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The recovery of species composition typical for ancient forests in recent woods is a very slow process and may last for decades or even centuries. It is enhanced only when postagricultural woods are adjacent to ancient ones. However, even in such a situation of the spatial contact of both forest types, colonization of recent woods by true forest species is a gradual process. According to studies focusing on the behaviour of individual species and their colonization rates into recent woods, it can be concluded that in more fertile habitats the migration process proceeds faster than on poorer sites. Thus, studies were conducted on light, acidic soils both in ancient and in adjoining post-agricultural pine woods (the Dicrano-Pinion Libb. 1933 alliance) and were focused on the process of the colonization of the herbaceous layer by woodland flora in recent woods. In eight transects 80 m in length perpendicular to the ancient/recent ecotone and consisting of 10 sample plots of 16 m2 laid out at intervals of 4 m, the percentage cover of herb layer species was recorded. The migration rates (based on the occurrence of the farthest individual and on the occurrence of the maximum cover of a species) for 12 forest species were calculated. The mean migration rate for all species reached 0.54 m yr–1 when based on maximum cover and 0.67 m yr–1 when based on the farthest individual and appeared to be lower than those reported in investigations in more fertile and moister habitats. The migration rates for individual species ranged from 0 to 1.21 m yr–1 and were also lower than in more fertile, black alder woodlands. The migration pattern of Vaccinium myrtillus L., the most abundant species in pine woods, fits the model based on the establishment of isolated individuals. The cover of most woodland species increased with the increasing age of a recent wood. Herb layer recovery on such sites is slower than in the more productive, fertile habitats of broadleaved forests. The ancient and recent pine woods investigated here differed in herb layer species composition despite the secondary succession having lasted for over 50–60 years.
The herb layer recovery in post-agricultural woods adjacent to ancient forests has not yet been studied for the wettest European woodlands, like those with black alders (Alnus glutinosa L. (Gaertn.)). Therefore, the studies aimed at: I. checking which herbs from the Polish list of ancient woodland species that are present in the alder woods show an association with these woods (AAWS=Ancient Alder Woodland Species); II. presenting their ecological profile (spectra of life forms, life strategies, dispersal modes, phytosociological affinity, and Ellenberg indicator values), and III. comparing the dispersal potential and other traits of species recorded more often in ancient woods (AAWS) vs the Polish ancient woodland indicators frequently present in ancient and recent alder woods (OAWS = Other Ancient Woodland Species). The survey was carried out in Alnus glutinosa-dominated woodlands, located in south-western Poland. The study sites are located within large forest complexes, where they occupy either periodically waterlogged sites or other places with a high level of groundwater. In the case of ancient woods, wet types of an oak-hornbeam community (Tilio-Carpinetum Tracz. 1962 or Galio-Carpinetum Oberd. 1957) (11 sites), alder-ash carrs (Fraxino-Alnetum W. Mat. 1952) (12 sites) and typical wet alder woods (Ribeso nigri-Alnetum Sol.-Górn. (1975) 1987) (10 sites) were investigated. The ancient woodland sites varied in size from 0.73 ha to 15.54 ha. Recent woods, adjacent to these sites, included black alder stands planted on former meadows. The area of their patches ranged from 0.72 ha to 8.6 ha. Post-agricultural woods represented the following age classes: up to 10 years, 11–20, 21–30, 31–40, and 41–50 years. The process of colonization of recent woods by woodland flora was investigated in 33 transects, approximately 80 m in length by 4 m in width, consisting of 10–12 quadrates, 16 m² each, laid out at intervals of 4 m, perpendicularly across the ancient-recent border. In total 131 quadrates in the ancient wood, 198 in the recent woodland, and 34 in the ecotone zone were investigated. The migration rates (m yr⁻¹) based on the occurrence of the farthest individuals, were calculated for over 50 woodland species. The original lists of species obtained from the transects were completed after detailed inspections of the whole area of adjacent forest sectors where the studies on the colonization process were undertaken. Then, the frequency of herb layer species in ancient and recent woods was compared (Fisher exact probability test). The mean migration rates of species from the AAWS and OAWS groups were calculated. Although 62 herbs from the group of ancient woodland indicators for Poland were recorded in the course of the studies, only 21 of them occurred significantly more often in alder woods. The mean migration rate for herbs from AAWS was significantly lower (0.68 m yr⁻¹) than in the case of the OAWS group (1.54 m yr⁻¹). This indicates that true woodland herbs differ distinctively in their dispersal potential. Species from those two sets also showed some differences in their ecological requirements. Such results allow a conclusion to be reached that in wet and fertile recent forests adjacent to ancient source woods, recolonization of the herbaceous layer by typical woodland flora proceeds faster than in other, less fertile and drier habitats. This in turn explains why many true woodland species do not occur in ancient woodland sites exclusively. They are often recorded in recent woods, as they are able to colonize such sites reasonably fast.
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