Changes in otolith microchemistry of the Japanese eel, Anguitta japonica, during its migration from the ocean to the rivers of Taiwan

The newly recruited Japanese eel, Anguilla japonica , elvers and 1-year-old eels collected in estuaries and in rivers, respectively, were studied. The microstructure and chemical composition of the sagittal otolith of these eels were examined by SEM and wavelength-dispersive spectrometer (WDS), A transition zone or'elver mark'was observed in the otolith of the young eels. A comparison of the otoliths of elvers with those from the 1-year-old eels suggests that this transition zone was deposited during upstream migration, a change from a marine to freshwater environment. Strontium (Sr) content in the primordium of the otolith of both elvers and young eels was low, probably due to the maternal or freshwater origin of the oocyte. The concentration of Sr in the otolith increased gradually during marine life and reached a peak approximately 1 month before upstream migration. As the elvers entered the estuary, the Src concentration dramatically decreased and remained at a low level thereafter. These findings indicate that the history of the migratory environment of the eel can be reconstructed from a combined study of otolith microstructure and microchemistry analysis.     

Determination of the age of young American eels, Anguilla rostrata, in fresh water, based on otolith surface area and microstructure

The time elvers of the American eel, Anguilla rostrata , spend in an estuary prior to their migration into fresh water was assessed. A distinct mark was formed on elvers' otoliths during their first 2 to 3 weeks in the river estuary. This mark was used to distinguish between growth in fresh water and in salt water. Migrating eels collected at a falls 4 km from the estuary exhibited bimodal length and weight distributions. Frequency distributions showed that eels collected in the estuary were smaller and had smaller otoliths than eels collected at the falls, indicating that elvers do not reach the falls in the same year as they enter the estuary. The three modal groups most probably represent three age–classes. However, the otoliths of elvers collected in the estuary had only the mark of transition whereas eels in the first and second mode at the falls usually had two rings (1–4) and four rings (3–6) per otolith, respectively, in addition to the mark of transition, as viewed under SEM. The possibility that ring formation is not annual means that the use of otoliths for the age determination of eels in this study has not been validated.     

The early life history of the tropical eel Anguilla marmorata (Quoy & Gaimard, 1824) from four Pacific estuaries, as revealed from otolith microstructural analysis

Anguilla marmorata glass eels or elvers were collected separately during anadromous migration from four Pacific estuaries: Hamuta, Poso, Shuang Hsi and Tanshui. The total length at arrival in these estuaries was (mean ± standard error) (51.50 ± 0.90) (51.80 ± 0.90) (46.95 ± 0.84) and (47.33 ± 0.80) mm, respectively. The sagittal otolith microstructure, increment patterns and daily age were examined by scanning electron microscope. Based on the number of increments of presumed daily deposition, the overall mean age at arrival in the estuaries was estimated to be about 3–4 months, with an estimated period of 73–86 days for the leptocephalus stage. Two zones, i.e. the leptocephalus growth zone (L) and the metamorphosis growth zone (M) were recognizable in the otolith cross section. The increment width of L and M varied from the otolith's centre to its margin, reflecting different growth rates. The spawning grounds of these eels are presumably not far from the estuary. Their locations are discussed.     

Age and growth of Saurenchelys (Nettastomatidae) and Dysomma (Synaphobranchidae) leptocephali in the East China Sea

The otolith microstructures of the leptocephali of Saurenchelys stylura and Dysomma sp., collected in November and December 2000 in the East China Sea, were examined to determine their larval ages and growth rates, and the spawning times of these two species of outer shelf and slope marine eels. Leptocephali ranging in size from 8 to 48 mm total length were examined, and the nettastomatid, S. stylura , and the synaphobranchid, Dysomma sp., had estimated ages that ranged from 16 to 75 days and 17 to 66 days, respectively. The overall growth rate of S. stylura was 0·68 mm day⁻¹( n  = 21), and of Dysomma sp. was 0·44 mm day⁻¹( n  = 22). These growth rates were similar or slightly faster than those observed for anguillid leptocephali in offshore areas of the western Pacific. The backcalculated hatching dates for these two species were from September to November. The otolith increment widths of S. stylura showed an increase before 20 to 30 days that were similar to those in anguillid species, but in Dysomma sp. there were no remarkable increases.     

鳗鲡幼鱼耳石日轮的研究

本文报道采自辽东半岛沿岸鳗鲡(Anguilla japonica)的白仔鳗和经人工培育的当年幼鳗耳石日轮生长的观察结果。白仔鳗和幼鳗耳石平均直径均与体全长成直线相关。12尾白仔鳗耳石的平均日轮数146.3,据此推测其产卵期为11—12月。观察证实从咸淡水转人到淡水生活的幼鳗耳石的环纹有过渡带存在。     

Otolith microstructure and daily age of Anguilla japonica, Temminck & Schlegel elvers from the estuaries of Taiwan with reference to unit stock and larval migration

To test the hypothesis that the Japanese eel, Anguillu japonica , elvers in the eastern and western coasts of Taiwan are recruited from two different spawning grounds and to increase the knowledge of the early life history of the eel, the otolith microstructure and daily age of elvers collected from five estuaries in the coast of Taiwan during December 1989 through February 1990 were examined by scanning electron microscopy. The total length of elvers at arrival in the estuaries was similar among estuaries, averaging c . 56.0 mm and showed a seasonal decrease. The maximum radius of the sagittal otolith of elvers ranged from 124.46 to 181.82μm with a mean of 143.15 ± 12.72 μm. The otolith from centre to edge included an organic-rich primordium (9.20 ± 2.02 μm in diameter), a diffusively calcified core (20.94 ± 1.99 μm), and the daily growth increments; these three layers were probably deposited during the embryonic, yolk sac and feeding period respectively. The growth rate of the otolith was higher at the beginning of early life (0.5−1.0 μm day ⁻¹), lowest at approximately 100-days old (<0.5 μm day⁻¹), and highest 1 month before arrival at the estuary (> 1.0 pm day⁻¹). The mean age for elvers arriving in the estuaries of the coasts of Taiwan was approximately 170.4 ± 21.02 days. Neither the growth pattern of the otolith nor the age of elvers arriving in the estuary were significantly different among estuaries, indicating that the elvers in both eastern and western Taiwan were probably recruited from the same spawning ground. The growth pattern of the otolith in relation to larval migration was analysed.     

Recruitment mechanism of the eel, Anguilla japonica, to the Japanese coast

A total of 149 Anguilla japonica elvers collected at 10 locations along the Japanese coast were aged according to otolith daily increments. The interrelationships among age, birth date, body size, pigmentation stage, sampling location and the timing of recruitment were examined in order to determine the recruitment mechanism of elvers to coastal waters.
First catches of eels were earlier in the locations at lower latitudes. Age at recruitment was roughly constant, 218 ± 29 (mean ± s.d.) days old, disregarding the localities, but a weak positive correlation was obtained between age and sampling date or timing of recruitment. Body length at recruitment was also constant, 56.3 ± 2.3 mm s.l., and showed no significant correlation with either locality or recruitment timing. Estimated birth date ranged from April to November, the mean ± s.d. being 22 July 1982 ± 42 days, suggesting a peak season spawning in summer. Birth date was closely related with both the latitude of location and sampling time. Pigmentation developed more at lower latitude. Recruitment mechanism of the Japanese eel was summarized as follows: the earlier-born individual recruits earlier at lower latitude and at younger age, but at a constant body size.     

Relationships between total length and otolith measurements for 36 fish species from Gökçeada Island,Turkey

The relationships between fish total length and otolith measurements (OL, OW and OR) were described by means of allometric power equation for 36 fish species from Gokceada Island, Turkey. Regressions were also estimated at genus level. A total of 14364 specimens were collected monthly using beach seine (0–2 m) and beam trawl (5–20 m) from June 2013 to June 2014. Generally, the otolith length showed the highest correlation for predicting fish total length. This paper represents the first relationships between otolith morphometrics and fish total length for 12 species. These relationships can be useful for researchers who examining stomach contents of piscivorous predators.     

Influence of water temperature and feeding regime on otolith growth in Anguilla japonica glass eels and elvers: does otolith growth cease at low temperatures?

The influences of water temperature and feeding regime on otolith growth in Anguilla japonica glass eels and elvers were investigated using individuals reared at 5, 10, 15, 20, 25 and 30° C and in fed or unfed conditions at salinity 32 after their otoliths were marked with alizarin complexone (ALC). To eliminate the difficulty of observing the edges of otoliths with optical (OM) or scanning electron (SEM) microscopes, three to 10 individuals were sampled from each tank at 10, 20 and 30 days during the experiment and reared for an additional 10 days at 25° C after their otoliths were marked a second time. Otolith growth and the number of increments were measured using both OM and SEM. Most A. japonica commenced feeding after 10 days at 20–30° C or after 20 days at 15° C, but no feeding occurred at 5 and 10° C. No otolith growth occurred at 5 and 10° C except in two individuals with minimal increment deposition at 10° C. Otolith growth was proportional to water temperature within 15–25° C and not different between 25 and 30° C. At 15, 25 and 30° C, the mean otolith growth rate in fed conditions was higher than in unfed conditions. The number of increments per day was significantly different among water temperatures (0·00–0·01 day⁻¹ at 5 and 10° C, 0·43–0·48 day⁻¹ at 15° C and 0·94–1·07 day⁻¹ at 20–30° C). These results indicated that otolith growth in A. japonica glass eels and elvers was affected by temperature and ceased at ≤10° C under experimental conditions. Hence, future studies analysing the otoliths of wild-caught A. japonica glass eels and elvers need to carefully consider the water temperatures potentially experienced by the juveniles in the wild.     

Morphology and taxonomic significance of the otoliths of some bathypelagic Anguilloidei and Saccopharyngoidei from the Sargasso Sea

The sagittal otoliths of seven anguilliform species belonging to the families Nemichthyidae, Serrivomeridae and Eurypharyngidae are described and illustrated, and a key for their identification is provided. Although the leptocephali of the various fish species treated here have similar otoliths, some species develop specific otolith characteristics during the adult stage. The shape as well as the ratio of fish length to otolith length ratio in adults may serve as a taxonomic aid. Since the sagittae of these fishes can be used for specific identification, the digested remains of prey in the stomachs and guts of predators can be identified.     

Discrepancies between otoliths of larvae and juveniles of the American eel: is something fishy happening at metamorphosis?

The use of otoliths to interpret early life history in fishes depends upon the assumptions that otoliths record past events accurately and consistently and that records of events in otoliths are continuous. Both the number of growth microincrements ( I ), and the radii ( R ,μm) of otoliths of American eel Anguilla rostrata , leptocephali increased linearly and highly significantly with leptocephalus body length ( L , mm), as expected on the above assumptions ( I , =2·29 L , − 5·75 and R , =1·05 L , + 12·02, r ²,=0·938 and 0·931, n , =20). In contrast, the number of increments and the radii of the leptocephalus growth zones of otoliths of glass-phase American eels were not related to body length, and they were lower than predicted by the relationships developed for leptocephali. Thus, otoliths of American eels apparently violate one or both assumptions. Possibly, the margin of the otolith is resorbed during metamorphosis from leptocephalus to glass eel, perhaps as part of calcium metabolism as skeletal elements are being formed.     

Ontogenetic and environmental effects on otolith shape variability in three Mediterranean European eel (Anguilla anguilla, L.) local stocks

Otolith morphology is an efficient tool for the discrimination of fish stocks, populations and species when comparative genetic data are not available. Currently, the relationship between environmental factors and otolith shape is poorly characterized for the European eel (Anguilla anguilla), a highly migratory catadromous species constituting a single, randomly mating stock. The present study analyses the differences in otolith morphology between three Mediterranean eel local stocks from different environmental contexts (i.e. two brackish lagoons and one river). The relationship between otolith shape and otolith size was studied by means of Elliptic Fourier analysis and multivariate statistics. Otolith profile was digitally acquired and Cartesian coordinates were extracted. Partial Least Square (PLS) analysis pointed to continuous allometric growth in size and shape in otoliths from all three sites. In the three environments, shape variations occurred during growth as indicated by the presence of a significant and positive relationship between otolith size and the first PLS latent vector (i.e. which bears most of the information regarding otolith outline). Differences between smaller and larger sized otoliths were investigated using PLS Discriminant Analysis (PLSDA) and cluster analysis. Results indicate that otolith shape is highly uniform at smaller than at larger sizes. These shape differences apparently overlap the initial differentiation of the small otolith outlines acquired by eels during the growing phase as elvers in the marine environment. Data were discussed considering that the physical and chemical habitat variability in brackish lagoons and river could underlie a marked change in otolith shape during the animals' growth.     

Age and growth of Anguilla bicolor bicolor leptocephali in the eastern Indian Ocean

A sampling survey for leptocephali was conducted in the eastern Indian Ocean to the west of Sumatra from 5 to 20 June 2003 in an overlapping area with the historical survey in September to November 1929 during the Danish Round the World Expedition. The age and larval growth rate of 34 Anguilla bicolor bicolor collected in 2003 were estimated using their otolith microstructure to obtain new information about the early life history of this sub-species. The total lengths and ages of these leptocephali were 44·1–55·5 mm and 114–158 days, respectively. Their hatching dates ranged from 3 January to 20 February 2003. Combining these age data and the estimated age of leptocephali collected by others in the same area, this sub-species was estimated to have a wide range of spawning periods. Individual growth rates of the leptocephali in 2003 ranged from 0·32 to 0·39 mm day⁻¹ with a mean ± s . d . of 0·35 ± 0·02 mm day⁻¹. These values were lower than the growth rates of leptocephali of other tropical eels such as Anguilla celebesensis or Anguilla borneensis , suggesting that A. b. bicolor from the eastern Indian Ocean have a longer leptocephalus period of oceanic migration.     

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.     

Der Einfluß von Temperatur,Futter, Größe und Herkunft auf die sexuelle Differenzierung von Glasaalen(Anguilla anguilla)

The effects of rearing and feeding conditions, as well as of body size and origin on sexual differentiation have been examined in elvers collected on the Atlantik coast (River Ems) and in the Tyrrhenian Sea. Raised at 17°, 20°, 23°, 26° or 29° C and at constant photoperiod, the elvers received either commercial fish food or cod roe. Eels from the Tyrrhenian Sea mostly developed into males. To some extent, at temperatures optimal for growth (26° C) and feeding a cod-roe diet, a shift of sex ratio in favour of females was observed in Atlantic eels. The results obtained contradict those ofFidora (1951), who, rearing elvers in ponds, found the percentage of male eels to be positively correlated with increasing stock density. Although in the present study, stock density was 200 times higher than inFidora's experiments, the percentage of females was much higher than that of males. The results obtained supportBellini's (1907) findings that big elvers preferentially develop into females, but small elvers into males. Irrespective of elvers' origin, water temperature and diet, the onset of sexual differentiation dependends upon attaining a certain body length (15–25 cm), but not on age. Whereas under natural conditions females are supposed to grow faster than males, under the conditions tested the males grew faster than the females. It is concluded, that, in addition to genetic factors, various environmental factors may influence sex determination in eels.     

Location,size and age at onset of metamorphosis in the Japanese eel Anguilla japonica

This study clarifies the location, size and age at the onset of metamorphosis in Japanese eels Anguilla japonica through oceanic surveys, rearing experiments and analyses of the morphology and otoliths of leptocephali and glass eels. Twenty‐eight metamorphosing leptocephali were collected in the mesoscale eddy region to the east of Taiwan during research expeditions in 2004. Rearing experiments showed that the total length (L_T) of leptocephali decreased by an average of 12·5% during metamorphosis and 13·9% during the 2–12 h after death. Thus, the mean back‐calculated L_T at the onset of metamorphosis for 630 glass eels from Taiwan and Japan was estimated at 67·8 ± 2·7 mm (mean ± S.D.). The estimated mean ante‐mortem size of the fully grown pre‐metamorphic leptocephali collected in 2004 was 64·6 ± 3·4 mm, which was consistent with the L_T estimate for glass eels. Otolith analysis showed that the mean age at the onset of metamorphosis was 137 ± 15 days and indicated that Japanese eels may have a recruitment route through the mesoscale eddies to the east of Taiwan in addition to the direct transfer route from the North Equatorial Current to the Kuroshio Current.     

Synchronized spawning ofanguilla japonica inferred from daily otolith increments in leptocephali

The exact timing ofAnguilla japonica spawning was determined from analyses of daily otolith increments in leptocephali collected near a spawning area west of the Mariana Islands on July 1–18, 1991. The birth dates of the 54 leptocephali examined (10.2 to 30.5 mm in total length) ranged from May 22 to June 24, 1991, the individuals clearly comprising two age groups, May-born fish (mode May 28) and June-born fish (mode June 21). The data showed thatA. japonica spawns intermittently during the spawning season, with fixed synchronized timing. Each group of leptocephali collected along three different north-south transects (131°, 134° and 137°E between 10° and 22°N) comprised both May-born and June-born fish. The latter were dominant along the easternmost and middle transects, whereas the May-born fish were more abundant along the westernmost transect. The modal ages of the June-born and May-born fish collected along 137°E on July 1–3 were 13 d and 35 d, respectively, while those of the two age groups collected along 134°E on July 17 and 18 were 28 d and 50 d, respectively. These data show that the interval between the sampling dates for the two transects (ca. 15 d) corresponded closely to the differences in modal ages of specimens from the two transects (15 d) for both the May- and June-born fish, and further, that the difference in modal age between the two age groups (22 d) was the same at both transects. A similar correspondence in total length was also observed between the two age groups at the above two transects. The findings clearly demonstrated parallel westward transport by the North Equatorial Current for both the May- and June-born eel leptocephali, which originated from a spawning area estimated as being between 141° and 143°E.     

Comparison of otolith growth and morphology with somatic growth and age in young-of-the-year bluefin tuna

Otolith morphological characteristics were studied using image analysis techniques and the relationships between otolith growth and somatic growth and age, as estimated from counting daily otolith increments, were examined in young-of-the-year (YOY) bluefin tuna Thunnus thynnus ranging in fork length ( L _F) from 8·5 to 55·5 cm. Whole otolith length, width, area and perimeter, and three shape indexes, circularity, E value and rectangularity, were extracted for each pair of sagittae. Since no statistical significant differences between left and right otolith morphometrics were found, only one otolith from each fish was used for correlations. Statistically significant relationships were observed between otoliths measurements and fish somatic growth when a linear regression was applied after logarithmic transformation of all variables tested. Among the variables, otolith length was the one that showed the highest correlation with L _F, followed by otolith area and perimeter, whereas otolith rectangularity exhibited the lowest correlation. Statistically significant relationships were also observed between the otolith variables tested and the age of the fish, which ranged from 20 to 129 days. The ages estimated using otolith mass were very close to those assessed using daily increment counts (bias ranged from 1 to 24 days). Therefore, otolith mass could represent a valuable criterion for age estimation in YOY bluefin tuna that is objective, economic and easy to perform compared to daily increment counting method.     

Relationship of otolith length to fish total length in six demersal species from the NW Mediterranean Sea

Relationships between otolith major axis length (mm) and fish size (total length, cm) were described by means of linear regression analysis for six demersal fish species from the NW Mediterranean: blue whiting (Micromesistius poutassou), greater forkbeard (Phycis blennoides), red mullet (Mullus barbatus), poor cod (Trisopetus minutus capelanus), horse mackerel (Trachurus trachurus), and Mediterranean mackerel (Trachurus mediterraneus). Results show that reconstruction of body size from otolith measurement is possible by applying this approach based on the relationship of otolith length – fish length.     

Growth variability in individually confined elvers, Anguilla anguilla (L.)

Newly caught elvers Anguilla anguilla (L.) were individually confined, induced to feed and their survival and growth variability compared to those of similar elvers held communally in lowdensity populations. Similar trials were conducted with fast-growing and slow-growing older elvers that had been induced to feed while cultured communally. It was not difficult to induce feeding in newly caught elvers, nor did it appear necessary for elvers to be stimulated to feed by the presence of others. Isolation seemed to enhance growth variability in newly caught elvers.
In older elvers growth was generally depressed by isolation. Following a period of stress, e.g. weighing, small fish tended to grow more slowly than larger fish in the individual groups. This suggested some permanency of stunting; however, some markedly stunted fish taken from large populations showed remarkable recovery when isolated and exhibited very high instantaneous growth rates, over 6.5% day⁻¹.