Control of panting in the desert iguana: roles for peripheral temperatures and the effect of dehydration

Although it is generally held that panting is a physiological mechanism for the regulation of brain temperature during heat stress, a number of studies have pointed to the importance of peripheral input for the initiation of the panting response in a variety of animals. By presenting ambient heat loads of 47 degrees, 54 degrees, 58 degrees, and 65 degrees C, and measuring skin, ear and core temperatures of the desert iguana, Dipsosaurus dorsalis, at the onset of panting, we found that the skin temperature at panting onset was independent of ambient heat load. This suggests that skin (peripheral) temperature is the body temperature on which the central thermoregulatory center cues to initiate thermal panting. Peripheral temperature control of panting was retained when the plasma osmolality of the desert iguana was increased by 100 mOsm/kg H2O to simulate dehydration. Dehydration to 80% initial body weight (IBW) resulted in a progressive increase in panting threshold (skin) from 42 degrees C for untreated lizards to 42.5 degrees C at 90% IBW to 43.3 degrees C at 80% IBW. Injection of 80% IBW lizards with a volume of 10 mM NaCl equivalent to weight loss resulted in a decrease in panting threshold to 40.8 degrees C. Injection with 1% body weight 3000 mM NaCl produced a dramatic increase in panting threshold to 45.9 degrees C. These data suggest that the desert iguana responds to dehydration by elevating panting threshold, thus promoting water conservation. These data also suggest that changes in plasma osmolality may be involved in the "setting" of panting threshold.     

High dietary sodium chloride and body temperature in the domestic fowl and the Glaucous-winged gull

Arad and Skadhauge (1986) correlated plasma sodium to calcium ratio and body temperature in domestic fowl (Gallus domesticus) during increased dietary sodium chloride intake which increased plasma sodium concentration. During acclimation to high dietary NaCl, body temperature should increase in proportion to the increase in plasma sodium concentration, and body temperature should increase less in gulls than in chickens because salt gland secretion of NaCl by gulls should prevent elevation of plasma sodium concentration. Plasma osmolality, plasma sodium concentration, plasma concentrations of total calcium and ionized calcium, and body temperature and panting threshold were measured in domestic roosters and Glaucous-winged gulls before and after exposure to high NaCl diets. Gull body temperature (40.4±0.2 °C) increased significantly (PM0.05) during salt acclimation. Rooster body temperature (41.0±0.2 °C) did not increase significantly. Plasma sodium concentration increased in gulls (5.4±0.5%, P<0.01) and was correlated with body temperature (r=0.497, P<0.05); the 3.8±1.0% increase in plasma sodium concentration in roosters (P<0.01) was not, suggesting that change in body temperature might be a response to the magnitude of increase in plasma sodium concentration. Plasma ionized calcium concentration increased by 12.9±4.6% (P<0.01) in gulls and by 5.3±1.0% (P<0.01) in roosters. Plasma sodium concentration was correlated with calcium ion concentration in both gulls (r=0.635, P<0.05) and roosters (r=0.664, P<0.05). In neither species were ratios of sodium to total calcium plasma concentration or sodium to ionized calcium concentration altered or related to body temperature. Panting threshold increased significantly in roosters following salt acclimation, but not in gulls due to high variability in response. The increase in gull plasma sodium concentration was small compared to previously reported (Saxena 1976; Denbow and Edens 1980, 1981; Maki et al. 1988) increases in hypothalamic and intraventricular sodium concentration following infusion of Na⁺, yet the effect on body temperature was similar in both types of studies. This suggests that sodium may have peripheral effects that augment the central effects imposed by altered hypothalamic interstitial sodium and calcium concentration.Abbreviations [Ca]_p1 total calcium concentration in plasma - [Ca²⁺] ionized calcium concentration in plasma - [Cl]_p1 chloride concentration in plasma - f respiratory frequency - Hct hematocrit - [K]_p1 potassium concentration in plasma - [Na]_p1 sodium concentration in plasma - osm_p1 plasma osmolality - PT panting threshold - T _a ambient temperature - T _b body temperature - V _t tidal volume     

Microscopic evaluation of vesicles shed by rat erythrocytes at elevated temperatures

It is hypothesized that the elevation of the temperature of the blood during heat stress may cause an increase of the shedding of erythrocyte membrane vesicles. Therefore, the increase of vesicle numbers following heat stress may be indicative of and proportional to the level heat stress. In order to test this hypothesis, erythrocytes and the vesicles shed by erythrocytes were collected from rat blood and analyzed after the elevation of body temperature by exposure to external heat. The images of erythrocytes and vesicles were analyzed by a custom light microscopy system with spatial resolution of better than 90 nm. The samples were observed in an aqueous environment and required no freezing, dehydration, staining, shadowing, marking or any other manipulation. The elevation of temperature from 36.7±0.3 to 40.3±0.4 °C resulted in significant increase of the concentration of vesicles in blood. At a temperature of 37 °C, mean vesicle concentrations and diameters found in rat blood were (1.4±0.2)×10⁶ vesicles/μL and 0.436±0.03 μm, respectively. The concentration of free vesicles increased after exposure to heat to (3.8±0.3)×10⁶ vesicles/μL. It was estimated that 80% of all vesicles found in rat blood are smaller than 0.45 μm. The increase in the number of vesicle associated with elevated temperatures may be indicative of the heat stress level and serve as diagnostic test of erythrocyte stability and heat resistance.     

Spermatozoa from the maned wolf (Chrysocyon brachyurus) display typical canid hyper-sensitivity to osmotic and freezing-induced injury,but respond favorably to dimethyl sulfoxide

We assessed the influences of medium osmolality, cryoprotectant and cooling and warming rate on maned wolf (Chrysocyon brachyurus) spermatozoa. Ejaculates were exposed to Ham’s F10 medium (isotonic control) or to this medium plus NaCl (350–1000 mOsm), sucrose (369 and 479 mOsm), 1 M glycerol (1086 mOsm) or dimethyl sulfoxide (Me₂SO, 1151 mOsm) for 10 min. Each sample then was diluted back into Ham’s medium and assessed for sperm motility and plasma membrane integrity. Although glycerol and Me₂SO had no influence (P > 0.05), NaCl and sucrose solutions affected sperm motility (P < 0.05), but not membrane integrity. Motility of sperm exposed to <600 mOsm NaCl or sucrose was less (P < 0.05) than fresh ejaculate, but comparable (P > 0.05) to the control. As osmolality of the NaCl solution increased, motility decreased to <5%. In a separate study, ejaculates were diluted in Test Yolk Buffer containing 1 M glycerol or Me₂SO and cooled from 5 °C to −120 °C at −57.8 °C, −124.2 °C or −67.0 °C/min, frozen in LN₂, thawed in a water bath for 30 s at 37 °C or 10 s at 50 °C, and then assessed for motility, plasma- and acrosomal membrane integrity. Cryopreservation markedly (P < 0.05) reduced sperm motility by 70% compared to fresh samples. Higher (P < 0.05) post-thaw motility (20.0 ± 1.9% versus 13.5 ± 2.1%) and membrane integrity (51.2 ± 1.7% versus 41.5 ± 2.2%) were observed in samples cryopreserved in Me₂SO than in glycerol. Cooling rates influenced survival of sperm cryopreserved in glycerol with −57.8 °C/min being advantageous (P < 0.05). The findings demonstrate that although maned wolf spermatozoa are similar to domestic dog sperm in their sensitivity to osmotic-induced motility damage, the plasma membranes tolerate dehydration, and the cells respond favorably to Me₂SO as a cryoprotectant.     

WATER-REGULATORY BEHAVIOUR IN TERRESTRIAL GASTROPODS

1. Terrestrial snails and slugs are exceedingly susceptible to dehydration due to evaporative water loss from the integument and lung surface, and the deposition of a dilute mucous trail. Active slugs can lose 30–40% of their initial body weight (IBW) within 2 h. 2. Both field and laboratory studies have revealed that habitat selection by snails and slugs is well correlated with the availability of water. In addition, numerous species display homing behaviour, returning directly to their moist secluded daytime resting sites at dawn. 3. Several aspects of locomotor activity are affected by body hydration and environmental conditions such as relative humidity. Moist conditions result in termination of aestivation in snails and a generally higher level of activity in both snails and slugs. In contrast, severe dehydration initiates aestivation in snails and an increase in the intensity and duration of circadian locomotor activity in slugs. 4. Huddling behaviour is a specialized example of the general preference of slugs for moist habitats. When groups of slugs are exposed to dry environmental conditions, they form closely packed aggregations. This response results in a decrease in the rate of dehydration of the individual slugs. 5. When slugs have been dehydrated to about 90% IBW, rhythmic closures of the pneumostome are initiated. As dehydration progresses there is a reduction in the open diameter of the pneumostome. These responses reduce the total exposure of the lung surface and thereby evaporative water loss. In slugs dehydrated to about 80 % IBW, these responses can result in a 7 % reduction in water loss. 6. When slugs have been dehydrated to about 65% IBW (67·6 ± 4·3% IBW) they move on to a moist surface, assume a characteristic flattened posture and remain quiescent while water is absorbed through the surface of the foot. Once they are rehydrated (to 93·5 ± 12·4% IBW) they move off the moist surface. Thus there exists a specific dehydration threshold for the initiation of contact-rehydration and a rehydration set-point at which the response is terminated. 7. Both initiation and termination of contact-rehydration are controlled by variations in haemolymph osmotic pressure. The behaviour can be experimentally initiated by injection of hyperosmotic mannitol solution and terminated by injection of dilute saline. 8. Contact-rehydration involves bulk flow of water through an epithelial paracellular pathway in the integument of the foot. The rate of absorption of [¹⁴C]inulin during contact-rehydration is similar to that of water. The efficacy of water movement through the pathway is modulated by body hydration, the pathway being opened only in dehydrated slugs. 9. By means of the dual-limit control of contact-rehydration slugs can behaviourally regulate their body hydration and haemolymph osmolality within the tolerable hydration range described by the upper and lower limits.     

Osmolality and volume factors in salt gland control of pekin ducks after adaptation to chronic salt loading

Summary Pekin ducks were adapted to permanent osmotic stress by rearing them on a NaCl solution of increasing concentration up to 2% as drinking water. Their salt and water balance was compared with that of non-adapted ducks maintained on tap water. Amounts and osmolalities of salt gland secretion and cloacal discharges, plasma osmolality and electrolytes were measured during stepwise osmotic loading by intravenous infusion of NaCl solution of about 740 mosm·kg^–1, at rates of 0.25, 0.45 and 0.65 ml·min^–1. Before loading, the plasma osmolality of the adapted ducks was about 22 mosm·kg^–1 higher than in non-adapted animals. The initial step of loading induced salt gland secretion in the adapted ducks after an average rise of plasma osmolality of 3.6 mosm·kg^–1 and in the non-adapted animals after a rise of 7.8 mosm·kg^–1. The method of osmotic loading enabled both groups of animals to balance their water input and output. However, only the adapted ducks were able to balance NaCl input and output, predominantly by salt gland secretion, thus maintaining a stable plasma osmolality. The nonadapted ducks retained 42% of the salt load which resulted in a rise of plasma osmolality of 49 mosm·kg^–1, more salt being excreted by the kidneys than by the salt glands.In the salt-adapted ducks, salt gland activity, plasma osmolality and Na⁺ concentration did not correlate during balanced states of salt input and output. The involvement of tonicity receptors in salt gland control was confirmed by the stimulating effects of various hypertonic solutions. On the other hand, continuous loading by a constant infusion of NaCl solution of 1,300 mosm·kg^–1 induced a steady salt gland secretion at a rising plasma osmolality and thus suggested that a volume factor is involved in salt gland control. Inhibition of salt gland activity by withdrawing blood and activation by blood infusion confirmed this assumption. While a direct cause and effect relationship between volume changes and salt gland secretion cannot be demonstrated, the results indicate that volume changes in one or more extracellular compartments do affect salt gland secretion.Supported by Deutsche Forschungsgemeinschaft (Si 320/2)     

Plasma levels of arginine vasotocin,prolactin, aldosterone and corticosterone during prolonged dehydration in the domestic flowl: effect of dietary NaCl

Three groups of White Plymouth Rock laying hens were adapted to three levels of dietary NaCl: low-NaCl food with tap water (LOW), high-NaCl food (1% NaCl w/w added) with tap water (HT), and high-NaCl food with 0.5% NaCl for drinking (HS). The birds were subjected to water deprivation (dehydration) for 18 days. Blood sampling was done at 2-4 day intervals. Plasma concentrations of arginine vasotocin (AVT), prolactin (PRL), aldosterone (ALDO) and corticosterone (CS) were determined by radioimmunoassay. Plasma osmolality, sodium, chloride, and potassium were also determined. In the normally hydrated hens fully adapted to the diets, there was a stepwise increase from LOW to HS in plasma osmolality (305, 315, 332 mOsm, for LOW, HT and HS, respectively), [Na+] (144, 153, 161 mM) and [Cl-] (109, 119, 127 mM) as well as in [AVT] (6, 14, 18 pg/ml) and [PRL] (16, 24, 34 ng/ml). Regressing [AVT] on osmolality gave a slope of 0.30 pg . ml-1/mOsm and a threshold of 273 mOsm. The slope of [PRL] on osmolality was 0.73 ng . ml-1/mOsm. The correlation coefficient of [AVT] and [PRL] was 0.67. LOW had high [ALDO] (165 pg/ml) which was suppressed to low levels in HT and HS (5-8 pg/ml), while [CS] was the same in all groups (0.9-1.1 ng/ml). Plasma [K+] was decreased in the high-NaCl groups (5.8 mM in LOW, 4.4 and 4.7 mM in HT and HS). Dehydration resulted within 2 days generally in a sharp (5-15%) increase in osmolality, [Na+] and [Cl-], which thereafter increased more slowly during the remaining 16 days in all groups, with the slowest increase in LOW. The levels of osmolality [Na+] and [Cl-] were 5% lower in LOW than in HT and HS, which showed the same levels during the dehydration period. Plasma [AVT] and [PRL] increased 2-4 fold within 2 days of dehydration; [AVT] reached a plateau at 29 pg/ml in all groups, but [PRL] continued to rise in all groups, fastest in LOW, reaching similar levels in all groups after 14-18 days of dehydration, about 85 ng/ml. The correlation coefficient of [AVT] and [PRL] was decreased by half (to 0.32) during dehydration. Plasma [ALDO] increased in all groups with dehydration, 1.7 fold in LOW and 3-6 fold in HT and HS, but the levels reached in HT and HS were only 15-30% of that seen in LOW.(ABSTRACT TRUNCATED AT 400 WORDS)     

Effect of freezing and dehydration on ion and cryoprotectant distribution and hemolymph volume in the goldenrod gall fly, Eurosta solidaginis

Extracellular freezing and dehydration concentrate hemolymph solutes, which can lead to cellular injury due to excessive water loss. Freeze tolerant larvae of the goldenrod gall fly, Eurosta solidaginis, may experience extreme cold and desiccation in winter. To determine whether larvae employ protective mechanisms against excessive cellular water loss we examined the effect of extracellular freezing and dehydration on hemolymph volume, and cryoprotectant and ion levels in the hemolymph. Dehydrated larvae or ones that had been frozen at −5 or −20 °C had a significantly smaller proportion of their body water as hemolymph (26.0-27.4%) compared to controls (30.5%). Even with this reduction in water content, hemolymph osmolality was similar or only slightly higher in frozen or dehydrated individuals than controls (908 mOsm kg⁻¹), indicating these stresses led to a reduction in hemolymph solutes. Hemolymph and intracellular content of ions remained largely unchanged between treatment groups; although levels of Mg⁺⁺ in the hemolymph were lower in larvae subjected to freezing (0.21 ± 0.01 μg mg⁻¹ dry mass) compared to controls (0.29 ± 0.01 μg mg⁻¹ dry mass), while intracellular levels of K⁺ were lower in groups exposed to low temperature (8.31 ± 0.21 μg mg⁻¹ dry mass). Whole body glycerol and sorbitol content was similar among all treatment groups, averaging 432 ± 25 mOsm kg⁻¹ and 549 ± 78 mOsm kg⁻¹ respectively. However, larvae subjected to dehydration and freezing at −20 °C had a much lower relative amount of cryoprotectants in their hemolymph (∼35%) compared to controls (54%) suggesting these solutes moved into intracellular compartments during these stresses. The correlation between reduced hemolymph volume (i.e. increased cellular water content) and intracellular movement of cryoprotectants may represent a link between tolerance of dehydration and cold in this species.     

The effects of temperature and housing on water balance in a burrowing mouse,Peromyscus polionotus

Summary The effects of temperature and humidity on the water balance of two races ofPeromyscus polionotus were compared to individuals of the same race given moist sand to burrow in. Temperature had the greatest effect on fluid consumption. A change from 20 to 30°C resulted in a significant decrease in the amount of water and 0.4 M NaCl solution consumed. Generally, there was no difference in the amount of water or 0.4 M NaCl consumed at 20°C under different housing conditions, but at 30°C both races consumed significantly more fluids at the low humidity than when occupying a burrow. Considering all types of housing, temperature had a significant effect on a mouse's ability to maintain body weight when stressed with salt water. Irrespective of temperature, weight loss was less and survival greater while drinking salt water for mice in a burrow (92% survival) compared with the high (77% survival) and low (67% survival) humidity conditions.     

The effect of heat acclimation on maximal urine osmolality in humans

The purpose of the current study was to determine the effect of 9 days of active heat acclimation on maximal urine osmolality (MUO) in humans. Eight subjects completed 9 days of heat acclimation, which consisted of a daily 90 min exercise session in a heated environmental chamber. Before and following heat acclimation the subjects abstained from drinking fluids for 15 h, and urine samples were collected to measure MUO. The subjects successfully heat acclimated as evidenced by a significant (P<0.05) decrease in the mean±SD exercise core temperature (37.7±0.3 °C on day 1 to 37.4±0.3 °C on day 9) and heart rate (143±17 bpm on day 1 to 128±14 bpm on day 9). The mean pre- and post-heat acclimation MUOs were 868±117 and 846±89 mmol kg⁻¹, respectively, which were not significantly different (P>0.05). Previous studies have shown that prolonged dehydration can increase the MUO in various mammalian species, including humans. In contrast, the results of the current study suggest that 9 days of active heat acclimation, without significant dehydration, does not affect the MUO in humans.     

Plant transpiration at high elevations: Theory,field measurements,and comparisons with desert plants

Summary The influence of elevational changes on plant transpiration was evaluated using leaf energy balance equations and well-known elevational changes in the physical parameters that influence water vapor diffusion. Simulated transpirational fluxes for large leaves with low and high stomatal resistances to water vapor diffusion were compared to small leaves with identical stomatal resistances at elevations ranging from sea level to 4 km. The specific influence of various air temperature lapse rates was also tested. Validation of the simulated results was accomplished by comparing actual field measurements taken at a low elevation (300 m) desert site with similar measurements for a high elevation (2,560 m) mountain research site. Close agreement was observed between predicted and measured values of transpiration for the environmental and leaf parameters tested.Substantial increases in solar irradiation and the diffusion coefficient for water vapor in air (D _wv) occurred with increasing elevation, while air and leaf temperatures, the water vapor concentration difference between the leaf and air, longwave irradiation, and the thermal conductivity coefficient for heat in air decreased with increasing elevation. These changes resulted in temperatures for sunlit leaves that were further above air temperature at higher elevations, especially for large leaves. For large leaves with low stomatal resistances, transpirational fluxes for low-elevation desert plants were close to those predicted for high-elevation plants even though the sunlit leaf temperatures of these mountain plants were over 10°C cooler. Simulating conditions with a low air temperature lapse rate (0.003° C m^-1 and 0.004° C m^-1) resulted in predicted transpirational fluxes that were greater than those calculated for the desert site. Transpiration for smaller leaves decreased with elevation for all lapse rates tested (0.003° C m^-1 to 0.010° C m^-1). However, transpirational fluxes at higher elevations were considerably greater than expected for all leaves, especially larger leaves, due to the strong influence of increased solar heating and a greater D _wv. These results are discussed in terms of similarities in leaf structure and plant habit observed among low-elevation desert plants and high-elevation alpine and subalpine plants.     

Effects of dehydration on plasma osmolality, thirst-related behavior, and plasma and brain angiotensin concentrations in Couch's spadefoot toad, Scaphiopus couchii

Under dehydrating conditions, many terrestrial vertebrates species exhibit increases in plasma osmolality and their drinking behavior. Under some circumstances, this behavioral change is accompanied by changes in plasma and central angiotensin concentrations, and it has been proposed that these changes in angiotensin levels induce the thirst-related behaviors. In response to dehydration, the spadefoot toad, Scaphiopus couchii, exhibits thirst-related behavior in the form of cutaneous drinking. This behavior has been termed water absorption response (WR) behavior. Spadefoot toads live in harsh desert environments and are subject annually to dehydrating conditions that may induce thirst-related behavior. We tested the hypothesis that an increase in WR behavior is associated with both an increase in plasma osmolality and an increase in plasma and brain angiotensin concentrations. First, we determined the degree of dehydration that was necessary to initiate WR behavior. Animals dehydrated to 85% of their standard bladder-empty weight via deprivation of water exhibited WR behavior more frequently than control toads left in home containers with water available. Next, using the same dehydration methods, we determined the plasma osmolality and sodium concentrations of dehydrated toads. Toads dehydrated to 85% standard weight also had a significant increase in plasma osmolality, but exhibited no overall change in plasma sodium concentrations, indicating that while an overall increase in plasma osmolality appears to be associated with WR behavior in S. couchii, changes in sodium concentrations alone are not sufficient to induce the behavior. Finally, plasma and brain angiotensin concentrations were measured in control toads and toads dehydrated to 85% standard weight. Plasma and brain angiotensin concentrations did not increase in dehydrated toads, indicating that dehydration-induced WR behavior that is associated with changes in plasma osmolality may not be induced by changes in endogenous angiotensin concentrations in S. couchii.     

Contributions of the kidneys and intestines to water conservation,and plasma levels of antidiuretic hormone,during dehydration in house sparrows (Passer domesticus)

Summary The contributions of the kidneys, the small intestine and the lower intestine (rectum plus cloaca) to water conservation during dehydration in unanaesthetized, unrestrained house sparrows (Passer domesticus) were assessed. Thirty hours of acute dehydration resulted in a 12% loss in body mass and a significant increase in plasma osmolality. Glomerular filtration rate declined by 55%, from 7.7 to 3.5 ml/h, and urine flow rate delined by more than 80%, from 0.2 to 0.03 ml/h. These changes are likely attributable to a large increase in plasma levels of arginine vasotocin during dehydration, from <26 pg/ml in hydrated birds to greater than 200 pg/ml after 30 h dehydration. Flow of water from the ileum to the lower intestine was reduced during dehydration, primarily because of a reduced flow of dry matter (with no significant reduction in water content). The rate of water loss in the excreta declined from 0.2 ml/h in hydrated birds to 0.04 ml/h in dehydrated birds. The rate of water reabsorption in the lower intestine (equal to the rate of water loss in the excreta minus the combined rates of inflow into the lower intestine from the urine and the ileal contents) slightly exceeded the rate of water flow from the ileum in both hydrated and dehydrated birds. We suggest that much of the water reabsorbed in the lower intestine of hydrated birds derives from the urine, but that primarily water from ileal contents is reabsorbed in dehydrated birds. That is, urine undergoes significant post-renal modification in hydrated but not dehydrated house sparrows.     

Effects of temperature on larval eclosion of the winter moth, Operophtera brumata

The developmental threshold and heat-unit requirements for larval eclosion of the winter moth, Operophtera brumata (L.) [Lepidoptera: Geometridae], were determined from experiments involving eggs exposed to various chilling and warming treatments. The developmental threshold was determined to be 4 °C. Eggs which were chilled below the developmental threshold required fewer heat-units for larval eclosion than did eggs not given a chill treatment. Eggs cultured at 14 °C required 470 (±47) degree-days for 50% larval eclosion. However, eggs chilled for 2 weeks at 1 °C and subsequently placed at 14 °C required 382 (±33) degree-days while eggs chilled for 12 weeks at 1 °C and subsequently placed at 14 °C required 156 (±12) degree-days. The results are discussed in relation to chilling intensity, diapause, and physiological-time models.

---

Résumé Le seuil de développement et la quantité de chaleur nécessaires pour l'éclosion larvaire chez Operophtera brumata (L.) (Lepidoptera: Geometridae) ont été déterminés en exposant les oeufs à différents régimes de refroidissement suivis de périodes de réchauffement. Le seuil de développement déterminé est de 4 °C. Les oeufs placés d'abord à des températures inférieures à celle du seuil de développement demandent moins de quantité de chaleur pour l'éclosion larvaire, que les oeufs qui n'ont pas été exposés à de basses températures. Les oeufs maintenus à 14 °C demandent 470 (±47) degrés-jours pour permettre 50% d'éclosion. Cependant, des oeufs maintenus pendant 2 semaines à 1 °C, puis à 14 °C, exigent 382 (±33) degrés-jours; ceux placés pendant 12 semaines à 1 °C, puis à 14 °C, en exigent 156 (±12). Les résultats sont discutés en relation avec l'intensité du refroidissement, la diapause et les modèles physiologico-temporels.

     

Effect of water temperature,salinity, and their interaction on growth,plasma osmolality,and gill Na,K-ATPase activity in juvenile GIFT tilapia Oreochromis niloticus (L.)

We used a central composite rotatable experimental design and response surface methodology to evaluate the effects of temperature (18–37 °C), salinity (0–20‰), and their interaction on specific growth rate (SGR), feed efficiency (FE), plasma osmolality, and gill Na⁺, K⁺-ATPase activity in GIFT tilapia juveniles. The linear and quadratic effects of temperature and salinity on SGR, plasma osmolality, and gill Na⁺, K⁺-ATPase activity were statistically significant (P<0.05). The interactive effects of temperature and salinity on plasma osmolality were significant (P<0.05). In contrast, the interaction term was not significant for SGR, FE, and gill Na⁺, K⁺-ATPase activity ⁽P>0.05). The regression equations for SGR, FE, plasma osmolality, and gill Na⁺, K⁺-ATPase activity against the two factors of interest had coefficients of determination of 0.944, 0.984, 0.966, and 0.960, respectively (P<0.01). The optimal temperature/salinity combination was 28.9 °C/7.8‰ at which SGR (2.26% d¹) and FE (0.82) were highest. These values correspond to the optimal temperature/salinity combination (29.1 °C/7.5‰) and the lowest plasma osmolality (348.38 mOsmol kg⁻¹) and gill Na⁺, K⁺-ATPase activity (1.31 µmol Pi. h⁻¹ g⁻¹ protein), and resulted in an energy-saving effect on osmoregulation, which promoted growth.     

Minimizing artifactual elevation of lipid peroxidation products (F2-isoprostanes) in plasma during collection and storage

F₂-isoprostanes (F₂-IsoP’s) are reliable measures of in vivo lipid oxidation, but care is required to prevent artifactual elevation. We examined the effects of blood collection and storage on plasma F₂-IsoP’s. Blood was collected into EDTA/butylated hydroxytoluene/reduced glutathione (EDTA/BHT/GSH) or EDTA, at 4 °C or room temperature. Plasma was stored at −20 or −80 °C for 1 or 6 months before F₂-IsoP’s were assayed by GC–MS. The temperature of blood collection did not affect F₂-IsoP’s. However, storage at −20 °C or collection into EDTA resulted in significant increases in F₂-IsoP’s. Blood collection into EDTA/BHT/GSH and storage at −80 °C minimizes artifactual elevation of plasma F₂-IsoP’s.     

Biology of the shore fly Scatella stagnalis in rockwool under greenhouse conditions

The development times and survival of immature stages in rockwool and the fecundity and longevity of adult Scatella stagnalis were determined and stage-specific life-tables constructed for the species at constant 20 and 25 °C and at a fluctuating temperature (23–34 °C, mean 28.5 °C). Development time from egg to adult decreased with temperature, being 15.9±0.1 days at 20 °C, 11.4±0.1 days at 25 °C and 10.1±0.2 days at fluctuating temperature with mean of 28.5 °C. The lower threshold for egg-to-adult development was 6.4±2.7 °C and the total quantity of thermal energy required to complete development was 212.8±.0 °C. The proportion of females in two populations studied was 0.521. High temperature increased the mortality of pupae from 7% (20 °C) and 10% (25 °C) to 29% at 28.5 °C. At 25 °C, female longevity was 15.5±0.7 days and fecundity 315±19 eggs/female (20.4 eggs/female/day). Males lived for 22.0±1.1 days. At constant 25 °C, the net reproductive rate was 126.1 female eggs/female, generation time was 18.4 days, the doubling time of the population 5.3 days, and the intrinsic rate of increase (r _m) 0.263 day^–1.     

Effect of ingestion pattern on rehydration and exercise performance subsequent to passive dehydration

Six male volunteers performed three tests, each comprising a passive heating session to obtain dehydration (loss of 2.6% body mass), followed by exercise on a treadmill until exhaustion (50% of maximal oxygen consumption) in a warm environment (dry bulb temperature 35° C, relative humidity 20%–30%). In one test, the subjects exercised without rehydration (Dh). In the two other tests, 50% of the fluid lost in the dehydration session was replaced by drinking mineral water given either in one amount [913 (SEM 23) ml] before the exercise (Rh1) or divided into four equal portions [228 (SEM 5) ml] before the exercise and on three occasions at 15-min intervals during exercise (Rh4). Rehydration increased exercise duration in Rh1 compared to Dh [112 (SEM 7) min and 82 (SEM 3) min, respectively;P < 0.05]. The difference was not significant with Rh4 [103 (SEM 9) min]. A restoration of the time course of changes in plasma volume, plasma osmolality, heart rate and rectal temperature occurred immediately in Rh1 and was delayed in Rh4 until after 60 min of exercise. Our results demonstrated that the swift replacement of the fluid loss in the dehydrated subjects was beneficial to exercise performance by rapidly correcting the disturbances in body fluid balance.     

Rehydration with fluid of varying tonicities: effects on fluid regulatory hormones and exercise performance in the heat.

This study examined the effects of rehydration (Rehy) with fluids of varying tonicities and routes of administration after exercise-induced hypohydration on exercise performance, fluid regulatory hormone responses, and cardiovascular and thermoregulatory strain during subsequent exercise in the heat. On four occasions, eight men performed an exercise-dehydration protocol of approximately 185 min (33 degrees C) to establish a 4% reduction in body weight. Following dehydration, 2% of the fluid lost was replaced during the first 45 min of a 100-min rest period by one of three random Rehy treatments (0.9% saline intravenous; 0.45% saline intravenous; 0.45% saline oral) or no Rehy (no fluid) treatment. Subjects then stood for 20 min at 36 degrees C and then walked at 50% maximal oxygen consumption for 90 min. Subsequent to dehydration, plasma Na(+), osmolality, aldosterone, and arginine vasopressin concentrations were elevated (P < 0.05) in each trial, accompanied by a -4% hemoconcentration. Following Rehy, there were no differences (P > 0.05) in fluid volume restored, post-rehydration (Post-Rehy) body weight, or urine volume. Percent change in plasma volume was 5% above pre-Rehy values, and plasma Na(+), osmolality, and fluid regulatory hormones were lower compared with no fluid. During exercise, skin and core temperatures, heart rate, and exercise time were not different (P > 0.05) among the Rehy treatments. Plasma osmolality, Na(+), percent change in plasma volume, and fluid regulatory hormones responded similarly among all Rehy treatments. Neither a fluid of greater tonicity nor the route of administration resulted in a more rapid or greater fluid retention, nor did it enhance heat tolerance or diminish physiological strain during subsequent exercise in the heat.     

Factors affecting low temperature preservation of the marine rotifer Brachionus rotundiformis Tschugunoff

Experiments were performed to determine suitable conditions for low temperature preservation of small S (Fukuoka) and ultra-small SS (Thai) strains of B. rotundiformis. For this, single rotifers (an adult bearing one egg or a 4-h neonate) were incubated for 10 days in 1 ml seawater (22 ppt salinity). The highest survival was achieved at 10 and 12 °C for S-strain and 12 °C for SS-strain. The effect of salinity, change of culture medium and feeding regime were further tested on rotifers (300 ind. ml^–1) cultured in vials containing 10 ml seawater and microalgae at 12 °C. Survival of S-strain was highest (55.5±0.8%) at 35 ppt, while SS-strain survived best (43.1±2.6%) at 17 ppt. Survival was suppressed by changing the culture medium every 4 days. Feeding rotifers every 2 days yielded better survival (66.2±6.6%: S-strains, cultured at 35 ppt and 81.8±5.2%, SS-strains cultured at 17 ppt) than feeding them only at the beginning of the experiment or at 4-day intervals. An acclimation at 20 °C for 24 h before transferring them from their usual culture temperature (28 °C) to 12 °C resulted in higher survival of SS-strain. For S-strain, however, no significant improvement resulted from acclimation. SS-strain was more susceptible to lower temperature and higher salinity than S-strain.