ in fished and protected areas within a marsh wetland (Brière, 7000 ha, Northwest France), using an intensive biological study (electrofishing and trapping) and a survey of the traditional fishery (licenses, questionnaires and creel surveys). First, we found that fishermen mainly targeted >320‐mm yellow eels (sedentary stage) using pots and square dipping nets and that harvest by fishermen was highly variable at different locations in the study area. Secondly, we found differences in the size‐class structures and mortality rates between protected and fished areas. Mortality rates of eels >320 mm was positively correlated with harvest by fishermen. Furthermore, the proportion of potentially migrating eels in the total population was found to be higher in the protected areas than in fished areas (6.38% vs. 1.42%, respectively). Thirdly, we found that protected areas potentially produce 8.4% of the total silver eel production whereas they only account for 2.4% of the aquatic habitat area. We estimated that a size adjustment of protected areas to 31.1% with maintaining the current fishery would produce 50% of the potential silver eel of a fully protected marsh. Protection of freshwater areas appears to be a promising management measure and a constructive consensual way to integrate the patrimonial and societal value of the traditional fishery and the international management plans for European eels. Furthermore, freshwater protective measures can be an effective local solution if they are integrated into the framework of freshwater biodiversity management and accompanied by other management measures that focus on all eel life stages.  相似文献   

16.
Aquaculture of Japanese eel Anguilla japonica relies upon the natural recruitment of their glass eels (juveniles); however, predation that could influence glass eel recruitment remains unknown. In the present study, we aimed to elucidate the proportion of predation on A. japonica glass eels through stomach content analysis of predatory fishes collected in the estuary region of the Tone River system and its vicinity in Japan. Species of the predated glass eels were identified by DNA barcoding. A total of 270 predatory fishes of 15 taxa was collected over 2 years. The overall proportion of predation on glass eels, genetically identified as Japanese eel, was 0.7%, but this rose to 2.0% when data were limited to fishes caught during the peak months of glass eel recruitment. A glass eel was found in the stomach contents of a channel catfish Ictalurus punctatus, an invasive species in this river system, and a blackfin sea bass Lateolabrax latus. These fishes are therefore considered potential predators of A. japonica glass eels. However, as the proportion of predation was low, and the glass eels represented only small proportions of predator stomach contents, further investigation is needed for a better understanding of predation on A. japonica glass eels, and its effects on the early life stages of this endangered species.  相似文献   

17.
The catadromous life cycle of the European eel encompasses a spawning migration to the Sargasso Sea. Prior to their migration, eels develop a silver coloration being referred to as “silver eels.” Due to the dramatic European eel recruitment decline, it is crucial to quantify silver eel escapement to evaluate the success of measures taken under Eel Management Plans (Regulation EC (1100/2007)). Thus, the percentage of silver eels escaping from the River Mondego (Portugal) was estimated during two consecutive spawning seasons (2014–2016) and their migratory behaviour was studied. Thirty-six male silver eels were tagged with acoustic transmitters and their downstream migration was tracked using automatic receivers deployed at four locations along the river course, from the first impassable obstacle up to the river mouth (67 km). Among the tagged eels, 15 (42%) escaped to the sea. In both years, individuals displayed faster migration speed in the downstream reaches of the river. BRT (“Boosted Regression Trees”) models were used to explain downstream migration and escapement of silver eels. The analyses revealed that the downstream migration is triggered by several environmental variables with water conductivity as the most influential predictor. Escapement of eels from the estuary occurred a few hours after their arrival and was primarily explained by the offshore wind intensity, which promotes a current in the coast that may favour their transport to the open sea. These findings contribute to a better understanding of silver eel migration in southern latitudes and highlight and reinforce the need to monitor spawner escapement.  相似文献   

18.
Abstract –  Knowledge of maturation state of eels ( Anguilla anguilla , L.) based on ocular index (OI) serves management and research functions, such as estimating how much silver eel actually could escape from a particular basin or determining more precisely the developmental biology of a particular eels. OI implies the measurements of five variables (total length and eyes diameters) in a formula which can be sensitive to measurement error. To investigate this issue, we carried out a comparative study using 13 European eels harvested in Camargue (Rhône Delta, France) and three replicated measurements by three different observers. The estimated amplitude of OI imprecision at a 95% confidence level was 1.8 whatever eel and observer. Such error may lead to classification problems particularly when OI values are close to the threshold values used to discriminate between yellow and silver stages. This study not only raised the problem of the OI imprecision but also brought up the need to develop standardised protocol for identifying silver eels. To reach this goal, two different ways are proposed in conclusion.  相似文献   

19.
Eels (Anguilla spp.) are in decline worldwide, and the signs of reduced recruitment have been observed in continental Europe since the early 1970s. To aid recovery of the European eel, stocking is used by many European countries as a management option. In this study, tagging experiments were conducted to follow eel migration from Lake Mälaren and four sites along the Swedish east coast in the Baltic Sea. The recaptured tagged eels were retrieved from fishermen, allowing for the opportunity to investigate their origin (brackish water, stocked in freshwater or a mix in between) by otolith microchemistry and to assess for morphological differences after tagging. Several changes took place; for example, eye index increased while weight and condition decreased with migrated distance and time until recapture. In Lake Mälaren, the majority of tagged eels did not migrate out of the outlets, irrespective of their origin. Most of them were caught in the opposite direction and continued to be caught in the lake 1–3 years after tagging, with significant weight losses. Overall, overwintering is suggested to be an inferior option, but it is uncertain whether this is a natural behaviour or a result of translocation and restocking. For coastal eels, origin had no effect on migratory behaviour; a majority of the tagged eels migrated towards the outlet of the Baltic Sea. Interestingly, a minority of the recaptured eels originated from stocked fish. Instead, recaptures were dominated by natural immigrants that had spent most of their lives in brackish waters.  相似文献   

20.
The pigmentation stages of Anguilla japonica were classified from the glass eel to yellow eel stage using 412 wild-caught eels from Hamana Lake and detailed developmental observations of 10 laboratory-reared eels. The sequential appearance of pigment was similar to that in A. anguilla, except for delayed pigment formation on the nerve cord of A. japonica. The general classification of pigmentation stages (VA–VIB) in A. anguilla was applicable to A. japonica, but the VB stage could be separated into two stages (VB1, VB2) in A. japonica. The completion of guanine deposition on the intra-abdominal membrane may be a trait to discriminate the yellow eel stage (VII) from the VIB stage. In natural conditions, wild-caught 0-age eels (n = 3,298) did not increase in size and retained a slender body form until VIA4, and then became thicker during VIB. The transition between body forms and growth may correspond to their ecological change from using passive transport in glass eels with tidal flow into rivers, to their settlement and further movements of elvers upstream. Considering this behavioral transition and pigmentation progression, it is proposed that the terms "glass eel" and "elver" could be defined as stages VA–VIA4 and VIB, respectively.  相似文献   

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