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Daily Energy Expenditure (daily + energy_expenditure)
Selected AbstractsDaily energy expenditure of singing great reed warblers Acrocephalus arundinaceusJOURNAL OF AVIAN BIOLOGY, Issue 4 2008Dennis Hasselquist According to honest signalling theory, signals must be costly to produce to retain information about the signaller's quality. The song produced by male birds during breeding is a vocal "ornament" used for intra- and inter-sexual purposes. The energetic cost of this vocal signal remains a contentious issue. We used the doubly labelled water method to measure field metabolic rate by estimating CO2 production and then convert this to daily energy expenditure (DEE) in great reed warbler males singing under natural conditions (10 at low to moderate intensity and 7 at very high intensity from dawn to dusk). There was a significant positive relationship between singing intensity and DEE. From this relationship we extrapolated the average DEE for intensely singing males (i.e., males producing song sounds 50% of the time and hence sitting at their elevated song post in the top of a reed stem more or less continuously throughout the ,20 h of daylight) to 3.3×BMR (basal metabolic rate) and for non-singing males to 2.2×BMR. The mean DEE measured for the seven males singing with very high intensity was 3.1×BMR. The maximum measured DEE for a single male was 3.9×BMR, i.e. close to the maximum sustainable DEE (4×BMR), and the minimum DEE was 2.1×BMR for a male singing at very low intensity. These results imply that producing intensive advertising song in birds may incur a substantial cost in terms of increased energy expenditure. [source] Geographical variation in the size of body organs in seabirdsFUNCTIONAL ECOLOGY, Issue 3 2000G. M. Hilton Abstract 1.,The size of body organs shows adaptive temporal variation in many animal species. The variation in the size of body organs was examined to see if it is also a component of local adaptation to geographical variation in ecological conditions. 2.,Major body organs were measured in five species of Icelandic seabirds, sampled from two areas where birds experience slightly different ecological conditions. Between-area differences in ecological conditions were consistent among the study species, allowing tests of the generality of ecological effects on organ size. 3.,All major body organs showed geographical size variation. Livers and kidneys were larger in locations where daily energy expenditure was expected to be higher; small intestines were heavier where food was of lower energy density; stomachs were heavier where food was less digestible; heart and flight muscle were larger where flight costs were greater. 4.,It is concluded that adaptive variation in organ size may be an important means by which animals optimize exploitation of their local environment, and may be a proximate factor in intraspecific life-history and metabolic variations between geographically separate populations. [source] Elevated metabolic costs while resting on water in a surface feeder: the Black-legged Kittiwake Rissa tridactylaIBIS, Issue 1 2007ELIZABETH M. HUMPHREYS Measurements of the energy costs of individual behaviours provide insights into how animals trade-off resource allocation and energy acquisition decisions. The energetic costs while resting on water are poorly known for seabirds but could comprise a substantial proportion of their daily energy expenditure. We measured the cost of resting on water in Black-legged Kittiwakes Rissa tridactyla, a species which does not fly during the night and for which estimating energy expenditure while resting on the water is therefore important. Their resting metabolic rate on water at 12.5 °C was at least 40% higher compared with resting at the same temperature in air. This indicates that, at comparable temperatures, metabolic costs are elevated for birds resting at sea compared with on land. We argue that Kittiwakes meet much of this extra thermoregulatory demand by dedicated metabolic activity. During the winter months, their costs are likely to be even higher owing to lower sea temperatures. Accordingly, we suggest that migration to milder latitudes, following breeding, will provide enhanced benefits, particularly to seabirds such as Kittiwakes which rest on the sea surface during darkness. [source] A fixed energetic ceiling to parental effort in the great tit?JOURNAL OF ANIMAL ECOLOGY, Issue 2 2000J. M. Tinbergen Summary 1.,To elucidate the links between avian brood size, parental effort and parental investment, we measured daily energy expenditure (DEEfem), condition (residuals of mass on tarsus) and feeding rate in female great tits Parus major L. rearing broods in which the number of young was either reduced, unmanipulated or enlarged. 2.,Female condition was negatively correlated with manipulation when measured at the nestling age of 8 days (measured during the day), which suggests a shift in allocation from self-feeding to chick-feeding. However, there was no detectable manipulation effect on condition measured at the nestling age of 12 days (measured during the night). Either female condition was only affected by manipulation in the early nestling phase or the females adjusted their diurnal mass trajectory in response to brood size manipulation. More detailed data are required to verify this point. There were no indications of a fitness cost associated with the condition during the day, but condition at night was positively related to winter survival. Since manipulation only affected condition during the day, there was no link between manipulation and winter survival. 3.,The duration of the working day was not affected by manipulation and female feeding rate tended to flatten off with manipulated brood size. Similarly, brood reduction resulted in a lower DEEfem, whilst brood enlargement had no effect. This suggests that females worked at an energetic ceiling when rearing an unmanipulated brood. However, the level of this ,ceiling' in DEEfem was not fixed: it differed between years. This leads us to conclude that the observed ceiling was imposed by extrinsic factors (e.g. available foraging time) and not by an intrinsic factor such as maximum energy assimilation rate. We hypothesize that time limitation was the cause for the observed ceiling in energy expenditure and that the annual variation in the level of this ceiling was due to annual variation in ambient temperature. 4.,A cost of reproduction was previously demonstrated in this population: brood enlargement caused a reduction in the incidence of second clutches. However, since DEEfem did not differ between control and enlarged broods, we judge it unlikely that daily energy expenditure is a general predictor for parental investment. [source] Daily energy expenditure of singing great reed warblers Acrocephalus arundinaceusJOURNAL OF AVIAN BIOLOGY, Issue 4 2008Dennis Hasselquist According to honest signalling theory, signals must be costly to produce to retain information about the signaller's quality. The song produced by male birds during breeding is a vocal "ornament" used for intra- and inter-sexual purposes. The energetic cost of this vocal signal remains a contentious issue. We used the doubly labelled water method to measure field metabolic rate by estimating CO2 production and then convert this to daily energy expenditure (DEE) in great reed warbler males singing under natural conditions (10 at low to moderate intensity and 7 at very high intensity from dawn to dusk). There was a significant positive relationship between singing intensity and DEE. From this relationship we extrapolated the average DEE for intensely singing males (i.e., males producing song sounds 50% of the time and hence sitting at their elevated song post in the top of a reed stem more or less continuously throughout the ,20 h of daylight) to 3.3×BMR (basal metabolic rate) and for non-singing males to 2.2×BMR. The mean DEE measured for the seven males singing with very high intensity was 3.1×BMR. The maximum measured DEE for a single male was 3.9×BMR, i.e. close to the maximum sustainable DEE (4×BMR), and the minimum DEE was 2.1×BMR for a male singing at very low intensity. These results imply that producing intensive advertising song in birds may incur a substantial cost in terms of increased energy expenditure. [source] Parkinson's disease patients with bilateral subthalamic deep brain stimulation gain weightMOVEMENT DISORDERS, Issue 2 2004Frédéric Macia MD Abstract Weight, body mass index (BMI) and energy expenditure/energy intake (EE/EI) was studied in 19 Parkinson's disease (PD) patients after subthalamic deep brain stimulation (STN-DBS) versus 14 nonoperated ones. Operated patients had a significant weight gain (WG, + 9.7 ± 7 kg) and BMI increase (+ 4.7 kg/m2). The fat mass was higher after STN-DBS. Resting EE (REE; offdrug/ON stimulation) was significantly decreased in STN-DBS patients, while their daily energy expenditure (DEI) was not significantly different. A significant correlation was found among WG, BMI increase, and pre-operative levodopa-equivalent daily dose, their reduction after STN-DBS, and the differential REE related to stimulation and the REE in the offdrug/OFF stimulation condition. In conclusion, STN-DBS in PD induces a significant WG associated with a reduction in REE without DEI adjustment. © 2003 Movement Disorder Society [source] Exercise tolerance and daily life in McArdle's diseaseMUSCLE AND NERVE, Issue 5 2005Karen Ollivier MSc Abstract McArdle's disease is a common disorder of muscle metabolism and is due to myophosphorylase deficiency. The major complaint of patients with this disease is effort intolerance. Although the clinical features of affected patients are well known, their daily lifestyle is not well documented. The main objective of this work was to assess their mean daily energy expenditure (DEE) and compare it with control subjects. Thirty patients and 87 control subjects completed a questionnaire. A 3-day self-record of daily physical activities was used to estimate the mean DEE for patients and control subjects. A separate section of the questionnaire was used to assess patients' clinical features and daily lifestyle. The DEE of patients (44.1 ± 6.9 kcal/kg) was not significantly different from control subjects (44.5 ± 5.6 kcal/kg). Half of the patients with McArdle's disease performed a daily physical leisure activity as sport, sometimes at a high level (17%). Despite large individual variation, physical abilities and patients' symptoms were negatively correlated. Physical leisure activity significantly decreased the sensation of muscle pain (P < 0.03). These findings show that patients with McArdle's disease do not have a strictly sedentary lifestyle. Moreover, physical exercise appears to have positive effects on the main clinical features, such as effort intolerance. Thus, regular, moderate physical activity may be beneficial in McArdle's disease. Muscle Nerve, 2005 [source] Energetic Adaptation to Chronic Disease in the ElderlyNUTRITION REVIEWS, Issue 3 2000Michael J. Toth Ph.D. Several chronic diseases occur with increased prevalence in the elderly. Body weight loss is a common feature of many chronic diseases. Weight loss increases the risk for morbidity and mortality and contributes to decreased functional independence and poor quality of life. Thus, an understanding of the effect of chronic disease on energy balance has important implications for nutritional supplementation and clinical outcome. This brief review will consider recent studies that have examined the effect of several chronic diseases (i.e., Alzheimer's disease, Parkinson's disease, and congestive heart failure) on daily energy expenditure in elderly individuals. Additionally, we put forth a model to explain the energetic adaptation to chronic disease in the elderly that is based on measurements of daily energy expenditure and its components. Studies suggest that chronic disease decreases daily energy expenditure in elderly individuals due to a marked reduction in physical activity energy expenditure. Moreover, these changes in daily energy expenditure often occur in the presence of increased resting energy expenditure. Thus, the net effect of chronic disease is to decrease daily energy expenditure. These results do not favor the hypothesis that increased energy expenditure contributes to disease-related weight loss. Instead, reduced energy intake appears to be a more likely mediator of the negative energy imbalance and weight loss that frequently accompany chronic disease in the elderly. [source] Climate variables as predictors of basal metabolic rate: New equationsAMERICAN JOURNAL OF HUMAN BIOLOGY, Issue 5 2008Andrew W. Froehle Estimation of basal metabolic rate (BMR) and daily energy expenditure (DEE) in living humans and in fossil hominins can be used to understand the way populations adapt to different environmental and nutritional circumstances. One variable that should be considered in such estimates is climate, which may influence between-population variation in BMR. Overall, populations living in warmer climates tend to have lower BMR than those living in colder climates, even after controlling for body size and composition. Current methods of estimating BMR ignore climate, or deal with its effects in an insufficient manner. This may affect studies that use the factorial method to estimate DEE from BMR, when BMR is not measured but predicted using an equation. The present meta-analysis of published BMR uses stepwise regression to investigate whether the inclusion of climate variables can produce a generally applicable model for human BMR. Regression results show that mean annual temperature and high heat index temperature have a significant effect on BMR, along with body size, age and sex. Based on the regression analysis, equations predicting BMR from body size and climate variables were derived and compared with existing equations. The new equations are generally more accurate and more consistent across climates than the older ones. Estimates of DEE in living and fossil humans using the new equations are compared with estimates using previously published equations, illustrating the utility of including climate variables in estimates of BMR. The new equations derived here may prove useful for future studies of human energy expenditure. Am. J. Hum. Biol., 2008. © 2008 Wiley-Liss, Inc. [source] Diet, energy expenditure, and body composition of lactating Ribeirinha women in the brazilian amazonAMERICAN JOURNAL OF HUMAN BIOLOGY, Issue 5 2007Barbara A. Piperata Lactation is the most energetically demanding part of human reproduction; yet, compared with pregnancy, we know little about the strategies women in different settings employ to cope with these increased energy demands. This paper takes a biocultural approach and reports longitudinal data on the anthropometry, dietary intakes and energy expenditure of a sample of 23 rural, lactating Ribeirinha women living in subsistence-based communities in the eastern Amazon. The dietary intakes of these lactating women were insufficient to meet their lactating energy needs and were least sufficient during resguardo, a 40-day period in the immediate postpartum when the women observed a series of food taboos and work restrictions. Instead, the women in this study met the increased energy demands of lactation by drawing on their energy reserves and reducing their energy expenditure in physical activity. The women showed a significant reduction in weight (P < 0.001), BMI (P < 0.001) and in circumferences (hip, P = 0.01; waist, P = 0.03) and skinfolds (thigh, P = 0.03) in the gluteal femoral region. Total daily energy expenditure (TDEE) was lowest during resguardo and increased as lactation progressed (P = 0.01). While the practice of resguardo reduced maternal energy expenditure and allowed women more time to spend with their newborn infants, it came at a cost (low dietary intake), which appears to be related to the loss of the adult woman from subsistence activities. By taking a biocultural approach this study illustrates the role the social environment plays in shaping the experience of lactating women. Am. J. Hum. Biol., 2007. © 2007 Wiley-Liss, Inc. [source] Measuring human energy expenditure: What have we learned from the flex-heart rate method?AMERICAN JOURNAL OF HUMAN BIOLOGY, Issue 4 2003William R. Leonard The measurement of daily energy expenditure is an important aspect of research on human health and nutrition. Over the last 30 years, G.B. Spurr has been a leader in developing and implementing methods for more effectively assessing energy expenditure and physical activity in traditional and modernizing populations. One of his most notable contributions has been the development of the "Flex Heart Rate" (flex-HR) method. Since its inception in the late 1980s, the flex-HR method has become a standard tool for measuring daily energy expenditure in free-living human populations. This article reviews the initial development and validation of the flex-HR technique, and examines recent refinements of the method and its application to research in biomedicine and human population biology. The review and analyses highlight how the flex-HR technique has improved on earlier methods of assessing energy expenditure and greatly advanced our understanding of variability in human energy requirements. Am. J. Hum. Biol. 15:479,489, 2003. © 2003 Wiley-Liss, Inc. [source] Physical Activity: Patterns of active transport in 11,12 year old Australian childrenAUSTRALIAN AND NEW ZEALAND JOURNAL OF PUBLIC HEALTH, Issue 2 2004Nathan Marten Objectives: To describe the habitual transport patterns of 11 to 12-year-old children in Australia, to determine the personal and environmental factors associated with active transport (AT), and to quantify how much AT contributes to overall daily energy expenditure (EE). Methods: The participants in this study were 136 children aged 11,12 year olds from eight randomly chosen primary schools in Adelaide, South Australia. Each child recalled their trips on two school days and a non-school day. Mass and stature were measured, and children completed a computerised activity recall and a neighbourhood satisfaction questionnaire. Trips were categorised according to their destination, child and parent dissatisfaction with the neighbourhood, and the gender, socio-economic status (SES), BMI and activity levels of the children undertaking them. These categories, along with the distance to the destination, were used as independent variables in a logistic regression model, with trip mode (passive versus active) as the dependent variable. Results: Children made an average of 1.0 active trips per day, with a median trip length of 0.63 km, while the median total distance covered actively per child per day was 0.61 km. Twenty-six per cent of children did no AT over the three days, and 67% did no AT on a weekend day. Distance was by far the strongest predictor of the likelihood that a trip would be active. Trips made by girls were less likely to be active compared with boys. Trips to the shops were less likely to be active than trips to school. Children's AT accounted for 1.3% of their daily EE. Conclusions and Implications: The active transport levels of children were very low. Interventions should focus on making neighbourhoods safer and more accessible to children and should promote bicycle use. [source] Uncoupled and surviving: individual mice with high metabolism have greater mitochondrial uncoupling and live longerAGING CELL, Issue 3 2004John R. Speakman Summary Two theories of how energy metabolism should be associated with longevity, both mediated via free-radical production, make completely contrary predictions. The ,rate of living-free-radical theory' (Pearl, 1928; Harman, 1956; Sohal, 2002) suggests a negative association, the ,uncoupling to survive' hypothesis (Brand, 2000) suggests the correlation should be positive. Existing empirical data on this issue is contradictory and extremely confused (Rubner, 1908; Yan & Sohal, 2000; Ragland & Sohal, 1975; Daan et al., 1996; Wolf & Schmid-Hempel, 1989]. We sought associations between longevity and individual variations in energy metabolism in a cohort of outbred mice. We found a positive association between metabolic intensity (kJ daily food assimilation expressed as g/body mass) and lifespan, but no relationships of lifespan to body mass, fat mass or lean body mass. Mice in the upper quartile of metabolic intensities had greater resting oxygen consumption by 17% and lived 36% longer than mice in the lowest intensity quartile. Mitochondria isolated from the skeletal muscle of mice in the upper quartile had higher proton conductance than mitochondria from mice from the lowest quartile. The higher conductance was caused by higher levels of endogenous activators of proton leak through the adenine nucleotide translocase and uncoupling protein-3. Individuals with high metabolism were therefore more uncoupled, had greater resting and total daily energy expenditures and survived longest , supporting the ,uncoupling to survive' hypothesis. 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