Marina Magaña

Natal dispersal in great bustards: the effect of sex, local population size and spatial isolation

1. We investigated the causes of natal dispersal in four Spanish areas where 35 breeding groups of the polygynous great bustard Otis tarda were monitored intensively. A total of 392 juveniles were radio-tracked between 1991 and 2006 by ground and via aeroplane to avoid potential biases derived from the non-detection of long-distance dispersers. 2. We explored 10 explanatory variables that were related to individual phenotypic features, habitat and conspecific traits in terms of group size and breeding performance, and spatial distribution of available breeding groups. Probability of group change and natal dispersal distances were investigated separately through multifactorial analyses. 3. Natal dispersal occurred in 47.8% of the birds and median natal dispersal distance of dispersers was 18.1 km (range 4.97-178.42 km). Sex largely determined the dispersal probability, with 75.6% of males being dispersers and 80.0% of females being philopatric, in contrast to the general pattern of female-biased dispersal found in most avian species. 4. Both the frequency of natal dispersal and dispersal distances were affected by the spatial distribution of breeding groups. More isolated groups showed a higher proportion of philopatric individuals, the effect being more evident in males than in females. This implies a reduction in gene flow in fragmented populations, as most genetic exchange is achieved through male dispersal. Additionally, dispersers hatched in more isolated groups tended to exhibit longer dispersal distances, which increases the associated energetic costs and mortality risks. 5. The dispersal decision was influenced by the number of conspecifics in the natal group. The individual probability of natal dispersal was related inversely to the size of the natal group, which supports the balanced dispersal model and the conspecific attraction hypothesis. 6. Overall, our results provide a good example of phenotypic plasticity and reinforce the current view that dispersal is an evolutionary complex trait conditioned by the interaction of individual, social and environmental causes that vary between individuals and populations.

Correlates of male mating success in great bustard leks: the effects of age, weight, and display effort

We examined how mating success varied in relation to age, weight, body size, and display behavior among great bustard Otis tarda males. The estimated mating success was strongly skewed, with 45% of adult males being involved in copulation attempts and only 9.7% actually seen copulating successfully. Unlike most birds, body size continued increasing in great bustards several years after reaching sexual maturity. Age, weight, and display effort were all significant and independent predictors of male mating success. The higher display effort involved performing longer full-display bouts. Older males could detach from the male flock earlier in the season as well as on each day and spend longer seasonal and daily periods displaying as solitary birds, which contributed to increase their mating success. In contrast, males weighing more did not invest more in display, which suggests that they could be recognized as dominants by other males and selected by females through assessment of their plumage sexual traits. In contrast to most other bird species, the system described for great bustards resembles that found in some lek-mating ungulates, where social rank is a complex trait determined by both age and mass, and as in these mammals, it suggests that sexual selection continues to favor a high male weight in this extremely sexually dimorphic species.

The Most Extreme Sexual Size Dimorphism Among Birds: Allometry, Selection, and Early Juvenile Development in the Great Bustard (Otis tarda)

ABSTRACT. The Great Bustard (Otis tarda) is one of the heaviest flying birds and the most sexually dimorphic living bird. Adult males weighed 2.48x more than females, and their linear measurements were 18–30% larger. Weight increased between the prebreeding and breeding seasons by 16% in females and 20% in males. Sexual size dimorphism emerges very early in development and explains why growth in males is so costly. Weight and central toe length were hyperallometric when related to wing length in males but isometric in females and varied more in males, as compared with females and with other male traits. Although hyperallometry and high variability have frequently been used to invoke sexual selection as a driving force, our results support different functional hypotheses for the evolution of each trait. Male—male competition is intense in this lekking species, and high rank among males and access to females are weight-dependent. Thus, sexual selection has likely pushed male weight close to the limit imposed by powered flight. Because Great Bustards are mostly cursorial, the hyperallometry of the central toes of males in relation to wing length most likely evolved for support and balance.

Side effects of rodent control on non-target species: Rodenticides increase parasite and pathogen burden in great bustards

For many years anticoagulant rodenticides have been used in vole control campaigns, in spite of the proven risk of secondary poisoning of non-target predators and scavengers. In this paper we analyse for the first time great bustard exposure and intoxication by anticoagulant rodenticides in Spain, based on residues found in the livers of 71 bustard carcasses collected during 1991-2010. Ten individuals contained chlorophacinone and one flocoumafen. Chlorophacinone level was significantly correlated with the pathogen and parasite burden of intoxicated birds. Moreover, through the last 12 years the annual number of great bustards that present chlorophacinone in liver collected in our study areas was correlated with vole peaks at a nearby area, suggesting that the ingestion of rodenticide was proportional to the amounts spread in the fields. We conclude that rodenticide consumption is a regular event among great bustards when baited cereal is spread on fields, and that this may cause chronic weakening of intoxicated individuals, possibly affecting their survival. Future rodent control actions should consider these negative side effects on non target granivorous steppe and farmland species, particularly when they are globally threatened.

Age-related dominance helps reduce male aggressiveness in great bustard leks

Stable dominance hierarchies have evolved in many socially living animals to reduce the negative consequences of agonistic interactions. To evaluate whether established dominance relationships reduce aggressive encounters among males during the mating season, we studied aggressive behaviour in lekking male great bustards, Otis tarda. This sexually dimorphic bird species is potentially subject to strong sexual selection operating through intramale competition. The strongly skewed mating success of males is mainly determined by their age and weight, which are reliably signalled through plumage traits. We observed that adult males lived in stable groups at traditional leks to which they remained faithful throughout their lives, a prerequisite for the establishment of stable dominance hierarchies. Males substantially reduced aggressive interactions during the mating period. Males involved in more aggressive interactions during the premating period had weakly expressed sexual traits and low courtship success, which suggests the existence of an age- and possibly also weight-determined lek hierarchy. This is supported by the increase with age in a male’s dominance index, and the absence of aggressive interactions at advanced ages. During the mating period, older males and those with higher courtship success were involved in fewer aggressive encounters, suggesting that other males respected their status. Subdominant males disrupted other males’ copulation attempts, perhaps to reduce their success or to gain copulations themselves. Our study supports the hypotheses that social dominance is largely age determined in the great bustard and that established dominance relationships help reduce intramale aggression during the mating period.

Genetic diversity of the great bustard in Iberia and Morocco: risks from current population fragmentation

We studied the genetic diversity of great bustards (Otis tarda) in Iberia and Morocco, the main stronghold of this globally endangered species. Samples were collected from 327 individuals covering most of the distribution range within the study area. Sequence variation in a 657 bp fragment of the mtDNA control region revealed 20 variable sites defining 22 haplotypes, two of them exclusive to Morocco. Genetic diversity showed marked regional differences (π = 0–0.53, h = 0–0.89). Multidimensional scaling analysis based on FST values showed a clear division between Morocco and the Iberian Peninsula, with no evidence of current gene flow between them. Our results suggest that Morocco, where few matrilines have persisted to present, was colonized from Iberia thousands of years ago. Last century reports suggest dispersal through Gibraltar, when the species was more abundant at both sides of the Strait but later population declines and the Strait’s barrier effect have favoured current genetic isolation. Within Iberia, only the most peripheral populations (Navarra, Aragón and Andalusia) differed significantly from the main ones in central Spain. The first two showed extremely low genetic diversity and are probably threatened by inbreeding depression. Diversity was higher in Andalusia, where three exclusive haplotypes were found, suggesting some degree of isolation from other populations. Andalusia and Morocco could be regarded as separate management units which hold a significant proportion of the current genetic diversity and thus deserve urgent conservation measures.

Field determination of age in male great bustards (Otis tarda) in spring

During a long-term study of individually marked, free-living male great bustards captured as chicks and radio-tracked through several years in Spain, we studied the development with age of two secondary sex traits, the moustachial feathers and the neck plumage pattern. Juvenile males acquired full adult plumage between their fourth and seventh years. The main changes occurred at the neck, coinciding with the onset of sexual maturity. The grey colour typical of immature males turned to ivory white around the fourth to fifth spring, and a gradual increase was appreciated in adults in the brightness of the white colour of the upper neck and in the contrast between this and a progressively more intense chestnut brown at the neck base. Based on these changes, we proposed four neck plumage patterns that can be used to differentiate male age classes during the mating period. The development of moustachial feathers showed more interindividual variability and was not as useful as the neck plumage to estimate male age.