Metabolism and evaporative water loss of Western Australian geckos (Reptilia : Sauria : Gekkonomorpha)

2000 ◽  
Vol 48 (2) ◽  
pp. 111 ◽  
Author(s):  
P. C. Withers ◽  
K. P. Aplin ◽  
Y. L. Werner

Resting metabolic rate (RMR) and evaporative water loss (EWL) were measured, and resistance (R) to evaporative water loss and water use index (WUI = EWL/RMR) were calculated, for 22 species of Western Australian gecko. For all available gecko data, body mass and temperature explained 85% of the variability in RMR (=14.5 mass0.833 100.0398 Ta µL h–1), and 70% of the variability in EWL (=0.126 mass0.539 100.049 Ta mg h–1 ). For Western Australian geckos, RMR and EWL were significantly influenced by body mass, using conventional regression and phylogenetic analyses. Resistance to evaporative water loss (R) was not significantly affected by body mass. Water use index was inversely related to body mass: WUI = 21.9 M–0.344 mg mL O2–1. There were significant differences between species for R and for standardised residuals of RMR, EWL and WUI. R was not correlated with phylogeny, and was significantly higher (P = 0.020) for saxicolous geckos (1467 s cm-1) than terrestrial geckos (797 s cm–1); arboreal geckos had an intermediate R (977 s cm–1). Species that ate termites had lower standardised linear regression residuals (P = 0.003) for RMR than did species that ate more general diets. Standardised residuals for EWL were almost significantly related to microhabitat (P = 0.053). Standardised residuals for WUI were significantly related to microhabitat (P = 0.016); saxicolous species had lower WUI than terrestrial species. Standardised linear regression residuals of the residuals from autoregression (which should be independent of both mass and phylogeny effects) still significantly correlated RMR and diet, but not EWL or WUI with microhabitat.

1997 ◽  
Vol 18 (2) ◽  
pp. 177-190 ◽  
Author(s):  
G.G. Thompson ◽  
P.C. Withers

AbstractThe common intra-specific mass exponent for the standard evaporative water loss was 0.86 for nine species of goanna (V. gilleni, V. caudolineatus, V. brevicauda, V. eremius, V. acanthurus, V. tristis, V. gouldii, V. rosenbergi and V. panoptes). The inter-specific mass exponent for evaporative water loss (EWL) was 0.95; EWL (mg h-1) = 2.149M0.95 The overall resistance to water loss was significantly lower inter-specifically for larger species than smaller species; however, there was no significant intra-specific relationship between resistance and body mass. The evaporative water loss of arboreal goannas (V caudolineatus, V gilleni and V. tristis) was less than that of terrestrial goannas (V brevicauda, V eremius, V acanthurus, V. gouldii, V rosenbergi and V. panoptes); this presumably reflects the exposure of these arboreal goannas to higher wind velocity and drier air. The more mesic V. rosenbergi had a higher evaporative water loss than the more arid species.


Water ◽  
2018 ◽  
Vol 10 (12) ◽  
pp. 1883 ◽  
Author(s):  
Angela Hof ◽  
Enrique Morán-Tejeda ◽  
Jorge Lorenzo-Lacruz ◽  
Macià Blázquez-Salom

The Balearic Islands are a major Mediterranean tourist destination that features one of the greatest swimming pool densities within Europe. In this paper, standard meteorological data were combined with a diachronic swimming pool inventory to estimate water evaporation from swimming pools over the Balearic archipelago. Evaporation was estimated using an empirical equation designed for open-water surfaces. Results revealed a 32% increase in swimming pools’ water use by 2015. Evaporation from swimming pools added 9.6 L of water to touristic consumption per guest night and person, and represented 4.9% of the total urban water consumption. In 2015, almost 5 hm3 (5 billion L) were lost from pools across the Balearic Islands. In several densely urbanized areas, evaporative water loss from pools exceeded four million litres per square kilometre and year. The water needed to refill the total of 62,599 swimming pools and to counteract evaporative water loss is equivalent to 1.2 pools per year. Swimming pools have rapidly proliferated across the islands. We have expounded on this development in view of much-needed responsible water management across the islands.


PeerJ ◽  
2019 ◽  
Vol 7 ◽  
pp. e7885 ◽  
Author(s):  
Mohlamatsane Mokhatla ◽  
John Measey ◽  
Ben Smit

Temperature and water availability are two of the most important variables affecting all aspects of an anuran’s key physiological processes such as body temperature (Tb), evaporative water loss (EWL) and standard metabolic rate (SMR). Since anurans display pronounced sexual dimorphism, evidence suggests that these processes are further influenced by other factors such as vapour pressure deficit (VPD), sex and body mass (Mb). However, a limited number of studies have tested the generality of these results across a wide range of ecologically relevant ambient temperatures (Ta), while taking habitat use into account. Thus, the aim of this study was to investigate the role of Ta on Tb, whole-animal EWL and whole-animal SMR in three wild caught African anuran species with different ecological specialisations: the principally aquatic African clawed frog (Xenopus laevis), stream-breeding common river frog (Amietia delalandii), and the largely terrestrial raucous toad (Sclerophrys capensis). Experiments were conducted at a range of test temperatures (5–35 °C, at 5 °C increments). We found that VPD better predicted rates of EWL than Ta in two of the three species considered. Moreover, we found that Tb, whole-animal EWL and whole-animal SMR increased with increasing Ta, while Tb increased with increasing Mb in A. delalandii and S. capensis but not in X. laevis. Whole-animal SMR increased with increasing Mb in S. capensis only. We did not find any significant effect of VPD, Mb or sex on whole-animal EWL within species. Lastly, Mb did not influence Tb, whole-animal SMR and EWL in the principally aquatic X. laevis. These results suggest that Mb may not have the same effect on key physiological variables, and that the influence of Mb may also depend on the species ecological specialisation. Thus, the generality of Mb as an important factor should be taken in the context of both physiology and species habitat specialisation.


2021 ◽  
Vol 224 (13) ◽  
Author(s):  
Emily S. Choy ◽  
Ryan S. O'Connor ◽  
H. Grant Gilchrist ◽  
Anna L. Hargreaves ◽  
Oliver P. Love ◽  
...  

ABSTRACT The Arctic is warming at approximately twice the global rate, with well-documented indirect effects on wildlife. However, few studies have examined the direct effects of warming temperatures on Arctic wildlife, leaving the importance of heat stress unclear. Here, we assessed the direct effects of increasing air temperatures on the physiology of thick-billed murres (Uria lomvia), an Arctic seabird with reported mortalities due to heat stress while nesting on sun-exposed cliffs. We used flow-through respirometry to measure the response of body temperature, resting metabolic rate, evaporative water loss and evaporative cooling efficiency (the ratio of evaporative heat loss to metabolic heat production) in murres while experimentally increasing air temperature. Murres had limited heat tolerance, exhibiting: (1) a low maximum body temperature (43.3°C); (2) a moderate increase in resting metabolic rate relative that within their thermoneutral zone (1.57 times); (3) a small increase in evaporative water loss rate relative that within their thermoneutral zone (1.26 times); and (4) a low maximum evaporative cooling efficiency (0.33). Moreover, evaporative cooling efficiency decreased with increasing air temperature, suggesting murres were producing heat at a faster rate than they were dissipating it. Larger murres also had a higher rate of increase in resting metabolic rate and a lower rate of increase in evaporative water loss than smaller murres; therefore, evaporative cooling efficiency declined with increasing body mass. As a cold-adapted bird, murres' limited heat tolerance likely explains their mortality on warm days. Direct effects of overheating on Arctic wildlife may be an important but under-reported impact of climate change.


1981 ◽  
Vol 54 (2) ◽  
pp. 195-202 ◽  
Author(s):  
James R. Spotila ◽  
Christina J. Weinheimer ◽  
Charles V. Paganelli

1986 ◽  
Vol 59 (1) ◽  
pp. 1-9 ◽  
Author(s):  
David S. Hinds ◽  
Richard E. MacMillen

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