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Tracking Ocean Wanders (PDF, 5 MB) - BirdLife International

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<strong>Tracking</strong> ocean wanderers: the global distribution of albatrosses and petrels – Methods<br />

2.2.2 Deriving density distribution maps<br />

In order to identify areas which are highly utilised by<br />

albatrosses and petrels, some indication of density needs to<br />

be derived from the PTT tracking data. However the<br />

sampling regime of these data is dependent on several<br />

factors: the speed at which the bird is travelling, its latitude<br />

(Georges et al. 1997), and the performance of the device<br />

itself. In order to provide a more regular sampling regime it<br />

was assumed that a bird flew in a straight line at constant<br />

velocity between two successive uplinks, where these uplinks<br />

were less than 24 hours apart. The path of the bird was then<br />

resampled at hourly intervals, any remaining time being<br />

added to the first segment of the next path between<br />

successive uplinks. If the interval between uplinks was more<br />

than 24 hours, no assumptions were made about the bird’s<br />

behaviour and these paths were not resampled. In this way<br />

devices with long duty cycles were also catered for as no<br />

assumptions were made about the bird’s location during<br />

‘OFF’ cycles. The resampling method also ensured that each<br />

trip was weighted by its duration when calculating density<br />

distributions. The process produced locations for the<br />

individual at hourly intervals, and thus density distribution<br />

maps derived from these locations were indicative of time<br />

spent (‘bird hours’) in a particular area.<br />

Albatrosses and petrels are central place foragers when<br />

breeding, so in any density distribution map the uplinks around<br />

the colony could potentially outweigh any more distant<br />

foraging area. If the commuting points to and from foraging<br />

areas are removed, this high density around the colony should<br />

be reduced. However this requires making assumptions about<br />

the bird’s activity based solely on the tracking data. In addition,<br />

commuting birds could still be at risk from fisheries interactions<br />

if they encounter a fishing vessel and stop to forage. To assess<br />

the effect of excluding commuting data, foraging points for<br />

Wandering Albatrosses were assumed to be those resampled<br />

points occurring between sunrise and sunset where the<br />

velocity was less than 20 km/hr. By excluding all other<br />

points, a density distribution of foraging locations was<br />

produced. This did not noticeably reduce the density around<br />

the colony, and there was little difference in areas of importance<br />

(Figure 2.2). Therefore foraging and commuting points<br />

were not separated out in the final maps. It is thus recognised<br />

that not all ‘hot spots’ identified by the kernel analysis will<br />

be foraging areas, but they still represent areas of risk.<br />

Kernel density estimators have been successfully used in<br />

several tracking studies to quantify habitat use and identify<br />

home ranges (e.g. Wood et al. 2000). The single most<br />

important step when using these estimators is the selection<br />

of the smoothing (or h) parameter. This can greatly<br />

influence the home range size and can also highlight or<br />

smooth over areas of high density (Annex 3), so it is<br />

necessary to explicitly report the methods used to ensure<br />

transparency and objectivity. Care needs to be taken when<br />

comparing different datasets, but current experience and<br />

practice is encouraging (e.g. Matthiopoulos 2003).<br />

As this study does not attempt to estimate range sizes,<br />

aiming instead to identify core areas of utilisation for<br />

conservation manage-ment, the selection of h was done by<br />

identifying the smallest practical unit of management on<br />

the high seas. For present purposes the workshop<br />

participants agreed this to be a 1 degree grid square.<br />

Although the use of 1 degree as a smoothing parameter<br />

means the shape of the kernel will vary with changes in<br />

latitude, it was agreed that the effects of this would be small<br />

in relation to the scales at which the data would be<br />

presented, and that this latitude-related distortion is widely<br />

understood.<br />

Kernel density distribution maps were derived using the<br />

kernel function in ArcGIS 8.2. The grid size was set at onetenth<br />

of the value of h i.e. 0.1 of a degree. If sample sizes<br />

were sufficiently large, separate kernel density distribution<br />

maps were produced for birds of different ages (juvenile,<br />

adult), breeding status, sex and breeding stage.<br />

2.2.3 Combining density grids (weighting)<br />

The density grids derived by kernel analysis of the<br />

resampled PTT locations for each part of the population<br />

were adjusted to reflect an index of ‘seabird at sea hours’ as<br />

follows: the kernel density estimate of each cell was divided<br />

by the number of resampled PTT locations for the dataset,<br />

and then weighted by the number of individuals at sea for<br />

that particular colony and breeding status/stage (e.g. Figure<br />

Figure 2.2. Kernel density distribution contours of breeding Wandering Albatrosses tracked from Iles Crozet, showing density contours using<br />

all locations (A) and foraging locations only (B).<br />

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