Hypoxia adaptation in the crayfish procambarus clarki

• 1.1. P. elarki is an oxyconformer, with an oxygen uptake rate of 144 ± 4 μl/g wet wt/hr at oxygen tensions above 90% saturation and an uptake rate of 18 ± 3 μl g wet wt/hr at 15 torr.
• 2.2. Between 159 and 40 tort, blood pH decreases slightly from 7.77 ± 0.03 to 7.65 ± .04, and at 15 torr, blood pH drops to 7.36 ± 0.06.
• 3.3. At normoxia, blood lactate levels are low at 0.66 ± 0.01 mM/l blood. After 2 and 5 hr exposure to 15 tort, blood lactate levels increase to 3.29 ± 0.47 and 8.91 ± 0.14 mM/l blood, respectively. Upon return to normoxia, blood lactate levels decrease and are comparable to normoxic controls after 13 hr.
• 4.4. During mild hypoxia, P. elarki maintains adequate oxygen transport by utilizing a high O₂ affinity hemocyanin in conjunction with a low metabolic demand by its tissues.

     

Laboratory studies on the oxygen consumption of the marine teleost,Lichia amia (Linnaeus, 1758)

• 1.1. The oxygen consumption of the marine teleost, Lichia amia was investigated under controlled laboratory conditions.
• 2.2. The routine oxygen consumption showed a strong circadian rhythm with the fish being mainly active during the light period.
• 3.3. The specific mass exponent (dimension: μg O₂/g/hr) is temperature independent and ranges from 0.27–0.29.
• 4.4. Starving the fish results in a mean decrease in active, routine and standard oxygen consumption of 21%, 24% and 20%, respectively.
• 5.5. Feecling led to an increase in the oxygen consumption of the teleosts, with the mean metabolic rate over the 24 hr that followed, being 58% and 50% higher for fish that had been starved for 162hr and 40 hr, respectively.
• 6.6. Apparent SDA showed some variation and ranged from 6.0 to 35.5%.
• 7.7. The results obtained are generally in agreement with those recorded for other teleosts.

     

Effect of temperature and salinity on the oxygen consumption of laboratory produced Penaeus californiensis postlarvae

• 1.1. The oxygen consumption by P. californiensis postlarvae (mean wt = 0.38 g) was determined at five different temperatures and four salinities.
• 2.2. The O₂ in each chamber was recorded at 10 min intervals for 1 hr. The time course of oxygen depletion was independent of O₂ concentration down to 1.6 mg/l.
• 3.3. Oxygen consumption increased with temperature from 0.0045 mg/g/min at 19°C, to 0.0142 mg/g/min at 35°C. The thermal coefficient (Q₁₀) indicated a very high sensitivity of the postlarvae to temperature variations at 19–23°C.
• 4.4. The results show that oxygen consumption significantly depends on temperature (P < 0.001) while salinity has only a marginal effect.

     

The oxygen consumption rates of three gastrotrichs

• 1.1. The oxygen consumption rates for three sympatric species of marine gastrotrichs (anatomically similar, except that one contains hemoglobin) were measured with a Cartesian diver microrespirometer.
• 2.2. The rates for the two species without hemoglobin, Turbanella ocellata and Dolichodasys carolinensis, were 307.2 μl O₂ g⁻¹ hr⁻¹ and 108.0 μl O₂ g⁻¹ hr⁻¹, respectively, while the rate for the hemoglobin-containing species, Neodasys, was 208.9 μl O₂ g⁻¹ hr⁻¹.
• 3.3. The possession of hemoglobin by Neodasys (14% by volume) cannot be explained by an unusually high demand for oxygen.
• 4.4. Instead, the hemoglobin may be useful as an oxygen store providing continued aerobic metabolism in anoxic conditions, thus allowing Neodasys to exploit a different niche.

     

Sodium balance in adult atlantic salmon (Salmo salar L.) during migration into neutral and acid fresh water

• 1.1. In sea-water, adult salmon (S. salar) exchange an average of 12.6% of total body sodium/hr.
• 2.2. Following transfer to fresh water sodium uptake follows Michaelis-Menton kinetics. F_max = 2.40 mmol Na/1 ECF/hr, K_m = 0.26 mmol Na/1. The uptake system is fully activated immediately following transfer to fresh water.
• 3.3. Post smolts adapted to sea-water for 3 months take up sodium at only one third of the rate of adult fish following return to fresh water.
• 4.4. The concentration of prolactin in the plasma is low in sea-water adapted fish and does not rise during the first 8 hr in fresh water.
• 5.5. At pH 5 sodium uptake is reduced by almost 90%, even in the absence of aluminium, but recovers immediately on return to neutral water.
• 6.6. At pH 5 and 20 μmol Al/1 there is little further effect on sodium uptake but after 6 hr in aluminium the inhibition of sodium uptake continues after return to neutral aluminium fresh water and uptake is only 50% of normal 24 hr later.

     

Increased muscle glucose uptake in response to chronic glyburide treatment is not related to changes in glucose transporter (GLUT4) protein

• 1.1. The mechanism of action of glyburide (a sulfonylurea) on muscle has been investigated by measuring glucose uptake and glucose transporter (GLUT4) protein levels after chronic glyburide treatment.
• 2.2. A dietary induced insulin resistant rat model (4 wk of high-fat, high-sucrose feeding) was given glyburide (2mg/kg/day) for 10 days and glucose uptake was measured in a perfused hindquarter preparation.
• 3.3. Protein levels of the GLUT4 glucose transporter were determined by Western analysis.
• 4.4. After 7 days of treatment, rats fed glyburide had lower blood glucose concentrations 2 hr (72 ± 5 vs 103 ± 12 mg/dl) and 24 hr (97 ± 7 vs 123 ± 7 mg/dl) after glyburide administration with no difference in serum insulin levels compared to vehicle treated animals.
• 5.5. Glucose uptake was approx doubled in basal state (0 insulin) in response to glyburide (2.8 + 0.4 vs 1.7 ± 0.2μ mol/g per hr).
• 6.6. Maximal insulin (100 nM) stimulated glucose uptake tended to be higher in the glyburide treated group, but did not reach statistical significance (8.0 ± 0.7 vs 7.0 ± 0.6 μmol/g per hr).
• 7.7. Western analysis revealed no significant effect of glyburide on the GLUT4 protein level in skeletal muscle.
• 8.8. These results suggest that glyburide alters glucose uptake through some mechanism other than alterations in the level of the GLUT4 glucose transporter protein.

     

Oxygen consumption and haemocyanin function in the freshwater snail Marisa cornuarietis (L.)

• 1.1. The MO₂ for branchial respiration in adult snails increased from 0.24 mmol/l/O₂ kg/hr at 18°C to 0.83 mmol/l/O₂ kg/hr at 40°C. Q₁₀ values were 2.75 between 35 and 40°C and 1.8 between 18 and 30°C.
• 2.2. The haemocyanin (31.9 ± 5.8 mg/ml) has a high oxygen affinity (6.28 ± 0.8 at 25°C) with a reversed Bohr effect measured between a pH of 6.80 and 7.95 with gelchromatographed haemolymph, and measured between a pH of 7.34 and 8.10 for native haemolymph.
• 3.3. Growth rate is optimal between 27 and 30°C whilst at 24°C stunted growth was found.
• 4.4. At 25°C the same MO₂ values were found for aerial and aquatic respiration.

     

The effect of inspired oxygen tension on oxygen uptake and tolerance to anoxia in the water snakes Helicops modestus and Liophis miliaris (Colubridae)

• 1.1. The effect of oxygen tension, p_o2, on oxygen uptake and tolerance to anoxia have been studied by exposure in nitrogen atmosphere and diving in the water snakes Helicops modestus and Liophis miliaris, at 25°C.
• 2.2. The critical P_o2, was the same (70mmHg O₂) for both species, but below that tension H. modestus showed a higher degree of dependence on P_o2.
• 3.3. Anoxia tolerance time was longer (14 min for H. modestus and 4 min for L. miliaris) during forced dive than during exposure to a 100% nitrogen atmosphere. No difference was found in pre- and post-forced dive oxygen uptake values in both species.
• 4.4. The maximum duration of a voluntary dive was shorter than the mean tolerance time to forced dives in L. miliaris. but longer in H. modestus.
• 5.5. H. modestus, the more aquatic species, is significantly more tolerant of complete anoxia (100% N₂ exposure) and submersion.

     

Effect of size and temperature on the oxygen consumption of the brown shrimp Penaeus californiensis (Holmes, 1900)

• 1.1. The routine rate of oxygen consumption by Peneaus californiensis was determined for the size groups with average weights of 0.26, 2.31 and 10.01 g at five temperatures (19, 23, 27, 31 and 35°C).
• 2.2. Oxygen consumption (mg O₂/g min) was independent of dissolved oxygen (DO) level down to 1.8mg/l, increased with temperature (P < 0.05) from 0.0015mg O₂/g min for the preadults at 19°C to 0.0106 mg O₂/g min at 35°C for the postlarvae, and was inversely proportional to weight (P < 0.05).
• 3.3. The thermal coefficient (Q₁₀) indicated a higher sensitivity by preadults to temperature variations.

     

The dependence of oxygen consumption of the common whelk (Buccinum undatum) on hypoxia,salinity and air exposure

• 1.1. Oxygen consumption of low salinity (20‰) acclimated whelks decreases markedly upon acute exposure to hypoxia (P_WO₂ = 35 Torr), but almost regenerates its original level within 48 hr exposure to the hypoxic condition.
• 2.2. This ability to regain the original level of oxygen consumption is not seen in high salinity (35‰) acclimated whelks.
• 3.3. Oxygen consumption in air at 10°C is more than twice the rate shown by low salinity acclimated whelks in normoxic water (P_WO₂ = 150 Torr).
• 4.4. Q₁₀ for oxygen consumption in air is about 1.0 in the temperature range 10–20°C.

     

Energy difference in lipid and glycogen metabolism of healthy and iridescent virus-infected Heliothis zea (Boddie)

• 1.1. Heliothis zea (Boddie) larvae infected with irridescent virus (IV) showed rapid cell dissolution in the fat bodies.
• 2.2. Fatty acid accumulation in healthy H. zea was significantly greater (P < 0.001) than in IV-infected larvae.
• 3.3. Healthy and IV-infected larvae accumulated glycogen at a rate of 3.86 cal and 0.19 cal/day/insect, respectively.
• 4.4. Total protein of healthy and IV-infected larvae showed no significant difference with time.

     

Oxygen uptake by Trypanosoma lewisi complex cells—III. C isolate

• 1.1. Standard Warburg techniques were employed to determine the oxygen uptake of two isolates (C and L) of Trypanosoma lewisi (Costa Rican and the U.S.). The C cell developed greater parasitemias in rat tail blood during the first 2 weeks after inoculation.
• 2.2. Oxygen uptake of both isolates progressively increased with time and was not related to rise in trypanosome populations in hosts. The C form (recently isolated) consumed 36 per cent more oxygen endogenously, 20 per cent more in glucose and 16 per cent more in serum than the L.
• 3.3. The metabolic capacity (Max./initial Q_O2) of the C cell was greater endogenously and in glucose; the L was superior in serum. Efficiency (substrate Q_O2 ratios) of the L cell was superior.

     

Juvenile hormone biosynthesis by corpus cardiacum-corpus allatum complexes of larval Lymantria dispar

• 1.1. A radiochemical assay was used to examine juvenile hormone (JH) synthesis and secretion in vitro by incubating two pairs of larval corpus cardiacum-corpus allatum complexes (CC-CA) from, Lymantria dispar, in 50 μl of osmotically balanced Grace's medium containing 1 μC1 [³H-methyl]-methionine for 6 hr.
• 2.2. For CC-CA of fourth instar female larvae, maximal incorporation of ³H-methyl was 0.15 pmol/pr/hr between days 2 and 3. High pressure liquid chromatographic (HPLC) analysis suggested that the biosynthetic products are mainly JH III with a little JH II at times.
• 3.3. For CC-CA of last instar female larvae, incorporation of ³H-methyl was 0.48 pmol/pr/hr at the beginning of the stadium and decreased to negligible levels by day 10. HPLC analysis suggested that CC-CA of last instar larvae produced only JH III. Volume increases in CA during the last instar were associated with declining activities of JH secretion.
• 4.4. Comparisons of maximal rates of ³ H-methyl incorporation by each unit volume of CA revealed that in the last instar each unit volume (μm³) of glandular tissue secreted 50% more JH than in the fourth instar.

     

The calcium uptake by larvae of the oyster,Crassostrea virginica,and the clam,Mulinia lateralis

• 1.1. The uptake of calcium by larvae of the oyster (Crassostrea virginica) and the clam (Mulinia lateralis) was measured using the ⁴⁵Ca isotope tracer method.
• 2.2. An equation was established for the calculation of true calcium uptake and the rates expressed as ng Ca/larva/hr were 0.39 and 0.34 ± 0.16 (n = 4) for 3- and 11-day-old oyster larvae, and 0.03 and 0.15 for 7- and 9-day-old clam larvae, respectively.
• 3.3. This system is sensitive, rapid, simple and potentially useful for the measurements of calcium metabolism, shell formation, aquaculture and toxicity.

     

Oxygen debt in reptiles: Relationship between the time required for repayment and metabolic rate

• 1.1. The increase in O₂ consumption in a 5 g lizard (Anolis carolinensis) after feeding and after maximal work was compared with that in a kilogram alligator (Alligator mississippiensis) treated similarly.
• 2.2. The amount of extra O₂ consumed/kg was the same in both. At the peak, there was a 2.6 fold increase in both animals following exhaustive work. Oxygen usage was elevated for 2 hr in the lizard and for 12 hr in the alligator, in inverse proportion to their respective metabolic rates.
• 3.3. Although the extra oxygen consumed was the same. feeding increased metabolic rate at the maximum by 300% in the alligator and by only 40% in the lizard.

     

Bioenergetics of abbreviated larval development in the bromeliad crab,Metopaulias depressus (Decapoda: Grapsidae)

• 1.1. Larvae of the bromeliad crab, Metopaulias depressus Rathbun, were reared in the laboratory, and changes in dry weight (W), ash-free W (AFW), carbon, nitrogen, hydrogen, protein, lipid, carbohydrates and respiration rate were measured during development from hatching to metamorphosis.
• 2.2. Development was successful in rain-water from bromeliads (pH < 5–6), but not in river water from the same region (pH 8). It is abbreviated, with two non-feeding zoeal stages (2.5–3.5 days each) and a feeding megalopa (8.5–10 days). Development to metamorphosis can also be completed in the absence of food (facultative lecithotrophy).
• 3.3. Dry weight and other absolute biomass values per individual vary significantly between different hatches, whereas changes in the relative (% of W or AFW) composition follow quite invariable patterns: ash increases from hatching through the first part of megalopa development, organic biomass decreases concurrently.
• 4.4. Elemental and biochemical data show that lecithotrophy of the zoeal stages as well as continued endotrophic development in the megalopa depend chiefly on degradation of lipid reserves and less on protein. No significant growth was observed in organic constituents when food was available, but without food the megalopa reached metamorphosis with only half the lipid and less than two thirds the protein of fed siblings.
• 5.5. The relationship between C and lipid is similar in M. depressus larvae as in planktotrophic marine crab larvae, whereas that between N and protein differs; it indicates the presence of unusually large quantities of unidentified non-protein N.
• 6.6. Exuvial losses of late premoult biomass or energy are very low in the zoeal stages (2 and 3%), but increase in the megalopa (16% in W, 10% in C, 7–8% in N, H and energy).
• 7.7. Respiration rate per individual increases gradually during larval development (0.6–0.8 μg O₂/hr). Starved megalopa larvae reveal lower individual but higher W-specific metabolism than fed larvae.
• 8.8. Bioenergetic traits of abbreviated larval development are discussed in relation to those known from regular (planktotrophic marine) development of brachyuran crabs. M. depressus is highly adapted to life and development in a physically extreme terrestrial environment.

     

The effect of a toxic dinoflagellate (Alexandrium tamarense) on the oxygen uptake of juvenile filter-feeding bivalve molluscs

• 1.1. Oxygen uptake and grazing rates of juvenile bivalve molluscs Mytilus edulis, Mya arenaria, Geukensia demissa, Placopecten magellanicus and Crassostrea virginica were measured following 1 hr exposure to bloom concentrations (10⁶ cells/1) of the toxic dinoflagellate Alexandrium tamarense (GT429) using a non-toxic clone of the same species (PLY 173) as control.
• 2.2. For all bivalves, prefeeding estimates of V̇O₂ were similar to postfeeding values and values recorded 24 hr after exposure to bloom conditions.
• 3.3. V̇O₂ was similar for bivalves fed on both the toxic and non-toxic strains of A. tamarense suggesting that there were no adverse effects on V̇O₂ following 1 hr exposure to toxic GT429.
• 4.4. Bivalves differed in their rates of grazing between toxic GT429 and non-toxic PLY 173. Similar grazing rates were recorded for M. edulis and G. demissa. For P. magellanicus and M. arenaria reduced rates of clearance were recorded in GT429 compared with the non-toxic strain.

     

Kinetic studies of catechol-o-methyltransferase from the brain of the African catfish,Clarias gariepinus

• 1.1. Optimum in vitro conditions, and kinetics of the enzyme catechol-O-methyltransferase from the brain of the male African catfish were studied.
• 2.2. A saturated level for S-adenosylmethionine, as methyldonor, and magnesium as cofactor was reached at 5 μM and 10 mM, respectively.
• 3.3. The addition of ascorbic acid, as an antioxidant, and tranylcypromine, as a MAO inhibitor, was not necessary, during incubations with fore-brain homogenates.
• 4.4. Kinetic analysis of the methylation of catecholestrone, catecholestradiol and dopamine showed K_m values of 1.2, 0.6 and 0.5 μM, respectively.
• 5.5. The affinity of the catecholsubstrates for the enzyme catechol-O-methyltransferase is much higher in the brain of the African catfish than in tissues of mammals.

     

The energy costs of temperature regulation in birds: The influence of quick sinusoidal temperature fluctuations on the gaseous metabolism of the japanese quail (Coturnix coturnix japonica)

• 1.1. Quick sinusoidal temperature fluctuations (constant average 10°C) cause an increase in metabolism in comparison to an invariable constant ambient temperature of the same dimension.
• 2.2. At the observed mean value of 10°C metabolism is increased by 0.8% per 1 K/hr based on the values of resting metabolic rate (correlation: M = 53.5 + 0.445 T_a, M in J/K g hr, T_a = ambient temperature change in K/hr) and 0.6% based on the values of activity metabolism (M = 70.4 + 0.425 T_a).
• 3.3. The absolute augmentation of metabolism per 1 K/hr is, by comparison, the same for day and night. Its amount is 0.42 and 0.43 J/K g hr respectively.
• 4.4. In the response of metabolism to temperature fluctuations no differences could be found with respect to the amplitude and frequency modifications of temperature.
• 5.5. The increase of energy consumption is probably caused to a greater extent by “overshoot” of the feedback control system in the course of adjusting metabolism to new levels according to the ambient temperature conditions.
• 6.6. Short term ambient temperature changes (i.e. measuring different temperature levels in one night to test basic metabolism vs ambient temperature) cannot produce reasonable values for basic metabolic rate, since these artificially high values reflect the testing procedure.

     

An in vitro study of short-chain fatty acid concentrations,production and absorption in pig (Sus scrofa) colon

• 1.1. Short-chain fatty acid concentration was 180mmol/l in the proximal colon and decreased to 108 mmol/l in the rectum.
• 2.2. Fermentation in chymus from different regions of the colon, showed the pattern of end products to reflect the substrate and not the site of the colon.
• 3.3. Isolated mucosa from proximal and distal colon had electroneutral sodium absorption of 4.8 ± 0.2 and 2.9 ± 0.8 μeq/cm² hr in bicarbonate free media, which was abolished in the absence of chloride.
• 4.4. Electroneutral sodium absorption was enhanced by short-chain fatty acids in the proximal colon and could be described by Michaelis-Menten kinetics with K_m 2.0–11 mmol/l and J_m 1.6–3.6μeq/cm² hr. In the distal colon the stimulation was smaller and propionate even inhibited sodium absorption.
• 5.5. Butyrate was absorbed in the proximal colon, whereas acetate and propionate, and butyrate in the distal colon had a flux ratio of one.
• 6.6. Amiloride (5 mmol/l) inhibited sodium absorption and net butyrate absorption.