scholarly journals Sources and significance of variation in basal, summit and maximal metabolic rates in birds

2010 ◽  
Vol 56 (6) ◽  
pp. 741-758 ◽  
Author(s):  
Andrew E. Mckechnie ◽  
David L. Swanson
Keyword(s):  
Metabolic Rate ◽  
Power Output ◽  
Power Production ◽  
Evolutionary Significance ◽  
Metabolic Reaction ◽  
Metabolic Rates ◽  
Metabolic Power ◽  
Metabolic Diversity ◽  
Upper Limits ◽  
The Relationship

Abstract The rates at which birds use energy may have profound effects on fitness, thereby influencing physiology, behavior, ecology and evolution. Comparisons of standardized metabolic rates (e.g., lower and upper limits of metabolic power output) present a method for elucidating the effects of ecological and evolutionary factors on the interface between physiology and life history in birds. In this paper we review variation in avian metabolic rates [basal metabolic rate (BMR; minimum normothermic metabolic rate), summit metabolic rate (Msum; maximal thermoregulatory metabolic rate), and maximal metabolic rate (MMR; maximal exercise metabolic rate)], the factors associated with this variation, the evidence for functional links between these metabolic traits, and the ecological and evolutionary significance of avian metabolic diversity. Both lower and upper limits to metabolic power production are phenotypically flexible traits, and vary in association with numerous ecological and evolutionary factors. For both inter- and intraspecific comparisons, lower and upper limits to metabolic power production are generally upregulated in response to energetically demanding conditions and downregulated when energetic demands are relaxed, or under conditions of energetic scarcity. Positive correlations have been documented between BMR, Msum and MMR in some, but not all studies on birds, providing partial support for the idea of a functional link between lower and upper limits to metabolic power production, but more intraspecific studies are needed to determine the robustness of this conclusion. Correlations between BMR and field metabolic rate (or daily energy expenditure) in birds are variable, suggesting that the linkage between these traits is subject to behavioral adjustment, and studies of the relationship between field and maximal metabolic rates are lacking. Our understanding of avian metabolic diversity would benefit from future studies of: (1) the functional and mechanistic links between lower and upper limits of metabolic power output; (2) the environmental and ecological cues driving phenotypically flexible metabolic responses, and how responses to such cues might impact population responses to climate change; (3) the shapes of metabolic reaction norms and their association with environmental variability; and (4) the relationship of metabolic variation to fitness, including studies of repeatability and heritability of minimum and maximum metabolic power output.

Testing the “rate of living” model: further evidence that longevity and metabolic rate are not inversely correlated in Drosophila melanogaster

2004 ◽  
Vol 97 (5) ◽  
pp. 1915-1922 ◽  
Author(s):  
Wayne A. Van Voorhies ◽  
Aziz A. Khazaeli ◽  
James W. Curtsinger
Keyword(s):  
Drosophila Melanogaster ◽  
Metabolic Rate ◽  
Recombinant Inbred ◽  
Recombinant Inbred Lines ◽  
Time Of Day ◽  
Metabolic Rates ◽  
Extended Longevity ◽  
Flow Through ◽  
The Relationship

In a recent study examining the relationship between longevity and metabolism in a large number of recombinant inbred Drosophila melanogaster lines, we found no indication of the inverse relationship between longevity and metabolic rate that one would expect under the classical “rate of living” model. A potential limitation in generalizing from that study is that it was conducted on experimental material derived from a single set of parental strains originally developed over 20 years ago. To determine whether the observations made with those lines are characteristic of the species, we studied metabolic rates and longevities in a second, independently derived set of recombinant inbred lines. We found no correlation in these lines between metabolic rate and longevity, indicating that the ability to both maintain a normal metabolic rate and have extended longevity may apply to D. melanogaster in general. To determine how closely our measurements reflect metabolic rates of flies maintained under conditions of life span assays, we used long-term, flow-through metabolic rate measurements and closed system respirometry to examine the effects of variables such as time of day, feeding state, fly density, mobility of the flies, and nitrogen knockout on D. melanogaster metabolic rate. We found that CO2 production estimated in individual flies accurately reflects metabolic rates of flies under the conditions used for longevity assays.

scholarly journals Basal metabolic rate of birds is associated with habitat temperature and precipitation, not primary productivity

2006 ◽  
Vol 274 (1607) ◽  
pp. 287-293 ◽  
Author(s):  
Craig R White ◽  
Tim M Blackburn ◽  
Graham R Martin ◽  
Patrick J Butler
Keyword(s):  
Metabolic Rate ◽  
Primary Productivity ◽  
Generalized Least Squares ◽  
Arid Environments ◽  
Metabolic Rates ◽  
Habitat Temperature ◽  
Ambient Temperatures ◽  
Temperature And Precipitation ◽  
The World ◽  
The Relationship

A classic example of ecophysiological adaptation is the observation that animals from hot arid environments have lower basal metabolic rates (BMRs, ml O 2  min −1 ) than those from non-arid (luxuriant) ones. However, the term ‘arid’ conceals within it a multitude of characteristics including extreme ambient temperatures ( T a , °C) and low annual net primary productivities (NPPs, g C m −2 ), both of which have been shown to correlate with BMR. To assess the relationship between environmental characteristics and metabolic rate in birds, we collated BMR measurements for 92 populations representing 90 wild-caught species and examined the relationships between BMR and NPP, T a , annual temperature range ( T r ), precipitation and intra-annual coefficient of variation of precipitation ( P CV ). Using conventional non-phylogenetic and phylogenetic generalized least-squares approaches, we found no support for a relationship between BMR and NPP, despite including species captured throughout the world in environments spanning a 35-fold range in NPP. Instead, BMR was negatively associated with T a and T r , and positively associated with P CV .

Cost of Sustained and Burst Swimming to Juvenile Coho Salmon (Oncorhynchus kisutch)

1984 ◽  
Vol 41 (11) ◽  
pp. 1546-1551 ◽  
Author(s):  
K. J. Puckett ◽  
L. M. Dill
Keyword(s):  
Oxygen Consumption ◽  
Metabolic Rate ◽  
Oxygen Consumption Rate ◽  
Sockeye Salmon ◽  
Consumption Rate ◽  
Coho Salmon ◽  
Oncorhynchus Kisutch ◽  
Metabolic Rates ◽  
Burst Swimming ◽  
The Relationship

The relationship between oxygen consumption rate (milligrams per kilogram per hour) and sustained swimming speed (calculated from tailbeat frequency) was determined for 1.2-g juvenile coho salmon (Oncorhynchus kisutch) at 15 °C. The data are best described by the following equation: log oxygen consumption rate = 2.2 + 0.13 (body lengths-s−1). This relationship is very similar to that extrapolated for sockeye salmon (O. nerka) of the same size, thus potentially enabling researchers to utilize the extensive sockeye data base to predict metabolic rates of coho. The oxygen consumption rate during burst swimming (9 body lengths∙s−1) was also determined. The burst swimming metabolic rate (38 000 mgO2∙kg−1∙h−1) is nearly 40 times greater than the maximum sustained swimming metabolic rate.

Selected Contribution: Long-lived Drosophila melanogaster lines exhibit normal metabolic rates

2003 ◽  
Vol 95 (6) ◽  
pp. 2605-2613 ◽  
Author(s):  
Wayne A. Van Voorhies ◽  
Aziz A. Khazaeli ◽  
James W. Curtsinger
Keyword(s):  
Drosophila Melanogaster ◽  
Metabolic Rate ◽  
A Priori ◽  
Model Organisms ◽  
Large Set ◽  
Metabolic Rates ◽  
Powerful Method ◽  
Wide Range ◽  
The Relationship ◽  
Average Adult

The use of model organisms, such as Drosophila melanogaster, provides a powerful method for studying mechanisms of aging. Here we report on a large set of recombinant inbred (RI) D. melanogaster lines that exhibit approximately a fivefold range of average adult longevities. Understanding the factors responsible for the differences in longevity, particularly the characteristics of the longest-lived lines, can provide fundamental insights into the mechanistic correlates of aging. In ectothermic organisms, longevity is often inversely correlated with metabolic rate, suggesting the a priori hypothesis that long-lived lines will have low resting metabolic rates. We conducted ∼6,000 measurements of CO2 production in individual male flies aged 5, 16, 29, and 47 days postemergence and simultaneously measured the weight of individual flies and life spans in populations of each line. Even though there was a wide range of longevities, there was no evidence of an inverse relationship between the variables. The increased longevity of long-lived lines is not mediated through reduction of metabolic activity. In Drosophila, it is possible to both maintain a normal metabolic rate and achieve long life. These results are evaluated in the context of 100 years of research on the relationship between metabolic rate and life span.

Hypoxic metabolic response of the golden-mantled ground squirrel

2001 ◽  
Vol 91 (2) ◽  
pp. 603-612 ◽  
Author(s):  
Renata C. H. Barros ◽  
Mary E. Zimmer ◽  
Luiz G. S. Branco ◽  
William K. Milsom
Keyword(s):  
Heart Rate ◽  
Body Temperature ◽  
Metabolic Rate ◽  
Small Mammals ◽  
Ground Squirrel ◽  
Metabolic Response ◽  
Ground Squirrels ◽  
Metabolic Rates ◽  
The Relationship ◽  
Primary Strategy

We examined the magnitude of the hypoxic metabolic response in golden-mantled ground squirrels to determine whether the shift in thermoregulatory set point (Tset) and subsequent fall in body temperature (Tb) and metabolic rate observed in small mammals were greater in a species that routinely experiences hypoxic burrows and hibernates. We measured the effects of changing ambient temperature (Ta; 6–29°C) on metabolism (O2 consumption and CO2 production), Tb, ventilation, and heart rate in normoxia and hypoxia (7% O2). The magnitude of the hypoxia-induced falls in Tb and metabolism of the squirrels was larger than that of other rodents. Metabolic rate was not simply suppressed but was regulated to assist the initial fall in Tb and then acted to slow this fall and stabilize Tb at a new, lower level. When Ta was reduced during 7% O2, animals were able to maintain or elevate their metabolic rates, suggesting that O2 was not limiting. The slope of the relationship between temperature-corrected O2 consumption and Taextrapolated to a Tset in hypoxia equals the actual Tb. The data suggest that Tset was proportionately related to Ta in hypoxia and that there was a shift from increasing ventilation to increasing O2extraction as the primary strategy employed to meet increasing metabolic demands under hypoxia. The animals were neither hypothermic nor hypometabolic, as Tb and metabolic rate appeared to be tightly regulated at new but lower levels as a result of a coordinated hypoxic metabolic response.

Metabolic correlates of selection for swim stress-induced analgesia in laboratory mice

1997 ◽  
Vol 273 (1) ◽  
pp. R337-R343 ◽  
Author(s):  
M. Konarzewski ◽  
B. Sadowski ◽  
I. Jozwik
Keyword(s):  
Metabolic Rate ◽  
Core Body Temperature ◽  
Metabolic Rates ◽  
Laboratory Mice ◽  
Swim Stress ◽  
Upper Limits ◽  
Maximal Metabolic Rate ◽  
Selection For ◽  
Core Body ◽  
Selection Agent

The upper limits of metabolic rates and the links between maximal and resting metabolic rates in vertebrates have recently received a lot of attention, mainly due to their possible relationship to the evolution of endothermy. We measured peak metabolic rates during 3 min swimming in 20 degrees C water (Vo2swim), maximal metabolic rate (Vo2max) in -2.5 degrees C Helox, and basal metabolic rate (BMR) in two lines of mice selected for high (HA) and low (LA) swim stress-induced analgesia (SSIA). We found that exercise combined with heat loss used for producing SSIA also acted as a selection agent, resulting in a 15% HA/LA line difference in Vo2swim. Core body temperature of HA mice (characterized by lower Vo2swim) was also on average 3.2 degrees C lower than that of LA mice. Furthermore, Vo2max of HA mice was lower than that of LA mice by 8% and accompanied by larger hypothermia. Thus mice with exceptionally high (or low) Vo2max tended to have exceptionally high (or low) Vo2swim, resulting in a positive correlation between Vo2swim and Vo2max. All these suggest that selection for SSIA produced genetically correlated responses in both Vo2swim and Vo2max. However, we did not observe HA/LA differences in BMR. Hence, changes in resting and maximum metabolic rates are not necessarily correlated. We hypothesize that the lack of such a correlation was partially due to the modulation of metabolic responses by SSIA.

scholarly journals Metabolic physiology explains macroevolutionary trends in the melanic colour system across amniotes

2018 ◽  
Vol 285 (1893) ◽  
pp. 20182014 ◽  
Author(s):  
Chad M. Eliason ◽  
Julia A. Clarke
Keyword(s):  
Metabolic Rate ◽  
Expression Patterns ◽  
Specific Gene ◽  
Rate Variation ◽  
Metabolic Rates ◽  
Melanocortin System ◽  
Metabolic Physiology ◽  
Colour System ◽  
The Relationship

Metabolism links organisms to their environment through its effects on thermoregulation, feeding behaviour and energetics. Genes involved in metabolic processes have known pleiotropic effects on some melanic colour traits. Understanding links between physiology and melanic colour is critical for understanding the role of, and potential constraints on, colour production. Despite considerable variation in metabolic rates and presumed ancestral melanic coloration in vertebrates, few studies have looked at a potential relationship between these two systems in a comparative framework. Here, we test the hypothesis that changes in melanosome shape in integumentary structures track metabolic rate variation across amniotes. Using multivariate comparative analyses and incorporating both extant and fossil taxa, we find significantly faster rates of melanosome shape evolution in taxa with high metabolic rates, as well as both colour- and clade-specific differences in the relationship between metabolic rate and melanosome shape. Phylogenetic tests recover an expansion in melanosome morphospace in maniraptoran dinosaurs, as well as rate shifts within birds (in songbirds) and mammals. These findings indicate another core phenotype influenced by metabolic changes in vertebrates. They also provide a framework for testing clade-specific gene expression patterns in the melanocortin system and may improve colour reconstructions in extinct taxa.

scholarly journals Metabolic rate covaries with fitness and the pace of the life history in the field

2016 ◽  
Vol 283 (1831) ◽  
pp. 20160323 ◽  
Author(s):  
Amanda K. Pettersen ◽  
Craig R. White ◽  
Dustin J. Marshall
Keyword(s):  
Growth Rate ◽  
Life History ◽  
Metabolic Rate ◽  
Reproductive Output ◽  
The Other ◽  
Metabolic Rates ◽  
Fitness Components ◽  
Entire Life ◽  
The Relationship ◽  
Growth And Reproduction

Metabolic rate reflects the ‘pace of life’ in every organism. Metabolic rate is related to an organism's capacity for essential maintenance, growth and reproduction—all of which interact to affect fitness. Although thousands of measurements of metabolic rate have been made, the microevolutionary forces that shape metabolic rate remain poorly resolved. The relationship between metabolic rate and components of fitness are often inconsistent, possibly because these fitness components incompletely map to actual fitness and often negatively covary with each other. Here we measure metabolic rate across ontogeny and monitor its effects on actual fitness (lifetime reproductive output) for a marine bryozoan in the field. We also measure key components of fitness throughout the entire life history including growth rate, longevity and age at the onset of reproduction. We found that correlational selection favours individuals with higher metabolic rates in one stage and lower metabolic rates in the other—individuals with similar metabolic rates in each developmental stage displayed the lowest fitness. Furthermore, individuals with the lowest metabolic rates lived for longer and reproduced more, but they also grew more slowly and took longer to reproduce initially. That metabolic rate is related to the pace of the life history in nature has long been suggested by macroevolutionary patterns but this study reveals the microevolutionary processes that probably generated these patterns.

scholarly journals Metabolic traits in brown trout (Salmo trutta) vary in response to food restriction and intrinsic factors

2020 ◽  
Vol 8 (1) ◽  
Author(s):  
Louise C Archer ◽  
Stephen A Hutton ◽  
Luke Harman ◽  
W Russell Poole ◽  
Patrick Gargan ◽  
...  
Keyword(s):  
Life History ◽  
Metabolic Rate ◽  
Intraspecific Variation ◽  
Brown Trout ◽  
Environmental Conditions ◽  
Food Restriction ◽  
Metabolic Rates ◽  
Intrinsic Factors ◽  
Metabolic Traits ◽  
Food Conditions

Abstract Metabolic rates vary hugely within and between populations, yet we know relatively little about factors causing intraspecific variation. Since metabolic rate determines the energetic cost of life, uncovering these sources of variation is important to understand and forecast responses to environmental change. Moreover, few studies have examined factors causing intraspecific variation in metabolic flexibility. We explore how extrinsic environmental conditions and intrinsic factors contribute to variation in metabolic traits in brown trout, an iconic and polymorphic species that is threatened across much of its native range. We measured metabolic traits in offspring from two wild populations that naturally show life-history variation in migratory tactics (one anadromous, i.e. sea-migratory, one non-anadromous) that we reared under either optimal food or experimental conditions of long-term food restriction (lasting between 7 and 17 months). Both populations showed decreased standard metabolic rates (SMR—baseline energy requirements) under low food conditions. The anadromous population had higher maximum metabolic rate (MMR) than the non-anadromous population, and marginally higher SMR. The MMR difference was greater than SMR and consequently aerobic scope (AS) was higher in the anadromous population. MMR and AS were both higher in males than females. The anadromous population also had higher AS under low food compared to optimal food conditions, consistent with population-specific effects of food restriction on AS. Our results suggest different components of metabolic rate can vary in their response to environmental conditions, and according to intrinsic (population-background/sex) effects. Populations might further differ in their flexibility of metabolic traits, potentially due to intrinsic factors related to life history (e.g. migratory tactics). More comparisons of populations/individuals with divergent life histories will help to reveal this. Overall, our study suggests that incorporating an understanding of metabolic trait variation and flexibility and linking this to life history and demography will improve our ability to conserve populations experiencing global change.

Metabolic Rate and Energy Expenditure of the Spiny Dogfish, Squalus acanthias

1978 ◽  
Vol 35 (6) ◽  
pp. 816-821 ◽  
Author(s):  
J. R. Brett ◽  
J. M. Blackburn
Keyword(s):  
Energy Expenditure ◽  
Metabolic Rate ◽  
Key Words ◽  
Swimming Performance ◽  
Squalus Acanthias ◽  
Spiny Dogfish ◽  
Metabolic Rates ◽  
Performance Curve ◽  
Power Performance ◽  
General Energy

The metabolic rate of spiny dogfish, Squalus acanthias, was determined in both a tunnel respirometer and a large, covered, circular tank (mass respirometer). Swimming performance was very poor in the respirometer, so that a power–performance curve could not be established. Instead, resting metabolic rates were determined, with higher rates induced by causing heavy thrashing (active metabolism). Routine metabolic rates were measured for the spontaneous activity characterizing behavior in the circular tank. For fish of 2 kg mean weight, the metabolic rates at 10 °C were 32.4 ± 2.6 SE (resting), 49.2 ± 5.0 SE (routine), and 88.4 ± 4.6 SE (active) mg O2∙kg−1∙h−1. Assuming that the routine rate represents a general energy expenditure in nature, this is equivalent to metabolizing about 3.8 kcal∙kg−1∙d−1 (15.9 × 103 J∙kg−1∙d−1). Key words: dogfish, metabolic rates, energetics, respiration

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