Effect of Light Intensity on Color Performance of False Clownfish,Amphiprion ocellaris Cuvier

Color performance of false clownfish, Amphiprion ocellaris Cuvier, was examined under three levels of light intensity (20–50 , 600–850 , and 2700–3500 lx) for 5 wk. The experiment was conducted in nine rectangular glass aquaria (25 × 25 × 20 cm) with three replicates. Each aquarium was stocked with 36 fish, and 3 fish were randomly sampled from each aquarium every other week. Digital images were taken weekly on each individual fish after it was anesthetized in MS‐222. The color performance in hue, saturation, and brightness was quantified using image analysis. In addition to the whole‐body analysis, each fish image was divided into ventral and dorsal parts to assess the body position‐dependent effect. Furthermore, color differences between dorsal fin, anal fin, ventral fin, and caudal fin were also quantified. The whole body was brighter at low light than at medium or at high light intensity. Irrespective of light intensity, the dorsal side was more orange but less bright than the ventral side. Brighter light strengthened overall orange color on fish fins. The dorsal fin and ventral fins appeared more orange than the anal and caudal fins regardless of light intensity and exposure duration. Similar to body color, low light also led to brighter fins, especially for caudal and dorsal fins. Our results indicate that ambient light could regulate fish color performance but could not change the pigment dominance by β‐carotene. Light intensity is unlikely to change the contrast between dorsal and ventral sides, but dim light tends to make fish body brighter, and bright light strengthens orange color on fins.     

Gross, histological and scanning electron microscopic appearance of dorsal fin rot in farmed Atlantic salmon, Salmo salar L., parr

The gross, histological and scanning electron microscopic appearance of dorsal fin rot in farmed Atlantic salmon parr, Salmo salar L. is described. The lesions were grouped into seven categories: (1) peripheral erosion and ray splitting; (2) peripheral erosion with some nodularity; (3) severe nodularity with differing degrees of tissue loss; (4) extensive to total loss of the dorsal fin; (5) smooth thickening of the dorsal fin; (6) haemorrhagic dorsal fin lesions; and (7) healed dorsal fin rot lesions. The main sign of injury was clefts extending through the epithelium. These injuries were consistent with bites from other parr. During healing from such wounds, damaged cells sloughed from the surface, and there was swelling and hyperplasia in the remaining cells. The majority of the thickening in the fins was the result of epithelial hyperplasia with a variable cellular inflammatory response. The distal epithelium of fins with severe fin rot (i.e. nodular and eroded) was rough, irregular and swollen with superficial nodular extensions. Wounds in all stages of repair were more numerous in such areas. Fin rays were frequently observed protruding from the abnormal epithelium at the distal edge of the fin. With the exception of the isolation of Aeromonas salmonicida from a small number of cases, no significant bacterial involvement was detected. Under scanning electron microscopy, bacteria were only detected on the exposed fin rays and not in association with the abnormal epithelium. In the majority of cases, the dorsal fin was either the only fin damaged or the most severely damaged. It is suggested that the hyperplastic response to numerous bite wounds is responsible for the accumulation of abnormal epithelium typical of dorsal fin rot in farmed Atlantic salmon parr.     

Impact of Background on Color Performance of False Clownfish,Amphiprion ocellaris,Cuvier

Color performance of false clownfish, Amphiprion ocellaris, Cuvier was first examined at four color backgrounds (blue, green red, and white) for 4 wk, then all fish were transferred to a white background for another 4 wk to test whether the impact of background colors on fish skin could have a lasting effect when the environment colors are changed. The experiment was conducted in 10‐L rectangular plastic buckets with three replicates. Thirty fish were stocked in each bucket and three fish were randomly sampled from each tank in Weeks 1, 4, and 8. The color hue, saturation, and brightness were quantified using image analysis. In addition to the whole body analysis, each fish image was divided into ventral and dorsal parts to examine the body position‐dependent response. Furthermore, color differences among the dorsal fin, anal fin, ventral fin, and caudal fin were also quantified. Blue or green background enhanced red orange color on fish skin, whereas white background made fish color brighter. Irrespective of background color, the dorsal side of fish exhibited more red orange, but the color was less bright and less saturated than that of ventral side. Upper fins (dorsal and caudal fins) were more red orange in a blue background than in a white background. Transferring fish from colored backgrounds to a white background made the fish skin and fins brighter, the color of ventral body and ventral fins less saturated, and the bottom fins more yellow orange. The results indicate that blue or green background could strengthen the orange color, whereas white background made fish color less saturated but brighter. The impact of background on the performance of fish color is temporary and likely to disappear when environmental color changes.     

Fin development in stream- and hatchery-reared Atlantic salmon

To determine the effect of development and environment on fin growth, we measured fin lengths of juvenile Atlantic salmon (Salmo salar) from two hatcheries (August, October and April–May), stream-reared fish (July and October) stocked as fry into two tributaries, and smolts from the main stem of the Connecticut River (May). For stream-reared parr, there was a linear relationship between the dorsal, caudal and anal fins with fork length, while the pectoral, pelvic and adipose fins exhibited a curvilinear relationship with fork length. Parr from a high gradient stream had larger caudal fins than fish from a low gradient stream, but other fins did not differ. Regression lines for the fins of stream-reared smolts were all linear when fin length was regressed against fork length. Stream-reared parr had larger pectoral, pelvic and anal fins than smolts of similar size while dorsal and caudal fin lengths did not differ. Regression equations formulated using the fins of stream-reared parr were used to calculate the percent difference (100×observed fin length/expected) in fin lengths between stream- and hatchery-reared parr. The pelvic, adipose, caudal and anal fins of hatchery-reared parr showed no signs of degeneration by the first sampling period 7 months after hatching, whereas degeneration in the pectoral (13–20%) and dorsal (15–18%) fins was evident at this time. By the end of the study, degeneration was present in every fin except the adipose, with the pectoral (35–65%) and dorsal (32–58%) fins exhibiting the greatest amount of fin loss. All fins of hatchery-reared parr became shorter with time. There were minor differences in fin degeneration among parr from the two hatcheries, but the overall pattern of decreasing fin size was similar, indicating a common cause of fin degeneration. Comparison of stream- and hatchery-reared fish is a valuable means of determining the impact of captive environments on fin growth.     

Interspecific comparison of experimental and natural routes of Lepeophtheirus salmonis and Caligus elongatus challenge and consequences for distribution of chalimus on salmonids and therapeutant screening

Although the gills have been reported as a site for settlement by sea lice attached stages in experimental challenges, the prevalence and abundance of infection on gills have not been reported in farmed fish and have been reported only rarely in wild salmonids. Disproportionate attachment to the gills may be significant in evaluation of new therapeutants and this study asks whether the efficacy data from studies of therapeutants based on experimental challenge can be extrapolated to the fish farm arena. The distribution of chalimus on gills, body and fins of farmed first sea year Atlantic salmon were examined in two Scottish sea lochs, each on two occasions (30 fish on each sampling date), fish from one farm with infection with Lepeophtheirus salmonis only and the other farm with exclusively Caligus elongatus. The dorsal fin was the primary attachment site of L. salmonis (50% and 33% in two samples respectively) with 29% and 32% on other fins and 20% and 29% on the body and head. Only one of 56 chalimus (1.8%) and four of 75 chalimus (5.3%) were attached to the gills. In contrast, the chalimus distribution of C. elongatus was predominantly on fins other than the dorsal, including the tail, 74% and 71%, on two sampling occasions, respectively, with only 4.2% and 3.6% of chalimus located on the dorsal fin. The pectoral fins were the most common location with 32%, followed by the tail 23%, pelvic fins 14% and only 3% on the anal fin. None of 287 and 111 chalimus in two samples, respectively, of C. elongatus was attached to the gills. The low abundance of lice on the gills indicated that non‐destructive sampling methods adequately represented lice infection. In three experimental challenges with L. salmonis, the gills were a major attachment location with 19.9–36.3% of chalimus, 9.9–26.9% on the body, 22–27% on the dorsal fin and 19–23% on the other fins. These differences with natural challenge in L. salmonis reported here and also in the literature suggest that the importance of the gills for chalimus location in the experimental model is atypical and an artefact of reduced host swimming speed in tanks that permits copepodids to attach to the gills. In natural infection, the flow over the gills is high and reduced flow is required for copepodid settlement. Greatest reductions (96%) in chalimus bath treated with cypermethrin occurred on the gills with no significant reductions in those located on the dorsal and other fins. It is possible that the efficacy of therapeutants may be higher in chalimus attached to the gills because of the higher concentration encountered of bath therapeutant and extrapolation of efficacy to farms may be misleading and progression to field testing is essential.     

背鳍缺失对胭脂鱼幼鱼游泳能力与反捕食能力的影响

为考察背鳍缺失对胭脂鱼( Myxocyprinus asiaticus )幼鱼游泳能力和反捕食能力的影响,将胭脂鱼幼鱼( 2.30 g±0.12 g, 4.59 cm±0.09 cm)随机分为对照组和背鳍缺失处理组(剪去背鳍),测定其临界游泳速度( U crit )及相关代谢参数、最大匀加速速度( U cat )、快速启动游泳能力以及捕食者存在条件下的存活率。结果显示:对照组和背鳍缺失组胭脂鱼幼鱼的 U crit 、最大代谢率( MMR)、 U cat 、快速启动过程的最大速度( V max )、最大加速度( A max )以及旋转角度与旋转率均无显著性差异。然而,背鳍缺失组胭脂鱼幼鱼在捕食者存在条件下的存活率显著低于对照组,背鳍缺失对胭脂鱼幼鱼的游泳能力没有明显影响,背鳍的存在可能是胭脂鱼幼鱼针对捕食者口裂限制的反捕食形态适应策略之一。     

鳜仔稚鱼骨骼系统骨化发育

采用软骨―硬骨双染色技术,描述了鳜(Siniperca chuatsi)仔稚鱼(1～35日龄)头骨、脊柱、附肢骨骼的骨化发育特征。结果显示:(1)头骨前鳃盖骨于14日龄最先骨化, 15日龄上下颌骨骨化,且上下颌骨相对长度呈现连续变化过程。17日龄后,颌齿、关节骨、舌颌骨骨化;19日龄,隅骨、间鳃盖骨、鳃盖骨、鳃条骨、额骨骨化。20日龄后,方骨、下鳃盖骨、辅上颌骨等骨化; 35日龄,头骨骨化基本完成。(2)脊柱于15日龄由前向后骨化, 20日龄背肋与腹肋由基部向末端骨化, 29日龄骨化完成。脉弓与脉棘、髓弓与髓棘均由前向后、由基部向末端骨化,脉棘与髓棘骨化时间晚于相应的椎体。(3)附肢骨骼骨化顺序依次为胸鳍、背鳍、臀鳍、腹鳍、尾鳍。胸鳍匙骨于16日龄骨化,乌喙骨与肩胛骨于25日龄骨化;背鳍、臀鳍分别于18日龄、20日龄骨化,骨化方式相似;腹鳍于23日龄骨化,骨化方式与胸鳍相反;尾杆骨、尾下骨于25日龄骨化,附肢骨骼于35日龄基本骨化完成。结果表明,鳜骨骼骨化发育与其早期运动、摄食与御敌等行为密切相关。     

鲔脊椎骨与附肢骨骼描述

为揭示鲔(Euthynnus affinis)的骨骼形态特征,采用X射线拍照法对鲔进行拍照及相关研究.研究发现,鲔脊柱由20枚躯椎和18枚尾椎构成,第4—第30枚脊椎骨连接27枚髓棘,第16—第28枚脊椎骨前后两端的椎体横突向下延伸后相互连接形成特殊骨骼结构,第35—第37脊椎骨上下两侧向斜后方延伸构成3块尾上骨和3块...     

Repeatability of fin length measurements using digital image analysis and studies of fin erosion as indicator of social interactions in Atlantic cod (Gadus morhua)

The aims of this study were to examine fin erosion caused by social interactions between Atlantic cod (Gadus morhua) juveniles, and to evaluate the repeatability of recorded fin length using digital image analysis (DIA). Fin length of 2100 juvenile Atlantic cod was analysed using DIA, during a 6 weeks experiment. The lengths of the three dorsal fins and the caudal fin were measured by three different assessors (M, K, B) three times during the experiment. Repeatability was based on a sub set of data from 42 randomly chosen fish. Assessor M measured the length of the fins of the 42 fish three times (M1, M2, M3). M1 and M2 were done on the same day, while M3 was conducted 2 weeks later. Assessor K measured two times with a 2‐year interval, and assessor B measured the fin length only once. The correlations between replicated measurements within assessor were highest for assessor M measured on the same day indicating an effect of memory. Repeatability of fin length ranged from 0.57 to 0.73 for the four fins. Social interaction with respect to fin erosion was studied using data on the four fins from all 2100 fish. ‘Relative fin length’ (fin length/total body length × 100) was calculated to assess fin erosion. Results indicated that all four fins were eroded due to social interactions, but the caudal fin was most severely eroded. In conclusion, DIA can be used to measured fin length but the method could be improved by using chromatic pictures.     

Genetic basis of pectoral fin deformities in the African catfish Clarias gariepinus (Burchell, 1822), Heterobranchus longifilis (Valenciennes 1840) and their hybrids

Morphological aberrations of the pectoral fins in nine mating combinations involving Clarias gariepinus (Burchell, 1822), Heterobranchus longifilis (Valenciennes, 1840) and their hybrids were investigated to determine the level and genetic basis of occurrence. The highest mean percentage survival in a Clarias× Clarias group was 75%, whereas the least mean percentage survival was 2% in the same group. The least mean percentage survival (40.3%) in the remaining three groups occurred in the cross of female hybrid (right pectoral fin absent) × male C. gariepinus (right pectoral fin absent). A maximum of nine types of aberrations was observed in the four mating groups – double dorsal fin, curved posterior dorsal fin, spineless right pectoral fin, right pectoral fin absent, left pectoral fin absent, rudimentary pectoral fin, both pectoral fins absent, double anal fin and curved anterior dorsal fin. These nine aberration types were recorded in the Clarias× Clarias group, with a total frequency ranging from 7.14% to 75.00%. The least number of aberrations was observed in the hybrid ×Clarias group (double dorsal fin and both pectoral fins absent) with a frequency range of 1.47–5.55%. No aberration was observed in two crosses involving female hybrid (right or left pectoral fin absent) × female C. gariepinus (normal). The level of aberrations in some of these crosses indicates the involvement of genotype rather than the influence of environment.     

Effects of baffles and isolation on dorsal fin erosion in steelhead trout, Oncorhynchus mykiss (Walbaum)

Abstract. Dorsal fin condition was evaluated in two groups of hatchery-reared steelhead trout, Oncorhynchus mykiss (Walbaum), and compared to wild fish. Hatchery fish were reared either in nursery tanks with baffles or in isolation (1 fish/rearing space). Evaluations were conducted to determine differences in dorsal fin condition between these groups and to monitor the progression and severity of fin damage. Isolated hatchery and wild steelhead trout maintained perfect dorsal fins with characteristic white margins. Hatchery fish reared in nursery tanks with baffles experienced dorsal fin erosion that started when the fish were about 40mm total length (30 days after being on feed). This erosion continued until dorsal fin length averaged only 2·3 mm in fish 161–200 mm total length in contrast to an average dorsal fin length of 20·9mm in wild fish of the same size.     

Skeletal development and abnormalities of the vertebral column and fins in larval stage of hatchery‐reared American shad,Alosa sapidissima

The present study describes the skeletal development and the occurrence of deformities in American shad, Alosa sapidissima, larvae from hatching to 45 days after hatching (DAH). The ontogeny of the vertebral column started at 16 DAH (days after hatching), with the formation of the posterior neural and haemal arches, and was complete at 28 DAH. In comparison, the vertebral centra started to form at 16 DAH, with ossification being visible in all centra at 38 DAH. The pectorals were the only fins that formed before the onset of feeding (at 2 DAH), with ossification being complete at 45 DAH. The caudal fin formed at 5 DAH, with ossification being complete at 40 DAH. Dorsal and pelvic fin development began at 6 DAH and 20 DAH respectively. The ossification of both the dorsal and pelvic fins was visible at 45 DAH. The anal fin began forming at 14 DAH, and was complete at 30 DAH. The ossification of the anal fin was complete at 45 DAH. Overall, 22 types of skeletal deformities were detected in about 41% of individuals. Most anomalies were detected in the haemal region, while the fewest anomalies were detected in the anal fin. In addition, the frequency of deformities gradually increased with fish age at the different developmental stages. Our results are expected to contribute baseline information on how rearing conditions impact skeletal development, in addition to identifying potential causative factors of skeletal deformities.     

Ontogeny of the shi drum Umbrina cirrosa (Linnaeus 1758), a candidate new species for aquaculture

The ontogeny of shi drum Umbrina cirrosa (Linnaeus 1758), a candidate new species for aquaculture, was studied throughout the entire larval phase. Geometric morphometric analysis revealed two clear inflection points (7.0 and 12.7 mm total length, TL) in the shape ontogeny of this species, separating the studied period into three phases of different allometric priorities. Spline graphs demonstrated that the major non‐uniform shape ontogeny correlated with the development of the fins, the anterior dorsal area of the body, the caudal peduncle, the eye and the mouth. Concerning the morphological features, shi drum larvae are characterized by an upward anterior bending of the notochord. The ontogeny of the fins began with the formation of the pectoral buds (2.9 mm TL), continued with the notochord flexion (4.3 mm TL, associated with the caudal fin development), the appearance of the pelvic buds, the first anal rays (4.5 mm TL) and the first dorsal rays (4.8 mm TL). Shi drum juveniles presented 25 vertebrae and the following dominant fin types: D XI,23, AII,6, VI,5, P17 and C17.     

Effect of vitamin A on the skeletal morphogenesis of European sea bass,Dicentrarchus labrax (Linnaeus, 1758)

The purpose of this study was to examine the effects of vitamin A levels in the larval diet of Dicentrarchus labrax, (a) on the shape of juvenile skeleton and (b) on the development of pelvic fins. To exclude the side‐effects of skeletal abnormalities on skeleton shape, morphometric analysis was performed on normal individuals only. Geometric morphometric analysis revealed a significant effect of larval nutrition on the shape of juvenile skeleton (Wilk's λ=0.0188, P<0.001), 55 days after the application of the different nutritional regimes. Between‐groups shape differences mainly concerned the position of anterior dorsal pterygiophore, which was associated with a significant (P<0.05) increase of the number of dorsal lepidotrichia and hard spines at low levels of vitamin A (3–9 × 10³ IU kg^?1 dry food). At the lowest vitamin A levels (3 × 10³ IU kg^?1 dry food), the development of pelvic fins was abnormal, with severe bilateral (44±10%, mean±SD) or unilateral (22±9%) lack of the fin lepidotrichia, hard spines and their supporting elements. In the 82–94% of the unilaterally deformed individuals, deformation concerned the left pelvic fin. Concerning the shape of pelvic fins in the normally developed individuals, results demonstrated a significant effect of nutritional conditions on the size and position of all the elements of the pelvic fin area (basipterygium, lower metacleithrum, cleithrum, scapula) (Wilk's λ=0.3087, P<0.001). Our results demonstrate a significant nutritionally driven phenotypic plasticity in D. labrax, with dietary levels of vitamin A determining the skeleton shape and the left–right symmetry of pelvic fins.     

Osteological development and anomalies in larval stage of hatchery‐reared yellow catfish Pelteobagrus fulvidraco

Comprehensive knowledge of osteological development of fish not only provides means for understanding its functional development, but also allows early detection of skeletal anomalies. The present study was conducted to determine osteological development and occurrence of anomalies from the first to the 40th day after hatching (DAH) for yellow catfish Pelteobagrus fulvidraco, a commercially important species in China. Vertebral ontogeny started with formation of anterior neural arches at 3 DAH, and completed at 6 DAH. Vertebral centra started to develop at 4 DAH and ossification in all centra was visible at 15 DAH. Caudal fin appeared at 2 DAH and ossification was visible at 26 DAH. The onset of dorsal and anal fins appeared at 4 DAH and their ossifications were visible at 20 DAH. Pectoral fins were present before first feeding and formed entirely at 9 DAH, and their ossifications were visible at 21 DAH. Pelvic fins appeared at 9 DAH, and formed completely at 21 DAH. The ossification of pelvic fins was not finished until the end of the experiment (40 DAH). 24 types of skeletal anomalies were observed. About 20% of individuals showed at least one anomaly. Haemal vertebrae anomalies occurred at the highest frequency, followed by pre‐haemal, caudal vertebrae and anal fin anomalies, and caudal fin had the lowest anomalies frequency. For the first time, our study determined osteological development and anomalies incidence in larval yellow catfish, which help further investigations into rearing conditions leading to appearance of these anomalies to prevent their incidence.     

美洲鲥仔稚鱼脊柱及附肢骨骼系统的早期发育

使用软骨-硬骨双染色技术,描述了美洲鲥(Alosa sapidissima)仔稚鱼(1~51日龄)脊柱、胸鳍、尾鳍、背鳍等附肢骨骼的形态发育特征。结果显示,脊柱的发育开始于10日龄仔鱼尾部的髓弓、脉弓和尾下骨的出现,16日龄髓弓和脉弓延伸形成髓棘和脉棘,19日龄脊柱出现分节的硬骨环,23日龄所有椎体形成。各附鳍支鳍骨发育顺序先后依次为胸鳍、尾鳍、背鳍、臀鳍和腹鳍。胸鳍在2日龄时出现乌喙骨,13日龄形成软骨质的胸鳍支鳍骨,19日龄仔鱼肩带和上匙骨开始骨化;尾鳍的尾下骨最早出现在5日龄,12日龄尾鳍形成2枚尾上骨、1枚尾杆骨和6枚尾下骨,19日龄仔鱼尾椎和尾鳍率先开始骨化,直至23日龄尾鳍骨骼系统钙化完全。最终背鳍和臀鳍分别形成18和22根鳍条。美洲鲥骨骼发育研究对其早期发育功能趋向、环境优化及分类鉴定有重要作用。     

中国南海银鲈科鱼类——新记录

2008年11月在广西北海市侨港镇码头采获银鲈科Gerreidae、银鲈属Gerres鱼类标本两尾,经鉴定为大棘银鲈Gerres macracanthus Bleeker,1854,系我国南海鱼类一新记录。其主要特征为：体长卵圆形,侧扁,体长为体高的2.2～2.3倍;体背腹缘均呈弧状隆起,体高以背鳍起点处最高。口小,能活动,伸出时略向下倾斜。体被薄圆鳞,易脱落;侧线鳞41～43枚。背鳍鳍棘部与鳍条部相连;背鳍IX-10,第2鳍棘延长呈丝状,压倒时末端伸达尾柄;臀鳍Ⅲ-7,以第3鳍棘最长;胸鳍长,末端可达臀鳍起点上方;尾鳍叉形。新鲜标本体背部银灰色,腹部银白色,体侧有7～10条青灰色横带;背鳍灰白色,第2鳍棘黑色;臀鳍、胸鳍和腹鳍淡黄色;尾鳍灰黄色,上、下叶内缘暗色,下叶外缘白色。     

鲫鱼背鳍棘的观察

１９８５年至１９９５年在上海对鲫鱼背鳍的进行了观察。结果表明，鲫属中金鲫、鲫、银鲫和大阪鲫的背鳍均具有４个棘。     

金鱼主要质量性状在杂交子一代中遗传规律的初步研究

为研究金鱼主要质量性状的遗传规律,将具有头瘤、龙睛、珍珠鳞、无背鳍、双尾、三尾等变异性状的金鱼与具正常性状的金鱼进行正交和反交,统计杂交子一代的性状表现。结果显示,头瘤、龙睛、珍珠鳞、双尾和三尾均为隐性性状;无背鳍金鱼与正常背鳍金鱼杂交的结果出现了高比例的残背个体,说明无背鳍不是单一性状。研究表明,在金鱼的杂交选育中,须遵循变异性状的遗传规律,才能更快更好地达到生产和繁育高品质金鱼的目的。     

A Survey of Trout Fin Erosion, Water Quality, and Rearing Conditions at State Fish Hatcheries in Utah

A total of 600 hatchery trout were examined for signs of fin erosion including rainbow trout Oncorhynchus mykiss , cutthroat trout O. clarki , brook trout Salvelinus fontinalis and brown trout Salmo trutta . A scoring system was used to evaluate erosion on all fins from 20 fish samples. Water quality and hatchery rearing variables were also determined for corresponding raceways or ponds. For rainbow trout groups ( N = 24), stepwise multiple linear regression was used to interpret the relationship between fin erosion and the other variables. These fish groups averaged between 92 and 243 mm in total length and no significant correlation was observed between length and a fin erosion index ( r = 0.045). The best-fit regression model (adjusted R² = 0.689) suggested that fin erosion was correlated with lower alkalinities, unnatural bottom substrates (concrete or steel), higher unionized ammonia levels, and higher fish densities. Despite significant variation between hatcheries, fin condition was significantly better in rainbow trout than in cutthroat trout in three of four hatcheries containing both species and the same substrate. Fin erosion in rainbow trout occurred primarily on dorsal fins, followed in order of decreasing severity, by pectoral, caudal, anal, and ventral fins.