Relationships between fish size and otolith size of four bathydemersal fish species from the south eastern Arabian Sea,India

The objective of this study was to estimate a prey body size from the hard parts (e.g. otoliths) of a fish species frequently found in the guts of predators. Length–weight relationships between otolith size (length, height, weight and aspect ratio) and fish size (total length and weight) were determined for four fish species captured in the Arabian Sea by bottom trawl (2015 survey on‐board FORV Sagar Sampada, 200–300 m depth), off the west coast of India: Psenopsis cyanea, Pterygotrigla hemisticta, Bembrops caudimacula and Hoplostethus rubellopterus. No significant differences were noted between the size of the left and right otoliths (t test) in any of the four species. The length–weight relationship of the otolith in all four species showed a negative allometric growth pattern (t test, p < .05). The data fitted well to the regression model for otolith length (OL), otolith height (OH) and otolith weight (OW) to total length (TL) and total weight (TW). Results showed that these relationships are a helpful tool in predicting fish size from the otoliths and in calculating the biomass of these less‐studied fish species during feeding studies and palaentology.     

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 growth of the Giant Kelpfish,Heterostichus rostratus Girard 1854, in Southern California,USA

In order to update existing life history parameters, age and growth patterns were determined for Giant Kelpfish, Heterostichus rostratus sampled from nearshore kelp forest and estuary habitats in southern California (USA) from April 2012 through June 2015. Fish were collected by pole spear, beach seine, beam trawl, purse seine, and square enclosure. Using age‐at‐length data derived from otolith readings, Giant Kelpfish were found to have a relatively short life span with the largest examined fish reaching a maximum total length of 413 mm at an age of 5 years. Von Bertalanffy growth parameters estimated for this species were: L_∞ = 45.1 cm, k = 0.25, t₀ = ?0.66. Standard length (SL, cm)‐total length (TL, cm) and total length (TL, cm)‐weight (W, g) relationships were described by the equations: SL = 0.90 TL – 1 and W = 2.21 × 10^?3 TL^3.39, respectively. Wild juvenile Giant Kelpfish collected for this study had a higher growth rate than laboratory‐reared fish from a previous study.     

Using otolith shape and morphometry to identify four Alburnus species (A. chalcoides,A. escherichii,A. mossulensis and A. tarichi) in Turkish inland waters

Asteriscus otolith shapes as well as their morphometry and shape contours were investigated in order to identify four allopatric Alburnus species: A. chalcoides (Güldenstädt, 1772) (Ordu), A. escherichii Steindachner, 1897 (Eski?ehir), A. mossulensis Heckel, 1843 (Tunceli), and A. tarichi (Güldenstädt, 1814) (Van) in Turkish inland waters. These were compared using the shape indices (form factor, roundness, circularity, ellipticity, rectangularity and aspect ratio), and the morphological characters [otolith weight (OWE), otolith length (OL), otolith width (OW), otolith perimeter (OP), and otolith area (OA)]. The overall canonical discriminant analysis (CDA) classification score was 93.8%, with the lowest score for A. escherichii (82.5%) and the highest for A. chalcoides (100%). The otolith shapes, morphology and shape contours of all sampled fish were a clear species differentiator, thereby demonstrating that the otolith shape is species‐specific. The current study presents for the first time comprehensive variation information on interspecific left‐right asteriscus otoliths in males and females of each Alburnus species: A. chalcoides from Ordu, A. escherichii from Eski?ehir, A. mossulensis from Tunceli and A. tarichi from Van, based on a total of 307 individuals. Scanning electron microscopy (SEM) images, shape contours and other otolith characters vary within the same genus; these differences should be investigated not only in other freshwater fish species or genera but also in the same species living in different habitats. In addition, further investigation is required not only with respect to the morphometry, biometry, shape, geometry, and shape contours of the otoliths, but also regarding the genetic methods for robust identification of various sympatric and allopatric fish populations.     

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.     

The relationships between fish size and otolith dimensions in the common sole (Solea solea (Linnaeus, 1758)) captured in the Northeastern Mediterranean

Fish specimens were captured by a commercial bottom trawler at a depth of 50–80 m from Iskenderun Bay (Hatay, Turkey) between December 2017 and May 2018. The bottom trawl gear used was equipped with a 44 mm stretched mesh size net at the cod-end. Blind side and eyed side otolith lengths (OL), otolith breadths (OB) and otolith weights (OW) were measured from each specimen to the nearest 0.001 mm and 0.0001g respectively. A total of 110 fish (43 females and 67 males) were collected. Total length ranged from 20.8 to 28.2 cm and 68.0 to 166.1 g (males) and 21.1 to −28.5 cm and 74.5 to 201.4 g (females). The coefficients of determination between fish weight and otolith weight, and total length and otolith weight (sexes combined) were found as R² = .7694 (0.77) and R² = .6274 (0.63), respectively. A moderate positive relationship between the total length-otolith dimensions, and fish weight-otolith dimensions, was also demonstrated.     

Relationships between fish and otolith size of nine deep‐sea fishes from the Andaman and Nicobar waters,North Indian Ocean

The study presents for the first time the otolith morphology of nine species of deep‐sea fishes. This study was based on sampling carried out on‐board FORV Sagar Sampada (Cruise No 349) during March‐April 2016, along the continental margin of the Andaman and Nicobar Islands in the Bay of Bengal using high speed demersal trawl. Unbroken (complete) otoliths from Polymixia fusca Kotthaus, 1970, Neoepinnula orientalis (Gilchrist & von Bonde 1924), Chlorophthalmus nigromarginatus (Kamohara, 1953), Cubiceps baxteri (McCulloch, 1923), Bembrops caudimacula (Steindachner, 1876), Neoscopelus microchir (Matsubara, 1943), Ostracoberyx dorygenis Fowler, 1934, Synagrops japonicus (Döderlein, 1883), and Bathyclupea hoskynii Alcock 1891) were used for this study. Length–weight relationships (LWR) and the regression between otolith size (width, weight, area and perimeter) and fish length (TL) of nine deep‐sea Fishes were considered. Numerical relationships derived from the relationship between otolith size and the fish can be used as predictors to estimate the prey size as well as to understand trophic relations and food web dynamics of these hitherto unexamined deep‐sea ichthyofauna. LWR showed negative allometric otolith growth in five species; four species showed positive allometric growth. Otolith size to fish size (TL) relation is explained by a simple linear regression considering otolith width (OW), otolith weight (OWe), otolith area (OA) and otolith perimeter (OP). Stronger r² values (>.76) indicate robustness, except for Cubiceps baxteri (r² = .65), and give better estimates for the TL of the fish.     

Comparison of scale and otolith age readings for trahira,Hoplias malabaricus (Bloch, 1794), from Paraná River,Argentina

The aim of this work was to compare age determinations and precision using two deposition structures of trahira Hoplias malabaricus (Bloch, 1794): the scales, which are most frequently used, and otoliths (lapilli). The length‐age relationships were obtained with both structures and compared with results from previous studies. The 163 sets of trahira otoliths (lapilli) and scales were 17–46 cm standard length (SL) from Cayastá (Santa Fe) and Islas Lechiguanas (Entre Ríos), Paraná River, Argentina. Three independent readings of each structure were conducted. An age bias plot was performed to compare age estimations from scales and otoliths. To assess the precision of age determinations using both structures, the percent agreement among readers for both structures and the coefficient of variation were calculated (%CV). The age‐length relationships were plotted and fitted with the von Bertalanffy growth function for both structures and compared with previous works. Age readings recorded for scales were lower than those recorded for otoliths for ages above or equal to 3 years. Percent agreement among readers was higher than 80% for otoliths and less than 65% for scales. The%CV obtained for scales was 20% for young fish and 17% for adults. For otoliths the %CV was 7% for young fish and 3% for adults. The %CV obtained for scales was over the recommended limit (>7.6%). The von Bertalanffy parameters for scales were L_inf = 45.80 mm; k = 0.29; t₀ = ?1.34 and for otoliths were L_inf = 40.76 mm; k = 0.39; t₀ = ?1.05. Precision of age estimations assessed from the percent agreement and the coefficient of variation indicates that the scales of the trahira are inappropriate to estimate age in population studies for juvenile and adult specimens.     

Growth and morphological development of sagittal otoliths of larval and early juvenile Trachurus japonicus

The daily periodicity of growth increment formation in sagittal otoliths of jack mackerel Trachurus japonicus was validated by marking otoliths with alizarin complexone (ALC). Analysis of otoliths of known‐age juveniles confirmed that the first increment formed on day 3 after hatching, and was associated with first feeding. A total of 198 specimens, ranging from 2·6 to 49·2 mm in body length (notochord length or standard length) and from 7 to 78 days in age, were collected in the East China Sea and Tosa Bay, and used to examine the association between otolith morphological development and ontogenetic development. The relationship between body length ( L ) and otolith radius ( R ) was significantly described by the linear function L  = 2·65 + 0·0425 R ( n  = 198, r ² = 0·99, P  < 0·001), indicating that somatic growth history can be reconstructed from otolith growth patterns. The otolith was primarily spherical in the preflexion larval stage, and became elongated with notochord flexion. The first secondary primordium formed at c . 25 days, during the middle postflexion stage, and was associated with metamorphosis. By c . 42 days the sagittal otolith was adult‐like in morphology, with the primary growth zone enclosed by the marginal growth zone, except in the anterior rostrum area. Thus age, growth and developmental stages were recorded in sagittal otoliths during the larval and early juvenile stages of jack mackerel.     

The relationship between otolith size and estimated age of tigertooth croaker (Otolithes ruber Bloch and Schneider, 1801) in Oman Sea,Iran

The relationships between somatic growth and otolith dimensions, otolith size to estimated age and growth parameters of the tigertooth croaker (Otolithes ruber) were investigated in 100 specimens (size range: 19.1–52.0 cm, total length) from the Oman Sea area, September 2014. All 100 otoliths were sectioned and determined by age. The oldest specimen was a 4.5‐year‐old female with a total length of 40.6 cm; the youngest specimen was also a female estimated at 1 year of age with a total length of 19.1 cm. The von Bertalanffy growth equation was estimated as L_t = 54.70 (1 ? exp (?0.37 (t + 0.21))). Concluded was that there is a significant relationship between body size, otolith dimensions and estimated age of Otolithes ruber.     

Exposure to thyroid hormone in ovo affects otolith crystallization in rainbow trout Oncorhynchus mykiss

Calcareous otoliths in the inner ears of fishes are necessary for proper hearing and vestibular function. Sagittal otoliths are usually composed of the calcium carbonate polymorph aragonite but may contain the polymorph vaterite, a phenomenon called otolith crystallization. The causes of otolith crystallization are poorly understood. Thyroid hormone (TH) can influence the chemical microenvironment and structure of the inner ear, suggesting that TH may influence otolith crystallization. The present study examined the effect of exogenous TH treatment on sagittal otolith crystallization and growth in larval and juvenile rainbow trout, Oncorhynchus mykiss. In the first experiment, 110?C179?day-old fish raised from TH-treated oocytes had significantly fewer sagittal otoliths containing the crystalline calcium carbonate polymorph vaterite as compared to untreated fish. Vaterite-containing otoliths were significantly longer than those containing the typical polymorph aragonite, although there was no effect of TH treatment on otolith length. In the second experiment, juveniles immersed in an exogenous solution of TH for 6?weeks had slightly longer otoliths (relative to fish length) than age-matched controls, but this effect was not significant. This juvenile population had a very high percentage (88.3?%) of vaterite sagittae overall and this percentage did not change significantly with treatment, suggesting the switch from aragonite to vaterite occurred prior to inclusion of the fish in the study. These results suggest that early manipulation of TH levels may affect calcium carbonate deposition on the otolith but that later TH exposure is unable to restore typical otolith composition.     

Using the otolith sulcus to aid in prey identification and improve estimates of prey size in diet studies of a piscivorous predator

Diet studies are fundamental for understanding trophic connections in marine ecosystems. In the southeastern US, the common bottlenose dolphin Tursiops truncatus is the predominant marine mammal in coastal waters, but its role as a top predator has received little attention. Diet studies of piscivorous predators, like bottlenose dolphins, start with assessing prey otoliths recovered from stomachs or feces, but digestive erosion hampers species identification and underestimates fish weight (FW). To compensate, FW is often estimated from the least affected otoliths and scaled to other otoliths, which also introduces bias. The sulcus, an otolith surface feature, has a species‐specific shape of its ostium and caudal extents, which is within the otolith edge for some species. We explored whether the sulcus could improve species identification and estimation of prey size using a case study of four sciaenid species targeted by fisheries and bottlenose dolphins in North Carolina. Methods were assessed first on otoliths from a reference collection (n = 421) and applied to prey otoliths (n = 5,308) recovered from 120 stomachs of dead stranded dolphins. We demonstrated in reference‐collection otoliths that cauda to sulcus length (CL:SL) could discriminate between spotted seatrout (Cynoscion nebulosus) and weakfish (Cynoscion regalis) (classification accuracy = 0.98). This method confirmed for the first time predation of spotted seatrout by bottlenose dolphins in North Carolina. Using predictive models developed from reference‐collection otoliths, we provided evidence that digestion affects otolith length more than sulcus or cauda length, making the latter better predictors. Lastly, we explored scenarios of calculating total consumed biomass across degrees of digestion. A suggested approach was for the least digested otoliths to be scaled to other otoliths iteratively from within the same stomach, month, or season as samples allow. Using the otolith sulcus helped overcome challenges of species identification and fish size estimation, indicating their potential use in other diet studies.     

Estimates on age,growth and mortality of the French angelfish Pomacanthus paru (Bloch, 1787) (Teleostei: Pomacanthidae) in the southwestern Atlantic

The aim of the present study was to determine age, growth and mortality of the French angelfish Pomacanthus paru. Age was solely determined by sectioned otoliths. All tetracycline‐treated otoliths were 1 year of age and revealed a clear fluorescent mark when observed under UV light. Otolith weight increased exponentially with standard length, and linearly with age, indicating that otolith growth continues with age and is independent of size. Age of fish in the sample ranged from 1 to 27 years. The von Bertalanffy growth equation was TLt = 36.33 (1 ? e^{?0.12 (t + 0)}). Total rate mortality (Z) was estimated to be 0.10. Attaining maximal size slowly, P. paru has a long life expectancy. Most linear growth is achieved within approximately 74% of the lifetime of the fish. Besides being an important ornamental species, P. paru has been commonly captured for decades as bycatch in trap fisheries. These growth parameters should be used with the purpose of managing fisheries targeting this species before more meaningful limits can be imposed. In the aquarium trade management, it is suggested that conservationist issues should be based on capture‐per‐area and the establishment of protected areas.     

Age and growth of damselfish Chromis notata (Temminck & Schlegel, 1843), Jeju Island,Korea

This study investigated the age and growth of damselfish, Chromis notate, from Jeju Island in Korea. Samples were collected monthly by lift net from September 2013 to August 2014. Total lengths of the damselfish ranged from 6.4 to 15.3 cm. The relationship between total length and wet weight was WW = 0.0125TL^3.1631 for females, and WW = 0.0091TL^3.2769 for males. The slopes in the relationship between length and weight were not significantly different between sexes, but were significantly different in the intercepts. There were more female than male specimens (1.3:1). Age determination was conducted using the otoliths. Marginal increment (MI) declined in summer and winter, which suggests that two rings are formed each year. Ages of sampled individuals ranged from 1 to 5 years. Length‐at‐age data were fitted using the von Bertalanffy growth model. The estimated growth functions were L_t = 19.93 [1 ? exp^{?0.21 (t + 0.811)}] total length and wet weight was females, and L_t = 16.47 [1 ? exp^{?0.32 (t + 0.499)}] for males.     

Lesser Sandplover,Charadrius mongolus,in Turkey

Sagittal otoliths are widely used to determine taxon, age and size of the teleost fishes, and are useful tools for studies of prey-predator relationships, population dynamics and ichthyo-archaeology. They can also be used to estimate the size of the prey. We examined the relationships between otolith measurements (length, height and weight) and fish size (total length and weight) for two species of Argentinidae (Argentina sphyraena and Glossanodon leioglossus) from the Southern Aegean Sea, Turkey. Length, height and mass of sagittae were shown to be good indicators for the length and weight of fish in both species. Glossanodon leioglossus has relatively larger sagittae than Argentina sphyraena. Linear and exponential functions provided the best fit for relations between otolith and fish measurements. No significant differences were found between left and right otolith sizes.     

Sexual dimorphism in the otolith shape of shi drum,Umbrina cirrosa (L.), in the eastern Mediterranean Sea: Fish size–otolith size relationships

Little is known about possible differences in sagitta otolith size and shape between sexes of the shi drum, Umbrina cirrosa, and relationships between their body and otolith size. Thus, this study aimed to fill this knowledge gap via examination of 414 sagittal otoliths from 108 male (total length 13.8–26.8 cm) and 99 female (13.5–26.7 cm) U. cirrosa caught between May 2017 and April 2018 in gillnets set at a depth of ~15 m in Mersin Bay, Eastern Mediterranean Sea. No statistical differences were observed between the shape indices of the left-sided and right-sided sagitta. However, there were significant differences in the size and shape of otoliths between males and females. The slopes of allometric power functions from otolith width × fish sizes gave significant differences between males and females (ANCOVA, P < 0.05). The relationship for length × weight of otoliths from both males and females showed isometric growth, whereas the relationship of otolith width × otolith weight showed positive allometry. Negative allometric growth was observed for the relationship otolith length × otolith width. In summary, this study revealed the presence of sexual dimorphism in the otolith shape of U. cirrosa, and the data on regression relationships of fish-otolith sizes can be used to estimate fish size from U. cirrosa otolith sizes.     

Age and growth characteristics of Schizopygopsis younghusbandi Regan, 1905 in the Yarlung Tsangpo River in Tibet,China

To better understand the biology of Schizopygopsis younghusbandi Regan, 1905 and its relationship with management considerations, this study describes the relationships between otolith size and fish length and age, verifies annual periodicity of otolith annulus formation, and estimates the S. younghusbandi growth parameters. These age and growth characteristics were studied using 694 specimens collected from August 2008 to August 2009. Otoliths grew asymmetrically throughout the range of standard length (SL) studied, showing a clear pattern of alternating translucent and opaque bands. Marginal increment ration (MIR) analysis of specimens up to 6 years of age indicated that one opaque band and one translucent band were laid down each year. Maximum observed age was 17 years, corresponding to a female of 35.8 cm SL and 589.1 g body weight (BW). The SL‐BW relationship was described as BW = 1.122 × 10^?5 SL^3.030 for sexes combined. The von Bertalanffy growth function was used to model back‐calculated lengths as L_t = 338.4 (1?e^{?0.233 (t + 0.403)}) for males, and L_t = 433.9 (1?e^{?0.194 (t + 0.397)}) for females. Growth performance of S. younghusbandi was relatively higher than those of other Schizothoracinaes inhabiting the same river.     

Age, growth, mortality and population characteristics of the pearl perch, Glaucosoma buergeri Richardson 1845, from deeper continental shelf waters off the Pilbara coast of north-western Australia

Pearl perch, Glaucosoma buergeri Richardson 1845, from deeper waters (> 100 m depth) on the continental shelf of north-western Australia were aged by examining transverse sections of their sagittal otoliths. Ages were assigned based on counts of alternating opaque and translucent zones (annuli). Otolith length and breadth (width) increased linearly with fish length, whereas otolith weight increased linearly with fish age. The continuous growth of the otoliths provides some evidence that the opaque and translucent zones used to estimate age in this study are formed on a regular basis. Parameters of the length–weight relationship were estimated, along with parameters of the von Bertalanffy growth function. The generalised von Bertalanffy growth function (total length-at-age, both sexes combined) for G. buergeri was L _t=512.7 (1 – e^{–0.139( t  + 0.89)}). There was no significant differential growth between the sexes in observed length-at-age. The oldest individual found was a male G. buergeri estimated to be 26 years of age. The annual instantaneous rate of natural mortality ( M ) was estimated to be 0.14. The slow growth, long life and low natural mortality rate indicate that G. buergeri is vulnerable to overfishing and that harvest strategies for this species should be conservative, given its low production potential.     

长江口鮻矢耳石形态特征及质量与年龄的关系

为研究长江口鮻矢耳石形态特征及其质量与年龄的关系,2017年2—6月从长江口水域采集鮻358尾,解剖并提取耳石324对,并对其形态学参数进行测量分析.结果表明:鮻矢耳石具有基叶和翼叶,中央听沟明显,矢耳石的大小和形状随个体生长变化明显,矢耳石由边缘规则的圆润瓜子状渐变为褊窄的叶片状,边缘波浪状突起逐渐变多.矢耳石平均密度为1.52 mg·mm^-2,平均矩形趋近率为0.68,耳石长占其体长的0.021%~0.047%,耳石宽占其体长的0.009%~0.021%,耳石质量占其体质量的0.045‰~0.731‰.鮻矢耳石长(OL)、宽(OW)、质量(OM)均与体长呈显著相关,耳石宽与耳石质量函数关系式的决定系数(R^2)最高(0.928).耳石质量与体长(BL)最佳拟合方程为幂函数:OM=0.0009BL1.8737(R2=0.967);耳石质量与年龄(A)以及体长与年龄的最佳拟合方程为多项式:OM=2.9262A^2+4.8437A+2.1894(R^2=0.847);BL=-3.2248A^2+102.54A+38.373(R^2=0.858),矢耳石质量与年龄呈显著线性相关,用耳石质量与年龄关系估算的年龄与从耳石上直接读取的年龄无显著差异,矢耳石质量可以作为鉴定鮻年龄的有效辅助手段.     

Age,growth and reproduction of the black sea bream Spondyliosoma cantharus (Linnaeus, ) (Sparidae) in the Gulf of Annaba (Algeria)

The objective of this study was to determine the basic population‐specific parameters necessary for fish stock assessment in the Gulf of Annaba and to compare these with data from other Mediterranean regions. Black sea bream Spondyliosoma cantharus (Linnaeus, 1758) (N = 501) were collected monthly from January to December 2008 along the Algerian eastern coasts. More than 22 fish were collected each month and ranged in size from 13.4 to 40 cm total length, weighing from 36 to 1080 g eviscerated weight. Biological sampling included weighing and measuring the fish, gonad weighing, sex and maturity stage determination, and age estimation through otolith readings. Validity of the otolith readings for estimating age and growth was supported using the back‐calculation method. Estimated parameters of the von Bertalanffy model are: L_∞ = 33.54 cm, W_∞ = 633.46 g, k = 0.52 year^?1 and t_o = ?0.04 year. The growth performance index (φ) is: 2.76. The length‐weight relationship is: EW = 4.4.10^?6 TL^3.23. The spawning period occurred from February to May, while the gamete emission peaked in April. Females reached sexual maturity at 19.3 cm (2 years) and males at 21.3 cm (3 years). Sexual inversion occurs at approximately 24.3 cm. Spondyliosoma cantharus was characterized as being a protogynic hermaphrodite.