An evaluation of the otolith characteristics of Conger conger during metamorphosis

A sample of 20 metamorphosing conger eel Conger conger leptocephali were collected from the Minho River, Portugal, in February 1999 and their sagittal otoliths were analysed by scanning electron microscopy. Four different etching agents were applied along both sagittal and frontal sections during otolith preparation to examine the microstructural growth in this species. Otolith growth increments were visible throughout the increment countable zone using all four treatments, but a permanent peripheral diffuse zone, where the daily increments were unclear, appeared on all otoliths, preventing accurate age estimation. To understand more about the nature of the diffuse zone, otoliths of 10 other metamorphosing leptocephali reared in aquaria were marked by immersion in tetracycline hydrochloride. The distance between the fluorescent marks and otolith edge, measured over a fixed period of time, was used to estimate the otolith growth rate. The application of this technique led to an anomalously high estimated otolith growth rate, probably as a result of the capture, marking and handling stress.     

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.     

Temperature effects on the incorporation of strontium in otolith of Japanese eel Anguilla japonica

The effects of temperature on somatic and otolith growth and the incorporation of strontium in otolith of the Japanese eel, were studied in laboratory-reared and field-caught eels. The somatic and otolith growth rates of the eel increased significantly with temperature and were estimated as approximately 0·096 mm t.l, (P<0·01) and 0·36 μm in otolith diameter per degree-day (0·01相似文献   

Assessment of growth zones on whole and thin-sectioned otoliths in <Emphasis Type="Italic">Sperata aor</Emphasis> (Bagridae) inhabiting the River Ganga,India

The present study was undertaken with the objective to assess the clarity of growth zones on whole and thin-sectioned otoliths in Sperata aor. A total of 125 sagittal otoliths of S. aor were collected monthly from the river Ganga during the period, April to December 2013 at Narora, Uttar Pradesh, India. Thin sections (approximately 0.5 mm) of one of the sagittal otoliths of each fish were cut using IsoMet® Low Speed Saw. Both whole otoliths and thin-sectioned otoliths were then examined under stereozoom microscope. Parameters of agreement on growth zones were calculated by comparing the number of growth zones obtained independentlyby the two readers (R1 and R2) from the two methods (whole otolith and thin-sectioned otolith method). Thin-sectioned otolith method exhibited higher agreement than whole otolith method based on linear regression analysis and growth zones bias plot. Between readers, higher agreement was noted for reader 1 than reader 2, plausibly due to his relatively more experience in examining the growth zones on the otoliths. However, both readers reported independently that the growth zones were clearer on thin sections than on whole otoliths especially those from older individuals. Thus, it may be concluded that the thin-sectioned otolith method should be utilized for assessment of growth zones in S. aor populations from the river Ganga.     

Age validation and growth of three commercially important hemiramphids in south-eastern Australia

The method of using sectioned otoliths to estimate age in three species of garfishes (family Hemiramphidae) was validated by: (1) staining fishes with the vital stain alizarin complexone (ALC) and periodically examining their otolith growth, and (2) marginal increment analyses. Staining fishes with ALC indicated that opaque zones were formed during winter and spring, but did not become visible on the otolith edge until late spring and summer. Hyporhamphus australis were found to be similar to the hemiramphids of the Atlantic in having fast growth rates and a maximum observed age of 4+ years old. Hyporhamphus regularis ardelio and Arrhamphus sclerolepis krefftii were found to be more similar to the southern sea garfish, Hyporhamphus melanochir , in being moderately long-lived, with maximum observed ages of 7+ years old for both species. Females grew faster and attained greater fork lengths than males for each species. Sectioned otoliths showed large variation in the appearance of opaque zones between the three species studied, with those from the wide-ranging, oceanic H. australis appearing inconsistent and diffuse when compared to the estuarine H. r. ardelio and A. s . krefftii . This variation was also apparent from fishes kept in aquaria, suggesting that the appearance of opaque zones in otoliths of these species is largely influenced by physiology, rather than by environmental conditions.     

Scanning electron microscopic analysis of annulus microstructure in otolith of European eel, Anguilla anguilla

To validate the yearly periodicity of annulus formation in the otolith of the eel, the structure of annuli in otoliths of the European eel, Anguilla anguilla , stocked for 7 and 12 years in Lake Ommen on the east coast of southern Sweden, was examined. The population was stocked from elvers imported both from France (Bay of Biscay) in April 1979 and England (River Severn) in March–April 1984. The microstructure of an annulus consisted of single, double and/or composite tings depending on the location in the otolith. The counts of annuli in otoliths of these eels were approximately consistent with the expected age. However, supernumerary false annuli and/or annulus underestimation frequently occurred. The methodology for annulus discrimination with light and scanning electron microscopes is described.     

All in the ears: unlocking the early life history biology and spatial ecology of fishes

Obtaining biological and spatial information of the early life history (ELH) phases of fishes has been problematic, such that larval and juvenile phases are often referred to as the ‘black box’ of fish population biology and ecology. However, a potent source of life‐history data has been mined from the earstones (otoliths) of bony fishes. We systematically reviewed 476 empirical papers published between 2005 and 2012 (inclusive) that used otoliths to examine fish ELH phases, which has been an area of increasing attention over this period. We found that otolith‐based research during this period could be split into two broad themes according to whether studies examined: (i) biological objectives related to intrinsic processes such as larval and juvenile age, growth and mortality, and/or (ii) spatial objectives, such as habitat use, dispersal and migration. Surprisingly, just 24 studies (5%) explored a combined biological–spatial objective by simultaneously exploiting biological and spatial information from otoliths, suggesting much more scope for such integrated research objectives to be answered via the use of multiple otolith‐based techniques in a single study. Mapping otolith analytical techniques across these two approaches revealed that otolith structural analysis was mainly used to investigate biological processes, while otolith chemical analyses were most often applied to spatial questions. Heavy skew in research effort was apparent across biomes, with most (62%) publications specific to marine species, despite comparable levels of species richness and the importance of freshwater taxa (just 15% of papers). Indeed, around 1% (380 species) of a possible 31400+ extant species were examined in our surveyed papers, with a strong emphasis on temperate marine species of commercial value. Potential model species for otolith‐based ELH ecology research are arising, with the eel genus Anguilla (24 studies) and the European anchovy Engraulis encrasicolis (14 studies) attracting more research effort than most other taxa. While there is a preponderance of common techniques (e.g. daily otolith increment counts, increment widths), novel techniques such as transgenerational marking and computed X‐ray tomography, are increasingly being applied in published studies. The application of an integrative approach based on a combination of emerging techniques and traditional methods holds promise for major advances in our understanding of ELH fish ecology and to shine light into the ‘black box’ of fish ecology.     

Fish otoliths: do sizes correlate with taxonomic group,habitat and/or luminescence?

Otoliths are dense structures in the ears of fishes that function in hearing and gravity perception. Otolith (sagitta) diameters, as percentages of standard length (% SL), are calculated for 247 marine fish species in 147 families and compared by taxonomic group (usually order), habitat and presence or absence of luminescence. Otolith sizes range from 0.4-31.4 mm and 0.08-11.2% SL. The eel and spiny eel orders Anguilliformes and Notacanthiformes have small to very small otoliths, as do the triggerfish order Tetraodontiformes, pipefish order Gasterosteiformes, billfish suborder Scombroidei and many of the dragonfish order Stomiiformes. The soldierfish order Beryciformes has moderate to very large otoliths. The perch order Perciformes has a wide range of otolith sizes but most have small to moderate otoliths 2-5% SL. Only 16 out of the 247 species have the relatively largest otoliths, over 7% SL. Seven out of these 16 species are also luminous from a variety of habitats. Luminous species have slightly to much larger otoliths than non-luminous species in the same family Both beryciforms and luminous fishes live in low-light environments, where acute colour vision is probably impossible. Most fishes of the epipelagic surface waters have very small otoliths, perhaps due to background noise and/or excessive movement of heavy otoliths in rough seas. Bathypelagic species usually have small otoliths and regressed or absent swimbladders. Other habitats have species with a range of otolith sizes. While the relationship between hearing ability and otolith length is unknown, at least some groups with modified swim-bladders have larger otoliths, which may be associated with more acute hearing.     

Differences in the Trace Element Deposition in Otoliths Between Marine- and Freshwater-resident Japanese Eels, Anguilla japonica, as Determined by Laser Ablation ICPMS

Synopsis In order to determine whether the trace element composition in otolith of the Japanese eel Anguilla japonica could be used to determine its habitat use, we used laser ablation inductivity coupled plasma mass spectrometry (LA-ICPMS) to assay sectioned otoliths of both marine-resident (sea eels) and freshwater-resident (river eels) eels. A close linear relationship in the Sr:Ca ratios between EPMA (X-ray analysis with an electron microprobe) and LA-ICPMS analyses was found, suggesting that the latter technique could be used to separate the marine and freshwater life phases. Elemental signatures in the otolith outside the elver mark showed significant differences in Cr:Ca, Mn:Ca, and Ba:Ca ratios as well as Sr:Ca ratios between sea and river eels. These results indicate that the elemental compositions may reflect environmental variability between marine and fresh water masses. Thus, those elemental ratios determined by LA-ICPMS analysis seem to have the potential to help distinguish the habitat of the eel.     

Historical changes in juvenile southern bluefin tuna Thunnus maccoyii growth rates based on otolith measurements

Suspected historic changes in juvenile southern bluefin tuna Thunnus maccoyii growth rates were investigated using otolith increment width data. Four hundred and ninety otoliths were selected from fish estimated to be between 1 and 41 years-old. The distance between the first five annuli were measured on the otoliths, giving estimates of otolith growth for age classes 1+ to 4+ years for fish spawned from the early 1960s to mid 1990s. The data showed that growth rates of juveniles (age 1+ and 2+ years) started to increase at around 1979–1980, and that growth continued to increase throughout the 1980s and early 1990s. Lee's phenomenon was not observed in the data. Correlation tests did not reveal clear relationships between annual otolith growth and regional environmental variables such as sea surface temperature or Southern Oscillation Index. The increase in otolith growth, however, was consistent with juvenile growth estimates obtained from other sources, and correlated with large-scale trends in population size and environmental conditions.     

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.     

Otolith growth and age estimation in the European hake

The internal sulcal rings in Merluccius merluccius otoliths cannot be considered as annuli. In the absence of a strong seasonal Zeitgeber, hake otoliths in the Mediterranean did not lay down an interpretable ring pattern that would be useful for age determination. A total of 484 sagittal otoliths from specimens ranging between 6 and 94 cm L T was studied in monthly samples from the Gulf of Lions in 1989–1990. Transverse, burnt otolith sections was analysed with an image analysis system using enhanced and filtered images and using a fast Fourier transform (FFT) function to avoid subjectivity in ring interpretation. The otolith radius-fish length relationship showed allometric growth and sexual dimorphism. The ring pattern was consistent for the sulcal rings in both sexes. Changes in the marginal increment showed the formation of multiple sulcal rings, of both environmental and physiological origin. The ring pattern depended on the sex and sexual activity.     

Neuron-specific enolase and serotonin in the Merkel cells of conger-eel (Conger conger) epidermis. An immunohistochemical study

Immunocytochemical techniques were used to investigate the distribution and co-localization of neuron-specific enolase (NSE) and serotonin (5-HT) in the skin of the conger eel, Conger conger. NSE and 5-HT immunoreactivity were found in Merkel cells; these cells were also identified at the electron-microscope level by the presence of characteristic granules and their association with an intraepithelial nerve ending. For the first time, it was demonstrated that Merkel-cell granules of vertebrate skin exhibit an immunoreaction with 5-HT. The production of amines may indicate that the Merkel cells of C. conger have both secretory capabilities and transduction functions. However, immunocytochemical investigation of the synaptic zones at the electron microscope level will be necessary to confirm this hypothesis. The present histochemical results suggest that NSE and 5-HT may be marker substances for Merkel cells, and that immunocytochemistry is a useful tool for the light-microscopic localization of these cells.     

Factors influencing otolith strontium/calcium ratios in Anguilla japonica elvers

The effects of temperature and salinity on the concentration ratios of strontium (Sr) to calcium (Ca) within the sagittal otoliths of elvers of the Japanese eel, Anguilla japonica, were studied by spot analysis using a wavelength dispersive X-ray electron microprobe. A total of 340 elvers were used: 100 elvers were reared for 15 days under various salinity conditions (freshwater, one-third seawater, two-thirds seawater and pure seawater at 22 °C; 240 elvers were reared for 58 days under various water temperature conditions (12, 17, 22, 27 °C) in either freshwater or pure seawater. Otolith Sr/Ca ratios were found to be positively correlated with water salinity. On the other hand, the Sr/Ca ratios were not found to be significantly different among the various temperature groups. The above results strongly suggest that the physiological mechanism of incorporation of Sr and Ca within the otolith of an eurythermal fish, Japanese eel, does not change within this range of temperatures (12–27 °C).     

用荧光物质浸泡标记胭脂鱼仔、稚鱼耳石

用茜素络合物和盐酸四环素溶液分别对胭脂鱼（Myxocyprinus asiaticus）仔、稚鱼浸泡标记,结果表明,100～200mg／L的茜素络合物溶液浸泡24h对胭脂鱼仔、稚鱼耳石有很好的标记效果。相同浸泡浓度下,随着日龄的增长,耳石上的荧光反应强度降低。三对耳石中,微耳石和矢耳石对茜素络合物较敏感,星耳石敏感性则较低。盐酸四环素溶液对仔、稚鱼耳石的标记效果很差,浸泡液浓度为100mg／L和120mg/L时,仅能在微耳石上检测到较弱的荧光标记,而150mg／L及以上浓度的浸泡液对稚鱼有较高的致死作用。因此,茜素络合物是对胭脂鱼早期鱼苗进行化学标记比较合适的荧光物质,而盐酸四环素不适于标记该鱼的耳石。在对标记鱼进行荧光检测时,矢耳石和微耳石是适合的材料。     

Three-dimensional imaging of walleye pollock otoliths: reconstruction from serial sections and fluorescent laser cytometry

Two techniques have been developed to examine the three-dimensional internal structure of otoliths. In the first, otoliths were sectioned serially, images were digitized, and the otolith was reconstructed as a computer model. In the second method growth increments were marked in vivo during their formation by immersing the fish in a fluorescent dye, and then the internal structure of the otolith visualized using laser cytometry. The results are useful for evaluating the potential for bias in otolith measurements and for determining the sectional plane with the least bias.     

Age determination and growth estimates of the white‐spotted conger eel,Conger myriaster (Brevoort, 1856) in marine waters of South Korea

The age and growth of conger eel, Conger myriaster, were investigated by measuring transversely sectioned sagittal otoliths samples from 635 individuals. Sample ages ranged from 1 to 13 years in the female data. Parameters of the von Bertalanffy growth function were estimated using nonlinear regression from back‐calculation, mean length of samples at age relationships, and otolith weight‐at‐age relationships. Best‐fitting value of the three methods was the otolith weight‐at‐age relationship (r² = .87). Parameters of otolith weight‐at‐age were estimated as L_∞ = 143.76 cm, K = 0.081, and t₀ = ?1.285. Maximum oocyte diameter (MOD) ranged from 50 to 430 μm. Reproductive traits of ovaries showed a positive relationship between GSI and MOD (r² = .8515). It is suggested that oogenesis begins to develop from 4 years of age and at lengths of about 45 cm TL. In conclusion, these data provide reliable fundamental data for the fish stock management of Conger myriaster in South Korea.     

Age and early life history of juvenile scotia sea icefish, <Emphasis Type="Italic">Chaenocephalus aceratus</Emphasis>, from Elephant and the South Shetland Islands

The otolith microstructure of juvenile Scotia Sea icefish (Chaenocephalus aceratus) was analyzed from samples collected around Elephant and South Shetland Islands, with the aim to validate previous annual ageing and to give new insight into its early life history timings. Fish were caught by bottom trawl fishing conducted on the continental shelf between 100 and 500 m depth. To determine the timing and position of the first annulus on sagittal otoliths, microincrements were counted on juvenile otoliths previously aged 1+ year old by counting annuli in sectioned otolith. Assuming that microincrements were laid down daily, age ranged from 406 to 578 days in fish measuring 13–19 cm TL, thus corroborating previous results. The relationship between fish size and otolith size/weight was estimated using the least square linear regression method. The relationship between age and otolith size was also estimated to determine the otolith length in 1-year old fish, which was approximately 1.58 mm. In all samples the otolith core was characterized by an evident strong check, assumed to be laid down at the beginning of exogenous feeding of yolk sac larvae. The yolk sac duration estimated from hatch to the first feeding check was longer than other channichthyids, lasting 29–45 days. Hatching dates were backcalculated from the date of capture using the age estimates, indicating C. aceratus sampled off Elephant and South Shetland Islands hatched over a long period lasting from July to December, with a peak in November. As a result, the potential larval dispersion driven by local oceanographic features is discussed.     

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.     

Is otolith science transformative? New views on fish migration

Publications focused on fish otolith applications grew exponentially from 1981–2000 but have subsequently stabilized, suggesting maturation of otolith applications. Over the past 30 years >3,500 primary journal publications were identified prompting the question, how have otoliths fundamentally changed our understanding of fishes and their environment? Has otolith science in this way been transformative? I use Harden Jones’ 1968 Fish Migration as a benchmark of fish migration concepts prior to Pannella’s 1971 breakthrough paper on otolith microstructure. For case study species I highlight how otolith science has informed migration concepts including, (1) parent stream theory (Atlantic bluefin tuna), (2) adoptive homing (Atlantic herring), and (3) partial migration (European eel). Harden Jones’ overall conclusion that life cycle closure leads to population structure (also known as the migration triangle) is a first principle in fisheries science, but in recent years has been challenged by otolith science. In particular, a transformative discovery attributable to otoliths is that life cycles vary substantially within populations. New avenues of otolith science are now exploring the causes and consequences of this life cycle diversity, and large advances are expected through integration of otolith approaches with electronic tagging, genetics, field manipulations, and modeling that will permit migration concepts to be tested at multiple ecological scales.