A biological analysis of eel catches, Anguilla anguilla L., from the lagoons of Lesina and Varano, Italy

A study of eel catches from Lesina (444 specimens) and Varano lagoons (325 specimens), in southern Adriatic, Italy, was made. Male silver eels in Lesina ranged from 33.4–51.5 cm in length, with a mean of 42.6 cm; from 50–240 g in weight, with a mean of 141 g and were 1.5–6.5 years old with a mean of 2.5 years. The average length of male silver eels in Varano lagoon was 40.5 cm (range 31–48.5 cm); the average weight was 122 g (range 80–220 g)and a mean age of 2.6 years (range 1.5–7.5 years).
The females are bigger, heavier and older than the males with, in Lesina, a mean length of 61 cm (range 50.9–74.3 cm), a mean weight of 438 g (range 240–730 g) and a mean age of 3.4 years (range 1.5–6.5). The average length of Varano female silver eels was 58 cm (range 50.8–72.5 cm), and the average weight was 383 g (range 225–840 g). They were 1.5–7.5 years old, with an average of 3.8 years. Female silver eels were only 20% of the population at Lesina and 10% at Varano.
In comparison with the silver eel populations of the North Adriatic lagoons, the North Sea or the Atlantic Ocean, the silver eels of Lesina and Varano show a greater growth rate, are younger and have a sex ratio in favour of the males.
The water temperature, higher than in other countries, could be an important factor affecting the differences in age and growth rates between Lesina and Varano silver eels and those of other waters.     

Histological study of the development and sex differentiation of the gonad in the European eel

The histological structure of the gonads was studied in yellow eels sampled from a coastal lagoon and from stocks reared in an aquaculture plant showing different sex ratios. Gonad development related to body size rather than to age and underwent an intermediate stage characterized by a structure of an early testis but containing oogonia and oocytes. This gonad was called the Syrski organ and the stage juvenile ambisexual. Ovaries were found in eels from 22–30 cm in length, possibly derived from undifferentiated gonads or from Syrski organs. Fully differentiated testes were found in eels >35 cm, derived from Syrski organs. These observations support the results of previous research. From elvers and in eels up to 15–16 cm in length, growth of the gonadal primordium is due to primordial germ cell migration. In eels > 15 cm multiplication of primordial cells begins. Oogonial clones were found in eels > 18 cm in length, whilespermatogonium B clones were observed in eels >30 cm in length. The dynamics of sex differentiation was different among stocks with different ultimate sex ratios: ovaries were found in shorter eels in stocks with a prevalence of females, in longer eels in stocks with a prevalence of males. This result supports the hypothesis of a metagametic (environmental) sex determination. The somatic cells in contact with germ cells and those in the interstitium appeared early during gonad development and preceded germ cell differentiation. This suggests that somatic cells are the targets of the environmental factors influencing sex differentiation.     

Biology of the annular seabream, Diplodus annularis (Sparidae), in coastal waters of the Canary Islands

The biology of the Canary Islands annular seabream Diplodus annularis (Linnaeus 1758) was studied from samples collected between January and December 1998. Fish ranged from 82 to 209 mm total length in size and from 8.7 to 137.1 g in weight. The mean length showed an increase with increasing water depth. Males showed a negative allometric growth and females isometric growth. The species was characterized by protandric hermaphroditism. The overall sex ratio was unbalanced in favour of males (1 : 0.79). The reproductive season extended from January to May, with a peak in spawning activity in March–April. Males reached maturity at a smaller length (103 mm, 1-year-old) than females (128 mm, 2-year-old). Fish aged 0–6 years were found. The von Bertalanffy growth parameters for all individuals were: L_∞=247.9 mm, k=0.268 years^–1, and t₀=–0.879 years.     

Biology of eelpout <Emphasis Type="Italic">Zoarces elongatus</Emphasis> (Zoarcidae) from Tauysk Bay,the Sea of Okhotsk

Based on the material collected in Tauysk Bay, the Sea of Okhotsk, from 1997 to 2014, the features of spatial distribution, body length and body weight composition, sex ratio, and some aspects of growth rate and reproduction of eelpout Zoarces elongatus are described. The representatives of the species prefer the biotopes with the littoral composed of large stones or pebbles, mainly from the upper border of the intertidal zone to the depths between 10 and 20 m. The catches mainly include the individuals with the body length 300?400 mm and body weight 0.1?100.0 g at the age between 5+ and 6+. Maximum registered body length, body weight, and age are as follows: 560.0 mm, 742 g, and 11+. The sex ratio (males: females) is 1: 1.2. In Tauysk bay, the release of juveniles occurs from November to December, and fecundity ranges from 20 to 185 eggs.     

Sexual dimorphism and gonadal development of the Australian longfinned river eel

The sex and stage of gonadal development of longfinned river eels Anguilla reinhardtii , captured from nine river catchments in New South Wales, Australia, between 1999 and 2001, were determined macroscopically. Sex was verified by histology. Histology was also necessary, however, to accurately define stages of gonadal development, particularly in individuals <600 mm in total body length. Anguilla reinhardtii displayed asynchronous gamete development. The most advanced cells present in migrating male and female A. reinhardtii were spermatocytes and pre-vitellogenic oocytes, respectively. Gonadal development stages were positively correlated with body size in both sexes. Females, however, were significantly larger than males and their gonads matured over a broader size range. Size at sexual differentiation (42–60 cm for males and 50–76 cm for females) was much larger than for most other anguillids that have been studied, with the exception of the New Zealand longfinned eel Anguilla dieffenbachii . Corresponding with its large range in size at sexual differentiation was a relatively large range in size at migration for both males (44–62 cm) and females (74–142 cm).     

Sex Determination in Freshwater Eels and Management Options for Manipulation of Sex

Catadromous eels enter fresh water as sexually undifferentiated glass eels and develop into males and females before migrating back to sea as silver eels. Females develop ovaries directly from the ambiguous primordial gonad whereas males pass through a transitional intersexual stage before developing testes. Eels have sex-specific life-history strategies. Males may grow faster than females initially, but this difference is soon reversed and females attain a greater age- and size-at-metamorphosis than males. Male fitness is maximized by maturing at the smallest size that allows a successful spawning migration (a time-minimizing strategy) whereas females adopt a more flexible size-maximizing strategy that trades off pre-reproductive mortality against fecundity. Although heteromorphic sex chromosomes have been identified in some species, the sex of developing gonads is labile and gender is determined principally by environmental factors. Individuals experiencing rapid growth prior to gonad differentiation tend to develop as males, whereas eels that grow slowly initially are more likely to develop as females. Paradoxically, males tend to predominate under conditions of high density, which may be because a male “grow quickly, mature early” strategy increases an individual’s chances of survival during periods of intraspecific competition. High temperatures and saline conditions have also been proposed to favor development as males but experimental studies have failed to demonstrate a clear effect of either on sex determination. High proportions of female silver eels migrating from some upstream areas, lakes and large rivers may be due to low population density or poor conditions for growth in these habitats. Manipulating sex ratios in favor of females has the potential to increase eel production in aquaculture and to buffer natural populations against fishing pressure. Sex steroids (oestrogens and phytoestrogens) have a strong feminizing effect on undifferentiated individuals and are most effective when targeted at younger eels and administered at high doses for prolonged periods. Modifying local environmental conditions, in particular reducing eel density and limiting interference and social stress, may also promote the development of females. Further research into the timing and mechanisms of sex determination in eels is required to effectively and efficiently manipulate sex for conservation and/or economic benefit.     

Evidence for Environmental Sex Determination in the American eel, Anguilla rostrata

Males have predominated among migrating silver eels in the Annaquatucket River, Rhode Island, for at least two decades, with no significant variation in mean total length in either sex. Because the species is panmictic (random breeding), this consistency suggests environmental sex determination (ESD). Most yellow (feeding phase) eels <300mm total length in the Annaquatucket are sexually undifferentiated, and in contrast to all other published sex ratios, males greatly outnumber females (3:1) among differentiated yellow eels. Estimates of yellow eel population densities are 4–10 times greater than published values for other habitats. We propose that this crowding results in a long period of undifferentiation and the suppression of femaleness. Published field and experimental evidence indicates that high population density results in high proportions of males in Atlantic Anguilla, and that low population density results in the predominance of females. This ESD may be adaptive, resulting in vast numbers of small males in coastal habitats, relatively close to the spawing area, and much larger and more fecund females that occupy most of the available eel habitat.     

Effects of diet supplementation with carp ovary on gonad differentiation and growth of the European eel

Treating elvers of European eel Anguilla anguilla with mature carp ovary for 3–6 months during early growth induced female differentiation in 51·6–66·7% of treated animals compared with c . 5% in controls. The treatment also induced differentiation of ovaries in eels <13 cm L _T and a higher number of Syrski organs with ambisexual characters, and was most effective when administered at an early growth stage. The results could be attributed to the natural steroid content of the carp ovary. The total weight of treated animals at the end of the farm experiment was 84·7% higher than controls. The specific growth rate for weight was significantly higher in female yellow eels than in males, for both control and treated groups. The enhanced growth was related to induced feminization. A diet supplementation with mature carp ovary could be a good approach to control of sex differentiation and growth in eels.     

Influence of different rations and water temperatures on the growth rates of shortfinned eels and longfinned eels

Juvenile (12–152 g) shortfinned eels Anguilla australis and longfinned eels A. dieffenbachia caught in New Zealand streams were fed squid mantle Nototodarus spp. 4 days per week in laboratory experiments. A linear multiple regression equation showed the amount of food eaten (0–2·7% w day⁻¹) explained 77·7% of the variation in specific growth rates (–0·60 to +1·07% w day⁻¹) among individual eels, while previous growth rates, water temperature (10·0–20·6°C), and eel weight (12–152 g) explained a further 5·6, 1·4 and 0·8%, respectively. Growth in length ranged from –0·3 to +0·9 mm day⁻¹. Eels which were starved and then given high rations grew substantially faster than expected. Once growth rates were adjusted for differences in ration and other factors, there were no significant differences in growth rates between species or individual fish. Growth of shortfinned eels fed maximum rations of commercial eel food depended on fish size and water temperatures and ceased below 9·0°C. Growth rates in the wild were substantially less than the maximum possible, after seasonal changes in water temperatures were taken into account, indicating that food supplies and not low water temperatures were controlling growth rates in the wild.     

Ecological aspects of the Japanese eel, Anguilla japonica, collected from coastal areas of Japan

The ecological characteristics of 597 yellow and silver-stage Japanese eels, Anguilla japonica, were examined and compared among collection sites located at three different latitudes of Japan (Amakusa Islands, Mikawa Bay, and Sanriku Coast) to provide basic data on this unusual catadromous fish species. Eels were sexed and their total length, body weight, age, and growth rate based on otolith analysis was compared among sexes, stages, and collection sites. The overall sex ratio favored females (94%), but the sex ratio differed among the three locations. The frequency of females was highest in the coastal waters at Sanriku in the north (100%), next highest at Mikawa Bay in central Japan (95%), and lowest in the Amakusa Islands in the south (70%). Silver eel males ranged from 41.2-66.3 cm in length and 4-10 years in age, and silver eel females from 44.3-97.2 cm in length and 5-17 years in age. Female eels generally grew faster (8.7+/-2.2 cm/year) than males (6.4+/-2.6 cm/year), and the growth rate slowed in the older eels. The growth rate of A. japonica at all three sites was much faster than that of other temperate anguillid species (< 4 cm/year), and their age at maturation was younger than that of other temperate species (approximately 7 to > 50 years), suggesting this species has important ecological differences from other similar species.     

The influence of growth rate on the size of migrating female eels in Lake Ellesmere, New Zealand

Lake Ellesmere, a large coastal lake in the South Island of New Zealand, supports an important commercial eel fishery, based mainly on migrating (silver) male Anguilla australis . Lengths of silver female eels from samples collected in 1942, 1974–1982 and 1998–1999 showed an initial decline between 1942 and 1974 but an increase from 1979 onwards. Back-calculated growth rates of 50 female silver eels caught in 1998 showed that most (90%) exhibited a period of accelerated linear growth commencing at lengths between 380 and 660 mm (mean 598 mm); this accelerated growth coincided with a change in diet to piscivory. The onset of maturity was more closely associated with length than age, condition, or growth rate. The increase in average length of female silver eels of 250 mm over the past 20 years is consistent with the hypothesis that female eels adopt a size-maximizing growth strategy to ensure maximum fecundity; this is the first time this hypothesis has been demonstrated from temporal changes within a single population.     

AGE, GROWTH, AND REPRODUCTION OF THE FINLESS PORPOISE, NEOPHOCAENA PHOCAENOIDES, IN THE COASTAL WATERS OF WESTERN KYUSHU, JAPAN

Abstract: In the coastal waters of western Kyushu, Japan, a total of 97 incidentally taken or stranded finless porpoises, Neophocaena phocaenoides , was collected for studying age, growth and reproduction. An additional 17 specimens from the Inland Sea were used for a comparison of life history. Mean neonatal body length was 78.2 cm. Both males and females grew to around 140 cm by 5 yr of age. The maximum body lengths of males and females in western Kyushu were 174.5 cm and 165.0 cm, respectively, which were smaller than those recorded in other Japanese waters. Females probably attain sexual maturity at ages of 6–9 yr and at body lengths of 135–145 cm. Males probably mature sexually at ages of 4–6 yr, at body lengths of 135–140 cm and at weight of testis of 40–150 g. The lack of females aged 5–6 yr and males aged 4–5 yr precluded firm conclusions on ages at sexual maturity. Parturition in western Kyushu was estimated to be prolonged from autumn to spring, whereas in the Inland Sea and Pacific waters it was restricted from spring to summer with a peak in April. These geographical differences and available information on distribution implies that the finless porpoises in western Kyushu constitute a local population.     

Sex differentiation in the European eel: histological analysis of the effects of sex steroids on the gonad

The effects of sex steroids on sex differentiation in the European eel were studied. The steroids, 17α-methyltestosterone (MT) and 17α-ethynylestradiol (EE), were given in the diet to 6–8 cm elvers and to 15–18 cm and 22–25 cm yellow eels. In our rearing conditions a very large percentage of the untreated eels developed as males. No masculinizing effect of MT could be demonstrated. The EE, administered at a dose of 10 mg kg^-1 of diet to 6–8 cm elvers and 15–18 cm eels, induced ovarian differentiation in about 90 and 65% of eels respectively, while in the control <5% of females was recorded. In 22–25 cm yellow eels a moderated feminizing effect was observed.
Histological analysis of the gonads of treated eels showed that sex steroids affect the gonadal structure. The androgen stimulates hypertrophy of compact connective tissue, early differentiation of Leydig cells, Sertoli cells and early formation of the spermatic duct. Oestrogen inhibits the differentiation of these structural components and stimulates the differentiation of follicular cells and an ovarian structure.
The involvement of gonadal structural components is discussed in relation to the effect of steroid treatment and to the peculiarities of sex differentiation in the European eel.     

Sex ratios in offspring of sex-reversed sea bass and the relationship between growth and phenotypic sex differentiation

Groups of sexually undifferentiated sea bass Dicentrarchus labrax were fed with the androgen 17α-methyltestosterone (MT) during sex differentiation. MT treatment increased males from 79±3% in the controls (the usual 3:1 male:female sex ratio of cultured sea bass) to 100±0%, implying that in the treated groups one out of each five resulting males was a masculinized female (neomale). Thirteen males from the MT treated groups were taken as the parental generation and their sperm used to individually fertilize a pool of eggs from unrelated females. The probability of having at least one neomale was 95% and most probably two or three of the males used were neomales. The offspring from each family were reared separately under the same environmental conditions. Samples were taken at 11 and 15 months of age, during and after sex differentiation, respectively. Results showed that females predominated among the larger fish whereas males and undifferentiated fish predominated among the smaller ones. Intersexes exhibited an intermediate size. All fish with a body length smaller than 12 cm were undifferentiated. These results suggest that sex differentiation is more dependent on length than on age. At 15 months, sex ratios were male-biased in all families, except one (females ranged from 5 to 50%) and only two families had sex ratios not significantly different from 1:1, suggesting that the mechanism of sex determination in the sea bass is not of a XX/XY or ZW/ZZ type since no family exhibited a female-biased progeny, as would be expected from both types. Results support the hypothesis that factors other than genetic, i.e., environmental, may act epigenetically on the sex determination mechanisms of sea bass, as has been demonstrated in other fishes.     

Effects of oestradiol—enriched diet and of feeding with porcine testicular tissue on macroscopic gonadal sex in European eels

Oestradiol–enriched food (25 mg kg^-1 oestradiol) fed for 91 days to small eels (2 or 7 g) with undifferentiated gonads (UD) significantly favoured development of gonads with the macroscopic appearance of ovaries (♀-gonads) during the next 8 months. Fifty-four and 51% of control eels and 75 and 78% ofoestradiol-treated eels developed ♀-gonads. Minced porcine testicular tissue fed to 2-g eels for up to 371 days had effects similar to oestradiol-enriched food (68% with ♀-gonads), whereas feeding for only 91 days had no effect during the next 8 months. Oestradiol-enriched food was also fed to larger eels with already macroscopically differentiated gonads (30–70 g; 95% with ♀-gonads, 5% with ♀-gonads). After 27 days significantly more eels with a ♀-gonad or with a mixture of ovary-like and testis-like regions in the gonads (♂+♀-gonads) were found. After 96 days there were 44% with ♀-gonads, 40% with ♂+♀-gonads and 16% with ♀-gonads. Oestradiol thus had a feminizing effect, not only on morphologically undifferentiated gonads but also on morphologically differentiated ♀-gonads. The presence of sex steroid hormones or their precursors in porcine testicular tissue may also exert a feminizing influence. In all experiments the hormone-fed groups showed a tendency (not significant) towards increased growth rate. In small eels early rapid growth and differentiation of ♀-gonads were clearly correlated, both in hormone treated and in control eels. Otherwise no correlation was found between growth rate and gonadal sex.     

Influence of stocking density of European eel (Anguilla anguilla, L.) elvers on sex differentiation and zootechnical performances

Survival rate, sex ratio and zootechnical performances were evaluated on 168 kg of Anguilla anguilla elvers (0.45 g) weaned into three groups (A1, A2, A3) at initial densities of 800, 1600 and 3200 g m⁻³, respectively. In order not to modify the sex ratio, animals weaned at the different densities were maintained separately during the trials, and no size grading was performed at the fattening phase.
Final mean weight achieved by females belonging to the different groups showed no statistically significant differences; weight of males was higher (P < 0.05) in A1 than in A3 where a higher percentage of males was observed. Sex ratio of eels was different among the groups, with a higher percentage of males in A3 (96%) than in A2 (78%) or in A1 (69%). This finding testifies to a sex differentiation strongly affected by pre-fattening stocking density of elvers. Final load showed an increase in males corresponding to a significantly reduced biomass between A1 and A2 (10.97 and 10.24 kg m⁻³) and A3 (8.44 kg m⁻³). Final survival rate ranged from 87% (A1) to 90% (A3). As to food conversion, a better rate was found in A1 (1.9:1) compared to A2 (2.1:1) and A3 (2.3:1) eels.     

Age and growth of yellow eels, Anguilla anguilla, in the estuary of the Guadalquivir river (south-west Spain)

A total of 1068 eels were examined from a population located in the Guadalquivir river estuary (37°N, 6°25'W). Maximum ages recorded were 4 + (males) and 7+ (females), and maximum lengths were 39-1 cm (males) and 54.1 cm (females). No growth was recorded between November and April, most occurring in May and, to a lesser extent, in June-October. Females grew to be larger than males. A classification analysis, based on 17 different European eel populations revealed that populations in brackish waters grew faster than those in fresh waters, but latitude also had an influence. Length-weight relationships obtained for three eel categories (males, females and undifferentiated) were used to estimate relative condition: condition cycles were similar between sexes, with increases in autumn and decreases in winter. There were monthly fluctuations in the sex ratio, and females dominated significantly in the combined catch (234 males/276 females).     

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.     

Survival, growth and sex ratios of gynogenetic diploid honmoroko

Survival, growth and sex ratios of gynogenetic diploid honmoroko Gnathopogon caerulescens induced by blocking the release of the second polar body were examined. Mean survival of gynogenetic juveniles at 130 days after hatching was about 33% lower than that of the controls. No significant difference was seen in early growth between control and gynogenetic diploids. Standard length and body weight in six groups of gynogenetic progeny were significantly greater but in two groups were significantly smaller than in the controls. Although 69% of gynogenetic diploids had well-developed gonads, the remaining 30% had undeveloped gonads (small in size or thread-like), and those gonads were divided into four types. The mean proportion of females in the 10 gynogenetic groups was 87·2% which was significantly ( P <0·01) higher than in the controls (44·7%). Gynogenetic diploids included 3·0–35·3% males. Most of those males produced a high proportion of female progeny, but the proportion of male offspring varied widely. From these results, the sex determining mechanism in honmoroko was presumed to be female homogamety, but other factors resulted in the production of males.     

Life-history patterns of the mosquito-fish, Gambusia affinis, in the estuary of the Guadalquivir river of south-west Spain

SUMMARY. 1. The age, growth and reproduction of the small, introduced fish Gambusia affinis (Baird & Girard, 1853) were studied in the estuary of the Guadalquivir river.
2. The life-span was very short, the stock contained only two age groups: with annulus (1+ group; 10–12 months old) and without annulus (0+ group).
3. In both sexes growth restarted in April when the annulus appeared, but whilst 1+ males stopped growth, 1+ females grew steadily to June. Growth of 0+ spawners was only evident in September, the last month of the reproductive period. A differential growth rate between sexes was also evident.
4. 1+ specimens reproduced during May and June and their offspring from July to September. In both age groups somatic condition progressively declined during the spawning period.
5. The loss of condition and the disappearance of 1 + and the larger 04-specimens after reproduction may indicate the cost of a prolonged high level of reproductive effort.
6. The total fecundity (taken as the number of embryos) of 1 + females was represented by the formula: Fec=5.08 T.L. (mm) -170.07 and that of 0+ specimens by: Fec=2.23 T.L. (mm) -42.92. The maximum average monthly fecundity was reached in June when the length of the mother was at its greatest.
7. Length at first maturity was smaller in 0+ group than in the 1 + group; the difference between the two groups was greater in males (≅5 mm, T.L.) than in females (≅3 mm, T.L.). Also the average total length of 14-spawners was greater than 0+ spawners. There were significant differences in the overall sex ratio of 956 males to 2057 females.
8. The differences found in growth and reproduction between the two age groups suggest that life-history tactics may vary not only between different stocks but also within the same stock among its different components.