Egg quality and parental ornamentation in the blue tit Parus caeruleus

Components of avian egg quality often show remarkable variation between females and yet the causes of variation in this fitness-related trait remain poorly understood. We investigated the egg size and yolk carotenoid investment of blue tit Parus caeruleus females in relation to multiple parental traits. We show that females produce eggs with more colourful yolks when mated to ultraviolet (UV) attractive males. Since yolk carotenoids may enhance offspring fitness, but may be available to females in limiting amounts, the correlation we found suggests adaptive egg quality adjustment in response to mate attractiveness, but an experimental approach is required to rule out alternative explanations. Yolk colour was also correlated with laying date and yolk mass. Though the effect of laying date could not be explained by ambient temperature during egg formation, it suggests a proximate constraint of general carotenoid availability on yolk composition. Egg size was not affected by male attractiveness; however, females with a brighter crown produced larger eggs, suggesting that crown coloration might indicate individual quality in females too.     

Habitat and laying date of Great and Blue Tit Parus major and P. caeruleus

Using 19 year's data from nine study areas at Ghent we investigated the effect of habitat on laying date, and found it to be quite different for Great and Blue Tits. In Great Tits we found a clear gradient in laying dates from urban over suburban to rural habitats. Blue Tits laid earliest in a suburban habitat and latest in a rural habitat. All other areas, including urban, suburban and rural ones, formed one intermediate group. The overall average laying date for the Great Tit, 18.9 April, was slightly earlier than that of the Blue Tit, 19.4 April. In urban areas Great Tits laid significantly earlier than Blue Tits, in optimal oak habitat and in one suburban area Blue Tits laid earlier, whereas in the five remaining areas no significant differences between the two species were found.
We argue that the differences in laying dates, although correlated to temperature, are probably caused by differences in the timing of food availability. We suggest that differences in laying dates of Great and Blue Tits are caused by a different response to environmental variations through differences in feeding ecology.     

Sex ratio and male sexual characters in a population of blue tits, Parus caeruleus

A. Dreiss, M. Richard, F. Moyen,     

Detection distance influences escape behaviour in two parids, Parus major and P. caeruleus

When birds are attacked by aerial predators they should benefit by adjusting their escape to the prevailing attack situation. One important factor likely to affect escape decisions of prey, to our knowledge not previously studied, is the distance at which the attacking predator is detected. We investigated if great tits Parus major and blue tits P. caeruleus alter their escape behaviour to two different detection distances (2.3 m and 1m) by simulating surprise attacks using a predator model. Both species used the information about detection distance when escaping by increasing the escape angle at the shorter detection distance. In addition, blue tits adjusted to the shorter detection distance by dodging sideways more frequently. Great tits escaped initially steeper and faster than blue tits, whereas blue tits increased escape angle and speed more than great tits along the measured distance after taking wing.     

Sex ratio and male sexual characters in a population of blue tits, Parus caeruleus

Sex allocation theory proposes that parents should bias thesex ratio of their offspring if the reproductive value of onesex is greater than that of the other. In the monogamous bluetit (Parus caeruleus), males have a greater variance in reproductivesuccess than females, and high-quality males have higher reproductivesuccess than high-quality females due to extrapair paternity.Consequently, females mating with attractive males are expectedto produce broods biased toward sons, as sons benefit more thandaughters from inheriting their father's characteristics. Songand plumage color in birds are secondary sexual characters indicatingmale quality and involved in female choice. We used these malesexual traits in blue tits to investigate adaptive sex ratiomanipulation by females. We did not find any relationship betweenmale color ornamentation and brood sex ratio, contrary to previousstudies. On the other hand, the length of the strophe bout (i.e.,the mean number of strophes per strophe bout) of fathers waspositively related with the proportion of sons in their broods.The length of the strophe bout is supposed to reflect male qualityin terms of neuromuscular performance. We further showed thatsons produced in experimentally enlarged broods had shorterstrophe bouts than sons raised in reduced broods. These resultsare consistent with the hypothesis that females adjust the sexratio of their broods in response to the phenotype of theirmate.     

Sex-specific recombination rates in Parus major and P. caeruleus, an exception to Huxley's rule

Huxley's rule predicts lower recombination rates in the heterogametic sex than in the homogametic one. The genotyping of Parus major and P. caeruleus families at 8 microsatellite and 4 enzyme loci yielded contradicting data. Significant genotypic disequilibrium was observed between esterase-1, esterase-2 and esterase-3 in adults of P. major and between esterase-2/esterase-3 and esterase-2/microsatellite PK-12 in P. caeruleus. Support comes from linkage analyses of nuclear families. In P. major, the recombination rate of esterase-2/esterase -3 in males is significantly lower than in females (theta(male) = 0.076, theta(female) = 0.145). The opposite is found for the recombination rates of esterase-1/esterase-2 and esterase-2/esterase-3 in P. caeruleus (EST-1/EST-2: theta(female) = 0.218, theta(male) = 0.5, EST-2/EST-3: theta(female) = 0.109, theta(male) = 0.194). We conclude that the basis of differences in recombination rates cannot be heterogamety, per se, but must have multiple genetic causes including chromosomal rearrangments that have evolved after the cladogenesis of the two species.     

Male-biased sex ratio among unhatched eggs in great tit Parus major, blue tit P. caeruleus and collared flycatcher Ficedula albicollis

An increasing number of studies have demonstrated that brood sex ratios are frequently unequal, but the proximate mechanisms underlying this deviation are largely unknown. In the current study we analysed deviation from expected 1:1 sex ratio among dead embryos from unhatched eggs collected from partially unhatched clutches of three passerine bird species. We showed that male embryos were significantly overrepresented among unhatched eggs of great tit Parus major , blue tit P. caeruleus and collared flycatcher Ficedula albicollis . Moreover, the bias in sex ratio differed among species and tended to differ among study years. We discuss several hypotheses to explain the observed male bias among unhatched eggs. We conclude that sex specific embryo mortality may contribute to explain the observed variation in sex ratios in several species of wild birds and that sexing unhatched eggs is important in studies of sex ratio allocation.     

The effect of old age on the reproduction of Great Tits Parus major and Blue Tits P. caeruleus

The results from two data sets show that in Great Tits Parus major and Blue Tits P. caeruleus reproduction is influenced by age. In both species, laying dates become earlier while clutch- and brood-size increase between the ages of 1 and 2, but there is no change in nesting success or post-fledging juvenile survival. Great Tits aged 5 or older are 'old' in that laying starts later and nesting success, brood-size and post-fledging juvenile survival decrease. Blue Tits become 'old' 1 year earlier than Great Tits: females aged 4 or older lay later, have a lower nesting success and smaller brood-size, and their young show a decreased post-fledging survival. The effect on laying date, in the Blue Tit, becomes apparent only for females aged 6 and older. It is concluded that ageing in small passerines is to be expected more generally, but that no extrapolations can be made as to the timing of the effect from one species to another.     

Leafing phenology and timing of egg laying in great tits Parus major and blue tits P. caeruleus

To evaluate the importance of tree leafing for the start of laying and clutch size of birds, we compared the breeding phenology of great tits Parus major and blue tits P. caeruleus between one coastal and two inland sites in the same geographical region. Because of the cooling influence of the sea, trees at the coastal site were known to initiate budburst about a week later than at the inland sites. During 5 years, breeding by the tits and the leaf phenology of birch Betula pendula , and oak Quercus robur were monitored. The leaf phenology of birch and oak explained a significant part of the between-year variation in the start of egg laying in blue and great tits, respectively. The tits started laying earlier at the sites with an early budburst, i.e. normally inland. However, leaf phenology was not an absolute cue to the start of laying, since blue tits laid earlier relative to leafing at the inland site than at the coastal site, and both tit species laid eggs earlier relative to leafing during late springs. In neither species was clutch size affected by leafing phenology. However, great tit females at the coastal site consistently produced fewer eggs than did those at the inland site. No such difference was found in the blue tits. Although leafing phenology may predict the start of laying in tits, other factors also influence its timing. These factors might include other cues, or differing life-history trade-offs depending on site or general climatic factors during the spring.     

Similarity of growth among Great tits (Parus major) and Blue tits (P. caeruleus)

Differences in morphology among species are proximately caused by changes in the ontogeny of individuals. It is therefore of importance to analyse possible differences in growth parameters among closely related species in order to understand what parameters are most and least likely, respectively, to change in evolution. In this paper I analyse growth in two closely related sympatric species, namely Great tit, Parus major, and Blue tit, P. caeruleus. The former is considerably larger than the latter in all external traits. The growth rates of the two species were found to be very similar for all traits, thus excluding differences in growth rate as a potential cause of evolutionary size changes. Offset of growth occurred at relatively similar times in the two species, excluding this factor as a major cause of the final size differences. However, size differences at hatching were pronounced and remained so throughout ontogeny, pointing to initial size (egg size or hatching size) as the target of factors promoting change. Bivariate allometric relations of traits vs. body size (mass) were similar between the two species at all ontogenetic stages. There was a high correlation among traits especially at intermediate age stages (5 and 8 days), but these correlations became weaker at older age and approached the low pattern of integration found in adults. All this suggests the operation of a general growth factor affecting all parts of the phenotype simultaneously, which has its major influence at the time of maximal growth. If closely related species in general have highly similar growth patterns, strong evolutionary allometry as found in many avian taxa is to be expected.     

Environmental factors shape cloacal bacterial assemblages in great tit Parus major and blue tit P. caeruleus nestlings

Despite their potential ecological and evolutionary importance, factors shaping the composition of bacterial communities in wild vertebrate populations remain poorly understood. The goal of this study was to examine the relative contributions of environmental factors and genetic factors (e.g. species and common origin) to the variation of cloacal bacterial assemblages in wild bird nestlings. We conducted a partial cross-fostering experiment with two passerine species, the great tit Parus major and the blue tit P. caeruleus, sharing similar habitats and breeding biology. Nestlings of the two species were exchanged four days after hatching and cloacal bacteria were sampled nine days later. The structure of cloacal bacterial communities was determined by Ribosomal Intergenic Spacer Analysis. Our results showed that each nestling displayed a unique bacterial community. Furthermore, nestlings raised in the same nest shared significantly similar bacterial communities. The similarity of bacterial community was higher among heterospecific siblings raised within the same nest than between biological siblings raised in separate nests. Effects of common origin between species could not be detected and, if present, were dominated by nest-based short-term environmental effects. Our results show that growth conditions within nests and individually based endogenous factors have significant effects on cloacal bacteria assemblages and could affect post-fledging condition.     

Sex ratio variation among broods of great reed warblers Acrocephalus arundinaceus

The sex of 746 great reed warbler fledglings (from 175 broods) was determined by the use of single primer polymerase chain reaction. The reliability of the technique was confirmed as 104 of the fledglings were subsequently recorded as adults of known sex. The overall sex ratio did not differ from unity. Variation in sex ratios between broods was larger than expected from a binomial distribution. Female identity explained some of the variation of brood sex ratio indicating that certain females consistently produced sex ratios that departed from the average value in the population. The theory of sex allocation predicts that parents should adjust the sex ratio of their brood to the relative value of sons and daughters and this may vary in relation to the quality of the parents or to the time of breeding. In the great reed warbler, the proportion of sons was not related to time of breeding, or to any of five female variables. Of five male variables, males with early arrival date tended to produce more daughters. The sex ratio of fledglings that were a result of extra-pair fertilizations did not differ from that of legitimate fledglings. Hence, there is currently no evidence of that female great reed warblers invest in a higher proportion of sons when mated with attractive males.     

Sex ratio manipulation within broods of house wrens, Troglodytes aedon

Trivers & Willard (1973, Science, 179, 90-92) developed an economic theory of parental investment to explain how the relative profitability of sons and daughters varies under specific ecological conditions. In their maternal condition hypothesis they proposed that in polygynous species, the sex of an offspring should be associated with the amount of parental care likely to be made available to it. In these species, the amount of parental investment directed towards offspring may differentially influence the fitness of male and female offspring because males in better than average condition as adults may enjoy larger fitness gains than a female would if she were in better than average condition, while the reverse may be true when conditions are poor. I tested this hypothesis by determining the sex of specific offspring within house wren broods. Because hatching is asynchronous and fledging is synchronous in this polygynous species, last-hatched young fledge having received less parental care than their broodmates. I predicted that last-hatched offspring would be more likely to be female. I found that these young were indeed more likely to be females, were more likely to have hatched from last-laid eggs and were fledging in poor condition relative to their broodmates. I propose that female house wrens behave in a manner consistent with the predictions of the Trivers & Willard hypothesis by producing female offspring last in the laying sequence of their clutches. Copyright 2000 The Association for the Study of Animal Behaviour.     

Foraging flight distances as a measure of parental effort in blue tits Parus caeruleus differ with environmental conditions

Life-history theory predicts that parental effort in nestling provisioning is optimised in relation to the quality of individuals and/or their habitat. We studied the investment of breeding pairs of blue tits Parus caeruleus for their reproduction during three breeding seasons in deciduous (high quality) vs. mixed (low quality) habitats in order to quantify to what extent habitat quality affects parental effort. Parental effort (costs) was related to their feeding rates and flight distances during foraging. In the deciduous habitat flight distances between nest and foraging patch were shorter than in the mixed habitat (22 m and 40 m, respectively), but the feeding rates did not differ between the habitats. The total flight distance per breeding pair from the first day after hatching until the 17th day of the nestling period was about half of the distance observed in the mixed habitat (375 km and 674 km, respectively). As the quality of fledglings did not differ between habitats, the higher number of fledglings per brood reflects better rewards per foraging trip in the deciduous than in the mixed habitat. Considering the parental foraging effort (costs) and, the quality and number of offspring (benefits), the benefit-cost-ratio was 2–3 times higher in the deciduous than in the mixed woodland.     

Weight loss of the female during the first brood as a factor influencing second brood initiation in Great Tits Parus major and Blue Tits P. caeruleus

We tested the hypothesis that the weight lost by female Great and Blue Tits Parus major and P. caeruleus while raising their first brood influences their ability to start a second brood. The evening weight of female parents was recorded when the nestlings were 5 and 13 days old, in different years and habitats. Several predictions were tested: (1) both species lose weight while raising nestlings and Great Tit females which start a second brood lose less weight than females which do not; (2) differences in the average weight lost between years and areas correlate with differences in the proportion of second broods; (3) the relative weight loss in Blue Tits, which only rarely undertake second broods, is higher than in Great Tits in which second broods are more common. Other factors also are related to the probability of undertaking a second brood: more second broods are undertaken by more successful females, adult females and females that lay earlier.
The comparison of Great and Blue Tits suggests that the two species use different reproductive strategies.     

Reproduction and survival of polygynous and monogamous Blue Tit Parus caeruleus

In a seven-year study of Blue Tits in optimal habitat near Antwerp, Belgium, 45 polygynous broods involving 22 males out of 667 successful first broods were found. In another 43 nests no male was found, although a major effort was made to trap all adults. The estimated proportion of polygynous males is 3.4%, if only confirmed cases are considered, but 10.8% if all possible cases are included. One male was paired simultaneously to three females.
Primary females (laying earliest in a triangle) were as successful as monogamous ones. Secondary (laying later in a triangle) and deserted females (nests in which no male was trapped), although still quite successful, raised fewer young and in one plot had a lower probability of recruiting offspring.
Both in males and females, the frequency of polygyny was independent of age. Adult survival did not differ between monogamous and polygynous males. Among females no effect of pairing status on survival was found in one plot, but in a second plot monogamous females survived better than others. It is concluded that in any study of Blue Tits in optimal habitat one could expect to find polygyny.     

Differences in reproductive success and parental qualities between habitats in the Great Tit Parus major

Reproductive success and parental attributes of Great Tits Parus major nesting in good and poor habitats were compared to investigate whether they differed and, if so, whether parental or environmental variation contributed most to the differences.
Monitored over 3 years, clutches in mature woodland were started earlier, were larger and produced larger broods of heavier chicks than those in marginal habitats such as gardens and hedgerows. Fledging success was significantly higher in woodland in 2 of the 3 years although egg weights were lower. Parents nesting in different habitats were very similar in body-size although those in woodland were in better condition. The prey delivered to nestlings in woodland was of significantly higher quality than that delivered in marginal habitats. Furthermore, the heritability of body-size (tarsus-length) was higher in woodland, suggesting that the environment limits nestling growth in poorer habitats. Reproductive success was considerably lower in poor habitats and appears to be constrained primarily by environmental quality, although this may operate partly through its affect on parental body condition.