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.     

Population structure, growth and reproduction of roughhead grenadier on the Flemish Cap and Flemish Pass

Roughhead grenadier Macrourus berglax were collected during the Flemish Cap bottom survey (1991–2001, NAFO division 3M, depth of 200–720 m) and on commercial vessels (1998–2000, NAFO divisions 3L, M and N, depth of 700–1700 m). The abundance of roughhead grenadier, as well as their average size, increased with depth. Age and length composition of the catches showed clear differences between the sexes. The proportion of males in the catch declined in the larger length classes and there were no males in the largest length classes (25 cm). There were differences in the growth trajectories of the two sexes; both sexes grew similarly up to 9 years, but the male growth was slower thereafter. The pre-anal fin length at first maturity ( L _PA50) for roughhead grenadier females was 28·5 cm, whilst the age at 50% maturity was 15–16 years. Individual total fecundity varied between 8522 and 61 844 oocytes. Macrourus berglax had a prolonged life cycle and multi-aged population structure, with differences in growth and mortality between males and females, slow maturation and low fecundity.     

Sexual maturation of cod (Gadus morhua L.) in the southern Baltic (1990–2006)

Baltic cod, like other species, is susceptible to inter‐annual fluctuations in sexual maturation, depending on the length, age, sex, extent of the habitat area, and stock abundance of the cod population. Maturity is one of the biological indicators used to detect changes in a stock that can be caused by fishing. To address these issues specifically for the eastern Baltic cod stock, long‐term data (1990–2006) from Polish research vessels in the southern Baltic were examined. To date, the ICES has used the same maturity ogives over extended periods and assumed invariant sex ratios for the assessment of eastern Baltic cod. The combined maturity ogives calculated in the present study were markedly lower, particularly for age groups 2–4 (5), in all periods, than those used in the ICES assessment. Moreover, the proportion of females increased with length and age, suggesting that annual verification of the sex ratio is needed. The present study also revealed that the total length (L_50%) and the age (mean age‐at‐maturity; MAM_50%) at which 50% achieved first sexual maturity were higher for females than for males in the study period. The long‐term mean L_50% and MAM_50% for females were 43.9 cm and 4.3 years, respectively, and for males 34.8 cm and 3.4 years. There was also a spatial difference between calculated maturity ogives, with slightly lower L_50% (range: 1.4–8.6 cm) in the Gdańsk Basin than in the Bornholm Basin. The increasing trend in fishing mortality observed in 1993–2004 (ICES data) did not translate into a temporal trend in calculated maturity ogives. However, changes in L_50% and MAM_50% reflected recruitment variations (ICES data). The significance of these findings is discussed in the context of the environment and recruits abundance.     

Reproductive aspects of the yellowtail snapper Ocyurus chrysurus from the southern Gulf of Mexico

In this study, sex ratio, spawning season, fork length (L(F)) at maturity (L(F50)), batch fecundity and spawning frequency were characterized for the continental population of Ocyurus chrysurus from the Campeche Bank, in the southern Gulf of Mexico. A total of 1657 specimens were collected from February 2008 to January 2009. The overall sex ratio (male:female) and sex ratios by size-class showed no significant differences from an expected 1:1 ratio. The Campeche Bank population did not conform to the reproductive seasonality pattern characteristic of a continental population. A protracted spawning season that extended from January to September with peaks occurring mainly between April and May and additionally in September was observed. The population conformed, however, to the sexual maturity pattern observed for populations and species associated with a continental margin. Fish of both sexes reached the onset of sexual maturity at a similar and small L(F) of c. 14 cm, and L(F50) (L(F) at which 50% of females and males become mature) was 21·3 and 19·4 cm. Asynchronous-type ovarian development was observed for this species and batch fecundity estimates ranged from 14,102 to 164,756 oocytes (mean ±S.D. = 43,852 ± 32,684 oocytes). The overall spawning frequency estimate was once every 8·3 days or 26 times during the 9 month spawning season.     

Biological vulnerability of two exploited sharks of the genus Deania (Centrophoridae)

Life-history parameters of Deania calcea and Deania quadrispinosa suggested that their productivity was very low. Maturity (L(T50) ) occurs at c. 80% of maximum observed total lengths (L(T) ) for both species and sexes. A large proportion of mature females were neither pre-ovulatory nor pregnant, and the reproductive cycle included a distinct resting phase after pregnancy. For D. calcea, mean ovarian fecundity was 12 and maximum observed litter size was 10 (average of six); D. quadrispinosa averaged 17 pups per litter. Birth L(T) was 28-33 cm for D. calcea and 23-25 cm for D. quadrispinosa. The male and female reproductive cycles were aseasonal, and consequently, the length of the reproductive cycle could not be determined. Preliminary ageing data from dorsal-spine growth bands suggested that female D. calcea lived to 31-36 years and males to 24-32 years. The L(T) -at-age data using external bands on the spines showed maturity occurring at 15·5 years (males) and 21·5 years (females), whereas banding on the internal dentine indicated maturity at 10·5 and 17·5 years for males and females. Thus, a female lifetime of 31-36 years allowed for a maximum of 7 litters if a 2 year cycle is assumed or only five litters with a 3 year cycle, resulting in a lifetime fecundity of only 42 pups (2 year cycle) or even lower (3 year cycle).     

Reproductive Biology of the Smooth Dogfish, Mustelus canis, in the Northwest Atlantic Ocean

Shark populations tend to be highly vulnerable to overexploitation due to low fecundity and slow growth rates. Recent fishing pressure on the smooth dogfish in the northwest Atlantic has created a necessity for more information about their basic biology. Length and age at maturity, fecundity, and reproductive season were estimated. Total length at 50% maturity was 102cm for females, and 86cm for males. The majority of females were mature at age 4 or 5, and all males were mature at 2 or 3 years of age. Females had an 11–12 month gestation with parturition occurring in May, ovulation occurring between May and July likely in late May and early June, and mating occurring between May and September. Fecundity ranged between 3 and 18 pups per litter, and was positively related to length and age, with a mean of 9.53 pups per litter. Sperm was found in the terminal zone of the oviducal gland of females throughout the year.     

Growth and reproduction in the Icelandic common seal (Phoca vitulina L., 1758)

Length, weight and maturity were studied in relation to age in the common seal (Phoca vitulina vitulina L., 1758), collected during the periods 1979-1983 and 1990-2000 in Icelandic waters. The maximum age of common seal observed was 36 years for females and 30 years for males. For common seal females and males, asymptotic length and weight were 161 cm and 93 kg and 174 cm and 97 kg, respectively, showing slight sexual dimorphism in size. The condition of adult females, measured as fat thickness at the lower end of the sternum, was lower in the period 1979-1983 than in 1990-2000 during June-September, the breeding and mating time of the Icelandic common seal. Males reached sexual maturity between 5 and 7 years, whereas 50% of females did so at age 4 years. Including the length and age interaction term in the logistic regression model for the maturity of females significantly improved it. Thus, body size matters in the onset of maturity. The mean birthing date for the Icelandic common seal was found to be in early June. A comparison of animals collected in the two periods 1979-1983 and 1990-2000 did not show significant differences in growth and the average age of sexual maturity for either males or females. The observed decline of the Icelandic common seal population is most probably caused by increased mortality, due to exploitation and accidental by-catch in gill-nets, rather than a decrease in fecundity.     

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 variables of Urotrygon rogersi (Batoidea: Urotrygonidae): a species with a triannual reproductive cycle in the eastern tropical Pacific Ocean

Reproductive aspects of the round ray Urotrygon rogersi were studied based on 2005 specimens obtained in the artisanal shrimp fishery operating on the Colombian Pacific coast. Females reached greater maximum total length (L(T) ), disc width (W(D) ) and mass (M) (38·0 cm, 19·9 cm and 348 g) than males (32·5 cm, 17·0 cm and 165 g). Sex ratio of juveniles and adults was 1:1. Clasper length increased rapidly between 10·0 and 12·5 cm W(D) . The smallest mature male measured 10·5 cm W(D) and the largest immature individual 13·7 cm W(D) . Male first maturity was reached at 61·8% of maximum W(D) , and estimated W(D50) was between 11·5 and 11·8 cm. The smallest mature female measured 10·5 cm W(D) ; the size at first maturity was 52·8% of maximum W(D) , and estimated W(D50) was between 11·8 and 12·3 cm. Embryos were found in females ≥ 10·5 cm W(D) and maximum fecundity was three embryos per female (mode = 1) and varied with maternal size. Embryos were found in all months, but three birthing peaks per year were identified and a gestation period of 4-5 months estimated. Based on ovulation time, embryonic growth and parturition dates, a triannual reproductive cycle was inferred for this species, with overlapping ovarian and uterine cycles. These results suggest that U. rogersi has a reproductive strategy based on low fecundity, a rapid reproductive cycle (short ovulation and gestation time), three birth peaks per year and large embryos. This strategy probably allows U. rogersi to withstand the fishing pressure they are subject to on the Colombian Pacific coast. The results also suggest that the study area is an important nursery and reproductive area for this species.     

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.     

Reproductive biology of the starry smooth-hound shark Mustelus asterias: geographic variation and implications for sustainable exploitation

Examination of the reproductive biology of Mustelus asterias in the north-east Atlantic Ocean highlighted apparent geographical variation in maturity, fecundity and ovarian cycle between Atlantic and Mediterranean populations. The stretch total length (L(ST) ) and age at 50% maturity for Atlantic males and females were estimated at 78 cm L(ST) and 4-5 years and 87 cm L(ST) and 6 years, respectively. Size at maturity of females was considerably smaller than in Mediterranean specimens (96 cm L(ST) ). Ovarian fecundity ranged from eight to 27 oocytes and uterine fecundity from six to 18 embryos. The gestation period was c. 12 months, followed by a resting period of c. 12 months, resulting in a biennial cycle. Females stored sperm in the oviducal gland and, unlike Mediterranean specimens, no uterine compartments were observed in Atlantic specimens. This study reveals the existence of strong, possibly adaptive, divergence in life-history traits in an elasmobranch, whose northern populations may be more susceptible to overexploitation than previously believed.     

Life history of the orange-striped emperor <Emphasis Type="Italic">Lethrinus obsoletus</Emphasis> from the Mariana Islands

The present study investigated the age-based demography of the orange-striped emperor, Lethrinus obsoletus, from commercial samples in the Commonwealth of the Northern Mariana Islands (CNMI), spanning a 24-month market sampling period. Information on growth, life span, mortality, and reproduction was derived through analysis of sectioned sagittal otoliths and gonad material. The species had a moderate longevity of 13 years while females and males reached 50% sexual maturity at 3.8 years (22.9 cm fork length) and 2.8 years (19.9 cm fork length), respectively. Histological examination of gonads and sex-specific age frequency distributions suggest the sexual ontogeny of the species conforms to juvenile hermaphroditism, whereby sexual transition from female to male occurred prior to maturation. No annual spawning periods were identified, but the ubiquitous presence of post-ovulatory follicles in females and spermatogenic material in males coupled with a consistent lunar trend in gonadosomatic index patterns suggests the species spawns every lunar cycle throughout the year with spawning activity potentially increasing around the new moon. Ratios of natural to fishing mortality indicate a moderate level of exploitation (0.37); however, a large portion of harvested females had not reached reproductive maturity, suggesting that formal assessments of stock status are warranted to ensure the sustainable harvest of the species in CNMI.     

Reproduction, age, growth and mortality of axillary seabream, Pagellus acarne (Sparidae), from the Canarian archipelago

Axillary seabream Pagellus acarne (Risso 1826) caught off the Canary Islands from January 1991 to December 1994 were studied. The length range of the catches was between 11 and 31 cm, with a modal distribution between 17 and 21 cm. The overall ratio of males to females was 1:1.74. Males were observed up to a length of 24 cm. Hermaphrodites were recorded at lengths between 15 and 23 cm. The species was characterized by protandric hermaphroditism. The reproductive season extended from October to March, with a peak in spawning activity in December–January. The size at sexual maturity was 15.8 cm total length (2 years old) for males and 19.4 cm total length (3 years old) for females. The total length–total weight relationship for the entire population is described by the parameters a = 0.0068, and b = 3.2401. Otolith age readings showed that the population exploited consisted of 10 age groups (1–10 years), including a very high proportion of individuals between 1 and 4 years old. The von Bertalanffy growth parameters for all individuals were L_∞ = 32.98 cm, k = 0.22 years⁻¹, and t₀ = −0.87 years. Males grew comparatively slower than females. The instantaneous rates of mortality for all fish were Z = 0.96 years⁻¹, M = 0.30 years⁻¹, and F = 0.66 years⁻¹. The exploitation ratio and the length at first capture were, respectively, E = 0.69 and LC₅₀ = 16.1 cm. The stock is overexploited, therefore measures such as closed seasons or changes in fishing patterns would be desirable to safeguard the spawning stock and recruits.     

绥芬河大麻哈鱼个体生物学研究

研究以2012至2017年在绥芬河东宁段采集的447尾大麻哈鱼(Oncorhynchus keta Walbaum)为材料,对其年龄与生长及繁殖特性等个体生物学特征进行研究分析。结果表明:绥芬河大麻哈鱼种群由1~+-5~+龄5个年龄组构成,其中雌性个体以3~+龄为主,雄性个体以2~+龄为主。大麻哈鱼雌、雄个体的体长-体重关系分别为:W=0.0082×L~(3.0604);W=0.0076×L~(3.0746),均属匀速生长类型;采用Von Bertalanffy生长方程拟合得到3~+龄大麻哈鱼雌、雄个体的叉长生长方程分别为:L_(t,F)=141.64×e~(-0.11)·(t+1.55));L_(t,M)=119.51×e~(-0.13·(t+1.45))。利用逻辑斯蒂方程估算大麻哈鱼雌、雄个体初次性成熟叉长(L_(50))分别为51.53和42.15 cm。ARSS分析显示雌、雄个体的L_(50)差异显著;大麻哈鱼的绝对繁殖力(F)、相对叉长繁殖力(F_L)和相对体重繁殖力(F_W)分别为3412粒、52.42粒/cm和1.17粒/g;F与叉长、体重、性腺重呈显著正相关关系,GSI与叉长、体重、F成显著负相关关系;F与叉长、体重的幂函数关系方程式分别为:F=0.0311×L~(2.7745)(R~2=0.638)和F=1.946×W~(0.9374)(R~2=0.704)。本研究为绥芬河大麻哈鱼资源保护工作提供基础资料。     

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.     

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.     

Age, growth and reproduction of Cobitis paludica in a seasonal stream

In the Iberian endemic loach Cobitis paludica , in a small seasonal tributary of the Guadalquivir River, 65–70% of the total growth in length occurred in the first year of life. The maximum ages observed were 3+ years in males and 4+ years in females. Both sexes matured at the beginning of their second year of life. There was a significant difference from 1: 1 in the overall sex ratio of 412 males to 674 females. Spawning began in late March and ended in July. Cobitis paludica is a multiple spawner that releases a minimum of two batches of eggs per female each year. Once spawning had started, however, there was no recruitment from the stock of transparent oocytes to the mature stock. The number of eggs decreased from the first batch to the second, but there was no significant difference in the mean egg diameter between batches. Compared with other populations of this species, the present population, from a low latitude, is characterized by a low number of age groups, fast growth, early maturity and high fecundity in multiple spawnings. These life-history characteristics are typical of species in unstable environments, where adult mortality is high, variable or unpredictable.     

Reproduction and population aspects of the yellownose skate, Dipturus chilensis (Pisces, Elasmobranchii: Rajidae), from southern Chile

The total length (TL) at sexual maturity by sex, fecundity characteristics, and some population aspects (size structures and sexual proportions) are presented for the yellownose skate, Dipturus chilensis , in the eastern South Pacific Ocean. Samples were taken between January 2003 and August 2004 from three zones (principal fishing grounds for the species) in Chile's southern channels (41°30'S–55°10'S). TL at which 50% of the individuals reach maturity was significantly different by sex, with females estimated to mature at 103.9 cm and males at 89.7 cm. The average estimated fecundity was 23.4 (SD 6.4) ova per female. We report on the relationships of clasper lengths and oviducal gland widths with TL and the stages of maturity. Length compositions were statistically different by sex in the same zone (P < 0.05) and between zones for combined sexes (P < 0.05). The proportion of females increased when these reached the TL at which 50% attained maturity, becoming highly available to the fishing gear, possibly in relation to the reproductive strategy. Finally, the results yielded valuable knowledge about population responses to exploitation through fishing.     

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.     

Population characteristics of pallid sturgeon (Scaphirhynchus albus (Forbes & Richardson, )) in the Lower Missouri River

Population characteristics of pallid sturgeon Scaphirhynchus albus in the lower Missouri River are relatively unknown. Therefore, data collected from the Nebraska Game and Parks Commission Pallid Sturgeon Population Assessment Program was synthesized to (i) document the population structure of pallid sturgeon by origin (hatchery‐reared or wild), gender, and reproductive readiness, (ii) document the minimum size and age‐at‐maturity by gender, and (iii) document the fecundity rates of the fish that were successfully spawned in the hatchery. During this 4‐year study (2008–2011), relative abundance for wild and hatchery‐reared pallid sturgeon collected with gill nets did not significantly change whereas relative abundance for wild fish using trot lines declined significantly. The proportion of hatchery‐reared pallid sturgeon increased annually, with the population being composed primarily of hatchery‐reared fish. The proportion of reproductively ready females to non‐reproductively ready females was 1 : 2.0, compared to male ratios at 1 : 0.9. Minimum fork length‐at‐maturity was estimated for females at 788 mm and for males at 798 mm. Minimum age‐at‐maturity for hatchery‐reared released fish was age‐9 for females and age‐7 for males. Highest relative fecundity, based on the ovosomatic index, was 10% with an overall mean of 7%. The number of eggs per ml (egg size) was not correlated with fork length (P = 0.0615) or weight (P = 0.0957). Relative condition factor (Kn) for females was significantly different by reproductive condition (P = 0.0014) and Kn for males did not differ between reproductive conditions (P = 0.2634). Detecting shifts in population characteristics are essential not only to understand population dynamics since hatchery inputs and natural perturbations continue to change the population structure but also to assess species recovery efforts to ensure long‐term species sustainability.