Abstract

In September 2019, a male wild boar was captured in the pre-Alps of Fribourg. It was equipped with a GPS collar and its movements could be followed for almost 2 whole years. The tracking of this wild boar was analyzed according to 4 aspects: global analysis of its movements, analysis of important points of presence, analysis of the use of the land cover and finally analysis of its activity patterns. The results show a great variability both in the territory occupied and in the use of the different covers. Hunting shows an important influence on its general activity. The results give a direction to future analyses that will be carried out on other individuals in the pre-Alps in order to confirm the elements found during this project.

No studies have been conducted on the movements of wild boar in the Pre-Alps. These analyses are done in the framework of a pre-study. The data are the property of the state of Fribourg and must be treated confidentially.

Introduction and research aim

Wild boars, sus scrofa, are common mammals in Europe (Suter & Fischer, 2021). The study of their movements and habits is used in particular within the framework of the management of their populations but also for the prevention of damage caused to agricultural crops and epidemiology management (Pelayo et al. 2014). Studies carried out within the framework of the EUROBOAR network initiative have shown that wild boars show a great behavioral plasticity and a great adaptability to their environment. This characteristic makes the study of this species complicated and implies that it must be studied in all environments where it is possible to meet it (Brivio et al. 2017). Many studies have been done to understand the spatio-temporal behavior of wild boars but none has been published on wild boars in the Pre-Alps. The pre-Alps present a particular territory due to their steep nature and their landscape coverage.

In this study, the movements of a male wild boar located in the Fribourg pre-Alps (Switzerland) were analyzed over almost two years. The first goal of these analyses was to define the animal’s home range and its use of it. The second goal was to analyze its habits and the effect of an anthropogenic disturbance, hunting, on its habits. As Ohashi and colleagues did in their study in 2013, the intensity of indirect daily disturbance caused by human activities was considered as a constant element. As hunting occurs only some months of the year and its directed toward wild animals, it’s considered here as an temporal element that can influence the boar’s habits.

The study of this data set was done from a global analysis to a more detailed analysis. Five elements guided the analysis with the following questions:

Due to the hilly topography and high elevations, the wild boar was expected to move to higher elevations on average in the summer months and then down in the cooler months with potential snowfall. Areas with high density of location points are assumed to be sources of food for this boar such as corn fields for example. Concerning the use of the landcover by this boar, the hypothesis is an important use of forest spaces, especially during the day, and also a variation in landcover use depending on season as shown by Morelle and Lejeune (2015). Finally, in view of the region where the boar is located, which is an area with many trails and anthropogenic activities, it is assumed that the boar presents mainly a nocturnal behavior. Hunting should have an influence on its movements and its use of the landcover.

Material and Methods

Spatiotemporal analysis of the data in this study was performed with R-Studio version 2022.02.3 and ArcGis Pro version 2.8.3.

Data set

The data set used in this project comes from the Forest and Nature Department of the canton of Fribourg. The 3rd September 2019, a male wild boar was captured in the Fribourg pre-Alps and fitted with a GPS collar. This collar transmitted the position of the animal every hour from 6pm to 6am and then once at noon. The collar was programmed by the nature and forest department based on the fact that the wild boar can be predominantly nocturnal in areas with anthropic disturbance (Ohashi et al., 2013 ; Podgorski et al., 2013) Location data could thus be obtained until July 2021. The animal then suddenly disappeared and so did the GPS transmission.

The data set contains 9431 lines, each corresponding to a location defined by X and Y coordinates according to the Swiss coordinate system (LV95/LV03, crs = 2056). The base file contains the following columns:

  • Date: date of the survey
  • Time: time of the survey
  • Altitude: altitude of the GPS point
  • X: X coordinate
  • Y: Y coordinate

Preprocessing

This data set required some additional columns derived from the base file data to allow for further analysis to answer the questions outlined in the introduction to this project. A first visual analysis of the file in excel was done to observe the data.

The analysis of the “Altitude” column revealed values that could not correspond to the region where the boar was located. Indeed, the highest point in the region is at 2014m (Dent de Lys) and some location points exceeded this value. These points were removed. The same was done for the location points below 500m altitude.

Fig 1: Map of the studied region

Fig 1: Map of the studied region

The dates were analyzed and a subclassification by months and years was done. These data were added as new columns to the available data. Date and time were also merged in a new column. a “Timelag” column was created which indicates the time elapsed between two locations, based on the “Datetime” column created during the previous manipulation of the “Date” and “Time” data. A “Daytime” column has been added. This one is based on the “Timelag” column. If the time difference is less than 65 minutes, it concerns measurements taken at night (from 6pm to 6am), if this difference is greater than 360 minutes, it concerns measurements taken during the day (between 6am and 6pm). The column therefore contains the information Day or Night.

To calculate the activity pattern of this boar, I decided to base my calculations on its speed. The speed is calculated by the distance traveled in a certain time lapse. A “Steplength” column was created. This one indicates the distance between two rows, i.e. two location points. Finally, a “Speed” column has been created. This one is the result of the “Steplength” column divided by the “Timelag” column.

Finally, to analyze the influence of hunting on the activity of this boar, two new columns were created. The first one is the hunting pressure which was evaluated according to the number of species hunted at the same time on a given date :

Wild boar

  • 2019 - 01.09 until 31.12

  • 2020 - 01.09 until 31.12

Roe deer

  • 2019 - 16.09 until 12.10

  • 2020 - 16.09 until 12.10

Chamois

  • 2019 - 16.09 until 28.09

  • 2020 - 21.09 until 03.10

Deer

  • 2019 - 14.10 until 26.10 and 02.11 until 16.11

  • 2020 - 19.10 until 31.10 and 07.11 until 21.11

This information was provided by the Forest and Nature Department of the Canton of Fribourg. Based on this information, four categories were established for hunting pressure:

  • 0 - no hunting

  • 1 - only wild boar hunting

  • 2 - hunting of wild boar + 1 other species

  • 3 - wild boar hunting + 2 other species

An additional column was created to indicate whether hunting was taking place, based on the hunting pressure (0 = no hunting, 1/2/3 = hunting)

Some analyses could only be done with the year 2020, the only full year of data. This is why a second data frame was created with only the points of 2020, subset of the original data frame.

Methods

I would like to point out that all of the methods described below can be applied to other similar data sets. These same manipulations will be used to study the movements of other wild boars in this same region in a future study.

Global analysis of the home range

Wild boars are territorial (Suter & Fischer, 2021). To understand the extent of the male boar’s territory in this study, a visual analysis of its presence was performed. I performed a mcp derived from the location points of this boar to identify its home range. For this purpose, the function st_convex_hull has been applied. It takes a point cloud as input and draws a convex hull around the most distant vertices. The area was then calculated using the chull.area function and compared to the results obtained on ArcGis Pro for validation. The home range was analyzed for all the data from 2019 to 2021

The altitude at which this boar was located is an important element considering the region in which it is located. Therefore, a boxplot analysis was performed to see the altitude the boar was located at as a function of the months in 2020.

Density and path

To visualize the areas where wild boar was most often (high density of location points), an analysis via ArcGis Pro was performed by Kernel Density approach. Following this result, and to understand if these areas correspond to areas where the wild boar stayed for a long time or if it came back all the time, an analysis of the path by ggplot with the geom_path function was performed for each month in 2020.

Land cover and use of it

With the help of ArcGis Pro, a geopackage regrouping the data of the departments of agriculture and forests of the canton of Fribourg for the year 2020 has been created. Not all parcels could be assigned to a surface category due to lack of the GIS layers. This was then imported into R-studio. As the GIS layer contained only categories in French or German, a column was added with the translation in English of the different types of surfaces for a better understanding. By analyzing the different types of surfaces and thinking about the behavior that a wild boar could have in them, I decided to create three surface overclasses: grassland areas which includes meadows, pastures and other rather open surfaces, forests and finally the surfaces corresponding to woodlands outside forests (Hedges-, fields- and riverbank woods). To facilitate the analysis of the data, I decided to work only with the main surface categories as well as the surface classes I created. For elements requiring detail such as a particular field, I worked with visualization in ArcGis Pro. The 2020 wild boar data frame and the geopackage data were then combined into a single data frame for further analysis.

A Bar plot was made to visualize the presence of wild boar on the different terrains.

To find out the exact use of surface types by wild boar, the percentage of location points present in each surface type was calculated. This manipulation was then refined to identify the type of surface used according to the time of day and according to the months.

Activity patterns

The speed of the boar was used as a basis for analyzing its activity rate. The GPS collar was programmed to transmit its position once an hour during the night from 6:00 p.m. to 6:00 a.m. and then once at noon. To verify this, two subsets were created: one for the day and one for the night. The average of the two subsets was calculated and then they were compared. For a better visualization, a boxplot was made. A day/night comparison was made by boxplot according to the months in 2020.

Finally, as speed can also depend on the type of surface on which the boar moves (behavior adapted to land cover), a boxplot analysis of the different speeds according to the type of surface was performed.

Effect of Hunting

Numerous studies demonstrated that hunting had an influence on boar movement speed. To understand the influence of hunting on this male boar, a boxplot analysis of travel speeds by hunting pressure was performed.

To analyze whether hunting also induced a change in the boar’s surface type use patterns, the percentage of location points in a surface type as a function of whether hunting occurred was performed.

Results

Home range and vertical migration

This male boar was moving in the region of the Fribourg pre-Alps. Its home range was limited by the freeway to the west and by the Sarine river to the east. Its home range from 2019 to 2021 was 158.97 km2.

Fig 2: Home range of the wild boar from september 2019 to july 2021

Fig 2: Home range of the wild boar from september 2019 to july 2021

The analysis of the altitude at which the boar was located from 2019 to 2021 shows that a vertical migration to higher altitudes took place in spring 2020 until June 2020. From July 2020 onwards, it can be observed that the boar again descended to lower altitudes. For the rest of the year 2020, the boar was located at approximately the same altitudes. In 2021, the boar was located within the same altitude range until July 2021 were i went up to higher altitudes (Figure 3, Table 1).

Fig 3: Altitude were the wild boar was, depending on the months and years

Fig 3: Altitude were the wild boar was, depending on the months and years

##         Monthyear Altitude
## 1      April 2020 1085.672
## 2      April 2021 1060.228
## 3     August 2020 1017.744
## 4   December 2019 1019.655
## 5   December 2020 1053.401
## 6   February 2020 1017.294
## 7   February 2021 1092.501
## 8    January 2020 1010.007
## 9    January 2021 1037.864
## 10      July 2020 1225.689
## 11      July 2021 1314.666
## 12      June 2020 1349.940
## 13      June 2021 1077.390
## 14     March 2020 1069.142
## 15     March 2021 1119.675
## 16       May 2020 1204.110
## 17       May 2021 1032.510
## 18  November 2019 1060.418
## 19  November 2020 1074.010
## 20   October 2019 1133.697
## 21   October 2020 1029.397
## 22 September 2019 1037.056
## 23 September 2020  968.587

Table 1 : Mean altitude for each month between September 2019 and July 2021.

Horizontal migration and land cover use in 2020

The point density analysis shows several areas of high density, including one in the northwest near the highway (Figure 4). The point analysis (Figure 5) of wild boar presence by month does not show that wild boar remained for a long time (minimum one month) in the same area. Path analysis by month confirms this trend, indicating that the boar was moving back and forth within its home range (Figure 6).

Fig 4: Density of location points of the wild boar in 2020

Fig 4: Density of location points of the wild boar in 2020

Fig 5: Location points by month in 2020

Fig 5: Location points by month in 2020

Fig 6: Path analysis by month in 2020

Fig 6: Path analysis by month in 2020

All the analyses carried out concerning the use of the different types of surface show that the wild boar was mainly located in the forest. Its presence in the forest did not vary much between months. Its presence in summer pastures was more important in May, June and July 2020 than in the other months. In January 2020, about 20% of the wild boar were in areas not identified in the available geopackage compared to 10% in December 2020 (Figure 7). The location points in 2020 were located this way : 50.5% Forest, 35.7% Grassland, 0,3% Hedges-, fields- and riverbank woods, 13,5% NA.

Fig 7: Land cover use per month in 2020.

Fig 7: Land cover use per month in 2020.

The wild boar was primarily located in the forest during the day (between 6:00 am and 6:00 pm) and diversified the areas where they were located at night (Figure 8).

Fig 8: Land cover use depending on daytime for each month in 2020

Fig 8: Land cover use depending on daytime for each month in 2020

An analysis on ArcGis Pro of areas with many location points showed that the GIS layer provided by the department for agriculture did not identify all areas (Figure 9).

Fig 9: Some location points could not be attributed to a specific land cover with the provided GIS layer

Fig 9: Some location points could not be attributed to a specific land cover with the provided GIS layer

Activity patterns

The speed of the boar does not show a big visual difference from month to month (Figure 10). It averages 0.64 m/min during the day (6am to 6pm) and 5.04 m/min at night (6pm to 6am).

Fig 10: Speed depending on daytime for each month in 2020

Fig 10: Speed depending on daytime for each month in 2020

The boar moved slower on average in the forest than in other surface types except for litter surfaces (Table 2).

##                            Landcover    Speed
## 1                            Forests 4.929045
## 2 Hedges, fields and riverbank woods 6.360040
## 3                    Litter surfaces 2.623450
## 4                  Permanent meadows 7.151576
## 5                 Permanent pastures 7.232080
## 6                    Summer pastures 6.431069
## 7             Tree, overlaying areas 8.110733

Table 2 : Mean speed for each landcover category in 2020.

Effect of hunting

Boxplot results show greater forest use during the hunting season in 2020 (Figure 11). Grassland use is similar between periods.

Fig 11: Landcover use depending on hunting in 2020

Fig 11: Landcover use depending on hunting in 2020

The boxplots show an increase in velocity when hunting pressure is present compared to a period without hunting (Figure 12). The mean of speed increased during the day and during the night with hunting pressure (Table 3, Table 4).

Fig 12: Speed depending on the hunting pressure from 2019 to 2021

Fig 12: Speed depending on the hunting pressure from 2019 to 2021

##   Huntpressure     Speed
## 1            0 0.6114687
## 2            1 0.5750352
## 3            2 0.8364226
## 4            3 0.6313324

Table 3 : Mean speed during day depending on hunting pressure from 2019 to 2021.

##   Huntpressure    Speed
## 1            0 4.700096
## 2            1 5.067419
## 3            2 6.327295
## 4            3 4.690600

Table 4 : Mean speed during night depending on hunting pressure from 2019 to 2021.

Discussion

Home range and vertical migration

The study of the movements of the wild boar in this study allowed a better understanding of its habits, its use of the land cover and the influence of the hunt on its spatial behavior. The data collected with the GPS collar allowed the study of its vertical and horizontal migration as well as the visualization of its home range. The results show that the boar in this study had a territory of 158.67 km2 which is about five times larger than the territories recorded for male boars which range from 4.5 to 30 km2 (Suter & Fischer, 2021). This difference could be explained by the hilly topography of the home range of this boar. Studies on other wild boars in the same region would allow us to establish whether this is an isolated case linked to this individual or a generalization for the Pre-Alps region.

One of the hypotheses of this study was to imagine a migration of wild boar to lower altitudes during the bad season because of the weather conditions and the possible difficulty to find food at higher altitudes in winter. The results showed a slight migration to higher elevations in spring and early summer of 2020 and then a return to elevations around 1000m. This trend was not repeated for the year 2021, except for a large ascent in July 2021.

One explanation for this would be the sometimes more difficult access at higher altitudes. Moreover, the Moléson and Dent de Lys regions are very popular hiking areas, making the higher altitudes no more interesting from a tranquility point of view than the areas where the wild boar were found most of the time. Furthermore, forest cover decreases with elevation. Since the wild boar observed here was mainly located in forests, the lack of forest cover towards higher elevations could also be an explanation for the limits of the animal’s vertical migration. The years studied may have had meteorological characteristics that could have influenced the movements of the boar. However, these were not investigated in these analyses. Further analysis of the weather conditions during the years of observation may provide more accurate answers to the question of whether wild boar move to certain elevations rather than others.

Horizontal migration and land cover use

Tracking analysis of the boar in this study showed that the animal was regularly traveling back and forth within its home range. Some geographic points seemed to be more popular than others and the analysis of the density of the location points clearly shows a geographic area particularly appreciated by the animal (Figure 4). Analysis of the GIS layer of surface cover compared with the location points was not sufficient in this study to explain all the location points. When the data was collected, the local wildlife ranger was asked to visit some of the plots to see what was there. For example, it appears that corn plots are not included in the GIS layer, but were particularly popular for this wild boar (Figure 9). Much of the data is thus biased because these types of plots fall into the NA category (about 13.5%) of our analysis and only an on-site analysis could answer questions related to these presence points. This indicates the limitation of the technique used in this study.

The boar in this study spent half of its time in the forest in 2020. This is consistent with data collected in other studies and in the general literature (Suter & Fischer, 2021). In 1991, Gerard et al. described that wild boar in their study in agricultural areas showed a tendency to move from their usual habitat areas to new areas between March and July. The results obtained in this study show a similar trend. In June 2020, the wild boar observed used less forest habitat than in other months of the year and increased its use of other areas. From March to July, plant growth is significant and moving to agricultural land provides an energetic advantage to the animals (Rosell et al. 2012). These larger out-of-forest excursions during this period could therefore have provided a clear advantage to the boar observed in this study. However, these results must be put into perspective as from May to July 2020, this boar also moved to higher elevations where there is less forest cover.

During 2020, the wild boar was primarily located in the forest during the day and exited onto other surface types during the night hours. The forest provides hiding places and allows the animal to rest in safety during day. This correlates with the results of Gerard et al. (1991) who showed that natural habitats are more favored during resting times than during activity phases.

Activity patterns

The boar showed an important nocturnal activity throughout the year and never reversed its daily rhythm. This nocturnal activity has also been noted in other studies and has been related to the greater anthropogenic disturbance during the day, forcing the animal to adapt (Ohashi et al. 2013; Podgorski et al. 2013). The results of this study are consistent with this trend. Indeed, the lower elevation areas are often close to dwellings and the area in general is a popular tourist area in both winter and summer, implying regular anthropogenic disturbance regardless of the season.

The type of surface in which the animal moved could potentially influence its activity. In general, wild boar moved slower on average in forests than in grassy areas. This can be explained by the day/night bias, as the boar most likely used forest areas for resting, but also by the denser vegetation that made movement more difficult. On the other hand, this could also be explained by the insecurity linked to open areas, forcing the animal to move more quickly in grassy areas.

Effect of hunting

Analyses of other publications could not show a trend in the influence of hunting on overall boar activity. In 2008, Keuling et al. and Ohashi et al. observed an increase in nocturnal activity during hunting. In 2013, Thurfjell et al. showed, on the contrary, a decrease in nocturnal activity during the hunting season. Brivio et al. (2017), on the other hand, observed no difference in nighttime activity of wild boars during the hunting season in their study. The main difference between these studies included the study region. In our study in the Fribourg pre-Alps, the overall day and night activity of wild boar increased with hunting pressure. The more species were hunted at the same time, the more hunters were present in the field. This pressure was reflected in the activity of this boar, indicating very clearly the disturbance caused to the fauna by the presence of these hunters, even if they were not looking for the boar. However, the results of this study do not show an increase in boar activity proportional to hunting pressure. In fact, hunting pressure category 3 indicates less disturbance than hunting pressure category 2. This result must be put into perspective because hunting pressure category 3 only concerns 2 weeks per year. In this study, this represents 4 weeks spread over almost 2 years of monitoring, implying a bias in the results. It might be appropriate to limit the number of hunting pressure categories to 3 instead of 4 in order to remove this bias.

Hunting can cause space use to be altered from its normal use (Scillitani et al. 2020). In this study, wild boar appeared to have increased use of forested areas during hunting. This result cannot be considered absolute. Indeed, the analysis of the GIS layer showed that a part of the parcels could not be attributed and are considered as NA. The wildlife warden indicated at the time that some of these plots contained corn and other crops. The hunting season is from September to December. During this period, migration to forested areas was described in other studies (Ballari et al. 2013 ; Massei et al. 1996) and migration to agricultural land occurs in the spring and summer, i.e. during the non-hunting period. The number of unallocated plots is increased in the non-hunting period, corresponding to the spring and summer months. Therefore, the migration to forested areas from September to December 2020 cannot be attributed solely to hunting pressure. 

Conclusion

The spatiotemporal use that an animal makes depends on many intrinsic and extra-intrinsic reasons. This study did not cover all possible aspects and further study would be needed to further understand this individual’s movements and motivations.

These results were validated by personal visualization and comparison with elements found in publications. Some answers were provided by discussion with the wildlife ranger of the region. A detailed statistical analysis is necessary to be able to affirm if the trends observed on the obtained graphs are significant or not. This analysis will be carried out in a second time, outside the framework of this work.

Finally, this study should be seen as a pre-study. Indeed, the study of a single individual does not allow us to draw conclusions for the local population, but it does allow us to determine in which direction further research could go in a study with more individuals.

References

Ballari S.A. & Barrios-Garcia M.N. (2013) : A review of wild boar Sus scrofa diet and factors affecting food selection in native and introduced ranges. Mammal Rev 44: 124-134. DOI : 10.1111/mam.12015

Brivio F., Grignolio S., Brogi R., Benazzi M., Bertolucci C. & Apollonio M. (2017) : An analysis of intrinsic and extrinsic factors affecting the activity of a nocturnal species : The wild boar. Mammalian Biology 84: 73-81.

Gerard J-F., Cargnelutti, Spitz F., Valet G. & Sardin T. (1991) : Habitat use of wild boar in a French agroecosystem from late winter to early summer. Acta theriologica 36 (1-2): 119-129.

Johann F., Handschuh M., Linderoth P., Heurich M., Dormann C.F. & Arnold J. (2020) : Variability of daily space use in wild boar Sus scrofa. Wildlife Biology. DOI : 10.2981/wlb.00609

Keuling O., Stier N. & Roth M. (2008) : How does hunting influence activity and spatial usage in wild boar Sus scrofa L. ? Eur. J. Wildl. Res 54: 729-737.

Massei G., Genov P.V. & Staines B.W. (1996) : Diet, food availability and reproduction of wild boar in a Meditterranean coastal area. Acta Theriol 41:307-320.

Morelle K. & Lejeune P. (2015) : Seasonal variations of wild boar Sus scrofa distribution in agricultural landscapes : a species distribution modelling approach. Eur. J. Wildl. Res. 61: 45-56.

Ohashi H. et al. (2013) : Differences in the activity pattern of the wild boar Sus scrofa related to human disturbance. Eur J. Wildl Res 59: 167-177.

Pelayo A., Quiros-Fernandez F., Casal J. & Vicente J. (2014) : Spatial distribution fo wild boar population abundance : Basic information for spatial epidemilogy and wildlife management. Ecological Indicators 36 : 594-600.

Podgorski T., Bas G., Jedrzejewska B., Sönnichsen L., Sniezko S., Jedrzejewski W. & Okarma H. (2013) : Spatiotemporal behavioral plasticity of wild boar (Sus scrofa) under contrasting conditions of human pressure : primeval forest and metropolitan area. J. Mammal. 94: 109-119.

Rosell C., Navas F. & Romero S. (2012) : Reproduction of wild boar in a cropland and coastal wetland area : implications for management. Anim Biodivers Conserv 35: 209-2017.

Scillitani L. et al. (2010) : Do intensive drive hunts affect wild boar (Sus scrofa) spatial behaviour in Italy ? Some evidences and management implications. Eur. J. Wildl. Res. 56: 307-318.

Suter S.M & Fischer C. (2021) : Wildschwein, p .316-139 in : Graf R.F. & Fischer C. (2021): Atlas der Säugetiere. Schweiz und Liechtenstein. Schweizerische Gesellschaft für Wildtierbiologie SGW, Haupt Verlag, Bern.

Thurfjell H., Spong G. & Ericsson G. (2013) : Effects of hunting on wild boar Sus scrofa behaviour. Wildlife Biology 19: 87-93.

Appendix :

Supplement R-Code

#Analyzing path in 2020 in a more funny way 

p <- ggplot(jojo2020, aes(X, Y)) + geom_path(show.legend = FALSE, mapping = aes(color = "indianred4")) + transition_time(Date) + labs(title = "Date : {frame_time}")
path2020 <- animate(p, duration = 120, render = gifski_renderer())
anim_save("jojo_path2020.gif", path2020)