Marcel M. Lambrechts
Centre national de la recherche scientifique
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Advances in Ecological Research | 2004
Marcel E. Visser; Christiaan Both; Marcel M. Lambrechts
Publisher Summary This chapter discusses the potential consequences of mistiming and identifies a number of ways in which either individual birds or bird populations potentially can adapt to reproductive mistiming. When different components of the food chain shift at different rates, this will lead to mistiming, and it is believed that such mistiming resulting from climate change will be a general phenomenon. The environment at the time avian produce their eggs is, in general much, earlier than the environment when selection will occur on, for instance, synchrony between offspring needs and prey availability. The evolved response mechanisms are appropriate for the range of prevailing conditions, and climate change is a trend that will at first fall within the normal range of temperatures. In the short term, an increase in temperatures may, therefore, allow birds to cope with their existing reaction norms. If these temperatures fall outside the normal range, or if periods in spring differ in their temperature change, the prevailing reaction norms become maladaptive. It is assumed that birds respond to climate change by changes in their laying date solely. However, investigation on pied flycatcher shows that rather than just using laying date as a way to advance hatching date, they use the whole complex of laying date, clutch size and start of incubation. Birds may also adjust other correlated life-history traits as some species show no change in laying date but do respond in whether or not they make a second brood.
Acta Ornithologica | 2010
Marcel M. Lambrechts; Frank Adriaensen; Daniel R. Ardia; Alexandr Artemyev; Francisco Atiénzar; Jerzy Bańbura; Emilio Barba; Jean Charles Bouvier; Jordi Camprodon; Caren B. Cooper; Russell D. Dawson; Marcel Eens; Tapio Eeva; Bruno Faivre; László Zsolt Garamszegi; Anne E. Goodenough; Andrew G. Gosler; Arnaud Grégoire; Simon C. Griffith; Lars Gustafsson; L. Scott Johnson; Wojciech Maria Kania; Oskars Keišs; Paulo E. Llambías; Mark C. Mainwaring; Raivo Mänd; Bruno Massa; Tomasz D. Mazgajski; Anders Pape Møller; Juan Moreno
Abstract. The widespread use of artificial nestboxes has led to significant advances in our knowledge of the ecology, behaviour and physiology of cavity nesting birds, especially small passerines. Nestboxes have made it easier to perform routine monitoring and experimental manipulation of eggs or nestlings, and also repeatedly to capture, identify and manipulate the parents. However, when comparing results across study sites the use of nestboxes may also introduce a potentially significant confounding variable in the form of differences in nestbox design amongst studies, such as their physical dimensions, placement height, and the way in which they are constructed and maintained. However, the use of nestboxes may also introduce an unconsidered and potentially significant confounding variable due to differences in nestbox design amongst studies, such as their physical dimensions, placement height, and the way in which they are constructed and maintained. Here we review to what extent the characteristics of artificial nestboxes (e.g. size, shape, construction material, colour) are documented in the ‘methods’ sections of publications involving hole-nesting passerine birds using natural or excavated cavities or artificial nestboxes for reproduction and roosting. Despite explicit previous recommendations that authors describe in detail the characteristics of the nestboxes used, we found that the description of nestbox characteristics in most recent publications remains poor and insufficient. We therefore list the types of descriptive data that should be included in the methods sections of relevant manuscripts and justify this by discussing how variation in nestbox characteristics can affect or confound conclusions from nestbox studies. We also propose several recommendations to improve the reliability and usefulness of research based on long-term studies of any secondary hole-nesting species using artificial nestboxes for breeding or roosting.
Behavioral Ecology and Sociobiology | 1986
Marcel M. Lambrechts; André A. Dhondt
SummaryThree possible measures of male quality (social dominance, song, and size), reproduction, and survival were studied in a single population of great tits. Winter dominance position on a feeder was related to strophe length (number of phrases per strophe), inversely related to positive drift (decrease of the singing rate of the phrases in a strophe), but not related to song repertoire size. Neither winter dominance position nor song were related to size (wing length, tarso-metatarsus length, weight).Singing capacity was not correlated with individual reproductive success in a single breeding season, using a rather limited data set. However, “better” singers (males which sing longer strophes, show less positive drift, and have larger song repertoires) survived better and had a higher individual lifetime reproductive success (on the basis of a males recruited offspring of all breeding seasons). Our results show that there exist measurable differences whereby birds that are dominant in winter sing “better”, survive longer, and produce more surviving offspring during their life time. We suggest that differences in male quality are the common cause (direct and indirect) of all these effects.
Animal Behaviour | 1988
Marcel M. Lambrechts; André A. Dhondt
Abstract This paper describes the results of a detailed analysis of 52 song bouts, recorded from 22 great tits, Parus major , during the dawn chorus. A song bout consists of a number of song bursts (called strophes) separated by periods of silence. High quality males, as measured by average strophe length, sang their bouts with a higher percentage performance time (i.e. the percentage of time spent singing in a bout), but the average number of strophes per bout was not related to male quality. In 31 of 52 bouts there was a systematic decrease in the percentage performance time throughout the bout. This was mainly caused by a prolongation of the pauses between the strophes, and sometimes by a shortening of the strophes. Both high and low quality males sang bouts with and without this decrease in the percentage performance time. Bouts that started with longer strophes and/or shorter inter-strophe pauses showed on average a more rapid decrease in the percentage performance time, and contained fewer strophes, than bouts that started with shorter strophes and/or longer inter-strophe pauses. After switching to another song type the males again used longer strophes and/or shorter inter-strophe pauses. An ‘anti-exhaustion’ hypothesis is proposed and discussed. This hypothesis gives a mainly causal explanation for the existence of song switching and song repertoires in passerine birds.
Ecology | 2003
Isabelle Tremblay; Donald W. Thomas; Marcel M. Lambrechts; Jacques Blondel; Philippe Perret
Food supply is widely considered to be a major factor in determining life history traits and reproductive performance of birds. However, large spatial and temporal variation in natural available food supply is not always paralleled by proportional changes in energy demand by breeding birds. This necessarily results in variation in the supply–demand ratio and the amount of food available per unit mass of nestling. Because reproductive performance should respond to increases in available supply as a saturation curve, reaching a plateau above a certain threshold of food supply, we predict that variation in supply should change the intensity of selection on reproductive traits. We first tested this prediction using long-term data on nestling growth and survival in Blue Tits (Parus caeruleus) breeding over a gradient of habitat richness in Corsica, France. This long-term data analysis evaluates the effect of variation in food supply available to breeding tits using three surrogate variables: interannual variation in peak caterpillar abundance (caterpillar frass fall), offset between breeding date and peak caterpillar abundance, and natural variation in clutch size. We also used an experimental brood size manipulation (±3 chicks) to test the effect of varying brood demand on nestling growth. Results of the long-term data analysis show that all three variables affect fledging mass and fledging success in poor habitats, while only fledging mass is affected by variation in offset in rich habitats. Moreover, mean annual fledging success and fledging mass is strongly affected by annual variation in peak caterpillar abundance at low levels of abundance, but these effects disappear when food becomes abundant (saturation threshold level of 373 and 560 mg frass·m−2·d−1 for fledging success and fledging mass, respectively). Brood size manipulations confirm these results. In rich habitats, breeding birds can raise three extra chicks without any apparent effects on chick growth, while in poor habitats, chick growth is significantly reduced with brood enlargement. Our study shows that although food limitation can play an important role, it may not always be the primary force shaping life history traits.
BioScience | 2006
Jacques Blondel; Donald W. Thomas; Anne Charmantier; Philippe Perret; Patrice Bourgault; Marcel M. Lambrechts
Abstract In recent years, the study of phenotypic and genetic variation has been enhanced by combining genetic, physiological, demographic, and behavioral components of life histories. Using these new approaches, we address the problem of adaptation to environmental heterogeneity by examining in detail the variation of several fitness-related traits in a small passerine bird, the blue tit, which has been extensively studied in habitat mosaics of the Mediterranean region. The response of blue tits to spatial habitat heterogeneity depends on their range of dispersal relative to the size of habitat patches. Dispersal over short distances leads to local specialization, whereas dispersal over long distances leads to phenotypic plasticity. Gene flow between habitats of different quality may produce local maladaptation and a source–sink population structure. However, when habitat-specific divergent selection regimes are strong enough to oppose the effects of gene flow, local adaptation may arise on a scale that is much smaller than the scale of dispersal.
Journal of Evolutionary Biology | 2008
Claire Doutrelant; Arnaud Grégoire; N. Grnac; Doris Gomez; Marcel M. Lambrechts; Philippe Perret
It is poorly understood whether female morphological and behavioural traits can be used as ‘signals’. In particular, experimental tests of the hypothesis that female ornaments reflect quality are scarce. Here, we experimentally examine whether female plumage coloration might signal maternal quality in the blue tit, Cyanistes caeruleus by forcing half of the females breeding in our population to produce a replacement clutch. Using statistical models that controlled for the effects of male coloration, and the effects of age and condition of both parents, we found that carotenoid‐based female coloration was positively linked to key proxies of bird lifetime reproductive success: clutch size, fledgling success and recruitment. Importantly, the relationships between maternal yellow carotenoid coloration and both clutch size and recruitment were stronger in the experimental group than in the control group, indicating that breeding females with higher values of yellow coloration were better able to handle the cost of producing a second clutch. Finally, UV‐blue female coloration was positively linked to female survival and marginally linked to laying date. Taken together, these results show for the first time in a natural population that female coloration can indicate individual and maternal quality under natural and adverse reproductive conditions. They highlight the potential for the evolution of female ornamental traits through sexual selection.
The American Naturalist | 2004
Bernt Erik Sæther; Steinar Engen; Anders Pape Møller; Henri Weimerskirch; Marcel E. Visser; Wolfgang Fiedler; Erik Matthysen; Marcel M. Lambrechts; Alexander V. Badyaev; Peter H. Becker; Jon E. Brommer; Dariusz Bukaciński; Monika Bukacińska; Hans Christensen; Janis L. Dickinson; Chris du Feu; Frederick R. Gehlbach; Dik Heg; Hermann Hötker; Juha Merilä; Jan Tøttrup Nielsen; Wallace B. Rendell; Raleigh J. Robertson; David Thomson; János Török; Piet Van Hecke
Comparative analyses of avian population fluctuations have shown large interspecific differences in population variability that have been difficult to relate to variation in general ecological characteristics. Here we show that interspecific variation in demographic stochasticity, caused by random variation among individuals in their fitness contributions, can be predicted from a knowledge of the species’ position along a “slow‐fast” gradient of life‐history variation, ranging from high reproductive species with short life expectancy at one end to species that often produce a single offspring but survive well at the other end of the continuum. The demographic stochasticity decreased with adult survival rate, age at maturity, and generation time or the position of the species toward the slow end of the slow‐fast life‐history gradient. This relationship between life‐history characteristics and demographic stochasticity was related to interspecific differences in the variation among females in recruitment as well as to differences in the individual variation in survival. Because reproductive decisions in birds are often subject to strong natural selection, our results provide strong evidence for adaptive modifications of reproductive investment through life‐history evolution of the influence of stochastic variation on avian population dynamics.
Evolutionary Ecology | 1997
Marcel M. Lambrechts; Jacques Blondel; Sylvie Hurtrez-Boussès; Marie Maistre; Philippe Perret
SummaryFew studies of natural populations have investigated how phenotypic variation across populations relates to key factors in the environment and landscape structure. In the blue tits of southern France, inter-population differences in reproductive life-history traits (e.g. laying date and clutch size) are small, whatever the timing of maximum caterpillar availability, a key factor for offspring survival in tits. These small differences are attributed to gene flow between local populations occupying different habitat types. In contrast, in blue tits on the island of Corsica, we noted large differences in reproductive life-history traits between two populations, where each population is synchronized with the peak-date of caterpillar abundance. These occur over a short geographical distance (25 km). Considering our study within a framework of long-term population studies in tits, our results support the hypothesis that different blue tit populations on Corsica show adaptive differences in life-history traits, and suggest that landscape structure at a small spatial scale can have profound effects on adaptive between-pop illation differentiation in life-history traits that are closely linked with fitness.
Oecologia | 2004
Marcel M. Lambrechts; Samuel P. Caro; Anne Charmantier; Nicolas Gross; Marie-Jo Galan; Philippe Perret; Mireille Cartan-Son; Paula C. Dias; Jacques Blondel; Donald W. Thomas
Vertebrate studies have rarely investigated the influence of spatial variation in habitat richness on both short-term (breeding) and long-term (offspring recruitment) reproductive performance using simultaneously multi-patch, multi-habitat type and multi-year approaches at landscape level. Here we present results of such an approach using the influence of two oak tree (Quercus ilex, Q. humilis) species on reproductive performance in Corsican blue tits (Parus caeruleus ogliastrae) as a model system. We found that blue tits breeding in rich broad-leaved deciduous patches consistently laid eggs earlier in the season, and produced larger clutches and more fledglings of higher quality, than those breeding in poor evergreen patches. Also, parents, especially males, were in better physical condition in the broad-leaved deciduous than in the evergreen patches. Surprisingly, estimates of long-term effects of reproduction, such as recruitment rates of locally born offspring, did not differ between the two habitat types. Our results suggest that short-term breeding performance and phenotypic quality of both chicks and parents do not necessarily provide reliable information about contributions to following generations at a scale larger than that of the local study plot. Differences in reproductive performance between the two oak habitat types could not be attributed to density-dependent effects, differences in levels of nest predation, or differences in age structure of the birds. We suggest that habitats that are optimal for breeding are not necessarily optimal for survival after the breeding season.