The role of torpor in the life of Australian arid zone mammals.

2004 ◽  
Vol 26 (2) ◽  
pp. 125 ◽  
Author(s):  
F Geiser

Approximately half of the Australian continent is arid and is characterised by low primary productivity, limited supply of food and pronounced daily fluctuations of ambient temperature (Ta). Despite these adverse conditions the diversity of small mammals in the Australian arid zone is high, although their abundance is generally low. The most successful groups of small arid zone mammals are the dasyurid marsupials, native rodents, and insectivorous bats. A probable reason for the success of the insectivorous dasyurids and bats, which must cope with strong fluctuations in food and water availability, is their extensive use of torpor. Mammalian torpor is characterised by substantial reductions of body temperature (Tb) metabolic rate (MR) and water loss. Small arid zone dasyurids use exclusively daily torpor, some even during the reproductive season, when most mammals maintain strict homeothermy. Dasyurids reduce Tb from ~ 35�C during normothermia to ~ 15�C during torpor, the MR during torpor (TMR) is ~ 30% of basal metabolic rate (BMR). Mass loss, and thus water loss, is related to the duration of torpor bouts. Dasyurids usually enter torpor at night or in the early morning and arouse around midday or in the afternoon. Recent evidence shows that desert dasyurids may bask in the sun during rewarming from torpor. This can minimise energetic cost of arousal to a fraction of that required for endogenous warming. Arid zone bats are also likely to use torpor extensively, but few species, specific to the arid zone, have been studied. Nevertheless, widely distributed bats that occur in the arid zone, such as Nyctophilus geoffroyi, enter brief torpor for part of the day in summer and prolonged torpor (hibernation) for up to two weeks in winter and can reduce Tb to a minimum of 2 - 3�C and TMR to ~ 3% of BMR; mass loss and water loss are minimal during torpor. Patterns of torpor similar to those in bats also have been observed in the insectivorous echidnas and two species of insectivorous / nectarivorous pygmy-possums, which have distribution ranges that include semi-arid and arid areas. In contrast to these species, no detailed information is available on torpor in native Australian rodents, because little work with respect to torpor has been conducted in Australia. However, many arid zone rodents on other continents employ torpor and it is likely that Australian rodents do as well. In addition to reducing energy expenditure and water loss, use of torpor also appears to prolong life span. This is important for bridging adverse conditions and for subsequent re-colonization of areas after droughts and fires in inland Australia. Thus it appears that the success of small insectivorous/nectarivorous mammals and perhaps rodents in the Australian arid zone is partially due to their use of torpor.

2001 ◽  
Vol 204 (13) ◽  
pp. 2301-2311 ◽  
Author(s):  
Joseph B. Williams ◽  
Stéphane Ostrowski ◽  
Eric Bedin ◽  
Khairi Ismail

SUMMARY We report on the energy expenditure and water flux, measured in the laboratory and in the field, of the Arabian oryx Oryx leucoryx, the largest desert ruminant for which measurements of the field metabolic rate of free-living individuals have been made using doubly labeled water. Prior to extirpation of this species in the wild in 1972, conservationists sequestered a number of individuals for captive breeding; in 1989, oryx were reintroduced in Saudi Arabia into Mahazat as-Sayd (2244km2). Apart from small pools of water available after rains, oryx do not have free-standing water available for drinking and therefore rely on grasses that they eat for preformed water intake as well as their energy needs. We tested whether oryx have a reduced fasting metabolic rate and total evaporative water loss (TEWL) in the laboratory, as do some other arid-adapted mammals, and whether oryx have high field metabolic rates (FMRs) and water influx rates (WIRs), as predicted by allometric equations for large arid-zone mammals. We measured FMR and WIR during the hot summer, when plant moisture content was low and ambient temperatures were high, and after winter rains, when the water content of grasses was high. For captive oryx that weighed 84.1kg, fasting metabolic rate averaged 8980kJday−1, 16.7% lower than predictions for Artiodactyla. Our own re-analysis of minimal metabolic rates among Artiodactyla yielded the equation: logV̇O2=−0.153+0.758logM, where V̇O2 is the rate of oxygen uptake in lh−1 and M is body mass in kg. Fasting metabolic rate of oryx was only 9.1% lower than predicted, suggesting that they do not have an unusually low metabolic rate. TEWL averaged 870.0mlday−1, 63.9% lower than predicted, a remarkably low value even compared with the camel, but the mechanisms that contribute to such low rates of water loss remain unresolved. For free-living oryx, FMR was 11076kJday−1 for animals with a mean body mass of 81.5kg during summer, whereas it was 22081kJday−1 for oryx in spring with a mean body mass of 89.0kg, values that were 48.6% and 90.4% of allometric predictions, respectively. During summer, WIR averaged 1310mlH2Oday−1, whereas in spring it was 3438mlH2Oday−1. Compared with allometric predictions, WIR was 76.9% lower than expected in summer and 43.6% lower in spring. We found no evidence to support the view that the WIR of large desert ungulates is higher than that of their mesic counterparts. On the basis of the WIR of the oryx averaged over the year and the water contents of plants in their diet, we estimated that an oryx consumes 858kg of dry matter per year.


2020 ◽  
pp. jeb.227264
Author(s):  
Miguel Leis ◽  
Claudio R. Lazzari

Active searching for vertebrate blood is a necessary activity for haematophagous insects, and it can be assumed that this search should also be costly in terms of energetic expenditure. Either if it is by swimming, walking, running or flying, active movement requires energy, increasing metabolic rates relative to resting situations. We analysed the respiratory pattern and the energetic cost of pedestrian locomotion in the blood-sucking bug Rhodnius prolixus using flow-through respirometry, by measuring carbon dioxide emission and water loss before, during and after walking. We observed an increase of up to 1.7-fold in the metabolic rate during walking as compared to resting in male R. prolixus and 1.5-fold in females, as well as a change in their respiratory pattern. The last switched from cyclic during resting to continuous, when the insects started to walk, remaining this condition unchanged during locomotion and for several minutes after stopping. Walking induced a significant loss of weight in both, males and females. This can be explained by the increase in both, the metabolic rate and the water loss during walking. These data constitute the first metabolic measures of active hematophagous insects and provide the first insights on the energetic expenditure associated to the active search for blood in this group.


2016 ◽  
Vol 94 (12) ◽  
pp. 829-836 ◽  
Author(s):  
B.J. Klüg-Baerwald ◽  
L.E. Gower ◽  
C.L. Lausen ◽  
R.M. Brigham

Winter activity of bats is common, yet poorly understood. Other studies suggest a relationship between winter activity and ambient temperature, particularly temperature at sunset. We recorded echolocation calls to determine correlates of hourly bat activity in Dinosaur Provincial Park, Alberta, Canada. We documented bat activity in temperatures as low as −10.4 °C. We observed big brown bats (Eptesicus fuscus (Palisot de Beauvois, 1796)) flying at colder temperatures than species of Myotis bats (genus Myotis Kaup, 1829). We show that temperature and wind are important predictors of winter activity by E. fuscus and Myotis, and that Myotis may also use changes in barometric pressure to cue activity. In the absence of foraging opportunity, we suggest these environmental factors relate to heat loss and thus the energetic cost of flight. To understand the energetic consequences of bat flight in cold temperatures, we estimated energy expenditure during winter flights of E. fuscus and little brown myotis (Myotis lucifugus (Le Conte, 1831)) using species-specific parameters. We estimated that winter flight uses considerable fat stores and that flight thermogenesis could mitigate energetic costs by 20% or more. We also show that temperature-dependent interspecific differences in winter activity likely stem from differences between species in heat loss and potential for activity–thermoregulatory heat substitution.


1983 ◽  
Vol 57 (3_suppl) ◽  
pp. 1255-1262 ◽  
Author(s):  
Michael A. Persinger

Mystical and religious experiences are hypothesized to be evoked by transient, electrical microseizures within deep structures of the temporal lobe. Although experiential details are affected by context and reinforcement history, basic themes reflect the inclusion of different amygdaloid-hippocampal structures and adjacent cortices. Whereas the unusual electrical coherence allows access to infantile memories of parents, a source of god expectations, specific stimulation evokes out-of-body experiences, space-time distortions, intense meaningfulness, and dreamy scenes. The species-specific similarities in temporal lobe properties enhance the homogeneity of cross-cultural experiences. They exist along a continuum that ranges from “early morning highs” to recurrent bouts of conversion and dominating religiosity. Predisposing factors include any biochemical or genetic factors that produce temporal lobe lability. A variety of precipitating stimuli provoke these experiences, but personal (life) crises and death bed conditions are optimal. These temporal lobe microseizures can be learned as responses to existential trauma because stimulation is of powerful intrinsic reward regions and reduction of death anxiety occurs. The implications of these transients as potent modifiers of human behavior are considered.


2019 ◽  
Vol 6 (4) ◽  
pp. 36-41
Author(s):  
Elaine Gleice Silva Moreira ◽  
Scarlet Aguiar Basílio ◽  
Mariany Dalila Milan ◽  
Natália Arruda ◽  
Katiane Santiago Silva Benett

Arugula is mainly cultivated by small producers, being a leafy vegetable susceptible to water loss and wilting after harvest, which may result in changes in appearance, texture, color (yellowing), and nutritional value of the product. Hydrocooling is a cooling method that stands out for being simple, practical and efficient. Its use is to reduce the temperature and respiratory rate of vegetables after harvesting by immersion in ice or cold water, so they can be packed and stored. This study was conducted to evaluate the hydrocooling efficiency when associated with the storage period in the postharvest shelf life of arugula leaves. Arugula leaves were subjected to ten days of storage, and measurements were taken at 0, 2, 4, 6, 8 and 10 days. The experimental design was completely randomized in a 3 × 6 factorial scheme, consisting of three hydrocooling treatments [control (without cooling), and hydrocooling at 0 °C and 10 °C] and for six storage periods (0, 2, 4, 6, 8 and 10 days) with three replicates. Fresh mass loss, soluble solids, titratable acidity, pH and subjective evaluation of product appearance were measured. Hydrocooling at 0 °C proved to be the most appropriate treatment when compared to control, as reported by the values of fresh mass loss, soluble solids, and titratable acidity. Hydrocooling to 0 °C slowed leaf water loss (lower respiratory rate) and resulted in better overall leaf appearance up to the sixth day of storage, thereby increasing shelf life of arugula leaves.


2021 ◽  
Author(s):  
Heiko T. Jansen ◽  
Brandon Evans Hutzenbiler ◽  
Hannah R. Hapner ◽  
Madeline L. McPhee ◽  
Anthony M. Carnahan ◽  
...  

ABSTRACTHibernation is characterized by suppression of many physiological processes. To determine if this state is reversible in a non-food caching species, we fed hibernating grizzly bears (Ursus arctos horribilis) glucose for 10 days to replace 53% or 100% of the estimated minimum daily energetic cost of hibernation. Feeding caused serum concentrations of glycerol and ketones (ß-hydroxybutyrate) to return to active season levels irrespective of the amount of glucose fed. By contrast, free-fatty acids and indices of metabolic rate, such as general activity, heart rate, and strength of the daily heart rate rhythm and insulin sensitivity were restored to roughly 50% of active season levels. Body temperature was unaffected by feeding. To determine the contribution of adipose to these metabolic effects of glucose feeding we cultured bear adipocytes collected at the beginning and end of the feeding and performed metabolic flux analysis. We found a roughly 33% increase in energy metabolism after feeding. Moreover, basal metabolism before feeding was 40% lower in hibernation cells compared to fed cells or active cells cultured at 37°C, thereby confirming the temperature independence of metabolic rate. The partial suppression of circulating FFA with feeding likely explains the incomplete restoration of insulin sensitivity and other metabolic parameters in hibernating bears. Further suppression of metabolic function is likely an active process. Together, the results provide a highly controlled model to examine the relationship between nutrient availability and metabolism on the hibernation phenotype in bears.


2019 ◽  
Vol 107 (1) ◽  
Author(s):  
Sofia Cividini ◽  
Spyros Sfenthourakis ◽  
Giuseppe Montesanto

AbstractThe capability of producing sounds and vibrations is well known in insects and is thought to be a form of intra- and interspecific communication. Sounds and vibrations are used and modulated for several aims such as interacting with conspecifics, getting information from the environment, and defending against predators. This phenomenon is less known but also present in other arthropods, including a few roller-type terrestrial isopods. In this study, we used a Y-shape test apparatus to investigate the behavior of adult individuals of Armadillo officinalis Duméril, 1816 (Crustacea: Isopoda: Oniscidea) when exposed to two particular vibrational stimuli, namely species-specific stridulations and non-specific substrate-borne vibrations. Our results showed that adults of A. officinalis significantly react to the presence of both types of vibrational stimuli, by moving away from the vibrational source as if they experienced these vibrations as a sign of danger or disturbance. A. officinalis can produce stridulations only when it rolls into a ball during the so-called conglobation, a possible defense mechanism against predators. Stridulation might thus be a secondary form of defense used during conglobation to deter a predator following contact with it and might be experienced as an alert by conspecifics nearby. The high sensitivity to non-specific substrate-borne vibrations might provide A. officinalis with the possibility to anticipate dangers and adverse conditions, giving it a better chance of survival.


1999 ◽  
Vol 77 (9) ◽  
pp. 1474-1485 ◽  
Author(s):  
Paul G Jensen ◽  
Peter J Pekins ◽  
James B Holter

For northern white-tailed deer (Odocoileus virginianus) fawns, the energetic cost of thermoregulation (HcE) during severe winters can result in substantial catabolism of body-tissue reserves. The heat increment of feeding (HiE) has the potential to offset thermoregulatory energy expenditure that would otherwise require the catabolism of these reserves. During winters 1996 and 1997, we conducted 18 fasting and 18 on-feed heat-production trials using indirect respiration calorimetry in a metabolic chamber. Nonlinear regression analysis was used to estimate the lower critical temperatures (Tlc) and determine the fasting metabolic rate (FMR) and resting metabolic rate (RMR). Resulting models were used to calculate HiE, HcE, and percent substitution of HiE for HcE. For fawns fed a natural browse diet, estimated FMR and RMR were 352 and 490 kJ·kg body mass (BM)-0.75·d-1, respectively; this 40% increase in thermoneutral heat production reduced Tlc from -0.8 to -11.2°C between the fasted and fed states, respectively, and reduced HcE by 59% for fed fawns. For fawns fed a concentrate diet, estimated FMR and RMR were 377 and 573 kJ·kg BM-0.75·d-1, respectively. Level of browse intake had a significant effect on RMR andTlc. RMR was 12% higher for fawns on a high versus a low level of intake, and estimated Tlc was -15.6 and -5.8°C, respectively. Our data indicate that the energetic cost of thermoregulation is probably a minor portion of the energy budget of a healthy fawn consuming natural forage.


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