Corticosterone Treatment Has Subtle Effects on Thermoregulatory Behavior and Raises Metabolic Rate in the New Zealand Common Gecko, Hoplodactylus maculatus

2008 ◽  
Vol 81 (5) ◽  
pp. 641-650 ◽  
Author(s):  
Marion R. Preest ◽  
Alison Cree
Keyword(s):  
New Zealand ◽  
Metabolic Rate ◽  
Thermoregulatory Behavior ◽  
Corticosterone Treatment

Daily Patterns of Metabolic Rate among New Zealand Lizards (Reptilia: Lacertilia: Diplodactylidae and Scincidae)

2006 ◽  
Vol 79 (4) ◽  
pp. 745-753 ◽  
Author(s):  
Kelly M. Hare ◽  
Shirley Pledger ◽  
Michael B. Thompson ◽  
John H. Miller ◽  
Charles H. Daugherty
Keyword(s):  
New Zealand ◽  
Metabolic Rate ◽  
Daily Patterns

Foraging energetics and diving behavior of lactating New Zealand sea lions, Phocarctos hookeri

2000 ◽  
Vol 203 (23) ◽  
pp. 3655-3665 ◽  
Author(s):  
D.P. Costa ◽  
N.J. Gales
Keyword(s):  
New Zealand ◽  
Metabolic Rate ◽  
Dive Depth ◽  
Diving Behavior ◽  
Metabolic Rates ◽  
Sea Lion ◽  
Water Turnover ◽  
Sea Lions ◽  
The Mean ◽  
Phocarctos Hookeri

The New Zealand sea lion, Phocarctos hookeri, is the deepest- and longest-diving sea lion. We were interested in whether the diving ability of this animal was related to changes in its at-sea and diving metabolic rates. We measured the metabolic rate, water turnover and diving behavior of 12 lactating New Zealand sea lions at Sandy Bay, Enderby Island, Auckland Islands Group, New Zealand (50 degrees 30′S, 166 degrees 17′E), during January and February 1997 when their pups were between 1 and 2 months old. Metabolic rate (rate of CO(2) production) and water turnover were measured using the (18)O doubly-labeled water technique, and diving behavior was measured with time/depth recorders (TDRs). Mean total body water was 66.0+/−1.1 % (mean +/− s.d.) and mean rate of CO(2) production was 0. 835+/−0.114 ml g(−)(1)h(−)(1), which provides an estimated mass-specific field metabolic rate (FMR) of 5.47+/−0.75 W kg(−)(1). After correction for time on shore, the at-sea FMR was estimated to be 6.65+/−1.09 W kg(−)(1), a value 5.8 times the predicted standard metabolic rate of a terrestrial animal of equal size. The mean maximum dive depth was 353+/−164 m, with a mean diving depth of 124+/−36 m. The mean maximum dive duration was 8.3+/−1.7 min, with an average duration of 3.4+/−0.6 min. The deepest, 550 m, and longest, 11.5 min, dives were made by the largest animal (155 kg). Our results indicate that the deep and long-duration diving ability of New Zealand sea lions is not due to a decreased diving metabolic rate. Individual sea lions that performed deeper dives had lower FMRs, which may result from the use of energetically efficient burst-and-glide locomotion. There are differences in the foraging patterns of deep and shallow divers that may reflect differences in surface swimming, time spent on the surface and/or diet. Our data indicate that, although New Zealand sea lions have increased their O(2) storage capacity, they do not, or cannot, significantly reduce their at-sea metabolic rates and are therefore likely to be operating near their physiological maximum.

scholarly journals The Paradox of Nocturnality in Lizards

2021 ◽  
Author(s):  
◽  
Kelly Maree Hare
Keyword(s):  
New Zealand ◽  
Metabolic Rate ◽  
Low Temperatures ◽  
Specific Activity ◽  
Glycolytic Enzyme ◽  
Activity Period ◽  
Energetic Cost ◽  
Metabolic Processes ◽  
Biochemical Adaptation ◽  
Daily Patterns

<p>Paradoxically, nocturnal lizards prefer substantially higher body temperatures than are achievable at night and are therefore active at thermally suboptimal temperatures. In this study, potential physiological mechanisms were examined that may enable nocturnal lizards to counteract the thermal handicap of activity at low temperatures: 1) daily rhythms of metabolic rate, 2) metabolic rate at low and high temperatures, 3) locomotor energetics, and 4) biochemical adaptation. A multi-species approach was used to separate evolutionary history of the species from any potential links between physiology and activity period. Four to eight species of lizards, encompassing nocturnal and diurnal lizards from the families Diplodactylidae and Scincidae, were used for all physiological measurements. Three daily patterns of metabolic rate (VO2) were apparent depending on the species: 24 h cycles, 12 h cycles, and no daily cycle. The daily patterns of VO2 and peak VO2 did not always coincide with the activity period of the species. All nocturnal lizards tested had a lower energetic cost of locomotion (Cmin) than diurnal lizards. Diurnal lizards from New Zealand also had low Cmin values when compared with nocturnal geckos and diurnal lizards from lower latitudes. Thus, a low Cmin appears to be related to activity at low temperatures rather than specifically to nocturnality. However, more data are required on lizards from high latitudes, including more New Zealand lizards, before the generality of this pattern can be confirmed. Also, based on correlations with lizards active at warmer temperatures, a low Cmin only partially offsets the thermal handicap imposed on lizards that are active at low temperatures. Nocturnal lizards were found to have lower thermal sensitivities of metabolism (lower Q10 values) than diurnal lizards, indicating that their energy-dependent activity was not as sensitive to changes in environmental temperature. The similarity of other metabolic processes among species with differing activity periods may be partly explained by the ability of nocturnal species to thermoregulate to achieve higher temperatures during the day. The amplitudes of daily VO2 cycles and mass-specific VO2 did not differ among nocturnal and diurnal New Zealand lizards at low temperatures. The specific activity of the glycolytic enzyme lactate dehydrogenase (LDH) isolated from the tail muscle of lizards was also comparable among nocturnal and diurnal lizards over a range of biologically relevant temperatures. Thus, activity of lizards at low temperatures is not enabled by lower energy requirements over a 24 h period, elevation of metabolic rates, or biochemical adaptation of LDH to specific temperatures. These results confirm that locomotion is more efficient in nocturnal lizards and diurnal lizards from New Zealand than lizards from elsewhere, but that other metabolic processes do not appear to differ among species. Additional physiological and behavioural adaptations may exist that complement the increased efficiency of locomotion, thus enabling nocturnal lizards to be active at low temperatures.</p>

Intracranial ethanol and ambient anoxia elicit selection of cooler water by goldfish

1989 ◽  
Vol 256 (1) ◽  
pp. R133-R137 ◽  
Author(s):  
L. I. Crawshaw ◽  
L. P. Wollmuth ◽  
C. S. O'Connor
Keyword(s):  
Temperature Gradient ◽  
Metabolic Rate ◽  
Survival Time ◽  
Control Group ◽  
Base Line ◽  
Thermoregulatory Behavior ◽  
Anterior Aspect ◽  
Normoxic Control ◽  
Selection Of ◽  
Effective Site

Goldfish were either subjected to anoxia for 5 h at 10 degrees C, normoxia for 5 h at 10 degrees C, or were implanted with an intracranial microinjection cannula. All groups were subsequently tested in a temperature gradient. The previously anoxic goldfish selected cooler temperatures (12.8 +/- 1.0 degrees C; mean +/- SE) than the corresponding normoxic control group (17.5 +/- 0.7 degrees C) for the first 20 min in the gradient. Intracranial microinjections of 0.0475 ng ethanol in 0.2 microliter 0.7% NaCl led to the immediate selection of water 8.7 +/- 1.5 degrees C below that of base-line levels, whereas control animals injected with 0.7% NaCl selected water 0.9 +/- 1.0 degree C cooler. Increased effects were obtained with higher concentrations of ethanol. The effective site was limited to the anterior aspect of the nucleus preopticus periventricularis; injections into 54 other loci were without effect. Goldfish tolerate anoxia by the conversion of lactate to ethanol, which diffuses across the gills. As the lost ethanol cannot be oxidatively metabolized, this process is energetically inefficient. Because the concentration of the ethanol injections was considerably lower than reported ethanol concentrations in the tissues of anoxic goldfish, endogenously produced ethanol may have induced the selection of cooler water by the anoxic goldfish. This alteration in thermoregulatory behavior would lead to a lower metabolic rate, significantly increasing survival time during anoxia.

scholarly journals Orderly recruitment of thermoeffectors in resting humans

2018 ◽  
Vol 314 (2) ◽  
pp. R171-R180 ◽  
Author(s):  
Zachary J. Schlader ◽  
James R. Sackett ◽  
Suman Sarker ◽  
Blair D. Johnson
Keyword(s):  
Blood Flow ◽  
Metabolic Rate ◽  
Thermal Behavior ◽  
Skin Temperature ◽  
Skin Blood Flow ◽  
Sweat Rate ◽  
Flow Behavior ◽  
Thermoregulatory Behavior ◽  
Physiological Cost ◽  
Heat And Cold Stress

The recruitment of thermoeffectors, including thermoregulatory behavior, relative to changes in body temperature has not been quantified in humans. We tested the hypothesis that changes in skin blood flow, behavior, and sweating or metabolic rate are initiated with increasing changes in mean skin temperature (Tskin) in resting humans. While wearing a water-perfused suit, 12 healthy young adults underwent heat (Heat) and cold stress (Cold) that induced gradual changes in Tskin. Subjects controlled the temperature of their dorsal neck to their perceived thermal comfort. Thus neck skin temperature provided an index of thermoregulatory behavior. Neck skin temperature (Tskin), core temperature (Tcore), metabolic rate, sweat rate, and nonglabrous skin blood flow were measured continually. Data were analyzed using segmental regression analysis, providing an index of thermoeffector activation relative to changes in Tskin. In Heat, increases in skin blood flow were observed with the smallest elevations in Tskin ( P < 0.01). Thermal behavior was initiated with an increase in Tskin of 2.4 ± 1.3°C (mean ± SD, P = 0.04), while sweating was observed with further elevations in Tskin (3.4 ± 0.5°C, P = 0.04), which coincided with increases in Tcore ( P = 0.98). In Cold, reductions in skin blood flow occurred with the smallest decrease in Tskin ( P < 0.01). Thermal behavior was initiated with a Tskin decrease of 1.5 ± 1.3°C, while metabolic rate ( P = 0.10) and Tcore ( P = 0.76) did not change throughout. These data indicate that autonomic and behavioral thermoeffectors are recruited in coordination with one another and likely in an orderly manner relative to the comparative physiological cost.

scholarly journals The Paradox of Nocturnality in Lizards

2021 ◽  
Author(s):  
◽  
Kelly Maree Hare
Keyword(s):  
New Zealand ◽  
Metabolic Rate ◽  
Low Temperatures ◽  
Specific Activity ◽  
Glycolytic Enzyme ◽  
Activity Period ◽  
Energetic Cost ◽  
Metabolic Processes ◽  
Biochemical Adaptation ◽  
Daily Patterns

<p>Paradoxically, nocturnal lizards prefer substantially higher body temperatures than are achievable at night and are therefore active at thermally suboptimal temperatures. In this study, potential physiological mechanisms were examined that may enable nocturnal lizards to counteract the thermal handicap of activity at low temperatures: 1) daily rhythms of metabolic rate, 2) metabolic rate at low and high temperatures, 3) locomotor energetics, and 4) biochemical adaptation. A multi-species approach was used to separate evolutionary history of the species from any potential links between physiology and activity period. Four to eight species of lizards, encompassing nocturnal and diurnal lizards from the families Diplodactylidae and Scincidae, were used for all physiological measurements. Three daily patterns of metabolic rate (VO2) were apparent depending on the species: 24 h cycles, 12 h cycles, and no daily cycle. The daily patterns of VO2 and peak VO2 did not always coincide with the activity period of the species. All nocturnal lizards tested had a lower energetic cost of locomotion (Cmin) than diurnal lizards. Diurnal lizards from New Zealand also had low Cmin values when compared with nocturnal geckos and diurnal lizards from lower latitudes. Thus, a low Cmin appears to be related to activity at low temperatures rather than specifically to nocturnality. However, more data are required on lizards from high latitudes, including more New Zealand lizards, before the generality of this pattern can be confirmed. Also, based on correlations with lizards active at warmer temperatures, a low Cmin only partially offsets the thermal handicap imposed on lizards that are active at low temperatures. Nocturnal lizards were found to have lower thermal sensitivities of metabolism (lower Q10 values) than diurnal lizards, indicating that their energy-dependent activity was not as sensitive to changes in environmental temperature. The similarity of other metabolic processes among species with differing activity periods may be partly explained by the ability of nocturnal species to thermoregulate to achieve higher temperatures during the day. The amplitudes of daily VO2 cycles and mass-specific VO2 did not differ among nocturnal and diurnal New Zealand lizards at low temperatures. The specific activity of the glycolytic enzyme lactate dehydrogenase (LDH) isolated from the tail muscle of lizards was also comparable among nocturnal and diurnal lizards over a range of biologically relevant temperatures. Thus, activity of lizards at low temperatures is not enabled by lower energy requirements over a 24 h period, elevation of metabolic rates, or biochemical adaptation of LDH to specific temperatures. These results confirm that locomotion is more efficient in nocturnal lizards and diurnal lizards from New Zealand than lizards from elsewhere, but that other metabolic processes do not appear to differ among species. Additional physiological and behavioural adaptations may exist that complement the increased efficiency of locomotion, thus enabling nocturnal lizards to be active at low temperatures.</p>

Magellanic Cloud Eclipsing Binaries: Primary Distance Indicators

1999 ◽  
Vol 190 ◽  
pp. 563-566
Author(s):  
J. D. Pritchard ◽  
W. Tobin ◽  
J. V. Clausen ◽  
E. F. Guinan ◽  
E. L. Fitzpatrick ◽  
...  
Keyword(s):  
New Zealand ◽  
Magellanic Cloud ◽  
Eclipsing Binaries ◽  
Fundamental Parameters ◽  
Distance Indicators

Our collaboration involves groups in Denmark, the U.S.A. Spain and of course New Zealand. Combining ground-based and satellite (IUEandHST) observations we aim to determine accurate and precise stellar fundamental parameters for the components of Magellanic Cloud Eclipsing Binaries as well as the distances to these systems and hence the parent galaxies themselves. This poster presents our latest progress.

Heat-Etching with a Bullivant Type II Simple Freeze-Cleave Device

1970 ◽  
Vol 28 ◽  
pp. 106-107 ◽  
Author(s):  
Ronald S. Weinstein ◽  
N. Scott McNutt
Keyword(s):  
New Zealand ◽  
General Hospital ◽  
Massachusetts General Hospital ◽  
Type I ◽  
Type Ii ◽  
Collaborative Effort ◽  
Temperature And Pressure ◽  
The University

The Type I simple cold block device was described by Bullivant and Ames in 1966 and represented the product of the first successful effort to simplify the equipment required to do sophisticated freeze-cleave techniques. Bullivant, Weinstein and Someda described the Type II device which is a modification of the Type I device and was developed as a collaborative effort at the Massachusetts General Hospital and the University of Auckland, New Zealand. The modifications reduced specimen contamination and provided controlled specimen warming for heat-etching of fracture faces. We have now tested the Mass. General Hospital version of the Type II device (called the “Type II-MGH device”) on a wide variety of biological specimens and have established temperature and pressure curves for routine heat-etching with the device.

A Cytochemical Study of Glucose-6-Phosphatase (G-6-PASE) in Cells Participating in Atherogenesis of Rabbit Aorta

1975 ◽  
Vol 33 ◽  
pp. 460-461
Author(s):  
Sidney D. Kobernick ◽  
Edna A. Elfont ◽  
Neddra L. Brooks
Keyword(s):  
Lipid Metabolism ◽  
New Zealand ◽  
Aortic Wall ◽  
Rabbit Aorta ◽  
Plaque Formation ◽  
Metabolic Changes ◽  
Atherosclerotic Plaques ◽  
Cytochemical Study ◽  
Cellular Alteration ◽  
New Zealand White Rabbits

This cytochemical study was designed to investigate early metabolic changes in the aortic wall that might lead to or accompany development of atherosclerotic plaques in rabbits. The hypothesis that the primary cellular alteration leading to plaque formation might be due to changes in either carbohydrate or lipid metabolism led to histochemical studies that showed elevation of G-6-Pase in atherosclerotic plaques of rabbit aorta. This observation initiated the present investigation to determine how early in plaque formation and in which cells this change could be observed.Male New Zealand white rabbits of approximately 2000 kg consumed normal diets or diets containing 0.25 or 1.0 gm of cholesterol per day for 10, 50 and 90 days. Aortas were injected jin situ with glutaraldehyde fixative and dissected out. The plaques were identified, isolated, minced and fixed for not more than 10 minutes. Incubation and postfixation proceeded as described by Leskes and co-workers.

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