Early post-fledgling survival in a fragmented population of a tropical cooperative breeding passerine

During the last years tropical forest has been a target of intense study especially due to its recent big scale destruction. Although a lot still needs to be explored, we start realizing how negative can the impact of our actions be for the ecosystem. Subsequently, the living community have been developing strategies to overcome this problem avoiding bottlenecks or even extinctions. Cooperative breeding (CB) has been recently pointed out as one of those strategies. CB is a breeding system where more than two individuals raise one brood. In most of the cases, extra individuals are offspring that delay their dispersal and independent breeding what allows them to help their parents raising their siblings in the subsequent breeding season. Such behavior is believed to be due, per example, to the lack of mates or breeding territories (ecological constraints hypothesis), a consequence of habitat fragmentation and/or disturbance. From this point, CB is easily promoted by a higher reproductive success of group vs pairs or single individuals. Accordingly, during this thesis I explore the early post-fledging survival of a cooperative breeding passerine, namely the impact of individual/habitat quality in its survival probability during the dependence period of the chicks. Our study species is the Cabanis’s greenbul (Phyllastrephus cabanisi), a medium-sized, brownish passerine, classified within the Pycnonotidae family. It is found over part of Central Africa in countries such as Angola, Democratic Republic of the Congo, Mozambique and Kenya, inhabiting primary and secondary forests, as well as woodland of various types up to 2700m of altitude. Previous studies have concluded that PC is a facultative cooperative breeder. This study was conducted in Taita Hills (TH) at the Eastern Arc Mountains (EAM), a chain of mountains running from Southeast Kenya to the South of Tanzania. TH comprises an area of 430 ha and has been suffering intense deforestation reflecting 98% forest reduction over the last 200 years. Nowadays its forest is divided in fragments and our study was based in 5of those fragments. We access the post-fledging survival through radio-telemetry. The juvenile survey was done through the breeding females in which transmitters were placed with a leg-loop technique. Ptilochronology is consider to be the study of feather growth bars and has been used to study the nutritional state of a bird. This technique considers that the feather growth rate is positively proportional to the individual capability of ingesting food and to the food availability. This technique is therefore used to infer for individual/habitat quality. Survival was lowest during the first 5 days post-fledging representing 53.3%. During the next 15 days, risk of predation decreased with only 14.3% more deceased individuals. This represents a total of only 33% survived individuals in the end of the 50 days. Our results showed yet a significant positive relationship between flock size and post-fledging survival as well as between ptilochronology values and post-fledgling survival. In practice, these imply that on this population, as bigger the flock, as greater the post fledging survival and that good habitat quality or good BF quality, will lead to a higher juvenile survival rate. We believe that CB is therefore an adaptive behaviour to the lack of mates/breeding territory originated from the mass forest destruction and disturbance. Such results confirms the critical importance of habitat quality in the post-fledging survival and, for the first time, demonstrates how flock size influences the living probability of the juveniles and therefore how it impacts the (local) population dynamics of this species. In my opinion, future research should be focus in disentangle individual and habitat quality from each other and verify which relationship exist between them. Such study will allow us to understand which factor has a stronger influence in the post-fledging survival and therefore redirect our studies in that direction. In order to confirm the negative impact of human disturbance and forest fragmentation, it would be of major relevance to compare the reproductive strategies and reproductive success of populations living in intact forests and disturbed patches.

A alimentação suplementar de aves necrófagas em comedouros

A alimentação artificial de aves necrófagas tem sido alvo de atenção e as suas vantagens e desvantagens ainda são discutidas. A habituação por parte dos abutres e a atracção de espécies oportunistas são vistas como um problema. Foi disponibilizado alimento em quatro comedouros durante três anos, de 2010 a 2012. Registaram-se todas as aves observadas nos comedouros, anotando-se a espécie, o número de indivíduos e o comportamento alimentar e/ou não alimentar a cada 5 minutos. Também foi monitorizado o número de casais e o sucesso reprodutor do Grifo e do Abutre do Egipto. Notou-se uma aparente relação positiva entre estas duas espécies. A frequência de alimentação e o número de indivíduos das duas espécies aumentou gradualmente ao longo dos três anos, enquanto os tempos de detecção e alimentação diminuíram. Uma tendência oposta foi obtida para espécies oportunistas como o Milhafre-preto e o Milhafre-real. Não foi possível concluir sobre o efeito da alimentação artificial na produtividade mas pode existir uma relação da frequência de alimentação com a fase da época de reprodução na qual as crias são um factor determinante. O máximo da frequência de alimentação e o mínimo geral de tempos coincidem com as primeiras semanas das crias, para o Abutre do Egipto, e com a fase de maior requerimento destas, para o Grifo. A evolução destes parâmetros pode definir habituação. Os nossos resultados mostram que esta habituação tornou a alimentação artificial mais eficaz, com pouca quantidade de alimento, maioritariamente obtido pelo Abutre do Egipto e pelo Grifo com menor presença de espécies oportunistas. As espécies que se alimentam nos comedouros apresentam diferentes estratégias na obtenção do alimento, contornando a monopolização apresentada pelo Grifo. Desta forma o Abutre do Egipto parece estar a conseguir tirar proveito do alimento que lhe é dirigido. A disponibilização de alimento regular em poucas quantidades, nas primeiras horas de luz do dia, alternando o local onde o alimento é colocado, podem ser estratégias acertadas na alimentação suplementar dirigida ao Abutre do Egipto e ao Grifo.