鳡鱼仔稚鱼耳石的标记和其日轮的确证

用茜素络合物对鳡鱼仔鱼进行了浸泡标记,耳石上能检测到橘红色荧光标记环。100mg/L茜素络合物溶液的标记效果较差;120mg/L和150mg/L溶液浸泡后微耳石的标记率很高,矢耳石和星耳石的标记率低。标记后耳石上的生长轮数与饲养天数间呈一一对应关系,相关方程为:N=0.2663 0.9276D(n=68,r~2=0.9664)。方程的斜率0.9276与1无显著差异,证明生长轮确系日轮。鱼体长与微耳石、矢耳石及星耳石的直径间呈显著的线性关系,相关方程为:BL=66.8723LD 2.7064(n=73,r~2=0.8867),BL=22.7839SD 6.6066(n=49,r~2=0.8525),BL=47.6079AD 3.5660(n=71,r~2=0.9012)。     

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。     

Daily increments on the otoliths of larval and juvenile Coregonus spp., and their modification by environmental factors

The sagittal otoliths of pre- and posthatch embryos, larval, and juvenile coregonids (Coregonus spp.) were examined for growth increments. Under laboratory conditions, a check is formed on the day of hatching and subsequently one growth increment per day is deposited during at least 265 days. Under the experimental conditions of this study, the age of young coregonids can therefore be determined with high accuracy.In starving larvae, both increment width and ring contrast decrease during the first 10 days after hatching until daily increments are no longer recognizable. A change from one diet to another, alteration of the water temperature, or a short starvation period lead to the formation of characteristic ring patterns which appear on the otoliths within 1 to 3 days. These patterns are highly reproducible among all specimens of each treatment group and can therefore be used as intrinsic marks. They could be applied to hatchery-reared coregonids, thus providing a basis for judging the efficacy of stocking operations.     

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.     

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 young-of-the-year mackerel in the Bay of Biscay

The first growth season of young-of-the-year (0+ year) mackerel Scomber scombrus , sampled in the Bay of Biscay, was parameterized to determine growth patterns. Daily increments were identified on sagittae otoliths, for calculation of age and growth of 92 larvae and 54 juveniles over the range 3·6–215·0 mm standard length ( L _S). A Gompertz curve was fitted to the length-at-age data. At the end of the first year of growth L _S was 194·2 mm, with a maximum growth increment of c . 2 mm day⁻¹, observed 62 days after hatching. Backcalculated growth increments for mackerel juveniles, during their larval stage, were higher than those observed for sampled larvae; only 10·9% of sampled larvae were estimated to survive. Growth for north-eastern Atlantic mackerel was slower than that published for north-western Atlantic mackerel. Backcalculated hatching dates for mackerel were consistent with the typical temporal distribution of mackerel spawning in the Bay of Biscay.     

Environmental effects on primary increment formation in the otoliths of newlyhatched Arctic charr

Otolith microincrements were investigated in Arctic charr Salvelinus alpinus , reared from hatching under various temperatures (1, 3, 5, 7° C) and feeding conditions (starved, fed every third day, fed daily). Larval charr otoliths were marked with oxytetracycline and alizarin complexone. Alizarin complexone was found to be 100 per cent successful in marking otoliths while oxytetracycline marks could be seen in <10 per cent of the otoliths viewed. Otolith microincrements were viewed by light and scanning electron microscopy to investigate the daily nature of increment deposition. Low temperatures (1 and 3° C) and starvation depressed daily increment formation. Increment deposition was found to be daily among the larvae reared at warmer temperatures (5 and 7° C) and fed at least every third day. Scanning electron microscopic analysis allowed us to confirm the results of light microscope increment counts from all temperatures except 1 ° C, where the number of increments enumerated were higher than the number obtained during light microscopy analyses. Increased feeding and warmer temperatures also resulted in increased increment width. The difference in increment number and width seems to be dependent upon fish growth rate which we have found to be affected by both temperature and feeding conditions.     

Growth and otolith microstructure of cod (Gadus morhua L.) larvae

Cod larvae from Irish Sea stocks were reared under differentgrowth conditions, and the otolith growth and increment formationexamined in sagittae and lapilli. Otolith increments were firstdeposited around the time of hatching and increment counts,on average, reflected larval age. The growth rate of fish larvaereared in different sized tanks was significantly different(P < 0.001), but there was no detectable effect on incrementformation. Otolith size was independent of larval size for individuals<5 mm in length. In larvae >6 mm, larger, faster growingindividuals had larger and faster growing otoliths.     

Otolith microstructure pattern in Oreochromis niloticus (L.)

The microstructure of otoliths from young and old Oreochromis niloticus (L.) were studied. Otoliths were prepared histologically except for those from newly hatched fish. Hatching results in the formation of a check in the otoliths, which appeared 1 day later. Other checks are rare in juvenile otoliths but common in adult otoliths. Faint and non-daily increments were observed within the hatching check. After hatching, increments were deposited daily. Sub-daily increments were faint and narrow, they were present in the area along the dorso-ventral axis of the otolith but did not continue into the lateral region. Discontinuous zones in the medial area appeared different from those in the lateral area. New growth centres were not only found in the juvenile fish otoliths, but also in adult fish otoliths.     

Immersion mass marking of pikeperch (<Emphasis Type="Italic">Sander lucioperca</Emphasis>) larvae in oxytetracycline hydrochloride and its detection using fluorescence microscopy

Fish marking is essential to distinguish between stocked and naturally reproduced fish. This procedure is challenging, especially in early life stages. Therefore the objective of this study was to investigate the possibility of oxytetracycline hydrochloride (800 mg L^?1 solution) immersion marking on 3–5 days old pikeperch larvae, with focus on durability and readability of marks on the otolith of marked individuals. The immediate mortality after marking was low (?5%) and growth of the pikeperch was continuous during the eight week study period. The fluorescent marks were detectable during the whole study period, but after the sixth week grinding of the otoliths was necessary. With grinding otoliths the processing time and the probability of damaging the mark increased significantly. Another critical period was the necessity of sample storage in a dark place due to the marks’ instability in light, in all phases before the final mark detection. The study confirmed the suitability of oxytetracycline hydrochloride marking for use in studies focused on pikeperch juveniles’ early growth, stocking success, distribution etc.     

Effects of growth rates on the otolith increments deposition rate in capelin larvae (Mallotus villosus)

Otolith microstructure analysis was applied to known age capelin larvae (Mallotus villosus) in order to examine the formation of daily increments. In two validation experiments, newly hatched yolk sac larvae were stocked into eight 10 m³ plastic bags where environmental conditions were kept as natural as possible. The bags were terminated after 35-79 days, the surviving larvae were collected and the otoliths were analysed. Survival in the bags varied between 39 - 71% with average individual length growth rates of 0.25 mm day^- 1. The ages of most larvae were underestimated and the accuracy in age estimation was generally low. Highest accuracy was found for fast growing larvae. On average, the larvae started to form increments about 12 days after hatching, and the increment width increased with age and/or length of the larvae. Larvae showing low body growth rates had fast otolith growth relative to body length.     

Microstructural growth in otoliths of black rockfish,sebastes schlegeli, from prenatal larval to early juvenile stages

Microstructural growth in the sagittae ofSeastes schlegeli, a viviparous scorpaenid, is described from prenatal larval to early juvenile stages, and related to morphological changes. Embryos and prenatal larvae were extruded from a gravid female from 21 d prior to birth onwards, and released larvae reared and sampled up to 58 d after birth. Eggs hatched in the ovary 14 d prior to birth. At this time, otoliths consisted of a core surrounded by a prominent check, similar to the otolith structure seen in oviparous fishes. Fourteen growth increments had been deposited by birth. The parturition mark it-self comprised a prominent check and narrow growth increment Growth increments were deposited daily from hatching up to 58 d after birth, whereas accessory primordia first appeared in otoliths by ca. 32 d after birth, at a specimen total length of ca. 13 mm. This corresponded to the period during which the larvae metamorphosed into juveniles. Otoliths grew exponentially during the larval stage and linearly during the juvenile stage. when plotted against total length. Growth in total length from hatching to 58 d after birth could be represented by the Gompertz curve.     

Daily growth increments in the larval otolith of the Japanese eel,Anguilla japonica

Early formation of otolith was studied on artificially hatched larvae of the Japanese eel,Anguilla japonica. Newly hatched larvae had a pair of sagittae which were flat and subelliptical with 8.3 μm in mean diameter. The diameter of the sagitta increased linearly with age. No growth increments were observed in the sagitta at hatching, while larvae which were 2, 4 and 6 days old had on average 2.1, 3.6 and 6.0 increments, respectively. The number of the increments (Y) and the age in days after hatching (X) showed a close linear relationship (Y=0.96X+ 0.06, r = 0.913, n = 40), suggesting daily deposition of sagittal increments. In 95 % of the field-caught elvers of this species, a distinct dark ring (check) with the diameter of 6–12 μm was found around the nucleus of the sagitta. This seems to be a “hatch check” deposited at hatching, since its diameter roughly agreed with that of the sagitta in the newly-hatched larvae. Possibly, the number of the increments outside the hatch check represents the age of the fish in days.     

The use of live and frozen Artemia salina nauplii enriched with fluorochromes for mass‐marking vendace Coregonus albula (L.) larvae

The aim of this study was to investigate the use of Artemia salina nauplii enriched with chosen fluorochromes for mass marking vendace Coregonus albula (L.) larvae. In the experiment, vendace larvae (6 DPH) were fed with live or frozen A. salina nauplii immersed in tetracycline hydrochloride (TC), calcein (Cal) or alizarin red S (ARS) for four subsequent days. More successful effects (marking otoliths) were obtained by feeding the fish with live nauplii enriched with fluorochromes, regardless of the dye type. The highest percentage of marked otoliths (100%) was recorded in the group fed with live nauplii immersed in TC. In the groups fed live or frozen nauplii enriched with Cal and ARS, a lower percentage of marked individuals (63.3%–73.7% and 56.7%–63.3%, respectively) were recorded. The survival rate of vendace larvae in particular groups oscillated between 93.7% and 95.7%. There were no significant differences in the total body length and body weight of the reared vendace larvae among different groups. In conclusion, for mass marking of vendace larvae using a feeding method, fish fed A. salinalive nauplii enriched with TC at a dose of 600 ppm is recommended for fishery practice.     

荧光物质浸泡标记稀有鮈鲫和彭泽鲫仔、稚鱼

研究了茜素络合物和盐酸四环素对稀有鮈鲫和彭泽鲫仔、稚鱼进行浸泡标记的方法和效果。茜素络合物在浸泡浓度５０—１００ｍｇ／Ｌ,浸泡时间持续６—２４ｈ的范围内,对两种鱼都有很好的标记效果;盐酸四环素在浸泡浓度１５０—２５０ｍｇ／Ｌ,浸泡时间１２—２４ｈ的范围内,对彭泽鲫有较好的标记效果,但对稀有　鲫有极高的致死率。在荧光显微镜下观察,茜素络合物呈橘红色、盐酸四环素标记区呈金黄色荧光反应。     

齐口裂腹鱼耳石早期生长发育与日轮特征研究

文章研究了在实验室条件下齐口裂腹鱼仔稚鱼耳石早期形态发育与生长特点、第一轮纹出现时间和轮纹沉积规律。结果表明: 在13.5-17.2℃孵化条件下,微耳石和矢耳石在出膜前形成,而星耳石于出膜后第12天出现。在仔稚鱼生长过程中,微耳石由近圆形发育成贻贝形,矢耳石经历近圆形、锲形后发育为箭矢状,星耳石形状由近圆形发育为星芒状。微耳石的前区、背区和腹区及矢耳石的背区和腹区生长呈幂函数关系,而微耳石的后区、矢耳石前区和后区生长以及两对耳石的前后区半径之和与全长均呈线性相关。在(18.50.5)℃和(15.61.1)℃条件下,50%矢耳石样本第一轮纹均在出膜后第 2 天形成(分别为出膜后18h和19h),以后每天形成一轮。微耳石和矢耳石轮纹数均与日龄呈线性相关,方程斜率均与1差异不显著(P0.05),表明两对耳石的轮纹沉积均为日周期性。这些结果为研究齐口裂腹鱼野生种群繁殖期和早期生活史特征等生态学问题提供了重要依据。     

Otolith Microstructure of Larval Gymnocypris potanini Herzenstein from the Minjiang River in China

Synopsis Otolith microstructure of about 120 Gymnocypris potanini larvae from the Minjiang River in China was examined and analyzed. Larvae had multiple primordia in most lapilli and sagittae, while had only one primordium in a few specimens. There had only one nucleus in otoliths of the larvae, except for some few specimens with 2 nuclei. The transparence of many otoliths differed from center to edge, and part of them could be divided into inner low optically dense zone (LODZ) and outer optically dense zone (ODZ). Based on increment clarity, otoliths of this species could be classified into three types, which were otolith with subtile increments, otolith with almost identified increments, and otolith with fairly clear increments characterized by high contrast. The last two types of otolith accounted for 87.07% in lapilli and 94.46% in sagittae, respectively. Increment clarity of sagitta was higher than that of lapillus. Natural checks were identified in 32.50% lapilli and 48.33% sagittae. These checks primarily located in the first to sixth increment. According to the number of increments in otoliths, the age of this batch larvae was 14 – 22 days, birth date was on June 17 – 25, and average growth rate of body length was 0.8936 ± 0.08769 mm/d.     

Verification of the eclossion mark on the sagittal otolith of the larvae of Sardinella aurita (Pisces: Clupeidae)

The study of otolith in larvae is important to determine fish age and growth, essential parameters in the study and management of fisheries resources. In this study, the formation of the hatching mark in Sardinella aurita was verified on ichthyoplankton samples collected off southern Cubagua island, Venezuela, from May 1998 to January 1999. The embryos were kept alive using a culture system until they hatched and daily a group of 10 to 30 larvae were fixed in 95% ethanol. An image analysis system was used to measure morphometric characteristics of larvae and sagittal otoliths. Following are mean values in newly hatched larvae: otolith hatching mark distance from nucleus 4.78 m (I.C. 0.36 m, p 0.05 n = 30), increase width 1.46 m (I.C. 0.17 microm, p 0.05, n = 30) and diameter 14.28 m (IC 1.11 m, p 0.05, n = 30). The mean standard length of larvae at age 0 was 3.31 mm (I.C. 0.08 mm, p 0.05, n = 200). The identification of the hatching mark allows the exact calculation of the number of rings in larvae from the natural environment.     

Otolith morphology, microstructure and ageing in the hedgehog seahorse, Hippocampus spinosissimus (Weber, 1913)

The life history characteristics of many species of seahorse, including the hedgehog seahorse Hippocampus spinosissimus, make them sensitive to exploitation. Consequently, proper management tools must be employed; these are often based on reliable ageing. The aim of the present study was to evaluate the possibility of using otoliths for ageing hedgehog seahorses from Vietnam. Asteriscus, lapillus and sagitta all showed moderate to strong correlations between fish standard length (SL), otolith length and number of increments in seahorses between 83 and 188 mm SL. There were no annual or seasonal marks in any of the three otolith pairs observed using dissecting or light microscopy, and only asteriscus revealed microincrements under light microscopy. The number of increments ranged between 71 and 137. A full trajectory of lapillar microincrements was only visible when using scanning electron microscopy, and then only in two of the examined individuals (88 and 115 increments). A validation experiment showed that the number of increments in the asterisci did not correspond to the age of seahorses bred and reared for 717 and 868 days. Furthermore, a second validation study using Alizarine Complexone (ALZ) otolith marking did not reveal any increments peripheral to the ALZ mark 30 days after marking. The conclusion of the study was that otoliths do not at present provide a reliable tool for estimating age in adult hedgehog seahorses, and therefore other tools have to be employed to improve their management.     

Otolith formation,microstructure and daily increment validation in juvenile perch Perca fluviatilis

The otoliths of laboratory‐reared larval and juvenile perch Perca fluviatilis of known age were analysed to determine the age of otolith formation and validate the formation of daily increments. There was a linear relationship between number of increments and age in days post‐hatching, although by 82 days post‐hatching daily increment counts underestimated actual age by an average of 5 days. Otolith dimensions in relation to standard length indicated allometric growth of otoliths until completion of yolk absorption, and isometric growth thereafter, up to 82 days post‐hatching.