O2 uptake through water during early life of Heteropneustes fossilis (Bloch)

The O₂ uptake through water has been measured in case of Heteropneustes fossilis during development and growth and its relationship to body size established. A higher rate of O₂ uptake during the early phase of ontogenesis is related to intense growth of the respiratory surface area and increasing metabolic demand of the fish.The logarithmic plot of data for O₂ uptake in relation to body size shows a statistically significant two-component curve; one related to the fish when it is a fully aquatic breather and the other when it changes to bimodal gas exchange. The onset of the air breathing habit brings about a 40% drop in O₂ uptake through water, which is made good through the newly developed air breathing organ.     

Oxygen uptake during early life in the fresh water fish, Esomus danricus (Ham) (Pisces, Cypriniformes)

O2 uptake in Esomus danricus has been determined in relation to body weight, length and thickness of the water-blood diffusion barrier at 27-28 degrees C temperature. Total O2 consumption in larvae was 1311 ml/kg/h but decreased significantly in juvenile fishes (720 ml/kg/h). The increase in the thickness of water-blood diffusion barrier at the secondary gill lamellae of the fish was found to be an important factor for the decrease in VO2. Logarithmic analyses of data for O2 uptake in relation to body weight gave a slope of 0.8865 for larvae and 0.5053 for juveniles. The exponent values of O2 uptake against diffusion barrier for larvae and juveniles were 1.7383 and 2.0956, respectively. The results obtained indicated that fish have an extra device which helps in extracting about 24% of the total VO2 required for the fulfilment of the metabolic oxygen demand of the body.     

Bimodal oxygen uptake in juveniles and adults amphibious fish,Channa (= Ophiocephalus) marulius

Oxygen uptake of Channa marulius was studied under water with and without access to air. There was a significant increase in the oxygen uptake through the gills when access to air was prevented. However, this value (0.863 ± 0.058 mlO₂/indiv./h) was quite low in comparison to the total bimodal oxygen uptake (2.04 ± 0.14 mlO₂/indiv./h) in juveniles. In adult fish the oxygen uptake per unit time increased appreciably (4.673 ± 0.404 mlO₂/indiv./h). In juveniles as well as in adults the air breathing dominated over aquatic breathing. This fish showed a definite circadian rhythm in the bimodal oxygen uptake during different hours of the day.This work was performed in the Ichthyology Laboratory, P. G. Dept. of Zoology, Bhagalpur University, and was supported by a research grant from Bhagalpur University     

Oxygen uptake capacity of gills and skin in relation to body weight of the air-breathing siluroid fish, Clarias batrachus (Linn.).

Oxygen consumption through gills and skin in relation to body weight was estimated in the air-breathing catfish, Clarias batrachus, under two experimental conditions, viz., (i) when access to air was allowed and (ii) when air-breathing was prevented. There was a positive correlation between VO2 (ml/hr) and body weight in both experimental conditions. Oxygen consumption (ml/hr) increased by a power of 0.869 when access to air was allowed whereas the power was slightly less (b = 0.841) when air-breathing was prevented. As the values for exponent (b) were less than 1.0, the weight specific VO2 (ml/kg/hr) decreased with increasing body weight. The decrease was more marked (b = - 0.180) in fishes which were not allowed air than in those where access to air was allowed (b = - 0.148). Under normal conditions of water and air-breathing the rate of VO2 (ml/kg/hr) via gills and skin from water ranged from 39.7 +/- 3.21 to 76.7 +/- 9.01 and this increased to 42.17 +/- 6.2 to 105.9 +/- 8.33 when air-breathing was prevented. The increase in the rate of VO2 was perhaps associated with the increase in the volume of water irrigating the gills per unit time.     

Cutaneous gas exchange in snakes

Summary Cutaneous aquatic gas exchange and pulmonary gas exchange have been compared in an aquatic snakeAchrochordus javanicus and the terrestrial snakeConstrictor constrictor.Gas exchange was measured by closed respirometry with the snakes in air and in water with access to air. Frequency of air breathing, tidal volumes and total lung volumes were also compared in the two species. All measurements were done at 20–22 ° C.The aquaticAchrochordus showed long periods of apnea in submerged condition interrupted by short periods of breathing activity at the surface. Average frequency of air breathing activity was 2.6 times per hour. Breathing in constrictor was more frequent but irregular with an average frequency of 143 breaths per hour.Total lung volume was 66±31 ml/kg body weight and 72.5±59 ml/kg body weight inAchrochordus andConstrictor, respectively. Tidal volumes were 41.5±4.4 ml/kg body weight and 29.5±14.8 ml/kg body weight, largest inAchrochordus. Constrictor had the highest total O₂ uptake ( ) correlating with a higher activity. Total gas exchange ratio (R _E ) was 0.69 forConstrictor and 0.77 forAchrochordus. InConstrictor air breathing accounted for 97% of the total whereas 21% of the CO₂ exchange was aquatic. Corresponding figures forAchrochordus were 92% of total by air breathing with as much as 33% of the CO₂ elimination as aquatic gas exchange.The results demonstrate that the trend among early air breathing vertebrates (fishes and amphibians) of a conservative evolution of CO₂ elimination by air breathing also extends to snakes.Significantly the cutaneous exchange component was highest in the more aquatic species.The results are discussed in relation to recent reports of a higher than alleged role of the skin of reptiles in evaporative water loss.This study was supported by grant HE 12071 from the National Institutes of Health in the U. S. A.     

Partitioning of respiration between the gills and air-breathing organ in response to aquatic hypoxia and exercise in the pacific tarpon, Megalops cyprinoides

The evolution of air-breathing organs (ABOs) is associated not only with hypoxic environments but also with activity. This investigation examines the effects of hypoxia and exercise on the partitioning of aquatic and aerial oxygen uptake in the Pacific tarpon. The two-species cosmopolitan genus Megalops is unique among teleosts in using swim bladder ABOs in the pelagic marine environment. Small fish (58-620 g) were swum at two sustainable speeds in a circulating flume respirometer in which dissolved oxygen was controlled. For fish swimming at 0.11 m s(-1) in normoxia (Po2 = 21 kPa), there was practically no air breathing, and gill oxygen uptake was 1.53 mL kg(-0.67) min(-1). Air breathing occurred at 0.5 breaths min(-1) in hypoxia (8 kPa) at this speed, when the gills and ABOs accounted for 0.71 and 0.57 mL kg(-0.67) min(-1), respectively. At 0.22 m s(-1) in normoxia, breathing occurred at 0.1 breaths min(-1), and gill and ABO oxygen uptake were 2.08 and 0.08 mL kg(-0.67) min(-1), respectively. In hypoxia and 0.22 m s(-1), breathing increased to 0.6 breaths min(-1), and gill and ABO oxygen uptake were 1.39 and 1.28 mL kg(-0.67) min(-1), respectively. Aquatic hypoxia was therefore the primary stimulus for air breathing under the limited conditions of this study, but exercise augmented oxygen uptake by the ABOs, particularly in hypoxic water.     

Air breathing of the neotropical fishes Lepidosiren paradoxa, Hoplerythrinus unitaeniatus and Hoplosternum littorale during aquatic hypoxia

The present study investigated the respiratory rates, frequency of air breathing and ability to extract oxygen from air compared to body mass of three neotropical air-breathing fishes (Lepidosiren paradoxa, Hoplerythrinus unitaeniatus and Hoplosternum littorale) with different accessory organs, under the same conditions of hypoxia (PO(2)<5 mm Hg) and temperature (25 degrees C), using the same apparatus. The results indicated a superior capacity of H. littorale (16.01 ml O(2) breath(-1) kg(-1)) compared to H. unitaeniatus (7.03 ml O(2) breath(-1) kg(-1)) and L. paradoxa (4.95 ml O(2) breath(-1) kg(-1)).     

Continuous measurement of oxygen tensions in the air-breathing organ of Pacific tarpon (Megalops cyprinoides) in relation to aquatic hypoxia and exercise

The Pacific tarpon is an elopomorph teleost fish with an air-breathing organ (ABO) derived from a physostomous gas bladder. Oxygen partial pressure (PO₂) in the ABO was measured on juveniles (238 g) with fiber-optic sensors during exposure to selected aquatic PO₂ and swimming speeds. At slow speed (0.65 BL s⁻¹), progressive aquatic hypoxia triggered the first breath at a mean PO₂ of 8.3 kPa. Below this, opercular movements declined sharply and visibly ceased in most fish below 6 kPa. At aquatic PO₂ of 6.1 kPa and swimming slowly, mean air-breathing frequency was 0.73 min⁻¹, ABO PO₂ was 10.9 kPa, breath volume was 23.8 ml kg⁻¹, rate of oxygen uptake from the ABO was 1.19 ml kg⁻¹ min⁻¹, and oxygen uptake per breath was 2.32 ml kg⁻¹. At the fastest experimental speed (2.4 BL s⁻¹) at 6.1 kPa, ABO oxygen uptake increased to about 1.90 ml kg⁻¹ min⁻¹, through a variable combination of breathing frequency and oxygen uptake per breath. In normoxic water, tarpon rarely breathed air and apparently closed down ABO perfusion, indicated by a drop in ABO oxygen uptake rate to about 1% of that in hypoxic water. This occurred at a wide range of ABO PO₂ (1.7–26.4 kPa), suggesting that oxygen level in the ABO was not regulated by intrinsic receptors.     

Amphibious adaptations in a newly recognized amphibious fish: Terrestrial locomotion and the influences of body size and temperature

Amphibious animals are adapted for both aquatic and terrestrial habitats. The conflicting requirements for dual habitats are perhaps most pronounced in the air‐breathing fishes, which represent an intermediate stage between the totally aquatic habitat and terrestrial colonization. A key requirement for amphibious fishes is terrestrial locomotion. The different densities and compositions of air and water impose constraints for efficient terrestrial locomotion that differ from those required for aquatic locomotion. I investigated terrestrial locomotion in a small South African fish, Galaxias ‘nebula’, by exposing 60 individual fish to air in specially designed raceways and quantifying movement type and occurrence as a function of availability of water, fish size and environmental temperature. Nebula showed a sustained undulating form of terrestrial locomotion characteristic of amphibious fishes and also a transient ballistic locomotion (jumps) typical of fully aquatic species. Terrestrial movement was influenced by fish size, with medium‐sized fish undertaking more jumps towards water, and fewer jumps away from water, than their smaller or larger conspecifics. In contrast, axial undulation was mainly influenced by temperature. However, there was no consistent pattern in temperature effects presumably because temperature is just one of a suit of environmental factors that may affect terrestrial locomotion. Nebula's amphibious adaptations allow it to cope with the unpredictability inherent in its natural environment.     

Respiratory gas exchange in the airbreathing fish,Synbranchus marmoratus

Synopsis The partitioning of O₂ uptake between aquatic and aerial gas exchange and its dependence on ambient water PO₂ was studied in the facultative air breathing teleost Synbranchus marmoratus, after acclimation to well aerated water and after acute and chronic exposure to hypoxic water. O₂ uptake was also studied following acute air exposure and after prolonged entrapment in soil. Breathing rates during water and air breathing in response to reduced water PO₂ and tidal volume during air breathing were also studied. S. marmoratus satisfies its O₂ requirement by water breathing alone until water PO₂ falls below 30–50 mm Hg (switching PO₂) depending on the acclimation history. Below the switching PO₂, air breathing is adopted while active water breathing stops. The O₂ uptake varied little for all groups when the principal mode of gas exchange changed at the switching PO₂. The highest O₂ uptake prevailed when the fish employed the mode of gas exchange in operation during the acclimation period (i.e. water breathing for normoxia-acclimated, air breathing for hypoxic-acclimated).Acclimation to chronic hypoxia gave a much higher switching PO₂ 55 mm Hg) than for the other groups (about 30 mm Hg). S. marmoratus maintained its O₂ uptake when acutely exposed to air. When entrapped in soil in an aestivating state, the O₂ uptake was reduced to 25% of that in water or during acute air exposure. The overall gas exchange ratio for air breathing was very low (R_E 0.1).Branchial water pumping increased with lowering of water PO₂. The rate of air breathing was independent of water PO₂.The findings are discussed in the light of the ecophysiological conditions confronting S. marmoratus.     

Oxygen uptake through water during early life of Anabas testudineus (Bloch)

The O₂ consumption (mg/hr) through water in case of Anabas testudineus during development and growth has been measured and its relationship to body weight or length studied.The logarithmic plot of 02 uptake through water either against body weight or length suggested a statistically significant (P > 3.53) two-component curve, the point of intersection being at 11 mg body weight and 1.78 cm body length. These are the theoretical values of weight or length at which the responsibility of supplementing nearly 40% of the total O₂ demand through the newly developed air breathing organ falls in the early life of the fish. One of the impelling causes forcing developing fry of Anabas to adopt a bimodal gas exchange machinery seems to be 4 fold increase in the diffusion distance at the gills.     

Oxygen consumption, carbon dioxide excretion and respiratory quotient of larval lampreys (Mordacia mordax) in air

The standard rates of O2 consumption of larval Mordacia mordax (weight range 1.3-2.3 g), after these ammocetes had been in humidified air for 18 hr, were 26.8, 46.3 and 71.2 microL x g(-1) x hr(-1) at 10, 15 and 20 degrees C, respectively. The corresponding rates of CO2 excretion were 20.7, 35.6 and 54.1 microL x g(-1) x hr(-1). The RQs at the three temperatures were essentially identical (0.76 or 0.77) and similar to that of adults of the lamprey Geotria australis in air at 15 degrees C. The above RQs for ammocoetes, which are probably similar to those that would be recorded in water, are consistent with the view that the aerobic respiration of these animals relies predominantly on lipid as an energy source, but that some energy is derived from carbohydrate and/or protein. The RQs for larval and adult lampreys in air lie well within the range recorded for amphibious fishes in air.     

Respiratory vasculatures of the intertidal air-breathing eel goby, <Emphasis Type="Italic">Odontamblyopus lacepedii</Emphasis> (Gobiidae: Amblyopinae)

Lacking a propensity to emerge over the mud surface, the eel goby, Odontamblyopus lacepedii, survives low tide periods by continuously breathing air in burrows filled with hypoxic water. As with most marine air-breathing fishes, O. lacepedii does not possess an accessory air-breathing organ, but holds air in the buccal–opercular cavity. The present study aimed to clarify how the respiratory vasculature has been modified in this facultative air-breathing fish. Results showed that the gills apparently lacked structural modifications for air breathing, whereas the inner epithelia of the opercula were richly vascularized. Comparison with two sympatric gobies revealed that the density of blood capillaries within 10μm from the inner opercular epithelial surface in O. lacepedii (14.5 ± 3.0 capillaries mm⁻¹; mean ± s.d., n = 3) was significantly higher than in the aquatic non-air-breathing Acanthogobius hasta (0.0 ± 0.0) but significantly lower than in the amphibious air-breathing mudskipper, Periophthalmus modestus (59.1 ± 8.5). The opercular capillary bed was supplied predominantly by the 1st efferent branchial arteries (EBA1) and drained by the opercular veins, which open into the anterior cardinal vein. Deep invaginations at the distal end of the EBA1 and the junction with EBA2 are suggestive of blood flow regulatory sites during breath-holding and apnoeic periods. It remains to be investigated how blood flow through the gills is maintained during breath holding when the buccal–opercular cavity is filled with air.     

Biological Control of Culex pipiens pattens (Diptera, Culicidae) by the Release of Fish Muddy Loach, Misgurnus mizolepis in Natural Ponds, Korea

ABSTRACT An assessment on the biological control potential with the fish muddy loaches (Misgurnus mizolepis) was conducted against naturally bred Culex pipiens pollens larvae in four ponds (A, B, C and D) in Busan from July through September, 2001. Predation of the fish at 3 different release rates of 4,5, and 6 fish/m² resulted in mostly over 90% mosquito control from the first week after treatment through the end of the survey period for 11 weeks. There were no significant difference among the release rates of fish at the 5% level of probability. However, substantial controls of 43.0% and 25.9% were obtained from pond C during the 3rd and 7th weeks after the fish introduction, respectively. The results of those two weeks showed a lower biological control by the introduced larvivorous fishes. This might be due to the presence of heavy organic matters including aquatic weeds and/or severely polluted water from sewage in pond C. The aquatic weeds covered the pond's water surface which may have affected the deterioration of mosquito preying in favor of aquatic weeds. Also, the fishes were observed to avoid severely contaminated sewage water in some parts of ponds A and C where more mosquito larvae were found.     

Gross and fine anatomy of the respiratory vasculature of the mudskipper,Periophthalmodon schlosseri (Gobiidae: Oxudercinae)

To illustrate vascular modification accompanying transition from aquatic to amphibious life in gobies, we investigated the respiratory vasculatures of the gills and the bucco‐opercular cavities in one of the most terrestrially‐adapted mudskippers, Periophthalmodon schlosseri, using the corrosion casting technique. The vascular system of Pn. schlosseri retains the typical fish configuration with a serial connection of the gills and the systemic circuits, suggesting a lack of separation of O₂‐poor systemic venous blood and O₂‐rich effluent blood from the air‐breathing surfaces. The gills appear to play a limited role in gas exchange, as evidenced from the sparsely‐spaced short filaments and the modification of secondary lamellar vasculature into five to eight parallel channels that are larger than red blood cell size, unlike the extensive sinusoidal system seen in purely water‐breathing fishes. In contrast, the epithelia of the bucco‐opercular chamber, branchial arches, and leading edge of the filaments are extensively laden with capillaries having a short (<10 μm) diffusion distance, which strongly demonstrate the principal respiratory function of these surfaces. These capillaries form spiral coils of three to five turns as they approach the epithelial surface. The respiratory capillaries of the bucco‐opercular chamber are supplied by efferent blood from the gills and drained by the systemic venous pathway. We also compared the degree of capillarization in the bucco‐opercular epithelia of Pn. schlosseri with that of the three related intertidal‐burrowing gobies (aquatic, non‐air‐breathing Acanthogobius hasta; aquatic, facultative air‐breathing Odontamblyopus lacepedii; amphibious air‐breathing Periophthalmus modestus) through histological analysis. The comparison revealed a clear trend of wider distribution of denser capillary networks in these epithelia with increasing reliance on air breathing, consistent with the highest aerial respiratory capacity of Pn. schlosseri among the four species. J. Morphol. 2011. © 2011 Wiley‐Liss, Inc.     

A comparison of adrenergic stress responses in three tropical teleosts exposed to acute hypoxia

Experiments were performed to assess the afferent and efferent limbs of the hypoxia-mediated humoral adrenergic stress response in selected hypoxia-tolerant tropical fishes that routinely experience environmental O(2) depletion. Plasma catecholamine (Cat) levels and blood respiratory status were measured during acute aquatic hypoxia [water Po(2) (Pw(O(2))) = 10-60 mmHg] in three teleost species, the obligate water breathers Hoplias malabaricus (traira) and Piaractus mesopotamicus (pacu) and the facultative air breather Hoplerythrinus unitaeniatus (jeju). Traira displayed a significant increase in plasma Cat levels (from 1.3 +/- 0.4 to 23.3 +/- 15.1 nmol/l) at Pw(O(2)) levels below 20 mmHg, whereas circulating Cat levels were unaltered in pacu at all levels of hypoxia. In jeju denied access to air, plasma Cat levels were increased markedly to a maximum mean value of 53.6 +/- 19.1 nmol/l as Pw(O(2)) was lowered below 40 mmHg. In traira and jeju, Cat release into the circulation occurred at abrupt thresholds corresponding to arterial Po(2) (Pa(O(2))) values of approximately 8.5-12.5 mmHg. A comparison of in vivo blood O(2) equilibration curves revealed low and similar P(50) values (i.e., Pa(O(2)) at 50% Hb-O(2) saturation) among the three species (7.7-11.3 mmHg). Thus Cat release in traira and jeju occurred as blood O(2) concentration was reduced to approximately 50-60% of the normoxic value. Intravascular injections of nicotine (600 nmol/kg) elicited pronounced increases in plasma Cat levels in traira and jeju but not in pacu. Thus the lack of Cat release during hypoxia in pacu may reflect an inoperative or absent humoral adrenergic stress response in this species. When allowed access to air, jeju did not release Cats into the circulation at any level of aquatic hypoxia. The likeliest explanation for the absence of Cat release in these fish was that air breathing, initiated by aquatic hypoxia, prevented Pa(O(2)) values from falling to the critical threshold required for Cat secretion. The ventilatory responses to hypoxia in each species were similar, consisting generally of increases in both frequency and amplitude. These responses were not synchronized with or influenced by plasma Cat levels. Thus the acute humoral adrenergic stress response does not appear to stimulate ventilation during acute hypoxia in these tropical species.     

Hydrogen shuttles in air versus water breathing fishes.

1. The malate-aspartate cycle was demonstrable in subcellular preparations of hearts from Arapaima, Lepidosiren, and Synbranchus (obligate air breathers), Hoplerythriunus (facultative air breather), and Osteoglossum and Hoplias (obligate water breathers). 2. Although no respiratory evidence for significant alpha-glycerophosphate cycle participation could be shown in the air breathers, this cycle was demonstrable in hearts of water breathers. 3. In agreement with the O2 uptake studies, it was possible to reconstruct the malate-aspartate, but not the alpha-glycerophosphate cycle, in isolated mitochondria from air breathers, while both shuttles could be reconstructed with heart mitochondria in the case of water breathing fishes.     

The occurrence of aerial respiration in Rhinelepis strigosa during progressive hypoxia

Rhinelepis strigosa did not surface for air breathing in normoxic or moderate hypoxic water. This species initiated air breathing when the P _io₂ in the water reached 22 ± 1 mmHg. Once begun, the air-breathing frequency increased with decreasing P _io₂. Aquatic oxygen consumption was 21·0 ± 1·9ml O₂ kg⁻¹h⁻¹ in normoxic water, and was almost constant during progressive hypoxia until the P _io₂ reached 23·9 mmHg, considered the critical oxygen tension (P_co₂). Gill ventilation increased until close to the P _co₂ (7·9-fold) as a consequence of a greater increase in ventilatory volume than in breathing frequency. Gill oxygen extraction was 42 ± 5% and decreased with hypoxia, but under severe hypoxia returned to values characteristic of normoxic. The critical threshold for air breathing was coincident with the P_co₂ during aquatic respiration. This suggests that the air-breathing response is evoked by the aquatic oxygen tension at which the respiratory mechanisms fail to compensate for environmental hypoxia, and the gill O₂ uptake becomes insufficient to meet O₂ requirements.     

Tolerance of forced air emergence by a fish with a broad vertical distribution, the rockpool blenny, Hypsoblennius gilberti (Blenniidae)

Many intertidal fishes, particularly among the Blenniidae and Cottidae, possess amphibious adaptations, including the ability to breathe in air and to avoid desiccation in terrestrial conditions. These traits are absent in subtidal species of blennies and cottids. Hypsoblennius gilberti, the rockpool blenny, is found in shallow rockpools in the mid to high intertidal areas of Southern California, and deeper to 18 m in the subtidal zone. This broad vertical distribution could indicate that this blenny is adapted for tidal air emergence, although H. gilberti has not been observed out of water in its natural habitat. H. gilberti does not emerge voluntarily from hypoxic sea water in the laboratory, but it easily withstands 3 h out of water. The aerial respiratory exchange ratio (CO2 released compared to O2 consumed) is 0.70, similar to that of amphibious intertidal fishes in air, indicating sufficient release of metabolically produced CO2 while emerged. There is no increase in aquatic respiration following emergence. However, unlike other amphibious fishes that maintain aerial oxygen consumption at a level similar to aquatic oxygen consumption, H. gilberti has an aerial oxygen consumption rate one-third that in water. H. gilberti can recover rapidly from terrestrial water loss, and shows no change in evaporative water loss rates at 93% and 77% relative humidities. The amphibious capabilities in H. gilberti, even if rarely used, permit survival in air during tidal emergence. These findings suggest that H. gilberti may demonstrate an intermediate condition between the amphibious species of intertidal fishes that regularly emerge from water, and the subtidal fishes that do not survive air emergence and are completely restricted to an aquatic habitat.     

Three species of fishes from an eutrophic, seasonally alkaline lake are not more tolerant to acute exposure to high pH in the laboratory

A number of different freshwater fish species (perch Perca fluviatilis , roach Rutilus rutilus and rudd Scardinius erythrophthalamus ) from either eutrophic (Slapton Ley, a seasonally alkaline lake) or non-eutrophic waters were compared with respect to their sodium uptake kinetics and tolerance to acute (1 h) exposure to pH 9·5. Further comparisons were made with rainbow trout Oncorhynchus mykiss and brown trout Salmo trutta . The influence of fish size was also investigated in rainbow trout. Exposure to pH 9·5 was found to disrupt sodium balance and inhibit ammonia excretion in all species and sizes of fishes. The origin of fishes did not have a significant effect on the sodium uptake kinetics or the physiological responses to high pH water. The fishes from the eutrophic lake therefore did not appear to have any increased tolerance to acute exposure to alkaline water. In contrast to previous studies there was no inhibition of Na⁺ uptake during exposure to high pH. Indeed in some groups of fish Na⁺ uptake was actually stimulated, as was Na⁺ efflux. These differences are attributed to experimental water composition and interspecific differences in physiology. It was not always possible to size-match fishes of the different species, so rainbow trout were used to assess the effect of body mass (from 2 to 40 g), on Na⁺ uptake kinetics and Na⁺ or ammonia fluxes during alkaline water exposure in rainbow trout. Size had no significant effect on these measurements within this narrow range, which helps validate the comparison between species in this study.