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Female Birds (female + bird)
Selected AbstractsHabitat utilisation during staging affects body condition in a long distance migrant, Branta bernicla hrota: potential impacts on fitness?JOURNAL OF AVIAN BIOLOGY, Issue 6 2008R. Inger There is considerable evidence to suggest that an animal's ability to access the appropriate resources at one time of year may profoundly restrict its performance at another. For migrants, wintering and breeding periods are often connected by refuelling or staging periods, critical (particularly for females) in attaining the body reserves required to ensure successful breeding. However in many instances there are differences in the extent to which different individuals gain access to the highest quality resources. Here we demonstrate how body condition in brent geese Branta bernicla hrota, during spring staging is related to differences in marine and terrestrial habitat utilisation (inferred from stable isotope analysis). Female birds with high fat scores feed to a greater extent on marine resources. Body mass and condition are also higher in individuals utilising more marine resources. Given that body mass at spring staging is correlated with reproductive success, the extent of marine habitat maybe critical to this population. Combining this with data from previous studies of dark-bellied brent geese Branta bernicla bernicla, we predict the potential impacts of spring staging resource utilisation on future breeding success. Although staging is of short duration compared to the other components of annual cycles of migratory species, our results suggest that the quality of staging grounds may be vitally important to population processes. [source] Age-dependent reproductive costs and the role of breeding skills in the Collared flycatcherACTA ZOOLOGICA, Issue 2 2007Joanna Sendecka Abstract This study addressed whether there are any age-related differences in reproductive costs. Of especial interest was whether young individuals increased their reproductive effort, and thereby their reproductive cost, as much as older birds when brood size was enlarged. To address these questions, a brood-size manipulation experiment with reciprocal cross-fostering of nestlings of young and middle-aged female Collared flycatchers, Ficedula albicollis, was performed on the Swedish island of Gotland. Nestlings' body mass, tarsus length and survival were recorded to estimate the parental ability and parental effort of the experimental female birds. Female survival and clutch size were recorded in the following years to estimate reproductive costs. We found that middle-aged female flycatchers coped better with enlarged broods than younger females or invested more in reproduction. In the following year, young female birds that had raised enlarged broods laid smaller clutches than the females from all the other experimental groups. This result shows that the young female birds pay higher reproductive costs than the middle-aged females. Both young and middle-aged female flycatchers seemed to increase their reproductive effort when brood size was increased. However, such an increase resulted in higher reproductive costs for the young females. The difference in reproductive costs between birds of different ages is most likely a result of insufficient breeding skills of the young individuals. [source] Incorporation of ZP1 into perivitelline membrane after in vivo treatment with exogenous ZP1 in Japanese quail (Coturnix japonica)FEBS JOURNAL, Issue 14 2008Mihoko Kinoshita In birds, the egg envelope surrounding the oocyte prior to ovulation is called the perivitelline membrane and it plays important roles in fertilization. In a previous study we demonstrated that one of the components of the perivitelline membrane, ZP3, which is secreted from the ovarian granulosa cells, specifically interacts with ZP1, another constituent that is synthesized in the liver of Japanese quail. In the present study, we investigated whether ZP1 injected exogenously into the blood possesses the ability to reconstruct the perivitelline membrane of Japanese quail. When ZP1 purified from the serum of laying quail was injected into other female birds, the signal of this exogenous ZP1 was detected in the perivitelline membrane. In addition, we revealed, by means of ligand blot analysis, that serum ZP1 interacts with both ZP1 and ZP3 of the perivitelline membrane. By contrast, when ZP1 derived from the perivitelline membrane was administered, it failed to become incorporated into the perivitelline membrane. Interestingly, serum ZP1 recovered from other Galliformes, including chicken and guinea fowl, could be incorporated into the quail perivitelline membrane, but the degree of interaction between quail ZP3 and ZP1 of the vitelline membrane of laid eggs from chicken and guinea fowl appeared to be weak. These results demonstrate that exogenous ZP1 purified from the serum, but not ZP1 from the perivitelline membrane, can become incorporated into the perivitelline membrane upon injection into other types of female birds. To our knowledge, this is the first demonstration that the egg envelope component, when exogenously administered to animals, can reconstruct the egg envelope in vivo. [source] Testosterone response to GnRH in a female songbird varies with stage of reproduction: implications for adult behaviour and maternal effectsFUNCTIONAL ECOLOGY, Issue 4 2007JODIE M. JAWOR Summary 1Despite considerable recent interest in plasma and yolk testosterone (T) in female birds, relatively little is known about environmental regulation of female T, individual variation in female T or the relationship between plasma and yolk T. 2In breeding females of a wild population of dark-eyed junco (Junco hyemalis), we assessed variation in the responsiveness of the hypothalamo-pituitary-gonadal (HPG) axis to a challenge with gonadotropin-releasing hormone (GnRH) by measuring circulating T before and 30 min after a standardized injection of GnRH. We asked whether response to challenge varied seasonally or with stage of reproduction and whether it was repeatable within individuals or related to T deposited in eggs. 3Initial and post-challenge levels of T were measured using enzyme immunoassay. In a subset of these females, luteinising hormone (LH) was measured using radioimmunoassay (RIA). In addition, eggs were collected from nests of 15 females that had received a GnRH challenge, and yolk T was measured using RIA. 4During most of the breeding season, plasma T did not increase in response to GnRH. GnRH consistently caused increases in plasma T only during the 7 days before oviposition, when females were rapidly depositing yolk in eggs but had not yet begun to lay them. Among a small subset of females we found a positive correlation between the magnitude of this increase in plasma T in response to GnRH during egg development and the amount of T deposited in the yolk of eggs collected at a later time. 5These results suggest that ovarian response to GnRH-induced increases in LH is greatest when females are actively depositing yolk into eggs. Factors that stimulate the release of GnRH during egg formation may result in higher levels of plasma T which could influence adult female behaviour. Further, because plasma T was correlated with later yolk T, factors that stimulate GnRH release may also lead to higher levels of yolk T potentially influencing offspring development or behaviour. [source] When heavier birds lose more mass during breeding: statistical artefact or biologically meaningful?JOURNAL OF AVIAN BIOLOGY, Issue 2 2000Sabine G. Gebhardt-HenrichArticle first published online: 30 OCT 200 Several studies on mass loss during breeding in female birds have shown a significant correlation between initial body mass and subsequent loss of body mass. The significant positive regression coefficient of mass loss on initial mass was interpreted as evidence for a greater mass loss of initially heavier birds. However, the positive correlation between mass loss and initial mass arises automatically even when initial and final body masses are uncorrelated and has no necessary biological meaning. This is shown analytically here. In general, a spurious correlation arises when one variable (e.g. mass loss) is part of another variable (e.g. initial mass) and then regressed on it. [source] | ||||||||||