华鲮鳃表面形态结构扫描电镜观察

应用扫描电镜对华鲮Sinilabeor rendahli鳃耙、鳃弓、鳃丝和鳃小片的形态结构进行了观察.鳃耙和鳃弓表面凹凸不平,分布着大量丘突.鳃丝和鳃耙表面有大量粘液细胞分布,鳃丝上皮细胞表面密布微嵴,氯细胞附着在鳃丝表面和鳃小片侧表面.鳃小片薄、表面凹凸不平,垂直排列在鳃丝上.鳃丝和鳃小片的表面形态结构特征有助于提高鱼鳃的气体交换效率.     

黄斑篮子鱼和金钱鱼鳃的扫描电镜观察

对两种鲈形目鱼类黄斑篮子鱼(Siganus oramin)和金钱鱼(Scatophagus argus)的鳃结构进行扫描电镜观察。结果表明,黄斑篮子鱼和金钱鱼鳃的表面结构及微细结构与其他硬骨鱼类基本相似,鳃丝表面都具有规则或不规则分布的环形微嵴、沟、坑、孔等结构。黄斑篮子鱼的鳃片中部鳃丝表皮有大量凸起,而端部鳃丝表皮的凹凸程度明显较低,黄斑篮子鱼的鳃小片高度较金钱鱼鳃小片高。黄斑篮子鱼和金钱鱼鳃上皮的扁平上皮细胞、氯细胞和黏液细胞的形态结构及数量分布存在细微的差异。黄斑篮子鱼鳃片鳃丝的端部和中部表面有黏液细胞,金钱鱼鳃丝表面的黏液细胞很难观察到,与大多数淡水鱼类相似。黄斑篮子鱼鳃丝表面分布的氯细胞数量多于金钱鱼,这可能与两种鱼生活环境、生活习性的长期演变相关。     

珠江口池养梭鱼鳃的光镜、扫描和透射电镜观察

应用光学显微镜、扫描电镜和透射电镜对珠江口池塘养殖梭鱼Liza haematocheila鳃的组织结构、表面形态特征及鳃小片超微结构进行了观察。结果表明梭鱼具有4对鳃,每个鳃由鳃弓、鳃丝、鳃小片和鳃耙组成。梭鱼鳃丝和鳃小片的表面结构和超微结构与其他硬骨鱼类的基本相似,鳃丝表面分布有众多规则或不规则的环形微嵴、沟、坑、孔等结构。鳃丝分为呼吸区和非呼吸区,呼吸区较为平滑,上皮细胞表面无微嵴,呈皱褶状;非呼吸区分布有沟、坑、孔等结构,上皮细胞有较规则的指纹状微嵴。鳃小片是最主要的呼吸场所,由基膜、上皮细胞、内皮细胞、柱细胞和毛细血管网组成。泌氯细胞主要分布在鳃小片基部,并有开口通往外界。本文还探讨了梭鱼鳃的结构与其功能的密切关系。     

不同生境下青海湖裸鲤(Gymnocypris przewalskii)两亚种鳃形态差异及其功能适应

该研究比较观察青海湖裸鲤(Gymnocypris przewalskii)两亚种(青海湖裸鲤指名亚种(Gymnocypris przewalskii przewalskii)和青海湖裸鲤甘子河亚种(Gymnocypris przewalskii ganzihonensis))鳃的形态及显微结构。结果显示,指名亚种的第一鳃弓鳃耙数多、密集且较长,而甘子河亚种则耙数少、稀疏且短;两者的鳃丝间距及鳃小片间距无明显差异,指名亚种的鳃丝较长;指名亚种扁平上皮细胞形态以不规则椭圆形为主,鳃丝表面有黏液细胞,其上分布的氯细胞数量多于甘子河亚种,而甘子河亚种扁平上皮细胞的形态以六边形为主,鳃丝表皮未观察到黏液细胞。由此推测,青海湖裸鲤两亚种鳃形态的差异与其食性和栖息环境相适应。     

不同盐度下鲻鱼幼鱼鳃和肾组织结构变化

采用组织切片技术,研究了不同盐度下鲻鱼幼鱼鳃和肾的显微结构变化,探讨这些变化与渗透压调节的关系。结果显示,随着盐度升高,鳃小片逐渐变窄,间距变小,鳃丝和鳃小片上泌氯细胞数量增多,体积变大。泌氯细胞集中分布在鳃小片基部,且向两侧扩布。高盐度组的S40组,鳃小片上皮出现分离脱落现象。随着盐度梯度的升高,肾小球及各级肾小管的结构上出现了不同程度的萎缩现象。     

鲑点石斑鱼和大眼鳜鳃的扫描电镜观察

对鲈形目科、底栖生活、凶猛肉食性的鲑点石斑鱼 (Epinephelusfario)和大眼鳜 (Sinipercakneri)鳃的结构进行扫描电镜观察。结果表明 ,两种鱼鳃的表面结构和微细结构与其他硬骨鱼类基本相似 ,鳃丝表面都具有规则或不规则分布的环形微嵴、沟、坑、孔等结构 ;然而两者的鳃小片都较高 ,表面更加凹凸不平 ,是对低溶氧环境的适应。鲑点石斑鱼的鳃丝表面一部分较为平坦 ,另一部分则凹凸不平 ,其鳃小片高度也高于大眼鳜 ,因而具有更大的表面积和较高的摄氧效率。在扫描电镜下能在鲑点石斑鱼和大眼鳜的鳃上分辨出扁平上皮细胞、氯细胞和粘液细胞 3种细胞 :前者鳃上的扁平上皮细胞界限清楚 ,而后者的界限模糊且表面遍布不规则的微嵴 ;前者的鳃丝和鳃小片上氯细胞的数量明显多于后者 ,两者细胞形态也存在差异 ;而鳃丝表面的粘液细胞的数量则是后者较多。两种鱼鳃上的细胞的形态结构及数量分布存在的差异 ,可能与前者生活于海水而后者生活于淡水的不同生活环境有关。     

斑马鱼鳃的光镜和透射电镜观察

应用光学显微镜和透射电镜对斑马鱼(Danio rerio)鳃的组织结构及鳃丝、鳃小片超微结构进行了观察。结果表明,斑马鱼有4对全鳃,鳃耙呈长锥状,鳃丝呈梳状排列在鳃弓上,鳃小片均匀排列在鳃丝两侧。鳃小片由上皮细胞、柱细胞、内皮细胞和毛细血管网组成,鳃小片基部和血管周围分布有泌氯细胞,胞内有丰富的线粒体和排泄小泡,根据线粒体形态特征和细胞质电子密度可将其分为两个亚型。黏液细胞通常与泌氯细胞对生存在,并且有通外的开口。斑马鱼鳃组织结构与其他硬骨鱼鳃结构相似,其结构和功能有密切的关系。     

波纹唇鱼鳃丝的光镜、扫描和透射电镜观察

应用光学显微镜、扫描电镜和透射电镜对波纹唇鱼(Cheilinus undulatus)鳃的组织结构、表面形态特征及鳃小片超微结构进行了观察.结果表明,波纹唇鱼有3对全鳃,1对半鳃和1对伪鳃,鳃丝呈梳状紧密排列在鳃弓上,鳃小片紧密地镶嵌排列在鳃丝两侧,入鳃动脉、出鳃动脉和鳃小片毛细血管网组成鳃的血液系统.鳃丝非呼吸区分布...     

盐度胁迫对尼罗罗非鱼鳃氯细胞调节变化的影响

采用扫描电镜和免疫组化技术,研究了尼罗罗非鱼(Oreochromis niloticus)鳃中氯细胞的分布,及其不同盐度(0、10、20、30)胁迫对氯细胞数目和形态变化的影响.扫描电镜结果表明:氯细胞分布在鳃丝的鳃小片基部,根据其表面开口长度,可分为Ⅰ型(＞6.5μm)、Ⅱ型(3.2～6.5μm)和Ⅲ型(＜3.2 μm)3种亚型;不同盐度下氯细胞总数目变化趋势为盐度10＜盐度20＜盐度0＜盐度30;从盐度0转移到盐度10后,氯细胞总数目减少,主要是由于Ⅰ型氯细胞数目显著下降;盐度20中的氯细胞数量高于盐度10,但不显著;盐度30中的氯细胞数量随Ⅲ型氯细胞数量的提高而显著增加.免疫组织化学进一步证实了不同盐度条件下Na+-K+-ATPase免疫反应性细胞均分布在鳃丝的鳃小片基部.本研究结果表明,尼罗罗非鱼可通过改变鳃氯细胞数量和形态结构来适应环境中的盐度变化,推测Ⅰ型氯细胞和Ⅲ型氯细胞分别在低盐、高盐适应中起着重要作用.     

小瓜虫在澳洲龙纹斑鳃器官上的分布及其影响

【目的】小瓜虫病是澳洲龙纹斑苗种阶段危害巨大的寄生虫病。探究小瓜虫在澳洲龙纹斑鳃器官上的分布及其影响可以丰富小瓜虫的致病性及病理学方面的研究内容,也可以为渔业生产中小瓜虫病的防治提供参考。【方法】采用光镜及扫描电镜技术确定病原,并观察小瓜虫在澳洲龙纹斑鳃丝、鳃小片及鳃盖上的分布情况及这些器官的变化情况。【结果】小瓜虫侵染澳洲龙纹斑的鳃器官后,分布在鳃丝、鳃小片及鳃盖的表面,上皮细胞之下及鳃小片之间,或是包裹在黏液细胞里,但侵染后期在鳃丝及鳃小片上的数量明显少于鳃盖。侵染后期,鳃丝、鳃小片及鳃盖出现一定程度的膨胀变形,黏液细胞分泌增多,鳃小片末端膨大变形甚至黏连融合,顶端充血呈球状或棒状。【结论】对于鳃部而言,侵染后期小瓜虫主要分布在澳洲龙纹斑的鳃盖上。小瓜虫主要通过侵染引发澳洲龙纹斑鳃部器官的变形膨大,使其丧失正常的功能,造成血液循环受阻、渗透压调节失衡,最终导致鱼体缺氧死亡。     

Comparative morphological and molecular studies on Myxobolus spp. infecting chub from the river Danube, Hungary, and description of M. muellericus sp. n

During a survey on fishes from the River Danube, the occurrence of 8 Myxobolus species (Myxozoa: Myxobolidae) was registered in chub Leuciscus cephalus L. Most species had a specific location within the fish host. M. cycloides was found in the wall of the swimbladder; the branched plasmodia of M. dujardini were located typically in the epithelium of the non-lamellar part of gill filaments; the plasmodia of M. ellipsoides infected fins between 2 fin rays; M. muelleri and Myxobolus sp. 2 formed large elongated plasmodia in the afferent gill artery of filaments, while the round cysts of M. muellericus sp. n. filled the capillary network of the gill lamellae. Intramuscular plasmodia of M. pseudodispar proved to be the most common, although large cysts of Myxobolus sp. 1 were also frequently found in the intestinal wall. Despite similarities of some species in spore morphology, 18S rDNA sequences showed clear differences between the species examined.     

Structural organization of the gills in pipefish (Teleostei,Syngnathidae)

Summary The morphology and structural features of the gills of the two Western Baltic pipefish Nerophis ophidion and Syngnathus rostellatus were investigated using scanning electron microscopy. The general anatomy of the gills complies with the general pattern in fish. Several adaptations though, show the highly specialized nature of pipefish gills. The filaments are extremely short, few in number and carry only a few lamellae due to the limited space in the branchial cavity. The lamellae have a widely projecting form yet still have a small area in comparison to other fish. Gill irrigation is performed by a specialized pumping mechanism which forces respiratory water through the small but densely packed gill sieve. Although both species live in the same habitat and belong to the same family, differences in gill morphology were found and are related to different lifestyles. S. rostellatus is the more active species and therefore has more filaments per gill arch, more lamellae per filament, wider projecting lamellae and a more extreme utilisation of available space in the gill cavity through a very densely packed gill sieve. N. ophidion has a stationary mode of life and therefore has a less extreme gill anatomy.     

The source of lamellar mitochondria-rich cells in the air-breathing fish, Trichogaster leeri

Pavement cells and the mitochondria-rich cells (MRCs) are two of the main types of cells in fish gill epithelia. The pavement cells are generally responsible for gas exchange and MRCs for ion regulation. MRCs are found especially in the trailing edge and the interlamellar region of gill filament. In some species, MRCs are also observed in the gill lamellae. A previous study reported the likelihood of having lamellar MRCs in air-breathing fishes. Nevertheless, the source of lamellar MRCs is unclear. We used the air-breathing fish, Trichogaster leeri, to investigate the source of proliferated cells on the lamellae when 5-bromo-2-deoxyuridine (BrdU) was injected at different times before fish were sampled from deionized water. There were two major findings in this study. First, undifferentiated cells were found in the lamellae, as well as in the filaments. And, within 12-24 hr, a proliferated cell, identified as BrdU cell, could differentiate to an MRC in the gill lamellae. Second, the filaments and the lamellae in T. leeri responded to ionic stress differently but the proportion of the proliferated MRCs to the BrdU cells remained constant. Our results suggested that the lamellar MRCs were mainly differentiated from the cells that proliferated earlier from the lamellae.     

Morphology and distribution of blood fluke eggs and associated pathology in the gills of cultured Pacific bluefin tuna, Thunnus orientalis

Infestations of blood flukes of the genus Cardicola have been observed in juvenile Pacific bluefin tuna (PBT) cultured in Japan. Infected fish harbor large numbers of parasite eggs in their gills. Although the link between blood fluke infection and juvenile mortality is not clear, accumulation of parasite eggs appears to be pathogenic to the fish. We investigated the origins, general morphology/distribution, and histopathology of these eggs in artificially produced 0 yr old PBT. Dead and live fish were sampled on several occasions from two culture facilities in Wakayama prefecture, Japan. The number of eggs in each gill filament was enumerated under a microscope. In addition, we estimated the total number of eggs by dissolving the gills in a weak NaOH solution. We observed two morphologically distinct egg types in the gill filaments, smaller, oval shaped eggs in the gill lamellae and larger, crescent shaped eggs that occurred primarily in the filamentary arteries. Based on the ITS2 sequence, the ovoid and crescent shaped eggs were identified as C. orientalis and C. opisthorchis, respectively. Eggs of the former species were more abundant (maximum: 6400 per filament) than the latter (maximum: 1400), but the number was highly variable among filaments. The eggs of the latter species were relatively evenly distributed among the filaments. In a heavily infected individual, we estimated a total of >4.5 million eggs were present in the gills on one side of the fish. The number of eggs from the two species was positively correlated to each other and the dead fish tended to harbor more eggs than the live fish. Histological observation revealed host responses around the eggs, including encapsulation by fibroblasts and nodule formation, as seen in response to other aporocotylid eggs. In addition, we observed widespread fusion of gill lamellae and blockage of the filamentary arteries in some instances. Our results provide information that can be used for routine diagnosis of Cardicola blood flukes in cultured tuna and suggest they represent a risk to juvenile PBT.     

Functional morphology of gills and respiratory area of two active rheophilic fish species, Plagioscion squamosissimus and Prochilodus scrofa

Measurements of gill dimensions were carried out on two ecologically distinct active rheophilic teleost species, the curvina Plagioscion squamosissimus and the curimbatá Prochilodus scrofa , and were analysed in relation to body mass according to the equation Y=aW^b . The gill respiratory areas of P. squamosissimus and P. scrofa were large as expected for active fish and increased with increasing body mass ( b =0.70 and 0.72, respectively) showing no significant difference between them. However, the large respiratory area of both species was realized in a different way revealing an adaptation to the plasticity of head components related to feeding habits. Consequently, significant differences were found between the number and average length of gill filaments and the bilateral area of secondary lamellae. The respiratory area of P. scrofa was due mainly to larger bilateral surface area of the secondary lamellae and its growth coefficient ( b =0.51) that was significantly higher ( P <0.05) than that found for P. squamosissimus ( b = 0.36). The frequency of secondary lamellae mm⁻¹ of filament was similar in both species (22 ± 2 on one side of gill filament). The dimensions of gill components and the respiratory area of these species suggest a complex interaction between head form, and feeding habits related to the functional morphology of the gills to meet the oxygen requirements of each species.     

Morphometric examination of the gills of walleye, Stizostedion vitreum vitreum (Mitchill) and rainbow trout, Salmo gairdneri Richardson

Observations on the gill morphology of individual gill arches of walleye, Stizostedion vitreum vitreum and rainbow trout, Salmo gairdneri suggest that the first two arches account for the highest proportion of gill filament number, secondary lamellae number, lamellae area, and gill surface area. Interspecific comparisons suggest walleye contain a larger number of gill filaments, with a lower secondary lamellae count, but a larger gill surface area than a trout of the same weight. This is partially attributed to the larger surface area of each lamella in a walleye than in a trout.
A detailed examination suggests the surface area of a lamella is dependent on its position on the gill filament, and the position of the gill filament on the gill arch.     

Morphological, histochemical and immunohistochemical study of the gill epithelium in the abyssal teleost fish Coelorhynchus coelorhynchus

Histochemical and immunohistochemical study was carried out on nitrinergic innervation and neuroendocrine system in the gill epithelium of the abyssal fish Coelorhynchus coelorhynchus. The results showed that nNOS-positive nerve fibers, originating from the branchial arch were present in the subepithelial tissue of branchial primary filament. nNOS-positive neuroendocrine cells were also present in the primary filaments and secondary lamellae. Numerous mucous cells in the gill epithelium were AB/PAS-positive, while sialic acid was absent as confirmed by neuraminidase reaction and WGA lectin histochemistry. The mucus compounds in abyssal teleost fish are different from those found in pelagic species, being related to their living conditions. In abyssal species, greater numbers of chloride and neuroendocrine cells are involved in the movement of water and electrolytes. Neuroendocrine cells possess oxygen receptors which mediate the cardiovascular and ventilatory response to oxygen deficiency, as reported in teleost species. Besides, NO contributes through nervous stimulation to the regulation of vascular tone and blood circulation in the gill.     

Site preference of fish myxosporeans in the gill

In addition to the morphological and size characteristics of the spores, indicating the exact location and tissue specificity is also essential for differentiation of the large number of species belonging to the group of gill-parasitic fish, the myxosporeans. According to the observations of the present author, Myxobolus, Henneguya and Thelohanellus species are characterised by strict tissue specificity, and species showing affinity to the epithelium, connective tissue, cartilage or vascular tissue usually occur in a strictly defined location within the gill apparatus. Some of the species typically form plasmodia in the lamellae of the gill and others in the gill filaments. Yet other species develop their plasmodia at the base of the gill filament or in the gill arch. Instead of the generally accepted but misleading terms 'intra-' and 'interlamellar', the present author distinguishes interlamellar-epithelial and intralamellar-vascular types in the case of plasmodia developing in the gill lamellae, and intrafilamental-epithelial, intrafilamental-vascular and intrafilamental-chondroidal types in the case of plasmodia developing in the gill filaments. Regarding site of development within the gill, the location of basifilamental plasmodia and that of plasmodia developing in the cartilaginous matrix, connective tissue or blood vessels of the gill arch are well distinguishable from the above types. The different types and their variations are shown in histological illustrations.     

Scanning electron microscopy of the gills of a freshwater catfish,Rita Rita

Variations in the gross morphology and surface architecture of the gill filaments and secondary lamellae of a freshwater catfish (Rita rita) have been investigated using scanning electron microscopy. Heterogeneity of the gill has been correlated with the distribution of lamellar water-flow at different regions of a gill filament. Higher lamellar water flow (cc/pore/cmH₂O/sec) was estimated for the middle region of the filaments. The filaments are covered with epithelial cells whose surface is provided with well-developed microridges. The lamellae are generally covered with microvillous epithelial cells. The variations in surface architecture of the gill filaments and secondary lamellae have been correlated with their probable functions.     

Myxobolus goensis n. sp. (Myxozoa, Myxosporea, Myxobolidae), a parasite of the gills of Mugil cephalus (Osteichthyes, Mugilidae) from Goa, India

Two species of Myxobolus are reported from the gills of Mugil cephalus collected at Goa, India: M. goensis n. sp. and M. parvus Shulman, 1962. Myxobolus goensis n. sp. forms digitiform or rounded plasmodia between the gill rakers. Their spores are oval in frontal view, with tapered anterior extremity, and lemon-shaped in lateral view, measuring 9.7 (9.5-10.5) microm in length, 6.6 (6-7.5) microm in width, and 5.2 (5-6) microm in thickness. The polar capsules are pyriform and unequal in size. The larger ones are 5.3 (4.5-6) microm long and 2.4 (2-3) microm wide; the smaller ones are 2.4 (2-3) microm long and 1.8 (1.5-2) microm wide. The polar filament forms five turns aligned perpendicularly to the longitudinal axis of the larger polar capsules. Within the smaller polar capsules the polar filament is difficult to observe and, apparently, forms three coils. The spores are distinctly different from other Myxobolus species infecting M. cephalus and other Mugil spp. Furthermore, the present material is also different from 204 Myxobolus species presenting differently sized polar capsules, representing nearly all the known species with this characteristic. The fact that only the M. cephalus specimens were infected among a sample of 206 fish specimens, comprising 27 different species, strongly suggests that this parasite is specific to M. cephalus.