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1.
Using video cameras and motion detection software, we examined sequential positions of the lizard Podarcis carbonelli in a temperature gradient to look for patterns in spatial and temporal thermoregulatory movements. As lizards shuttled between warm and cool areas, their movements were typically slow; punctuated by bursts of speed. The animals were relatively inactive when heating, moved almost continually when cooling, and spent less time heating than cooling. Traditional modeling techniques proved unsuccessful, so we assessed the movement patterns with nonlinear dynamical techniques. The shuttling frequency, and the pattern of velocity changes, both met the qualitative attributes (self similarity, strange attractors, and noisy power spectra) and the quantitative criteria (positive Lyapunov exponent and capacity and/or correlation dimensions less than 5) that suggest deterministic chaos. These movement patterns appear regular, but at unpredictable times the patterns become disturbed before returning to regulation. There are both behavioral and physiological advantages to movements that follow a model of deterministic chaos control. 相似文献
2.
We examined the contributions of alterations in daily activity and behavioral selection of microhabitat to thermoregulation in a population of the lizard, Ameiva exsul (Teiidae), by combining data on lizard activity with data on the availability of sun-shade patches and operative temperatures (Te). By comparing Te distributions predicted by “no thermoregulation” and “only thermoregulation” hypotheses to those predicted by random use of thermal habitat, we assessed the relative contributions of microhabitat selection and daily activity to regulation of body temperature (Tb). Over the course of a day lizards maintained Tb very close to optimal temperature (Tsel) despite Tes that deviated substantially from Tsel. Data demonstrating a unimodal daily activity pattern reject the hypothesis of uniform activity throughout the day. Also, lizard activity was not positively correlated with the proportion of Tes within Tsel nor negatively correlated with the absolute deviation of available Te from Tsel (de) (“only thermoregulation”). Microsite use by A. exsul deviated significantly from predictions of the “no thermoregulation” hypothesis, but our data could not reject predictions of the “only thermoregulation” hypothesis that lizards would use sun-shade patches relative to the proportion of microsites where Te is within Tsel. Also, lizards appeared to actively select sunlit and partially shaded microsites at different times of day. Thus, despite thermal constraints imposed by the habitat, A. exsul maintained high and relatively constant Tbs throughout its daily activity period and thermoregulated effectively. This appears to be generally representative of West Indian species of Ameiva. 相似文献
3.
We investigate how a unique dietary specialist, the Gila monster (Heloderma suspectum), uses behavioral thermoregulation to elevate body temperature (Tb) after feeding. Lizards in a laboratory thermal gradient were fed rodent meals of three different sizes (5, 10, or 20% of body mass), or sham fed (meal of 0% body mass), and Tbs were recorded for three days before feeding and seven days after feeding. Gila monsters selected a mean Tb of 25.2 °C while fasting (set-point range 23.6–27.1), and increased Tbs after feeding. The magnitude and duration of post-prandial Tb increases are positively related to meal size, and Gila monsters selected mean Tbs up to 3.0 °C higher and maintain elevated Tbs for 3–6 days after feeding. Selection of Tb does not appear to differ between day and night time periods, and because the lizards are both diurnal and nocturnal (at different times of year), photoperiod may not be an important influence on Tb selection. 相似文献
4.
To investigate patterns of thermoregulation in free-ranging and captive southern brown bandicoots Isoodon obesulus, we measured abdominal body temperature (Tb) of five free-ranging bandicoots over 42 days using implanted data loggers and Tb of three captive bandicoots over 3 months using implanted temperature-sensitive radio transmitters. Bandicoots in the wild had a mean Tb of 36.5±1.0 °C (range 33.4–39.8 °C) and showed a pronounced nychthemeral pattern with two distinct temperature phases. Tb increased at 13:30±2.6 h each day and remained high for 10.65±2.07 h, suggesting a crepuscular and early evening activity pattern. Daily Tb variation of I. obesulus would save considerable energy by reducing daytime thermoregulatory costs in the wild. Captive bandicoots had a similar mean body temperature (36.9±0.2°C) and range (33.0–39.9°C) as free-ranging bandicoots. However, the nychthemeral Tb pattern of captive bandicoots was different from free-ranging bandicoots, with a less pronounced daily cycle and the nocturnal rise in Tb occurring mainly at sunset and the daily decline occurring mainly at dawn. 相似文献
5.
Ectotherms in water experience rates of heat transfer at least two orders of magnitude greater than in air, seriously constraining their thermoregulatory capabilities. Yet, even in water, individuals may exert control over body temperature (Tb) via behaviors such as selecting thermally favorable microhabitats. The interactions among body size, physiology, and behavior on the thermal biology of large, entirely aquatic, ectotherms is poorly understood. We tested the hypothesis that alligator snapping turtles (Macroclemmys temminckii) selected microhabitats based on temperature by comparing temperatures at sites used by turtles to temperatures at randomly selected sites. These large turtles selected a narrow range of microhabitats that were significantly warmer and less variable in temperature than random sites. Cooling trials in the laboratory indicated larger turtles equilibrated more slowly to ambient temperature (Ta) than smaller turtles. We recorded Ta and body temperature (Tb) of turtles in the field continuously throughout the year. The Tb generally conformed to Ta but there were periods when Tb−Ta differences were great. These results suggest that while physiology and size of aquatic turtles can affect Tb transiently, microhabitat selection may be the only meaningful mechanism for large, entirely aquatic, turtles to control Tb. 相似文献
6.
Liu C Li R Liu Z Yin S Wang Z 《Journal of comparative physiology. B, Biochemical, systemic, and environmental physiology》2006,176(4):321-328
Typically, small lizards rely heavily on behavioral thermoregulation rather than physiological mechanisms to control their rates of warming and cooling. We tested the hypothesis that prostaglandins participate in mediating the cardiovascular response to heating and cooling and temperature regulating neurons in the hypothalamus of the small lizard Phrynocephalus przewalskii. In vivo and in vitro treatments, heart rates (HRs) were all found to be higher during heating than during cooling, hysteresis was distinct below 30 and 26°C, respectively. In vivo, as administration of COX inhibitor, there were no differences in HR between heating and cooling at any body temperature and administration of agonist prostaglandins only produced a significant effect on HR below 25°C. Single-unit activity was recorded extracellularly in vitro with microelectrodes, found the firing rate of the continuous unit increased 23% when the temperature of the artificial cerebrospinal fluid dropped from 30–20°C. We conclude that prostaglandins appear to play only a limited role in modulating heart activity in Phrynocephalus przewalskii and suggest that cold-sensitive neurons in the preoptic and anterior hypothalamus (PO/AH) are involved in thermoregulatory control during heating or cooling. 相似文献
7.
Arthur Georges 《Journal of thermal biology》1979,4(3):213-217
When heated radiantly, head-body temperature gradients developed in both live and dead Tiliqua scincoides. The gradients were consistently larger in live than in dead individuals, indicating they were enhanced by a physiological component superimposed on the more basic physical components. Large gradients in the initial phases of heating represented a lag effect, the head core beginning to receive heat before the body core because it is closer to the heated surface. Once this lag effect subsided, the body heated more rapidly than the head because it presented a greater incident surface area per unit mass than did the head. Living lizards appeared to maintain head-body temperature differences until the maximum voluntary temperature was approached. 相似文献
8.
中华花龟幼体热耐受性、体温昼夜变化和运动表现的热依赖性 总被引:3,自引:3,他引:3
为研究中华花龟(Ocadia sinensis)幼体的热耐受性和运动表现热依赖性,设计了具有和缺乏温度梯度两种热环境,研究幼龟体温的昼夜变化。高、低温耐受性分别用临界高温和临界低温表示,体温为泄殖腔温度,水温和气温分别是幼龟所处位置的水温和1cm高气温。临界高温和临界低温分别为41.9℃和1.8℃。在有温度梯度的热环境中,体温、水温和气温平均值有显著的昼夜差异,水温和体温的日平均值无显著差异,两者均大于气温的日平均值。在缺乏温度梯度的热环境中,体温、气温和水温平均值亦有显著的昼夜差异,但气温、水温和体温的日平均温度无显著差异。温度梯度是幼龟进行体温调节不可或缺的条件,选择体温有显著的昼夜变化,最大值和最小值分别为29.2℃和25.4℃。在02:00—06:00时间段内,幼龟选择体温明显较低,其它测定时刻的选择体温无显著差异。幼龟各测定时刻的平均体温与平均气温和水温均呈正相关。处于温度梯度中幼龟特定气温的体温比处于缺乏温度梯度中的幼龟高3.7℃,这种差异是前者利用温度梯度进行体温调节的结果;处于不同热环境中幼龟特定水温的体温无显著差异。体温显著影响幼龟的运动表现。18—39℃体温范围内,疾跑速随体温增加而增加,36℃和39℃体温的幼龟疾跑速最大;体温达到41℃时,疾跑速显著下降。体温较高的幼龟的最大持续运动距离大于体温较低的幼龟。偏相关分析显示,疾跑速与最大持续运动距离和停顿次数呈显著的正相关,停顿次数与最大持续运动距离呈负相关。 相似文献
9.
1. We compared the mean, limits and breadth of the preferred thermal range (PTR) of two Iberian populations of the lizard Psammodromus algirus separated by 700 m altitude in May and July. 相似文献
10.
Geiser F Brigham RM 《Journal of comparative physiology. B, Biochemical, systemic, and environmental physiology》2000,170(2):153-162
Previous studies have suggested that Australian long-eared bats (Nyctophilus) differ from northern-hemisphere bats with respect to their thermal physiology and patterns of torpor. To determine whether
this is a general trait of Australian bats, we characterised the temporal organisation of torpor and quantified metabolic
rates and body temperatures of normothermic and torpid Australian bats (Nyctophilus geoffroyi, 7 g and N. gouldi, 10 g) over a range of air temperatures and in different seasons. The basal metabolic rate of normothermic bats was 1.36 ± 0.17 ml g−1 h−1 (N. geoffroyi) and 1.22 ± 0.13 ml g−1 h−1 (N. gouldi), about 65% of that predicted by allometric equations, and the corresponding body temperature was about 36 °C. Below an air
temperature of about 25 °C bats usually remained normothermic for only brief periods and typically entered torpor. Arousal
from torpor usually occurred shortly after the beginning of the dark phase and torpor re-entry occurred almost always during
the dark phase after normothermic periods of only 111 ± 48 min (N. geoffroyi) and 115 ± 66 min (N. gouldi). At air temperatures below 10 °C, bats remained torpid for more than 1 day. Bats that were measured overnight had steady-state
torpor metabolic rates representing only 2.7% (N. geoffroyi) and 4.2% (N. gouldi) of the basal metabolic rate, and their body temperatures fell to minima of 1.4 and 2.3 °C, respectively. In contrast, bats
measured entirely during the day, as in previous studies, had torpor metabolic rates that were up to ten times higher than
those measured overnight. The steady-state torpor metabolic rate of thermoconforming torpid bats showed an exponential relationship
with body temperature (r
2 = 0.94), suggesting that temperature effects are important for reduction of metabolic rate below basal levels. However, the
75% reduction of metabolic rate between basal metabolic rate and torpor metabolic rate at a body temperature of 29.3 °C suggests
that metabolic inhibition also plays an important role. Torpor metabolic rate showed little or no seasonal change. Our study
suggests that Australian Nyctophilus bats have a low basal metabolic rate and that their patterns of torpor are similar to those measured in bats from the northern
hemisphere. The low basal metabolic rate and the high proclivity of these bats for using torpor suggest that they are constrained
by limited energy availability and that heterothermy plays a key role in their natural biology.
Accepted: 22 November 1999 相似文献
11.
Birds exposed to seasonal environments are faced with the problem of maintaining thermogenic homoeostasis. Previous studies have established that birds native to the Holarctic increase their Resting Metabolic Rate at different ambient temperatures (RMRTa) and Basal Metabolic Rate (BMR) in winter as an adaptation to cold temperature since winters are more severe, while their non-Holarctic counterparts generally decrease their winter BMR as an energy saving mechanism during unproductive and dry winter months. In this study, we examined seasonal thermoregulation in the burrowing parrot (Cyanoliseus patagonus), a colonial psittacine native to the Patagonian region of Argentina, a region with an unpredictable environment. We found significantly higher mass specific RMRTa and BMR in summer than in winter. Both summer and winter BMR of the species fell within the predicted 95% confident interval for a parrot of its size. Body mass was significantly higher in winter than in summer. The burrowing parrot had broad thermo-neutral zones in winter and summer. The circadian rhythm of core body temperature (Tb) of burrowing parrots was not affected by season, showing that this species regulated its Tb irrespective of season. These results suggest that the burrowing parrots' seasonal thermoregulatory responses represent that of energy conservation which is important in an unpredictable environment. 相似文献
12.
- 1.
- Thermoregulatory behavior of fed and fasted desert hamsters (Phodopus roborovskii) acclimated to summer- [16 light (L):8 dark (D), ambient temperature (Ta)=26.5 °C] and winter-like (8L:16D, Ta=10 °C) conditions was studied. Body temperature (Tb), selected temperature and activity were measured in hamsters placed in a thermal gradient system for 48 h. 相似文献
13.
Variations in body temperature (Tb) of lizards can be partially explained by intrinsic factors such as sex, ontogeny and body size. Liolaemus lutzae is a lizard species restricted to restingas in the Brazilian coast in the state of Rio de Janeiro. Herein, we studied sexual dimorphism and influences of sex, ontogeny, and body size to the Tb of L. lutzae. Adult males were larger than adult females, probably due to both intersexual selection and intra-sexual selection. There was intersexual difference in lizards' Tb (males hotter than females), but Tb did not differ after factored out for the effects of body size. The mean Tb of juvenile lizards was higher than that of adults after factored out for the effect of body mass. It is possible that adults may have excluded juveniles from microhabitats with better thermal regimes. Also, this might have occurred due to requirements of juveniles to maintain high growth rates. Forage searching for prey by juveniles also exposes them to high environmental temperatures. Juveniles also may have higher Tb than co-specific adults (relative to body mass) to favor prey capture. In absolute values, adult lizards tended to use microhabitats with lower temperatures than that used by juveniles, possibly to avoid risks of overheating and death. Body temperature and snout–vent length were positively related, as well as body temperature and body mass, presumably caused by the thermal inertia of the bodies (trend of a body to resist to changes in its temperature). Intrinsic factors such as sex, ontogeny and body size can affect the thermal ecology of L. lutzae, despite coastal habitat features to which they are exposed also influences the body temperature of active lizards in restinga habitats. 相似文献
14.
- 1.
- Various factors affect a reptile's capacity for thermoregulation and most studies have focussed on terrestrial species.
- 2.
- We investigated the thermoregulatory abilities of the yellow anaconda (Eunectes notaeus) in terms of selected body temperature (Tsel), set-point range (Tset) and body posture in terrestrial and aquatic thermal mosaics.
- 3.
- Yellow anacondas selected higher body temperatures (Tb) and have a narrower Tset in a terrestrial environment than in an aquatic one.
- 4.
- Coiled body postures were most frequently observed and were generally associated with higher Tb.
15.
We studied the ecology of Tropidurus itambere and T. oreadicus that occur syntopically in rocky habitats of Cerrado vegetation in central Brazil during the dry season (April to September 2000). The two species are ecologically similar, but somewhat differentiated in vertical microhabitat use. The two species preferred rocky surface microhabitat. Both species demonstrated a unimodal activity pattern, with a peak between 10 and 15 h. Their diets were similar in composition and prey size. The most frequent item used by both species was ants, whereas the most important preys volumetrically were termites and ants. Small morphological differences observed between the two Tropidurus species could explain minor microhabitat divergence: T. itambere is slightly smaller, heavier, and more robust, and uses lower perches. T. oreadicus is larger, lankier, with longer extremities (tail, fore- and hindlegs), and uses a larger vertical microhabitat range. These ecological differences are slight, when compared with those observed between sympatric species of Tropidurus in spatially more heterogeneous landscapes. Considering the slight ecomorphological divergence between the two Tropidurus species and their high abundance in outcrops, we suggest that interspecific territoriality is the mechanism of coexistence. 相似文献
16.
Seasonal variations in ambient temperature (Ta) require changes in thermoregulatory responses of endotherms. These responses vary according to several factors including taxon and energy constraints. Despite a plethora of studies on chiropteran variations in thermoregulation, few have examined African species. In this study, we used the Wahlberg's epauletted fruit bat (Epomophorus wahlbergi, body mass≈115 g) to determine how the thermoregulatory abilities of an Afrotropical chiropteran respond to seasonal changes in Ta. Mass specific Resting Metabolic Rates (RMRTa) and basal metabolic rate (BMR) were significantly higher in winter than in summer. Furthermore, winter body mass was significantly higher than summer body mass. A broad thermoneutral zone (TNZ) was observed in winter (15–35 °C) compared with summer (25–30 °C). This species exhibited heterothermy (rectal and core body temperature) during the photophase (bats' rest-phase) particularly at lower Tas and had a low tolerance of high Tas. Overall, there was a significant seasonal variation in the thermoregulatory abilities of E. wahlbergi. The relative paucity of data relating to the seasonal thermoregulatory abilities of Afrotropical bats suggest further work is needed for comparison and possible effects of climate change, particularly extreme hot days. 相似文献
17.
Cameron J. van den Heuvel Sally A. Ferguson Saul S. Gilbert Drew Dawson 《Journal of thermal biology》2004,29(7-8):457-461
Sleepiness and changes in body temperature are temporally associated. (2) There is mounting evidence that insomnia may be caused by impaired heat loss capacity. (3) New techniques such as infrared thermal imaging may be useful tools to investigate thermoregulatory changes associated with sleep in humans. 相似文献
18.
Peter H. Brice Gordon C. Grigg Lyn A. Beard Janette A. Donovan 《Journal of thermal biology》2002,27(6):355-457
(1) Echidnas occur throughout the hot arid zone of Australia yet laboratory studies have concluded that they are ill equipped physiologically to manage Ta higher than 35°C. (2) Consequently, it is generally assumed that echidnas must rely on behavioural thermoregulation, being nocturnal in hot weather and seeking less extreme microclimates during the day. (3) By monitoring Tb of echidnas in the field and relating these to Ta within their day time shelters in Western Queensland during summer, this study showed that echidnas are able to tolerate Ta of 35–40°C in hollow logs for up to 10 h. (4) Further, as Tb remains < Ta in these situations, echidnas may have physiological mechanisms for dealing with the heat after all. 相似文献
19.
Color and color patterns in animals are important characteristics that bring protection, by dampening the ability of predators that depend on their sight to detect their preys. In lizards, the dorsal coloration plays a key role in communication of intraspecific signals such as social cues. In this study, we evaluated the seasonal changes in the dorsal coloration of the wide foraging lizard A. costata costata, in Tonatico, State of Mexico, Mexico. The seasonal evaluation included: the rainy season from mid June to mid September (can also include the end of May to early October); and the dry season for the rest of the year. The dorsal coloration of A. costata costata and their microhabitats were evaluated by contrasting the color pattern with an identification guide and the control colors of Pantone, during 11 samplings carried out from February-October 2007. Individual lizard analysis recorded snout-vent length, sex and stage (juveniles and adults). Besides, all animals were marked by toe-clipping, allowing to distinguish dorsal coloration between seasons, sex and stage. A total of 95 lizards were analyzed (53 and 42 for the dry and rainy seasons respectively). We found that the dorsal coloration in A. costata costata varies seasonally and with microhabitats: during the dry season individuals show a brown coloration whereas during the rainy season becomes greener, as the background dominant vegetation color. The results of the present study suggest that: 1) the variation in dorsal coloration in A. costata costata plays an important role in the survival (by cryptic camouflage) of this widely foraging species; 2) the changes in the dorsal coloration of A. costata costata are individually expressed traits, since the coloration of the same lizard is either brown or green depending on the season; and 3) the cryptic functions of the dorsal coloration in widely foraging species have been largely underestimated. We discuss the possible influence of the changes in coloration in an habitat that changes drastically between both dry and rainy seasons. 相似文献
20.
- 1.
- Field body temperatures (Tb's) of Chamaeleo chamaeleon in southwestern Spain averaged 28 °C in October and 30 °C in June. Slopes of regressions of Tb on Ta (ambient temperature at perch height) indicated that individuals were able to maintain a preferred body temperature of about 30 °C in June but not in October. 相似文献