No abstract

Since the mid-19th century, Pinus nigra plantations have played a key role in the restoration of degraded European landscapes. Nowadays, these plantations are aging and prone to natural disturbances, insect infestations, and diseases. For their successful gradual conversion, knowledge of optimal gap spatiotemporal dynamics is crucial. We studied herb and natural regeneration patterns along with site factors on 477 subplots within 44 plots distributed over four stand types: closed stand (14% diffuse light), open stand (21%), gap edge (23%), and gap (57%). Despite the abundant Quercus petraea, Q. cerris, and Q. pubescens mast year, no one-year seedlings were recorded, which is likely due to the summer drought. Short seedlings (h < 20 cm) of Quercus sp., Fraxinus ornus and Ostrya carpinifolia were more successful within closed stands. Short Quercus seedlings were positively associated with soil depth and negatively associated with soil nutrients, distance to seed trees, and Sesleria autumnalis coverage. Taller Quercus seedlings required more light than both of its strongest competitors and were positively related to humid soils and less rocky sites. Ungulate overbrowsing significantly impeded natural regeneration. The results indicate a satisfactory Quercus density for conversion and the importance of advanced regeneration, which should be gradually, but persistently, released by progressively widening gaps.

In the last century, a synchronous beech expansion has been observed for many mixed mountain forests in southeastern Europe. This change is associated with the interaction of various disturbances. We analyzed structural changes in the Pecka old-growth forest in Slovenia during the last century, using several inventories of the tree layer, regeneration, and site factors. Throughout the observation period, the density of silver fir in the regeneration layer and in the overstory steadily decreased. In 1893, silver fir accounted for about 60% of the growing stock, whereas in 2013 it accounted for less than 13%. This is likely because of silver fir’s decline in the canopy layer due to air pollution, successive windthrows, and overbrowsing. However, climate change may also have played an important role, as silver fir also declined in southeastern European old-growth forests where air pollution was less pronounced and ungulate densities were low. A gradual decline of silver fir in the overstory resulted in a decrease of overall tree density to 231 trees ha–1, while growing stock remained relatively high at 712 m3 ha–1. Median diffuse light at 1.3 m was 3.7% and regeneration density was 19,954 ha–1. Beech was dominant (94%), followed by silver fir (4%), and sycamore maple (2%). No silver fir seedlings larger than 0.2 m were recorded. Silver fir, sycamore maple, and beech regeneration showed 87, 76, and 45% browsing damage, respectively. Regression models indicated some evidence of niche partitioning between silver fir and beech. However, many processes may be masked by the silver fir’s avoidance strategy. Given current red deer densities, climate change, and existing forest structure, the Pecka old-growth forest will likely reach an alternative stable state dominated by beech in a few decades. This calls for immediate reduction of ungulate populations. Despite the interaction of multiple disturbances, the Pecka old-growth forest has maintained a relatively high overall growing stock, a favorable microclimate, and succession pathway with shade-tolerant beech. This indicates the intrinsic resilience of natural forests. The mechanisms discussed here can be applied to the future governance of old-growth and managed montane mixed forests.