Search results for "Cooperative breeding"
showing 10 items of 10 documents
Stepping stones of life: natal dispersal in the group-living but noncooperative speckled warbler
2003
In most cooperatively breeding birds the offspring of one sex, usually male, delays dispersal to remain on the natal territory and helps its parents to rear subsequent young. Thus delayed dispersal could be the first step in the evolution of cooperative breeding. We studied natal dispersal in a population of the group-living speckled warbler, Chthonicola sagittata, based on observations of a colour-banded population over 3 years. Unlike other group-living members of the Acanthizinae, all juvenile males in this population dispersed to settle on foreign territories as subordinates, which do not help rear the young. Speckled warblers showed all the life history traits that are thought to resul…
Information transfer determined by association of neighbours in European bee-eater (Merops apiaster) colonies
2007
The Information Centre Hypothesis (ICH) and the Two-Strategies Hypothesis (TSH) predict that foraging success is enhanced by information exchanged among individuals within a colony or roost. Nest location within a colony may be critical in this regard, as individuals with abundant, nearby neighbours likely have greater access to information regarding a new food resource than relatively isolated breeders. To determine how the availability of neighbours influences information transfer, we quantified foraging success in a population of European bee-eaters (Merops apiaster) provided with a honey bee (Apis mellifera) hive as a new food resource. To quantify potential information transfer we deve…
No synergy needed: ecological constraints favor the evolution of eusociality.
2015
In eusocial species, some individuals sacrifice their own reproduction for the benefit of others. It has been argued that the evolution of sterile helpers in eusocial insects requires synergistic efficiency gains through cooperation that are uncommon in cooperatively breeding vertebrates and that this precludes a universal ecological explanation of social systems with alloparental care. In contrast, using a model that incorporates realistic ecological mechanisms of population regulation, we show here that constraints on independent breeding (through nest-site limitation and dispersal mortality) eliminate any need for synergistic efficiency gains: sterile helpers may evolve even if they are …
No Evidence for Enforced Alloparental Care in a Cooperatively Breeding Parrot
2016
In cooperatively breeding species, in which non-breeding helpers assist in rearing the offspring of breeding individuals, conflicts of interest commonly occur between breeders and helpers over their respective contributions to offspring care. During such conflicts, breeders might use aggressive behavior to enforce contributions of helpers to offspring care, especially if helpers are not related to the breeders and their offspring and thus do not stand to gain indirect fitness benefits by helping. Using a combination of behavioral and genetic data, we investigated in the cooperatively breeding El Oro parakeet Pyrrhura orcesi (i) whether breeders are commonly dominant over helpers, (ii) wheth…
The age and evolution of sociality in Stegodyphus spiders: a molecular phylogenetic perspective
2006
Social, cooperative breeding behaviour is rare in spiders and generally characterized by inbreeding, skewed sex ratios and high rates of colony turnover, processes that when combined may reduce genetic variation and lower individual fitness quickly. On these grounds, social spider species have been suggested to be unstable in evolutionary time, and hence sociality a rare phenomenon in spiders. Based on a partial molecular phylogeny of the genus Stegodyphus , we address the hypothesis that social spiders in this genus are evolutionary transient. We estimate the age of the three social species, test whether they represent an ancestral or derived state and assess diversification relative to s…
When should cuckolded males care for extra-pair offspring?
2012
In socially monogamous species with bi-parental care, males suffer reduced reproductive success if their mate engages in extra-pair copulations (EPCs). One might therefore expect that males should refuse to care for a brood if they can detect that an EPC has occurred. Here, we use a game-theory model to study male brood care in the face of EPCs in a cooperatively breeding species in which offspring help to raise their (half-) siblings in their parents' next breeding attempt. We show that under certain conditions males are selected to care even for broods completely unrelated to themselves. This counterintuitive result arises through a form of pseudo-reciprocity, whereby surviving extra-pair…
Winter male plumage coloration correlates with breeding status in a cooperative breeding species
2007
The function of colored ornaments is usually related to the signaling of individual quality in intra- and intersexual interactions. In cooperative breeding species, where only a fraction of the male population access the breeding status and the other fraction has the option to help breeding pairs, colored traits might provide the females with a reliable information on the quality of potential mate. Males of the cooperative breeding azure-winged magpies (Cyanopica cyanus) display conspicuous blue plumage coloration. Here we explored the role played by structural blue coloration of males and the probability of becoming a breeder or a helper. Birds were trapped during 4 consecutive years, and …
Dynamics of the caring family
2003
When several individuals simultaneously provide for offspring, as in families, the effort of any one individual will depend on the efforts of the other family members. This conflict of interest among family members is made more complicated by their relatedness because relatives share genetic interest to some degree. The conflict resolution will also be influenced by the differences in reproductive value between breeders and helpers. Here, we calculate evolutionarily stable provisioning efforts in families with up to two helpers. We explicitly consider that the behavioral choices are made in a life-history context, and we also consider how group sizes change dynamically; this affects, for ex…
Parental Care and Investment
2017
Parental care is common throughout the animal kingdom, and much variation exists among species in how, and how much, parents care for their offspring. In most species, females care more; in others, males care more and in some, caring is more or less equally shared between the sexes. Several hypotheses have been proposed to explain patterns of parental care within and among species. These hypotheses invoke factors such as the relatedness (parentage certainty) of each parent to the brood; the sex ratio at maturation; the strength of sexual selection faced by each sex and the exact nature of any trade-offs between caring and other activities. Work is still ongoing to develop an overarching hyp…
New insights on the role of ecology and life-history in social evolution
2017
Biological altruism, defined as a behaviour that benefits others at an apparent cost to the focal individual, is found abundantly across different levels of biological organization. While kin selection has been useful for explaining both cooperation and conflict in specialized cooperative societies, more theoretical work has to be done to develop models for realistic ecological and life-history contexts. This thesis aims to fill this gap by providing several new insights on the role of ecology and life-history in various social systems. Firstly, I propose a model that incorporates realistic ecological mechanisms of population regulation and study how different population regulation mechanisms affe…