Validation of daily otolith increments in larval and juvenile Chinese sucker, <Emphasis Type="Italic">Myxocyprinus asiaticus</Emphasis>

Otolith development was observed and the formation of daily growth increments in otoliths of Chinese sucker, Myxocyprinus asiaticus, was validated by monitoring known-age larvae and juveniles in the laboratory from 2003 to 2005. Otolith shape changed with larval and juvenile development, and there was an exponential relationship until a body length of 16 mm or so, and a linear relationship after a body length of 16 mm between otolith size and fish size. The first increment was identified in larvae 1 day after hatching. The regressed equations between daily age (D) and increment number in otoliths (N) were N = −0.64 + 0.96D in lapillus, and N = −0.31 + 0.98D in sagitta. The slopes were not significantly different than 1.0. This demonstrated that otolith increments in this species were formed daily and can be used for daily age determination.     

Growth of larval and juvenile Diaphus theta (Pisces: Myctophidae) in the transitional waters of the western North Pacific

Diaphus theta is one of the most common myctophid fish species in the subarctic and transitional waters of the North Pacific. The growth of larval and juvenile D. theta was investigated using sagittal otolith increment analysis of specimens caught in transitional waters of the western North Pacific. Samples taken over a 24-h period demonstrated that otoliths exhibited daily growth cycles, allowing accurate determination of age. Calcification of the incremental zone of otoliths took place only at night, suggesting that the formation cycle of the increment of juvenile D. theta was different from that of shallow-water fishes and would be related to their diel vertical migration. The relationships between standard length (SL) and daily growth increment (D) were expressed as linear equations: SL = 2.65 + 0.141D (r ² = 0.942) for larvae of 5.1–9.6 mm SL and SL = 3.54 + 0.129D (r ² = 0.933) for juveniles of 13.7–27.6 mm SL. The growth rates were 0.14 mm d⁻¹ in larvae and 0.13 mm d⁻¹ in juveniles; this is slow compared with tropical or subtropical mycto-phid species, in which growth occurs at about twice these rates. The larval period, including the metamorphic stage, was long compared with species at lower latitudes and was estimated to be 71 days. The slow growth rate and long period of larval stage of D. theta would be the life history pattern of high-latitudinal species adapted to a low-temperature habitat. Received: March 23, 2001 / Revised: July 5, 2001 / Accepted: July 19, 2001     

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.     

Fast versus slow growing tuna species: age,growth, and implications for population dynamics and fisheries management

Growth models describe the change in length or weight as a function of age. Growth curves in tunas can take different forms from relatively simple von Bertalanffy growth curves (Atlantic bluefin, albacore tunas) to more complex two- or three-stanza growth curves (yellowfin, bigeye, skipjack, southern bluefin tunas). We reviewed the growth of the principal market tunas (albacore, bigeye, skipjack, yellowfin and the three bluefin tuna species) in all oceans to ascertain the different growth rates among tuna species and their implications for population productivity and resilience. Tunas are among the fastest-growing of all fishes. Compared to other species, tunas exhibit rapid growth (i.e., relatively high K) and achieve large body sizes (i.e., high L _∞ ). A comparison of their growth functions reveals that tunas have evolved different growth strategies. Tunas attain asymptotic sizes (L _∞ ), ranging from 75 cm FL (skipjack tuna) to 400 cm FL (Atlantic bluefin tuna), and reach L _∞ at different rates (K), varying from 0.95 year^?1 (skipjack tuna) to 0.05 year^?1 (Atlantic bluefin tuna). Skipjack tuna (followed by yellowfin tuna) is considered the “fastest growing” species of all tunas. Growth characteristics have important implications for population dynamics and fisheries management outcomes since tunas, and other fish species, with faster growth rates generally support higher estimates of Maximum Sustainable Yield (MSY) than species with slower growth rates.     

Early otolith development in the critically endangered tooth-carp, <Emphasis Type="Italic">Aphanius farsicus</Emphasis> (Teleostei: Cyprinodontidae)

Otolith morphology in the tooth-carp/killifish genus Aphanius is a source of informative taxonomic characters at both the species and population level. Most work on otoliths has focused on adult specimens, while evidence of ontogenetic variation is rarely provided. In this study we describe the development of otolith morphology during the early life stages of an endangered and endemic species, the Fars tooth-carp Aphanius farsicus from southern Iran. The study material comprises 34 larvae and early juveniles representing nine different developmental stages (0–120 days post hatching), all reared under the same laboratory conditions. The results reveal (i) a significant correlation between standard length and otolith size (length) in larval and early juvenile stages, (ii) clear differences in otolith morphology between larvae/early juveniles and adults, and (iii) a temporal link between the appearance of the sulcus on the otolith’s inner face and the emergence of the dorsal and anal fins. Our results indicate that otoliths of Aphanius can be recognized as originating from larval or early juvenile fish based on their short rostrum and antirostrum lengths and wide excisura, in addition to their small size. These immature otoliths are, however, not diagnostic at the species level in A. farsicus, nor most probably in other species of tooth-carp. The outcome of our study is also of interest to palaeontologists working with fossil killifish otoliths, as it can help avoid misinterpretation of ancient species diversity.     

Effects of starvation on the formation of daily growth increments in the otoliths of milkfish, Chanos chanos (Forsskål), larvae

The effects of starvation on daily growth and increment formation in the otolith were examined using a double oxytetracycline-labelling method on larval milkfish, Chanos chanos (Forsskål), reared under different feeding regimes. The results indicated that the differences in body and otolith growth between the larvae fed once and three times a day were not significant, and that the otolith growth increment was deposited daily in both groups of fed larvae. In contrast, the starved larvae grew at a slower rate than fed larvae in body length and otolith dimensions, and the otolith growth increment in the starved larvae was not deposited on a daily basis. After undergoing starvation, the larvae were unable to recover their normal growth either in otolith increment deposition or in body and otolith growth even though they were fed. Therefore, the application of ageing techniques based on counting otolith growth increments seems to be inaccurate for starved larvae.     

Early life‐history of the spiny siganid Siganus spinus (Linnaeus 1758) inferred from otolith microstructure

Juveniles of the spiny siganid Siganus spinus were sampled from three sources in April, May and June 2008 for a study of its early life‐history through otolith microstructure analysis. Specimens were obtained from bagnet catches in off‐reef sites and seine nets in seagrass beds operating in Lagonoy Gulf, Philippines, and from the guts of skipjack tuna Katsuwonus pelamis caught by hand‐line in an offshore area about 72 km east of the mouth of the gulf. The core, hatch ring, first feeding rings, and settlement increment of spiny siganid were identified and their widths measured. Mean daily otolith ages were 20.6, 22.1 and 21.7 of specimens from the gut, off‐reef site and seagrass bed, respectively. Sagittae of the youngest (17‐, 18‐ and 19‐day‐old) specimens from the tuna gut do not have settlement marks. Planktonic larval duration is 17 days. Most settlement (59%) occurred at the 20th increment on the evidence of its highest reduction in width and lessening of opacity. During the settlement process the juveniles swim from the fringing coral reefs to the seaweed beds then finally to the seagrass beds, wherein settlement volume is highest on or about the new moon date. The short, pelagic larval duration and restricted settlement timed on or 1–2 days near the new moon are integral elements in the settlement strategy of the fish.     

Otolith microstructure of Japanese sea bass larvae and juveniles: interpretation and utility for ageing

This paper interprets and discusses the usefulness of otolith microstructure for ageing Japanese sea bass ( Lateolabrax japonicus ) larvae and juveniles. Samples were collected from the Tango Sea along the Japan Sea coast, January–March 2007. Known-age (0-day and 10-day-old) larvae were obtained from the Ibaragi Prefectural Hatchery, Japan. Sagittal and lapillar otolith were processed and read using an otolith reading system. Clearly discernible hatch- and first-feeding marks were evident on sagitta, and development of accessory premordia (AP) appeared to be associated with larva-juvenile transition; however, no other marks indicating metamorphosis or settlement were evident. In lapillus, no discernible check mark was found. Known-age larvae showed that deposition of the first daily increment (DI) corresponded to first-feeding, which occurred at day-4 post-hatch. However, mean increment counts were significantly lower in lapillus than in sagitta, caused by poorly expressed increments around the centrum as well as relatively unclear centrum of the lapillus. The authors suggest that the use of lapillus can cause significant underestimation of age. Therefore, the sagitta is recommended for age and growth estimations of larvae and juveniles, although the presence of numerous subdaily increments warrants careful preparation and interpretation of the microstructure. A test for asymmetry showed the right and left otoliths to be quite symmetrical and their DI counts not significantly different, suggesting that either otolith can be used for studying age and growth of Japanese sea bass larvae and juveniles.     

Growth during the early life history of the Pacific tarpon,Megalops cyprinoides

The early growth of the Pacific tarpon,Megalops cyprinoides, was studied by larval otolith analysis and rearing of larvae and juveniles in the laboratory. Morphology of the sagitta, validation of sagittal daily increments, age at the start of metamorphosis, decrement of standard length in early metamorphosis, and growth under rearing conditions are described. The sagitta of fully-grown Pacific tarpon leptocephali were transparent and circular, with regular intervals between the neighboring rings becoming wider at the onset of metamorphosis. Alizarin complexone treatment of larvae confirmed the daily formation of the sagittal rings. Metamorphosis was estimated to start about one month after hatching. After drastic shrinkage during the first several days of metamorphosis, the body length more or less stabilized for one month and then resumed rapid growth. The early growth of Pacific tarpon was divided into four phases as follows: A) leptocephalus positive growth phase; B) leptocephalus negative growth phase; C) sluggish growth phase; and D) juvenile growth phase.     

Otolith variation in Pacific herring (<Emphasis Type="Italic">Clupea pallasii</Emphasis>) reflects mitogenomic variation rather than the subspecies classification

Pacific herring (Clupea pallasii) is divided into three subspecies: two in northeast Europe and one in the north Pacific Ocean. Genetic studies have indicated that the populations in northeast Europe have derived from the northwest Pacific herring recently, or during the last 10–15 kyr, and that they are distinct from the population in the northeast Pacific. In addition, hybridization between the Pacific herring and the Atlantic herring has been documented. Otolith variation has been considered to be largely affected by environmental variation, but here we evaluate whether the genetic differentiation is reflected in otolith shape differences. A clear difference in otolith shape was observed between the genetically differentiated herring species Clupea harengus from the Atlantic and C. pallasii. The otolith shape of C. p. suworowi in the Barents Sea was different from the shape of C. pallasii in northern Norway and C. p. pallasii from the Pacific. Populations of C. p. pallasii, sampled east and west of the Alaska Peninsula, which belong to two genetically different clades of the C. p. pallasii in the Pacific Ocean, show a clear difference in otolith shape. C. p. suworowi and the local C. pallasii peripheral population in Balsfjord in northern Norway are more similar to the northwest Pacific herring (C. p. pallasii) than to the northeast Pacific herring (C. p. pallasii), both genetically and in otolith shape. The Balsfjord population, known to be influenced by introgression of mtDNA from the Atlantic herring, does not show any sign of admixture in otolith shape between the two species. A revised classification, considering the observed genetic and morphological evidence, should rather group the northwest Pacific herring in the Bering Sea together with the European populations of C. pallasii than with the northeast Pacific herring in the Gulf of Alaska.     

Otolith shape analysis and daily increment validation during ontogeny of larval and juvenile European chub Squalius cephalus

This assesses features of otoliths from laboratory-reared embryos, larvae and juvenile European chub Squalius cephalus from hatching to 180 days post-hatching (dph). We observed the development of the three pairs of otoliths (lapilli, sagittae and asterisci) and more precisely shape changes, as well as timing and deposition rate of increments of the lapilli. The lapilli and the sagittae were present at hatching, whereas the asterisci formed between 20 and 30 dph. The lapillus and sagitta shapes were round until 20 dph. From 60 dph the anterior and the posterior rostra of the sagittae were well developed, but very thin, making this otolith too fragile to manipulate for further studies of shape and validation of otolith increment deposition rate. The lapilli provided reliable age estimates for free embryos, larvae and juveniles up to 120 dph. However, caution should be taken when ageing fish older than 150 dph as an underestimation was noticeable. The regression of the number of otolith increments on age showed a slope and an intercept not significantly different from 1 and 0, respectively, which indicated that otolith growth increments were deposited on a daily basis, with the first microincrement occurring at hatching. Increment counts were consistent between three interpreters, indicating a consistent and reliable age estimate. This study validates that the otolith increment deposition rate can be used to assess hatching dates and daily growth of wild S. cephalus under 150 dph and in environments similar to the conditions used in this study.     

Occurrence of Larval and Juvenile Japanese Snook, <Emphasis Type="Italic">Lates japonicus</Emphasis>, in the Shimanto Estuary,Japan

A total of 54 postlarval, 12 juvenile and six young Lates japonicus were collected in the Shimanto estuary from August 1985 to January 1987. The larvae (4.3–7.6 mm SL) and juveniles (8.1–28.0 mm SL) occurred only in areas with eelgrass beds from late July to middle August. Temperatures and salinities at waters where any number of them were collected ranged from 27.8 to 31.9°C and from 2.8 to 18.2%, respectively. The larvae are very similar in general morphology to those of Mugilidae and some of Gobiidae, but are distinguished from others by the spines of preopercle, position of the anus and pigmentation patterns in the posterior part of body.     

Factors affecting morphological development of the sagittal otolith in juvenile and adult small yellow croaker (Larimichthys polyactis Bleeker, 1877)

The morphology and morphometrics of the sagittal otoliths of small yellow croaker (Larimichthys polyactis) from the southern Yellow Sea were investigated. Study objectives were to evaluate the shape variability and morphometric variables of sagittae of juveniles and adults as related to developmental changes and habit shift. A total of 152 fish were sampled from April to June of 2012 and 2013, along the coastal waters of the Lüsi spawning ground in the southern Yellow Sea. Changes in otolith shapes from the juvenile to the adult were presented with the rim development through the entire‐lobed‐entire transition and with the curvature of the cauda toward the ventral margin. The otolith elongation in the juvenile stage occurred at 10–20 mm standard length (SL) and was likely associated with the formation of otolith accessory growth centers from larvae to juvenile. The L. polyactis sagittal otoliths acquired their definitive shape at 130 mm SL maturity. Ontogeny on otolith shape might be related, for example, to the factors of metamorphic development, feeding habitat, and ambient water salinity, which varied throughout the growth of L. polyactis.     

Is the marginal otolith increment width a reliable recent growth index for larval and juvenile herring?

Marginal otolith increment width analysis was performed on field‐collected larval and juvenile spring‐spawned herring Clupea harengus that experienced variable feeding conditions and high temperatures that were above the optimum for growth. Although drastic zooplankton biomass reduction had a significant effect on increment width, a delay of a few days in the otolith response was observed. More importantly, a very clear, positive temperature effect on marginal increment width was demonstrated in fish characterized by temperature independent somatic growth. These results indicate that under natural conditions it may be impossible to distinguish increment width changes related to variation in feeding conditions from changes caused by temperature fluctuations. Therefore, it was concluded that marginal otolith increment width analysis could not be used as a recent growth index ( I _G) for herring larvae and juveniles exposed to drastic temperature fluctuations. The implication of these results is significant not only for the use of marginal increments as a recent growth index, but also if growth rate backcalculation is to be used as a research method.     

Verification of growth dependent survival in early life history of Pacific saury <Emphasis Type="Italic">Cololabis saira</Emphasis> using laboratory experiment

To understand the survival processes in Pacific saury during the early life stages, growth histories were compared between individuals that died and those that survived under laboratory conditions. The morphology of Pacific saury drastically changed by 40 day after hatching (DAH) under 20°C, and during this period most individuals reached the juvenile stage (40 mm knob length (KnL)). From hatch to this period, high levels of mortality were observed. The back-calculated growth rates analyzed from otolith microstructure were compared among individuals that died and those that survived this period of metamorphosis. Growth rates of individuals that died were significantly lower since 1 DAH than surviving individuals. Factors contributing to mortality are considered to be the cumulative effects of their delayed growth and their less favorable body conditions (growth dependent survival). The body size (40 mm KnL) that is currently used to estimate the recruitment is concluded to be valid for evaluating the recruitment in the field.     

Variation in growth performance of Ryukyu-ayu, <Emphasis Type="Italic">Plecoglossus altivelis ryukyuensis</Emphasis>, inferred from otolith analysis

Ryukyu-ayu (Plecoglossus altivelis ryukyuensis) is an amphidromous fish species that migrates between the sea and rivers over its one-year life span. Although growth performance during the early marine stage may affect growth in the later riverine stage of this species’ life cycle, no studies have specifically examined this relationship in P. a. ryukyuensis. In the present study, we reconstructed the growth trajectories of P. a. ryukyuensis individuals collected from the Yakugachi River, Amami-Oshima Island, Japan in 2016 (n?=?47) throughout their growth period in both the sea and river by using otolith analysis. Using this, we determined the age and body size of individuals at the time of their upstream migration, as well as their growth rates during the marine and riverine stages. Results showed that body size at upstream migration significantly affected body size at the riverine stage, indicating that juveniles with larger body size in the sea had better growth performance in the river. Individuals with higher growth rates during the marine stage tended to enter the river younger and at larger body sizes than those with lower marine growth rates. Our results demonstrated the close linkage between the growth performance in the sea and in rivers of P. a. ryukyuensis. This information will contribute to better understanding variations in growth patterns of this endangered species and potentially aid in its conservation.     

Peculiarities of early ontogenesis of the tubenose poacher, <Emphasis Type="Italic">Pallasina barbata</Emphasis> steindachner, 1876 (Pisces,Agonidae) from Peter the Great Bay (Sea of Japan)

Based on the analysis of original material (52 specimens of Pallasina barbata larvae and juveniles), sampled in the Peter the Great Bay (Sea of Japan) from 1992 to 2006, the ontogenetic stages of this species were described for the first time. It is shown that P. barbata has a planktonic larval stage in its development. The major morphologic features that are typical for larvae and juveniles during their development were revealed. It was shown that snout length, head length and pectoral fin size are increased with growth; at the same time body height and eye diameter are decreased, and the nature of larval pigmentation is changed. The main differences between P. barbata and close species are shown. Original illustrations of larvae and juvenile are provided.     

Review of the <Emphasis Type="Italic">Chromis xanthura</Emphasis> species group (Perciformes: Pomacentridae), with description of a new species

A taxonomic review of the Chromis xanthura species group, defined here as having 13 dorsal-fin spines, three upper and three lower procurrent caudal-fin rays, two black bands at the preopercular and opercular margins, and a yellow caudal fin when juvenile, resulted in the recognition of three species, Chromis xanthura (Bleeker 1854), Chromis opercularis (Günther 1867), and Chromis anadema sp. nov. Chromis xanthura and C. opercularis, the Pacific and Indian Ocean paired sister species, respectively, are redescribed, with confirmation of two color types of C. xanthura (having a white or black caudal peduncle and fin) as a single species on the basis of morphological and molecular analyses. Chromis anadema sp. nov., described from the oceanic islands of the Pacific Ocean on the basis of 21 specimens, is characterized by having 28–33 gill rakers; longest dorsal-fin soft ray length 20.0–24.7% of standard length (SL); first anal-fin spine length 5.0–6.1% of SL; caudal-fin length 33.4–43.8% of SL; posterior tips of caudal-fin lobes not filamentous in adults; broad black bands along preopercular and opercular margins, sum width of two bands 28.9–38.7% of head length; distal half of soft-rayed portion of dorsal fin transparent in adults; triangular black blotches at upper and lower caudal-fin base in adults; caudal peduncle and fin bluish black in adults; and body grayish, and all fins (except for pectoral fin) bright yellow in juveniles.     

Is skipjack tuna the fastest-growing teleost fish on earth?

Using a genetic marker mitochondrial DNA control region, Nikolic et al. (Environ Biol Fish 99:171-178, 2016) recently reported the identification of two juveniles of tuna as skipjack (Katsuwonus pelamis) recovered from the mouth of dolphinfish in the vicinity of Reunion Island, western Indian Ocean. Based on the age estimates of the two specimens from opercular bones at about 16–20 days and the increased occurrence of skipjack in the catch of Japanese longliners during October–January, the authors indicate that their results suggest a specific seasonal spawning area of skipjack around Reunion Island. We challenge the validity of age estimates and the interpretation of the results published by Nikolic et al. (Environ Biol Fish 99:171-178, 2016). Current knowledge of skipjack tuna biology indicates that the paper of Nikolic et al. (Environ Biol Fish 99:171-178, 2016) contains misinterpretation of field observations that led the authors to misunderstandings on skipjack tuna ecology.     

Distribution and microhabitat associations of the juveniles of a high-value sea cucumber, <Emphasis Type="Italic">Stichopus</Emphasis> cf. <Emphasis Type="Italic">horrens,</Emphasis> in northern Philippines

There is considerable global interest in rebuilding depleted populations of sea cucumbers (Echinodermata, Holothuroidea) to address conservation and economic goals. For the vast majority of holothurian species, the habitat and food requirements of the juvenile stage are poorly understood. We investigated the distribution and microhabitat associations of juveniles of a commercially important sea cucumber, Stichopus cf. horrens, in the shallow, shoreward side of a coral reef (or backreef) in northern Philippines (16°21′38.7″N, 119°59′47.9″E). Relationships between juvenile density and the physical, chemical and biological characteristics of their habitat were examined. Potential food sources of the juveniles were also investigated using elemental and stable isotope analysis. Results showed that juveniles are more abundant in seagrass areas and the transition zone between seagrass and the rubble-dominated reef flat. A non-metric multidimensional scaling (MDS) plot indicated that juvenile density was most positively associated with coarser sand and rubble (>0.5 mm) and seagrass (Thalassia hemprichii) abundance (2D stress = 0.11). Juvenile density was also positively associated with sediment organic matter from plant detritus to a lesser extent. Elemental and isotope analysis of one site indicated that epiphytes were the primary food source of juveniles, while sediment detritus from microalgae and seagrass was a secondary food source. This study corroborates anecdotal evidence regarding the importance of seagrass to S. cf. horrens as potential refugia and source of high-quality food for its juveniles. These findings underscore the need to protect the nursery habitats of wild juveniles and provide critical information for the selection of suitable natural habitats for releasing cultured juveniles of this important species.