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1.
  • 1.1. The food consumption, energy, nitrogen, fat, ash, calcium, phosphate and magnesium balances of the Eurasian kestrel (Falco tinnunculus), and screech owl (Otus kennicotti) are compared.
  • 2.2. Eurasian kestrel sample values were significantly greater than screech owl sample values in the energy, nitrogen, calcium, phosphate and magnesium content in pellets, and calcium content in excrement. Phosphate content in excrement was significantly greater in screech owl samples than in Eurasian kestrel samples.
  • 3.3. The Eurasian kestrel ingested significantly greater amounts of calcium and phosphate, egested via excrement significantly greater amounts of ash, excreted or egested significantly greater amounts of energy, nitrogen, calcium and phosphate via excrement and pellets, and excreted significantly greater amounts of magnesium via excrement than did the screech owl. The screech owl assimilated significantly greater amounts of ash than did the Eurasian kestrel.
  • 4.4. The metabolizability coefficient averaged 48.32% for the Eurasian kestrel, and 49.62% for the screech owl.
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2.
  • 1.1. Lactating ewes were treated with mouse epidermal growth factor (EGF) at a dose rate of 0.5 mg/day for 4 days and its effects on the electrolyte profile were observed.
  • 2.2. There was no effect of EGF on plasma concentrations of sodium or potassium, although urinary and total (in urine and milk) losses of both were reduced.
  • 3.3. EGF-induced hypocalcaemia was associated with reduced milk calcium secretion and increased urinary calcium excretion whereas EGF-induced hypermagnesaemia was associated with reduced urinary and total magnesium losses.
  • 4.4. Glomerular filtration rate was reduced during EGF infusion.
  • 5.5. Chronic intravenous EGF infusion affects the electrolyte profile by altering electrolyte secretion by the mammary gland and renal electrolyte excretion.
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3.
  • 1.1. Physiological responses of 13 adult female collared peccaries (Tayassu tajacu) to high quality and low quality diets, fed for 15 weeks, were examined. The low quality diet simulated energy and protein intake of peccaries during poor range conditions resulting from drought. Blood samples were collected after 10 and 15 weeks of dietary treatment; urine samples were collected after 15 weeks of treatment.
  • 2.2. Females receiving the low quality diet for 15 weeks lost 27.4% of their original body weight, compared to no weight change among high quality-fed females.
  • 3.3. Red blood cell counts, hematocrits, and hemoglobin concentrations were significantly greater among females fed a high quality diet compared to those receiving a low quality diet. High quality-fed females also had a higher mean corpuscular hemoglobin concentration. Plasma fibrinogen concentration was nearly twice as great among females receiving the low quality diet compared to the high quality group.
  • 4.4. Consumption of the low quality diet resulted in significantly elevated serum levels of nonesterified fatty acids, alkaline phosphatase, phosphorus, alpha-2 globulin and alpha globulin: beta globulin ratio.
  • 5.5. Consumption of the low quality diet resulted in significantly lowered serum levels of urea nitrogen, calcium, zinc, calcium: phosphorus, urea index, beta-1 flobulin, beta globulin: albumin ratio, thyroxine and triiodothyronine.
  • 6.6. Serum levels ofcreatinine, total bilirubin, glucose, cholesterol, gamma glutamyltransferase, aspartate aminotransferase, alanine aminotransferase, lactate dehydrogenase, potassium, copper, magnesium, sodium chloride, total protein and gamma globulin were unaffected by diet quality.
  • 7.7. Urine chemistry results suggested pH, osmolarity, albumin, creatinine phosphokinase, calcium and phosphorus concentrations might be useful indices for assessing nutritional status in female peccaries.
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4.
  • 1.1. The subcellular distribution of nine transition metals (plus four additional elements) was measured in the kidney tissue of the quahog, Mercenaria mercenaria.
  • 2.2. Elemental analyses of the subcellular fractions indicated three main patterns of metal distribution within kidney cells.
  • 3.3. Barium, iron, manganese and lead were associated primarily with kidney granules.
  • 4.4. Cadmium, copper, potassium and magnesium were found mainly in the cytosolic fraction.
  • 5.5. Calcium, phosphorus and zinc were found in all isolated fractions, probably reflecting the important roles that these elements play in bivalve metabolism.
  • 6.6. The organelle composition of the isolated subcellular fractions was determined using marker enzyme assays and microscopic techniques.
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5.
  • 1.1. Eyestalk unablated and unilaterally ablated Penaeus monodon juveniles had survival rates after 5 months of 75–72.5 and 67.5–60%, respectively.
  • 2.2. Unilaterally ablated shrimps had significantly higher (P < 0.05) growth rate than unablated shrimps.
  • 3.3. Eyestalk-ablatement resulted in a decrease in the haemolymph sodium concentration and an increase in the potassium and calcium concentration of shrimps.
  • 4.4. The osmolarity of haemolymph and total protein concentration of unablated shrimps were demonstrated to be higher than those of unilaterally ablated shrimps.
  • 5.5. The eyestalk-ablated shrimps possess higher total ATPase and Na+,K+-ATPase activities in the gill than those of unablated shrimps.
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6.
  • 1.1. Renal function in migrating adult Atlantic salmon was studied in sea-water (SW) and following abrupt transfer to fresh water (FW).
  • 2.2. Urine flow rate of SW-adapted fish, 0.72 ml/kg/hr, increased 6.3-fold to 4.55 ml/kg/hr after 2–3 days in FW, later decreasing to around 1 ml/kg/hr.
  • 3.3. Changes in glomerular filtration rate and ion filtration rates largely paralleled changes in urine flow. In SW-adapted salmon about 4% of excreted magnesium is filtered. Tubular magnesium secretion declined within 1 day of FW transfer.
  • 4.4. During the period of maximum diuresis, urinary sodium loss is 77% of the branchial sodium uptake rate. This falls to less than 20% in FW-adapted fish.
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7.
  • 1.1. Simultaneous measurement of calcium fluxes in brown trout, at low external [Ca] (20 μ mol 1−1), provided evidence of active uptake of Ca from the medium.
  • 2.2. At pH 4.5, calcium influx was inhibited and efflux was stimulated.
  • 3.3. Cd and Mn, but not Al, at concentrations within the ranges found in acid waters experiencing fish population decline, inhibited calcium influx. Efflux was unaffected.
  • 4.4. Cd and Mn stimulated sodium influx and efflux.
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8.
  • 1.1. Milk samples of 4 ml or more were obtained from guinea pigs (Cavia porcellus), dairy cattle (Bos taurus), horses (Equus caballus) and humans (Homo sapiens). The milks were analysed for minerals including calcium (Ca), phosphorus (P), magnesium (Mg), potassium (K) and sodium (Na) by Inductively Coupled Plasma-Optical Emission Spectroscopy (ICP-OES).
  • 2.2. Calcium was approximately twice as concentrated in guinea pig milk as in cows' milk, which was twice as much as the level in mares' milk, and this, in turn, was twice as concentrated as human milk.
  • 3.3. The ratio of Ca to P in guinea pig milk was 1.66:1, while it was 1.24:1 in cows' milk, 1.56:1 in mares' milk and 2.07:1 in human milk.
  • 4.4. Potassium was the most abundant mineral in the milks of cows, mares and humans, but not in guinea pig milk, and was much higher in cows' milk than in others.
  • 5.5. Sodium was highest in guinea pig milk with cows' milk being a close second.
  • 6.6. Magnesium was one-tenth as concentrated as Ca.
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9.
  • 1.1. Over an 8-year period, 19 biochemical parameters have been determined at various ages in the blood serum of 92 clinically healthy Lechwe waterbucks (Kobus leche), 33 males and 59 females.
  • 2.2. Significant differences have been noted with age. In neonates, the lowest values of total proteins, glucose, creatinine, urea, AST, ALT and iron have been noted; the highest ones have been seen for cholesterol, alkaline phosphatase, calcium and phosphorus.
  • 3.3. With regard to sex, raised values of glucose, urea, alkaline phosphatase and ALT, and lowered values of cholesterol, have been noted in juvenile females compared with males of the same age.
  • 4.4. In adult females, higher levels of urea and cholesterol and lower levels of glucose, triglycerides and natrium have been recorded compared with males.
  • 5.5. With sex and age, no significant changes have been found in the levels of GGT, magnesium, chlorides and copper.
  • 6.6. Out findings are discussed with those abstracted from the literature for related species.
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10.
  • 1.1. Metabolic rate (MR) and water budget (WB) components of cave and camel crickets are directly related to size and temperature.
  • 2.2. MR increases most rapidly with size for insects in general followed by cave crickets (females > males), and lastly, camel crickets (no sex differences).
  • 3.3. Metabolic thermal sensitivity of cave crickets (males > females) is much greater than camel crickets.
  • 4.4. WB components parallel MR relations.
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11.
  • 1.1. The pump-leak hypothesis of transmembrane ion distribution implicitly poses the operational immobilization of a fraction of intracellular potassium and extracellular sodium.
  • 2.2. Subtraction of operationally immobilized ion fractions from total intracellular potassium and extracellular sodium concentrations leads to Donnan ratios of the mobile fractions consistent with the transmembrane distribution of the chloride ions and potentials derived from the constant field equation.
  • 3.3. The predictions of this simple approach agree with the experimental observations regarding ionosmotic processes in several types of aquatic animal cells.
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12.
  • 1.1. Cells of tentacles and body wall of the sea anemone Condylactis gigantea behaved as simple osmometers during 5hr exposure to 50, 67, 83, 100 and 125% sea-water.
  • 2.2. All intracellular water appeared to be osmotically active.
  • 3.3. Cell sodium, chloride and total osmolyte content remained invariable, with taurine decreasing and potassium increasing as sea-water concentration was reduced.
  • 4.4. Tissues, as a whole, exhibited a pseudoregulatory response to changes in salinity as the large and osmotically inert extracellular space buffered volume changes to a considerable extent.
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13.
  • 1.1. Measurements of the rate of nitrogen consumption, total nitrogen and ammonia excretion and nitrogen absorption of bream, Abramis brama L. (body weight range 0.4–519 g wet wt) were made at 10, 15 and 20 C.
  • 2.2. Fish were fed once daily on live zooplankton collected in Lake Balaton and cultured Tubifex sp. at 5–15% of their body weight.
  • 3.3. Fish size and temperature had a combined effect on the rate of total nitrogen excretion. Total nitrogen excretion did not increase proportionally with an increase in consumption.
  • 4.4. On average, 52–80% of the nitrogen consumed with food was excreted by bream.
  • 5.5. The greatest part of total nitrogen excretion was ammonia and its proportion in the total ranged between 53 and 75%.
  • 6.6. Temperature did not have any significant effect on the proportion of excreted ammonia and the rate of excreted total nitrogen was the only factor determining its proportion in the total.
  • 7.7. The rate of nitrogen absorption of bream was surprisingly very high.
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14.
  • 1.1. Scale regeneration was examined in Oreochromis niloticus under normal, dietary calcium-deficient, and both dietary and ambient water calcium-deficient conditions.
  • 2.2. Calcium contents of regenerating scales were dependent on the calcium status of the fish, but areal growth of the scales was independent.
  • 3.3. Transient hypocalcemia accompanied with a loss of calcium from original scales was observed in descaled fish in dietary calcium deficiency, and intact and descaled fish in both dietary and ambient water calcium deficiency.
  • 4.4. The results suggested that calcium mobilized from internal sources was insufficient and both water and dietary calcium were necessary for normal calcification of the regenerating scales.
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15.
  • 1.1. Brain trehalase specific activity and trehalosemia were measured during the end of the developmental life cycle in non-diapausing and diapausing insects.
  • 2.2. During non-diapausing development, trehalosemia reached maximum values at the beginning of pupal life. Then a constant decrease was observed up to the end of adult life.
  • 3.3. The specific activity of brain trehalase was maximum when the insects were in active feeding periods, minimum activity appearing during moulting phases.
  • 4.4. During diapausing development, trehalosemia was very high at the beginning of pupal life, particularly when insects were exposed to wintering conditions.
  • 5.5. When diapause was broken, trehalosemia fell, announcing adult emergence.
  • 6.6. Brain trehalase activity showed the same qualitative variations as in non-diapausing larvae, but with rather lower values.
  • 7.7. During pupal life, brain trehalase activity decreased markedly during the long period necessary to obtain diapause breakdown.
  • 8.8. Wintering conditions allow a progressive increase of brain trehalase activity, which preceded the fall of trehalosemia.
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16.
  • 1.1. Both the post-moult, rockhopper (Eudyptes crestatus) and magellanic penguins (Spheniscus magellanicus) had significantly lower plasma total protein, albumin, urate, iron and potassium and higher alkaline phosphatase activity than pre-moult birds. In addition creatinine, conjugated bilirubin and inorganic phosphate in the magellanics; globulin, urate, calcium, alanine and aspartate transaminases in the rockhoppers were significantly decreased.
  • 2.2. There were significant differences in plasma bicarbonate, inorganic phosphate, alkaline phosphatase and iron concentrations between non-moulting adult and post-moult gentoo penguin (Pygoscelis papua) chicks.
  • 3.3. Absence or scarcity of the preferred nutrient requirement during the period preceding moulting could threaten the survival of any of the species, particularly of those of narrow dietary speciality.
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17.
  • 1.1. Gastric mucosal calcium channel complex was isolated from the solubilized epithelial cell membranes by affinity chromatography on wheat germ agglutinin.
  • 2.2. The complex following labeling with [3H]PN200-110 was reconstituted into phosphatidylcholine vesicles which exhibited active 45Ca2+ uptake into intravesicular space as evidenced by La3+ displacement and osmolarity measurements. The 45Ca2+ uptake was independent of sodium and potassium gradients indicating the electroneutral nature of the process.
  • 3.3. The gastric mucosal channels on epidermal growth factor binding in the presence of ATP responded by an increase in protein tyrosine phosphorylation of 55 and 170 kDa subunits of calcium channel.
  • 4.4. The phosphorylated channels following reconstitution into vesicles displayed at 48% greater 45Ca2+ uptake, thus indicating the tyrosine kinase involvement in EGF dependent activation of calcium channel.
  • 5.5. The results point towards the importance of epidermal growth factor in the maintenance of gastric mucosal calcium homeostasis.
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18.
  • 1.1. The activity of brush border enzymes (alkaline phosphatase, maltase, sucrase, trehalase, leucine amino peptidase) was higher in purified membranes prepared with calcium. The contamination of these membranes with basolateral membranes was also lower (1.27 for Na-K-ATPase activity ratio).
  • 2.2. The extraction of brush border lipids was carried out according to Folch adapted method. Two dimensional thin layer chromatography was used to separate the phospholipidic fractions. Fatty acids of phospholipids were analysed using gas chromatography after acid transmethylation (column SP 2330).
  • 3.3. Phospholipids are composed of phosphatidylcholine (PC: 33%), phosphatidylethanolamine (PE: 30%), sphingomyeline (SM: 21%), phosphatidylserine (PS: 14%) and phosphatidylinositol (PI: 2%). 4. PC, PE and PS are characterized by high levels of unsaturated fatty acids (monounsaturated MUFA: 21.5% and polyunsaturated PUFA: 34.9%). The most abundant PUFA belong to the (n-3) family [18:3 (n-3), 20:5 (n-3) and 22:6 (n-3)].
  • 4.5. Fatty acids from sphingomyelin of purified membranes have low proportions of PUFA (13.5%) but higher proportions of MUFA (39.5%).
  • 5.6. No specific differences were found between calcium and magnesium prepared membranes.
  • 6.7. The low content in LPC and the absence of LPE confirmed the absence of major structural lipids transformation during the membrane purification with calcium or magnesium.
  • 7.8. Glycine transport was measured during 10 sec at different temperatures using the rapid filtration technique. Glycine transport was higher with Na+ than with K+. In the presence of Na+, this transport increases with temperature.
  • 8.9. Arrhenius curves were mono phasic without obvious breakpoint and indicated no phase transition in the lipid bilayer.
  • 9.10. A significant Na+ dependent glycine transport has been characterized at low temperatures (0°C) which suggests a possible role of membrane polyunsaturated fatty acids in the control of glycine transport.
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19.
  • 1.1. Responses of channel catfish (Ictalurus punctatus) swim-up fry to dietary calcium in soft (< 1 mg/1 as CaCO3) and hard (> 100 mg/1 as CaCO3) water were determined by feeding purified egg-white diets containing 0, 0.5, 1.0, or 2.0% calcium from CaCO3 for 8 weeks.
  • 2.2. Catfish fry fed the basal diet (0.03% Ca) in hard and soft water had lower whole-body ash and whole-body calcium concentrations but higher weight gain and survival than those fed calcium-supplemented diets.
  • 3.3. Fry in soft water generally had lower whole-body ash, whole-body calcium, and survival, as well as a higher incidence of spinal deformities than fry in hard water.
  • 4.4. Feeding higher levels of calcium to fry reared in soft water did not increase whole-body calcium levels or decrease spinal deformities to the levels observed for fry reared in hard water and fed supplemental calcium.
  • 5.5. These data indicate that calcium derived solely from dietary or environmental sources was not sufficient for optimum health of channel catfish fry.
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20.
  • 1.1. In crayfish, light stimulation of the retinular cells induces a depolarizing receptor potential.
  • 2.2. Experiments were designed to determine the role of Na+ and Ca2+ on receptor potential during dark And light states.
  • 3.3. Depolarization depends on Na+ and Ca2+ availability to the retinular cell.
  • 4.4. Repolarization velocity and response duration depend on extracellular Ca2+ availability.
  • 5.5. Light adaptation increases receptor potential dependence on calcium and sodium ions.
  • 6.6. We analyse these results with respect to other invertebrate photoreceptors.
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