Incubation

About: Incubation is a research topic. Over the lifetime, 5748 publications have been published within this topic receiving 126541 citations.

Effects of interferon-gamma and tumor necrosis factor-alpha on the expression of an Ia antigen on a murine macrophage cell line.

Abstract: Cultures of the murine myelomonocytic cell line, WEHI-3, can be induced to express the Class II MHC antigen, I-A, by incubation with rMuIFN-gamma and/or rHuTNF-alpha. A 24-hr incubation with the combination of rMuIFN-gamma (5.6 ng/ml) and rHuTNF-alpha (13 ng/ml) induced the highest level of expression in the cell population (more than 90%), followed by rMuIFN-gamma (75%) and rHuTNF-alpha (33%). Comparison of the level of mRNA for the heavy chain subunit of the I-A molecule, A alpha, indicates that the combination is 10 and 40 times as stimulatory as rMuIFN-gamma and rHuTNF-alpha alone, respectively. Each cytokine treatment induced a time-dependent increase in the level of A alpha mRNA over the 72 hr of incubation examined, although the combination continued to elevate the level of A alpha mRNA above that induced by either cytokine alone. The findings reported here demonstrate that the monokine rHuTNF-alpha can induce I-A antigen expression and A alpha mRNA. Furthermore, stimulation by the combination of rHuTNF-alpha and rMuIFN-gamma is more than additive, relative to the effects of each cytokine as individual agents.

Energetic Cost of Incubation in the Zebra Finch

Abstract: -At temperatures below 28”C, rate of oxygen consumption (vjo2) of Zebra Finches (Poephila guttuta) incubating eggs averaged 20% higher than the \ioz of non-incubating Zebra Finches sitting in a nest at the same temperature. This increase represents the energetic cost of incubation. The O,, of non-incubating birds sitting in a nest was lower than values reported for birds perched in the open at the same temperature. In the Zebra Finch, the ameliorating effects of the nest microclimate approximately compensate for the increment in metabolic rate due to incubation. The energetic cost of incubation increased when birds had to rewarm cold eggs. Incubating birds responded to artificially cooled eggs by elevating their metabolic rate and increasing heat flow to the clutch. The pattern of adult attentiveness at the nest determines the number of times and amount by which the eggs must be rewarmed. Because it is energetically more expensive to rewarm eggs than to maintain temperature once the eggs are warm, the cost of incubation depends in part on the attentiveness pattern. Reproduction, especially the care of eggs and young, places special demands on the way birds allocate available energy. Various techniques have been used to estimate the energetic costs associated with territorial defense (Stiles 1971, Wolf and Hainsworth I971), nest building (Collias and Collias 1967, Withers 1977a), egg production (King 1973), and the feeding of nestlings (Utter and Lefebvre 1973). These activities, together with incubation of the eggs, include most of the time and energy that birds devote to reproductive activities. However, the costs of incubation, an activity that takes up a significant portion of the reproductive cycle, are difficult to measure and have been the subject of controversy (Kendeigh 1973, King 1973). Linear heat flow models have been used to make indirect estimates of the energetic cost of incubation based on the assumption that heat loss from eggs must be balanced by extra heat production by the parent (Kendeigh 1963, Ricklefs 1974). For example, Drent (1970) found that Kendeigh’ s (1963) model accurately described the heat input required to keep the eggs of Herring Gulls (Larus urgentu Mertens 1977) and Baird’ s Sandpiper, (Calidris hairi Norton 1973). However, neither author compared the oxygen consumption of incubating and non-incubating birds, and consequently it is impossible to estimate the energy expended solely for incubation. In contrast, Biebach (1977, 1979) measured the oxygen consumption of both incubating and non-incubating Starlings (Sturnus dgaris) and calculated the energetic cost of incubation at several nest temperatures. Gessaman and Findell (1979) measured CO, production of three incubating and non-incubating American Kestrels (F&o sparzjerius) but their results are ambiguous. Mertens (1980) measured heat loss from the nest of a Great Tit, using heat flux disks mounted in the nestbox walls, and found that heat loss from the bird and nest increased considerably during incubation. The energetic cost of warming cooled eggs “to the incubation temperature” has not been determined. Kendeigh et al. (1977) suggested that energy expended to rewarm eggs could be calculated from estimates of the heat needed to rewarm eggs, but this procedure ignores the inefficiency of heat transfer from the parent to the eggs. If a bird increases its heat production in order to re-

Temperature effects on release and ecologically relevant properties of dissolved organic carbon in sterilised and biologically active soil samples

Abstract: To evaluate the effects of temperature and biological activity on the release and quality of dissolved organic carbon (DOC), incubation experiments were conducted with soil from the Ap-horizon of a Gleyic Fluvisol (sandy clay loam, pH 7.2; 6.4% C org ). Samples were either non-sterile, sterilised by γ-irradiation or reinoculated after sterilisation. Incubations were performed at three temperatures: 5, 20 and 35 °C for 12 days with continuous CO 2 -monitoring. DOC was obtained by percolating the samples before and after incubation with 1 mM CaCl 2 solution. DOC quality was assessed by ultra-filtration, UV-absorbance, Cu-complexation capacity and biodegradability. In the sterile samples, DOC-concentrations were hardly affected by incubation temperature and among the quality parameters, only the UV-absorbance of DOC decreased with increasing incubation temperature in all size fractions. In the reinoculated and non-sterile samples, DOC-concentrations decreased strongly with increasing incubation temperature. This was closely related to respiration activity and accompanied by increases in Cu-complexation capacity and biodegradability. In the larger DOC size fractions separated by ultra-filtration (MWCO>1000), UV-absorbance increased after incubation at higher temperatures. The results show that DOC is readily utilised as substrate by microorganisms and at the same time modified in its composition by selective degradation of UV-inactive compounds and by the release of low molecular, easily degradable compounds with high Cu-complexation capacity.

Phenotypic Plasticity for Growth in the Common Snapping Turtle: Effects of Incubation Temperature, Clutch, and Their Interaction

Abstract: Abstrcact.-We examined a critical component of the Charnov-Bull hypothesis of temperaturedependent sex determination (TSD) by determining the reaction norms of hatchling growth to embryonic incubation temperature in the common snapping turtle, Chelydra serpentina. Hormone manipulations of eggs produced females at male temperatures and vice versa, which thereby permitted same-sex comparisons of hatchling growth across a range of incubation temperatures. In this way, the normally confounded effects of incubation temperature and sex were dissociated experimentally. The resultant hatchlings, including controls and experimentals, exhibited normal gonadal structure and sex steroid profiles. The subsequent growth of hatchlings monitored for 6 mo was strongly affected by embryonic incubation temperature but not by sex. As predicted, growth was enhanced at incubation temperatures that produced males. Clutch effects and interaction effects (clutch by incubation temperature) on growth were significant. In addition, there was a positive genetic covariance among incubation temperatures, but incubation temperature effects varied among clutches. The variation in growth plasticity among clutches was consistent with Charnov-Bull predictions. In this TSD species, incubation temperature is likely to have differential fitness effects on the sexes mediated via differences in growth.