Surface area of the respiratory organs of the Climbing perch, Anabas testudineus (Pisces: Anabantidae)

Measurements have been made of the surface area of the gills and accessory respiratory organs of Anabas in the weight range 1–120 g, and the data analysed with respect to body weight using logarithmic transformations. The slope of the regression line for total gill area (0–615) is less than that found in most fish, the number of secondary lamellae/mm decreased more rapidly with body weight than for most water-breathing species (h = -0.152). The gill area of Anabas is relatively small but when the area of the accessory organs is added, the total respiratory area is of the same order as inactive water-breathing fish. The regression coefficient for combined areas of labyrinthine organs and lining of the suprabranchial chambers (0.713) exceeds that for the gills and together with other evidence (including estimates of diffusing capacity from morphological measurements), indicates an increasing importance of air-breathing of larger specimens. The average surface area of the accessory organs available for 1 ml of air within the suprabranchial chambers was found to be 2226 mm².     

Scanning electron microseopy of the respiratory surfaces of trout gills

Fixation of trout gills with different concentrations of glutaraldehyde has shown that the more concentrated solutions (25%) tended to produce clearer material for inspection under the scanning electron microscope. All gradations in surface sculpturing, from microvilli to microridges of about 13– 7–0 μm length have been observed, and their distribution on different parts of individual secondary lamellae is described. The possible significance of the types of sculpturing and their distribution is discussed in relation to the likely pattern of water flow across the secondary lamella during gill ventilation.     

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.     

A morphological study on posterior gills of the mangrove crab Ucides cordatus

Morphological and histological studies on posterior gills of the mangrove crab Ucides cordatus showed that the 5th gill (of 7) has a larger surface area and a greater number of lamellae compared to the 6th gill. Regular separation of gill lamellae, important when the gill is in air, is maintained by enlargements of the marginal canals. Conical, spine-like structures along the efferent vessel of both 5th and 6th gills were also observed. In addition, pillar cells, a discontinuous lamellar septum and a hypobranchial artery were observed. The presence of valve-like structures near the efferent vessel was also indicated. These structures, together with the pillar cells, may have a role in directing the hemolymph flow towards certain gills during particular physiological states. Localization of osmoregulatory epithelia in the lamellae of both gills was inferred from dimethylaminostyrylethylpyridiniumiodine staining. Apparently gills 5 and 6 have osmoregulatory epithelial cell patches of similar area, corresponding to 43% and 38% of the total lamellae area, respectively. However, their localization is quite different. Gill number 5 osmoregulatory patches seem to be restricted to the afferent region of the lamella whereas in gill number 6, they are more dispersed over the entire lamella. These differences may be related to the particular functional characteristics of these gills.     

Gross structure of the respiratory organs and dimensions of the gill in the mud–skipper, Periophthalmodon schlosseri (Bleeker)

In Periopkrlialnwdon scldosseri the respiratory organs consist of the gills, the suprabranchial and opercular chambers. The gills are more suited for aerial than aquatic respiration as is shown by the presence of the vascular papillae, blood sinusesand dilated blood vessels in their lamellae. The gill lamellae possess a surface coat of sulphated mucopolysaccharides that prevents water loss during exposure to the air. The filaments of the outer hemibranchs in the first gill arch are reduced to nearly one quarter of those of its posterior hemibranch. The gill area in relation to body weight shows a high slope value ( b =0·93).     

Morphometric analysis of the gills of the European eel, Anguilla anguilla

The gills of the European eel, Anguilla unguilla L. were analysed morphometrically. Fresh (unfixed) gills and resin-replica casts of the branchial vascular system were examined. The total gill surface area was found to be proportional to (body mas) 0-715 for fish of between 60 and 1 160 g. This relationship between gill surfxe area and body mass was maintained irrespective of a reduction in body mass produced by fasting. Vessel dimensions were obtained from the vascular casts. Calculations made using these values suggest that the major sites of gill vascular resistance lie at the level of the afferent lamellar arterioles and the secondary lamellae.     

Functional respiratory anatomy of a deep-sea orbiniid polychaete from the Brine Pool NR-1 in the Gulf of Mexico

Abstract. An undescribed species of Orbiniidae (Annelida; Polychaeta) is found in large numbers associated with communities of the mussel, Bathymodiolus childressi at hydrocarbon seeps on the Louisiana slope (Gulf of Mexico). Their microhabitat is often hypoxic and sulfidic, which poses serious respiratory challenges for an aerobic metazoan. They display several anatomical features that are quite unusual for this family, which likely allow them to live in their food-rich, but oxygen-limited, habitat. The anterior gills are hypertrophied whereas the posterior gills are not. These anterior gills provide the worms with a large gill surface area (≤9.9 cm²/g wet weight), which represents 90–95% of the total gill surface area. The gills contain two blood vessels: a central blood vessel, delimited by a coelomic epithelium, and an intra-epidermal vessel. The diffusion distance between this latter and the environment is only 3 μ-m in the anterior gills, which facilitates gas diffusion. Only the anterior gills are ciliated, which may also facilitate gas exchange across this respiratory surface. The gill cells also contain numerous mitochondria and other electron-dense organelles that might be involved in sulfide detoxification.     

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.     

Scanning electron microscopy of the respiratory surfaces of Saccobranchus (=Heteropneustes) fossilis (Bloch)

Summary The gill secondary lamellae are generally covered with epithelial cells whose outer surfaces form numerous microvilli. The surface of the primary lamellae is characterised by microridges. A particular type of surface sculpturing seems to be associated with given cell boundaries.Further evidence for the derivation of the air tube and fans which guard its entrance by modification of the basic gill structure has been obtained from both the gross surface architecture and microstructure of the individual cell surfaces. Secondary lamellae are represented by stubby projections which generally have a biserial arrangement. The outer surfaces of the epithelia overlying the capillaries of these respiratory islets are coated with microvilli as in the secondary lamellae. On the other hand, the relatively smooth-surfaced lanes between groups of respiratory islets have a microridged surface similar to that of the primary gill lamellae.It is suggested that previous estimates of surface area, and consequently diffusing capacities of the air-breathing organ, have been low in view of the increased surface, due to both their gross and microstructure. Estimates for gill surface area may need very little correction as the spaces between the microvilli and microridges are probably filled with mucus under normal conditions.We thank Mr. John Clements for his excellent technical assistance and the Department of Botany, Bristol University for the use of their scanning electron microscope     

The gill of fish larvae. Is it primarily a respiratory or an ionoregulatory structure?

Based on surface area and chloride cell number, rainbow trout Oncorhynchus mykiss gills appear initially to be more important in terms of ion balance than gas exchange. Chloride cells appear on the gill 3–6 days before hatch at 10°C. This is about 9 days before secondary lamellae, the definitive adult gas exchange structure, begin to form. At hatch, 22% of all chloride cells but only 7% of total surface area are located on the gill. This discrepancy gradually diminishes but even at complete yolk absorption the gill still seems to be about twice as important in terms of ion balance (75% of chloride cells) as gas exchange (37% of total surface area represented by gill filaments and lamellae combined). Surface area measurements and chloride cell counts reported in the literature for larvae of other species show a similar pattern suggesting that this may be a general phenomenon. If true, the implications are profound not only for developmental physiologists but also for those interested in the evolutionary history of gills and their function in adult fish.     

Estimation of oxygen-diffusing capacity in the gills of different sizes of a tilapia, Oreochromis niloticus

Measurements on gills of features that affect gas exchange have been studied in relation to body weight in specimens (0.0112–812.3 g) of a tilapia, Oreochromis niloticus . The data were analysed with respect to body weight by means of logarithmic transformations (log Y = log a+b log W ). The slopes ( b ) of the log/log regression lines for the gill area, harmonic mean diffusion distance and oxygen diffusing capacity were 0.777, 0.077 and 0.700, respectively. The gill respiratory area of O. niloticus (Trewavas) increases as the fish develops because the number and bilateral area of secondary lamellae increase. The scaling value for oxygen-diffusing capacity is less than the value for gill area because of the slight increase in harmonic mean diffusion distance with development.     

Gill Morphometrics of the Lampreys Lampetra fluviatilis (L.) and Lampetra planeri (Bloch)

Morphometric measurements have been made on various gill components of different stages in the life cycle of the anadromous parasitic lamprey, Lampetra fluviatilis, and its nonparasitic derivative Lampetra planeri. The total gill area, expressed in terms of body weight, of both larval (1462–2717 mm² g^–1) and adult (1402–2337 mm² g^–1) L. fluviatilis are greater than those previously recorded in the rather meagre literature on lamprey gill measurements and are comparable with those found in the most active teleosts. The gills of the two Lampetra species are apparently identical in the larval stages and those of metamorphosing and adult L. planeri are similar to those of metamorphosing L. fluviatilis. Although the pharyngeal arrangement of lampreys differs greatly from that of teleosts, there are many features of the gills indicative of convergence between the two groups. Thus, in a given stage in the life cycle of lampreys, the secondary lamellae on either side of the filaments also alternate, become more widely spaced as the filament length increases and increase in area as the body weight becomes greater. Furthermore, the fractional cumulative increase in secondary lamellae area along a line following the presumed direction of water flow is also represented by a sigmoid curve. While at metamorphosis the pharynx becomes considerably modified to accommodate the change from a unidirectional to a tidal respiratory water flow, the total gill areas of the ammocoete are similar to those of metamorphosing stages which have attained adult characteristics. However, there are clearly differences in some of the components that influence and contribute towards the total gill area. Thus, in terms of body weight, the number and total length of the filaments and the total number of secondary lamellae, together with the number of secondary lamellae found on a given distance of filament, are greater in late metamorphosing stages, while the reverse is true for the average bilateral area of the secondary lamellae which is considerably greater in ammocoetes.     

Studies on the extent of gill surface in a fresh water cat-fish Bagarius bagarius (Ham.).

The total gill area of the fish ranges from 37,537 to 56,551 lamellae. The number of lamellae per mm of the gill filament and area of lamellae knowing the respiratory gill area, the gill area per g of body weight and per cm3 of body volume were calculated to correlate the variation in gill surface area per unit weight and volume of the fish. The fish can survive for quite long out of water as the lamallae are spaced wide apart and do not adhere together.     

Gross structure and dimensions of the gill in an air-breathing estuarine goby,Pseudapocryptes lanceolatus

The gills of the air-breathing estuarine goby,Pseudapocryptes lanceolatus, are reduced owing to the development of a specialized organ of O₂ uptake from air. In the first gill arch, the filaments of the outer hemibranch are reduced to nearly one-half in comparison to those of its inner hemibranch. A smaller number of secondary lamellae per mm (27.6) occurring on one side of the gill filament reduces the gill surface area. A bilogarithmic plot of the gill area and the body weight indicates a curve with two significantly different components, one (b = 0.924) related to the fish weighing up to 6 g and the other (b = 0.405) to the fish weighing 8 g and above.     

The structure of the gill of the trout,Salmo gairdneri (Richardson)

Summary A light and electron microscopic study was made of the structure of the gill arch, filament and secondary lamella of Salmo gairdneri R. Blood pathways through the gill were traced from serial histological sections, and from the examination of ink perfused tissue and perspex casts formed following resin injection of the circulatory system.The epithelium covering the gill consists of unspecialized, dark, chloride and mucous cells. The distribution of specialized cells appears to be related to gill function. The basement membrane underlying the epithelium consists of three layers, the inner collagen layer being continuous with the connective tissue core of the gills.Blood supply to the secondary lamellar respiratory surface is via branchial, filament and secondary lamellar arteries. Blood spaces of the secondary lamellae are delimited by pillar cells containing what appears to be contractile material. The marginal channel of each lamella is bounded distally by cells of endothelial origin. A network of lymph spaces within the filaments connects with efferent branchial arteries. Nutritionary capillaries within the filaments connect with afferent branchial arteries. No shunts between afferent and efferent filament arteries were found.Data from this study and previous physiological and histopathological studies suggest a mechanism for the control of blood flow to suit the respiratory requirements of the fish. This mechanism involves a system of recruitment of additional respiratory units and changes in overall blood flow patterns.This work formed part of a thesis submitted for the degree of Doctor of Philosophy in 1971 and for which M. M. was in receipt of a studentship from the Natural Environmental Research Council. The authors are grateful for the support given by research grants from the M.R.C (P.T.) and the N.E.R.C. (M.M.), and to Prof. G. M. Hughes in whose department the work was carried out.     

Functional Organization of the Teleost Gill

The circulation of the gills has been studied in the perch, trout and eel combining the conventional histological methods and casting techniques. The existence of two blood pathways in each gill arch was confirmed. 1 — An arterio-arterial pathway assuming the respiratory function. It includes the afferent branchial artery and in each primary lamella the afferent primary artery, the secondary lamellae capillaries and the primary and branchial efferent arteries. 2 — An arterio-venous pathway arising from both the branchial artery, in the gill arch, and the primary arteries in each primary lamella. This pathway includes the central venous sinus of the primary lamella, several small veins and is finally connected with the branchial veins. 3 — The lack of connections between afferent primary arteries and cvs in the trout and the perch makes impossible a direct blood flow from the afferent to the efferent artery (shunt). In the eel connections between cvs and both afferent and efferent arteries do not mean that a shunt is operating according to the pressure gradient.     

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 STRUCTURE OF FISH GILLS IN RELATION TO THEIR RESPIRATORY FUNCTION

1. The general structure of the gills of different fishes is compared and it is concluded that, though essentially the same, there are certain differences by which they can be recognized. Possible ways in which they may have evolved from one another are considered. 2. A detailed account is given of the structure of the secondary lamellae, where gaseous exchange takes place, and it is shown that two epithelial sheets are separated by a vascular axis mainly composed of pillar cells overlain by a basement membrane on each side. Blood pathways through the gills are discussed in relation to their respiratory function. 3. The embryonic development of gills is described and evidence regarding homo-logies of different structures, particularly the pillar cells, is reviewed. 4. The gills of fish having different modes of life show variations in (a) the number of arches, (b) the number and length of the gill filaments, and (c) the size and frequency of the secondary lamellae. Ways in which measurements of gill area may be carried out and some of the complications involved are reviewed and a summary given of measurements made for a wide variety of species. Measurements of the thickness of the water-blood barrier are also discussed; the more active fish generally have thinner water-blood barriers and larger gill areas. 5. The different mechanisms of gill ventilation are summarized and characteristics of gill resistance in elasmobranchs and teleosts are compared. Gas exchange is discussed in relation to available techniques and the current terminology and symbols, and to indicate the value of analogies between gill exchangers and systems studied by engineers. 6. It is outlined how studies of the functioning of gills during coughing, parasitic infection, and in polluted waters add to knowledge of their role in respiration.     

Respiratory gill surface of the serrasalmid fish, Piaractus mesopotamicus

Gill element dimensions of pacu Piaractus mesopotamicus were estimated and correlated to body mass ( W ), according to the power equation Y=aW^b . The filament number ( b =0.154) and length ( b =0.457) increased with body mass, markedly influencing the respiratory gill surface area ( b =0.769). The high filament number and length, associated with a high secondary lamellae frequency ( a =40.21), are typical of active fish species and may be an adaptation to its migratory movements during reproduction. The comparatively small dimensions of its secondary lamellae are found more commonly in less active species, and may be related to the environmental conditions prevailing in lentic environments, where the species is normally found most of the year. Such features, together with its ability to compensate for oxygen reduction by means of a high ventilatory volume, and the use of aquatic surface respiration (ASR), may account for its adaptative capacity to withstand hypoxic conditions, with a low respiratory energy cost.