Reproduction,growth and feeding habits of stout beardfish Polymixia nobilis (Polymixiidae) off the Canary Islands (NE Atlantic)

The present study provides fisheries biology knowledge which will allow the implementation of regulatory measures contributing to the sustainability of the fisheries and the conservation of the stout beardfish Polymixia nobilis Lowe, 1838 off the Canary Islands, north eastern Atlantic Ocean. Males ranged between 16.5 and 38.4 cm fork length (FL) and females from 14.2 to 46.5 cm FL. Sex ratio by size classes provided significant differences in classes higher than 36 cm, being clearly unbalanced in favour of females. Individuals in maturing and mature stages were present during all months sampled, although a spawning peak is evident between April and June. Size at first maturity was estimated as 26 cm FL for females and 30 cm FL for males. Age was determined from annuli in whole otoliths. Age range was found to be 0–14 years for fish measuring 14.2 to 46.5 cm FL. It is a slow‐growing and long‐lived species. Significant differences in the growth parameters between sexes were detected. The von Bertalanffy growth parameters estimated for females (n = 213) were L_∞ = 45.92 cm LF, k = 0.16 years^?1 and t₀ = ?2.84 years; and for males (n = 186) L_∞ = 36.44 cm LF, k = 0.26 years^?1 and t₀ = ?2.16 years. Stomach analysis indicated some variations in the feeding habits with growth: individuals of small and medium sizes preyed on crustaceans and fishes, while large specimens preyed mainly on fishes.     

Aspects of the reproductive biology of two pelagic sharks in the eastern Atlantic Ocean

This study used data provided by the Chinese Longline Fishery Scientific Observer Programme from the tropical eastern Atlantic Ocean to estimate the reproductive parameters of the blue shark (Prionace glauca) and crocodile shark (Pseudocarcharias kamoharai). Sizes ranged from 80 to 298 cm fork length (FL) for blue sharks and from 48 to 99 cm FL for crocodile sharks. Sexual segregation was observed during different months for both sharks. The sex ratio for blue sharks was 1.38 F:1 M, and 1 F:2.79 M for crocodile sharks. The size of adult blue sharks ranged from 144 to 280 cm for males and from 174 to 298 cm for females; and that of crocodile sharks from 63 to 97 cm for males and 78–99 cm for females. The size at 50% of maturity for blue sharks was estimated at 191.7 cm FL for females and 197.5 cm FL for males, and that of crocodile sharks was assessed at 84.9 cm FL for females and 78.5 cm FL for males. Most sexually matured females were pregnant; their means were 207.2 ± 16.4 cm FL for blue sharks and 89.4 ± 4.3 cm FL for crocodile sharks. Mature sizes for both species were significantly different among months. Embryonic sizes also varied widely among months for crocodile sharks, but a slight change was recorded for those of blue sharks. The observed mean size at birth and litter size were 34.5 cm FL and 37 ± 12 for the blue sharks, and that of the crocodile sharks, 39.5 cm FL and a dominant four embryos in the uterus. Due to the observed increasing catch trend of blue sharks and the slow reproductive cycle of crocodile sharks, this study presents the need of implementing conservation measures to ensure the sustainability of both species in their habitat.     

Age and growth of Atlantic bluefin tuna, Thunnus thynnus (Osteichthyes: Thunnidae), in the Mediterranean Sea

The objective of the study was to describe the biometry of Mediterranean bluefin tuna, Thunnus thynnus, the biology of which is not yet well understood. A total of 504 specimens was collected from 1998 to 2005 in the central part of the Mediterranean basin. They were sexed and measured; fork lengths (FL) ranged from 51.0 to 255.0 cm while body weights (W) ranged from 2.6 to 247.0 kg. The first spiniform ray (spine) of the first dorsal fin was removed and cross‐sectioned near the condyle base in order to count annuli for age estimation. The regression coefficient (b) of the female FL–W relationship was significantly higher than that of the male, and both sexes displayed a negatively allometric growth (b < 3); male regression equation: ln W = ?2.942 + 2.730 ln FL; female regression equation: ln W = ?3.660 + 2.878 ln FL. Based on counts of the translucent zones in the sections of the first ray of the first dorsal fin, estimated ages ranged from 1 to 15 years for males and 1 to 14 years for females. The correlation between the spine ray (R) and FL fit the allometric model best; the R–FL regression equations of the two sexes did not differ significantly and the overall equation was: ln FL = 3.721 + 0.851 ln R. Due to the R–FL allometric correlation, estimates of fork lengths at previous ages, FL_i, were back‐calculated with a body proportional hypothesis. Von Bertalanffy growth equations were derived from both observed and back‐calculated FLs‐at‐age, which did not differ significantly. Moreover, no significant difference was found between the growth equations of the two sexes; the overall equation was FL_t = 373.08 [1?e^{?0.07(t + 1.76)}]. Weight‐at‐age values were derived from the von Bertalanffy predicted FLs‐at‐age by the FL–W correlation equations for males and females. The paper represents the first comprehensive study on the biometry, including age and growth, of bluefin tuna captured in the Mediterranean Sea.     

Reproduction in Bagre marinus (Ariidae) off Pernambuco, northeastern Brazil

Throughout 1997, the catches of artisanal gillnetters working off the coast of northeastern Brazil were sampled monthly for Bagre marinus (Mitchill 1815). Significantly more females (n = 207) than males (n = 82) were caught, although there was no significant difference in their size compositions (21–47 cm fork length, FL). All males sampled (21–40 cm FL) had developed gonads and were classified as sexually mature. According to macroscopic and microscopic examination of their reproductive tract, females were separated into four reproductive stages (immature, maturing, mature, and resting). Size at 50% sexual maturity for females was estimated to be 33 cm FL. A positive linear relationship was detected between the size of mature females and their fecundity (between 11 and 32 oocytes). Clear reproductive progress indicated a spawning period between March and May. We conclude that further fishery‐independent data are required to determine patterns of male abundances and distributions.     

Age and growth of the sand smelt, Atherina boyeri (Risso 1810), in the Mar Menor coastal lagoon (SE Iberian Peninsula)

The age and growth of sand smelt, Atherina boyeri (Risso 1810), in the Mar Menor (SE Iberian Peninsula) were studied in samples taken from catches of local fishermen obtained between November 1997 and September 1998. The maximum lengths were 94 mm (FL, fork length) in females and 87 mm (FL) in males. Age determination based on scale readings and validated by length frequency analysis shows that the population has a 3‐year life cycle. Females were significantly longer than males in each of the age classes. Both sexes of the sand smelt grow allometrically (b = 3.113 males; b = 3.043 females) and attain approximately 56.2% of their maximum fork length in their immature first year, after which the annual growth rate drops quickly. The highest growth rate was observed from winter to spring (G_L = 16.01 males 1+; G_L = 11.25 males 2+; G_L = 17.18 females 1+; G_L = 9.62 females 2+). The condition cycles were similar for both sexes, with a minimum in June–July and two maximums in April and November.     

Gonad maturation and spawning of cobia,Rachycentron canadum (Linnaeus, 1766) off the Dungun coast,Malaysia

The reproductive biology of cobia, Rachycentron canadum, from the coastal waters of Dungun, Malaysia was studied from June 2014 to May 2015. From commercial trawls, a total of 201 samples (combined sexes) were collected (fork lengths [FL] 37.5–124.0 cm; body weights 0.5–20.4 g). The overall sex ratio of females to males was 1:0.9, which was not significantly different (χ² = 2.12, df = 1; p < .05). Estimations of length at 50% maturity (L₅₀) showed that both sexes matured at approximately 75 cm FL; estimated spawning frequency was 6 days. Mean batch fecundity (BF) ranged from 0.55 to 4.32 million eggs. The average number of eggs per gram of ovary was from 2,100 to 5,400 eggs, and relative fecundity 147 eggs/g. There was a weak positive correlation (r² = .48) between BF and female FL as well as BF with an ovary‐free body weight (r² = .56), possibly due to females being in a continuous spawning condition and some possibly half‐spent, based on the histological examination of the female gonads. Despite cobia being asynchronous spawners, the gonadosomatic index in both males and females showed peaks in June, November, and particularly March. Based on histological examination, spawning‐capable males were encountered throughout the study period, whereas spawning‐capable females in the late developing subphase were found mostly in March and April. This is the first study on the reproductive aspects of cobia in Malaysian waters.     

Age-based life history of humpback red snapper,Lutjanus gibbus,in New Caledonia

This paper examines the life history of humpback red snapper Lutjanus gibbus, an important fishery species for coastal communities across the Indo-Pacific, in southern New Caledonia, where the species is lightly exploited. A total of 243 L. gibbus were sampled between January 2013 and December 2016 from occasional harvests of commercial fishers. Examination of sectioned otoliths revealed that opaque increment formation occurred annually between November and March, coinciding with the species' spawning season. Estimates of maximum age were similar between sexes, with observed ages of 38 and 36 years for females and males, respectively, extending the reported longevity of this species by at least 11 years. Growth differed significantly between sexes, with males reaching greater length at age and greater asymptotic length than females (38.88 v. 31.46 cm fork length (L_F). Total mortality for all samples was estimated as 0.13 and was slightly higher for males (0.16) than females (0.11). Estimates of natural and fishing mortality were low and slightly higher for males than females. Male L. gibbus were found to mature at slightly greater lengths and younger ages than females, with the length and age at which 50% of individuals attained maturity estimated to be 25.8 cm L_F and 3.9 years of age for females and 26.8 cm L_F and 3.4 years of age for males. The results provide key baseline information from which to assess the effect of fishing on the species for populations in New Caledonia and adjacent locations and, when viewed with those of other studies, highlight the importance of understanding spatial patterns in demography of harvested fish species across gradients of exploitation and environmental influences.     

Validated age and growth estimates for the shortfin mako, Isurus oxyrinchus, in the North Atlantic Ocean

Age and growth estimates for the shortfin mako, Isurus oxyrinchus, derived from vertebral centra of 258 specimens (118 males, 140 females), ranging in size from 64 to 340 cm fork length (FL) were compared with data from 22 tag–recaptured individuals (74–193 cm FL) and length–frequency data from 1822 individuals (1035 males, 787 females; 65–215 cm FL). Annual band-pair deposition, confirmed by a concurrent bomb radiocarbon validation study, was used as the basis for band interpretation. Validation was further confirmed with a tetracycline-injected male shortfin mako recaptured after being at liberty off South Africa for 1 year and aged at 18 years. Growth rates from tag–recapture analysis (GROTAG) were higher than those derived from vertebral annuli and were only available from sharks up to 193 cm FL at recapture. Modal length–frequency data were used to verify the first four age classes. Growth curves were fit using both von Bertalanffy and Gompertz models. The 3-parameter version of the von Bertalanffy growth function produced the most biologically reasonable values for males, based on observed data (L _∞  = 253 cm FL, K = 0.125 year^?1 (estimated longevity = 21 year), and L ₀ = 72 cm). The 3-parameter version of the Gompertz growth function produced the most biologically reasonable estimates, for females (L _∞  = 366 cm FL, K = 0.087 year^?1 (estimated longevity = 38 year) and L ₀ = 88 cm. Males and females were aged to 29 (260 cm FL) and 32 years (335 cm FL), respectively. Both sexes grew similarly to age 11 (207 cm FL, 212 cm FL for males and females, respectively) when the curve leveled in males and continued to rise in females. Age at 50% maturity was estimated at 8 years for males (185 cm FL) and 18 years for females (275 cm FL). The species grows slower, matures later and has a longer life span than previously reported in North Atlantic waters.     

Population biology of the red gurnard (Aspitrigla cuculus L.; Triglidae) in the inshore waters of Eastern Anglesey and Northwest Wales

ICES has identified red gurnard Aspitrigla cuculus (L.) as a potential commercial species and recommended that monitoring programmes should be conducted to derive information on biological parameters for stock assessment purposes. In this paper, data on the population biology of red gurnard in the coastal waters of Northwest Wales and Eastern Anglesey are presented. Total length (TL) of fish sampled ranged from 15.4 to 35.0 cm (males) and 10.5 to 43.1 cm (females), with the majority of females between 20 and 30 cm TL (70.0%) and males between 20 and 30 cm TL (71.0%). TL/weight (W) relations were similar between immature and mature individuals for both sexes and between both sexes (all maturity stages combined), producing a combined data equation W = 0.005 TL^3.19. Age of fish ranged from 1 to 7 years and 1 to 6 years, respectively, for females and males, with the majority of females age 3 (37%) and the majority of males age 2 (49%). The age structures of female and male red gurnards were significantly different, with the older age classes consisting predominantly of female fish. Both males and females exhibited similar asymptotic growth patterns; the combined von Bertalanffy growth function was . Instantaneous rates of total mortality were calculated as 1.13 year^?1 for males and 0.98 year^?1 for females. The size (L₅₀) and age at first maturity (A₅₀) were estimated to be 26.3 cm TL and 3.6 years for males, 28.1 cm TL and 3.5 years for females and 25.6 cm TL and 3.7 years for both sexes combined.     

Reproductive biology of Bagrus docmak in the Victoria Nile,Uganda

Aspects of the reproductive biology of Bagrus docmak in the Victoria Nile were investigated between November 2005 and October 2006. Macroscopic and histological analysis of the gonads confirmed it as an asynchronous batch spawner which spawns throughout the year with bimodal spawning peaks coinciding with rainfall seasons. The first spawning peak occurred from March to May, the second from September to November. The sex ratio did not significantly deviate from 1:1. Length at sexual maturity was 33.6 cm and 31.6 cm fork length (FL) for females and males, respectively. Batch fecundity ranged from 1 000 eggs in 34 cm FL fish to 43 000 eggs in 79 cm FL fish, and correlated linearly with FL (r = 0.72) and body weight (r = 0.79). Mean relative batch fecundity was 6 eggs g^?1 (SE 2). These results could guide research into the possibility of artificially inducing the fish to spawn, and its subsequent culture.     

Reproductive biology and implications for management of the painted sweetlips Diagramma pictum in the southern Arabian Gulf

The reproductive biology of the painted sweetlips Diagramma pictum was determined from 487 individuals collected between January and December 2010 in the southern Arabian Gulf. There was no evidence of sex change and the combination of histological results with the sex composition of the size and age structures indicated a gonochoristic sexual pattern. There were peaks in gonado-somatic indices for females in March and October with spawning occurring during two seasons (April to May and November). The mean size and age at sexual maturity (L(m50) and A(m50) ) were 35·7 cm fork length (L(F) ) and 2·9 years for females and 26·7 cm L(F) and 0·5 years for males. The maximum recorded age (11 years) and small mean size and young age at sexual maturity for males may be a direct result of intensive demersal fishing in the southern Arabian Gulf. There was an exponential increase in the cumulative reproductive potential with size and a linear increase with age for both sexes. The mean L(F) (L(c50) ) at which D. pictum became vulnerable to capture was 33·3 cm, which corresponded to only 3 and 7% of the cumulative reproductive potential of males and females, respectively. Size-specific and age-specific reproductive potential indicated that conventional regulations that equate the mean size at first capture to sexual maturation are unsuitable for the management of D. pictum.     

Size and age at sexual maturity of female bluefin tuna (Thunnus thynnus L. 1758) from the Mediterranean Sea

The ovaries of 501 female eastern Atlantic bluefin tuna (Thunnus thynnus Linnaeus, 1758) captured in the Mediterranean Sea from May to September between 1998 and 2004 were analysed histologically. Body size at median sexual maturity (L₅₀) was 103.6 cm fork length (FL), while 100% maturity was reached above 135 cm FL. The age analysis, based on the count of the translucent zones of the first spiniform ray of the first dorsal fin, showed that most of the specimens with FL = L₅₀ were 3 years old while 100% maturity was reached between 4 to 5 years. The reported evidence indicates that for the eastern Atlantic bluefin tuna stock, the size and age of first sexual maturity of females was lower than in the western Atlantic stock.     

Reproduction, diet and population structure of the mountain mullet, Agonostomus monticola, in Jamaica, West Indies

Reproduction, feeding and population structure were investigated in the mountain mullet, Agonostomus monticola, in eastern Jamaica between 1982 and 1986. Female fishes just outnumbered males 1.2 : 1. Minimum size at maturity for females was 123 mm fork length (FL) and 96 mm FL for males. Mean size at maturity for females was 165.8 mm FL (S.D.=1.61) and for males was 148.4 mm FL (S.D.=2.97). Fecundity was 340 000 eggs for a 25 g ovary. Fecundity (F) was related to size by the equation F=153.8 FL^1.36. Mean lengths of males and females captured by all methods were 129.4 mm (S.D.=5.56) and 160.4 mm FL (S.D.=0.70), respectively. A. monticola was found to be chiefly an insectivorous feeder. The major food items found in stomach contents in ranked sequence were insects, freshwater prawns, plant detritus and algae.     

Mitochondrial and nuclear DNA analyses reveal fine scale geographic structure in bottlenose dolphins (<Emphasis Type="Italic">Tursiops truncatus</Emphasis>) in the Gulf of Mexico

There is a need for biological information to support current stock designations of bottlenose dolphins (Tursiops truncatus) in the Gulf of Mexico. The existence of many inshore, resident “communities” raises questions as to the relationship these dolphins may hold with dolphins inhabiting neighboring inshore and coastal areas. In this study, population subdivision was examined among four resident, inshore bottlenose dolphin stocks (Sarasota Bay, FL, Tampa Bay, FL, Charlotte Harbor, FL and Matagorda Bay, TX) and one coastal stock (1–12 km offshore) in the Gulf of Mexico. Evidence of significant population structure among all areas was found on the basis of both mitochondrial DNA (mtDNA) control region sequence data and nine nuclear microsatellite loci. Estimates of relatedness showed no population contained a significantly high number of related individuals, while separate AMOVAs for males and females indicated that both sexes exhibit a significant level of site philopatry. Results presented here provide the first genetic evidence of population subdivision between the coastal Gulf of Mexico and adjacent inshore areas along the central west coast of Florida. Such strong genetic subdivision is surprising given the short geographical distance between many of these areas and the lack of obvious geographic barriers to prevent gene flow. These findings support the current, separate identification of stocks for bottlenose dolphins inhabiting the eastern coastal and inshore areas of the Gulf of Mexico.     

Age, growth and reproduction of the barbel, Barbus sclateri (Günther, 1868), in a first-order stream in southern Spain

This study was based on examination of 1476 barbels from a first-order stream located in the Guadalquivir River basin (38°N, 4°43'W). This stock comprised nine age groups of male and 11 of females. No growth was recorded between October and March, most occurring in April–June and, to a lesser extent, in July–September. A classification analysis revealed that this stock had the lowest growth rate of 37 different European barbel populations. Length–weight relationships were obtained for 12 barbel categories and used to estimate both condition and instantaneous growth rate. Relative condition (before and after subtracting gonad weight) was similar in both sexes and was affected by gonad growth and environmental summer conditions.
Spawning occurred during the second half of May (15 May is suggested as the birthday). Gonads began to develop in September (females) and in February (males). Males matured at between 7 and 9 cm fork length (f.l.) (2–4 years old) and females between 11 and 16 cm (6–7 years). The fecundity of this stock was represented by the formula F =6.07 10 ⁴ f.l. (mm)^3.0667. Larger and older fish showed a higher fecundity and bigger eggs. The overall sex ratio did not differ from 1:1.     

Reproductive biology of brown trout, Salmo trutta macrostigma Dumeril 1858, in a tributary of the Ceyhan River which flows into the eastern Mediterranean Sea

The study describes some key elements of the reproductive biology, including spawning season, age at sexual maturity, fecundity and egg diameter of the native brown trout, Salmo trutta macrostigma, in a tributary of the Ceyhan River. A total of 197 brown trout (118 females and 79 males) were captured in 2000–2001 by electric fishing. In observations on monthly changes, the gonadosomatic index (GSI) and the monthly frequency distribution of egg diameter confirmed that spawning lasted from November to January. Some 27.7% of the females and 62.5% of the males attained sexual maturity in their second year. The smallest fork length (FL) of brown trout attaining sexual maturity was 17.4 cm for males and 17.8 cm for females. Mean fecundity in age groups II, III, IV and V were 360, 452, 693 and 1283 eggs per female, respectively. One 9‐year‐old female had a unique 3232 egg count. The mean fecundity of the sampled population was 554 eggs per fish, positively correlated with the FL (mm) (R = 0.8227 ) and body weight (R = 0.8130). The diameter of mature eggs in the spawning season ranged from 3.250 to 5.930 mm, with a 4.146 mm average. Mean egg diameter in age groups II, III, IV and V in the spawning season were 0.813, 3.799, 4.663 and 5.243 mm, respectively. Fecundity, egg weight and diameter were statistically different in all age groups.     

Differences in size and growth rates of male and female migrating Japanese eels in Pearl River, China

The Sr/Ca ratios in otoliths of silver Japanese eels Anguilla japonica , in Pearl River, China, indicated that both sexes did not stay in brackish water and grew in fresh water from the glass eel stage until spawning migration. This did not support the hypothesis that females tended to distribute upstream and males might be restricted to estuaries. The back-calculated total length of males at glass eel stage was not significantly different from that of females, indicating that the hypothesis that small glass eels became males and larger ones became females may not be true. The mean (±S.D.) age and total length of males at migration were 6·4±1·6 years and 48·3±4·5 cm, which were significantly smaller than for females, 8·3±1·6 years and 61·4±4·1 cm. The age of migration was related inversely to growth rate for both sexes. Growth parameters of the von Bertalanffy growth equation were K =0·21 cm year°1, L _∞=55·7 cm and t _o=-0·55 year for males and K =0·14 cm year⁻¹, L _∞=77·5 cm and t _o=-0·60 year for females. The difference in asymptotic length ( L _∞) between males and females may be because females postpone migration to achieve larger size for maximizing reproductive success.     

Reproductive biology of alfonsino Beryx splendens

The main aim of this work is to provide a detailed analysis of the reproductive cycle of Beryx splendens in the Juan Fernández Archipelago. The gonadosomatic index (I(G) ) and maturity ogives in both sexes were estimated using an extensive database collected by onboard scientific observers between January 2006 and October 2009. A histological analysis of maturation was also completed for females collected between May and December 2001. Variations in both I(G) and proportion of mature individuals were observed in fish with a fork length (L(F) ) >37 cm for females and >33 cm for males. The main reproductive season was in the austral winter and spring (June to November). Fork length at 50% maturity (L(50) ) was estimated as 39·67 cm for females (95% c.i. =39·34, 40·02 cm) and 36·88 cm for males (95% c.i. =36·45, 37·36 cm) using macroscopic analysis of gonads. Estimates for females using histological data varied slightly with an estimated L(50) of 43·67 cm (95% c.i. =42·82, 44·91 cm). Changes in I(G) and maturity were modelled as a function of month and L(F) within a generalized additive model framework. A high porportion of immature individuals were found throughout the year. The results of this study are compared with reproductive traits reported for B. splendens in other areas of its distribution and are discussed with reference to exploitation, vulnerability and conservation of the B. splendens stock in Juan Fernández Archipelago.     

Age, growth and reproductive parameters of the Mediterranean cardinal fish, Apogon imberbis

Life history parameters (age, growth and reproductive characteristics) of the Mediterranean paternal mouthbrooding cardinal fish, Apogon imberbis, were investigated at a coastal locality off Blanes, NW Mediterranean Sea. Maximum age was found to be 5 years for both sexes. Age was validated with an otolith chemical (tetracycline) marking experiment. Both females and males reached maturity at length >5.5 cm, corresponding to 1 year of age in both sexes. The spawning season ranges from July to October, with a peak in August. The number of eggs in the mouths of males increased linearly with fish total length.     

Age, sex ratio and timing of the catch of kelts and ascending Atlantic salmon in the subarctic River Teno

By 15 June, 82% of the catch of Atlantic salmon Salmo salar kelts had been taken from the middle part of River Teno, northern Scandinavia. The median date of capture was 4 June for males and 8 June for females. Salmon of 1–4 sea–winters (SW) of both sexes survived spawning to return to sea as kelts. Among males, 1 SW kelts were caught earliest in the spring and 3 SW latest, but among females 4 SW were earliest, then 3 SW and finally 1 and 2 SW. There were 17 river and sea–age combinations among the kelts compared with 23 among the ascending salmon. The smolt age distribution and the mean smolt age differed significantly only between female 2 SW ascending salmon (3·97 years) and kelts (4·14 years). The proportion of 1 SW females was higher and that of 3 SW males lower among kelts than among ascending salmon. The proportion of males among 1 SW ascending salmon was 80% but among kelts only 57%. Similarly, the proportion of males among 3 SW fish was 21% for ascending salmon but only 7% for kelts. Hence overwinter mortality was higher among males. Male and female kelts of 1 and female kelts of 2 SWhad a greater mean length than ascending salmon in corresponding groups indicating a better survival of larger fish within an age group. Grilse ascend rivers after most kelts have left, but the main catch of ascending 2–3 SW salmon takes place concurrently with kelts leaving the river, inadvertently targeting kelts in the fishery.