The Structure of Saproxylic Beetle Assemblages in View of Coarse Woody Debris Resources in Pine Stands of Western Poland

: Background: Resources of dying and dead trees, decaying fragments of stems, stumps and branches, i.e., coarse woody debris (CWD), are an important structural element of biocenoses and are drivers of biodiversity. The aim of this study was to describe assemblages of saproxylic beetles in pine stands of western Poland in view of dead wood resources. We present faunistic (species identity) and quantitative (species and individual counts) data from two types of stands: 1. unmanaged pine stands, in which no trees have been extracted for over 30 years, with processes connected with tree dying and self-thinning of stands being undisturbed, 2. managed pine stands, in which routine tending operations extracting trees are performed in accordance with forest management plans and naturally dying trees are removed in the course of tending and sanitary logging; Methods: Beetles were captured in the years 2013–2014 using window ﬂight traps. Assemblages of saproxylic beetles were assessed based on the indices of dominance, diversity (the Shannon–Weiner index), and species richness (Margalef’s index) as well as the estimated habitat ﬁdelity index, feeding habits, and zoogeo-graphical distribution. Similarity between the assemblages was evaluated applying cluster analysis. Dependence between dead wood resources and the diversity and species richness indices were analysed; Results: A total of 2006 individuals classiﬁed to 216 species were captured. Assemblages show considerable similarity on the local scale. Higher values of species diversity indicators were observed in unmanaged stands, in which no sanitation cuttings are performed; Conclusions: The decision to refrain from sanitation logging in pine monocultures results in increased CWD resources, which nevertheless does not lead to a marked increase in the values of biodiversity indicators. Unmanaged stands were characterised by a high share of zoophagous, mycetophagous, and saproxylic species. In contrast, managed stands were characterised by a high share of xylophagous beetles.


Introduction
The present-day European forest management system is considered to be multifunctional (serving social, economic, and ecological functions) and sustainable [1]. A major objective of such a management is to preserve biodiversity. Forest habitats in Central Europe are characterised by high species diversity (with approx. 65% plant and animal species being forest species) [2,3]. Factors threatening species diversity include increased timber harvesting combined with reduced rotation, promotion of fast-growing species significant differences in saproxylic beetle assemblages between hurricane-damaged stands cleared after the hurricane and unaffected managed stands. The rapid accumulation of dead wood resources resulted in an increase in the number of individuals and the concentration of some species on the local scale, although it did not affect the number of species.
Pine coniferous forests were also investigated in areas of high nature value with the aim of finding model patterns. Examples in this respect include the Kampinos Forest [51] and the Białowieża Forest, in which the structure of subcorticular beetle assemblages was analysed [11,52] as a tool in the assessment of anthropogenic transformations of primeval forest habitats. In pine coniferous forests of the Białowieża Forest, observations were also made on the impact of fire on alfa and gamma diversity of beetles [53]. In the initial period of habitat regeneration, the diversity indices were higher for the fire-affected stand; however, in the successive years of observations the differences between the stand destroyed by the fire and the control stand were disappearing.
The aim of this study was to identify dependencies between CWD resources and characteristics of assemblages of saproxylic and subcorticular beetles in lowland pine stands differing in the management system (unmanaged vs. managed), determining dead wood resources.

Materials and Methods
Investigations were conducted in the years 2013-2014 in central-western Poland in terms of its landscape representing the North European Plain (Figure 1).
The objects of the study included stands of similar valuation parameters, such as age and species composition, but differing in intensity of snag removal, based on which it was divided into two categories: A. unmanaged stands, originally commercial forests, with established protection functions, such as, e.g., landscape, water, or soil protection), in which no logging operations have been conducted for over 30 years and in which tree dieback and self-thinning processes have been undisturbed. They are permanent experimental sites of the Department of Silviculture, PULS, in the Torzym and Gubin Forest Districts [54,55] as well as a stand in the Drawieński National Park subjected to the same principles.
B. managed stands, in which routine tending operations (logging) are performed in accordance with the forest management plan, and naturally dying trees are removed in the course of tending operations and sanitation cuttings.
In these experimental sites, CWD resources were measured, stand dynamics trends were assessed, beetles and saproxylic fungi were inventoried [57,58], and losses of benefits due to the allocation of wood to decompose naturally were estimated [59] (Table 1).
Mean volume in unmanaged stands was 356.7 m 3 /ha, at the mean volume of dead wood (CWD) of 12.99 m 3 /ha, the percentage share of dead wood in relation to growing stock was 3.63%. In managed stands the mean volume was higher and amounted to 389 m 3 /ha, while values of the other parameters were approx. 3-fold lower; the mean volume of dead wood was 4.04 m 3 /ha and the share of dead wood in relation to growing stock was 1.05%.
Identification of species diversity in Coleoptera. Insects were captured with window flight traps commonly used in inventorying saproxylic beetles in Poland and considered to be highly effective [10,50,[60][61][62]. Two traps of 3800 cm 2 were hung in each of the experimental sites using for this purpose dying trees, windsnaps as well as broken branches and parts of the crown lying on the ground. Beetle capture operations were conducted from 23 April 2013 to 15 November 2014. Window flight traps were operating for a total of 1692 trap-days (the number of days of trap operation × the number of traps).
The beetles for determination were prepared using techniques recommended for individual families (e.g., with separation of mating apparats). The available keys and guides for family and species identification as well as taxonomic revisions of selected groups of beetles were used for the determinations. It was used for this, among others: series of keys for determination of beetles in Poland for example [63][64][65] and Central Europe [66,67], taxonomic monographs of beetle families [68][69][70]. The markings were verified using illustrated keys and beetle iconography [71,72]. The specimens are deposited in the authors' collections at the Department of Forest Entomology and Pathology, Poznan University of Life Sciences, Poland. In these experimental sites, CWD resources were measured, stand dynamics trends were assessed, beetles and saproxylic fungi were inventoried [57,58], and losses of benefits due to the allocation of wood to decompose naturally were estimated [59] (Table 1). Results of capture operations from individual stands were totalled, distinguishing beetle assemblages, which were assessed based on such parameters as the number of species (S), the number of individuals (n), Margalef's index (d-species richness) [73], Shannon's index (H'-species diversity) [74,75] and the percentage share of trophic forms (zoophagous, mycetophagous, xylophagous, saproxylophagous). Identified species in terms of their trophic levels were divided into five groups: xylophagous, mycetophagous, zoophagous, saproxylic species, and the other trophic groups. Next species richness and the number of individuals in each of the groups were determined. Among the captured insects, also the percentage shares of species were calculated. The species, the share of which exceeded 5%, were considered dominant, while codominant species were those whose share ranged from 2% to 5%.
Similarity between the Coleoptera assemblages was assessed using cluster analysis. The analysis used the species dominance index (where the number of individuals n = 2006, the number of taxa S = 244) in the studied stands. The Euclidean distance was taken as the measure of clustering distances. The analyses were performed using the Statistica13.3 software by StatSoft ® . The volume of dead wood, the number of species in an assemblage as well as percentage shares of individual trophic groups were vectors of observations. The Euclidean distance was applied as the metric. Assessment of specificity of Coleoptera assemblages. Characteristics of species and their relationships with the habitat were based on the estimated fidelity classes proposed by A. Szujecki [76,77] and their later modifications taking into consideration the character of the study and the specific nature of beetle groups [78][79][80] as well as the Catalogue of Polish Fauna and the National Biodiversity Information System website [81].
The following modified estimated fidelity classes were adopted: F4: obligate characteristic species-strictly (obligately) related, i.e., in terms of their trophic levels and biology, with processes of dieback in coniferous trees, cambio-, xylo-, and endophytophagous (the first stages in the succession chains in the subcorticular habitat).
F3: selective characteristic species-found numerously in a given habitat, although also present in other habitats; included predatory, parasitic, and ambrosia beetles as well as mycetophagous species, the occurrence of which is dependent on the presence of host organisms.
F2: auxiliary (accompanying) species-found in the subcortical habitat less numerously than in other habitats or showing no preference to any habitat type; included species facultatively (periodically) appearing in the subcortical habitat, searching for shelter or food. F1: species alien to a given habitat. F0: ubiquitous, cosmopolitan species. R: relic species, of special faunistic value, reported in single localities, related with primeval forests.
Data on the occurrence of clown beetles (Histeridae) was published in a study by Mazur et al. [61].
Saproxylic beetles (understood as species in terms of their ecology associated with dying, dead, and decaying trees, in which the utilisation of wood has led to morphological, anatomical, and metabolic adaptations to the habitat) [82,83] were classified in further analyses to species from fidelity classes R, F4, F3, and F2.

Results
A total of 2006 beetles belonging to 244 taxa were captured in the period of the study. Of that number, 1820 individuals were identified to species, which accounts for 90.7% all captured insects. They were classified to 216 species, whereas the other beetles (9.3%) were identified to the level of genus or family (Supplementary Materials). Among them 194 (89.8%) are species permanently or periodically associated with wood, they were represented by 1702 (93.7%) individuals. Characteristics of assemblages in the investigated stands are given in Table 2. Table 2. Characteristics of Coleoptera assemblages in managed and unmanaged pine stands in western Poland. In unmanaged stands, a total of 167 beetle species were reported, which were represented by 936 individuals, whereas in managed stands 153 species were captured, represented by 1067 individuals. On average, in each of the unmanaged stands 55.5 species (SD = 14.8) were identified, while in managed stands it was 46.6 species (SD = 22.6).
Analyses of individual stand showed the highest number of beetle species in the oldest stands (UG1, MD5, UD4), aged over 140 years, which was reflected in the high values of species richness (d) and species diversity (H'). An exception in this respect was found for the commercial (managed) pine stand established on former farmland (MC8), in which biodiversity indices were relatively high ( Table 2). The lowest qualitative and quantitative richness of beetles was recorded in commercial stands in the Gubin and Torzym Forest Districts (MG6, MT7) (  (Table 3). Only Enicmus rugosus reached the dominance index above 5% in five stands. Species, which were dominant (D > 5%) in at least three stands included Phloeostiba lapponica reported with a very high dominance index in the protected stand in the Torzym Forest District (UT3) and in two managed stands (MT7, MG6); Spondylis buprestoides dominant in managed stands as well as Nicrophorus vespilloides recorded as dominant only in managed stands. Although Ampedus balteatus was the most numerously represented among the captured insects, it was dominant only in one of the analysed stands (MD5).
Ampedus balteatus Crypturgus hispidulus Results of the analyses of Coleoptera assemblages indicate considerable similarity between the stands located the closest geographically ( Figure 2). The assemblages form three basic agglomerations: 1. beetles found in unmanaged stands in the Gubin Forest District (UG1, UG2), 2. beetle assemblages in managed stands in the Gubin and Torzym Forest Districts together with the protected stand in the Torzym Forest District (MT7, UT3, MG6), and 3. beetle assemblages in the managed stand in the Jarocin Forest District and assemblages found in the Drawieński National Park (MC8, MD5, UD4). The assemblage of beetles found in stand MD5 is the most distant from all analysed. between the stands located the closest geographically ( Figure 2). The assemblages form three basic agglomerations: 1. beetles found in unmanaged stands in the Gubin Forest District (UG1, UG2), 2. beetle assemblages in managed stands in the Gubin and Torzym Forest Districts together with the protected stand in the Torzym Forest District (MT7, UT3, MG6), and 3. beetle assemblages in the managed stand in the Jarocin Forest District and assemblages found in the Drawieński National Park (MC8, MD5, UD4). The assemblage of beetles found in stand MD5 is the most distant from all analysed. The percentage shares of individual trophic groups in the beetle assemblages differ in the analysed stands (Table 4).
When comparing mean shares of species in the trophic groups in both stand management types, most identified species were zoophages. Species richness of xylophagous and mycetophagous beetles is similar. The lowest share was recorded for saproxylophagous species. In managed stands, a greater share of xylophagous species was reported, while unmanaged stands are generally characterised by a greater share of all trophic The percentage shares of individual trophic groups in the beetle assemblages differ in the analysed stands (Table 4). When comparing mean shares of species in the trophic groups in both stand management types, most identified species were zoophages. Species richness of xylophagous and mycetophagous beetles is similar. The lowest share was recorded for saproxylophagous species. In managed stands, a greater share of xylophagous species was reported, while unmanaged stands are generally characterised by a greater share of all trophic groups except for xylophages. The shares of species belonging to the other trophic groups are practically identical.
In unmanaged stands, the highest frequency was recorded for specimens of zoophagous species. The shares of xylophagous and mycetophagous beetles exceeded 10%, while the lowest values were found for saproxylophages and the other trophic groups. In managed stands, the highest number of individuals was also reported in the group of zoophagous specimens; however, their share was much lower than in unmanaged stands. The other trophic groups account for approx. 1/5 of all the individuals, while the frequency of xylophagous and mycetophagous beetles was high, considerably exceeding that in unmanaged stands. The shares of individuals classified to the adopted fidelity classes varied in the investigated stands (Figure 3). This pertains particularly to the shares of individuals representing alien species in managed stands, which may even exceed 30% (the managed stand in the Torzym Forest District, MT7). Shares of individuals representing obligate characteristic species ranged from 15% to 39%. The highest share of these species was observed in unmanaged stands in the Gubin Forest District (UG1) and the Drawieński National Park (UD4) (Figure 3a). The shares of individuals classified to the adopted fidelity classes varied in the investigated stands (Figure 3). This pertains particularly to the shares of individuals representing alien species in managed stands, which may even exceed 30% (the managed stand in the Torzym Forest District, MT7). Shares of individuals representing obligate characteristic species ranged from 15% to 39%. The highest share of these species was observed in unmanaged stands in the Gubin Forest District (UG1) and the Drawieński National Park (UD4) (Figure 3a). The total number of species belonging to the four fidelity classes most strongly associated with the subcorticular habitat (R, F4, F3, F2) is higher in unmanaged stands compared to managed stands (Figure 3b). Occurrence of single relic species (R) was observed in almost all the stands, both unmanaged and managed, with the exception of MT7, where no species from that fidelity class were recorded. Selective characteristic species (F3) and alien species (F1) were more numerous in managed stands, whereas ubiquitous species (F0) had only a slight share in the assemblage (Figure 4). The total number of species belonging to the four fidelity classes most strongly associated with the subcorticular habitat (R, F4, F3, F2) is higher in unmanaged stands compared to managed stands (Figure 3b). Occurrence of single relic species (R) was observed in almost all the stands, both unmanaged and managed, with the exception of MT7, where no species from that fidelity class were recorded. Selective characteristic species (F3) and alien species (F1) were more numerous in managed stands, whereas ubiquitous species (F0) had only a slight share in the assemblage (Figure 4).
Indices of species richness (Margalef's index) and species diversity (Shannon's index) in the investigated stands reached higher values in the group of unmanaged stands ( Table 2).
The total number of species belonging to the four fidelity classes most strongly associated with the subcorticular habitat (R, F4, F3, F2) is higher in unmanaged stands compared to managed stands (Figure 3b). Occurrence of single relic species (R) was observed in almost all the stands, both unmanaged and managed, with the exception of MT7, where no species from that fidelity class were recorded. Selective characteristic species (F3) and alien species (F1) were more numerous in managed stands, whereas ubiquitous species (F0) had only a slight share in the assemblage (Figure 4).  Table  2).

Discussion
Information on saproxylic beetles of pine coniferous forests in view of the area covered by these forests and their role in the forest management system in central Europe is not proportional. Data comes mainly from northern and central Europe [40,42,43]. In turn, studies in Poland were conducted primarily in the eastern part of the country [10,11,50,51,53], which differs significantly in terms of climate from western Poland, which results in different habitats and plant communities [84]. Western Poland is under the influence of the Atlantic climate, and the pine forests form communities in the type of

Discussion
Information on saproxylic beetles of pine coniferous forests in view of the area covered by these forests and their role in the forest management system in central Europe is not proportional. Data comes mainly from northern and central Europe [40,42,43]. In turn, studies in Poland were conducted primarily in the eastern part of the m which differs significantly in terms of climate from western Poland, which results in different habitats and plant communities [84]. Western Poland is under the influence of the Atlantic climate, and the pine forests form communities in the type of sub-Atlantic fresh forest-Leucobryo-Pinetum. Northeast Poland, on the other hand, is under the influence of a subcontinental climate, it is an area of pine forests of the Peucedano-Pinetum type [85]. This affects the length of the growing season, which may determine the distribution of some beetle species (including saproxylic beetles) [86].
The use of screen traps as the only trapping method was dictated by utilitarian goals. In managed stands, standing dead trees and broken tree crowns were the most common microbiotopes, where saproxylic species may occur. One trapping method, although assessed as very effective, narrows the scale of captured species and does not allow direct comparison of the results. The use of various types of traps (e.g., emergence, screen traps in different colours, etc.), dedicated to specific ecological groups of beetles, results in an increase in the number of species caught [61].
Species richness of saproxylic beetles in the investigated pine stands of western Poland differs from that observed in central and eastern parts of the country [50,52,53,80]. Studies conducted to date were frequently based on many methods of insect capture and observation, which considerably hinders comparability of the obtained results. Nevertheless, in relation to forest ecosystems considered natural, which often are treated as a model, to which research results on species diversity are referred, the number of recorded species was lower. In the Białowieża Forest, a total of 630 species were reported [53], while in mixed coniferous forests of the Kampinos Forest it was 433 species [51]. However, they are one of richest and best preserved forest ecosystems in this part of Europe. On the other hand, studies on the fauna of pine stumps showed 178 species [87], whereas assemblages of saproxylic beetles in boggy pine coniferous forests it was as few as 121 species [50].
As it was shown by the studies conducted in stands affected by hurricane and wild fires, a rapid increase in CWD resources does not cause an equally dynamic increase in species diversity [88,89]. Already in the 5th year after stand damage the diversity indices were more favourable for undamaged unmanaged stands with dead wood resources of 7.8-15 m 3 /ha. For damaged stands, this index reached a similar value, with a slight advantage of unclear stands (mean CWD resources of 225.5 m 3 /ha) over cleared stands (94.5 m 3 /ha) [50]. These observations show that for the maintenance of species diversity continuous access to dead wood is more important than its abundance. Natural selfthinning processes, which are less dynamic, facilitate full utilisation of microhabitats formed over the years. A broad spectrum of trees at various stages of dieback and wood decomposition distributed as a mosaic in the ecosystem promotes survival of individual species more effectively than a large amount of substrate of similar parameters. This was confirmed by extensive research conducted in France [24,90], showing a significant effect of not only CWD resources, but also the presence of den trees, diversity of arboreal fungi and openness of the habitat providing available light and an advantageous microclimate. Moreover, for saproxylic species developing in dying pine trees a significant role is played by the diameter of the stem or branches, the presence of bark, as well as height above the ground [47].
Presented results show the course of transformation of managed forests into forests with the dominant protection function focused on saproxylic insects. The reported observations confirm that the decision to cease removing dying and dead trees has an advantageous effect on species diversity. Analysis of Coleoptera assemblages showed that sites located closest geographically are most similar (Figure 2), while higher values of diversity and species richness indices within agglomerations were recorded for unmanaged forests ( Table 2).
In unmanaged forests, the shares and numbers of obligate characteristic and characteristic species were greater. It is also of interest that the shares of species being strictly saproxylic in both stand categories were comparable. Thus, how can the relatively high share of this trophic group be explained in managed stands, where CWD resources are much smaller?
Such a situation may be explained by the specific character of individual forest ecosystems, determined by their history and intensity of management operations affecting the continuity of natural processes of tree dieback and accumulation of dead wood with all its specific microhabitats. Thus, utilisation of the current abundance of dead wood as an indicator feature of biodiversity may lead to a bias. This parameter does not take into consideration the size and degree of decomposition of dead wood, which determine the occurrence of several specific/stenotopic beetle species [91]. It is obvious that in the case of the accumulation of large CWD amounts a wider spectrum of microhabitats is more probable, although some cases suggest that it is not always the rule [28].
Observed high values of diversity and species richness indices at limited CWD resources in managed stands may be explained as a certain island effect [92]. Dying trees constitute a biotope for several species, while in sterile managed forest they may function as hotspots in a microscale.
Probably a reduced number of dying and dead trees of a given species within a certain range may cause the accumulation of specific fauna, and thus increased species richness on individual trees.
In stands not covered by sanitation regime, in which tree dieback is a common process taking place over larger areas, with an increase in CWD resources the concentration of fauna is observed, which in turn may result in a decrease in the values of diversities and species richness indices.
Posing questions on the volume of dead wood resources as the only factor determining insect assemblages associated with this habitat is an oversimplification of the complex biocenotic associations taking place during tree dieback and wood decomposition between several organisms, among which beetles constitute a considerable group. Assessment and strategies to preserve biodiversity need to take into consideration not only α-diversity, but also βand γ-diversity [93].
A characteristic differentiating the investigated pine stands in western Poland is connected with the share of species dominant on the local scale. Ampedus balteatus (Elateridae) is a superdominant, found at a very high frequency in stand MD5. Ampedus balteatus is a zoophagous species developing in pine stumps [80,94], an obligatory saproxylic species [95].
It was captured in traps with retusol and sulcatol in southern Finland [96] and in fermental traps [40], while in studies on subcorticular beetles in natural and managed forests with a share of pine and spruce it was recorded only in managed forests [41]. In hurricane-affected stands in the Piska Forest it was co-dominant and found commonly, although its population size did not increase under the influence of the accumulation of hurricane-damaged timber [50]. Its presence in the investigated stands needs thus to be associated with the intensive process of tree dieback and increased presence of organisms constituting its food source.
A list of species dominant in the analysed stands indicates that most identified assemblages have different dominant species. Only Enicmus rugosus (Latridiidae) and Phloeostiba lapponica (Staphylinidae) were found with the dominant share in three or more assemblages ( Table 3). The minute brown scavenger beetle E. rugosus is a mycetophagous species, with an extensive distribution in Europe, obligatorily associated with hardwood CWD as well as softwood CWD of larger diameters [95,97]. It does not show a close association to a specific type of forest habitat [95,98], colonising wood dominated by slime mould Eumycetozoa [99]. In many forest habitats it is found as a dominant [79,87,100], colonising tall stumps [87,101], tree hollows [102], and lying boles (trunks) [103] as well as old, solitary oak trees [104].
Another species recorded with high frequency was Phloeostiba lapponica, a holarctic species [105]. It is a small, predatory subcorticular beetle staying under tree bark, typically in bark beetle galleries on coniferous trees. In eastern Finland it was reported with high frequency on burnt trees, in habitats subjected to controlled burns to renaturalise managed boreal forests [106].
It also needs to be stressed here that groups of dominant species, which are unique rather than common indicate high specificity of each of the assemblages. A comparison of the dominant species systems between the group of managed vs. unmanaged stands identifies dominant species for each category of stands. In unmanaged stands the most numerous were Enicmus rugosus and Phloeostiba lapponica, while in managed stands it was Ampedus balteatus, Nicrophorus vespilloides, Melanotus villosus, and Tomicus piniperda. The presence of large subcorticular predators (Ampedus, Melanotus) accompanying cambiophages (Tomicus) may indicate the initiated processes of tree dieback, in which the first succession stages are taken by cambiophages of large body size (part of Scolytinae, Cerambycidae, Buprestridae) [107,108].
When analysing the frequency of families (Supplementary Materials), it is noticed that representatives of families Bothrideridae, Dryophthoridae, Eucnemidae, Trogossitidae, and Zopheridae occur only in unmanaged stands. However, in these stands with a greater frequency than in managed stands, species from the following families occur: Ciidae, Melandryidae, Monotomidae, and Scydmaenidae. They are representatives of typically saproxylic families [6]. Only species of Silvanidae have been found in the managed stands, and bark beetles (Curculionidae) are more numerous than in unmanaged stands.
Research results indicate that the leaving naturally dying trees in pine stands results in a slow accumulation of CWD resources and influences directions of succession for assemblages of subcorticular and saproxylic beetles.
This study may illustrate an example of the transition of a stand from the managed type to the unmanaged type as well as changes in fauna with an increase in CWD resources and directions of succession for beetle assemblages associated with processes of dieback and dead wood accumulation.

Conclusions
These analyses showed differences between assemblages of saproxylic beetles found in managed and unmanaged stands. These differences are smaller in terms of the number of species, while they are higher in terms of the frequency of individuals in the identified ecological and trophic groups of beetles. However, the number of saproxylic species greater by eight percentage points recorded in unmanaged stands shows that the management method affects species diversity in this group of insects.
Clustering being the result of analysis of similarity between the analysed stands indicates a significant role of the geographical location of these sites. The closer they were located to one another, the greater the similarity despite their different management methods.
Based on the identified objects, no relationship was confirmed between the species diversity indices and growing CWD resources; however, a trend may be observed for the organisation of Coleoptera assemblages towards an increase in the share of zoophagous, saproxylic, mycetobiontic, and relic species. Managed stands with the implemented sanitation cutting regime, in which trees naturally dying are removed, are characterised by lower species diversity indices and a greater share of xylophages.
Simulated dependencies between dead wood resources and species richness and diversity indices in pine coniferous forest with different management regimes may indicate that at a comparable level of biodiversity in managed stands trends are evident towards a grouping (concentration) of fauna dependent on dead trees, while in unmanaged stands with an increase in CWD resources saproxylic beetles are scattered.
Pine coniferous forests of central Europe may serve a considerable role in the system of protection for saproxylic beetles. These forests are habitats transformed by traditional forestry towards monocultures of limited diversity and low dead wood resources, particularly large-sized wood. Nevertheless, this habitat is colonised by numerous saproxylic species, in which numbers of individuals and concentration are directly dependent on the presence of coarse woody debris. Thus, active protection of the forest habitat needs to be focused on increasing this parameter through protection of natural and spontaneous phenomena of tree dieback.