Monthly changes in the swim bladder morphology of the female Japanese eel <Emphasis Type="Italic">Anguilla japonica</Emphasis> in the coastal waters of Mikawa Bay,Japan

In the coastal area of Mikawa Bay, central Japan, specimens of the female Japanese eel Anguilla japonica could be divided into two groups according to the degree of swim bladder development. In one case, they were undeveloped, and in the other, they were highly developed with large rete mirabile, thick submucosa, and a well-developed gas gland. The morphology of the swim bladder in the latter group was comparable with that in the artificially fully maturated eel. The specimens with an undeveloped swim bladder were caught during all months, although their number was small. The specimens with a highly developed swim bladder were most abundant in November and December. During these months, catch of the specimens also increased sharply, by more than 10 fold compared to that in other months. These observations indicate that most of the eel appearing in coastal Mikawa Bay from October to January have a highly developed swim bladder adapted for a deep-sea environment. It was also conjectured that these specimens most likely migrated from rivers feeding into Mikawa Bay, toward spawning grounds in the open sea, and that this occurred after development of their swim bladders was completed. Actually, the specimens caught in the upstream of the Toyo River feeding into Mikawa Bay from late August to early October already had highly developed swim bladders.     

Comparisons between the age structures, growth and reproductive biology of two co-occurring sillaginids, Sillago robusta and S. bassensis, in temperate coastal waters of Australia

Sillago robusta and S. bassensis occupy the open sandy areas of the deeper waters (20–35 m) of the inner continental shelf of the lower west coast of Australia. Comparisons were made of their age and size compositions, growth rates, ages and sizes at first maturity, and spawning times. Most S. robusta were less than 3 years old (maximum 7 years), while S. bassensis often reached 7 years of age (maximum 10 years). The maximum length of S. robusta (200 mm) was far shorter than S. bassensis (328 mm), whereas the reverse pertained for the von Bertalanffy growth coeffcient (K), i.e. c. 1.0 v. c. 0.3. Differences in K reflect the fact that c. 80% of the asymptotic length is achieved by S. robusta after 2 years, but not until 6 years of age by S. bassensis. Sexual maturity was reached by up to 50% of S. robusta at the end of their first year of life, and by almost all fish at the end of their second year of life. Most S. bassensis did not reach maturity until the end of their third year of life. In both species, those individuals that reached maturity early, were significantly longer than those that did not reach maturity at the same age. The gonadosomatic indices and proportions of mature gonads, and the numbers of vitellogenic and hydrated oocytes and post-ovulatory follicles, were relatively high in ovaries of both species between December and March. Although both species spawn in these 4 months, some S. bassensis also spawn between September and November and in March and April. In the middle of the spawning period, the ovaries of S. robusta and S. bassensis frequently contained oocytes that ranged widely in size and development, together with post-ovulatory follicles, suggesting that both species are multiple spawners. Juveniles of S. robusta remain in the deeper waters of the inner continental shelf, whereas those of S. bassensis migrate inshore to their nursery areas in surf zones. As S. robusta reaches sexual maturity at an earlier age and smaller size than S. bassensis, it is probably more advantageous for the juveniles of this species to remain in deeper water, and thereby conserve energy for gonadal maturation, rather than migrating into shallow waters for only a very few months.     

Timing and rate of sexual maturation of European eel in brackish and freshwater environments

Maturation rates in three European eel Anguilla anguilla populations increased from September to October and were slightly lower in fresh water than in brackish waters. Average and variance of total length at maturation were larger in females than males.     

An Examination of Utilizing External Measures to Identify Sexually Maturing Female American Eels, Anguilla Rostrata, in the St. Lawrence River

It is well established that Anguillid eels undergo a complex suite of morphological and physiological changes during their transformation from resident, yellow-phase juveniles to actively migrating silver-phase eels. While it has been shown that some morphological measures can be used successfully to identify sexually maturing European eels, Anguilla anguilla, as well as Australian short fin, Anguilla australis, and long fin, Anguilla dieffenbachii eels, this relationship has never been quantitatively assessed for American eels, Anguilla rostrata. American eels of varying sexual development were collected from three locations on the St. Lawrence River: Lake St. Lawrence, Quebec City and Kamouraska. Sexual development of each eel was assessed with gonadosomatic index (GSI), oocyte diameter and degree of oocyte development. Morphological measures of total length, weight, head width, pectoral fin length and vertical and horizontal eye diameters were obtained from each fish. We used this data to test two hypotheses: (i) resident yellow phase eels, suspected migrants and known migrants are morphologically indistinguishable; and (ii) if differences exist, they cannot be used to reliably predict gonadal development or migratory status. Univariate analysis (ANOVA and ANCOVA) indicated that there were highly significant differences in all of the measured parameters and thus we were able to reject the first hypothesis. However, we failed to reject the second hypothesis as the high degree of overlap between groups eliminated the ability of any single measure to differentiate between resident and migratory eels. A multivariate discriminant model was developed that could classify only 72–80% of the eels correctly based on their morphological characters. While morphological measures may have some potential as a rapid, cost-effective method of pre-screening individual eels, morphological measures should not be considered a definitive indicator of sexual maturity or migratory status for female American eels in the Upper St. Lawrence River.     

Advanced sexual maturation before marine migration of Anguilla bicolor bicolor and Anguilla marmorata at Réunion Island

Maturing sub-adults of two species of anguillid eels (a female Anguilla bicolor bicolor and a male Anguilla marmorata ) were collected for the first time at Réunion Island, western Indian Ocean. Both were silver eels, i.e. maturing eels at the onset of their spawning migration, and characterized by advanced sexual maturation that has been only observed in Anguilla dieffenbachii from New Zealand.     

The fatty acid chain elongase,Elovl1, is required for kidney and swim bladder development during zebrafish embryogenesis

Very long chain fatty acids are required for sphingolipid synthesis, lipid homeostasis, myelin formation, epidermal permeability, and retinal function. Seven different enzymes are known to be involved in the elongation cycle of fatty acids, with different chain-length specificities. Elovl1 is one of those enzymes whose function has been linked mainly to the synthesis of sphingolipids and the epidermal barrier. However, the role of Elovl1 in organogenesis is not clear. In zebrafish, 2 Elovl1 genes, elovl1a and elovl1b, are highly expressed in the swim bladder, and elovl1b is also expressed in the kidney. We found that both elovl1 knockdown embryos contain increased levels of long chain fatty acids from carbon number 14 to 20 as compared to control embryos. Oil-Red-O staining shows that yolk lipid consumption is greatly reduced, whereas lipid droplets accumulate within the swim bladder. Notably, knockdown of either elovl1a or elovl1b affects the expression of genes involved in swim bladder development and impairs inflation of the swim bladder. Consistent with its expression in the pronephros, knockdown of elovl1b alone affects the expression of genes required for kidney development and reduces renal clearance. Our findings strongly suggest that both elovl1 genes are a key determinant of swim bladder and kidney development in zebrafish, which may be comparatively applicable to lung and kidney development in humans.     

Does a 5500-km swim trial stimulate early sexual maturation in the European eel (Anguilla anguilla L.)?

The catadromous European eel (Anguilla anguilla L.) undertakes a 6000-km spawning migration from its freshwater habitats to the Sargasso Sea. In large Blazka swim tunnels of 127 l, the physiological effect of such a prolonged swimming performance on sexual maturation in adult female eels was investigated. Two groups of eels were placed in swim tunnels for 173 days, one group was able to swim at 0.5 body lengths/second (Swim group) covering a distance of c. 5500-km over the experimental period, and one group kept in static (End Control group). A control group was sampled at the start of the experiment in order to determine the initial stage of reproductive development (Initial Control group). At the end of the swim trial, the maturation parameters 11-ketotestosterone, pituitary levels of LH and plasma levels of estradiol were higher (although not significantly) in the Swim compared to the End Control group. In addition, no significant differences were observed in most measured morphometric and reproductive parameters, including eye-index, gonadosomatic index, hepatosomatic index, and plasma levels of vitellogenin, cortisol and melanophore-stimulating hormone (MSH). Also, pituitary levels of both MSH, and adrenocorticotropic hormone (ACTH) were unaffected. In contrast, the oocyte diameter was found to be significantly higher in the Swim compared to the End Control group. Based on these observations we conclude that a period of prolonged swimming might be a physiological stimulus necessary for the onset of maturation in the European eel.