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Is a wind-power plant acting as a barrier for reindeer Rangifer tarandus tarandus movements?

A major increase in human-made structures, such as roads, hydroelectric dams, wind-power plants (WPs), power lines and buildings, has occurred in arctic regions over the last 50 years, especially in Scandinavia (Klein 2000). There is considerable concern for the ecological effects of human development, in particular for species that range over expansive areas such as reindeer Rangifer tarandus tarandus (Reimers & Colman 2006). Some studies report negative effects of roads and power lines for reindeer or caribou Rangifer tarandus when dispersing from one side of these linear structures to the other (Vistnes & Nellemann 2008), others are vague in their statements about barrier effects (Dahle et al. 2008), while some report lack of negative effects from these structures using indirect measurement on vegetation (e.g. Reimers et al. 2007). To further clarify, we needed first to separate the animals' reduced use of areas close to the infrastructure, due to avoidance behaviour, from the role of the infrastructure in acting as a barrier in the landscape to hinder movement from one side to the other. We define: 1) a physical barrier as an aspect in the landscape that creates a physical obstacle that an animal has difficulty in crossing, such as a fence, wall or road-divider, and 2) a behavioural barrier as a behavioural response to a stimulus or stimuli preventing an animal from crossing a 'zone' in the landscape, such as under power lines, past WPs or over roads. A behavioural barrier is not a physical obstacle but caused by the animals' reaction towards the anthropogenic stimuli in the landscape. This might be the case for linear corridors in forested areas where habitat characteristics are altered under power lines or along roads (e.g. Dodd et al. 2004), along with increased risk of predation (Frid & Dill 2002) related to such habitat/landscape alterations.

The demand for 'green energy' from WPs is increasing dramatically (EWEA 2008), while studies addressing effects of WPs on free-ranging ungulates are lacking. WPs can impact ungulates directly through visual dominance in the landscape and high turbulent noise, and indirectly through additional infrastructure (power lines and access roads) and human activity. Many sites for existing and planned WPs in Scandinavia are found within important reindeer habitat (NVE 2012). In Norway alone, six WPs have been built within semi-domestic reindeer (reindeer herded by Sami pastoralists) habitats and many more are in the planning (NVE 2012). When migrating into their summer habitat, reindeer in northern Norway cross into numerous peninsulas along the northern coast of Norway. The debate over large losses of outlying pastures found on peninsulas affected by infrastructure has been especially important because of the possibility for barrier effects impeding dispersal into the outer sections of the peninsulas. This is potentially a more severe effect of WPs than just avoidance of the immediate surroundings.

We tested for behavioural barrier effects of a WP on reindeer, as opposed to avoidance effects. Reindeer use two smaller peninsulas (Dyfjord and Skjotningberg) on the west coast of the larger Nordkinn peninsula in Norway as their summer range. Both peninsulas have potential behavioural barrier effects from a road and a power line bisecting them in a north-south direction, but only one with a WP, making it possible to decipher the influence of the WP installations themselves. We tested the prediction that infrastructure on the two peninsulas affects the area use of the reindeer by 1) reducing the number of animals on the western, outer section of the infrastructure, and 2) reducing the number of animal crossings, both from the eastern and the western side of the infrastructure. We also tested whether the WP had added a stronger, cumulative behavioural barrier effect than the effects of the roads and power lines in both peninsulas, and whether this effect was strongest during the construction period.

Materials and methods

Study areas

We studied semi-domesticated reindeer on two peninsulas; Dyfjord and Skjotningberg on the larger Nordkinn peninsula in Finnmark, northern Norway (Fig. 1). Both peninsulas constitute good summer pastures approximately below 250 m a.s.l. (constituting 87% and 78% of the total area in Dyfjord and Skjotningberg, respectively) with rocky low productive areas above this elevation. The average elevation is similar on Skjotningberg (187 m a.s.l.) and Dyfjord (167 m a.s.l.). The climate is oceanic characterised by mild winters, low summer temperatures and a yearly precipitation between 500 and 700 mm (Moen 1998). The two peninsulas have a similar area (61.9 [km.sup.2] in Dyfjord and 71.0 [km.sup.2] in Skjotningberg; see Fig. 1) excluding water, and both the landscape and vegetation follow a similar pattern along an east-west gradient. The vegetation types, including impediment (areas covered either by rocks or sand/gravel with no vegetation), are similar in the western parts of both peninsulas. However, the proportion of impediment in the eastern part of Skjotningberg (29%) is relatively higher than in Dyfjord east (15%). Nevertheless, the impediment in Skjotningberg east is located in the north-east and does not influence the movement across the barrier. Moreover, the proportions of other poor vegetation types (e.g. ridges) are high in Dyfjord east (20%) compared to Skjotningberg east (7%) and therefore makes the difference in impediment even less significant. Because of the east-west alignment and the north-south bisecting infrastructure through the middle of both peninsulas, we were able to divide the study areas into east and west of the bisecting infrastructure (see Fig. 1). The existing power line on Dyfjord and both the existing power lines and dirt road on Skjotningberg have existed since the 1960s.

Semi-domesticated reindeer in northern Norway experience close contact with herders during marking of calves, slaughtering and when herded between seasonal pastures (Tveraa et al. 2007). Otherwise, they are free-ranging, while occasional herding may occur if animals move into terrain outside their given pasture area. The reindeer in our study are actively herded into and out of the main Nordkinn peninsula where they spend the summer season. However, once on the peninsula, the reindeer are allowed to disperse freely in and out of, within and between the two peninsulas during the entire summer season, up until the autumn gathering when they are herded back to their winter range. There is one gathering period during September for calf marking and slaughtering when the reindeer are herded into corrals. Before and after this, they are free ranging. We did not conduct any fieldwork within at least one week after these gathering periods in the end of September or beginning of October.

In 2006, a WP was built in the middle of Dyfjord, while no infrastructure was built on Skjotningberg during the course of our study (2006-2010). The WP consisted of 17 wind turbines with a base height of 70 m and a rotor diameter of 82.4 m and was connected by an internal road located on top of Gartefjellet, positioned close to the centre of the Dyfjord peninsula (see Fig. 1). An 8. 5 km dirt access road (5 m wide) connected the WP with the state road. Assuming the infrastructure in our study areas represented potential behavioural barriers, we defined a buffer zone of 50 m on either side of the barrier. Because herded reindeer can be assumed to have similar or less fright and flight reactions towards anthropogenic activities as wild reindeer, we based this 50-m zone on approximations to the shortest fright and flight reactions of wild reindeer in Norway (Reimers et al. 2009). It was assumed that when reindeer were outside of the barrier zone, they could be considered on one side or the other, while if they were inside the zone, we could not be certain whether they would cross it or not.

Data collection

Reindeer positions in our entire study areas were surveyed by direct observations from the ground using binoculars (12 x 42; Colman et al. 2003). This was done one day in each month from June to October 2006-2010 on both peninsulas, except for October 2007-2008 and June-September 2010. We followed a predetermined route and targeted hilltops providing optimal visibility. The locations of reindeer were marked on a map using GPS, in combination with compass direction, topographic information in the field and estimated distance between ourselves and the animals. When reindeer were in groups of any number of individuals interacting with each other and moving together, the position of the middle of the group was mapped.

Data analysis

We performed two analyses to assess the possibility for barrier effects impeding reindeer movements in relation to east and west of the infrastructure, excluding reindeer < 50 m away from these. First, we compared the observed and expected numbers of reindeer east and west of the peninsulas for each year using a test comparing expected density based on area available (Neu et al. 1974, Cronin 1998) for testing our first prediction of reduced number of animals on the western side of the infrastructure. The size of the area east and west of the barrier was used to calculate the expected number relative to the observed numbers, removing areas covered with water. We assumed that all areas were equally available to reindeer.

Secondly, we analysed the proportion of reindeer crossings (our second prediction) to test differences between the WP construction period (2006) and operative years after construction (2007-2009) using a generalised linear model. We used an indirect measure of crossings, i.e. proportional change in number of reindeer from month to month. We calculated the proportion of reindeer crossings as follows: [P.sub.i] = [absolute value of ([M.sub.i+1] - [M.sub.i])]/([M.sub.i+1] or [M.sub.i]), where [P.sub.i] refers to the proportion of reindeer crossings in two consecutive months, Mi refers to the number of animals in the ith month and [M.sub.i+1] refers to the number of animals for the consecutive month. Either of the [M.sub.i] or [M.sub.i+1] that had the largest number was used as a denominator, as this was the maximum number of reindeer in the area in the course of the two consecutive months. The year 2010 was excluded from this analysis as data was recorded only for October. In the model, we included site (Dyfjord vs Skjotningberg), years (2006 vs operative years after the construction), and the interaction between site and year. The analyses were performed in R statistical software version 2.12.0 (R Development Core Team 2011).


We observed more reindeer relative to available area on Dyfjord compared to Skjotningberg in all years, but in 2008 the numbers for both peninsulas were similar to expected (Table 1). Comparing the four locations together, Dyfjord west had more reindeer than expected for all five years except 2008, which was as expected, while the number of animals observed for the other three areas varied among years (see Table 1). Despite the lower densities on Skjotningberg, we observed a higher number of animals than expected west of the infrastructure when we compared east and west of Skjotningberg alone (for all years except 2008; see Table 1). Considering only Dyfjord, the number of reindeer west of the WP was as expected in all years, but was more than expected in 2010. Similarly, the number of reindeer east on Dyfjord was as expected for all years, except some variation in 2009 (more) and 2010 (less; see Table 1).

Dyfjord and Skjotningberg had no significant difference in the proportions of reindeer crossings (Table 2). However, the estimates were negative during the construction period for Dyfjord (see Table 2) and in all years for Skjotningberg except for 2006. The proportion of reindeer crossings on Dyfjord was relatively lower during the WP construction period (2006; 49%) compared to the operative years after the construction period (2007-2009; 62%). However, a positive trend during the operative years in Dyfjord suggests absence of a barrier effect from the WP (see Table 2). On Skjotningberg, crossings did not vary significantly between the construction period (2006; 74%) and operative years (2007-2009; 67%).


Contrary to our predictions, there was no clear evidence for a barrier effect from the WP and associated infrastructure that could potentially cut off the Dyfjord peninsula for reindeer use. Presence of lower number of animals using Dyfjord west relative to Skjotningberg west except in 2008 and 2010 when looking at each peninsula separately, may indicate a slightly decreased preference for using Dyfjord west, relative to Skjotningberg west. However, a smaller number of animals than expected for Skjotningberg west compared to Dyfjord west (for three out of five years) when comparing the four halves showed the opposite effect. The preference was thus not consistent among locations and varied between years, and more importantly, the lack of a significant difference in the proportions of reindeer crossings for both areas supported our inference of no clear evidence for a barrier effect. The decision to construct a WP at the Dyfjord peninsula in Kjollefjord brought concern among reindeer management authorities and the local reindeer herdsmen, for reindeer pasture being lost due to a barrier effect from the WP (Colman et al. 2002). This concern was emanated from studies showing negative barrier effects for reindeer towards linear structures like roads and power lines (Klein 1991, Wolfe et al. 2000, Dyer et al. 2001, Vistnes et al. 2001, Nellemann et al. 2003, Vistnes & Nellemann 2008).

Generally, reindeer continued using both sides of the WP during both the construction period (2006) and after (2007-2010). It is thus unlikely that the WP had a major negative effect on movements of reindeer within the summer grazing areas of the Dyfjord peninsula. We expected a strong barrier effect during the WP's construction period, with considerable ground transportation, construction work and human activity, but the number of reindeer west of the barrier on Dyfjord in 2006 was not affected. However, a lower proportion of reindeer crossings in 2006 than in other years (but not significantly different) on Dyfjord suggested a weak barrier effect during this period. The construction work might have influenced the reindeer from going back east, crossing the barrier, once they had moved into the western section of Dyfjord. Nevertheless, we did not find significant differences in the proportion of reindeer crossings when comparing the two peninsulas. Importantly, a higher number of reindeer more than expected, coupled with a positive trend in the proportion of reindeer crossings on Dyfjord during the operative years supported the absence of a barrier effect from the WP. Unfortunately, no survey data before the construction of the WP were available. Our comparison between the two peninsulas controlled for potential yearly variation within each separate peninsula, as suggested by Reimers & Colman (2006).

Rangifer habitat use, movement patterns and feeding preferences are governed by a complexity of natural interacting factors (Reimers & Colman 2006, Skarin et al. 2010). The barrier and the avoidance effects are two key aspects of ungulate disturbance-reactions relating to linear structures like roads and power lines. Unless limiting or preventing crossings all together (the barrier effect: Forman & Alexander 1998, Trombulak & Frissell 2000, Nellemann et al. 2001, Vistnes et al. 2004), linear and non-linear structures, like cabins, may cause an avoidance of or aversion towards adjacent areas (e.g. Nellemann et al. 2001, Vistnes et al. 2001, Vistnes & Nellemann 2008). The barrier and avoidance effects can occur in unison or independently, and the 'strength' of either effect can vary considerably with time and in spatial scale. In our study, we have focused on the behavioural barrier effect only, as it may be particularly important in our setting if WPs limit reindeer use of entire peninsulas. Rangifer and other ungulates are also well known for their ability to habituate towards many types of stimuli, including anthropogenic activities and structures (e.g. Reimers & Colman 2006, Stankowich 2008). Based on aerial surveys of the distribution of reindeer and lichen measurements, Reimers et al. (2007) reported that reindeer crossed underneath, and grazed under and on both sides, of a 66 KV power line transecting the range of wild reindeer in northern Ottadalen, Norway. However, a negative barrier effect is expected to be especially strong for progressive, cumulative effects from parallel roads and power lines and when expansive structures like WPs are concerned (see review by Vistnes & Nellemann 2008). Despite this, we found no cumulative effects of the new access road built parallel to existing power line, or the WP. However, we were unable to determine whether the east-west alignment of the wind turbines in our study may have influenced the reindeers' perceptions towards the WP.

The potential loss of outlying pasture on peninsulas is especially important in the discussion of management of reindeer and other wildlife. The reindeer in our study are semi-domesticated and may therefore be less susceptible to negative behavioural reactions towards human activities compared to wild reindeer (Reimers & Colman 2006). Nevertheless, our study suggests that this WP does not represent a behavioural barrier for the movements of reindeer on summer pasture, while further analyses are needed to determine whether local avoidance might exist in the neighbourhood of the WP and its associated infrastructure.

DOI: 10.2981/11-116

Acknowledgements--financing was provided by the Norwegian Science Council, The Norwegian Water Resource and Energy Directorate, The Norwegian Reindeer Herding Management, Statkraft, Troms Kraft, Nordkraft Vind, Hydro, Statoil, Fred Olsen Renewable, Agder Energi, Statnett, Statskog and the Reindeer Husbandry Research Fund. We thank the members of the Wind-Rein Project reference group for their valuable input. C. Pedersen, M.A. Gaup, N.M.A. Gaup, A. Mann, J.N. Dyrhaug, J. Holmen, O. T. Rannestad, M. Lilleeng, H. Ronning, B. A. Buvarp, I. Mikalsen, B.A. Mikalsen, E. Nilsen and N.L. Colman provided excellent field assistance.


Colman, J.E., Eftestol, S., Gaup, M.A., Reimers, E. & Flydal, K. 2002: Kjollefjord vindpark, Lebesby kommune. - Konsekvensutredning for reindriften.--Biologisk institutt, Universitetet i Oslo, Oslo, Norway, 35 pp. (In Norwegian).

Colman, J.E., Pedersen, C., Hjermann, D.0., Holand, 0., Moe, S.R. & Reimers, E. 2003: Do wild reindeer exhibit grazing compensation during insect harassment? - Journal of Wildlife Management 67(1): 11-19.

Cronin, M.A., Amstrup, S.C., Durner, G.M., Noel, L.E., McDonald, T.L. & Ballard, W.B. 1998: Caribou distribution during the post-calving period in relation to infrastructure in the Prudhoe Bay oil field, Alaska. - Arctic 51(2): 85-93.

Dahle, B., Reimers, E. & Colman, J.E. 2008: Reindeer (Rangifer tarandus) avoidance of a highway as revealed by lichen measurements.--European Journal of Wildlife Research 54(1): 27-35.

Dodd, C.K., Jr., Barichivich, W.J. & Smith, L.L. 2004: Effectiveness of a barrier wall and culverts in reducing wildlife mortality on a heavily travelled highway in Florida.--Biological Conservation 118(5): 619-631.

Dyer, S.J., O'Neill, J.P., Wasel, S.M. & Boutin, S. 2001: Avoidance of industrial development by woodland caribou. --Journal of Wildlife Management 65(3): 531-542.

EWEA 2008: Pure Power: Wind Energy Scenarios up to 2030.--European Wind Energy Association (EWEA), Brussels, Belgium, 57 pp.

Forman, R.T.T. & Alexander, L.E. 1998: Roads and their major ecological effects.--Annual Review of Ecology and Systematics 29(1): 207-231.

Frid, A. & Dill, L. 2002: Human-caused disturbance stimuli as a form of predation risk.--Conservation Ecology 6(1): 11.

Klein, D.R. 1991: Caribou in the changing North.--Applied Animal Behaviour Science 29(1): 279-291.

Klein, D.R. 2000: Arctic grazing systems and industrial development: can we minimize conflicts? - Polar Research 19(1): 91-98.

Moen, A. 1998: Nasjonalatlas for Norge: Vegetasjon. Statens kartverk, H0nefoss, Norway, 199 pp. (In Norwegian).

Nellemann, C., Vistnes, I., Jordhoy, P. & Strand, O. 2001: Winter distribution of wild reindeer in relation to power lines, roads and resorts.--Biological Conservation 101(3): 351-360.

Nellemann, C., Vistnes, I., Jordhoy, P., Strand, O. & Newton, A. 2003: Progressive impact of piecemeal infrastructure development on wild reindeer.--Biological Conservation 113(2): 307-317.

Neu, C.W., Byers, C.R. & Peek, J.M. 1974: A technique for analysis of utilization-availability data.--Journal of Wildlife Management 38(3): 541-545.

NVE 2012: Vindkraft.--Norges Vassdrags- og Energidirektorat (NVE). Available at (Last accessed on 20 February 2012). (In Norwegian).

R Development Core Team 2011: R: A language and environment for statistical computing.--R Foundation for Statistical Computing, Vienna, Austria. Available at (Last accessed on 17 February 2011).

Reimers, E. & Colman, J.E. 2006: Reindeer and caribou (Rangifer) response to human activities.--Rangifer 26(2): 55-71.

Reimers, E., Dahle, B., Eftestol, S., Colman, J.E. & Gaare, E. 2007: Effects of a power line on migration and range use of wild reindeer.--Biological Conservation 134(4): 484-494.

Reimers, E., Loe, L.E., Eftestol, S., Colman, J.E. & Dahle, B. 2009: Effects of Hunting on Response Behaviors of Wild Reindeer.--Journal of Wildlife Management 73(6): 844851.

Skarin, A., Danell, O., Bergstrom, R. & Moen, J. 2010: Reindeer movement patterns in alpine summer ranges. Polar Biology 33(9): 1263-1275.

Stankowich, T. 2008: Ungulate flight response to human disturbance: A review and meta-analysis.--Biological Conservation 141(9): 2159-2173.

Trombulak, S.C. & Frissell, C.A. 2000: Review of ecological effects of roads on terrestrial and aquatic communities. Conservation Biology 14(1): 18-30.

Tveraa, T., Fauchald, P., Yoccoz, N.G., Ims, R.A., Aanes, R. & H0gda, K.A. 2007: What regulate and limit reindeer populations in Norway?--Oikos 116(4): 706-715.

Vistnes, I. & Nellemann, C. 2008: The matter of spatial and temporal scales: a review of reindeer and caribou response to human activity.--Polar Biology 31(4): 399-407.

Vistnes, I., Nellemann, C., Jordhoy, P. & Strand, O. 2001: Wild reindeer: impacts of progressive infrastructure development on distribution and range use.--Polar Biology 24(7): 531-537.

Vistnes, I., Nellemann, C., Jordhoy, P. & Strand, O. 2004: Effects of infrastructure on migration and range use of wild reindeer.--Journal of Wildlife Management 68(1): 101-108.

Wolfe, S.A., Griffith, B. & Wolfe, C.A.G. 2000: Response of reindeer and caribou to human activities.--Polar Research 19(1): 63-73.

Jonathan E. Colman & Diress Tsegaye, University of Oslo, Department of Biology, P.O. Box 1066 Blindern, NO-0316 Oslo, Norway, and Norwegian University of Life Sciences, Department of Ecology and Natural Resource Management, P.O.Box 5003, NO-1432 As, Norway--e-mail addresses: (Jonathan E. Colman); (Diress Tsegaye)

Sindre Eftestol & Kjetil Flydal, University of Oslo, Department of Biology, P.O. Box 1066 Blindern, NO-0316 Oslo, Norway--e-mail addresses: (Sindre Ef testol); (Kjetil Flydal)

Atle Mysterud, Centre for Ecological and Evolutionary Synthesis (CEES), Department of Biology, University of Oslo, P.O. Box 1066 Blindern, NO-0316 Oslo, Norway--e-mail address:

Corresponding author: Diress Tsegaye

Received 29 November 2011, accepted 7 May 2012

Associate Editor: Hans Christian Pedersen

Table 1. Use-availability analysis for reindeer distribution in
relation to the inner eastern and outer western sections of the
barrier on the Dyfjord and Skjotningberg peninsulas, summer
2006-2010. Available area, excluding the barrier zone and water,
was 14.20 [km.sup.2], 40.13 [km.sup.2], 35.80 [km.sup.2] and
30.50 km2for East Dyfjord, West Dyfjord, East Skjotningberg and
West Skjotningberg, respectively. The letters in parenthesis in
the body of the table indicate whether the number of reindeer
observed was similar to expected (E), significantly less (L) or
more (M) than expected from availability. In 2010, observation
was made only for October.


                                       Proportion of     Number
Site              Location             available area   observed

Dyfjord           East                     0.261        146 (E)
                  West                     0.739        648 (E)
Skjotningberg     East                     0.540         81 (L)
                  West                     0.460        218 (M)
Both peninsulas   East Dyfjord             0.118        146 (E)
                  West Dyfjord             0.333        648 (M)
                  East Skjotningberg       0.297         81 (L)
                  West Skjotningberg       0.253        218 (L)

Overall           All Dyfjord               0.45        794 (M)
                  All Skjotningberg         0.55        299 (L)

                      2006         2007                      2008

                                  Number                    Number
Site                 95% CI      observed      95% CI      observed

Dyfjord           (0.24, 0.27)   375 (E)    (0.26, 0.32)    162(E)
                  (0.72, 0.75)   932 (E)    (0.66, 0.78)   557 (E)
Skjotningberg     (0.38, 0.41)   180 (L)    (0.23, 0.33)   482 (E)
                  (0.59, 0.63)   474 (M)    (0.64, 0.82)   335 (E)
Both peninsulas   (0.16,0.17)    375 (M)    (0.17,0.21)     162(E)
                  (0.46, 0.49)   932 (M)    (0.44, 0.51)   557 (E)
                  (0.13,0.15)    180 (L)    (0.08, 0.11)   482 (E)
                  (0.21,0.23)    474 (E)    (0.22, 0.27)   335 (E)

Overall           (0.63, 0.65)   1307 (M)   (0.62, 0.72)   719 (E)
                  (0.35, 0.37)   654 (L)    (0.31,0.37)     817(E)

                      2008         2009

Site                 95% CI      observed      95% CI

Dyfjord           (0.19,0.27)    467 (M)    (0.27, 0.34)
                  (0.69, 0.87)   1077 (E)   (0.65, 0.75)
Skjotningberg     (0.53, 0.66)   245 (L)    (0.30, 0.40)
                  (0.34, 0.47)   458 (M)    (0.59, 0.73)
Both peninsulas   (0.09, 0.12)   467 (M)    (0.19,0.23)
                  (0.33, 0.40)   1077 (M)   (0.45, 0.52)
                  (0.28, 0.35)   245 (L)    (0.10,0.12)
                  (0.19,0.25)    458 (L)    (0.18,0.23)

Overall           (0.43, 0.51)   1544 (M)   (0.64, 0.73)
                  (0.49, 0.58)   703 (L)    (0.29, 0.34)


Site              observed      95% CI

Dyfjord            17 (L)    (0.03, 0.10)
                  274 (M)    (0.79, 1.11)
Skjotningberg      95 (L)    (0.24, 0.39)
                  215 (M)    (0.58, 0.83)
Both peninsulas    17 (L)    (0.02, 0.05)
                  274 (M)    (0.39, 0.53)
                   95 (L)    (0.13, 0.20)
                  215 (M)    (0.31, 0.42)

Overall           291 (E)    (0.42, 0.56)
                  310 (L)    (0.45, 0.59)

Table 2. Proportion of reindeer crossings in reference to the
outer western section of the barrier on the Dyfjord and
Skjotningberg peninsulas. Skjotningberg and year 2006 (wind-
power plant construction period) were used as reference levels
for site and year categorical variables.

Coefficients     Estimate   Standard error   t value   P value

Intercept          0.83          0.16          5.32    < 0.001
Dyfjord           -0.34          0.21         -1.64      0.12
2007              -0.33          0.22         -1.48      0.16
2008              -0.12          0.22         -0.55      0.59
2009              -0.06          0.21         -0.30      0.77
Dyfjord * 2007     0.40          0.30          1.34      0.20
Dyfjord * 2008     0.33          0.30          1.11      0.28
Dyfjord * 2009     0.17          0.28          0.60      0.56
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Title Annotation:Short communication
Author:Colman, Jonathan E.; Eftestol, Sindre; Tsegaye, Diress; Flydal, Kjetil; Mysterud, Atle
Publication:Wildlife Biology
Article Type:Report
Geographic Code:4EXNO
Date:Dec 1, 2012
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