Abstract:-Pinus nigra and Robinia pseudoacacia are exotic trees used for afforestation in Hungary. Pinus nigra was non-invasive, however R. pseudoacacia escaped from cultivation and invaded several vegetation types including pine plantations. It has recently been planned to cut P. nigra plantations and replace them by native tree stands, especially in nature reserves. The scattered presence of R. pseudoacacia specimens in pine stands might place constraints on planned tree replacement because of their vegetative respro… Show more
“…While all these factors can act simultaneously, other unidentified biotic or abiotic factors may be also be at play. Finally, SV relationships may be common in plant invasion biology, especially for invasive leguminous trees and shrubs that constitute large seed banks throughout the world (Paynter et al, 2003;Richardson and Kluge, 2008;Cseresnyés and Csontos, 2012;Strydom et al, 2017). In this case, SV relationships can serve as a starting point to predict seed bank dynamics, and evaluate their state compared with native areas and the efficiency of control programs, and can help to focus on the main factors likely to contribute to the accumulation of many seeds in soil.…”
Background and aims-Large, persistent seed banks contribute to the invasiveness of non-native plants, and maternal plant size is an important contributory factor. We explored the relationships between plant vegetative size (V) and soil seed bank size (S) for the invasive shrub (Ulex europaeus) in its native range and in non-native populations, and identified which other factors may contribute to seed bank variation between native and invaded regions. Methods-We compared the native region (France) with two regions where Ulex is invasive, one with seed predators introduced for biological control (New Zealand) and another where seed predators are absent (La Réunion). We quantified seed bank size, plant dimensions, seed predation, and soil fertility for six stands in each of the three regions. Key results-Seed banks were 9 to 14 times larger in the two invaded regions compared to native France. We found a positive relationship between current seed bank size and actual plant size, and that any deviation from this relationship was probably due to large differences in seed predation and/or soil fertility. We further identified three possible factors explaining larger seed banks in non-native environments: larger maternal plant size, lower activity of seed predators and higher soil fertility. Conclusions-In highlighting a positive relationship between maternal plant size and seed bank size, and identifying additional factors that regulate soil seed bank dynamics in non-native ranges, our data offer a number of opportunities for invasive weed control. For non-native Ulex populations specifically, management focusing on 'S' (i.e. the reduction of the seed bank by stimulating germination, or the introduction of seed predators as biological control agents), and/or 'V' (i.e. by cutting mature stands to reduce maternal plant biomass) offers the most probable combination of effective control options.
“…While all these factors can act simultaneously, other unidentified biotic or abiotic factors may be also be at play. Finally, SV relationships may be common in plant invasion biology, especially for invasive leguminous trees and shrubs that constitute large seed banks throughout the world (Paynter et al, 2003;Richardson and Kluge, 2008;Cseresnyés and Csontos, 2012;Strydom et al, 2017). In this case, SV relationships can serve as a starting point to predict seed bank dynamics, and evaluate their state compared with native areas and the efficiency of control programs, and can help to focus on the main factors likely to contribute to the accumulation of many seeds in soil.…”
Background and aims-Large, persistent seed banks contribute to the invasiveness of non-native plants, and maternal plant size is an important contributory factor. We explored the relationships between plant vegetative size (V) and soil seed bank size (S) for the invasive shrub (Ulex europaeus) in its native range and in non-native populations, and identified which other factors may contribute to seed bank variation between native and invaded regions. Methods-We compared the native region (France) with two regions where Ulex is invasive, one with seed predators introduced for biological control (New Zealand) and another where seed predators are absent (La Réunion). We quantified seed bank size, plant dimensions, seed predation, and soil fertility for six stands in each of the three regions. Key results-Seed banks were 9 to 14 times larger in the two invaded regions compared to native France. We found a positive relationship between current seed bank size and actual plant size, and that any deviation from this relationship was probably due to large differences in seed predation and/or soil fertility. We further identified three possible factors explaining larger seed banks in non-native environments: larger maternal plant size, lower activity of seed predators and higher soil fertility. Conclusions-In highlighting a positive relationship between maternal plant size and seed bank size, and identifying additional factors that regulate soil seed bank dynamics in non-native ranges, our data offer a number of opportunities for invasive weed control. For non-native Ulex populations specifically, management focusing on 'S' (i.e. the reduction of the seed bank by stimulating germination, or the introduction of seed predators as biological control agents), and/or 'V' (i.e. by cutting mature stands to reduce maternal plant biomass) offers the most probable combination of effective control options.
“…Although these plantations occupy only 3.7% of the total forested lands of the country, P. nigra is responsible for some serious ecological and nature conservation problems (Tamás, 2003). Several studies called the attention to the various aftermaths of the creation of pine stands, such as to the effects on the soil and ground layer including serious impoverishment of the species-rich native grassland vegetation (Bódis, 1993;Csontos et al, 1997, Szalai et al, 2012, the promoted spreading of other alien plants (Török et al, 2003;Cseresnyés and Csontos, 2012a), as well as the highly increased fire risk as a consequence of the considerable accumulation of resinous needle litter (Cseresnyés et al, 2011).…”
Phytosociological and nature conservation assessment of the herb layer of 6-, 15-and 20-yearold post-mining Austrian pine stands was conducted in reclaimed bauxite quarries in Hungary. Great differences among the vegetations were found. Disturbance-tolerant species were dominant, subdominant and subordinated in the youngest, middle-aged and oldest pine stand, respectively. In parallel, proportion of the species characteristic for natural habitats increased gradually, leading to growing diversity and naturalness. The increasing pine cover reduced the species number and the coverage of herb layer. Postmining flora differed significantly from both the potential mature oak forest vegetation of the areas and from the associations developed through regenerative succession on clear-cut areas of oak forests. Vegetation of the reclaimed quarries had lower naturalness: relative abundances of disturbance-tolerant and ruderal species were higher, but ratio of natural broad-leaved forest's species was smaller than in the potential vegetation. Similar differences were shown by comparison of the flora of bauxite quarries with the same-aged stages of regenerative succession of oak forests. In pine stands the repression of weeds parallel to the spreading of natural competitors was slower, and natural geophytes and protected species remained absent. Deficiency of propagule sources in reclaimed areas could contribute to the retentive effect of Austrian pine on vegetation succession.
“…As a N-fixing species, black locust creates irreversible changes in physico-chemical and biological soil properties. It influences the species composition of ground flora under its canopy by favouring ruderal and species-poor neutrophilous weed associations, eliminating oligotrophic and acidophilous ones typical of forests, thereby reducing plant diversity (Kleinbauer et al 2010;Benesperi et al 2012;Cseresnyés and Csontos 2012;Dimitrova 2012;Vuković et al 2013). In invaded stands, as soil pH is significantly lower and soil NO 3 − significantly higher, soil microarthropode communities suffer significant loss of abundance and richness while nematode taxon richness is significantly lower (Lazzaro et al 2018).…”
wood, fodder, and a source of honey as well as bio-oil and biomass. It is also important for carbon sequestration, soil stabilization and re-vegetation of landfills, mining areas and wastelands, in biotherapy and landscaping. In Europe, black locust is drought tolerant so grows in areas with annual precipitation as low as 500-550 mm. It tolerates dry, nutrient poor soils but grows best on deep, nutrient-rich, well-drained soils. It is a fast-growing tree and the height, diameter and volume growth peak before the age of 20. It mostly regenerates vegetatively by root suckers under a simple coppice system, which is considered the most cost-effective management system. It also regenerates, but less frequently, by stool sprouts. Its early silviculture in production forests includes release cutting to promote root suckers rather than stool shoots, and cleaning-respacing to remove low-quality stems, reduce the number of shoots per stool, and adjust spacing between root suckers. In addition, early, moderate and frequent thinning as well as limited pruning are carried out focusing on crop trees. The species is regarded as
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