首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献,搜索用时 15 毫秒
1.
Costs and benefits of natal dispersal have not been fully evaluated in birds. We compared timing of breeding and nesting success for yearling female mallards Anas platyrhynchos returning to or dispersing from their natal areas. Information about natal origins was discerned with feather‐isotopes and combined with detailed reproductive histories for 503 radio‐marked females monitored at 16 study sites across the Canadian Aspen Parklands, during 1993–2000. A natal origin assignment model based on feather‐ δ34S, δD, δ15N, and δ13C values correctly assigned 81% (112 of 138) of known‐source yearlings to region of origin; region‐specific rates ranged from 70–90%. Timing of breeding and nesting success was not related to whether or not a female had dispersed from its region of natal origin in Aspen Parkland (i.e. short‐distance dispersal) versus the southern prairies or boreal forest regions (i.e. long‐distance dispersal). Rather, nesting success was best modeled to include effects of site‐specific wetland and breeding pair abundances and an interaction between local breeding pair and wetland densities. Nest success performance relative to dispersal distance varied among study sites but was unrelated to local upland nest cover, wetland habitat conditions, or conspecific density. Thus, we detected no strong costs of dispersal but some evidence that long‐distance dispersers presumably benefitted when they were able to acquire better nest sites.  相似文献   

2.
3.
In conspecific brood parasitism (CBP), a parasitic female takes advantage of the parental care performed by a host female by laying eggs in the nest of the host. The host female raises the offspring of the parasitic female as well as her own. In species where local females are related, direct costs for the host might be more than compensated for by gains in inclusive fitness through increased reproduction of a related parasite, but the role of relatedness in CBP is debated. This inclusive-fitness model of parasitism, structured as a game between host and parasite, suggests that both females can gain inclusive fitness and that host-parasite relatedness can therefore facilitate the evolution of CBP. Crucial assumptions are that there is kin discrimination and a potential for host resistance to parasitism by unrelated females but close relatives are accepted. The cost of parasitism in terms of reduced clutch size or offspring survival for the host must not be large; otherwise, parasitism will reduce her inclusive fitness. Therefore, if these costs are high, it does not benefit a host to accept a parasite, even if the parasite is closely related. The secondary female may still have higher fitness from parasitism, but if the costs are high, she should parasitize an unrelated host, not a relative. This requires that the reduction in parasite success that a host can cause by resistance is not too large; otherwise, it will be better for the secondary female to parasitize an accepting related host or to nest solitarily. For these reasons, host-parasite relatedness is most likely to occur in animals where costs of being parasitized are low and host resistance can markedly reduce the success of an unrelated parasite. When costs are higher, parasitism of unrelated hosts may be better, and if host resistance strongly reduces parasite success, solitary breeding is preferable. In some cases, CBP is directly advantageous for the host, and it may sometimes evolve in close connection with cooperative breeding, which is also considered in the model. Some but not all empirical results support these ideas, and more detailed studies of behavior, relatedness, and reproduction of host and parasite are needed for critical tests.  相似文献   

4.
For passerines the starvation‐predation risk theory predicts that birds should decrease their body mass to improve escape flight performance, when predation pressure increases. To investigate whether this theory may apply to large birds, which manage body reserves differently from small passerines, we experimentally increased the predation risk in mallards Anas platyrhynchos. Two groups were disturbed at different frequencies during experimental sessions lasting one week, while a control group was left undisturbed. We found that body mass loss and final wing loading were similar in both disturbed groups and significantly differed from the control group. Food intake in disturbed groups was reduced up to day four of the disturbance session and was lower than in the control group. Altogether our results suggest that disturbed mallards may adjust their body mass to reach a more favorable wing loading, supposedly to improve escape flight performance. Nevertheless, body mass loss in our mallards was double than what has been observed in passerines. This greater mass decrease might be explained by different strategies concerning energy storage. Furthermore, in large birds the predation component of the starvation‐predation trade‐off might be of greater importance. Hence, the observed relevance of this trade‐off over a large size range suggests that the starvation‐predation risk theory is of major ecological significance for many animal species.  相似文献   

5.
Eadie J  Lyon BE 《Molecular ecology》2011,20(24):5114-5118
Conspecific brood parasites lay their eggs in the nests of other females in the same population, leading to a fascinating array of possible ‘games’ among parasites and their hosts ( Davies 2000 ; Lyon & Eadie 2008 ). Almost 30 years ago, Andersson & Eriksson (1982) first suggested that perhaps this form of parasitism was not what it seemed—indeed, perhaps it was not parasitism at all! Andersson & Eriksson (1982) observed that conspecific brood parasitism (CBP) was disproportionally common in waterfowl (Anatidae), a group of birds for which natal philopatry is female‐biased rather than the more usual avian pattern of male‐biased natal philopatry. Accordingly, Andersson (1984) reasoned (and demonstrated in an elegantly simple model) that relatedness among females might facilitate the evolution of CBP—prodding us to reconsider it as a kin‐selected and possibly cooperative breeding system rather than a parasitic interaction. The idea was much cited but rarely tested empirically until recently—a number of new studies, empowered with a battery of molecular techniques, have now put Andersson’s hypothesis to the test ( Table 1 ). The results are tantalizing, but also somewhat conflicting. Several studies, focusing on waterfowl, have found clear evidence that hosts and parasites are often related ( Andersson & Åhlund 2000 ; Roy Nielsen et al. 2006 ; Andersson & Waldeck 2007 ; Waldeck et al. 2008 ; Jaatinen et al. 2009 ; Tiedemann et al. 2011 ). However, this is not always the case ( Semel & Sherman 2001 ; Anderholm et al. 2009 ; and see Pöysa 2004 ). In a new study reported in this issue of Molecular Ecology, Jaatinen et al. (2011a) provide yet another twist to this story that might explain not only why such variable results have been obtained, but also suggests that the games between parasites and their hosts—and the role of kinship in these games—may be even more complex than Andersson (1984) imagined. Indeed, the role of kinship in CBP may be very much one of relative degree!
Table 1. A summary of recent studies that have tested for evidence of relatedness between hosts and parasites in avian conspecific brood parasites
Species Evidence of host–parasite relatedness? Evidence of local kin structure? Relatedness > expected spatially r Host–Parasite r Population Costs or benefits measured? Method Source
Common moorhen (Gallinula chloropus) Mixed
Some parasitism between relatives
Yes
Limited dispersal of both sexes
No
Not greater than expected
No (but discussed) DNA minisatellite fingerprints McRae & Burke (1996 )
Common goldeneye (Bucephala clangula) Yes
Number of parasitic eggs also increased with relatedness
Not tested; high female philopatry Yes 0.132 No Protein fingerprints 50 bands Andersson & Åhlund (2000 )
Wood duck (Aix sponsa) No (parasites avoid relatives) Not tested; high female philopatry No
Significantly less likely to parasitize local kin
No Behavioural observation Semel & Sherman (2001 )
Common goldeneye (B. clangula) No
Relatedness unlikely to explain CBP
Not tested Not measured Yes Field measures Pöysa (2004 )
Wood duck (A. sponsa) Yes (for primary parasites) No Yes (for primary parasites) 0.04 (all) 0.11 (primary parasites) 0.01–0.02 No 5 microsatellites Roy Nielsen et al. (2006 )
Common eider (Mollissima somateria) Yes No Yes 0.122 (all) 0.126, 0.162 (two colonies) ?0.065 (neighbours 1–10 m) No Protein fingerprints 30 bands Andersson & Waldeck (2007 )
Common eider (M. somateria) Yes
Number of parasitic eggs also increased with relatedness
Yes
Relatedness declined with distance
Possibly
Host–parasite relatedness > close neighbours in 1 of 2 analyses
0.18–0.21 0.09 (neighbours) No Protein fingerprints 51 bands Waldeck et al. (2008 )
Barnacle goose (Branta llucopsis) No Weak
Females within 40 m more closely related
No 0.04 ?0.0008 No Protein fingerprints 28 bands Anderholm et al. (2009 )
Barrow’s goldeneye (Bucephala islandica) Yes
Number of parasitic eggs increased with relatedness
Weak
Slight decline in relatedness with distance
No
Host–parasite relatedness similar to neighbours
0.08 ?0.015
0.11 (neighbours)
No 19 microsatellites Jaatinen et al. 2009
Common eider (M. somateria) Yes
Interaction with parasite status
No Yes 0.39 (mean) 0.48, 0.28 (different sites) 0.0 No 7 microsatellites Tiedemann et al. (2011 )
  • CBP, conspecific brood parasitism.
Jaatinen et al.’s (2011a) study highlights several intriguing and as yet not fully resolved issues. First, they confirm results from an earlier study ( Jaatinen et al. 2009 ) showing that relatedness influences conspecific brood parasitism (CBP) in the Barrow’s goldeneye (Bucephala islandica; Fig. 1 ), a species of cavity‐nesting sea duck well known to engage in parasitic egg‐laying ( Eadie 1989 ; Eadie & Fryxell 1992 ). CBP in this species was more frequent among related females that nested in close proximity ( Jaatinen et al. 2009, 2011a ). Female natal philopatry is pronounced in the Barrow’s goldeneye ( Eadie et al. 2000 ), and it is possible the spatial proximity of kin could account for this pattern. However, Jaatinen et al. (2011a) show that relatedness and distance independently affected the extent of parasitism, suggesting that natal philopatry alone cannot provide an explanation. Similar patterns of elevated host–parasite relatedness after controlling for spatial proximity of kin have been reported for other species ( Table 1 ). The novel observation of Jaatinen et al.’s newest study is that the nesting status of the parasite profoundly altered the influence of relatedness on host–parasite interactions. Parasitic females that also had a nest of their own (‘nesting parasites’) increased the number of eggs laid in a host nest with increasing relatedness to the host, whereas parasites without a nest of their own (‘non‐nesting parasites’) did not. Apparently, females within the same population may be using different decision rules with respect to relatedness, and the effects of kinship on CBP may be far more subtle than previously appreciated.
Figure 1 Open in figure viewer PowerPoint A pair of Barrow’s goldeneyes (Bucephala islandica) in central British Columbia. Photo credit: Bruce Lyon.  相似文献   

6.
Generalizations used to support hypotheses about the evolutionof fidelity to breeding areas in birds include the tendencyfor fidelity to be greater in adult birds than in yearlings.In ducks, in contrast to most bird species, fidelity is thoughtto be greater among females than males. Researchers have suggestedthat fidelity in ducks is positively correlated with pond availability.However, most estimates of fidelity on which these inferenceshave been based represent functions of survival and recapture—resightingprobabilities in addition to fidelity. We applied the modelingapproach developed by Burnham to recapture and band recoverydata of mallard ducks to test the above hypotheses about fidelity.We found little evidence of sex differences in adult philopatry,with females being slightly more philopatric than males inone study area, but not in a second study area. However, yearlingfemales were more philopatric than yearling males in both studyareas. We found that adults were generally more philopatricthan yearlings. We could find no relationship between fidelityand pond availability. Our results, while partially supportingcurrent theory concerning sex and age differences in philopatry,suggest that adult male mallards are more philopatric thanonce thought, and we recommend that other generalizations aboutphilopatry be revisited with proper estimation techniques.  相似文献   

7.
The latitudinal increase in extra‐pair paternity (EPP) rates in birds suggests broad selective benefits to low EPP rates in the tropics. However, we have few EPP data from tropical birds, particularly from species with close relatives at high latitudes. Here, we report EPP rates in two resident equatorial populations of rufous‐collared sparrow Zonotrichia capensis, a genus well‐represented at high latitudes. We found 64% and 60% of broods contained extra‐pair offspring, and 42% and 52% of all young were extra‐pair. EPP rates were similar in these populations, despite clear differences in elevation, temperature, rainfall, and breeding season length. These findings provide evidence that EPP rates in tropical birds can be as high as those observed in temperate birds, and suggest that the selective pressures acting on EPP rates vary markedly across tropical birds.  相似文献   

8.
Numerous methods have been proposed to indirectly detect conspecific brood parasitism (CBP) in birds. Egg morphology has been suggested as a predictor of parasitism, assuming that variation in egg size is greater among females than within females. Here we use microsatellite data to assess the use of egg morphology to detect CBP in a sample of black brant Branta bernicla nigricans nests. We attempted to repeat a previously demonstrated technique using cluster analysis and maximum Euclidean distance (MED) to detect parasitized nests within black brant. Additionally we attempted a new technique based on a discriminant function analysis of egg morphology in an attempt to detect brood parasitic eggs. When detecting parasitized nests using egg morphology, the cluster analysis revealed that the MED between the two most dissimilar eggs in each nest was significantly greater for parasitized nests than for non‐parasitized nests (1.62±0.06 and 1.43±0.08, respectively). The extent of overlap in sizes of eggs between parasitized and non‐parasitized nests, however, was such that we were unable to effectively identify parasitized nests. In most cases for each parasitized nest correctly identified, 3 non‐parasitized nests were incorrectly identified as parasitic. When we attempted to detect parasitic eggs we found that parasitic eggs were more different from the expected egg volume than host eggs: mean absolute residual volume of parasitic eggs=2.59±5.79 cm3 while that for host eggs=1.82±2.14 cm3. Overall, we found that the discriminant function analysis was moderately effective in determining whether eggs belonged to the host female using a resubstitution technique (error rate=9.71%) or a jackknife technique (error rate=6.12%). Additionally, we found a higher but moderate error rate when using an independent data set to validate the function (error rate=14.07%). In both cases, however, parasitic eggs accounted for most of the error and were not correctly classified 75%, 70% and 100% of the time respectively. We suggest when developing a predictive function for detecting conspecific brood parasitism based on egg morphology that an appropriate technique be used to validate the function, particularly those techniques that utilize unambiguous identifiers such as molecular and protein fingerprinting techniques.  相似文献   

9.
In winter, pen-reared and wild black ducks (Anas rubripes), and game farm and wild mallards (Anas platyrhynchos), maintained on pelleted feed, were sham-dosed or given one number 4 lead shot. After 14 days, dosed birds were redosed with two or four additional lead shot. This dosing regimen also was repeated in summer using pen-reared black ducks and game farm mallards. Based upon mortality, overt intoxication, weight change, delta-aminolevulinic acid dehydratase activity and protoporphyrin concentration, black ducks and mallards were found to be equally tolerant to lead shot. However, captive wild ducks were more sensitive than their domesticated counterparts, as evidenced by greater mortality and weight loss following lead shot administration. This difference may be related to stress associated with captivity and unnatural diet.  相似文献   

10.
We examined the effects of lead ingestion on in vitro and in vivo indices of immune function in mallards (Anas platyrhynchos). Twenty-four mallard drakes were randomly divided into three groups (I, II, III), then assigned to treatment or control subgroups (n = 4). On day 0, all treatment birds were dosed orally with one number 4 lead shot (mean = 0.2 g). We challenged all individuals in each group with washed sheep red blood cells (SRBC) injected intraperitoneally on days 0 (Group I), 7 (Group II) or 14 (Group III), and collected blood for analyses 7 and 8 days after SRBC challenge. We measured and compared blood lead concentrations, in vitro lymphocyte transformation responses to phytohemagglutinin A and lipopolysaccharide, and hemagglutination titers to SRBC. Mean blood lead concentrations were elevated (P less than or equal to 0.04) in treatment birds at each sampling period. Large individual variability in lymphocyte stimulation responses precluded further analysis of those data. Hemagglutination titers to SRBC were lower (P less than 0.0001) in lead-poisoned ducks than in controls, suggesting that ingested lead may have immunosuppressive effects on mallards.  相似文献   

11.
Genes of the Major Histocompatibility Complex (MHC) represent an essential component of the vertebrate acquired immune system. In the last decades, the role of MHC genes in mate choice has been subject of particular scientific interest. However, results of studies dealing with this topic in different species are equivocal and mechanisms conducting MHC‐based mate choice are still puzzling. We investigated the impact of MHC class I variability on within‐pair and extra‐pair fertilisation success in a wild population of a socially monogamous passerine bird with considerable rates of extra‐pair paternity, the scarlet rosefinch Carpodacus erythrinus. We found some support for the ‘good‐genes‐as‐heterozygosity model’, as social males of high MHC‐heterozygosity were cheated by their females less frequently than less MHC‐heterozygous males. However, cuckolding males were not more MHC‐heterozygous than the cheated social males, nor were extra‐pair young more MHC‐heterozygous than within‐pair young. We did not find any evidence for mating preferences according to the complementarity model.  相似文献   

12.
13.
The mallard Anas platyrhynchos is the world’s most widespread and numerous dabbling duck. It is also farmed and released to the wild by the millions each year, but the effects of this on wild populations remain little studied. By using historical national ringing–recovery data from Sweden and Finland, we here address three predictions based on previous studies: (1) longevity is higher in wild than in hand-reared mallards, (2) wild mallards migrate longer than hand-reared, and (3) migration distance in wild ducks surviving long enough to start fall migration has decreased over the last 50 years. Indeed, wild mallards lived longer than hand-reared (19 versus 9 months in Swedish birds and 13 versus 4 months in Finnish birds). Compared to wild mallards, a smaller proportion of hand-reared birds survived long enough to have the chance to enter the wild breeding population; less than 25 % of the Swedish birds and less than 10 % of the Finnish birds lived a year or longer. Wild birds migrated farther than hand-reared (mean distance in Swedish birds, 676 versus 523 km; in Finnish birds, 1,213 versus 157 km), a pattern caused by both shorter life span and lower migration speed in hand-reared birds. Mean migration distance in wild Swedish mallards was 787 km in 1947–1972 but 591 km in 1977–1993. This difference was not statistically significant, though, possibly due to the limited sample size and lack of data from the last two decades. In general, our study provides a conservative test of the predictions addressed, calling for more research about the consequences of restocking duck populations.  相似文献   

14.
Conspecific brood parasitism (CBP) is a common strategy in several species of birds. Currently, some studies suggest that relatedness between host and parasite enhances CBP, since indirect fitness benefits could select for acceptance of related eggs by hosts. Conversely, parasites should avoid laying eggs in nests of relatives if this is costly for the host. Based on the latter argument, kinship should not promote brood parasitism. A recent model clarified this relationship, and showed that kinship can promote brood parasitism, assuming kin recognition. However, in that model kin recognition was assumed perfect. Here we present a model that addresses the role of relatedness and kin selection in CBP, when kin recognition is not perfect and hosts do not always detect parasitism. We consider both the indirect fitness of the parasite and the possible responses of the host. Our results indicate that the existence and accuracy of a kin recognition system is crucial to the final outcome. When CBP represents a cost to the host, a parasitic female that has the choice should avoid parasitizing relatives, unless (1) the costs are not too high and (2) hosts can accurately enough recognize eggs laid by relatives, rejecting them less often than eggs laid by nonkin. But if ‘parasitism’ enhances the direct fitness of the host (which is possible in species with precocial young) parasites should choose relatives whenever possible, even if hosts do not recognize kin eggs. Copyright 2002 The Association for the Study of Animal Behaviour. Published by Elsevier Science Ltd. All rights reserved.  相似文献   

15.
16.

Introduction

The monk parakeet (Myiopsitta monachus) is a widespread invasive species native to southern South America that has become established in many regions of the world. Monk parakeets breed in a large, fully enclosed structure built from twigs, which consist of one to many individual brooding chambers. The species has been considered to be socially and genetically monogamous. However, genetic relatedness of adults to juveniles in the native area was found to be lower than expected for monogamy. To assess the significance of this discrepancy, we examined individual and population genetic patterns of microsatellite loci at two sites in Córdoba province, Argentina.

Results

We sampled 154 nestlings and 42 adults in Córdoba, Argentina. Mean value of pairwise relatedness of nestlings within chambers was about 0.40. Contrarily, relatedness of nestlings between chambers was close to zero. We found a considerable degree of variation in nestling pairwise relatedness and parentage within chambers, including chambers with combinations of unrelated, half-sib, and full-sib nestlings. The proportion of sibling relatedness indicated monogamy in 47% and extra pair-paternity in 40% of the chambers. We also found intra-brood parasitism in 3% of the chambers.

Conclusions

Our results indicate that the monk parakeet is sexually polygamous in its native range in Argentina, which is consistent with the observed mean value of relatedness of adults to juveniles of about 0.4. We also confirm the existence of intra-brood parasitism. High density of monk parakeets may favor occurrence of extra-pair paternity and intra-brood parasitism in the native sites.
  相似文献   

17.
Captured free‐living male mallard Anas platyrhynchos at Abberton in southern Britain showed peak mass gain immediately prior to simultaneous remex moult. Individuals of both sexes were heavier before shedding wing feathers than when flightless confirming literature accounts that show mallard accumulate fat stores in anticipation of moult to contribute to meeting energy needs during remex re‐growth. Over the course of four seasons, males lost 13 17% of initial body mass on average during re‐growth of flight feathers, females 13 23%. Based on energy expenditure of 1.3 times BMR, male mallard were estimated to be able to fulfil 42 60% and females 41 82% of their energy needs throughout moult from stores. Free‐flying male mallard fed ad libitum in a predator‐free environment did not differ in starting body mass or rate of mass loss during wing moult compared to free‐living Abberton birds, suggesting depletion of fat stores, irrespective of available sources of exogenous energy. Based on this evidence, we reject that the hypotheses that mass loss in moulting mallard is due to 1) simple energy stress and 2) restrictions on feeding and consider that 3) attaining the ability to fly at an earlier stage on incompletely grown flight feathers is not the primary factor shaping this trait. Rather, we consider the accumulation and subsequent depletion of fat stores, together with reductions in energy expenditure, enable mallard to re‐grow feathers as rapidly as possible by exploiting habitats that offer safety from predators, but do not necessarily enable them to balance energy budgets during the flightless period of remex feather re‐growth.  相似文献   

18.
Eadie (1989) developed a method based on variation between females in egg length, width and weight to detect conspecific brood parasitism in the field: using these three egg measures, Euclidean distance between all pairs of eggs within a clutch is calculated, and if maximum Euclidean distance (MED) between any two eggs exceeds a threshold value the nest is considered parasitized. The MED method has been tested in Finnish and Scottish common goldeneye Bucephala clangula populations but the results have been contradicting. Here we use protein fingerprinting to assess the validity of the MED method. Data comprised 35 clutches of which we knew, based on protein fingerprinting, how many different females laid the clutch (range 1–5 females). The mean MED of non-parasitized clutches (laid by 1 female only) was 1.470 (95% CI: lower 1.169, upper 1.771; n=21) and that of parasitized clutches (laid by 2 or more females) was 3.654 (95% CL: lower 3.083, upper 4.225; n=14). Using a MED>3.0 as a criterion to identify parasitized clutches 89% of all clutches were classified correctly either parasitized or non-parasitized when compared to the identification based on protein fingerprinting. Clutch size and the number of females (beyond 2 females) did not affect the clutch MED, whereas the status of parasitism did. Repeatability of egg length, width and weight were: 0.63, 0.76 and 0.80, respectively, implying that, variation in these egg measures occurs among rather than within females. Our new results confirm that the MED method is reliable enough to detect parasitism in common goldeneye.  相似文献   

19.
Ideal preemption and conspecific attraction are alternative hypotheses of the habitat selection rules used by individuals. According to the former an occupied site is assumed to be preempted and therefore not available for later arriving individuals, whereas according to the latter individuals are assumed to be attracted by conspecifics to occupied sites, rather than avoiding them. We studied these competing hypotheses in breeding mallards (Anas platyrhynchos) by a cross-over experiment in 2 years, introducing birds onto lakes before migratory wild mallards arrived. If mallards use the ideal preemptive rule, breeding density of wild mallards in experimental lakes should be lower and they should be occupied less frequently than control lakes, but if mallards use the conspecific attraction rule the reverse should be true. Our results allowed us to reject the ideal preemptive rule whereas the conspecific attraction rule was to some extent supported. We discuss these findings in relation to population limitation. The results suggest that the local breeding population studied is not limited by spacing behaviour related to habitat selection. Received: 14 July 1997 / Accepted: 17 November 1997  相似文献   

20.
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号