Incubation of penguin eggs

The preservation of rare and endangered species of birds requires finding efficient, and above all successful, methods of breeding them in captivity. One strategy adopted is to remove eggs from the mother, making her lay more eggs, and then incubating the removed eggs artificially. Artificial incubation machines must attempt to replicate the conditions of natural incubation as closely as possible. Aside from careful control of temperature and humidity within the artificial incubator, an important factor to reproduce is that eggs must be turned about their long axis from time to time. Hatching will not occur in an egg that is not subjected to some form of occasional rotation. The reason why eggs are turned and the way in which they should be turned are still not well understood. The Study Group attempted to gain some insight into why eggs have to be turned from a fluid dynamic perspective. A simple egg-turning model for an egg at the first stages of incubation was constructed, based on lubrication theory

Evolutionary dynamics of incubation periods

The incubation period of a disease is the time between an initiating pathologic event and the onset of symptoms. For typhoid fever, polio, measles, leukemia and many other diseases, the incubation period is highly variable. Some affected people take much longer than average to show symptoms, leading to a distribution of incubation periods that is right skewed and often approximately lognormal. Although this statistical pattern was discovered more than sixty years ago, it remains an open question to explain its ubiquity. Here we propose an explanation based on evolutionary dynamics on graphs. For simple models of a mutant or pathogen invading a network-structured population of healthy cells, we show that skewed distributions of incubation periods emerge for a wide range of assumptions about invader fitness, competition dynamics, and network structure. The skewness stems from stochastic mechanisms associated with two classic problems in probability theory: the coupon collector and the random walk. Unlike previous explanations that rely crucially on heterogeneity, our results hold even for homogeneous populations. Thus, we predict that two equally healthy individuals subjected to equal doses of equally pathogenic agents may, by chance alone, show remarkably different time courses of disease.Comment: 24 pages, 8 figures, 1 tabl

Directed percolation with incubation times

We introduce a model for directed percolation with a long-range temporal diffusion, while the spatial diffusion is kept short ranged. In an interpretation of directed percolation as an epidemic process, this non-Markovian modification can be understood as incubation times, which are distributed accordingly to a Levy distribution. We argue that the best approach to find the effective action for this problem is through a generalization of the Cardy-Sugar method, adding the non-Markovian features into the geometrical properties of the lattice. We formulate a field theory for this problem and renormalize it up to one loop in a perturbative expansion. We solve the various technical difficulties that the integrations possess by means of an asymptotic analysis of the divergences. We show the absence of field renormalization at one-loop order, and we argue that this would be the case to all orders in perturbation theory. Consequently, in addition to the characteristic scaling relations of directed percolation, we find a scaling relation valid for the critical exponents of this theory. In this universality class, the critical exponents vary continuously with the Levy parameter.Comment: 17 pages, 7 figures. v.2: minor correction

Influence of incubation temperature on morphology and locomotion performance of Leatherback (<i>Dermochelys coriacea</i>) hatchlings

The journey of Leatherback (Dermochelys coriacea (Vandelli, 1761)) hatchlings from nest to the sea is a vulnerable life-history stage. Studies have shown that nest incubation temperatures influence hatchling morphology and locomotor performance, which may affect hatchling fitness. We obtained incubation temperature profiles from 16 Leatherback nests in Tobago, West Indies, during the 2008 nesting season (March-June). There was significant variation among mean nest incubation temperatures, which had a significant influence on hatchling morphology. Using principal components analysis, we determined the morphological traits that explained the most variation among hatchlings, which allowed investigation of the relationship between hatchling morphology and terrestrial locomotion speed. Hatchlings with a narrower carapace width and longer flipper reach (produced at lower incubation temperatures) had significantly faster terrestrial speed and total run time than those with opposite characteristics (produced at higher incubation temperatures). Our results demonstrate that lower incubation temperatures produce hatchlings with traits that are significantly advantageous to terrestrial locomotion. These findings suggest that nest incubation temperature is important in determining hatchling fitness, as nest incubation temperature significantly influences hatchling morphology and locomotor capabilities. This study supplements related findings in Green Turtles (Chelonia mydas (L., 1758)), but also illustrates some unique features in Leatherbacks

Sharing the burden : on the division of parental care and vocalizations during incubation

In species with biparental care, individuals only have to pay the costs for their own parental investment, whereas the contribution of their partner comes for free. Each parent hence benefits if its partner works harder, creating an evolutionary conflict of interest. How parents resolve this conflict and how they achieve the optimal division of parental tasks often remains elusive. In this study, we investigated whether lesser black-backed gulls (Larus fuscus) divide parental care during incubation equally and whether this correlates with the extent of vocalizations between pair-members during incubation. We then investigated whether pairs showing more evenly distributed incubation behavior had a higher reproductive success. To this end, we recorded incubation behavior and vocalizations for 24-h time periods. Subsequently, we experimentally increased or decreased brood sizes in order to manipulate parental effort, and followed offspring development from hatching till fledging. Although incubation bouts were, on average, slightly longer in females, patterns varied strongly between pairs, ranging from primarily female incubation over equal sex contributions to male-biased incubation. Pairs contributing more equally to incubation vocalized more during nest relief and had a higher reproductive output when brood sizes were experimentally increased. Thus, vocalizations and a more equal division of parental care during incubation may facilitate higher levels of care during the nestling period, as suggested by a greater reproductive success when facing high brood demand, or they indicate pair quality

Business Incubation Developmentin India

The paper provides the experience of setting up first incubator for grassroots innovations in the form of GIAN (Grassroots Innovation Augmentation Network) and make a case for replicating this model elsewhere in the developing world.