Flying at no mechanical energy cost: disclosing the secret of wandering albatrosses

ALBATROSSES DO SOMETHING THAT NO OTHER BIRDS ARE ABLE TO DO: fly thousands of kilometres at no mechanical cost. This is possible because they use dynamic soaring, a flight mode that enables them to gain the energy required for flying from wind. Until now, the physical mechanisms of the energy gain in terms of the energy transfer from the wind to the bird were mostly unknown. Here we show that the energy gain is achieved by a dynamic flight manoeuvre consisting of a continually repeated up-down curve with optimal adjustment to the wind. We determined the energy obtained from the wind by analysing the measured trajectories of free flying birds using a new GPS-signal tracking method yielding a high precision. Our results reveal an evolutionary adaptation to an extreme environment, and may support recent biologically inspired research on robotic aircraft that might utilize albatrosses' flight technique for engineless propulsion.     

Behavioral responses to encounter of fishing boats in wandering albatrosses

Animals are attracted to human food subsidies worldwide. The behavioral response of individuals to these resources is rarely described in detail, beyond chances of encounters. Seabirds for instance scavenge in large numbers at fishing boats, triggering crucial conservation issues, but how the response to boats varies across encounters is poorly known. Here we examine the behavioral response of wandering albatrosses (Diomedea exulans), equipped with GPS tags, to longline fishing boats operating near their colony for which we had access to vessel monitoring system data. We distinguish between encounters (flying within 30 km of a boat) and attendance behavior (sitting on the sea within 3 km of a boat), and examine factors affecting each. In particular, we test hypotheses that the response to encountered boats should vary with sex and age in this long‐lived dimorphic species. Among the 60% trips that encountered boats at least once, 80% of them contained attendance (but attendance followed only 60% of each single encounter). Birds were more attracted and remained attending longer when boats were hauling lines, despite the measures enforced by this fleet to limit food availability during operations. Sex and age of birds had low influence on the response to boats, except the year when fewer boats came fishing in the area, and younger birds were attending further from boats compared to older birds. Net mass gain of birds was similar across sex and not affected by time spent attending boats. Our results indicate albatrosses extensively attend this fishery, with no clear advantages, questioning impacts on foraging time budgets. Factors responsible for sex foraging segregation at larger scale seem not to operate at this fleet near the colony and are not consistent with predictions of optimal foraging theory on potential individual dominance asymmetries. This approach complements studies of large‐scale overlap of animals with human subsidies.     

Comparison of census methods for black-browed albatrosses breeding at the Ildefonso Archipelago,Chile

A breeding population of black-browed albatrosses has been known to exist at the Ildefonso Archipelago, Chile, for >90 years but the population has never been censused using scientifically defendable methods. To estimate population size, and examine the accuracy and practicality of various census methods, the population was censused in the 2002/2003 breeding season using (a) ground-truthed aerial photography, (b) yacht-based photography, (c) ground counts, (d) quadrat sampling and (e) point-distance sampling. Compared to ground-truthed aerial photography (judged the most accurate) yacht-based photography underestimated population size by 55%, ground counts by 13%, quadrat sampling by 11% and point-distance sampling by 9%. Ground-truthed air photography revealed that in the 2002/2003 breeding season 47,000 pairs of black-browed albatrosses bred at the Ildefonso Archipelago. A repeat aerial census in 2006 suggested the size of the breeding population had not changed in the 4 years between the two censuses. After the Falkland Islands/Islas Malvinas, South Georgia and Diego Ramirez, the Ildefonso Archipelago holds the fourth largest population of black-browed albatrosses in the world.     

Postnatal dispersal of wandering albatrosses Diomedea exulans: implications for the conservation of the species

Many large marine vertebrates are today threatened by human activities and it is therefore crucial to obtain information on their distribution and behaviour at sea. In particular little is known about the time necessary for juveniles to acquire the foraging skills of adults. We tracked 13 juvenile wandering albatrosses Diomedea exulans by satellite telemetry during their first year at sea. They covered an average distance of 184,000 km during the first year and restricted their dispersal to the unproductive waters of the subtropical Indian Ocean and Tasman Sea. This region of low wind velocities does not overlap with the foraging areas used by adults. After an innate phase of rapid dispersal with a fixed flight direction, young birds progressively increased their daily flight distances and attained adult flight efficiency within their first six months at sea. The complete overlap of the juveniles' foraging ranges with major long-line fisheries in the subtropical waters constitutes a major threat that could jeopardize the long term recovery ability of populations of the endangered wandering albatross in the Indian Ocean.     

Female great tits Parus major do not increase their daily energy expenditure when incubating enlarged clutches

Several studies have shown that enlargement of clutches during incubation reduces the long-term survival of parents. In line with these findings, studies on the energetic costs of nocturnal incubation show an increase in energy expenditure with clutch enlargement. Studies on daily energy expenditure during incubation (DEE_inc), however, do not consistently show such a negative effect of clutch enlargement. To determine whether differential survival results from a direct increase in energy costs or rather from costs associated with compensatory behaviour, we studied the DEE_inc (kJ day⁻¹), change in body mass and nest attendance behaviour of free-living female great tits Parus major that incubated either control or experimentally enlarged clutches. DEE_inc did not differ between the two treatment groups, but was negatively related to mean ambient temperature over the 24-h measuring period, and to the fraction of daytime females spent on the nest. Controlling for these two factors, females incubating enlarged clutches did not spend more energy per 24 h period than females incubating control clutches. Clutch enlargement also did not affect body mass of incubating females, or their nest attendance behaviour. Yet, in the enlarged group body mass change and nest attentiveness were negatively correlated, suggesting that females responded differently to the experimental treatment and thereby preventing us from finding an effect of clutch enlargement.     

Postnatal dispersal of wandering albatrosses Diomedea exulans: implications for the conservation of the species

Many large marine vertebrates are today threatened by human activities and it is therefore crucial to obtain information on their distribution and behaviour at sea. In particular little is known about the time necessary for juveniles to acquire the foraging skills of adults. We tracked 13 juvenile wandering albatrosses Diomedea exulans by satellite telemetry during their first year at sea. They covered an average distance of 184,000 km during the first year and restricted their dispersal to the unproductive waters of the subtropical Indian Ocean and Tasman Sea. This region of low wind velocities does not overlap with the foraging areas used by adults. After an innate phase of rapid dispersal with a fixed flight direction, young birds progressively increased their daily flight distances and attained adult flight efficiency within their first six months at sea. The complete overlap of the juveniles’ foraging ranges with major long‐line fisheries in the subtropical waters constitutes a major threat that could jeopardize the long term recovery ability of populations of the endangered wandering albatross in the Indian Ocean.     

Regulation of foraging trips and incubation routine in male and female wandering albatrosses

The resolution of the conflict between eggcare and foraging was studied in male and female wandering albatrosses. The foraging zone and range, duration of incubation shifts and foraging trips, and associated changes in body mass were studied. Costs during incubation, expressed as the time spent incubating and the proportional loss of body mass, were similar for both sexes. The mass gained at sea was related to the duration of foraging trips, but the relationship was much less significant in males, where foraging ranges, though similar on average to those of females, were very variable. Males foraged in more southerly waters than females, and gained mass more rapidly. Only females appeared to regulate the duration of foraging trips, and this compensated for the mass lost during the incubation fast. Previous breeding experience had no influence on foraging efficiency. Egg desertion because of depletion of body reserves was very rare because birds have a wide safety margin, i.e. the difference between the average body mass when relieved and that at nest desertion. This safety margin enables the birds to compensate for the high variability in the duration of foraging trips, and is probably a reason for the high breeding success of wandering albatrosses. Decisions to return from the sea to the nest or to desert the nest are probably related to the status of body reserves, and have been selected in the large wandering albatross so that both present and future reproductive success are maximised.     

能量消耗C指标在评价乒乓球运动员多球练习中能量消耗的应用*

目的:研究周期类运动能量消耗^C指标在评价乒乓球多球练习中能量消耗应用的可行性。方法:11名某大学代表队的乒乓球运动员(18±1 yrs, 177±2 cm, 71±3 kg,运动水平≥二级)自愿参加了1次跑台递增负荷测试和2次(正手和反手)发球机多球递增频率测试(3 min × 6级,频率为35~85 stroke·min^-1)。用便携式气体代谢仪和心率监测仪检测3次测试的呼吸气体和心率,计算每种频率下每次击球所消耗的能量;采集运动前后的耳血进行血乳酸分析。结果:乒乓球前冲弧圈多球练习的能量消耗^C随击球频率的增加而下降(P＜0.05)。6种击球频率下,正手前冲弧圈的能量消耗^C都高于反手,且差异在35、45、55、65和85 stroke·min^-1时显著(P＜0.05)。能量消耗^C与频率的关系公式分别为y=166.4x^-0.731(R²=0.9731)和y=33.21x^-0.392(R²=0.8423),其中y为能量消耗^C(单位为J·stroke^-1·kg^-1),x为击球频率(单位为stroke·min^-1)。结论:周期类运动项目的能量消耗^C可应用于评价乒乓球运动员单一技术动作多球练习的能量消耗,反映乒乓球运动员在不同击球频率下的击球效率。     

Status and distribution of wandering, black-browed and grey-headed albatrosses breeding at South Georgia

Long-term studies at Bird Island, South Georgia, show that numbers of wandering, black-browed and grey-headed albatrosses have been decreasing since the late 1970s. To determine the status of the total South Georgia population, all known colonies were censused in 2003/2004 using a combination of yacht-based digital photography and ground counts. The breeding population estimates from this census are 1,553 pairs of wandering albatross, 74,296 pairs of black-browed albatross and 47,674 pairs of grey-headed albatross. A 30% decline since 1984 was recorded for wandering albatross, and comparison of a sample of black-browed and grey-headed albatross colonies on the mainland of South Georgia photo-censused in both 1985/1986 and 2003/2004 indicates similarly substantial population declines. Unless these decreases can be halted or reversed, doubt will exist as to the long-term viability of these species of albatross at South Georgia.     

Sensitivity of methods for calculating energy expenditure by use of doubly labeled water

Attempts to estimate human energy expenditure by use of doubly labeled water have produced three methods currently used for calculating carbon dioxide production from isotope disappearance data: 1) the two-point method, 2) the regression method, and 3) the integration method. An ideal data set was used to determine the error produced in the calculated energy expenditure for each method when specific variables were perturbed. The analysis indicates that some of the calculation methods are more susceptible to perturbations in certain variables than others. Results from an experiment on one adult human subject are used to illustrate the potential for error in actual data. Samples of second void urine, 24-h urine, and breath collected every other day for 21 days are used to calculate the average daily energy expenditure by three calculation methods. The difference between calculated energy expenditure and metabolizable energy on a weight-maintenance diet is used to estimate the error associated with the doubly labeled water method.     

Comparison of energy expenditure elevations after submaximal and supramaximal running

Laforgia, J., R. T. Withers, N. J. Shipp, and C. J. Gore.Comparison of energy expenditure elevations after submaximal andsupramaximal running. J. Appl.Physiol. 82(2): 661-666, 1997.Although exerciseintensity has been identified as a major determinant of the excesspostexercise oxygen consumption (EPOC), no studies have compared theEPOC after submaximal continuous running and supramaximal intervalrunning. Eight male middle-distance runners [age = 21.1 ± 3.1 (SD) yr; mass = 67.8 ± 5.1 kg; maximal oxygen consumption(O_{2 max}) = 69.2 ± 4.0 ml ^· kg^{1 ·} min¹] thereforecompleted two equated treatments of treadmill running (continuousrunning: 30 min at 70%O_{2 max}; intervalrunning: 20 × 1-min intervals at 105%O_{2 max} withintervening 2-min rest periods) and a control session (no exercise) ina counterbalanced research design. The 9-h EPOC values were 6.9 ± 3.8 and 15.0 ± 3.3 liters (t-test:P = 0.001) for the submaximal andsupramaximal treatments, respectively. These values represent 7.1 and13.8% of the net total oxygen cost of both treatments. Notwithstanding the higher EPOC for supramaximal interval running compared with submaximal continuous running, the major contribution of both to weightloss is therefore via the energy expended during the actual exercise.

     

Extrapair paternities in black-browed Thalassarche melanophris, grey-headed T. chrysostoma and wandering albatrosses Diomedea exulans at South Georgia

Extrapair paternities (EPP) are relatively common in passerines, but rare in seabirds. Like most seabirds, albatrosses are long lived, form long-term pair bonds and require biparental care for chick-rearing. Microsatellite analyses of 327 chicks from black-browed Thalassarche melanophris , grey-headed T. chrysostoma and wandering albatrosses Diomedea exulans over two breeding seasons revealed the presence of EPP in all three species. Though EPP rates varied between species and years, up to 21% of offspring were the result of extrapair matings. Rates were highest in wandering albatrosses (6–21%) followed by grey-headed (3–10%) and black-browed (0–9%) albatrosses. EPP rates were lower in 1998 compared to 1999 in both black-browed and grey-headed albatrosses, whereas the reverse was true for wandering albatrosses. Interspecific differences in EPP rates may reflect differences in breeding phenology and sexual size dimorphism. Differences in timing and frequency of breeding may promote different opportunities for interactions with birds other than their normal partner. The different breeding habitat, dispersion and mate-attraction rituals in wandering albatross, together with the disparity in size between the sexes may also offer more scope for higher rates of EPP. Despite extensive sampling within each colony, we were unable to identify sires for many of the extrapair young; however males from other colonies were involved, raising interesting questions regarding the timing and nature of such events.     

Bioimpedance for severe obesity: comparing research methods for total body water and resting energy expenditure

Objective: As the acceptance of surgical procedures for weight loss in morbid obesity is increasing, clinically useful baseline and follow‐up measures of total body water (TBW) and resting energy expenditure (REE) are important. Research methods such as deuterium (D²O) dilution and metabolic carts are problematic in the clinical setting. We compared bioimpedance analysis (BIA) predicted (Tanita TBF‐310) and measured TBW and REE. Methods and Procedures: Forty‐two paired presurgery studies were completed using BIA and D²O in patients with BMI (mean ± s.d.) 50.2 ± 8.8 kg/m² for TBW, and 30 patients with BMI 51.0 ± 13 kg/m² completed paired determinations of REE with metabolic carts and the Tanita balance with weight, height, sex, and age modifiers. Regression analysis and Bland‐Altman plots were applied. Results: When regression analysis was completed for TBW, regression line was consistent with the identity line “y = x.” The intercept was not different from 0 (95% confidence interval ?2.5 ± 7.0). The slope of the line was not different from 1.0 ± 0.1. The measured TBW 51.2 ± 10.1 l had a correlation with the predicted 49.5 ± 11.27 l of 0.92. There also was no significant difference (P = 0.33) between predicted (2,316 ± 559 kcal/day) and measured REE (2,383 ± 576 kcal/day);δ 66.7 ± 273 kcal/day. The two measures were highly correlated (r = 0.88) with no bias detected. Discussion: These observations support the use of the BIA system calibration in subjects with severe obesity. Without the use of complex, costly equipment and invasive procedures, BIA measurements can easily be obtained in clinical practice to monitor patient responses to treatment.     

Annual energy budget and food requirements of breeding wandering albatrosses (<Emphasis Type="Italic">Diomedea exulans</Emphasis>)

Energy budgets form an integral part of our understanding of animal energetics, particularly when presented in the context of reproduction. In this paper, I created a time-energy budget for a breeding pair of wandering albatrosses (Diomedea exulans) to estimate the annual breeding costs and food requirements of the population at Possession Island, Crozet Archipelago. For a breeding cycle that lasts 356 days on average, a pair uses 2,733 MJ to raise a single chick to fledging. This estimate is 1.21 times higher than previously calculated for wandering albatrosses breeding at Marion Island. Unlike the current analysis, the previous study assumed that foraging costs were constant across all stages of the breeding cycle. Recent evidence shows that foraging costs vary during breeding for wandering albatrosses at Crozet and this is probably true for all populations. Incubation costs have also been shown to be substantially lower than previously determined. Therefore, if a wandering albatross pair at Crozet uses a total of 2,733 MJ to breed, they would need to consume at least 1.7 kg bird^–1 day^–1 of fresh food, on average, to balance their own energy requirements and to provision a single chick for approximately 278 days. At this rate of food consumption, the breeding population at Crozet would consume approximately 340 tonnes of fresh food per breeding season.