Home About us Contact | |||
Size Manipulation (size + manipulation)
Selected AbstractsA 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] Experimental reduction of incubation temperature affects both nestling and adult blue tits Cyanistes caeruleusJOURNAL OF AVIAN BIOLOGY, Issue 5 2008Johan F. Nilsson Incubation was for a long time considered to be a period of decreased activity and low cost for parents. It was therefore ignored as a potential factor affecting life-history trade-offs in birds. Lately this view has started to change, and studies now show that there might be considerable costs connected to incubation. We experimentally reduced the nest temperature during incubation in blue tits Cyanistes caeruleus, thus increasing the energetic cost of incubation, to test the importance of incubation as a component of reproductive costs and for nestling quality. While most other studies use brood size manipulation to manipulate reproductive costs, we were able to separate treatment effects acting during the incubation period from those acting on later reproductive performance by applying a cross-foster design. We were also able to isolate the effects of decreased incubation temperature on the nestlings from treatment effects acting on incubating females. We found no experimental effect on the length of the incubation period or on hatching success. The lower temperature during incubation, however, caused lower growth rates in nestlings and reduced chick rearing capacity in adults. We conclude that incubation is a costly period, with the potential to affect both the trade-off between current and future reproduction and the one between parental effort and offspring quality within the current breeding attempt. [source] Genetic and environmental effects on morphology and fluctuating asymmetry in nestling barn swallowsJOURNAL OF EVOLUTIONARY BIOLOGY, Issue 3 2000Cadée A barn swallow Hirundo rustica partial cross-fostering experiment with simultaneous brood size manipulation was conducted in two years with contrasting weather conditions, to estimate heritable variation in tarsus, tail and wing size and fluctuating asymmetry. Environmental stress had contrasting effects depending on trait type. Significant heritabilities for tarsus, tail and wing size were found only in enlarged broods irrespective of year effects, while tarsus asymmetry was significantly heritable in the year with benign weather conditions irrespective of brood size manipulation effects. Tail, wing and composite (multicharacter) asymmetry were never significantly heritable. The environment with the higher heritability generally had higher additive genetic variance and lower environmental variance, irrespective of trait type. Heritability was larger for trait size than for trait asymmetry. Patterns of genetic variation in nestlings do not necessarily translate to the juvenile or adult stage, as indicated by lack of correlation between nestling and fledgling traits. [source] Two-point dixon fat,water separation: Improving reliability and accuracy in phase correction algorithmsJOURNAL OF MAGNETIC RESONANCE IMAGING, Issue 5 2008Maria A. Schmidt PhD Abstract Purpose To propose an advanced phase-correction region-growing algorithm for two-point fat,water separation suitable for parotid assessment, and to evaluate the general performance of phase-correction algorithms. Materials and Methods Two region-growing algorithms were evaluated in test objects and in head images: the original phase-correction algorithm (OPC) and the advanced phase-correction algorithm with voxel size manipulation (VSM) which includes: 1) starting the region-growing process from images of lower resolution and subsequently stepping toward the original matrix size, and 2) limiting the use of low-pass filters to fat,water interfaces with partial volume effects Results Fundamental problems relate to biological tissue spectrum being poorly approximated by two discrete peaks for fat and water. The VSM algorithm was shown to be less noise-sensitive, faster, and to produce a better approximation for the field inhomogeneity map. In head images (6 volunteers, 10 slices each) 43 errors were found with the OPC algorithm and only 6 errors with the VSM algorithm. Only the OPC algorithm produced errors surrounding the parotids (10 errors). Conclusion The VSM algorithm provides a more accurate and less noise-sensitive fat,water separation. This highly significant performance improvement allows the application of phase-correction algorithms to a wider range of clinical applications. J. Magn. Reson. Imaging 2008. © 2008 Wiley-Liss, Inc. [source] Inter-sexual differences in the immune response of Eurasian kestrel nestlings under food shortageECOLOGY LETTERS, Issue 1 2002Juan A. Fargallo When resources are limited, parents should decide the optimal number, size, and sex of progeny, and offspring should decide the optimal allocation of resources to different costly functions, such as growth and immunity. We manipulated clutch sizes of Eurasian kestrels by one egg to estimate possible cumulative effects of incubation and chick rearing costs on parental body condition, feeding effort, and offspring viability. No obvious effects of clutch size manipulations on feeding effort were found while feeding effort was adjusted to the original clutch size. Enlarged and control nests suffered from higher nestling mortality than reduced nests, and chicks of the enlarged group were in poorer body condition than chicks of the reduced group. Controlling for body mass, male chicks exhibited lower cell-mediated immunity assessed by a cutaneous hypersensitivity response than females, but only in treatments suffering from food restrictions, as indicated by chick starvation. These novel results reveal inter-sexual differences in physiological strategies in early life, suggesting sex-related differences in susceptibility to disease and consequently in survival prospects of offspring. [source] How do changes in parental investment influence development in echinoid echinoderms?EVOLUTION AND DEVELOPMENT, Issue 6 2009Nicholas J. Alcorn SUMMARY Understanding the relationship between egg size, development time, and juvenile size is critical to explaining patterns of life-history evolution in marine invertebrates. Currently there is conflicting information about the effects of changes in egg size on the life histories of echinoid echinoderms. We sought to resolve this conflict by manipulating egg size and food level during the development of two planktotrophic echinoid echinoderms: the green sea urchin, Strongylocentrotus droebachiensis and the sand dollar, Echinarachnius parma. Based on comparative datasets, we predicted that decreasing food availability and egg size would increase development time and reduce juvenile size. To test our prediction, blastomere separations were performed in both species at the two-cell stage to reduce egg volume by 50%, producing whole- and half-size larvae that were reared to metamorphosis under high or low food levels. Upon settlement, age at metamorphosis, juvenile size, spine number, and spine length were measured. As predicted, reducing egg size and food availability significantly increased age at metamorphosis and reduced juvenile quality. Along with previous egg size manipulations in other echinoids, this study suggests that the relationship between egg size, development time, and juvenile size is strongly dependent upon the initial size of the egg. [source] |