Browse Subject Areas

Click through the PLOS taxonomy to find articles in your field.

For more information about PLOS Subject Areas, click here.

  • Loading metrics

Sparse trees and shrubs confers a high biodiversity to pastures: Case study on spiders from Transylvania

  • Róbert Gallé ,

    Contributed equally to this work with: Róbert Gallé, István Urák

    Roles Conceptualization, Formal analysis, Investigation, Methodology, Writing – original draft, Writing – review & editing

    Affiliation Department of Ecology, University of Szeged, Szeged, Hungary


  • István Urák ,

    Contributed equally to this work with: Róbert Gallé, István Urák

    Roles Conceptualization, Investigation, Resources, Writing – original draft, Writing – review & editing

    Affiliation Ecosystem Services Laboratory, Department of Environmental Sciences—Sapientia Hungarian University of Transylvania, Cluj-Napoca, Romania

  • Gallé-Szpisjak Nikolett,

    Roles Investigation, Visualization

    Affiliation Department of Ecology, University of Szeged, Szeged, Hungary

  • Tibor Hartel

    Roles Conceptualization, Formal analysis, Funding acquisition, Investigation, Methodology, Writing – original draft, Writing – review & editing

    Affiliations Ecosystem Services Laboratory, Department of Environmental Sciences—Sapientia Hungarian University of Transylvania, Cluj-Napoca, Romania, Department of Taxonomy and Ecology, Faculty of Biology, Babes-Bolyai University, Cluj-Napoca, Romania

Sparse trees and shrubs confers a high biodiversity to pastures: Case study on spiders from Transylvania

  • Róbert Gallé, 
  • István Urák, 
  • Gallé-Szpisjak Nikolett, 
  • Tibor Hartel


The integration of food production and biodiversity conservation represents a key challenge for sustainability. Several studies suggest that even small structural elements in the landscape can make a substantial contribution to the overall biodiversity value of the agricultural landscapes. Pastures can have high biodiversity potential. However, their intensive and monofunctional use typically erodes its natural capital, including biodiversity. Here we address the ecological value of fine scale structural elements represented by sparsely scattered trees and shrubs for the spider communities in a moderately intensively grazed pasture in Transylvania, Eastern Europe. The pasture was grazed with sheep, cattle and buffalo (ca 1 Livestock Unit ha-1) and no chemical fertilizers were applied. Sampling sites covered the open pasture as well as the existing fine-scale heterogeneity created by scattered trees and shrub. 40 sampling locations each being represented by three 1 m2 quadrats were situated in a stratified design while assuring spatial independency of sampling locations. We identified 140 species of spiders, out of which 18 were red listed and four were new for the Romanian fauna. Spider species assemblages of open pasture, scattered trees, trees and shrubs and the forest edge were statistically distinct. Our study shows that sparsely scattered mature woody vegetation and shrubs substantially increases the ecological value of managed pastures. The structural complexity provided by scattered trees and shrubs makes possible the co-occurrence of high spider diversity with a moderately high intensity grazing possible in this wood-pasture. Our results are in line with recent empirical research showing that sparse trees and shrubs increases the biodiversity potential of pastures managed for commodity production.


The integration of commodity production and biodiversity conservation in agricultural landscapes is an increasing challenge for sustainability [1]. Traditional farming landscapes are especially important in meeting this challenge because these landscapes have exceptional ecological values and evolved as commodity (food, timber, vine) production landscapes [2], [3], [4]. Within this context, traditionally managed pastures with small natural features such as the sparse trees and shrubs are considered archetypes of traditional landscapes with high natural and cultural values in Europe [5]. Sparse mature trees and shrubs provided several benefits for the local farmer communities including shadow for livestock, fruits, halting soil erosion and cultural-aesthetic values (overviewed e.g. in [6]). Besides their important socio-economic roles, scattered trees are considered keystone habitat structures [7], [8]. Solitary trees on pastures significantly increased the overall diversity of lichens [9], vascular plants and bryophytes [10]. Sparse trees are important breeding sites for birds [11], [12] and they may also harbor a great invertebrate diversity [13], [14]. Trees create a distinct microclimatic conditions on grasslands and this results in distinct arthropod species assemblages, including several rare species [15], [16], [17]. Despite their several ecological and socioeconomic values, the sparse woody vegetation from pastures is seriously threatened because the current formal institutions (e.g. the Common Agricultural Policy (CAP) and the national level institutions) does not explicitly recognize their multiple values and potentials [16]. CAP negatively affects sparse trees on pastures mainly through the lack of explicit recognition of their socio-economic values, lack of incentives to farmers to regenerate them and their removal when these trees are perceived as ‘damaged’ (e.g. hollowing) [18]. Without an explicit policy recognition and support, sparsely scattered trees are going to disappear from pastures [5]. The removal of sparse trees from pastures will have substantial impact on the overall biodiversity, adaptive potential and ecological resilience of these commodity production landscapes [6]. The main goal of this contribution is to document the ecological importance of sparse trees and shrubs for the overall pasture biodiversity in a moderately intensively grazed pasture from (Transylvania, Romania).

Spiders are abundant invertebrate predators in several terrestrial ecosystems and their taxonomy together with their life histories are relatively well-known [19]. Spiders respond to structural changes in vegetation, soil moisture and shade even in very small spatial scales [20], [21], [22]. The importance of fine-scale habitat heterogeneity created by woody vegetation for spider species assemblages was explored by several studies in Europe. These studies targeted a wide range of ecosystems including riparian areas e.g. [23], [24], dry steppe woodlands e.g. [25], subalpine forests e.g. [26], [27], mature forests e.g. [28], coppice forests e.g. [29], retention trees on clear-cuts e.g. [30] or the Mediterranean regions e.g. [31]. To the best of our knowledge, traditional pastoral systems such are those from Eastern Europe are still not explored regarding the importance of sparse trees on pastures to spider communities. In order to fill this knowledge gap, we selected a lowland area within a highly productive region of Transylvania (Romania), which was managed by grazing since historical times (see below). Agricultural production is typically intensified in such landscapes when modern technology becomes available and as a result, sparse trees are likely to be removed [32]. The aim of the present study was to assess the importance of scattered trees in an open grazed landscape for spider communities. More specifically, we hypothesized that sparsely scattered trees and shrubs creates distinct spider species assemblages compared to the pasture surfaces without these structural elements and thus confers a high beta diversity value for the grazed system.

Materials and methods

Study area and methods

The description of the pasture and its management.

The studied pasture was situated in the Transylvanian region of Romania at an altitude of ca 430 m (central coordinates: Lat: 46.9198°; Long: 23.5053°). The surface area of the pasture was ca 250 hectare (see Fig 1 for map). The study site was situated within the continental biogeographic region. The temporal continuity of livestock grazing in the study area covered at least two centuries. This area was visualized as semi-open landscape in the 18th century Josephine maps and historical descriptions of woodland management in Transylvania e.g. [33] suggests that these landscapes were grazed either with pig or by cattle.

Fig 1. Species accumulation curves for the four habitat types of the studies wood-pasture.

Gray shades represent 95% confidence intervals.

The current physiognomy of the pasture is presented in S1 Fig. The pasture contains sparse trees, in an overall density of ca 1 tree per hectare. This physiognomy emerged likely in the end of the 19th–early 20th century, when several woodlands were opened and transformed in open pastures while sparsely scattered trees were maintained for shadow and/or fruits [33]. At the eastern part, the pasture is bordered by a high oak forest managed for timber production where grazing is prohibited. The sparse trees on the studied pasture were represented mainly by mature oak (Quercus robur and Q. cerris in equal proportion) while shrubs were represented by Prunus. sp, Rosa. sp and Crataegus sp. During the period of our study the pasture was grazed by sheep, cattle and buffalo with an overall ca 0.93–1.1 livestock unit per hectare (local shepherds, personal communication), this grazing management being applied for at least four consecutive years. No chemical fertilizers were applied to this pasture at least for the past 50 years (shepherds and locals, personal communication). While the cattle and buffalo were allowed on the pasture typically in the period of May-November, the sheep grazing occurs through the whole year (local shepherds, personal communication, and author’s personal observation).

Sampling design and procedure.

In order to assess the ecological importance of sparsely scattered trees on the grazed pasture, we placed 40 sampling sites were across the pasture, each site consisting from three square meter plots situated in a triangle, with 4–5 m distance between them. In the case of forest edge (see below) the three plots were situated in a linear way along the edge of the forest.

When selecting the sites we considered the following aspects: (i) To capture the existing structural gradients represented by woody vegetation across the pasture. In this way we ended up in studying four habitat types, which are presented below. (ii) To assure an even distribution of the sampling sites across the studied pasture surface and (iii) To assure that the neighboring sampling locations are distant enough to consider them ‘independent’ sampling units (see below). The distance between the neighboring sampling sites was set to at least 110 m (mean ± SD = 149.8 ± 33.4 m) in order to assure their spatial independence. We distributed the sampling sites across the pasture to cover the main structural (and grazing) gradients ranging from pasture surfaces without any tree and shrub to pasture surfaces with sparse trees and shrubs. These are detailed in the following. (i) The open pasture surfaces contained no woody vegetation. These sites were dominated by Agrostis capillaris and Festuca stricta. Based on the personal communication of shepherds, these pasture surfaces contained no woody vegetation for at least two decades and were continuously grazed. (ii) Scattered open grown mature oak trees. The tree sampling plots for this habitat were situated under the tree canopy positioned in a triangle around the trunk of the tree. The girth of the trees in the sampling sites was ranging between 2 and 3 m trunk circumference measured at cca 130 cm height (iii) Sparse trees with shrubs under their canopy, with the dominant shrubs Prunus sp., Rosa sp. and Crataegus sp. We considered ‘shrubs’ as present when we found a substantial coverage of shrub of at least 50 cm height under the tree canopy and/or in the very close vicinity (i.e. at least up to cca 2–3 m distance from the crown) of the tree. Shrubs typically develop in pastures from this region as a result of the decreasing grazing intensity. Indeed, the grazing intensity in Transylvania decreased with the overall abandonment of the farming landscape management in the decade following the collapse of the communism (i.e. 1989) [34] (iv) Forest edges with the herbaceous vegetation characterized by several forest and edge specialist plant species. Since the forest edges was regularly used as shading place by sheep, the forest-pasture transition (i.e. the ‘ecotone’) was abrupt, shrubs being only scarcely developed along the forest edge. In the following we refer to the above four structural elements as ‘habitat types’. Ten sites were selected in each of the four habitat types. The distance to the closest forest did not differ significantly between open pasture, scattered oak, tree and shrub sites (ANOVA, F = 1.298, p = 0.29), hence we assume that the variation in the spider communities detected in our study did was not related to the distance of the site from the forest. No autocorrelation of the spider fauna was detected by the mantel test between the Bray-Curtis dissimilarity matrix of spiders and the Euclidian distance between sampling sites (Mantel z = 4.693, p = 0.473).

The description of the habitat types was performed on 7–9 June in 2015 before the start of the spider sampling. We described each habitat type with four structural variables. Each of these variables were quantified in the 1m2 square plots which formed a sampling site (see above). These variables were: (i) Average herbaceous vegetation height: the height of the vegetation in cm, measured in three random points; the average value of these measurements were used for each site (ii) Herbaceous vegetation cover: the average percentage of vegetation cover. (iii) Liter coverage: the leaf litter coverage, estimated visually by three persons. (iv) Bare ground coverage: the percentage of bare ground, estimated visually by three persons and averaged. The variables characterizing the sampling sites were presented using descriptive statistics: average, 95% confidence intervals (Table 1).

Table 1. Descriptive characteristics of the vegetation cover of the habitat types.

Spiders were collected in middle of May (two consecutive days: 12 and 13) and early June (three consecutive days (07–09) in 2015 using a ‘D-vac’ suction sampler. Spiders were collected only from the herbaceous vegetation; no sampling occurred from the canopy of shrubs and trees. The ‘D-vac’ head was placed near the ground in order to increase efficiency in sampling the ground dwelling spiders. Spiders caught with suction sampling were placed in 70% alcohol-water solution and adult specimens were identified to species level in the laboratory.

Data analysis

The effect of habitat type on species richness of spider species of conservation interest were tested with general linear model (GLM) with Poisson error term and log-link function. We tested the effect of habitat type on abundance of spider species of conservation interest with negative binomial GLM with logit link function, followed by the Tukey type pairwise comparisons using the glht function with p<0.05 from the multcomp library [35]. We computed species accumulation curves on the basis of pooled individual-based abundance data for open pasture, scattered oak, forest edge and tree and shrub sites to compare the species richness of spiders [iNEXT package, 36]. We also estimated the number of species and Shannon diversity for the pooled data of each habitat type with the ChaoRichness and ChaoShannon functions, iNEXT package [36].

The multivariate response of spider communities to habitat type was studied with Non-metric Multidimensional Scaling (NMDS) on the basis of Bray-Curtis dissimilarity matrix. We pooled the data from the two collection dates and the three samples per site for this analysis. A Hellinger transformation was applied to the data prior to the ordination [37]. The abundance of each trait was fitted passively onto the NMDS ordination plot and the correlation between the species traits and habitat types (see above) was tested by 5000 Monte-Carlo permutations [38] and traits with significant correlation (p<0.05) were displayed on NMDS plot. Analysis of Similarities (ANOSIM) with 5000 permutations was performed to test the difference among the four habitat types based on Bray-Curtis dissimilarity matrices. ANOSIM is a multivariate analysis of variance that uses dissimilarity between pairs of samples [39]. We considered each site as a replicate, we summed abundances of each species over three plots and two sampling periods. All habitats were compared by pairs to test whether there is a significant difference among them (ANOSIM, Bray-Curtis dissimilarity; 5000 permutations followed by a Bonferroni-Holm adjustment of P-values).


Characterizing the four habitat types

The average height of the herbaceous vegetation across the four habitat types varied very narrowly between 10 and 12 cm (Table 1). The herbaceous vegetation cover was highest as expected in the open pasture habitat (99%) and lowest (64%) in the forest edge (Table 1). The coverage of bare ground was highest on the forest edges (12%) while in the other three habitat types was below 5% (Table 1). Finally, the litter cover was highest in the forest edges (31%) followed by tree and shrub habitat (17%) and scattered tree habitat (5%), while the open pasture habitat had no litter (Table 1).

Spider fauna

We collected 2697 spider specimens (1461 adults), belonging to 140 species from 21 families (S1 Table). Two species of spiders were new for the Romanian fauna (Synageles subcingulatus, one specimen at scattered tree habitat and Talavera parvistyla one specimen at tree and shrub habitat). Two species (Dipoena erythropus, two individuals identified from open pasture and scattered tree sites habitats and Philodromus praedatus, two individuals from open pasture and forest edge habitats) with uncertain presence for the Romanian fauna were confirmed by the present study. We found 25 species of spiders which are considered rare (Table 2). These species are typically considered as preferring ‘climax’, ‘non-disturbed’ and ‘natural habitats’ in Europe e.g. [40], [41][42]. We found no significant effect of habitat type on species richness of rare species according to the Poisson GLM and the following pairwise comparisons. However sparse trees with shrubs had significantly higher abundance of rare species than scattered oaks (z = 3.213, p = 0.006).

Table 2. Abundances of species of conservation interest.

Species and categories according to [41] and [42].

Spider communities

Tree and shrub sites had the highest spider species richness (19.3, 95% confidence interval [CI]: 16.3–22.2) followed by forest edge (17.3, 95% CI, 13.8–20.7), scattered tree (14.5 95% CI, 12.1–16.8) and open pasture (12.8, 95% CI, 9.58–16.01) habitats. The number of spider species detected exclusively in the open pasture habitat was seven (representing 16% of the species found in this habitat type), while for the scattered tree habitat this value was eight (13%), for tree and shrub 25 (32%) and for forest edge 25 (30%). The estimated species richness Shannon diversity and species accumulation curves also detected lower diversity of open pasture sites compared to sampling sites with woody vegetation (Table 3, Fig 1).

Table 3. Estimated species richness and Shannon diversity of the four habitat types.

Mean values and 95% confidence intervals are given.

Ordination by NMDS indicated a clear separation of species composition among the habitat types with relatively small overlap between the polygons grouping the four habitat types (Fig 2). The ANOSIM statistic highlighted significant difference among the four habitat types (R = 0.611, P<0.001). Furthermore, the subsequent comparison of habitat types showed significant differences in spider community structure between all pairs of habitat types (ANOSIM, Padjusted<0.01).

Fig 2. Non-metric multidimensional scaling of spider species assemblages of the four habitat types studied.

Open circles represent the sampling sites. Stress: 0.201.


We explored the importance of fine-scale heterogeneity for spider assemblages in a moderately intensively grazed pasture from Eastern-Europe). We highlight a remarkably high number of spider species in the studied pasture, which also includes four previously unknown species for Romania and several species which are considered rare in Europe. Fine-scale structural elements represented by sparse trees and shrubs had significant influence on the spider species assemblages from the ground and low vegetation.

Our results showed that small natural features such as the sparsely scattered trees and shrubs confers a high biodiversity value–as measured through spider communities—for managed pastures, this is in line with several studies investigating the effect of sparsely scattered trees on Arthropods (Table 4). Scattered trees with shrubs had higher spider species richness than the other three habitat types but each of the four habitat type contributed to the beta diversity of the studied pasture through statistically distinct spider community assemblages. The high potential of the scattered trees on pastures for spiders of conservation interest is also highlighted by the fact that we identified new species for the Romanian spider fauna under the canopy of these trees. Solitary trees had different spider species assemblages than the surrounding open landscape in the alpine timberline [42] while open-grown tree canopies harbored high number of spider species and high of conservation value assemblages in a lowland area from Czech Republic [15].

Table 4. Examples of studies investigating the effect of solitary large old trees and shrubs on different Arthropod taxa.

Sparse trees and shrubs on pastures results in a substantial improvement of the ecological conditions of the pasture by creating habitat niches for several species of spiders. Several of these species may have high conservation status (see Results). This result was surprising and unexpected, since the studied pasture was relatively intensively managed by livestock grazing. In this respect, our results suggest that the pasture with sparse trees grazed by livestock may act as ‘wild’ landscape for several species of spiders.

The statistical differentiation of the spider species assemblages in the four habitat types was possible due to the ‘unique’ spider species which were associated to specific habitats (see Results).

Vegetation structure, shading and microclimate are considered major divers of spider community structure [22]. Scattered trees provide shade and moist and intercept direct radiation and precipitation [54], [55]. Significant litter accumulation under scattered trees provides habitat and food resources for several invertebrate decomposers which may act as prey items for spiders [56], [57]. Soil nutrient levels under oaks are enhanced by livestock excrement [7] while trampling by livestock represent disturbance; this results in distinct herbaceous plant and insect herbivore species communities which in turn also affects spider communities in these habitats (see our results).

Sparse woody vegetation is of crucial importance for the overall biodiversity of pastures [7], [8], [11], [12] (Table 4) and contributes to the soil fertility [14]. Still, this vegetation elements are not explicitly recognized by major policies and institutions responsible for the governance of the management of the pastoral systems [18]. Sparse trees are typically disfavored both by agricultural policies (either by the Common Agricultural Policy, and the national level agricultural policies) and the forestry policies. This situation resulted in the decline of treed pastures all over Europe [5], [58]. We showed that sparse woody vegetation can bring substantial contribution to the biodiversity of pastures. Hence it is of utmost importance to harmonize various policies relevant for the sustainability of these pasture ecosystems e.g. [5], [18], [59]. Pastures with sparse trees may well integrate food production and biodiversity conservation; our study suggest that the biodiversity and structural properties of these pastures are tightly linked.

Supporting information

S1 Fig. The map of the studied pasture with the four habitat types sampled.

The physiognomy of the pasture and typical pictures representing the sampled habitats are also shown.


S1 Table. List of collected species spider species and number of individuals collected in the wood-pasture with and without arboreal and shrub vegetation in Transylvania in May and June 2015.

Significant indicator values (IndVal, Dufrêne & Legendre, 1997) are indicated with stars (p<0.05).



TH received funding from the European Community’s Seventh Framework Programme under Grant Agreement No. 613520 (Project AGFORWARD, 2014-present).


  1. 1. Fischer J, Abson DJ, Butsic V, Chappell MJ, Ekroos J, Hanspach J, et al. Land Sparing Versus Land Sharing: Moving Forward Conserv Lett. 2014;7:149–157.
  2. 2. Halada L, Evans D, Romão C, Petersen J-E. Which habitats of European importance depend on agricultural practices? Biodivers Conserv. 2011;20: 2365–2378.
  3. 3. Wright HL, Lake IR, Dolman PM. Agriculture—a key element for conservation in the developing world. Conserv Lett. 2011;5: 11–19.
  4. 4. Košulič O, Michalko R, Hula V. Recent artificial vineyard terraces as a refuge for rare and endangered spiders in a modern agricultural landscape. Ecol Eng. 2014;68: 133–142.
  5. 5. Plieninger T, Hartel T, Martín-López B, Beaufoy G, Bergmeier E, Kirby K, et al. Wood-pastures of Europe: Geographic coverage, social-ecological values, conservation management, and policy implications. Biol Conserv. 2015 190: 70–79.
  6. 6. Hartel T, Plieninger T. European wood-pastures in transition: A social-ecological approach. London and New York: Earthscan from Routledge, 2014.
  7. 7. Manning AD, Fischer J, Lindenmayer DB. Scattered trees are keystone structures–implications for conservation. Biol Conserv. 2006;132: 311–321.
  8. 8. Lindenmayer DB. Conserving large old trees as small natural features. Biol Conserv. 2017;
  9. 9. Paltto H, Nordberg A, Nordén B, Snäll T Development of secondary woodland in oak wood pastures reduces the richness of rare epiphytic lichens. PLoS ONE 2011;6, e24675. pmid:21961041
  10. 10. Kiebacher T, Scheidegger C, Bergamini A. Solitary trees increase the diversity of vascular plants and bryophytes in pastures. Agr Ecosyst Environ. 2017;239: 293–303.
  11. 11. Hartel T, Hanspach J, Abson DJ, Máthé O, Moga CI, Fischer J. Bird communities in traditional wood-pastures with changing management in Eastern Europe. Basic Appl Ecol. 2014;15: 385–395.
  12. 12. Jakobsson S, Lindborg R. The importance of trees for woody pasture bird diversity and effects of the EU tree density policy. J Appl Ecol. 2017;
  13. 13. Seibold S, Bässler C, Brandl R, Büche B, Szallies A, Thorn S, et al. Microclimate and habitat heterogeneity as the major drivers of beetle diversity in dead wood. J Appl Ecol. 2016;53: 934–943.
  14. 14. García-Tejero S, Taboada Á. Microhabitat heterogeneity promotes soil fertility and ground-dwelling arthropod diversity in Mediterranean wood-pastures. Agr Ecosyst Environ. 2017;233: 192–201.
  15. 15. Lindsay EA, Cunningham SA. Livestock grazing exclusion and microhabitat variation affect invertebrates and litter decomposition rates in woodland remnants. Forest Ecol Manag. 2009;258: 178–187.
  16. 16. Taboada A, Kotze DJ, Salgado JM, Tarrega R. The influence of habitat type on the distribution of carabid beetles in traditionally managed ‘dehesa’ ecosystems in NW Spain. Entomol Fennica. 2006;17: 284–295.
  17. 17. Sebek P, Vodka S, Bogusch P, Pech P, Tropek R, Weiss M, et al. Open-grown trees as key habitats for arthropods in temperate woodlands: The diversity, composition, and conservation value of associated communities. Forest Ecol Manag. 2016;380: 172–181.
  18. 18. Beaufoy G (editor) Europe's wood-pastures: condemned to a slow death by the CAP? A test case for EU agriculture and biodiversity policy. Booklet produced for the wood-pasture policy seminar in the European Parliament, Brussels, in 17th of November, 2015. Available from:
  19. 19. Cardoso P, Pekár S, Jocqué R, Coddington JA. (2011) Global patterns of guild composition and functional diversity of spiders. PLoS ONE, 6, e21710. pmid:21738772
  20. 20. Cattin MF, Blandenier G, Banašek-Richter C, Bersier LF. The impact of mowing as a management strategy for wet meadows on spider (Araneae) communities. Biol Conserv. 2003;113: 179–188.
  21. 21. Gallé R, Erdélyi N, Szpisjak N, Tölgyesi C, Maák I. The effect of the invasive Asclepias syriaca on the ground-dwelling arthropod fauna. Biologia 2015;70, 104–112.
  22. 22. Entling W, Schmidt MH, Bacher S, Brandl R, Nentwig W. Niche properties of Central European spiders: shading, and the evolution of the habitat niche. Global Ecol Biogeogr. 2007;16: 440–448.
  23. 23. Bonn A, Hagen K, Reiche DWV. The significance of flood regimes for carabid beetle and spider communities in riparian habitats—a comparison of three major rivers in Germany. River Res Appl. 200218, 43–64.
  24. 24. Lambeets K, Hendrickx F, Vanacker S, Van Looy K, Maelfait JP, Bonte D. Assemblage structure and conservation value of spiders and carabid beetles from restored lowland river banks. Biodiver Conserv. 2008;17: 3133–3148.
  25. 25. Gallé R, Torma A. Epigeic spider (Araneae) assemblages of natural forest edges in the Kiskunság (Hungary). Community Ecol. 2009;10: 146–151.
  26. 26. Muff P, Schmidt MH, Frick H, Nentwig W, Kropf C. Spider (Arachnida: Araneae) distribution across the timberline in the Swiss Central Alps (Alp Flix, Grisons) and three morphologically remarkable species. Arachnol Mitt. 2007;34: 16–24.
  27. 27. Frick H, Nentwig W, Kropf C. Influence of stand-alone trees on epigeic spiders (Araneae) at the alpine timberline. Ann Zool Fenn. 2007;44: 43–57.
  28. 28. Hsieh YL, Linsenmair KE. Underestimated spider diversity in a temperate beech forest. Biodiver Conserv. 2011;20: 2953–2965.
  29. 29. Košulič O, Michalko R, Hula V. Impact of Canopy Openness on Spider Communities: Implications for Conservation Management of Formerly Coppiced Oak Forests. PLoS ONE, 2016;11, e0148585. pmid:26845431
  30. 30. Matveinen-Huju K, Niemelä J, Rita H, O’Hara RB. Retention-tree groups in clear-cuts: Do they constitute ‘life-boats’ for spiders and carabids? Forest Ecol Manag, 2006;230: 119–135.
  31. 31. Moreno G, Gonzalez-Bornay G, Pulido F, Lopez-Diaz ML, Bertomeu M, Juárez E, et al. Exploring the causes of high biodiversity of Iberian dehesas: the importance of wood pastures and marginal habitats. Agroforest Syst. 2016;90: 87–105.
  32. 32. Lindenmayer DB, Laurance WF. The ecology, distribution, conservation and management of large old trees. Biol Rev. 2017, pmid:27383287
  33. 33. Oroszi S. The forest management of Transylvanian Saxons. Erdészeti Egyesület. Erdészettörténeti közlemények 2004;63: 1–153, Budapest (in Hungarian).
  34. 34. Német E, Ruprecht E, Gallé R, Markó B. Abandonment of crop lands leads to different recovery patterns for ant and plant communities in Eastern Europe. Community Ecol. 2016;17: 79–87.
  35. 35. Hothorn T, Bretz F, Westfall P, Heiberger RM, Schuetzenmeister A, Scheibe S, et al. Package ‘multcomp’. Simultaneous inference in general parametric models. Project for Statistical Computing, Vienna, Austria;2016.
  36. 36. Hsieh TC, Ma KH, Chao A. iNEXT: an R package for rarefaction and extrapolation of species diversity (Hill numbers). Methods Ecol Evol. 2016;7: 1451–1456.
  37. 37. Legendre P, Gallagher ED. Ecologically meaningful transformations for ordination of species data. Oecologia. 2001;129: 271–280. pmid:28547606
  38. 38. Oksanen J, Blanchet FG, Kindt R. Vegan: community ecology package. R Package Ver 2; 2013
  39. 39. Clarke KR, Warwick RM. Change in Marine Communities: An Approach to Statistical Analysis and Interpretation, 2nd edn. Primer-E Ltd, Plymouth, UK;2001.
  40. 40. Buchar J, Ruzicka V. Catalogue of spiders of the Czech Republic. Peres, Prague; 2002.
  41. 41. Gajdoš P, Moscaliuc LA, Rozwalka R. Red list of spiders (Araneae) of the Carpathian Mts. In: Kadlečík J, editor. Draft Carpathian red list of forest habitats and of species draft Carpathian list of invasive alien species, Štátna ochrana prírody Slovenskej republiky, [State Nature Conservancy of the Slovak Republic]. Banská Bystrica, 2014. pp. 118–170.
  42. 42. Řezáč M, Kůrka A, Růžička V, Heneberg P. Red List of Czech spiders: adjusted according to evidence-based national conservation priorities. Biologia 2015;70: 645–666.
  43. 43. Ranius T, Wilander P. Occurrence of Larca lata HJ Hansen (Pseudoscorpionida: Garypidae) and Allochernes wideri CL Koch (Pseudoscorpionida: Chernetidae) in tree hollows in relation to habitat quality and density. J Insect Conserv. 2000;4: 23–31.
  44. 44. Rossetti I, Bagella S, Cappai C, Caria MC, Lai R, Roggero PP. Isolated cork oak trees affect soil properties and biodiversity in a Mediterranean wooded grassland. Agr Ecosyst Environ. 2015;202: 203–216.
  45. 45. García-Tejero S, Taboada Á. Microhabitat heterogeneity promotes soil fertility and ground-dwelling arthropod diversity in Mediterranean wood-pastures. Agr Ecosyst Environ. 2016;233: 192–201.
  46. 46. Galante E, Garcia-Roman M, Barrera I, Galindo P. Comparison of spatial distribution patterns of dung-feeding scarabs (Coleoptera: Scarabaeidae, Geotrupidae) in wooded and open pastureland in the Mediterranean ‘‘Dehesa” area of the Iberian Peninsula. Environ Entomol. 1991;20: 90–97.
  47. 47. Galante E, Mena J, Lumbreras C. Dung beetles attracted (Coleoptera, Scarabaeidae, Geotrupidae) to fresh cattle dung in wooded and open pastures. Environ Entomol. 1995;24: 1063–1068.
  48. 48. Taboada A, Kotze J, Tarrega R, Salgado J. Traditional forest management: do carabid beetles respond to human-created vegetation structures in an oak mosaic landscape? For Ecol Manage. 2006; 237: 443–449.
  49. 49. Falk S. Wood-pastures as reservoirs for invertebrates. In Hartel T, Plineninger T, editors. European wood-pastures in transition: A social-ecological approach. Taylor and Francis, London and New York; 2014. pp. 132–148.
  50. 50. Torres-Vila LM. Reproductive biology of the great capricorn beetle, Cerambyx cerdo (Coleoptera: Cerambycidae): a protected but occasionally harmful species. Bull Entomol Res. 2017; pmid:28397625
  51. 51. Reyes-Lopez J, Ruiz N, Fernandez-Haeger J. Community structure of ground-ants: the role of single trees in a Mediterranean pastureland Acta Oecol. 2003;24: 195–202.
  52. 52. Freese A, Benes J, Bolz R, Cizek O, Dolek M, Geyer A, et al. Habitat use of the endangered butterfly Euphydryas maturna and forestry in Central Europe. Anim Conserv. 2006;9; 388–397.
  53. 53. Sutcliffe L, Öllerer K, Roellig M. 2014 Wood-pasture management in southern Transylvania (Romania). European Wood-pastures in Transition: A Social-ecological Approach. Taylor and Francis, London and New York, 2014 pp. 219–234.
  54. 54. Muff P, Kropf C, Frick H, Nentwig W, Schmidt-Entling MH. Co‐existence of divergent communities at natural boundaries: spider (Arachnida: Araneae) diversity across an alpine timberline. Insect Conserv Diver. 2009;2: 36–44.
  55. 55. Mistry J. Savannas. Progress in Physical Geography, 2000;24, 601–608.
  56. 56. Heisler GM, Grant RH, Gao W. Individual-and scattered-tree influences on ultraviolet irradiance. Agr Forest Meteorol. 2003;120: 113–126.
  57. 57. Mcelhinny C, Lowson C, Schneemann B, Pachon C. Variation in litter under individual tree crowns: Implications for scattered tree ecosystems. Austral Ecol. 2010;35: 87–95.
  58. 58. Hartel T, Plieninger T, Varga A. Wood-pastures of Europe. In Kirby K, Watkins C, editors. Europe’s changing woods and forests: from wildwood to managed landscapes. CABI Press, Oxfordshire, UK;2015. pp. 61–76.
  59. 59. Bergmeier E, Petermann J, Schröder E. Geobotanical survey of wood-pasture habitats in Europe: diversity, threats and conservation. Biodiver Conserv. 2010;19: 2995–3014.