Differences in fungal contamination of broiler litter between summer and winter fattening periods

This study aimed to compare fungal contamination of poultry litter between warm and cold seasons. It was carried out in commercial production conditions over two five-week fattening periods: one in the summer (July-August) and one in the winter (December-January). Broilers were reared on a litter composed of chopped straw and sawdust. Litter fungal concentration and composition were investigated weekly, along with litter temperature, moisture, and pH. Litter concentration of total fungi increased over both fattening periods, with no differences in median concentrations between them. Season also had no effect on yeast, Aspergillus section Nigri, and Cladosporium, Fusarium, and Rhizopus spp. concentrations, while the Aspergillus section Flavi and Aspergillus spp. combined showed higher concentrations in the summer, and Mucor and Penicillium spp. in the winter. Total fungal concentration highly correlated with litter temperature, moisture, and pH, regardless of the season. Our findings can be useful in the assessment and control of potential harmful effect of fungi on the health of poultry and poultry farm workers.

Pre-winter fattening and fat loss during wing moult: the annual cycle of fat deposition in captive barnacle geese (branta leucopsis)

Many different physiological changes have been observed in wild waterfowl during the flightless stage of wing moult, including a loss of body mass. Previously we established that captive barnacle geese (Branta leucopsis) underwent this characteristic decrease in body mass during their wing moult, even though they had unlimited and unrestricted access to food. In the present study we aimed to determine if this body mass loss during moult comprised mainly a reduction in fat stores, and to ascertain if the captive geese undergo pre-migratory and pre-winter fattening over a similar temporal scale to their wild conspecifics. The non-destructive technique of deuterium oxide isotope dilution was employed to provide repeated measurements of estimated fat deposition from a captive flock of fourteen barnacle geese. Birds were injected with deuterium oxide at 7 distinct intervals for one annual cycle. During the flightless period of the moult, body fat decreased by approximately 40% from the pre-moult value. During late-September and early October, body fat reached its highest point in the annual cycle, both as an absolute value and as a percentage of total body mass. We propose that while the energetic cost of wing moult is not the ultimate cause of fat loss in moulting barnacle geese, the approximate 212 g of fat catabolised during moult would provide sufficient energy to cover the cost of the replacement of the flight feathers, estimated to be 6384 kJ, over an approximate 42 day period. We conclude that the previously recorded increase in metabolism during moult in the geese, led to the use of endogenous fat reserves because the birds reduced rather than increased their food intake rates owing to the increased risk of predation when flightless. We also conclude that captive barnacle geese do undergo pre-winter and pre-migratory fattening, providing further evidence of the innate nature of these fat deposition cycles.

Seasonal Body Weight Variation in Five Species of Woodpeckers

We investigated patterns of seasonal variation in body weight in six populations of five resident species of temperate-zone woodpeckers: Acorn Woodpecker (Melanerpes formicivorus), Red-bellied Woodpecker (M. carolinus), Red-cockaded Woodpecker (Picoides borealis), Downy Woodpecker (P. pubescens), and Great Spotted Woodpecker (Dendrocopos major). After controlling for time of day and overall body size, annual variation in body weight was small and generally not statistically significant. However, analysis revealed evidence of significant “winter fattening,” comparable in magnitude to other temperate-zone resident species, in three of the species. The degree of winter fattening did not correlate with either the size of the acorn crop (for the Acorn Woodpecker) or latitude, two variables potentially related to predictability of food resources. However, the smaller species exhibited significantly greater winter fattening than the larger species, as predicted by the hypothesis that energy storage should be more important for small-bodied species. Furthermore, the food-storing Acorn Woodpecker exhibited considerably less winter fattening than the nonfood-storing species, supporting the hypothesis that food storage provides an ecological alternative to winter fattening.

Seasonal and Diurnal Body-Mass Fluctuations for two Nonhoarding Species of Parus in Sweden Modeled Using Path Analysis

According to the hypothesis that has been invoked most frequently to explain seasonal fattening patterns for birds—the “adaptive winter-fattening hypothesis”—individuals respond to worsening foraging conditions by increasing body mass and energy reserves. Two hypotheses have been proposed equally frequently to explain daily weight gain patterns for birds: according to the “state-dependent foraging hypothesis,” energy reserves should be amassed early during the day, when starvation risk increases; according to the “mass-dependent predation-risk hypothesis,” mass gain should be delayed for as long as possible, to minimize predation risk. Those hypotheses have been tested previously, using statistical methods (e.g. multiple-regression analysis) that assume independence among environmental variables (e.g. photoperiod and temperature). We conducted path analyses that included four predictor variables (day-in-season, hour-in-day, mean daily temperature, and daily precipitation) to model body-mass fluctuations for two small, nonhoarding (noncaching) passerine species that inhabit central eastern Sweden. Data were partitioned hierarchically into species, age class, gender, and season subgroups. As reported in many small passerine species studies, body mass increased during the day and maximized at dusk; over seasons, body mass increased during autumn, maximized by midwinter, and declined toward breeding in spring. Path analysis models accounted for 9.5–49.9% (mean 26.3%) for Blue Tit (Parus caeruleus) body mass variance and 1.8–52.3% (mean 16.8%) for Great Tit (P. major) body mass variance; for both species, accountability was lowest for autumn (Blue Tit,12.2%; Great Tit, 7.3%), highest for winter (Blue Tit, 33.4%; Great Tit, 21.9%), and intermediate for spring (Blue Tit, 22.7%; Great Tit, 11.8%); for Blue Tits, it was greater for adults than for juveniles (33.2 and 21.7%); whereas negligible for Great Tits (15.9 and 17.3%) and slightly greater for males than for females (Blue Tit, 27.4 and 23.5%; Great Tit, 23.1 and 21.3%). Those results are consistent with predictions formulated on the basis of the adaptive winter-fattening, partially with state-dependent foraging, and, possibly, mass-dependent predation-risk hypothesies and reveal that body-mass fluctuations are associated to a greater extent with photoperiod than with temperature.

Seasonal variation in body mass and blood oxygen carrying capacity of the superb fairy-wren (Malurus cyaneus)

The responses of small birds to many seasonal energy challenges include enhancement of aspects of aerobic metabolism, sometimes involving an increase in the rate of oxygen delivery to the metabolising tissues. One such mechanism that enhances oxygen delivery seasonally is an increase in blood oxygen carrying capacity. This response is enhanced in birds because of their rapid erythrocyte turnover rate. Some small birds have also evolved winter fattening, which helps them to meet the energy challenge presented by winter conditions. Such adaptations, while well documented for North Temperate birds, have received little attention in birds inhabiting temperate Australia. Over a two-year period, we examined seasonal changes in mass, an approximate indicator of fattening, and the parameters determining blood oxygen carrying capacity in a population of superb fairy-wrens (Malurus cyaneus) in outer Melbourne, Australia. Body mass did not vary significantly seasonally, but haematocrit and whole blood haemoglobin were significantly higher in the breeding season than at other times of year and the erythrocyte count was significantly higher in spring than in autumn. We conclude that the failure of the fairy-wrens to increase mass in winter (i.e. show marked winter fattening) was probably due to the comparative mildness of the climate and to the known fitness costs of fat storage. The significant 18% increase in blood oxygen carrying capacity in spring probably helped the birds to meet the additional energy requirements of breeding, particularly the likely increase in flight activity. However, given the magnitude of the increase, other mechanisms must have been involved in meeting breeding costs. The seasonal peak in blood oxygen carrying capacity did not coincide with the time when moulting was most pronounced.