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1.
  • 1.1. A half platelet preparation from Chinese crab (Eriocheir sinensis) gill is described which allows electrophysiological investigations of ion transport by gill epithelial monolayer when mounted in a modified Ussing chamber.
  • 2.2. The resistance of these preparations equals half that of complete gill platelets (containing the gill epithelium and cuticle twice) indicating that cell damage during preparation of half platelets is negligible.
  • 3.3. The transepithelial resistance (resistance of cuticle subtracted previously) was determined to be about 140 Ω cm2 when both sides are bathed with identical salines.
  • 4.4. Similarities to the results obtained with perfused complete gills demonstrates the reliability of this preparation.
  • 5.5. When identical salines are applied on both sides of the epithelium an outside positive transepithelial potential difference (PDte) up to 40 mV was measured.
  • 6.6. The occurrence of such a high PDte under symmetric conditions and its sensitivity to CN suggests the PDte to be generated by active transport processes.
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2.
  • 1.1. Semaphore crabs (Heloecius cordiformis) are active in air at low tide. Their branchial chambers are lined with a vascular epithelium and are expanded above the gills (five pairs) to form air cavities which could function as lungs. Water is continuously circulated over the gills.
  • 2.2. The relative contribution made by the gills and lungs to gas exchange in semaphore crabs active in air and circulating branchial water, was determined by measuring oxygen consumption (at 25°C) in crabs with and without branchial water, and in crabs with their lungs subsequently occluded.
  • 3.3. Activity levels and VO2 were unaffected by the absence of branchial water.
  • 4.4. With their lungs occluded, VO2 dropped (on average) by 61% in crabs with branchial water (i.e. gills still functional) and by 81% in crabs without branchial water (gill function impaired).
  • 5.5. It is concluded that semaphore crabs are obligate air breathers while active on land, despite carrying water within their branchial chambers. Lung development and gill reduction in land crabs is discussed briefly in relation to “terrestriality”.
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3.
  • 1.1. Subcellular distribution of (NA+, K+-ATPase and ouabain-insensitive ATPase (Mg2+-ATPase) are compared in branchial tissues of the euryhaline crab, Eriocheir sinensis, acclimated to fresh water.
  • 2.2. Both the anterior and posterior gills contain cAMP-dependent protein kinase and endogenous protein substrate for phosphorylation.
  • 3.3. Phosphorylation occurs in both “particulate” and “soluble” subcellular fractions but its stimulation by cAMP is restricted to the “soluble” fraction.
  • 4.4. serotonin (5-HT) and dopamine receptors are present only in the “light particulate” fraction isolated from the posterior gills.
  • 1.(a) Serotonin and dopamine have no effect on the phosphorylation observed in a subcellular fraction alone.
  • 2.(b) Activation of the phosphorylation by serotonin and dopamine is found when the soluble fraction (source of cAMP-dependent protein kinase) is added to the fraction P3 from the posterior gills.
  • 3.(c) No activation occurs with the fractions P3 as well as P1 or P2 (not shown) from anterior gills of fresh water crab.
  • 4.(d) Cyproheptadine, a serotonin receptor antagonist, inhibits the 5-HT dependent increase in phosphorylation.
  • 5.(e) The dopamine receptor antagonist, chlorpromazine, inhibits dopamine-stimulated phosphorylation.
  • 6.5. Ouabain mimics the effect of cyproheptadine on the serotonin-stimulated phosphorylation found in the posterior gills.
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4.
  • 1.1. Freshwater gammarids from 900–1400 m depths lose Na at 1 atm, 4°C, while related shallow water gammarids are near neutral Na balance.
  • 2.2. Na+ influx rates are similar at 1 atm, 4°C, for abyssal and shallow water gammarids of similar weight.
  • 3.3. Na+ efflux is faster for abyssal gammarids than for comparable shallow water gammarids.
  • 4.4. Compressing abyssal gammarids to 90–140 atm increases Na+ influx rates enough to restore neutral Na balance, while in shallow water crustaceans, compression decreases Na+ influx.
  • 5.5. Na+ influx rates in Baikalian gammarids vary with the 0.55 power of weight.
  • 6.6. The equation Fma × t = 1.3 × W0.55 μEq/hr/animal applies to freshwater crustaceans over the weight range from 0.03 to 35 g.
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5.
  • 1.1. Cutaneous O2 uptake in the carp, Cyprinus carpio, was determined at various water flow rates across the skin (.V) ranging from 2.5 to 40 ml/min, using flow-through respirometers.
  • 2.2. When thickness of water flow was 2mm, cutaneous O2 uptake remained stable (about 3.8 nmol/cm2/min) at a .V of 20–40 ml/min and decreased with .V below 20 ml/min.
  • 3.3. When thickness of water flow was 4 mm, cutaneous O2 uptake decreased with .V below 40 ml/min.
  • 4.4. Apparent water velocity (U') was calculated dividing .V by an area of a cross section of the water flow (0.5 and 1.0 cm2 respectively). In both experiments, cutaneous O2 uptake decreased with U' below 0.7 cm/sec.
  • 5.5. This suggests that cutaneous O2 uptake in the carp is limited at a low water velocity by a resistance of the hypoxic boundary layer.
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6.
  • 1.1. The structure of the gills of skipjack tuna (Katsuwonus pelamis) is reviewed and the pattern of water flow in front of, and through, the gills is described. The tuna system is attractive for analysis of this type because water flow is continuous rather than pulsatile and the gill system is more rigid than that of other fish. In addition, oxygen uptake rates are the extreme case (i.e. highest values) for water-breathers.
  • 2.2. Flow into the slits between the gill bars is rectilinear and nearly uniform, and therefore irrigation at the gill sieve should be nearly uniform.
  • 3.3. Reynolds numbers are so low that turbulent flow is unlikely and entrance effects are negligible.
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7.
  • 1.1. The specific activity of Na-K ATPase was determined from the microsomal preparation of gills dissected from adult Macrobrachium rosenbergii.
  • 2.2. Maximal ATPase activity was achieved at a substrate concentration of 0.5 mM ATP.
  • 3.3. Optimal enzyme activity was obtained at pH of 7.5.
  • 4.4. The Arrhenius plot of Na-K ATPase activity revealed a marked discontinuity at 30°C. “Mg” ATPase activity did not exhibit a marked discontinuity.
  • 5.5. The Ea for Na-K ATPase and “Mg” ATPase was 14.6 kCal/mole and 9.31 kCal/mole respectively. Q10 values for Na-K ATPase was 2.34 and for “Mg” ATPase 1.65.
  • 6.6. ATPase activity and gill homogenate protein concentration exhibited a linear relationship up to 130 μg protein/ml.
  • 7.7. Na-K ATPase activity was inhibited by 10−3 M ouabain. It was equally inhibited by the removal of K+ from the reaction medium.
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8.
  • 1.1. Cadmium (Cd) and zinc (Zn) were inhibitory to calcium uptake by isolated gills of Fundulus heteroclitus in vitro. The metals appeared to act by displacing Ca2+ ions from protein carriers involved in facilitated diffusion.
  • 2.2. In saltwater fish, transport of calcium across the serosal membrane of gill chloride cells is partly energy dependent and is likely mediated by Ca2+-ATPase. However, much of the calcium transport through the gill epithelium appears to occur by passive processes.
  • 3.3. Cd (10−5M—10−3M) and Zn (10−7M—10−3 M) inhibited calcium uptake by isolated scale patches incubated in a physiological saline.
  • 4.4. Cyanide, oubain, and quercetin treatment of scale patches produced results similar to those of the Cd and Zn treatments suggesting that metal-induced inhibition of ATPases may be responsible for reduced calcium transport by scale osteoblasts.
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9.
  • 1.1. Observation of ventilation in immersed Pholis gunnellus showed a linear relationship between ventilatory rate and temperature between 8 and 20°C.
  • 2.2. At 13°C and after 30 min emersion, ventilatory rate was initially lower than prior to emersion, providing evidence of adequate uptake of O2 for standard metabolism during the emersion period.
  • 3.3. This species has a laterally elongate body form with reduced scales and extensive mucus secretion.
  • 4.4. During emersion, gaping behaviour probably exposes the gills and extensively vascularised oesophageal regions to air.
  • 5.5. These are considered to be morphological and behavioural adaptations by P. gunnellus, to aerial respiration in the intertidal habitats occupied by this species.
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10.
  • 1.1. Specific activity and kinetic characteristics of the (Na+ + K+)ATPase have been investigated in the gill epithelium of the hyper-hypoosmoregulator crab Uca minax.
  • 2.2. (Na+ +K+)ATPase activity is shown to be at least three times higher in the posterior gills.
  • 3.3. The kinetic study supports the hypothesis of the existence of two different (Na+ + K+)ATPases: the enzyme activity in the posterior gills could be involved in the transepithelial transport of Na+ while the activity of the anterior gills could be responsible for the intracellular regulation of Na+ and K+.
  • 4.4. Significant and specific changes in (Na+ +K+)ATPase activity occur upon acclimation to media of various salinities.
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11.
  • 1.1. Salmon calcitonin binding by isolated gill cells from rainbow trout, Salmo gairdneri has been investigated.
  • 2.2. The calcitonin receptor interaction is time- and temperature-dependent.
  • 3.3. 50% of inhibition of the 125I labeled calcitonin binding is observed in presence of 1.5 ng/ml unlabeled salmon calcitonin.
  • 4.4. Two types of receptors are described: a high affinity-low capacity site and a low affinity-large capacity site.
  • 5.5. These studies strongly support the role of calcitonin as a hormone regulating the gill function in physiological conditions.
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12.
  • 1.1. The diffusional water permeability (Pd) of rabbit red blood cell (RBC) membrane has been monitored by a doping nuclear magnetic resonance (NMR) technique on control cells and following inhibition with p-chloromercuribenzene sulfonate (PCMBS).
  • 2.2. The values of Pd were around 6.3 × 10−3 cm/sec at 15°C, 7.0 × 10−3cm/sec at 20°C, 8.0 × 10−3 cm/sec at 25°C, 9.1 × 10−3 cm/sec at 30°C and10.7 × 10−3 cm/sec at 37°C.
  • 3.3. Systematic studies on the effects of PCMBS on water diffusion indicated that the maximal inhibition was reached in 15 min at 37°C with 0.5 mM PCMBS.
  • 4.4. The values of maximal inhibition were around 71–74% at all temperatures.
  • 5.5. The basal permeability to water was estimated as 1.6 × 10−3cm/sec at 15°C, 2.0 × 10−3cm/sec at 20°C, 2.4 × 10−3cm/sec at 25°C, 2.6 × 10−3cm/sec at 30°C, and 3.1× 10−3 cm/secat 37°C.
  • 6.6. The activation energy of water diffusion was around 18 kJ/mol and increased to 27 kcal/mol after incubation with PCMBS in conditions of maximal inhibition of water diffusion.
  • 7.7. The membrane polypeptide electrophoretic pattern of rabbit RBCs has been compared with its human counterpart.
  • 8.8. The rabbit membrane contained a higher amount of spectrin (bands 1 and 2), while the band 6 (glyceraldehyde-3-phosphate dehydrogenase) was markedly less intense.
  • 9.9. Considerable differences in the electrophoretic patterns of the two sources of RBC membranes appeared in the bands migrating in the band 4.5 region and in front of band 7, where some polypeptides were apparent in higher amounts in the rabbit RBC membrane.
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13.
  • 1.1. Carp red cells were treated with drugs that affect the cell membranes. The water content of the cells and the accumulation of cAMP in the cells were measured in normoxia and in hypoxia using non-stimulated and adrenergically stimulated cells.
  • 2.2. WGA, DIDS + CCCP and A23187 increased the water content of nonstimulated normoxic cells.
  • 3.3. In hypoxia ouabain and DIDS + CCCP increased the water content but cytochalasin B, NPM, DIDS, CCCP and A23187 + CA2+ abolished the hypoxia-induced swelling.
  • 4.4. Any membrane perturbation induced some cAMP formation, Sophora and Anquilla lectins being most potent.
  • 5.5. Also in adrenergically stimulated cells, membrane perturbation generally increased cAMP formation.
  • 6.6. However, cAMP accumulation diminished in cells treated with cytochalasin B, CCCP and DIDS + CCCP.
  • 7.7. The adrenergic swelling of carp red cells was reduced in normoxia by DIDS. NPM and CCCP increased the adrenergic swelling in normoxia to hypoxic level.
  • 8.8. In hypoxia WGA and Anquilla lectin decreased the swelling.
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14.
  • 1.1. Rainbow trout were acclimated to salt water (1.5, 2.0 or 3.0%, which means 40, 60 or 85% concentrated sea-water) and the electrolyte, glucose and cortisol concentrations of the plasma as well as the extra- and intracellular muscle space, the muscle electrolyte concentrations and the ATPase activity were analysed.
  • 2.2. Plasma osmolality, Na+, Ca2+ and Mg2+ concentrations of the plasma had a maximum at 24 hr after the start of acclimation when acclimated to 3.0% salt water. Plasma osmolality, Na+ and Mg2+ concentrations were significantly higher during the whole acclimation time when exposed to 3.0% salt water.
  • 3.3. Variations and regulations of ECS and ICS were clearly demonstrated. The intracellular electrolyte concentrations were also maximal at 24 hr.
  • 4.4. The plasma glucose level was just slightly elevated, but the cortisol level clearly indicated a stress response at 24 hr.
  • 5.5. The activity of gill Na-K-ATPase increased during the acclimation time.
  • 6.6. The regulatory processes in trout during acclimation to salt water are compared with those occurring in tilapia and carp.
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15.
  • 1.1. Compositions of lipids and proteins of erythrocytes (RBC) and gills from Japanese charr (Salvelinus leucomaenis) which were exposed to 0.4 and 0.7 ppm ozone for 30 min were compared with those of the control.
  • 2.2. On exposure to ozone, both RBC and gill membrane phospholipid content, especially phosphatidylethanolamine (PE), dropped.
  • 3.3. The decrease of PE was brought about by the decrease of docosahexaenoic acid content which comprised the major component of PE.
  • 4.4. RBC membrane protein with 215 and 225 kDa, which is equivalent to cytoskeletal protein, selectively disappeared on exposure to ozone.
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16.
  • 1.1. The Parstrogylus megistus (assassin bug) somatic muscle membrane has low excitability.
  • 2.2. Its Em measured in normal Ringer is — 55 mV.
  • 3.3. Its Rm and Cm measured by low current injection are 2kΩ/cm2 and 7μF/cm2.
  • 4.4. Rectification appears only when the membrane potential was displaced for more than 60 mV in both directions.
  • 5.5. The Em is maintained by EK, ECl and passive Na permeability.
  • 6.6. The EK is maintained by metabolic processes.
  • 7.7. Ca depolarizes this membrane through its effect of increasing gK and an unspecific effect.
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17.
  • 1.1. The pathway leading to the excretion of ammonia in the crustacean, Cherax destructor, has been investigated.
  • 2.2. Injection of ammonium chloride and of serine into the haemolymph always led to a rapid increase in the excretion of ammonia. This was not the case with other amino acids. Isolated gills incubated with serine and threonine but not glutamate and glutamine produced ammonia.
  • 3.3. Serine dehydratase was present in the gills, midgut gland and tail muscle and serine (0.1 mM) was present in the haemolymph.
  • 4.4. The hypothesis is put forward that serine may be the ultimate source of ammonia and that this deaminating reaction is not restricted to the gill. Such a hypothesis sees the formation and deamination of serine—from 3-phosphoglycerate to pyruvate (lactate) as a modified glycolytic pathway.
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18.
  • 1.1. Rainbow trout (Salmo gairdneri Rich.) heads were perfused with phosphate buffered saline containing 10 μM adrenaline. The gills were ventilated with aerated water (PIO2 = 20.7–20.9 kPa). PvO2 and PaO2 were measured and PIO2 controlled.
  • 2.2. An equilibrium between PIO2 and PaO2 when PvO2 = 0 kPa, was never observed. The reasons for this difference in O2 tensions were evaluated.
  • 3.3. Perfusion with nitrogen equilibrated saline (PvO2 = 0 kPa) resulted in PaO2 of 16.4 ± 0.4 kPa. After a change to aerated saline (PvO2 20.7–20.9 kPa) PaO2 increased to 17.6 ± 0.5 kPa. In this situation when PvO2 = PIO2 the PIO2 − Pao, difference showed that gill tissue consumed O2 from the saline.
  • 4.4. As expected, an inhibition of this O2 consumption with cyanide in the ventilation water increased PaO2 to 20.1 ± 0.3 kPa. However a return to the N2-equilibrated saline (PvO2 = 0 kPa), still in presence of cyanide, decreased PaO2 to 17.2 ± 0.5 kPa. This indicates that O2 consumption of gill tissue is not the only factor limiting O2- transfer.
  • 5.5. An increase of perfusion flow (Q) within a physiological flow rate from 0.5 to 3.0 ml min−1 (100 g fish)−1 did not significantly affect PaO2 Thus, the O2 transfer in the perfused gills appear to be rather limited by perfusion than by diffusion.
  • 6.6. Ventilation at the rate used (800–1000 ml min−1 (100 g fish)−1)did not limit O2-transfer. The PIO2–PaO2 difference was not caused by a “water shunt”.
  • 7.7. We suggest therefore, that the PIO2-PaO2 difference in saline perfused gills is a result of a shunt, i.e. perfusate flow by-passing the gas exchange area in the gill circulation. The shunt was calculated to 11–22 of the total perfusion flow (Q).
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19.
  • 1.l. High amino acid concentrations were found in the anterior coelomic fluid of a Polychaeta (Sabella pavonina Savigny).
  • 2.2. The concentrations being much higher in the fluid which penetrates the nephrostomia into the nephridia lumen than in the final urine indicates that the nephridia reabsorbs large amounts of amino acids.
  • 3.3. Nephridial perfusion experiments showed that an amino acid analogue (α-amino-iso-butyric acid, AIB) is transported by the nephidia.
  • 4.4. The transport took place across the nephridial wall owing to the presence of a carrier-mediated transport system and a diffusion system.
  • 5.5. For the carrier-mediated transport, the Vmax was 0.234 ± 0.025 nmol·min and the Km 3.715 ± 0.315mmol·l.
  • 6.6. AIB accumulated in the nephridial cells up to a maximum rate of 01.17 nmol·min.
  • 7.7. Intracellular accumulation stopped increasing when the Vmax for reabsorption was reached.
  • 8.8. These results indicate that the carrier-mediated transport of AIB is located at the apical membrane of the nephridial cell, and that AIB transport by simple diffusion takes place through the paracellular pathway.
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20.
  • 1.1. The shell side of the mantle of Achatina fulica is several millivolts positive to the blood side in vitro.
  • 2.2. The electrical potential does not depend on Na+, Ca2+, Mg2+, K+ or HCO3 but requires the presence of chloride on the shell side.
  • 3.3. The potential difference and short-circuit current ranged from 3.0 to 30.0 mV and 15.0 to 75 μA/cm2 with averages at 10m V and 50 μA/cm2 respectively.
  • 4.4. The electrical gradient is reduced by 2,4-dinitrophenol, thiocyanate and furosemide but not by ouabain, CO2 or acetozolamide.
  • 5.5. It is suggested that the nature and mechanism of electrogenesis in Achatina parallels that of the Helix mantle.
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