Using measurements from high resolution monitoring of radial tree-growth we present new data of the growth reactions of four widespread broadleaved tree-species to the combined European drought years ...2018 and 2019. We can show that, in contrast to field crops, trees could make better use of the winter soil moisture storage in 2018 which buffered them from severe drought stress and growth depressions in this year. Nevertheless, legacy effects of the 2018 drought accompanied by sustained low soil moisture conditions (missing recharge in winter) and again higher than average temperatures and low precipitation in spring/summer 2019 have resulted in severe growth reductions for all studied tree-species in this year. This highlights the pivotal role of soil water recharge in winter. Although short term resistance to hot summers can be high if sufficient winter precipitations buffers forest stands from drought damage, legacy effects will strongly impact tree growth in subsequent years if the drought persists. The two years 2018 and 2019 are extreme with regard to historical instrumental data but, according to regional climate models, resemble rather normal conditions of the climate in the second half of the 21st century. Therefore the observed strongly reduced growth rates can provide an outlook on future forest growth potential in northern Central Europe and beyond.
More than 60% of the flora of the Galapagos Islands is introduced and some of these species have become invasive, severely altering ecosystems. An example of an affected ecosystem is the Scalesia ...forest, originally dominated by the endemic giant daisy tree Scalesia pedunculata (Asteraceae). The remnant patches of this unique forest are increasingly being invaded by introduced plants, mainly by Rubus niveus (blackberry, Rosaceae). To help large-scale restoration of this ecologically important forest, we seek to better understand the natural regeneration of S. pedunculata after invasive plant control. We monitored naturally recruited S. pedunculata saplings and young trees over five years in an area where invasive plant species are continuously being removed by manual means. We measured survival, height and growth of S. pedunculata saplings and young trees along permanent transects. Percent cover of surrounding plant species and of canopy shade directly above each S. pedunculata individual were determined, as well as distance to the next mature S. pedunculata tree. We identified potential factors influencing initial sapling survival and growth by applying generalized linear models. Results showed a rapid growth of saplings and young trees of up to 0.45 cm per day and a high mortality rate, as is typical for pioneer species like S. pedunculata. Sapling survival, growth and mortality seemed to be influenced by light availability, surrounding vegetation and distance to the next adult S. pedunculata tree. We concluded that natural regeneration of S. pedunculata was high only five months after the last herbicide application but that 95% of these recruits had died over the 5-year period. Further studies are needed to corroborate whether the number of surviving trees is sufficient to replace the aging adult trees and this way maintain remnants of the Scalesia forest. Urgent action is needed to help improve future restoration strategies to prevent further degradation of this rapidly shrinking threatened forest ecosystem.
Distance to grazing hotspots like watering points or farms is regularly used as proxy for grazing intensity in extended rangelands. In many studies the resulting patterns between distance and grazing ...dependent variables are nonlinear with strong changes in the vicinity of the centre, a distinct transition zone, and hardly any changes on remote sites. Here we propose that this typical pattern just reflects the nonlinear relationship between grazing intensity and distance in circular grazing hotspots. Theoretical considerations as well as other proxies of grazing intensity like dung density or salinity suggest that reciprocal distance better represents grazing intensity. It is a more realistic description of the temporal distribution of livestock and often reveals linear relationships to grazing dependent variables preventing misinterpretations of thresholds that might be important for rangeland management.
Aim
Species–area relationships (SARs) are fundamental scaling laws in ecology although their shape is still disputed. At larger areas, power laws best represent SARs. Yet, it remains unclear whether ...SARs follow other shapes at finer spatial grains in continuous vegetation. We asked which function describes SARs best at small grains and explored how sampling methodology or the environment influence SAR shape.
Location
Palaearctic grasslands and other non‐forested habitats.
Taxa
Vascular plants, bryophytes and lichens.
Methods
We used the GrassPlot database, containing standardized vegetation‐plot data from vascular plants, bryophytes and lichens spanning a wide range of grassland types throughout the Palaearctic and including 2,057 nested‐plot series with at least seven grain sizes ranging from 1 cm2 to 1,024 m2. Using nonlinear regression, we assessed the appropriateness of different SAR functions (power, power quadratic, power breakpoint, logarithmic, Michaelis–Menten). Based on AICc, we tested whether the ranking of functions differed among taxonomic groups, methodological settings, biomes or vegetation types.
Results
The power function was the most suitable function across the studied taxonomic groups. The superiority of this function increased from lichens to bryophytes to vascular plants to all three taxonomic groups together. The sampling method was highly influential as rooted presence sampling decreased the performance of the power function. By contrast, biome and vegetation type had practically no influence on the superiority of the power law.
Main conclusions
We conclude that SARs of sessile organisms at smaller spatial grains are best approximated by a power function. This coincides with several other comprehensive studies of SARs at different grain sizes and for different taxa, thus supporting the general appropriateness of the power function for modelling species diversity over a wide range of grain sizes. The poor performance of the Michaelis–Menten function demonstrates that richness within plant communities generally does not approach any saturation, thus calling into question the concept of minimal area.
Questions
Which environmental factors influence fine‐grain beta diversity of vegetation and do they vary among taxonomic groups?
Location
Palaearctic biogeographic realm.
Methods
We extracted 4,654 ...nested‐plot series with at least four different grain sizes between 0.0001 m² and 1,024 m² from the GrassPlot database, covering a wide range of different grassland and other open habitat types. We derived extensive environmental and structural information for these series. For each series and four taxonomic groups (vascular plants, bryophytes, lichens, all), we calculated the slope parameter (z‐value) of the power law species–area relationship (SAR), as a beta diversity measure. We tested whether z‐values differed among taxonomic groups and with respect to biogeographic gradients (latitude, elevation, macroclimate), ecological (site) characteristics (several stress–productivity, disturbance and heterogeneity measures, including land use) and alpha diversity (c‐value of the power law SAR).
Results
Mean z‐values were highest for lichens, intermediate for vascular plants and lowest for bryophytes. Bivariate regressions of z‐values against environmental variables had rather low predictive power (mean R² = 0.07 for vascular plants, less for other taxa). For vascular plants, the strongest predictors of z‐values were herb layer cover (negative), elevation (positive), rock and stone cover (positive) and the c‐value (U‐shaped). All tested metrics related to land use (fertilization, livestock grazing, mowing, burning, decrease in naturalness) led to a decrease in z‐values. Other predictors had little or no impact on z‐values. The patterns for bryophytes, lichens and all taxa combined were similar but weaker than those for vascular plants.
Conclusions
We conclude that productivity has negative and heterogeneity positive effects on z‐values, while the effect of disturbance varies depending on type and intensity. These patterns and the differences among taxonomic groups can be explained via the effects of these drivers on the mean occupancy of species, which is mathematically linked to beta diversity.
We analysed fine‐grain beta diversity of grasslands and other open habitats in the Palaearctic using 4,654 nested‐plot series and the z‐values of power‐law species–area relationships. Mean z‐values were highest for lichens, intermediate for vascular plants and lowest for bryophytes. The strongest environmental predictors of z‐values were herb layer cover (negative), elevation (positive), rock and stone cover (positive) and the c‐value (U‐shaped). In a conceptual figure, we summarize the resulting hypotheses how different predictors could influence z‐values via mean occupancy.
Sal (Shorea robusta) forests, a dominant forest type in Nepal, experience different disturbance intensities depending on management regimes. This study compares the impact of disturbance on Nepalese ...Sal forests, which are managed on three major management regimes: protected area, state-managed forest, and buffer zone community forest. Using a systematic sampling approach, we sampled 20 plots, each covering 500 square meters, and nested plots within each main plot to measure pole and regeneration for each management regime. We recorded forest characteristics including tree species, counts, diameter, height, crown cover, and disturbance indicators. We compared forest attributes such as diversity indices, species richness, and stand structure by management regime using analysis of variance and regression analysis. The forest management regimes were classified into three disturbance levels based on disturbance factor bundles, and the buffer zone community forest was found to have the highest disturbance while the protected forest had the lowest disturbance. Species richness, diversity, evenness, abundance, density and basal area were higher, but regeneration was lower in protected area and state-managed forest compared to the buffer zone community forests. This suggests positive impacts of moderate disturbance on regeneration. The management plan should prioritize the minimization of excessive disturbance to balance forest conservation and provide forest resources to local users.
Logging and sawing of timber using conventional tools by unskilled workers causes enormous damage to the valuable timber, residual stand, regeneration, and forest soil in Nepal. The purpose of this ...study was to find out the volume reduction factor and identify major strategies to reduce timber losses in the tree harvesting process in the Terai Shorea robusta forest of Nepal. Field measurements and product flow analysis of 51 felled trees from felling coupes and randomly selected 167 sawed logs were examined to study harvesting losses. Responses from 116 forest experts were analyzed to explore strategies for reducing harvesting and processing losses. The results showed that timber losses in the felling and bucking stage with and without stem rot were 23% and 22%, respectively. Similarly, timber losses in the sawing stage with and without stem rot were 31% and 30%, respectively. Paired t-test at 5% level of significance revealed that there was significant loss in both tree felling and log sawing stages with present harvesting practice. The most leading factor contributing to timber loss in all of the three stages was the use of inappropriate equipment during tree harvesting. Use of synthetic ropes for directional felling and skidding as well as flexible and portable sawing machine with size adjustment options during sawing were mainly recommended as strategies to reduce timber losses. This study serves as a baseline study to identify and quantify timber losses in different stages of tree conversion and also formulate their reduction strategies in Nepal.
Questions: How are plant species distributed along grazing gradients? What is the shape of species richness patterns? How can we test for the existence of potential discontinuities in species ...turnover pattern? Location: Semi-deserts in the eastern Caucasus, Azerbaijan, Gobustan district. Methods: We studied the distribution of vascular plant species along transects 900-m long, perpendicular to five farms, and estimated grazing intensity as current livestock units per distance. We modelled species response curves with Huismann-Olff-Fresco (HOF) models and calculated species turnover by accumulating the first derivatives of all response curves. To test for potential discontinuities in changes of vegetation composition along the grazing gradient, we introduce a new null model based on the individualistic continuum concept that uses permutations of the observed pattern of species responses. Results: Most species show a sigmoidal negative response to grazing intensity, while a few species respond with a unimodal pattern. The monotonic decrease in species richness with increasing grazing intensity marks a process of overgrazing that leads to the complete extirpation of plant species. Although the species turnover pattern shows a clear peak, it does not deviate significantly from the null model of individualistic continuous changes. Conclusions: Our approach offers a method for differentiating between transition zones and continuous shifts in species composition along ecological gradients. It also provides a valuable tool for rangeland management to test state-and-transition concepts and gives deeper insights into ecological processes affected by grazing.
Shrub expansion in alpine and arctic areas is a process with possibly profound implications for ecosystem functioning. The recent shrub expansion has been mainly documented by remote sensing ...techniques, but the drivers for this process largely remain hypotheses. Here, we outline a dendrochronological method, adapted to shrubs, to address these hypotheses and then present a mechanism for the current shrub expansion by linking recent climate change to shrub growth performance in northern Sweden. A pronounced increase in radial and vertical growth during recent decades along an elevational gradient from treeline to shrubline indicates an ongoing shrub expansion. Age distribution of the shrub population indicates the new colonization of shrubs at high elevations. Shrub growth is correlated with warm summers and winter snow cover and suggests the potential for large-scale ecosystem changes if climate change continues as projected.
► Dendrochronological investigations of beech and oak along precipitation gradient. ► Growth strongly depends on water availability especially during June and July. ► Sensitivity of tree growth and ...correlations to climate increase along gradient. ► Numbers of pointer years increase, changes more pronounced for beech. ► oak might gain competitive advantages under the projected drier climate.
For north-eastern Germany regional climate models project rising temperatures in combination with decreasing summer and increasing winter precipitation. The resulting overall drier conditions during the growing season will considerably impact forest growth there. We evaluate the consequences of increasing drought on the growth of the two locally most important broadleaf tree species common beech (
Fagus sylvatica L.) and pedunculate oak (
Quercus robur L.). Three mixed forests of beech and oak were sampled along a west-east gradient of declining precipitation. In total we used 257 ring-width samples from 133 trees to build six species and site specific chronologies. Additionally, we modelled the soil water budget for each site. We performed continuous and discontinuous (pointer year) analysis of climate-tree-growth relationships with particular emphasis on inter-annual-variations and their dependence upon climatic factors (temperature, precipitation, soil moisture) and on the stability of the obtained relationships. Results of climate-growth correlations together with pointer year analysis indicate a strong dependency of growth of both species from water availability, especially during early summer (June and July). General correlation pattern between growth and climate are similar for both species, but climate sensitivity of beech is generally higher. We identified drought as the main driver of negative growth depressions in both species. Increasing drought stress along the gradient is expressed in higher correlations to climatic variables, higher sensitivity (variance) of growth, and a higher number of negative pointer years for both species. For beech we also found a significant trend of decreasing average growth rates along the gradient. Growth superiority of beech compared to oak declines with decreasing precipitation. The relationships were generally stable throughout the 20th century. A rise of sensitivity together with a higher frequency of negative pointer years during the last decades suggests that increasing climatic variability together with rising temperatures might be influencing growth of
Fagus at the more humid sites. If we substitute space by time it seems that already small changes in precipitation regime can have considerable impact, especially on the growth of beech. Other, more drought tolerant species like oak might gain competitive advantages under the projected climatic changes.
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