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Changes in mountain birch forests and reindeer management: Comparing different knowledge systems in Sápmi, northern Fennoscandia

Published online by Cambridge University Press:  07 February 2020

Bruce C. Forbes
Affiliation:
Arctic Centre, University of Lapland, Rovaniemi, Finland
Minna T. Turunen
Affiliation:
Arctic Centre, University of Lapland, Rovaniemi, Finland
Päivi Soppela
Affiliation:
Arctic Centre, University of Lapland, Rovaniemi, Finland
Sirpa Rasmus*
Affiliation:
Arctic Centre, University of Lapland, Rovaniemi, Finland
Terhi Vuojala-Magga
Affiliation:
Arctic Centre, University of Lapland, Rovaniemi, Finland
Heidi Kitti
Affiliation:
Saami Regional Education Centre, Inari, Finland
*
Author for correspondence: Sirpa Rasmus, Email: [email protected]
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Abstract

Mountain birch forests in the northern areas of Sápmi, the Saami homeland, serve as pastures for semi-domesticated reindeer. Recent reindeer management of the area has, to date, proceeded with little involvement of reindeer herders or their knowledge. To get more in-depth understanding of recent changes, we present together herders’ knowledge and scientific knowledge concerning the impacts of herbivory and climate change on mountain birch forests in three Saami communities in Norway and in Finland. Most of the herders interviewed reported changes in weather during the preceding decades. Herders agreed that the canopy and understorey of mountain birch forests have changed. The observed transformations in the quality of pastures have increased the financial costs of reindeer husbandry. Our study demonstrates that herders have practical knowledge of the present state and recent changes of birch forests, and of the responses of reindeer caused by these. This knowledge generally coincides with scientific knowledge. We call for better integration of knowledge systems and a better protocol for co-production of knowledge as it relates to more adaptive future reindeer management regimes. Such integration will facilitate understanding of cultural adaptation within rapidly changing social-ecological systems in which sustainable reindeer husbandry continues to be an important livelihood.

Type
Review Article
Creative Commons
Creative Common License - CCCreative Common License - BY
This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited.
Copyright
© The Author(s) 2020

Introduction

Mountain birch (Betula pubescens spp. czerepanovii) is the predominant tree within the sub-arctic forest zone of northern Fennoscandia, which is situated between treeless upland fells and the coniferous forest zone at lower elevations (Fig. 1). As such, the mountain birch forest ecosystems are the most important source of primary production in the northern areas of Sápmi, the Saami homeland that encompasses much of northern Fennoscandia, including parts of Kola Peninsula (Lehtola, Reference Lehtola2002; Wielgolaski, Reference Wielgolaski, Kankaanpää, Müller-Wille, Susiluoto and Sutinen2002).

Fig. 1. Northern Fennoscandia and Sápmi (dashed line, Lehtola, Reference Lehtola2002). Research communities of Máze, Guovdageaidnu and Gáregasnjárga are marked, and the solid black lines mark the herding districts of the communities (Guovdajohtolat in Norway and Báišduottar in Finland). The mountain birch ecoregion of northern Fennoscandia is shaded in the map. Area used by reindeer stretches also south, outside Sápmi (Johansen unpublished; Käyhkö & Horstkotte, Reference Käyhkö and Horstkotte2017). White squares mark the meteorological stations of Guovdageaidnu, Suolovuopmi and Kárášjohka (Karasjok).

Indigenous Saami have used mountain birch forests for several centuries in various ways: as a pasture for semi-domesticated reindeer (Rangifer tarandus tarandus) and for hunting, trapping, fishing, food and fuel gathering, raw material for handicrafts and construction, and also for spiritual purposes (Aikio & Müller-Wille, Reference Aikio, Müller-Wille, Kankaanpää, Müller-Wille, Susiluoto and Sutinen2002; Crate, Forbes, King, & Kruse, Reference Crate, Forbes, King, Kruse, Larsen, Schweitzer and Fondahl2010; Itkonen, Reference Itkonen1984). The mountain birch region is utilised also by other inhabitants of the area and it serves as an important resource for recreation and for land uses like tourism and wind power. Mountain birch forests are cultural landscapes; intensity and spatial distribution of land uses, specifically reindeer grazing, has been shaped by cultural activities and socio-political processes for centuries (Bernes, Bråthen, Forbes, Speed, & Moen, Reference Bernes, Bråthen, Forbes, Speed and Moen2015; Uboni et al., Reference Uboni, Horstkotte, Kaarlejärvi, Sévêque, Stammler, Olofsson and Moen2016).

Mountain birch is an important source of summer forage for reindeer; during winter reindeer feed mainly on the terricolous lichens, as well as dwarf shrubs, that grow on the forest floor. Access to winter forage is often difficult and energy expenditure of moving and foraging is increased, due to snow conditions (Kitti, Gunslay, & Forbes, Reference Kitti, Gunslay, Forbes, Forbes, Bölter, Müller-Wille, Hukkinen, Müller, Gunslay and Konstantinov2006; Riseth et al., Reference Riseth, Tømmervik, Helander-Renvall, Labba, Johansson, Malnes and Callaghan2011). Deep or icy snow during the winter or late snow melt during the following spring may lead to high winter mortality of reindeer as well as to low calf survival (Eira, Reference Eira2012; Kitti et al., Reference Kitti, Gunslay, Forbes, Forbes, Bölter, Müller-Wille, Hukkinen, Müller, Gunslay and Konstantinov2006; Turunen, Rasmus, Bavay, Ruosteenoja, & Heiskanen, Reference Turunen, Rasmus, Bavay, Ruosteenoja and Heiskanen2016). As high latitudes warm, more frequent formation of ice crusts in the snow cover is expected (Meredith et al., Reference Meredith, Pörtner, Roberts, Masson-Delmotte, Zhai, Tignor, Poloczanska, Mintenbeck, Nicolai, Okem, Petzold, Rama and Weyer2019; Rasmus, Kivinen, Bavay, & Heiskanen, Reference Rasmus, Kivinen, Bavay and Heiskanen2016). When the snow cover is deep or icy, reindeer look for the arboreal lichens that grow on the upper trunks and branches of birch (Sonesson, Reference Sonesson and Wielgolaski2001).

In addition to accessibility of forage, the state of the understorey vegetation (ground lichen, graminoids and shrubs) is crucial when considering mountain birch forests as reindeer pastures. Herbivory and climate are considered as main factors affecting the mountain birch forests ecosystems of the region (Cairns, Lafon, Moen, & Young, Reference Cairns, Lafon, Moen and Young2007; Moen, Cairns, & Lafon, Reference Moen, Cairns and Lafon2008; Tømmervik et al., Reference Tømmervik, Johansen, Tombre, Thannheiser, Høgda, Gaare and Wielgolaski2004; Wielgolaski, Reference Wielgolaski, Kankaanpää, Müller-Wille, Susiluoto and Sutinen2002). Reindeer themselves affect soil properties and microbial processes, plant species and vegetation diversity by grazing, trampling and through excrements (Bernes et al., Reference Bernes, Bråthen, Forbes, Speed and Moen2015; Väisänen et al., Reference Väisänen, Ylänne, Kaarlejärvi, Sjögersten, Olofsson, Crout and Stark2014). Geometrid moths including autumnal (Epirrita autumnata) and winter moths (Operophtera brumata) have periodically great effect on the mountain birch (Helle, Reference Helle and Wielgolaski2001; Neuvonen, Bylund, & Tømmervik, Reference Neuvonen, Bylund, Tømmervik and Wielgolaski2005; Fig. 2). Other herbivores (voles, lemmings and some invertebrates) (Anschlag, Broll, & Holtmeier, Reference Anschlag, Broll and Holtmeier2008), fire (Stocks et al., Reference Stocks, Fosberg, Lynham, Mearns, Wotton, Yang and McKenney1998), forest cutting (Veijola, Reference Veijola1998) and tourism (Forbes, Tolvanen, Wielgolaski, & Laine, Reference Forbes, Tolvanen, Wielgolaski, Laine and Wielgolaski2005) also affect these ecosystems.

Fig. 2. Mountain birch forest before an autumnal moth outbreak without (a) and with (b) intensive reindeer herbivory, and after the outbreak (c). Photos: Otso Suominen.

Autumnal moths appear episodically at approximately 10-year intervals (Tenow & Nilssen, Reference Tenow and Nilssen1990). A severe autumnal moth outbreak was experienced in our research area in 1965–66; significant outbreaks have been documented also in 1927 and 1955 (Kallio & Lehtonen, Reference Kallio and Lehtonen1973). In the 1960s, autumnal moths defoliated sizeable areas of mountain birch forest in Ohcejohka commune in northernmost Finland; these areas have regenerated extremely slowly over the intervening five decades and are presently mostly treeless tundra (Neuvonen et al., Reference Neuvonen, Bylund, Tømmervik and Wielgolaski2005). During the years 2002–2008, both autumnal and winter moths caused spatially variable defoliation within the region (Jepsen, Hagen, Ims, & Yoccoz, Reference Jepsen, Hagen, Ims and Yoccoz2008; Klemola, Andersson, & Ruohomäki, Reference Klemola, Andersson and Ruohomäki2016).

Studies in Arctic North America and northwest Eurasia have indicated an increase in tall deciduous shrub cover and abundance in response to climate change (Forbes, Macias-Fauria, & Zetterberg, Reference Forbes, Macias-Fauria and Zetterberg2010; Macias-Fauria, Forbes, Zetterberg, & Kumpula, Reference Macias-Fauria, Forbes, Zetterberg and Kumpula2012; Myers-Smith et al., Reference Myers-Smith, Forbes, Wilmking, Hallinger, Lantz, Blok and Hik2011; Tape, Sturm, & Racine, Reference Tape, Sturm and Racine2006; Tømmervik et al Reference Tømmervik, Johansen, Tombre, Thannheiser, Høgda, Gaare and Wielgolaski2004). Higher temperature and increased precipitation are favourable for seed production of birch trees near the tree line (Wielgolaski, Reference Wielgolaski, Kankaanpää, Müller-Wille, Susiluoto and Sutinen2002). In the past, the tree line has migrated further north and to higher elevations when air temperatures have been high enough (Kullman, Reference Kullman2002). The effects of climate change on the mountain birch tree line can be difficult to isolate from other factors that affect it simultaneously (Emanuelsson, Reference Emanuelsson1987; Hofgaard, Reference Hofgaard1997). For example, in northern Sweden, reindeer grazing keeps landscapes open and controls the deciduous tree line (Cairns & Moen, Reference Cairns and Moen2004).

In this work we relate two different knowledge systems, scientific knowledge and practitioners’ knowledge of local herders, to gain more in-depth understanding of the recent changes in the mountain birch forests of our research area. Scientific knowledge is accumulated through a formalised process and is most often explicit (written) and quantitative. Ecological and meteorological research is based on measurements (observations, monitoring, remote sensing), retrospective analyses, experimental manipulation of environment or on mathematical modelling. It aims at generalisations, replicability and objectivity (Huntington, Callaghan, Fox, & Krupnik, Reference Huntington, Callaghan, Fox and Krupnik2004; Raymond et al., Reference Raymond, Fazey, Reed, Stringer, Robinson and Evely2010). In recent decades, a large and fast-growing body of literature has addressed the cultures carrying Indigenous Knowledge, Traditional Knowledge and Traditional Ecological Knowledge (TEK) (e.g. Agrawal, Reference Agrawal1995; Alexander et al., Reference Alexander, Bynum, Johnson, King, Mustonen, Neofotis and Weeks2011). The commonly used term TEK can be defined as “knowledge, practice and beliefs about the dynamic relationship of living beings with one another, and with their environment, which has evolved by adaptive processes, and has been handed down from generation to generation” (Berkes, Reference Berkes2008). In our case TEK can be understood as local, practitioners’ knowledge possessed by herders. Local knowledge is a wide term including several knowledge systems, also those classified as traditional and indigenous. It is thought to be developed by societies with long histories of interaction with their natural surroundings but it is not confined to certain inhabitant groups of the area (FAO, 2017; UNESCO, 2017). Also practitioners’ knowledge widens the scope of TEK to acknowledge the non-ethnic nature of knowledge gained in certain livelihoods by spending time on the land and evolving knowledge through practice and experience (Ingold, Reference Ingold2000). This knowledge has been gained over decades, most often since childhood, and reflected in local practices (Forbes, Reference Forbes, Forbes, Bölter, Müller-Wille, Hukkinen, Müller, Gunslay and Konstantinov2006; Helander-Renvall, Reference Helander-Renvall, Marvin and McHugh2014; Vuojala-Magga, Turunen, Ryyppö, & Tennberg, Reference Vuojala-Magga, Turunen, Ryyppö and Tennberg2011).

Practitioners’ knowledge of local herders has only relatively recently been integrated into studies on the status and management of mountain birch forests. Themes covered range from mountain birch forests as reindeer pastures (Aikio & Müller-Wille, Reference Aikio, Müller-Wille, Kankaanpää, Müller-Wille, Susiluoto and Sutinen2002; Inga, Reference Inga2007; Kitti et al., Reference Kitti, Gunslay, Forbes, Forbes, Bölter, Müller-Wille, Hukkinen, Müller, Gunslay and Konstantinov2006; Vuojala-Magga & Turunen, Reference Vuojala-Magga and Turunen2015) to vegetation dynamics within the area (Horstkotte et al., Reference Horstkotte, Utsi, Larsson-Blind, Burgess, Johansen, Käyhkö, Oksanen and Forbes2017; Huntington et al., Reference Huntington, Callaghan, Fox and Krupnik2004). Also, the roles of extreme weather events (Vuojala-Magga et al., Reference Vuojala-Magga, Turunen, Ryyppö and Tennberg2011) and snow conditions (Eira et al., Reference Eira, Jaedicke, Magga, Maynard, Vikhamar-Schuler and Mathiesen2013; Riseth et al., Reference Riseth, Tømmervik, Helander-Renvall, Labba, Johansson, Malnes and Callaghan2011) in herding have been discussed.

The understanding gained through relating different knowledge systems is especially needed in the planning of the northern land use and the management of reindeer herds. The post-WWII management regimes of reindeer herds within the respective Nordic countries have adhered to increasingly strict agricultural norms geared to maximise meat production, and while sustaining ground lichen reserves within winter pastures (Forbes, Reference Forbes, Forbes, Bölter, Müller-Wille, Hukkinen, Müller, Gunslay and Konstantinov2006; Forbes & Stammler, Reference Forbes and Stammler2009). This approach has, to date, proceeded with little to no involvement of herders or their knowledge (Heikkinen, Sarkki, & Nuttall, Reference Heikkinen, Sarkki and Nuttall2012; Sarkki, Heikkinen, Herva, & Saarinen, Reference Sarkki, Heikkinen, Herva and Saarinen2018). This contrasts with the situation in Arctic North America, where co-management of renewable resources has been legally codified since the 1970s (Forbes & Stammler, Reference Forbes and Stammler2009). Participatory action research, in which stakeholders and scientists collaborate and reflect on research implementation and interpretation, is relatively new in Nordic reindeer management (Hukkinen et al., Reference Hukkinen, Müller-Wille, Aikio, Heikkinen, Jääskö, Laakso and West2006). As recently as 15 years ago, research directly involving reindeer herders was deemed too “political” in Finland (Kitti, Reference Kitti2004), and the admission of access to an area of science by “primitive and illiterate reindeer herders” (Magga, Reference Magga and Forbes2006) was disapproved. Since then, however, participatory approaches to connect science, policy and society have become increasingly common (Armitage, Berkes, Dale, Kocho-Schellenberg, & Patton, Reference Armitage, Berkes, Dale, Kocho-Schellenberg and Patton2011; Nilsson et al., Reference Nilsson, Carson, Cost, Forbes, Haavisto, Karlsdottir and Pelyasov2019). New types of participatory methods are developing into a new norm in Nordic Arctic renewable resource management (Adenskog, Reference Adenskog2018; Huntington et al., Reference Huntington, Carey, Apok, Forbes, Fox, Holm and Stammler2019; Jäske, Reference Jäske2018); participatory decision-making is believed to lead to more long-term, deliberate, inclusive and sustainable governance solutions. Emphasis on participation has been established as a general frame also in research funding (Armitage et al., Reference Armitage, Berkes, Dale, Kocho-Schellenberg and Patton2011). Both national and EU Arctic strategies (European Commission, 2016; Prime Minister’s Office, 2013) have been developed to explicitly engage local stakeholders in research projects and land use planning processes. All of these developments call for research that is participatory, acknowledging the characteristics and potential of different knowledge systems.

This study is intended as a contribution towards the integration of distinct knowledge systems in Nordic mountain birch forests in the service of developing a better protocol for co-production of knowledge as it relates to more adaptive future reindeer management regimes. Our overall aim is to understand how the mountain birch forests dynamics are perceived, respectively, in reindeer herders’ and scientific knowledge systems. Specifically, we concentrate on knowledge pertaining to potential pathways from relatively closed mountain birch forest to open tundra, following massive herbivorous moth outbreaks in three localities within the Saami reindeer management region. To do so, we have collected the scientific and practitioners’ “ways of knowing” (sensu Kendrick, Reference Kendrick and Berkes2003) relevant to such moth outbreaks and describe the processes underlying the disappearance and regeneration, where relevant, of mountain birch forests, which function as reindeer rangelands. The main objectives are therefore to:

  1. (1) assess herders’ perceptions of the key ecological drivers of birch forest rangeland dynamics following massive herbivorous moth outbreaks;

  2. (2) present together herders’ perceptions of change and relevant findings within the scientific literature; and

  3. (3) discuss the potential for future integration of practitioners’ knowledge in reindeer management regimes of Sápmi.

Material and methods

Research area

The research area included the Saami communities of Máze (Masi) and Guovdageaidnu (Kautokeino) in Norway and Gáregasnjárga (Karigasniemi) in Finland (Fig. 1, Table 1 ). They are all situated within the sub-arctic zone; seasonal snow cover forms in the area typically in October and melts in May. The dominant tree in the area is mountain birch. The villages of Máze and Guovdageaidnu are located in Guovdajohtolat herding district, and in Guovdageaidnu (Kautokeino) municipality in Finnmark county; it is the largest municipality in Norway. Máze has approximately 400 inhabitants and about 1300 people live in Guovdageaidnu. Gáregasnjárga is located in the Báišduottar herding district, and in Ohcejohka (Utsjoki) municipality; it has about 300 inhabitants. In the municipality of Ohcejohka, more than half of the inhabitants speak Saami as their native tongue and in the Guovdageaidnu municipality over 90%

Table 1. Characteristics and mean climate conditions 1 of the research communities

1 Data for Máze from meteorological station of Suolovuopmi (381 m.a.s.l, 19 km away) and for Gáregasnjárga from station of Kárášjohka (129 m.a.s.l, 19 km away).

2 Administrative units of reindeer management; their organisation and activities are guided by the law. Village of Guovdageaidnu is situated at the western border of the herding district Guovdajohtolat (Kautokeino midtre sone) and the district Oarjjabealli (Kautokeino Vestre sone). Village of Máze is situated close to the eastern border of the district Guovdajohtolat. Village of Gáregasnjárga is located in the district Báišduottar (Paistunturi). Reindeer data are for the year 2015–2016, Finland from RHA (2017) and Norway from Landbruksdepartementet (2016).

In each village, reindeer husbandry is an important livelihood; the surrounding territories serve as reindeer pastures, and 8–25% of the inhabitants of the Ohcejohka and Guovdageaidnu municipalities are reindeer herders (see Table 1). There are also other land users, for example tourism, of which the most important form is moose (Alces alces L.) hunting. Herding practices of the area are based on Saami tradition. In this tradition (compared to small-scale herding combined with other livelihoods, practised in more southern, forested herding districts of Finland) herds are bigger, herding is more often based on pastoralism, and intensive supplementary winter feeding, especially feeding in enclosures, is seldom used (Helle and Jaakkola, Reference Helle and Jaakkola2008; Kitti et al., Reference Kitti, Gunslay, Forbes, Forbes, Bölter, Müller-Wille, Hukkinen, Müller, Gunslay and Konstantinov2006). Herding work is organised through herding groups, siidas (Vuojala-Magga, Reference Vuojala-Magga and Tennberg2012). Differences nevertheless exist between the practices of the herding communities. In northern Norway, reindeer generally move long distances between their summer and winter pastures. In Guovdageaidnu and Máze the winter pasture areas are situated inland, where lichen heaths dominate and summer pastures are by the sea, where vegetation consists of herbs and shrubs and there are also fewer biting insects compared to more heavily forested inland pastures. This represents a natural seasonal pasture rotation for reindeer. In difficult years (deep snow, icing of the ground), reindeer are given supplemental winter feed. The vicinities of the villages of Guovdageaidnu and Máze are utilised as transitional autumn/spring pastures. In Gáregasnjárga, Finland, reindeer graze more or less on the same areas year-round, even though some areas are protected from summer trampling. Annual slaughtering is nowadays conducted in autumn; this practice protects lichens pastures since fewer animals remain alive to forage throughout the winter. The reindeer have been herded with the aid of supplemental feeding (i.e. provided with forage along the way from one pasture area to another) in late winter since the 1990s. This practice is intended to reduce natural mortality, especially of pregnant females, during winters with deep or icy snow and maintain relatively consistent calf birth rates and weights from year to year. Detailed descriptions of the mountain birch forests of the research area are found in Neuvonen et al. (Reference Neuvonen, Bylund, Tømmervik and Wielgolaski2005) and in Vuojala-Magga & Turunen (Reference Vuojala-Magga and Turunen2015), of meteorological conditions in Vikhamar-Schuler, Hanssen-Bauer, & Førland (Reference Vikhamar-Schuler, Hanssen-Bauer and Førland2010) and in Rasmus et al. (Reference Rasmus, Kumpula and Jylhä2014), and of reindeer population dynamics in Uboni et al. (Reference Uboni, Horstkotte, Kaarlejärvi, Sévêque, Stammler, Olofsson and Moen2016).

Knowledge systems on the impacts of herbivory and climate change on mountain birch forests

Interview methods

Semi-directed interviews were conducted with altogether 22 reindeer herders during 2007–2008. This comprises approximately 2.6 % of the herders of the Báišduottar and Guovdajohtolat herding districts (Table 1). Ten herders were interviewed in Gáregasnjárga, nine in Máze and three in Guovdageaidnu. We knew most of the herders beforehand in Gáregasnjárga, but not in Máze and Guovdageaidnu. One of us lived in two different families altogether one month. The interactions between the researchers and informants were thus not only based on interviews but on a mutual trust due to shared living experience. Participant observation transitioned to thematic interviews. Informants were found through the “snowball-method” meaning that we asked each informant whom we should interview next. For interviews, we adhered to the research principles of the International Arctic Social Sciences Association (IASSA, 1998). The informants, all adults, consented to be interviewed and have approved the information and the sharing of it publicly, albeit anonymously. Sixteen of the herders were men and six were women. Their ages varied between 30 and 75 years, but most of them were 60–70 years old. People from different age groups were interviewed to obtain a broad sample set among the active and retired herders. The interviews were conducted either in Saami or in Finnish by two biologists and an anthropologist. It was an advantage that most of the participant observation and interviews could be conducted in Saami as this was the native language of most of the informants. In this paper, we present some Saami terms related to phenomena discussed when appropriate, but we do not present comprehensive analogues for all terminologies used. Saami terminology is designated via the use of italics throughout the text. The interviews were thematic, enabling the discussion of matters that the herders found interesting and important. As starting questions the herders were asked about the main characteristics of their pastures (e.g. topography, vegetation and the significance of mountain birch forests), their management practices, effects of geometrid moths, reindeer foraging and variation in weather on the amount and accessibility of forage on the pastures, and effects of these on reindeer husbandry. Subsequent to this step, discussions were left unstructured, but followed the themes which came naturally up. The temporal perspective of the processes discussed varied according to the theme: variation of weather was most often considered during the last 10–20 years, but for moth outbreaks and other rare events the time perspective was approximately 50 years.

The interview material was gone through and analysed thematically using a qualitative content analysis approach (Krippendorf, Reference Krippendorf1980). We sought to gain an interpretive understanding of the material, making comparison with scientific knowledge possible. From the material arose two central themes: changes in winter weather during recent decades, and changes in vegetation and effects of herbivory on reindeer pastures. Subthemes were: implications of changes in winter weather for reindeer husbandry; changes in birch forests; changes in understorey vegetation; effects of the moth outbreaks; and effects of reindeer grazing. Material related to these compiles the practitioners’ knowledge set used in this study. To protect the privacy of the informants, each person was assigned a code. Informants in Gáregasnjárga have codes G1–G10, in Máze the codes are M1–M9 and in Guovdageaidnu the codes are GG1–GG3. Letters without numbers (G, M, GG) refer to the reindeer herders of each village in general. Excerpts from 13 interviews are quoted in the text.

Literature review methods

Results of a complete meta-analysis of all studies on drivers of reindeer rangeland dynamics in northern Fennoscandia would not be commensurate with the practitioners’ knowledge described above and would not allow relevant comparison. Scientific knowledge concerning the central themes of the interviews was therefore compiled through a targeted literature review. A standard internet search using Google Scholar was performed from the recent literature starting with the broadest possible search terms. The main search terms were Betula pubescens spp. czerepanovii (or simply Betula pubescens) and mountain birch forest (or simply mountain birch). The approach was therefore comparable to the “snowball-method” utilised in the herders’ interviews (see Interview methods above), in that if a publication’s bibliography contained seemingly relevant citations, then those older publications would be checked as well. The time frame was eventually selected as the 1970s, when the outcomes of major moth outbreaks relevant for our study were first reported, up to the present. After the first step, publications were discarded if they were based on B. pubescens woodlands outside the geographical area of the study (e.g. Greenland, Iceland or central Norway). Similarly, if the study did not address central themes of the interviews (see Interview methods above), it was excluded. The publication types included in our review were peer-reviewed papers, book chapters and scientific reports. The literature search was performed both in English and Finnish. Approximately 200 references were screened, and about 80 cited. Of these, altogether 40 locally relevant references comprise the core of the scientific knowledge used in this study. The main results of these publications are collected in Tables 2 and 4, together with herders’ knowledge on central themes of the interviews. We compared the different knowledge systems both according to consideration of certain phenomena or process (has the issue been discussed?), and also according to the considered substance (i.e. coincidence of the knowledge systems; Huntington et al., Reference Huntington, Callaghan, Fox and Krupnik2004). Knowledge gaps and inconsistencies between the knowledge systems were also mapped.

Table 2. Comparison of herders’ knowledge and scientific knowledge concerning the changes in weather during the last decades in the research area

1 Periods with snow-free ground and air temperature below 0°C during 1 September–31 August.

References to scientific literature have been sorted according to the local relevance, ** meaning high relevance (studies conducted in the same locations than our interviews) and * meaning some relevance (studies conducted in the northern Fennoscandian mountain birch region).

Results

In this section, we go through the themes of the study, beginning by presenting herders’ experiences, based on interviews. These results are then discussed in the light of previous studies. See Tables 2 and 4 for summaries comparing herders’ knowledge and scientific knowledge concerning the changes in winter weather, and the changes in the vegetation cover in the research area, respectively.

Changes in winter weather during recent decades

Most of the herders reported specific changes in winter weather during the last 10–20 years (Table 2). Herders said that forecasting weather has become increasingly difficult and that weather changes more quickly. It has become more common even in midwinter that first it is raining and the next day the temperature is below 0°C. There are more often episodes of thawing (njáhcu) in midwinter, as well as extended periods of mild weather with a concomitant reduction in long periods of freezing temperatures (GG2). “For example, we were herding reindeer during Christmas 2007 and it was incomplete snow cover (girjebievla)” (GG2). Herders observe the quality and quantity of snow to estimate the conditions for moving, access to forage and herding (Eira et al., Reference Eira, Jaedicke, Magga, Maynard, Vikhamar-Schuler and Mathiesen2013). The Saami snow concept goavvi relates to extremely poor grazing conditions due to deep or icy snow. According to herders, icing of the ground (bodneskárta) has become more frequent, as well as ice layers (geartnit) within the snow column. Herders have observed delayed snow cover formation in the autumn and earlier snowmelt in the spring.

Herders’ observations about warmer winters and shortened periods below 0°C coincide with the measurements of long-term climate trends for the Guovdageaidnu area (Vikhamar-Schuler et al., Reference Vikhamar-Schuler, Hanssen-Bauer and Førland2010, Reference Vikhamar-Schuler, Isaksen, Haugen, Tømmervik, Luks, Schuler and Bjerke2016) and northern Finland (Lépy & Pasanen, Reference Lépy and Pasanen2017; Vuojala-Magga et al., Reference Vuojala-Magga, Turunen, Ryyppö and Tennberg2011). Delayed snow cover formation has been observed in some meteorological stations of the area by Rasmus et al. (Reference Rasmus, Kumpula and Jylhä2014), but Vikhamar-Schuler et al. (Reference Vikhamar-Schuler, Hanssen-Bauer and Førland2010) observed no significant change in the first day of the snow season. Studies have not observed significant changes in the maximum annual snow depth of the area (Rasmus et al., Reference Rasmus, Kumpula and Jylhä2014; Lépy and Pasanen Reference Lépy and Pasanen2017; Vikhamar-Schuler et al., Reference Vikhamar-Schuler, Hanssen-Bauer and Førland2010). Herders observations about earlier snowmelt agree with the meteorological records (Lépy and Pasanen Reference Lépy and Pasanen2017; Rasmus, Kumpula, & Jylhä, Reference Rasmus, Kumpula and Jylhä2014; Vikhamar-Schuler et al., Reference Vikhamar-Schuler, Hanssen-Bauer and Førland2010).

Kivinen, Rasmus, Jylhä, and Laapas (Reference Kivinen, Rasmus, Jylhä and Laapas2017) found that extremely cold weather events have significantly declined in all seasons during the past 100 years and extremely warm weather events increased particularly in spring and autumn. Vikhamar-Schuler et al. (Reference Vikhamar-Schuler, Isaksen, Haugen, Tømmervik, Luks, Schuler and Bjerke2016) concentrated on exceptionally warm winter periods during the past century, often associated with rainfall and subsequent ground ice formation. These warm events have been frequent during 2000s, increasing in frequency during the study period.

Implications of changes in winter weather for reindeer husbandry

The general consensus among interviewed herders was that the changes in the quality of pastures, particularly decreased access to forage and the amount of forage, have increased the number of working hours and altered herding practices (Table 3). Changes in snow conditions have negatively affected access to forage such that herding has become more difficult overall as a result (Table 3). There is a sense that pastures are becoming “locked” more often, meaning conditions which prevent reindeer reaching forage beneath the snow (heajos guohtun). “Locking” can be caused by (i) icing of the ground layer, which results from rain followed by freezing temperatures before there is adequate snow cover, or if the snow cover has melted completely during the winter; (ii) ice layers (geardni), which are caused by winter rain-on-snow or thaw events followed by freezing temperatures (one herder said that three discrete ice layers could effectively “lock” the pastures (GG3)); and (iii) snow drifts resulting from high snowfall in late winter, increased winds and high density of birch stems (Table 3). Two reindeer herders noted, “When there are more [shrub and mountain] birch, there will be more snow drifts” (GG1, GG2). Enhanced formation of snow drifts means that access to ground lichens can locally decrease, even if lichen cover remains undiminished.

Table 3. The effects of climate change during the year on the quality of the pastures and working conditions of herders as revealed by the interviews

↑ increasing effect, ↓ reducing effect, (↑) increasing effect on summer forage.

Table 4. Comparison of herders’ knowledge and scientific knowledge concerning the changes in the vegetation cover in the research area

1 Chronic, low-intensity leaf damage by defoliating, mining and gall-forming invertebrates such as sawflies (Hymenoptera: Tenthredinidae).

References to scientific literature have been sorted according to the local relevance, ** meaning high relevance (studies conducted in the same locations than our interviews) and * meaning some relevance (studies conducted in the northern Fennoscandian mountain birch region).

Another finding reported by herders concerns the amount and consistency of snow. Animals keep busy and remain in one place when digging for forage below the snow (fieski). Adequate snow depth is needed for this, and as the timing of a complete snow cover has more frequently been delayed until late autumn, conditions for fieski tend to occur later than previously (GG2). One result is that herders are forced to manage their reindeer more intensively (GG2) (Table 3). When a complete snow cover was present earlier, the winter flocks used to be tamer and easier to handle since reindeer tended not to move outside of the fieski zone but turned back by themselves. Now herders have to make temporary enclosures to keep reindeer within the designated areas (Table 3). At the same time, the aforementioned icing of the ground requires more effort, as herders need to move animals to unaffected areas or furnish animals with supplemental forage.

Interviewed herders have noted that the prolonged snow-free periods in both spring and fall have improved the availability of forage for reindeer and contributed to good condition of reindeer. “Snow melts here [in Gáregasnjárga] normally during Mother’s Day (11st May), but in the 2000’s it has not been the case, snow has melted earlier, but it has then snowed sometimes afterwards. Early snowmelt, mild weather and early start of the grass growth would be ideal for reindeer, it does not matter if it was cold in early summer, so long as snow melted, ponds of the mires dried, no insects developed” (G).

The effects of snow conditions reported by herders are congruent with scientific studies on this subject. Research has shown that deep or icy snow or late snow melt may lead to high winter mortality of reindeer as well as to low calf survival during the following spring (Helle & Kojola, Reference Helle and Kojola2008; Kumpula & Colpaert, Reference Kumpula and Colpaert2003; Lee, Press, Lee, Ingold, & Kurttila, Reference Lee, Press, Lee, Ingold and Kurttila2000). Especially, detrimental is the formation of ice on pastures if supplementary winter feeding of reindeer is not in use (Rasmus, Kivinen, & Irannezhad, Reference Rasmus, Kivinen and Irannezhad2018; Riseth et al., Reference Riseth, Tømmervik, Helander-Renvall, Labba, Johansson, Malnes and Callaghan2011; Turunen et al., Reference Turunen, Rasmus, Bavay, Ruosteenoja and Heiskanen2016). The prevalence and frequency of ground ice formation events have rarely been studied within the research area, although Eira (Reference Eira2012) and Rasmus et al. (Reference Rasmus, Kivinen and Irannezhad2018) have reported increased frequency of goavvi events or extensive basal ice formation.

Changes in vegetation and effects of herbivory on reindeer pastures

Changes in vegetation cover

Herders reported changes in vegetation cover, for example, an increase in the abundance of mountain birch; birch grows faster and at higher elevations than previously (GG1, GG2). This has been observed particularly in coastal areas, but also further inland (Table 4). Willow does not spread as quickly as birch, but it is still expanding by increasing rapidly in height and cover (GG1). Herders generally felt that graminoids had become more abundant than before (Table 4). According to one herder, there are more mushrooms now than before, “reindeer are behaving crazier about them than in the past” (GG2).

At certain places within valleys, the mountain birch forest has become so dense that it is not possible for reindeer to utilise the areas (GG2). Within inland lichen heaths, the increase in birch forests and certain vascular understorey plants affect reindeer husbandry and pasture quality negatively by reducing the amount of ground lichen cover. One mechanism is that the dense cover of fallen leaves in autumn within relatively closed forest canopies suppresses the growth of ground lichens. A positive effect of the increase in the birch forest is that the availability of fresh green forage in early summer during the lactation period is improved for the reindeer and their newly born calves.

Herders’ observations of decrease in lichens while birch and some graminoids (Deschampsia cespitosa, D. flexuosa) increase are consistent with research (Myers-Smith et al., Reference Myers-Smith, Forbes, Wilmking, Hallinger, Lantz, Blok and Hik2011; Walker et al., Reference Walker, Wahren, Hollister, Henry, Ahlquist, Alatalo and Wookey2006). Satellite imagery from the Guovdageaidnu and Kárášjohka areas (Tømmervik et al., Reference Tømmervik, Johansen, Tombre, Thannheiser, Høgda, Gaare and Wielgolaski2004) parallels herders’ observations on increases in the abundance of mountain birch. Abundance and height of woody plants are also increasing in other Arctic regions (Käyhkö & Horstkotte Reference Käyhkö and Horstkotte2017; Myers-Smith et al., Reference Myers-Smith, Forbes, Wilmking, Hallinger, Lantz, Blok and Hik2011; Normand et al., Reference Normand, Høye, Forbes, Bowden, Davies, Odgaard and Wischnewski2017; Tape et al., Reference Tape, Sturm and Racine2006).

Climate variability and change affect the growth conditions for mountain birch forests: temperature, precipitation and atmospheric nitrogen (Tømmervik et al., Reference Tømmervik, Johansen, Tombre, Thannheiser, Høgda, Gaare and Wielgolaski2004). In recent decades, both forest and understorey vegetation of Finnmark have developed in ways that reflect more oceanic conditions. For example, lichens have decreased and according to Tømmervik et al. (Reference Tømmervik, Johansen, Tombre, Thannheiser, Høgda, Gaare and Wielgolaski2004) one reason for this is that lichens grow slowly and some vascular plant species (like Cornus suecica, Vaccinium myrtillus) are better competitors under moist conditions. The documented increase in precipitation in the Finnmark area during the last century (Vikhamar-Schuler et al., Reference Vikhamar-Schuler, Hanssen-Bauer and Førland2010) is believed to be favourable for seed germination and growth of birch near the tree line (Kullman, Reference Kullman2002; Wielgolaski, Reference Wielgolaski, Kankaanpää, Müller-Wille, Susiluoto and Sutinen2002). Research on the abundance of mushrooms is scarce. Some results suggest that belowground fungal communities could be controlled by herbivory, and moth outbreaks could have a cascading effect on root-associated fungi (Saravesi et al., Reference Saravesi, Aikio, Wäli, Ruotsalainen, Kaukonen, Huusko and Markkola2015).

Changes in vegetation caused by moth outbreaks

Despite herders’ observation about more abundant mountain birch within wooded areas, the effects of mass outbreaks of moths can overshadow this trend locally. Herders had noticed that there have been moth outbreaks more often than earlier (Table 4). This has had significant effects on the use of mountain birch forests as reindeer pastures. In areas affected by extensive outbreaks in Gáregasnjárga, herders observed that the vegetation composition and cover have changed, with important implications for reindeer husbandry. Defoliation and mortality of birch trees have impacts not only on the availability of winter forage, but also on the availability of summer forage. As one of the herders said: “Defoliation of birch forests by moth is significant for our [summer pasture] areas in Ohcejohka municipality and northern parts of Anár…. one just cannot understand it… the summer of 2008 was saved for example because there was plenty of mushrooms, so that it was not possible to see the effect of birch defoliation by moths on calf slaughter weights [in autumn], it saved the calves, because there was so many mushrooms, it was a good time for reindeer” (G). Ohcejohka and Gáregasnjárga herders reported that both ground and arboreal lichens and birch have decreased and the abundance of graminoids has increased. They largely link these changes to the large autumnal moth outbreak in the 1960s, which affected upland mountain birch forest and fell areas. For reindeer husbandry, the net result was that winter pasture quality has declined because lichens constitute important winter forage (Table 3). The negative effects for reindeer husbandry are increased expenses and working hours because animals require more frequent movements in search of lichens and require costly supplemental feeding. A potential positive effect of the decrease in mountain birch forest is that when the areas have become treeless, there is less snow cover than earlier and the area can be used longer in late winter. Currently, these areas can serve as calving grounds (G).

Herders in Gáregasnjárga state that due to attacks by autumnal moths, most old birch trees died; in some areas, nearly all trees have disappeared and the ground vegetation cover has changed. “Defoliated forests are still visible, in 1968 from Gáregasnjárga to Inari for over 10–15 km, there used to be a birch forest, then green larvae came, there were 2–3 larvae on each leaf. There used to be a lichen pasture, a couple of years after autumnal moth came, grass started to grow, wavy hairgrass, which killed the lichen, reindeer were fat due to grass which grew there for several years, when grass was finished, mosses came, soil became nutrient-poor, trees were decayed…” (G). In Guovdageaidnu and Máze, there have not been severe autumnal moth attacks, though in recent years moth damages have increased (GG, M). Herders reported outbreaks of winter moth during the 2000s in these areas; even the leaves of cloudberries were eaten by moths in summer 2008 (GG2).

The greatest change is the increased amount of graminoids and a decrease in ground lichens, in particular fruticose forms (Table 4). This has had a clear effect on the forage quality of winter pastures. In the herders’ words, “Grasses destroyed the pastures” (G). One of the herders (G6) noted that the quality of pastures has decreased because the amount of star-tipped reindeer lichen (Cladina stellaris) has declined. Herders claim that the forage value of winter pastures has declined because lichens, which form the basis of the winter diet of reindeer, have decreased though animals also consume some graminoids and shrubs in winter. Herders say that the decline in old birch trees means that arboreal lichens growing on the stems have also disappeared (Table 4). In earlier times, during late winter after the snow cover had hardened, reindeer would walk from tree to tree feeding on arboreal lichens, when available. Regeneration of the birch forest has been spatially variable in the Gáregasnjárga area. According to herders, forests have not recovered from previous autumnal moth outbreaks in fell areas, although at lower elevations there has been noticeable regeneration.

Scientific knowledge parallels herders’ observations that autumnal moth has a clear effect on birch forests and tree line. Severe outbreaks are known to have a long-term influence on mountain birch ecosystems (Tenow, Bylund, Nilsen, & Karlsson, Reference Tenow, Bylund, Nilsen, Karlsson and Wielgolaski2005). Herders in Gáregasnjárga and the scientific literature have both linked the loss of birch forest to major outbreaks of the autumnal moth, which in 1965–66 defoliated about 60% (1350 km2) of forested area in the vicinity of the community (Tenow et al., Reference Tenow, Bylund, Nilsen, Karlsson and Wielgolaski2005). Herders’ observation that more birches died in fell areas than in the lowlands is congruent with research done in Ohcejohka commune (Lehtonen, Reference Lehtonen1987). Especially in the vicinity of Geavvu (Kevo), birch grew very slowly and the area has long ago become treeless (Kallio & Lehtonen, Reference Kallio and Lehtonen1973). Regeneration has been unsuccessful partly due to root rot that developed in the aftermath of the moth outbreak (Lehtonen & Heikkinen, Reference Lehtonen and Heikkinen1995). Extensive autumnal moth damage had not been reported in the scientific literature in the Guovdageaidnu–Máze areas. However, during the years 2002–2008, outbreaks of autumnal and winter moths have been reported. The latest moth outbreak causing significant damage in the area was caused by winter moth during years 2006–2008. The rise in winter minimum temperatures is assumed to favour moth outbreaks, and warming facilitates the range expansion of autumnal and winter moth (Helander-Renvall, Reference Helander-Renvall, Marvin and McHugh2014; Jepsen et al., Reference Jepsen, Hagen, Ims and Yoccoz2008; Klemola et al., Reference Klemola, Andersson and Ruohomäki2016). In addition to moth outbreaks, foraging by small mammals like Norwegian lemmings (Lemmus lemmus) and grey‐sided voles (Clethrionomys rufocanus), and background herbivory by invertebrates have been shown to be significant factors in tundra ecosystems (Barrio et al., Reference Barrio, Lindén, Te Beest, Olofsson, Rocha, Soininen and Kozlov2017; Olofsson, Hulme, Oksanen, & Suominen, Reference Olofsson, Hulme, Oksanen and Suominen2004). Damages due to the low-intensity but widespread herbivory are assumed to grow with increasing temperature and precipitation (Barrio et al., Reference Barrio, Lindén, Te Beest, Olofsson, Rocha, Soininen and Kozlov2017).

Changes in vegetation caused by reindeer grazing

Herders in both Gáregasnjárga and Máze were certain that reindeer herbivory does not harm healthy birch forest but, rather, stimulates growth. One herder summarised this as follows, “Birch need reindeer. We have had reindeer here for so long so that if the animals would harm birch, we would not have birch here” (G3). According to herders, reindeer do not browse all the leaves but carefully select some; these are assumed to be of highest quality. Therefore, reindeer keep old forests “clean”. Dense woodlands are not perceived as good pastures because reindeer cannot access the forest and there are no ground lichens growing there due to low light conditions. In late winter, reindeer graze moderately intensively on lichens growing on birch stems. Herders claim this does not have any effect on birch. According to some informants (M11, M12), moose are more destructive for birch because it browses bark to the extent that the stem becomes wounded.

Herders have observed that intensive grazing and trampling by reindeer prevent birch seedling growth and regeneration of forests in summer pastures, including those affected by moth herbivory (Table 4). Herders in Gáregasnjárga say that young and damaged forests (e.g. autumnal moth) do not tolerate as much grazing as mature ones. One informant said that “reindeer can prevent the growth of the seedlings” (G2) in the areas with large numbers of animals, for example, inside the enclosure or on an island. Via grazing and trampling, reindeer might destroy some shoots as well (M11). According to herders, another way reindeer may have a negative effect on birch is that in autumn animals rub their antlers against saplings and in doing so can mortally wound them. In addition to root rot that developed in the aftermath of the moth outbreak, the consensus among herders is that reindeer themselves inhibit the regeneration of birch forests. Some contend that damages could have been prevented: “All the adult birch should have been cut when the moon is growing (when evaporation is strongest), then the shoots would have grown back. Now the birch died along the roots” (G7). Herders also had a concrete suggestion for renewal of the area: “Defoliated areas should be left in peace even for a couple of years, so that seedlings could be growing in peace” (G).

As a key reason for the long-term loss of lichens, at least in Gáregasnjárga, herders see soil erosion related to the retreating forest due to moth outbreaks. One informant said: “Earlier birch protected the earth; now wind and water erode the soil” (G4). Nevertheless, some herders said that the large number of generally unsupervised reindeer in the 1980s also had an effect on the decrease in ground lichen. Reindeer were both from Finland and Norway, as the fence between Norway and Finland was not complete (G). In the vicinity of Gáregasnjárga, there is also a certain amount of overlap in the territories where reindeer graze and trample year-round.

Based on scientific knowledge, healthy mountain birch forests tolerate moderate grazing and may benefit from it and grow faster (Helle, Reference Helle and Wielgolaski2001). Reindeer grazing can also facilitate the establishment of birch because trampling creates gaps in the vegetation for seedlings to grow on the fell areas, thus affecting the growth of birch up to 300 m in elevation (Lempa, Neuvonen, & Tømmervik, Reference Lempa, Neuvonen, Tømmervik and Wielgolaski2005; Tømmervik et al., Reference Tømmervik, Johansen, Riseth, Karlsen, Solberg and Høgda2009; Wielgolaski, Reference Wielgolaski, Kankaanpää, Müller-Wille, Susiluoto and Sutinen2002). However, strong grazing and trampling pressure are known to negatively affect the birch forests, and death of seedlings is a common phenomenon in intensively grazed birch forests (Helle, Kajala, Niva, & Särkelä, Reference Helle, Kajala, Niva, Särkelä, Hyppönen, Penttilä and Poikajärvi1998; den Herder, Kytöviita, & Niemelä, Reference den Herder, Kytöviita and Niemelä2003; Lehtonen and Heikkinen Reference Lehtonen and Heikkinen1995). Herders’ observations agree with the scientific literature that damaged (autumnal moth) or limited areas (enclosures, islands) affected by heavy grazing and trampling regenerate very slowly if grazing is continuous (Vuojala-Magga & Turunen, Reference Vuojala-Magga and Turunen2015). Herders stated that regeneration of mountain birch forests has not succeeded near Gáregasnjárga because reindeer trample the areas and eat seedlings. This is in agreement with many published scientific studies (Biuw et al., Reference Biuw, Jepsen, Cohen, Ahonen, Tejesvi, Aikio and Ims2014; Bråthen et al., Reference Bråthen, Ims, Yoccoz, Fauchald, Tveraa and Hausner2007; Kallio & Lehtonen, Reference Kallio and Lehtonen1973; Lehtonen & Heikkinen, Reference Lehtonen and Heikkinen1995; Moen & Danell, Reference Moen and Danell2003; Tenow et al., Reference Tenow, Bylund, Nilsen, Karlsson and Wielgolaski2005). Reindeer browsing has also been shown to be an important mortality factor for saplings in mountain birch forests defoliated by the outbreaks (Lehtonen & Heikkinen Reference Lehtonen and Heikkinen1995).

The decrease in lichens in places where graminoids increase has been both observed by herders and also reported in the scientific literature (Table 4), but the explanations differ somewhat. There is agreement within the scientific literature that high reindeer density has negative effects on lichen cover. A decrease in lichen biomass due to reindeer grazing has been shown in several studies (Bråthen et al., Reference Bråthen, Ims, Yoccoz, Fauchald, Tveraa and Hausner2007; Lempa et al., Reference Lempa, Neuvonen, Tømmervik and Wielgolaski2005; Moen & Danell, Reference Moen and Danell2003; Reinert & Benjaminsen, Reference Reinert and Benjaminsen2015), and significant grazing pressure seems to also benefit graminoids to the detriment of lichens (Bråthen & Oksanen, Reference Bråthen and Oksanen2001; Eskelinen & Oksanen, Reference Eskelinen and Oksanen2006). Especially, detrimental is year-round grazing with no pasture rotation, as dry lichens are easily crushed and the shattered fragments are susceptible to wind and water erosion (Forbes & Kumpula, Reference Forbes and Kumpula2009; Kumpula, Kurkilahti, Helle, & Colpaert, Reference Kumpula, Kurkilahti, Helle and Colpaert2014; Kumpula, Stark, & Holand, Reference Kumpula, Stark and Holand2011). In some experiments, increases in vascular plant biomass due to decreased reindeer grazing have caused lichen biomass to decrease (Virtanen, Reference Virtanen2000). After grazing pressure has decreased, regeneration of lichen pastures can be relatively rapid (Pajunen, Virtanen, & Roininen, Reference Pajunen, Virtanen and Roininen2008; Tømmervik, Bjerke, Gaare, Johansen, & Thannheiser, Reference Tømmervik, Bjerke, Gaare, Johansen and Thannheiser2012).

Discussion

All of the interviewed herders had observed that both the canopy and understorey of mountain birch forests in Guovdageaidnu–Máze and Gáregasnjárga areas have changed during the past 50 years. The changes in weather conditions and vegetation have significantly affected reindeer husbandry by transforming herding practices and increasing expenses.

Even though we do not aim at validation of either of the two “ways of knowing” presented here, such general comparisons enrich our understanding of recent changes and clarifies the useful features of the respective knowledge systems. The knowledge of herders concerning Nordic mountain birch forest dynamics in large part coincides with the existing scientific knowledge base. Active and retired herders possess practitioners’ knowledge that is clearly grounded in, and related to, specific events and processes. This extends back several decades, so within the lifespan of retired herders. Yet knowledge pertaining to extreme events may also be handed down for several generations (Forbes et al., Reference Forbes, Kumpula, Meschtyb, Laptander, Macias-Fauria, Zetterberg and Bartsch2016; Huntington et al., Reference Huntington, Callaghan, Fox and Krupnik2004). There were also interesting inconsistencies between the knowledge systems, as well as knowledge gaps. Scientific and practitioners’ knowledge may have relevance at different temporal or spatial scales. In climate research, the most common temporal depth is approximately 30 years, whereas ecological research (apart from long-term ecological monitoring) often concentrates on certain short periods (e.g. part of the growing season) within a long continuum. Quantitative measurements are often spatially limited, especially in sparsely populated areas. They may also be seasonally biased. Herders’ memories, on the other hand, may emphasise recent and extreme conditions, and to seasons and phenomena which are most relevant to reindeer herding. Emphasis on extreme events, and paying most attention to variables and changes which are most relevant to herding, such as “locked” winter pastures, are very useful for understanding what adaptive strategies have been deployed in different times and places and how they may be deployed in the future as the Arctic climate most likely continues to warm (Forbes et al., Reference Forbes, Kumpula, Meschtyb, Laptander, Macias-Fauria, Zetterberg and Bartsch2016; IPCC, Reference Pörtner, Roberts, Masson-Delmotte, Zhai, Tignor, Poloczanska, Mintenbeck, Nicolai, Okem, Petzold, Rama and Weyer2019). It has been suggested that public debate, for example, on climate change impacts may influence herders’ perceptions on this topic. However, according to a global analysis by Marin and Berkes (Reference Marin and Berkes2013), herders, hunters and fishers are well aware of the mainstream public climate change narrative, yet the media discourse does not override the knowledge gained through practice and direct experience.

Some phenomena observed by herders have not been reported within the scientific literature. These include, for example, changes in abundances of mushrooms. Beyond our study, the increase in weather variability has been reported by several northern or Arctic communities (ACIA, 2004; Huntington et al., Reference Huntington, Callaghan, Fox and Krupnik2004; Krupnik and Jolly Reference Krupnik and Jolly2002; Meredith et al., Reference Meredith, Pörtner, Roberts, Masson-Delmotte, Zhai, Tignor, Poloczanska, Mintenbeck, Nicolai, Okem, Petzold, Rama and Weyer2019). Scientific knowledge on the subject is scarce, regarding our research area, and results can be contradictory, partly due to incomplete understanding of the scales involved and measures of variability (e.g. Fischer and Knutti, Reference Fischer and Knutti2014). In our interpretation, our informants were most often considering the rapid, intermittent changes in daily weather. In meteorological terms, this would mean a perceived decrease in weather persistence from one day to the next. To our knowledge, weather persistence of sub-Arctic Fennoscandia has not been explicitly studied.

On the other hand, not all processes or events reported by scientists were mentioned by our informants. The combined effects of herbivory and climate change on northern ecosystems have been recently studied (Biuw et al., Reference Biuw, Jepsen, Cohen, Ahonen, Tejesvi, Aikio and Ims2014; Cairns & Moen, Reference Cairns and Moen2004; den Herder et al., Reference den Herder, Virtanen and Roininen2004; Vowles, Lovehav, Molau, & Björk, Reference Vowles, Lovehav, Molau and Björk2017), as well as combined effects of historical human activities and climate change (Normand et al., Reference Normand, Høye, Forbes, Bowden, Davies, Odgaard and Wischnewski2017) and potential feedbacks of herbivory on climate. Examples of these feedbacks include the reduction in deciduous shrub cover and height (cf. Kitti et al., Reference Kitti, Forbes and Oksanen2009; Kolari et al., Reference Kolari, Kumpula, Verdonen, Forbes and Tahvanainen2019), and the loss of fruticose lichen (Forbes & Kumpula, Reference Forbes and Kumpula2009; Helle & Jaakkola, Reference Helle and Jaakkola2008; Kumpula et al., Reference Kumpula, Kurkilahti, Helle and Colpaert2014). The former increases albedo, especially during the snow-covered period, meaning decreased absorption of heat at the ground level or snow cover surface (stabilising feedback); the latter decreases albedo during the snow-free period, resulting in increased absorption of heat (reinforcing feedback) (Cohen et al., Reference Cohen, Pulliainen, Ménard, Johansen, Oksanen, Luojus and Ikonen2013; Olofsson et al., Reference Olofsson, Oksanen, Callaghan, Hulme, Oksanen and Suominen2009). Although important, our analysis does not encompass these complex issues as they did not explicitly stand out from our interview material. In previous studies, the effect of summer temperature and insect harassment during hot summers on reindeer condition and reindeer husbandry has been seen as significant (e.g. Weladji, Holand, & Almøy, Reference Weladji, Holand and Almøy2003). This did not appear as a central theme in our interviews.

Another example of contrasting views arose in the discussion of lichen pasture deterioration, erosion and potential overgrazing by reindeer herds. Herders openly acknowledge the keystone role of reindeer, especially regarding how heavy trampling and grazing of seedlings impeded regeneration of mountain birch forests following massive moth outbreaks. The role of herbivorous moths is nevertheless seen as highly significant in terms of triggering a sequence of events in the transition from mountain birch forest to treeless tundra, and the well-documented retreat of the forest after massive moth outbreaks is considered to be the overriding driver in this transition. In the scientific literature, and in the media (Ruukki Reference Ruukki2016), reindeer trampling is often seen as a main explanatory factor of erosion (e.g. Uhlig & Zink Reference Uhlig, Zink, Forbes, Bölter, Müller-Wille, Hukkinen, Müller, Gunslay and Konstantinov2006; Helle & Jaakkola Reference Helle and Jaakkola2008).

The scientific observations reviewed had varying relevance across scales (Tables 2 and 4). Most of the scientific literature on weather changes (Table 2) had high local relevance (conducted in the same locations as our interviews) and coincided with local practitioners’ knowledge. Scientific knowledge on changes in the vegetation cover (Table 4) is, in some cases, based on literature with lower local relevance (conducted in the northern Fennoscandian mountain birch region, but not in the same locations as our interviews). This was the case with research on increases in shrubs and graminoids. Several studies concentrating on decreases in lichen cover and increases in birch and vascular plants had high local relevance. In addition, literature on decreases in mountain birch due to moth outbreaks and inhibited regeneration due to reindeer grazing included several locally relevant studies.

Our results confirm the conclusions of recent studies in which local or practitioners’ knowledge on northern ecosystems have been related with scientific findings (e.g. Riseth et al., Reference Riseth, Tømmervik, Helander-Renvall, Labba, Johansson, Malnes and Callaghan2011; Eira et al., Reference Eira, Jaedicke, Magga, Maynard, Vikhamar-Schuler and Mathiesen2013; Helander-Renvall, Reference Helander-Renvall, Marvin and McHugh2014; Horstkotte et al., Reference Horstkotte, Utsi, Larsson-Blind, Burgess, Johansen, Käyhkö, Oksanen and Forbes2017).

There is a need to better understand and relate herders’ knowledge of past and ongoing changes with scientific studies in order to more sustainably manage reindeer rangelands in the contemporary milieu of multiple users (Bernes et al., Reference Bernes, Bråthen, Forbes, Speed and Moen2015; Horstkotte et al., Reference Horstkotte, Utsi, Larsson-Blind, Burgess, Johansen, Käyhkö, Oksanen and Forbes2017). As national and international research funding calls and Arctic strategies demand more inclusive stakeholder involvement (European Commission, 2016; Prime Minister’s Office, 2013), it is critical to see where scientific and practitioners’ knowledge both converge and diverge, so that future research and decision-making can better incorporate different “ways of knowing” (sensu Kendrick, Reference Kendrick and Berkes2003). Especially, important is that practitioners can put observed events and processes into a locally relevant perspective, and enrich the meteorological and ecological data with aspects like experiences, impacts and coping. Also, local herding practices leading to measurable outcomes (e.g. vegetation changes, cf. Cohen et al., Reference Cohen, Pulliainen, Ménard, Johansen, Oksanen, Luojus and Ikonen2013; Horstkotte et al., Reference Horstkotte, Utsi, Larsson-Blind, Burgess, Johansen, Käyhkö, Oksanen and Forbes2017; Kolari et al., Reference Kolari, Kumpula, Verdonen, Forbes and Tahvanainen2019) can be afforded their proper social-ecological context. Practitioners’ view can also bring forth new research questions.

The herders interviewed have applied their knowledge to comprehend remarkably detailed patterns of pasture extent, conditions and forage dynamics in space and time. Reindeer husbandry has functioned within the region for centuries, while simultaneously altering mountain birch forests (Horstkotte et al., Reference Horstkotte, Utsi, Larsson-Blind, Burgess, Johansen, Käyhkö, Oksanen and Forbes2017). The determining role of scientific knowledge in the management regime of reindeer herds of our research area has still been indisputable during the past decades (Hukkinen et al., Reference Hukkinen, Müller-Wille, Aikio, Heikkinen, Jääskö, Laakso and West2006), as has been the low local decision-making power (Heikkinen et al., Reference Heikkinen, Sarkki and Nuttall2012, Sarkki et al., Reference Sarkki, Heikkinen, Herva and Saarinen2018). Herders have seldom been seen as “local managers”, making the actual management decisions based on their practitioners’ knowledge.

An example of the very recent emphasis on participation, and approaches that connect science, policy and society, is the process of setting the maximum reindeer numbers in Finland. Reindeer management in Finland belongs under the jurisdiction of the Ministry of Agriculture and Forestry (MAF). Every 10 years, MAF sets the maximum number of reindeer for each herding district. Already 30 years ago (MAF, 1989), it was suggested to allow more decision-making power to herding districts. However, maximum numbers have continuously been set according to the ecological carrying capacity of winter pastures, as estimated by the state-funded and mandated processes aimed at minimising conflicts with forestry and agriculture (MAF, 1989, 1999). The most recent process, setting the maximum numbers for the period of 2020–2030, generally succeeded in involving several stakeholders, including local herding communities, and recommendations were at least partly based both on the scientific and practitioners’ knowledge (MAF, 2019). It is noteworthy that researchers involved in the process considered co-planning and local participation as central methods in the northern land use management (Kumpula et al., Reference Kumpula, Siitari, Siitari, Kurkilahti, Heikkinen and Oinonen2019a, Reference Kumpula, Jokinen, Tauriainen, Pekkarinen, Tahvonen, Stark and Oinonen2019b).

Reindeer husbandry shares the same operational space with several other land users in northern Fennoscandia, encompassing the Sápmi region. Intensifying land use such as forestry, mining industry and tourism has contributed to decrease, fragmentation and degradation of the pastures (Kumpula et al., Reference Kumpula, Kurkilahti, Helle and Colpaert2014; Pape & Löffler, Reference Pape and Löffler2012). Unlike in North America, where Arctic indigenous people have a legal right to participate in the co-management of living resources, access to reindeer rangelands in Sápmi depends on usufruct rights (Forbes and Stammler, Reference Forbes and Stammler2009). Decades of top-down reindeer management have led to distrust of governance institutions (Forbes et al., Reference Forbes, Forbes, Bölter, Müller-Wille, Hukkinen, Müller, Gunslay and Konstantinov2006). A central question in future land use planning is how different actors can use the natural resources without significantly degrading the resources and reducing the range of options for use by others. Co-production of knowledge where both scientific findings and local information are combined facilitates the incorporation of qualitative aspects into the discussion (Markkula, Turunen, & Kantola, Reference Markkula, Turunen and Kantola2019). It provides locally valid information concerning how to prepare for the future (Huntington et al., Reference Huntington, Callaghan, Fox and Krupnik2004; UNESCO, 2017) and facilitates integrated understanding needed in land use planning processes (Horstkotte et al., Reference Horstkotte, Utsi, Larsson-Blind, Burgess, Johansen, Käyhkö, Oksanen and Forbes2017; Raymond et al., Reference Raymond, Fazey, Reed, Stringer, Robinson and Evely2010; Sandström et al., Reference Sandström, Pahlén, Edenius, Tømmervik, Hagner, Hemberg and Mikael2003).

All knowledge systems involved need to participate in a mutually respectful dialogue to determine which approach is the most desirable, and to what outcome. True integration in fact is the crux of the interactions among knowledge systems (cf. Gratani et al., Reference Gratani, Butler, Royee, Valentine, Burrows, Canendo and Anderson2011). As the de facto practitioners of reindeer management over generations in the mountain birch forest and adjoining fell tundra zones, a meaningful role for Saami reindeer herders would be justifiable in the process. Viable reindeer rangelands should meet not only the biological needs of the reindeer itself, but also suit the herders’ sociocultural imperatives, such as passing on their particular ways of knowing in variable geographical and social-ecological contexts, to the next generation (Forbes et al., Reference Forbes, Forbes, Bölter, Müller-Wille, Hukkinen, Müller, Gunslay and Konstantinov2006; Laakso Reference Laakso2008; Ostrom, Reference Ostrom2011).

Conclusions

Our results show that through a participatory research approach a rich body of knowledge can be assembled, and that the different knowledge systems, or “ways of knowing”, can coalesce from distinct yet complementary bases. It is nevertheless anticipated that further integration of these knowledge systems and better protocols for co-production of knowledge are critically needed in the near future. Learning on “how to relate knowledge from different systems for the purpose of improved decisions and solutions” is called for by IPCC (Reference Pörtner, Roberts, Masson-Delmotte, Zhai, Tignor, Poloczanska, Mintenbeck, Nicolai, Okem, Petzold, Rama and Weyer2019), as well.

This study has demonstrated that reindeer herders have relevant and practical knowledge of the present state and recent historic changes of the mountain birch forest ecosystem in northern Fennoscandia. In northern Canada and Alaska, the value of practitioners’ knowledge has been recognised legally through land claims and has become progressively integrated into research and administration (Forbes & Stammler Reference Forbes and Stammler2009). At present, ecosystem management of Fennoscandia is based primarily on scientific knowledge when it comes to state administrative and regulatory regimes. Practitioners’ knowledge does not have the same status and has not been properly accounted for in laws and regulations. As such, the acceptance of practitioners’ knowledge is generally much more contested and conflicted in the policy arena, than as an academic inevitability (cf. Sara Reference Sara2011; Turi and Keskitalo Reference Turi and Keskitalo2014; Benjaminsen, Reinert, Sjaastad, & Sara, Reference Benjaminsen, Reinert, Sjaastad and Sara2015). We conclude that better integration of practitioners’ knowledge with scientific knowledge will improve critical understanding of cultural land use patterns, cultural adaptation to local ecosystems and sustainable development of local communities where reindeer husbandry remains an important livelihood.

Acknowledgements

The authors would like to thank the informants from Guovdageaidnu and Máze in Norway and from Gáregasnjárga in Finland. Otso Suominen from the Kevo Subarctic Research Institute, University of Turku provided the photos for the article, which we warmly acknowledge. We would also like to thank Dagrun Vikhamar-Schuler from the Norwegian Meteorological Institute for the help with the meteorological data, Tove Aagnes Utsi from the Arctic University of Norway for the help with the reindeer data and Risto Viitanen from the Arctic Centre, University of Lapland for technical help. Klemetti Näkkäläjärvi from the University of Lapland is acknowledged for revising the Saami terminology used.

Financial support

This work was supported by EU 5th Framework Programme RENMAN (no. QLK5-CT-2000-0745), NCoE TUNDRA, and Academy of Finland projects RISES (no. 256991) and HUMANOR (no. 251111; also JPI Climate no. 291581). Heidi Kitti was financed by a PhD student position of the Arctic Graduate School (Arktis) during the years 2005–2007 and 2009 at the Arctic Centre through funding from the Academy of Finland and Finland’s Ministry of Education.

Footnotes

a

First author: [email protected]

References

ACIA. (2004). Impacts of a Warming Arctic: Arctic Climate Impact Assessment (ACIA) overview report. Cambridge: Cambridge University Press.Google Scholar
Adenskog, M. (2018). Democratic innovations in political systems—Towards a systemic approach. Örebro Studies in Political Science, 42.Google Scholar
Agrawal, A. (1995). Dismantling the divide between indigenous and scientific knowledge. Development and Change, 26(3), 413439.CrossRefGoogle Scholar
Aikio, M. S., & Müller-Wille, L. (2002). Living at the timberline: The Sámi and the mountain birch forests in northernmost Europe. In Kankaanpää, S., Müller-Wille, L., Susiluoto, P., & Sutinen, M.-L. (Eds.), Northern Timberline Forests: Environmental and Socio-economic Issues and Concerns (pp. 4056). Jyväskylä: Finnish Forest Research Institute.Google Scholar
Alexander, C., Bynum, N., Johnson, E., King, U., Mustonen, T., Neofotis, P., … Weeks, B. (2011). Linking indigenous and scientific knowledge of climate change. BioScience, 61(6), 477484.CrossRefGoogle Scholar
Anschlag, K., Broll, G., & Holtmeier, F.-K. (2008). Mountain birch seedlings in the treeline ecotone, subarctic Finland: Variation in above- and below-ground growth depending on microtopography. Arctic, Antarctic, and Alpine Research, 40, 609616.CrossRefGoogle Scholar
Armitage, D., Berkes, F., Dale, A., Kocho-Schellenberg, E., & Patton, E. (2011). Co-management and the co-production of knowledge: Learning to adapt in Canada’s Arctic. Global Environmental Change, 21, 9951004. doi: 10.1016/j.gloenvcha.2011.04.006 CrossRefGoogle Scholar
Barrio, I., Lindén, E., Te Beest, M., Olofsson, J., Rocha, A., Soininen, E., … Kozlov, M. (2017). Background invertebrate herbivory on dwarf birch (Betula glandulosa-nana complex) increases with temperature and precipitation across the tundra biome. Polar Biology, 40(11), 22652278. doi: 10.1007/s00300-017-2139-7 Google Scholar
Benjaminsen, T. A., Reinert, H., Sjaastad, E., & Sara, M. N. (2015). Misreading the Arctic landscape: A political ecology of reindeer, carrying capacities, and overstocking in Finnmark, Norway. Norsk Geografisk Tidsskrift-Norwegian Journal of Geography, 69(4), 219229.CrossRefGoogle Scholar
Berkes, F. (2008). Sacred Ecology. New York: Routledge.CrossRefGoogle Scholar
Bernes, C., Bråthen, K., Forbes, B., Speed, J., & Moen, J. (2015). What are the impacts of reindeer/caribou (Rangifer Tarandus L.) on arctic and alpine vegetation? A systematic review. Environmental Evidence, 4(1), 126.CrossRefGoogle Scholar
Biuw, M., Jepsen, J., Cohen, J., Ahonen, S., Tejesvi, M., Aikio, S., … Ims, R. A. (2014). Long-term impacts of contrasting management of large ungulates in the arctic tundra-forest ecotone: Ecosystem structure and climate feedback. Ecosystems, 17, 890905.CrossRefGoogle Scholar
Bråthen, K. A., Ims, R., Yoccoz, N., Fauchald, P., Tveraa, T., & Hausner, V. (2007). Induced shift in ecosystem productivity? Extensive scale effects of abundant large herbivores. Ecosystems, 10(5), 773–89.CrossRefGoogle Scholar
Bråthen, K. A., & Oksanen, J. (2001). Reindeer reduce biomass of preferred plant species. Journal of Vegetation Science, 12(4), 473480.CrossRefGoogle Scholar
Cairns, D. M., Lafon, C., Moen, J., & Young, A. (2007). Influences of animal activity on treeline position and pattern: implications for treeline responses to climate change. Physical Geography, 28, 419433.Google Scholar
Cairns, D. M., & Moen, J. (2004). Herbivory influences tree lines. Journal of Ecology, 92, 10191024.CrossRefGoogle Scholar
Cohen, J., Pulliainen, J., Ménard, C.B., Johansen, B., Oksanen, L., Luojus, K., & Ikonen, J. (2013). Effect of reindeer grazing on snowmelt, albedo and energy balance based on satellite data analyses. Remote Sensing of Environment, 135, 107117.CrossRefGoogle Scholar
Crate, S. A., Forbes, B. C., King, L., & Kruse, J. (2010). Contact with nature. In Larsen, J. N., Schweitzer, P., & Fondahl, G. (Eds.), Arctic Social Indicators: A Follow-up to the Arctic Human Development Report (TemaNord 519) (pp. 109127). Copenhagen: Nordic Council of Ministers.Google Scholar
den Herder, M., Kytöviita, M.-M., & Niemelä, P. (2003). Growth of reindeer lichens and effects of reindeer grazing on ground cover vegetation in a Scots pine forest and a subarctic heathland in Finnish Lapland. Ecography, 26, 312.CrossRefGoogle Scholar
den Herder, M., Virtanen, R., & Roininen, H. (2004). Effects of reindeer browsing on tundra willow and its associated insect herbivores. Journal of Applied Ecology, 41, 870879.CrossRefGoogle Scholar
Eira, I. M. G. (2012). The silent language of snow: Sámi traditional knowledge of snow in times of climate change. PhD dissertation. Tromsø: University of Tromsø.Google Scholar
Eira, I. M. G., Jaedicke, C., Magga, O. H., Maynard, N. G., Vikhamar-Schuler, D., & Mathiesen, S. D. (2013). Traditional Sami snow terminology and physical snow classification – Two ways of knowing. Cold Regions Science and Technology, 85, 117130. doi: 10.1016/j.coldregions.2012.09.004 CrossRefGoogle Scholar
Emanuelsson, U. (1987). Human influence on vegetation in the Torneträsk area during the last three centuries. Ecological Bulletins, 38, 95111.Google Scholar
Eskelinen, A., & Oksanen, J. (2006). Changes in the abundance, composition and species richness of mountain vegetation in relation to summer grazing by reindeer. Journal of Vegetation Science, 17(2), 245254.CrossRefGoogle Scholar
European Commission. (2016). An integrated European Union policy for the Arctic. URL: https://eeas.europa.eu/arctic-policy/eu-arctic-policy_en (assessed 20 November 2019).Google Scholar
FAO (Food and Agriculture Organization of United the Nations). (2017). What is local knowledge? URL: http://www.fao.org/docrep/007/y5610e/y5610e01.htm (assessed 24 October 2018).Google Scholar
Fischer, E., & Knutti, R. (2014). Impacts: Heated debate on cold weather. Nature Climate Change, 4, 537538. doi: 10.1038/nclimate2286 Google Scholar
Forbes, B. C. (2006). The challenges of modernity for reindeer management in northernmost Europe. In Forbes, B. C., Bölter, M., Müller-Wille, L., Hukkinen, J., Müller, F., Gunslay, N., & Konstantinov, Y. (Eds.), Reindeer Management in Northernmost Europe: Linking Practical and Scientific Knowledge in Social-ecological System (Ecological Studies 184) (pp. 1125). Berlin: Springer-Verlag.CrossRefGoogle Scholar
Forbes, B. C., Macias-Fauria, M., & Zetterberg, P. (2010). Russian Arctic warming and “greening” are closely tracked by tundra shrub willows. Global Change Biology, 16(5), 15421554.CrossRefGoogle Scholar
Forbes, B. C., & Kumpula, T. (2009). The ecological role and geography of reindeer (Rangifer tarandus) in northern Eurasia. Geography Compass, 3/4, 13561380.CrossRefGoogle Scholar
Forbes, B. C., Kumpula, T., Meschtyb, N., Laptander, R., Macias-Fauria, M., Zetterberg, P., … Bartsch, A. (2016). Sea ice, rain-on-snow and tundra reindeer nomadism in Arctic Russia. Biology Letters, 12. doi: 10.1098/rsbl.2016.0466 CrossRefGoogle ScholarPubMed
Forbes, B. C., & Stammler, F. (2009). Arctic climate change discourse: the contrasting politics of research agendas in the West and Russia. Polar Research, 28(1), 2842.CrossRefGoogle Scholar
Forbes, B. C., Tolvanen, A., Wielgolaski, F. E., & Laine, K. (2005). Rates and processes of natural regeneration in disturbed habitats. In Wielgolaski, F. E. (Ed.), Plant Ecology, Herbivory and Human Impact in Nordic Mountain Birch Forests (pp. 193202). Berlin: Springer.Google Scholar
Gratani, M., Butler, J. R., Royee, F., Valentine, P., Burrows, D., Canendo, W. I., & Anderson, A. S. (2011). Is validation of indigenous ecological knowledge a disrespectful process? A case study of traditional fishing poisons and invasive fish management from the Wet Tropics, Australia. Ecology and Society, 16(3).CrossRefGoogle Scholar
Heikkinen, H. I., Sarkki, S., & Nuttall, M. (2012). Users or producers of ecosystem services? A scenario exercise for integrating conservation and reindeer herding in northeast Finland. Pastoralism, 2(11).CrossRefGoogle Scholar
Helander-Renvall, E. (2014). Relationships between Sami reindeer herders, lands, and reindeer. In Marvin, G. & McHugh, S. (Eds.), Routledge Handbook of Human-Animal Studies (pp. 246258). London and New York: Routledge.Google Scholar
Helle, T. (2001). Mountain birch forests and reindeer husbandry. In Wielgolaski, F. E. (Eds.), Nordic Mountain Birch Ecosystems (pp. 279291). Paris and Parthenon, New York and London: UNESCO.Google Scholar
Helle, T., & Jaakkola, L. M. (2008). Transitions in herd management of semi-domesticated reindeer in northern Finland. Annales Zoologici Fennici, 45(2), 81101. doi: 10.5735/086.045.0201 CrossRefGoogle Scholar
Helle, T., Kajala, L., Niva, A., & Särkelä, M. (1998). Poron laidunnuksen vaikutus tunturikoivikoiden rakenteeseen (Effect of reindeer grazing on the structure of mountain birch forests). In Hyppönen, M., Penttilä, T., & Poikajärvi, H. (Eds.), Effect of Reindeer on Forest and Fell Environments (Finnish Forest Research Institute Research Papers 678) (pp. 132141). Helsinki: Finnish Forest Research Institute.Google Scholar
Helle, T., & Kojola, I. (2008). Demographics in an alpine reindeer herd: effects of density and winter weather. Ecography, 31, 221230. doi: 10.1111/j.2008.0906-7590.04912.x CrossRefGoogle Scholar
Hofgaard, A. (1997). Inter-relationships between treeline position, species diversity, land use and climate change in central Scandes Mountains of Norway. Global Ecology and Biogeography Letters, 6, 419429.CrossRefGoogle Scholar
Horstkotte, T., Utsi, T. A., Larsson-Blind, Å., Burgess, P., Johansen, B., Käyhkö, J., Oksanen, L. & Forbes, B. C. (2017). Human–animal agency in reindeer management: Sámi herders’ perspectives on vegetation dynamics under climate change. Ecosphere, 8(9), e01931. doi: 10.1002/ecs2.1931 Google Scholar
Hukkinen, J., Müller-Wille, L., Aikio, P., Heikkinen, H., Jääskö, O., Laakso, A., … West, N. (2006). Development of participatory institutions for reindeer management in Finland: A diagnosis of deliberation, knowledge integration and sustainability. Ecological Studies, 184, 4771.CrossRefGoogle Scholar
Huntington, H., Callaghan, T., Fox, S., & Krupnik, I. (2004). Matching traditional and scientific observations to detect environmental change: a discussion on Arctic terrestrial ecosystems. Ambio Special Report, 13, 1823.Google Scholar
Huntington, H. P., Carey, M., Apok, C., Forbes, B.C., Fox, S., Holm, L.K., … Stammler, F. (2019). Climate change in context: putting people first in the Arctic. Regional Environmental Change, 19(4), 12171223. doi: 10.1007/s10113-019-01478-8 CrossRefGoogle Scholar
IASSA (International Arctic Social Sciences Association). (1998). URL: https://iassa.org/about-iassa/research-principles (assessed 15 March 2018).Google Scholar
Inga, B. (2007). Reindeer (Rangifer tarandus tarandus) feeding on lichens and mushrooms: traditional ecological knowledge among reindeer-herding Sami in northern Sweden. Rangifer, 27, 93106.CrossRefGoogle Scholar
Ingold, T. (2000). The Perception of the Environment: Essays in Livelihood, Dwelling and Skill. London: Routledge.Google Scholar
IPCC. (2019). Chapter 1: Framing and Context of the Report. In Pörtner, H.-O., Roberts, D.C., Masson-Delmotte, V., Zhai, P., Tignor, M., Poloczanska, E., Mintenbeck, K., Nicolai, M., Okem, A., Petzold, J., Rama, B., & Weyer, N. (Eds.), IPCC Special Report on the Ocean and Cryosphere in a Changing Climate. In press.Google Scholar
Itkonen, T. (1984 and 1948). Suomen lappalaiset I-II (Lapps in Finland I-II). Porvoo: WSOY.Google Scholar
Jäske, M. (2018). Participatory innovations and maxi-publics: The influence of participation possibilities on perceived legitimacy at the local level in Finland. European Journal of Political Research, 58(2), 603630.CrossRefGoogle Scholar
Jepsen, J., Hagen, S., Ims, R., & Yoccoz, N. (2008). Climate change and outbreaks of the geometrids Operophtera brumata and Epirrita autumnata in subarctic birch forest: Evidence of a recent outbreak range expansion. Journal of Animal Ecology, 77(2), 257264.CrossRefGoogle ScholarPubMed
Kallio, P., & Lehtonen, J. (1973). Birch forest damage caused by Oporinia autumnata (Bkh.) in 1965-66 in Ohcejohka, N Finland. Reports of Kevo Subarctic Research Station, 10, 5569.Google Scholar
Käyhkö, J., & Horstkotte, T. (Eds). (2017). Reindeer Husbandry under Global Change in the Tundra Region of Northern Fennoscandia. Turku: Painosalama Oy.Google Scholar
Kendrick, A. (2003). Caribou co-management in northern Canada: fostering multiple ways of knowing. In Berkes, F. et al., (Ed.), Navigating Social–Ecological Systems. Building Resilience for Complexity and Change. Cambridge: Cambridge University Press.Google Scholar
Kitti, H., Gunslay, N., & Forbes, B. C. (2006). Defining the quality of reindeer pastures: The perspectives of Sámi reindeer herders. In Forbes, B. C., Bölter, M., Müller-Wille, L., Hukkinen, J., Müller, F., Gunslay, N., & Konstantinov, Y. (Eds.), Reindeer Management in Northernmost Europe: Linking Practical and Scientific Knowledge in Social-ecological Systems (Ecological Studies 184), (pp. 141165). Berlin: Springer.CrossRefGoogle Scholar
Kitti, J. (2004). No new information about reindeer husbandry. Lapin Kansa, 30 August 2004, p. 5. (in Finnish)Google Scholar
Kitti, H., Forbes, B.C., & Oksanen, J. (2009). Long- and short-term effects of reindeer grazing on tundra wetland vegetation. Polar Biology, 32, 253261. doi: 10.1007/s00300-008-0526-9 CrossRefGoogle Scholar
Kivinen, S., Rasmus, S., Jylhä, K., & Laapas, M. (2017). Climate variations over the past century (1914–2013) in Northern Fennoscandia: Trends and extreme events. Climate, 5(1), 16. doi: 10.3390/cli5010016 CrossRefGoogle Scholar
Klemola, T., Andersson, T., & Ruohomäki, K. (2016). No regulatory role for adult predation in cyclic population dynamics of the autumnal moth, Epirrita autumnata . Ecological Entomology, 41(5), 582589.CrossRefGoogle Scholar
Kolari, T., Kumpula, T., Verdonen, M., Forbes, B. C., & Tahvanainen, T. (2019). Reindeer grazing controls willows with minor effects on plant communities in Fennoscandian oroarctic mires. Arctic, Antarctic, and Alpine Research, 51, 506520. doi: 10.1080/15230430.2019.1679940 CrossRefGoogle Scholar
Krippendorf, K. (1980). Content Analysis: An Introduction to its Methodology. Beverly Hills, CA: Sage.Google Scholar
Krupnik, I., & Jolly, D. (Eds.). (2002). The Earth is Faster Now: Indigenous Observations of Arctic Environmental Change. Fairbanks: ARCUS.Google Scholar
Kullman, L. (2002). Rapid recent range-margin rise of tree and shrub species in the Swedish Scandes. Journal of Ecology, 90, 6877.CrossRefGoogle Scholar
Kumpula, J., & Colpaert, A. (2003). Effects of weather and snow conditions on reproduction and survival of semi-domesticated reindeer (R.t. tarandus). Polar Research, 22(2), 225233.CrossRefGoogle Scholar
Kumpula, J., Jokinen, M., Tauriainen, J., Pekkarinen, A.-J., Tahvonen, O., Stark, S., … Oinonen, K. (2019b). Reindeer Herding Inventory and Sustainable Bioeconomy with Reindeer Pastures. Summary report, project KEBIPORO. Helsinki: LUKE, University of Helsinki, University of Lapland. (in Finnish)Google Scholar
Kumpula, J., Kurkilahti, M., Helle, T., & Colpaert, A. (2014). Both reindeer management and several other land use factors explain the reduction in ground lichens (Cladonia spp.) in pastures grazed by semi-domesticated reindeer in Finland. Regional Environmental Change, 14(2), 541559.CrossRefGoogle Scholar
Kumpula, J., Siitari, J., Siitari, S., Kurkilahti, M., Heikkinen, J., & Oinonen, K. (2019a). Reindeer herding area winter pasture inventory 2016–2018: Changes in winter pasture status and reasons for changes. Natural Resources and Bioeconomy Research 33/2019. Helsinki: Natural Resources Center. 86 pp. (in Finnish)Google Scholar
Kumpula, J., Stark, S., & Holand, Ø. (2011). Seasonal grazing effects by semi-domesticated reindeer on subarctic mountain birch forests. Polar Biology, 34, 441453.CrossRefGoogle Scholar
Laakso, A. M. (2008). The shadow field of reindeer management: a case study from Finland. Acta Borealia, 25(2), 138159. doi: 10.1080/08003830802496703 CrossRefGoogle Scholar
Landbruksdepartementet. (2016). Ressursregnskapet for reindritsnæringen 2015–2016 (Report of reindeer herding 2015–2016). Landbruksdepartementet Rapport 24/2016.Google Scholar
Lee, S. E., Press, M. C., Lee, J. A., Ingold, T., & Kurttila, T. (2000). Regional effects of climate change on reindeer: A case study of the Muotkatunturi region in Finnish Lapland. Polar Research, 19, 99105.CrossRefGoogle Scholar
Lehtola, V.-P. (2002). The Sámi People. Traditions in Transition. Inari: Kustannus-Puntsi.Google Scholar
Lehtonen, J. (1987). Recovery and development of birch forests damaged by Epirrita autumnata in Ohcejohka area, north Finland. Reports of Kevo Subarctic Research Station, 20, 3539.Google Scholar
Lehtonen, J., & Heikkinen, R. K. (1995). On the recovery of mountain birch after Epirrita damage in Finnish Lapland, with a particular emphasis on reindeer grazing. Écoscience, 2, 349356.CrossRefGoogle Scholar
Lempa, K., Neuvonen, S. & Tømmervik, H. (2005). Effects of reindeer grazing on pastures in a mountain birch system. In Wielgolaski, F. E. (Ed.), Plant Ecology, Herbivory and Human Impact in Nordic Mountain Birch Forests (pp. 157164). Berlin: Springer.CrossRefGoogle Scholar
Lépy, E., and Pasanen, L. (2017). Observed regional climate variability during the last 50 years in reindeer herding cooperatives of Finnish fell Lapland. Climate, 5(4), 81. doi: 10.3390/cli5040081 CrossRefGoogle Scholar
Macias-Fauria, M., Forbes, B. C., Zetterberg, P., & Kumpula, T. (2012). Eurasian Arctic greening reveals teleconnections and the potential for structurally novel ecosystems. Nature Climate Change, 2(8), 613618.CrossRefGoogle Scholar
Magga, J. (2006). Reindeer herder lost in the jungle of science. In Forbes, B. C. (Ed.) et al., Reindeer Management in Northernmost Europe: Linking Practical and Scientific Knowledge in Social-Ecological Systems. Ecological Studies, Vol. 184, pp. 381383. Berlin, Heidelberg: Springer.Google Scholar
Marin, A., & Berkes, F. (2013). Local people’s accounts of climate change: To what extent are they influenced by the media? WIREs Climate Change, 4, 18. doi: 10.1002/wcc.199 CrossRefGoogle Scholar
Markkula, I., Turunen, M. T., & Kantola, S. (2019). Traditional and local knowledge in land use planning: insights into the use of the Akwé: Kon Guidelines in Eanodat, Finnish Sápmi. Ecology and Society, 24(1), 20. doi: 10.5751/ES-10735-240120 CrossRefGoogle Scholar
Meredith, M. et al. (Eds.) (2019). Chapter 3: Polar Regions. In Pörtner, H.-O., Roberts, D.C., Masson-Delmotte, V., Zhai, P., Tignor, M., Poloczanska, E., Mintenbeck, K., Nicolai, M., Okem, A., Petzold, J., Rama, B., & Weyer, N. (Eds.), IPCC Special Report on the Ocean and Cryosphere in a Changing Climate. In press.Google Scholar
Ministry of Agriculture and Forestry. (1989). Maximum number of reindeer winter stocks, proposal by the working group. MAF memorandum 1989. (in Finnish)Google Scholar
Ministry of Agriculture and Forestry. (1999). Maximum number of reindeer winter stocks, proposal by the working group. MAF memorandum 1999:20. (in Finnish)Google Scholar
Ministry of Agriculture and Forestry. (2019). Maximum number of reindeer winter stocks, proposal by the working group. MAF memorandum 2019. (in Finnish)Google Scholar
Moen, J., Cairns, D. M., & Lafon, C. W. (2008). Factors structuring the treeline ecotone in Fennoscandia. Plant Ecology and Diversity, 1, 7787.CrossRefGoogle Scholar
Moen, J., & Danell, Ö. (2003). Reindeer in the Swedish mountains: An assessment of grazing impacts. Ambio, 32(6), 397402.CrossRefGoogle ScholarPubMed
Myers-Smith, I.H., Forbes, B. C., Wilmking, M., Hallinger, M., Lantz, T., Blok, D., … Hik, D. S. (2011). Shrub expansion in tundra ecosystems: dynamics, impacts and research priorities. Environmental Research Letters, 6, 045509. doi: 10.1088/1748-9326/6/4/045509 CrossRefGoogle Scholar
Neuvonen, S., Bylund, H., & Tømmervik, H. (2005). Forest defoliation risks in birch forests by insects under different climate and land use scenarios in northern Europe. In Wielgolaski, F. E. (Ed.), Plant Ecology, Herbivory and Human Impact in Nordic Mountain Birch Forests (pp. 125138). Berlin: Springer.CrossRefGoogle Scholar
Nieminen, M. (1994). Poro – ruumiinrakenne ja elintoiminnat. Rovaniemi: Riista- ja kalatalouden tutkimuslaitos.Google Scholar
Nilsson, A. E., Carson, M., Cost, D.S., Forbes, B.C., Haavisto, R., Karlsdottir, A., … Pelyasov, A. (2019). Towards improved participatory scenario methodologies in the Arctic. Polar Geography, doi: 10.1080/1088937X.2019.1648583 Google Scholar
Normand, S., Høye, T., Forbes, B. C., Bowden, J., Davies, A., Odgaard, B., … Wischnewski, J. (2017). Legacies of historical human activities in Arctic woody plant dynamics. Annual Review of Environment and Resources, 42, 541567.CrossRefGoogle Scholar
Olofsson, J., Hulme, P. E., Oksanen, L., & Suominen, O. (2004). Importance of large and small mammalian herbivores for the plant community structure in the forest tundra ecotone. Oikos, 106(2), 324334.CrossRefGoogle Scholar
Olofsson, J., Oksanen, L., Callaghan, T., Hulme, P. E., Oksanen, T., & Suominen, O. (2009). Herbivores inhibit climate-driven shrub expansion on the tundra. Global Change Biology, 15, 26812693. doi: 10.1111/j.1365-2486.2009.01935.x CrossRefGoogle Scholar
Ostrom, E. (2011). Background on the Institutional Analysis and Development Framework. The Policy Studies Journal, 39(1).CrossRefGoogle Scholar
Pajunen, A., Virtanen, R., & Roininen, H. (2008). The effects of reindeer grazing on the composition and species richness of vegetation in forest–tundra ecotone. Polar Biology, 31(10), 12331244.CrossRefGoogle Scholar
Pape, R., & Löffler, J. (2012). Climate change, land use conflicts, predation and ecological degradation as challenges for reindeer husbandry in Northern Europe: What do we really know after half a century of research? Ambio, 41(5), 421434. doi: 10.1007/s13280-012-0257-6 CrossRefGoogle ScholarPubMed
Prime Minister’s Office. (2013). Finland’s Strategy for the Arctic Region. URL: https://vnk.fi/en/arctic-issues/finlands-arctic-policy (assessed 20 November 2019).Google Scholar
Rasmus, S., Kivinen, S., Bavay, M., & Heiskanen, J. (2016). Local and regional variability in snow conditions in northern Finland: a reindeer herding perspective. Ambio, 45(4), 398414. doi: 10.1007/s1328015-0762-5 CrossRefGoogle ScholarPubMed
Rasmus, S., Kivinen, S., & Irannezhad, M. (2018). Basal ice formation in Northern Finland snow covers during 1948–2016. Environmental Research Letters, 13, 114009. doi: 10.1088/1748-9326/aae541 CrossRefGoogle Scholar
Rasmus, S., Kumpula, J., & Jylhä, K. (2014). Suomen poronhoitoalueen muuttuvat talviset sää-ja lumiolosuhteet (Changing winter conditions in the Finnish reindeer herding area). Terra, 126(4), 169185.Google Scholar
Raymond, C., Fazey, I., Reed, M., Stringer, L., Robinson, G., & Evely, A. (2010). Integrating local and scientific knowledge for environmental management. Journal of Environmental Management, 91, 17661777. doi: 10.1016/j.jenvman.2010.03.023 CrossRefGoogle ScholarPubMed
Reinert, H., & Benjaminsen, T. (2015). Conceptualizing resilience in Norwegian Sámi reindeer pastoralism. Resilience, 3(2), 95112.CrossRefGoogle Scholar
RHA (Reindeer Herders Association ). (2017). Statistics of Reindeer Numbers, 2015–2016. Rovaniemi: RHA.Google Scholar
Riseth, J. Å., Tømmervik, H., Helander-Renvall, E., Labba, N., Johansson, C., Malnes, E., … Callaghan, T. V. (2011). Sámi traditional ecological knowledge as a guide to science: snow, ice and reindeer pasture facing climate change. Polar Record, 47(3), 202217. doi: 10.1017/S0032247410000434 CrossRefGoogle Scholar
Ruukki, J. (2016). Reindeer factory farming is an environmental risk. Helsingin Sanomat, 19.09.2016. (in Finnish)Google Scholar
Sandström, P., Pahlén, T. G., Edenius, L., Tømmervik, H., Hagner, O., Hemberg, L., … Mikael, E. (2003). Conflict resolution by participatory management: Remote sensing and GIS as tools for communicating land-use needs for reindeer herding in northern Sweden. Ambio, 32, 557567.CrossRefGoogle ScholarPubMed
Sara, M. N. (2011). Land usage and siida autonomy. Arctic Review, 2(2).CrossRefGoogle Scholar
Saravesi, K., Aikio, S., Wäli, P. R., Ruotsalainen, A. L., Kaukonen, M., Huusko, K., … Markkola, A. (2015). Moth outbreaks alter root-associated fungal communities in subarctic mountain birch forests. Microbial Ecology, 69(4), 788797. doi: 10.1007/s00248-015-0577-8 CrossRefGoogle ScholarPubMed
Sarkki, S., Heikkinen, H.I., Herva, V.-P., & Saarinen, J. (2018). Myths on local use of natural resources and social equity of land use governance: Reindeer herding in Finland. Land Use Policy, 77, 322331. doi: 10.1016/j.landusepol.2018.05.055 CrossRefGoogle Scholar
Sonesson, M. (2001). Ecology of some epiphytic lichens on the mountain birch. In Wielgolaski, F. E. (Ed.), Nordic Mountain Birch Ecosystems (pp. 6376). Paris and Parthenon, New York and London: UNESCO.Google Scholar
Stocks, B.J., Fosberg, M. A., Lynham, T. J., Mearns, L., Wotton, B. M., Yang, Q., … McKenney, D. W. (1998). Climate change and forest fire potential in Russian and Canadian boreal forests Climatic Change, 38, 113.CrossRefGoogle Scholar
Tape, K., Sturm, M., & Racine, C. H. (2006). The evidence for shrub expansion in northern Alaska and the Pan-Arctic. Global Change Biology, 12, 686702.CrossRefGoogle Scholar
Tenow, O., Bylund, H., Nilsen, A. C., & Karlsson, P. S. (2005). Long-term influence of herbivores on northern birch forests. In Wielgolaski, F. E. (Ed.), Plant Ecology, Herbivory and Human Impact in Nordic Mountain Birch Forests (pp. 165181). Berlin: Springer.CrossRefGoogle Scholar
Tenow, O., & Nilssen, A. (1990). Egg cold hardiness and topoclimatic limitations to outbreaks of Epirrita autumnata in northern Fennoscandia. Journal of Applied Ecology, 27, 723734.CrossRefGoogle Scholar
Tømmervik, H., Bjerke, J., Gaare, E., Johansen, B., & Thannheiser, D. (2012). Rapid recovery of recently overexploited winter grazing pastures for reindeer in northern Norway. Fungal Ecology, 5(1), 315.CrossRefGoogle Scholar
Tømmervik, H., Johansen, B., Riseth, J. A., Karlsen, S. R., Solberg, B., & Høgda, K. A. (2009). Above ground biomass changes in the mountain birch forests and mountain heaths of Finnmarksvidda, northern Norway, in the period 1957–2006. Forest Ecology and Management, 257, 244257.CrossRefGoogle Scholar
Tømmervik, H., Johansen, B., Tombre, I., Thannheiser, D., Høgda, K. A., Gaare, E. & Wielgolaski, F. E. (2004). Vegetation changes in the Nordic mountain birch forest: the influence of grazing and climate change. Arctic, Antarctic and Alpine Research, 36, 323332.CrossRefGoogle Scholar
Turi, E. I., & Keskitalo, E. C. H. (2014). Governing reindeer husbandry in western Finnmark: Barriers for incorporating traditional knowledge in local-level policy implementation. Polar Geography, 37(3), 234251.Google Scholar
Turunen, M., Rasmus, S., Bavay, M., Ruosteenoja, K., & Heiskanen, J. (2016). Coping with increasingly difficult weather and snow conditions: Reindeer herders’ views on climate change impacts and coping strategies. Climate Risk Management, 11, 1536.CrossRefGoogle Scholar
Uboni, A., Horstkotte, T., Kaarlejärvi, E., Sévêque, A., Stammler, F., Olofsson, J., … Moen, J. (2016). Long-Term trends and role of climate in the population dynamics of Eurasian Reindeer. PLoS ONE, 11(6), e0158359. doi: 10.1371/journal.pone.0158359 CrossRefGoogle ScholarPubMed
Uhlig, C., & Zink, A. (2006). Changes in organic horizon soil properties due to reindeer herding and changing management. In Forbes, B. C., Bölter, M., Müller-Wille, L., Hukkinen, J., Müller, F., Gunslay, N., & Konstantinov, Y. (Eds.), Reindeer Management in Northernmost Europe: Linking Practical and Scientific Knowledge in Social-Ecological Systems (Ecological Studies 184) (pp. 245264). Berlin: Springer.CrossRefGoogle Scholar
Väisänen, M., Ylänne, H., Kaarlejärvi, E., Sjögersten, S., Olofsson, J., Crout, N., & Stark, S. (2014). Consequences of warming on tundra carbon balance determined by reindeer grazing history. Nature Climate Change, 4, 384388. doi: 10.1038/NCLIMATE2147 CrossRefGoogle Scholar
Veijola, P. (1998). Suomen metsärajametsien käyttö ja suojelu (Use and conservation of the tree line forests in Finland). Finnish Forest Research Institute, Research Papers 692, Helsinki, Finland.Google Scholar
Vikhamar-Schuler, D., Hanssen-Bauer, I., & Førland, E. (2010). Long-term climate trends of Finnmarksvidda, Northern-Norway. Norwegian Meteorological Institute, Report 6, Oslo, Norway.Google Scholar
Vikhamar-Schuler, D., Isaksen, K., Haugen, J. E., Tømmervik, H., Luks, B., Schuler, T. V., & Bjerke, J. W. (2016). Changes in winter warming events in the Nordic Arctic Region. Journal of Climate, 29, 62236244.CrossRefGoogle Scholar
Virtanen, R. (2000). Effects of grazing on above-ground biomass on a mountain snowbed, NW Finland. Oikos, 90(2), 295300.CrossRefGoogle Scholar
Vowles, T., Lovehav, C., Molau, U., & Björk, R. (2017). Contrasting impacts of reindeer grazing in two tundra grasslands. Environmental Research Letters, 12(3), 34018.CrossRefGoogle Scholar
Vuojala-Magga, T. (2012). Adaptation of Sámi reindeer herding: EU regulation and climate change. In Tennberg, M. (Eds.), Governing the Uncertain: Adaptation and Climate Change in Russia and Finland (pp. 101122). Dortrecht, Hedelberg, London, NY: Springer.CrossRefGoogle Scholar
Vuojala-Magga, T., & Turunen, M. (2015). Sámi reindeer herders’ perspective on herbivory of subarctic mountain birch forests by geometrid moths and reindeer: a case study from northernmost Finland. SpringerPlus, 4, 134. doi: 10.1186/s40064-015-0921-y CrossRefGoogle ScholarPubMed
Vuojala-Magga, T., Turunen, M., Ryyppö, T., & Tennberg, M. (2011). Resonance strategies of Sami reindeer herding during climatically extreme years in northernmost Finland in 1970–2007. Arctic, 64(2), 227241.Google Scholar
Walker, M. D., Wahren, C. H., Hollister, R. D., Henry, G. H. R., Ahlquist, L. E., Alatalo, J. M., … Wookey, P. A. (2006). Plant community responses to experimental warming across the tundra biome. Proceedings of the National Academy of Sciences of the USA 103, 13421346. doi: 10.1073/pnas.0503198103 CrossRefGoogle ScholarPubMed
Weladji, R. B., Holand, Ø., & Almøy, T. (2003). Use of climatic data to assess the effect of insect harassment on the autumn weight of reindeer (Rangifer tarandus) calves. Journal of Zoology, 260, 7985. doi: 10.1017/S0952836903003510 CrossRefGoogle Scholar
Wielgolaski, F.E. (2002). Nordic mountain birch forest. In Kankaanpää, S., Müller-Wille, L., Susiluoto, P., & Sutinen, M.-L. (Eds.), Northern Timberline Forests: Environmental and Socio-Economic Issues and Concerns (Finnish Forest Research Institute, Research papers 862) (pp. 7690). Helsinki: Finnish Forest Research Institute.Google Scholar
Figure 0

Fig. 1. Northern Fennoscandia and Sápmi (dashed line, Lehtola, 2002). Research communities of Máze, Guovdageaidnu and Gáregasnjárga are marked, and the solid black lines mark the herding districts of the communities (Guovdajohtolat in Norway and Báišduottar in Finland). The mountain birch ecoregion of northern Fennoscandia is shaded in the map. Area used by reindeer stretches also south, outside Sápmi (Johansen unpublished; Käyhkö & Horstkotte, 2017). White squares mark the meteorological stations of Guovdageaidnu, Suolovuopmi and Kárášjohka (Karasjok).

Figure 1

Fig. 2. Mountain birch forest before an autumnal moth outbreak without (a) and with (b) intensive reindeer herbivory, and after the outbreak (c). Photos: Otso Suominen.

Figure 2

Table 1. Characteristics and mean climate conditions1 of the research communities

Figure 3

Table 2. Comparison of herders’ knowledge and scientific knowledge concerning the changes in weather during the last decades in the research area

Figure 4

Table 3. The effects of climate change during the year on the quality of the pastures and working conditions of herders as revealed by the interviews

Figure 5

Table 4. Comparison of herders’ knowledge and scientific knowledge concerning the changes in the vegetation cover in the research area