التفاصيل البيبلوغرافية
| العنوان: |
Data from: Relative contributions of fixed and dynamic heterogeneity to variation in lifetime reproductive success in kestrels (Falco tinnunculus) |
| المؤلفون: |
Bol, B.J., Broekman, M.J.E., Jongejans, E., Tuljapurkar, S. |
| بيانات النشر: |
Zenodo |
| سنة النشر: |
2020 |
| المجموعة: |
Radboud University: DSpace |
| مصطلحات موضوعية: |
Survival, Reproduction, Capture-mark-recapture multistate model, Dynamic heterogeneity, Lifetime reproductive success, Sensitivity, Variance partitioning, Animal Ecology and Physiology |
| الوصف: |
Item does not contain fulltext ; These data contain information about the survival and reproduction of Common kestrels in the Haarlemmermeer, The Netherlands. This dataset was used by Broekman et al. (2020) to fit a capture-mark-recapture multistate model, which was subsequently used to analyse relative contributions of fixed and dynamic heterogeneity to variation in lifetime reproductive success. The Common Kestrel (Falco tinnunculus) is a small raptor that is widespread in Europe and is the most common bird of prey in the Netherlands. It is a short-lived species and can start breeding in their second calendar year (Village 1990). We studied a kestrel population in the Haarlemmermeer (185 km2), which contains Amsterdam Schiphol Airport. This area has on average 56 breeding pairs per year (varying between 36 and 73 breeding pairs per year, see table S1 in Broekman et al. 2020), with clutch sizes ranging from 1 to 8 eggs. The Life-time Reproductive Success (LRS) in this population ranges between 0-42 for females and 0-38 for males, with the majority of the offspring produced by a small fraction of the population (4% of the kestrels produce around 30% of the offspring). Data on this population were collected by Bert Jan Bol between 1993-2015 and entailed capturing and individually marking of birds, as well as observing the success of all nests (mainly in nest boxes) in the study area (Bol 1997). In addition, breeding biology data were gathered, which included, among others, the location, the number of fledglings and the identity and age of the parents. The identity of the mother was known for 81% of the nests and the identity of the father was known for 29% of the nests (N = 1194). Furthermore, in a previous study on this population we determined the amount of extra-pair paternities in 109 different nests from 2011-2014, including years with both low and high prey abundance and did not find any extra-pair paternities (Broekman 2016). We can therefore assume that the identified father of a nest is the father off ... |
| نوع الوثيقة: |
dataset |
| اللغة: |
unknown |
| Relation: |
https://hdl.handle.net/2066/221200 |
| DOI: |
10.5281/zenodo.3957759 |
| الاتاحة: |
https://hdl.handle.net/2066/221200
https://doi.org/10.5281/zenodo.3957759 |
| رقم الانضمام: |
edsbas.693BE3A9 |
| قاعدة البيانات: |
BASE |