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1.
Ecol Evol ; 6(4): 1092-103, 2016 02.
Article in English | MEDLINE | ID: mdl-26941945

ABSTRACT

The White-headed Vulture Trigonoceps occipitalis (WhV) is uncommon and largely restricted to protected areas across its range in sub-Saharan Africa. We used the World Database on Protected Areas to identify protected areas (PAs) likely to contain White-headed Vultures. Vulture occurrence on road transects in Southern, East, and West Africa was adjusted to nests per km(2) using data from areas with known numbers of nests and corresponding road transect data. Nest density was used to calculate the number of WhV nests within identified PAs and from there extrapolated to estimate the global population. Across a fragmented range, 400 PAs are estimated to contain 1893 WhV nests. Eastern Africa is estimated to contain 721 nests, Central Africa 548 nests, Southern Africa 468 nests, and West Africa 156 nests. Including immature and nonbreeding birds, and accounting for data deficient PAs, the estimated global population is 5475 - 5493 birds. The identified distribution highlights are alarming: over 78% (n = 313) of identified PAs contain fewer than five nests. A further 17% (n = 68) of PAs contain 5 - 20 nests and 4% (n = 14) of identified PAs are estimated to contain >20 nests. Just 1% (n = 5) of PAs are estimated to contain >40 nests; none is located in West Africa. Whilst ranging behavior of WhVs is currently unknown, 35% of PAs large enough to hold >20 nests are isolated by more than 100 km from other PAs. Spatially discrete and unpredictable mortality events such as poisoning pose major threats to small localized vulture populations and will accelerate ongoing local extinctions. Apart from reducing the threat of poisoning events, conservation actions promoting linkages between protected areas should be pursued. Identifying potential areas for assisted re-establishment via translocation offers the potential to expand the range of this species and alleviate risk.

2.
Behav Processes ; 88(1): 1-6, 2011 Sep.
Article in English | MEDLINE | ID: mdl-21736928

ABSTRACT

We currently have little understanding of how birds know what nest to build and what little we do know has been gained largely from investigations of the completed structures (morphology of finished nests) or of material selection. Here we looked at the behaviours performed by male Southern Masked weaverbirds when building their nests. During the two earliest phases of construction individual males varied in the direction in which they carried and inserted grass into their developing nest, the speed at which they completed phases of nest construction and in the frequency with which they dropped grass during weaving. Behaviours performed during the initial attachment phase, when grass is being secured to a bare branch, were not repeatable within males, whereas during the subsequent "ring" phase behaviours tended to be repeatable. Some males were biased as to which side of the nest they inserted grass blades and strongly lateralized individuals completed phases of nest-building more quickly. The lack of repeatability of most nest-building behaviours and the changes in those behaviours as males build more nests seems most readily explained by increasing dexterity. Further work is required to confirm any role for cognition in these experience-dependent changes.


Subject(s)
Individuality , Nesting Behavior/physiology , Passeriformes/physiology , Animals , Functional Laterality , Male
3.
Biol Lett ; 6(2): 149-51, 2010 Apr 23.
Article in English | MEDLINE | ID: mdl-19846449

ABSTRACT

It is generally assumed that birds build nests according to a genetic 'template', little influenced by learning or memory. One way to confirm the role of genetics in nest building is to assess the repeatability of nest morphology with repeated nest attempts. Solitary weaver birds, which build multiple nests in a single breeding season, are a useful group with which to do this. Here we show that repeatability of nest morphology was low, but significant, in male Southern Masked weaver birds and not significant in the Village weavers. The larger bodied Village weavers built larger nests than did Southern Masked weavers, but body size did not explain variation in Southern Masked weaver nest dimensions. Nests built by the same male in both species got shorter and lighter as more nests were constructed. While these data demonstrate the potential for a genetic component of variation in nest building in solitary weavers, it is also clear that there remains plenty of scope in both of these species for experience to shape nest construction.


Subject(s)
Nesting Behavior/physiology , Passeriformes/genetics , Passeriformes/physiology , Animals , Body Size , Body Weights and Measures , Botswana , Male , Species Specificity
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