Forest microclimates contrast strongly with the climate outside forests. To fully understand and better predict how forests' biodiversity and functions relate to climate and climate change, ...microclimates need to be integrated into ecological research. Despite the potentially broad impact of microclimates on the response of forest ecosystems to global change, our understanding of how microclimates within and below tree canopies modulate biotic responses to global change at the species, community and ecosystem level is still limited. Here, we review how spatial and temporal variation in forest microclimates result from an interplay of forest features, local water balance, topography and landscape composition. We first stress and exemplify the importance of considering forest microclimates to understand variation in biodiversity and ecosystem functions across forest landscapes. Next, we explain how macroclimate warming (of the free atmosphere) can affect microclimates, and vice versa, via interactions with land‐use changes across different biomes. Finally, we perform a priority ranking of future research avenues at the interface of microclimate ecology and global change biology, with a specific focus on three key themes: (1) disentangling the abiotic and biotic drivers and feedbacks of forest microclimates; (2) global and regional mapping and predictions of forest microclimates; and (3) the impacts of microclimate on forest biodiversity and ecosystem functioning in the face of climate change. The availability of microclimatic data will significantly increase in the coming decades, characterizing climate variability at unprecedented spatial and temporal scales relevant to biological processes in forests. This will revolutionize our understanding of the dynamics, drivers and implications of forest microclimates on biodiversity and ecological functions, and the impacts of global changes. In order to support the sustainable use of forests and to secure their biodiversity and ecosystem services for future generations, microclimates cannot be ignored.
Below‐canopy forest microclimates contrast strongly with the climate outside forests due to the presence of trees and shrubs. Here we review the drivers and the importance of forest microclimates in the face of climate change, and perform a priority ranking of future research avenues.
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BFBNIB, FZAB, GIS, IJS, KILJ, NLZOH, NUK, OILJ, SAZU, SBCE, SBMB, UL, UM, UPUK
Climate change is pushing species towards and potentially beyond their critical thermal limits. The extent to which species can cope with temperatures exceeding their critical thermal limits is still ...uncertain. To better assess species' responses to warming, we compute the warming tolerance (ΔTniche) as a thermal vulnerability index, using species' upper thermal limits (the temperature at the warm limit of their distribution range) minus the local habitat temperature actually experienced at a given location. This metric is useful to predict how much more warming species can tolerate before negative impacts are expected to occur. Here we set up a cross‐continental transplant experiment involving five regions distributed along a latitudinal gradient across Europe (43° N–61° N). Transplant sites were located in dense and open forests stands, and at forest edges and in interiors. We estimated the warming tolerance for 12 understory plant species common in European temperate forests. During 3 years, we examined the effects of the warming tolerance of each species across all transplanted locations on local plant performance, in terms of survival, height, ground cover, flowering probabilities and flower number. We found that the warming tolerance (ΔTniche) of the 12 studied understory species was significantly different across Europe and varied by up to 8°C. In general, ΔTniche were smaller (less positive) towards the forest edge and in open stands. Plant performance (growth and reproduction) increased with increasing ΔTniche across all 12 species. Our study demonstrated that ΔTniche of understory plant species varied with macroclimatic differences among regions across Europe, as well as in response to forest microclimates, albeit to a lesser extent. Our findings support the hypothesis that plant performance across species decreases in terms of growth and reproduction as local temperature conditions reach or exceed the warm limit of the focal species.
The warming tolerances of understory plant species varied with macroclimatic differences among regions across Europe, as well as in response to forest microclimates, albeit to a lesser extent. Plant performance across species decreases in terms of growth and reproduction as local temperature conditions reach or exceed the warm limit of the focal species.
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BFBNIB, FZAB, GIS, IJS, KILJ, NLZOH, NUK, OILJ, SAZU, SBCE, SBMB, UL, UM, UPUK
Abstract Questions Forests are highly fragmented across the globe. For urban forests in particular, fragmentation increases the exposure to local warming caused by the urban heat island (UHI) effect. ...We here aim to quantify edge effects on herbaceous understorey vegetation in urban forests, and test whether these effects interact with forest structural complexity. Location We set up a pan‐European study at the continental scale including six urban forests in Zurich, Paris, Katowice, Brussels, Bremen, and Stockholm. Methods We recorded understorey plant communities from the edge towards the interior of urban forests. Within each urban forest, we studied edge‐to‐interior gradients in paired stands with differing forest structural complexity. Community composition was analysed based on species specialism, life form, light, nutrient, acidity and disturbance indicator values and species' thermal niches. Results We found that herbaceous communities at urban forest edges supported more generalists and forbs but fewer ferns than in forests' interiors. A buffered summer microclimate proved crucial for the presence of fern species. The edge communities contained more thermophilous, disturbance‐tolerant, nutrient‐demanding and basiphilous plant species, a pattern strongly confirmed by corresponding edge‐to‐interior gradients in microclimate, soil and light conditions in the understorey. Additionally, plots with a lower canopy cover and higher light availability supported higher numbers of both generalists and forest specialists. Even though no significant interactions were found between the edge distance and forest structural complexity, opposing additive effects indicated that a dense canopy can be used to buffer negative edge effects. Conclusion The urban environment poses a multifaceted filter on understorey plant communities which contributes to significant differences in community composition between urban forest edges and interiors. For urban biodiversity conservation and the buffering of edge effects, it will be key to maintain dense canopies near urban forest edges.
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BFBNIB, FZAB, GIS, IJS, KILJ, NLZOH, NUK, OILJ, SAZU, SBCE, SBMB, UL, UM, UPUK
Abstract
Aim
The soil seed bank is a key component of the biodiversity of plant communities, but various aspects of its functioning in temperate forest ecosystems are still unknown
.
We here adopted ...a trait‐based approach to investigate the effects of macro‐ and microclimatic gradients on the juvenile plant communities from the realized seed bank of two types of European temperate forest.
Location
Oak‐dominated forests in Italy and Belgium.
Methods
We analysed the variation of key functional traits (plant height, leaf area, leaf dry weight, specific leaf area and leaf number) of juvenile plants from the realised soil seed bank in relation to elevation (from 0 to 800 m a.s.l.), forest type (thinned and unthinned forest) and distance to the forest edge. We translocated soil samples from the forest core to the edge (and vice versa) and from high‐ to low‐elevation forests to test the effects of edge and warming respectively.
Results
Taller communities developed at the forest edge due to higher light availability and warmer temperatures. The translocation from the core to the edge did not significantly modify mean trait values. Instead, the shadier and cooler microclimate of the forest core reduced the mean leaf area, mean dry weight, height and leaf number in the communities realised from the edge soil. The translocation from high‐ to lowland forests led to increased values for all traits (except specific leaf area). Edge vs core trait variation was more driven by intraspecific variability, whereas the translocation from high‐ to low‐elevation forests caused trait changes mostly due to species turnover.
Conclusions
Global warming might result in a functional shift of the understorey due to both an early filtering effect on the seedlings from soil seed banks and their adaptive trait adjustments to temperature increase. Furthermore, our study underpins the importance of edge vs core microclimate in driving the functional composition of the realised soil seed bank.
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BFBNIB, DOBA, FZAB, GIS, IJS, IZUM, KILJ, NLZOH, NUK, OILJ, PILJ, PNG, SAZU, SBCE, SBMB, UILJ, UKNU, UL, UM, UPUK
Aim
The microclimate and light conditions on the forest floor are strongly modified by tree canopies. Therefore, we need to better consider the micro‐environment when quantifying trait–environment ...relationships for forest understorey plants. Here, we quantify relationships between micro‐environmental conditions and plant functional traits at the community level, including intraspecific trait variation, and their relationship with microclimate air temperature, light and soil properties.
Location
Deciduous temperate forests across Europe.
Time period
2018.
Major taxa studied
Herbaceous vegetation.
Methods
We sampled 225 plots across 15 regions along four complementary gradients capturing both macro‐ and microclimatic conditions including latitude, elevation, forest management and distance to forest edges. We related the community‐weighted mean of five plant functional traits (plant height, specific leaf area SLA, plant carbon C, plant nitrogen N and plant C:N ratio) across 150 vascular plant species to variation in local microclimate air temperature, light and soil properties. We tested the effect of accounting for intraspecific variation in trait–environment relationships and performed variation partitioning to identify major drivers of trait variation.
Results
Microclimate temperature, light availability and soil properties were all important predictors of community‐weighted mean functional traits. When light availability and variation in temperature were higher, the herb community often consisted of taller plants with a higher C:N ratio. In more productive environments (e.g. with high soil nitrogen availability), the community was dominated by individuals with resource‐acquisitive traits: high SLA and N but low C:N. Including intraspecific trait variation increased the strength of the trait–micro‐environment relationship, and increased the importance of light availability.
Main conclusions
The trait–environment relationships were much stronger when the micro‐environment and intraspecific trait variation were considered. By locally steering light availability and temperature, forest managers can potentially impact the functional signature of the forest herb‐layer community.
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BFBNIB, FZAB, GIS, IJS, KILJ, NLZOH, NUK, OILJ, SAZU, SBCE, SBMB, UL, UM, UPUK
Forest microclimatic variation can result in substantial temperature differences at local scales with concomitant impacts on plant defences and herbivory. Such microclimatic effects, however, may ...differ across abiotically contrasting sites depending on background environmental differences. To test these cross‐scale effects shaping species ecological and evolutionary responses, we experimentally tested the effects of aboveground microhabitat warming on insect leaf herbivory and leaf defences (toughness, phenolic compounds) for saplings of sessile oak Quercus petraea across two abiotically contrasting sites spanning 9° latitude. We found higher levels of herbivory at the low‐latitude site, but leaf traits showed mixed patterns across sites. Toughness and condensed tannins were higher at the high‐latitude site, whereas hydrolysable tannins and hydroxycinnamic acids were higher at the low‐latitude site. At the microhabitat scale, experimental warming increased herbivory, but did not affect any of the measured leaf traits. Condensed tannins were negatively correlated with herbivory, suggesting that they drive variation in leaf damage at both scales. Moreover, the effects of microhabitat warming on herbivory and leaf traits were consistent across sites, i.e. effects at the microhabitat scale play out similarly despite variation in factors acting at broader scales. These findings together suggest that herbivory responds to both microhabitat (warming) and broad‐scale environmental factors, whereas leaf traits appear to respond more to environmental factors operating at broad scales (e.g. macroclimatic factors) than to warming at the microhabitat scale. In turn, leaf secondary chemistry (tannins) appears to drive both broad‐scale and microhabitat‐scale variation in herbivory. Further studies are needed using reciprocal transplants with more populations across a greater number of sites to tease apart plant plasticity from genetic differences contributing to leaf trait and associated herbivory responses across scales and, in doing so, better understand the potential for dynamics such as local adaptation and range expansion or contraction under shifting climatic regimes.
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FZAB, GIS, IJS, KILJ, NLZOH, NUK, OILJ, SAZU, SBCE, SBMB, UL, UM, UPUK
Brief introduction: What are microclimates and why are they important?
Microclimate science has developed into a global discipline. Microclimate science is increasingly used to understand and ...mitigate climate and biodiversity shifts. Here, we provide an overview of the current status of microclimate ecology and biogeography in terrestrial ecosystems, and where this field is heading next.
Microclimate investigations in ecology and biogeography
We highlight the latest research on interactions between microclimates and organisms, including how microclimates influence individuals, and through them populations, communities and entire ecosystems and their processes. We also briefly discuss recent research on how organisms shape microclimates from the tropics to the poles.
Microclimate applications in ecosystem management
Microclimates are also important in ecosystem management under climate change. We showcase new research in microclimate management with examples from biodiversity conservation, forestry and urban ecology. We discuss the importance of microrefugia in conservation and how to promote microclimate heterogeneity.
Methods for microclimate science
We showcase the recent advances in data acquisition, such as novel field sensors and remote sensing methods. We discuss microclimate modelling, mapping and data processing, including accessibility of modelling tools, advantages of mechanistic and statistical modelling and solutions for computational challenges that have pushed the state‐of‐the‐art of the field.
What's next?
We identify major knowledge gaps that need to be filled for further advancing microclimate investigations, applications and methods. These gaps include spatiotemporal scaling of microclimate data, mismatches between macroclimate and microclimate in predicting responses of organisms to climate change, and the need for more evidence on the outcomes of microclimate management.
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BFBNIB, FZAB, GIS, IJS, KILJ, NLZOH, NUK, OILJ, SAZU, SBCE, SBMB, UL, UM, UPUK
Summary
Species are altering their phenology to track warming temperatures. In forests, understorey plants experience tree canopy shading resulting in light and temperature conditions, which strongly ...deviate from open habitats. Yet, little is known about understorey phenology responses to forest microclimates.
We recorded flowering onset, peak, end and duration of 10 temperate forest understorey plant species in two mesocosm experiments to understand how phenology is affected by sub‐canopy warming and how this response is modulated by illumination, which is related to canopy change. Furthermore, we investigated whether phenological sensitivities can be explained by species' characteristics, such as thermal niche.
We found a mean advance of flowering onset of 7.1 d per 1°C warming, more than previously reported in studies not accounting for microclimatic buffering. Warm‐adapted species exhibited greater advances. Temperature sensitivity did not differ between early‐ and later‐flowering species. Experimental illumination did not significantly affect species' phenological temperature sensitivities, but slightly delayed flowering phenology independent from warming.
Our study suggests that integrating sub‐canopy temperature and light availability will help us better understand future understorey phenology responses. Climate warming together with intensifying canopy disturbances will continue to drive phenological shifts and potentially disrupt understorey communities, thereby affecting forest biodiversity and functioning.
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BFBNIB, FZAB, GIS, IJS, KILJ, NLZOH, NUK, OILJ, SAZU, SBCE, SBMB, UL, UM, UPUK
Understanding the distinct impacts of temperature and light on seedling growth is crucial for predicting forest regeneration trajectories under future climate change and forest disturbance. This is ...because temperature and light can change independently or together, influencing the competitive status of tree seedlings and forest herbs. However, most prior studies tend to explore temperature and light effects either separately or in combination, lacking comprehensive full-factorial designs. Here, we utilized two large-scale full-factorial experiments to explore warming and light effects on tree seedlings growing in mesocosms with herbaceous plants. We found that light increased seedling height, diameter, and biomass, while warming alone had no significant effects. Moreover, we observed that there was an interaction effect between light and warming, where warming increased seedling height, diameter, and biomass under illumination. Understory herbaceous plant cover alone did not affect seedling height, diameter, and biomass, but it decreased seedling biomass when mesocosms were warmed or illuminated. This highlights the importance of considering the indirect negative effects induced by the interaction between forest opening and understory herbaceous plants. By disentangling the effects of increased temperature and light availability on understory seedling height, diameter, and biomass, our results contribute valuable knowledge for future forest management. It is imperative to carefully control the size of the gaps artificially created to facilitate the understory regeneration. Small gaps are recommended considering that the herbaceous plants may interact with both warming and light to negatively affect seedlings.
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GEOZS, IJS, IMTLJ, KILJ, KISLJ, NLZOH, NUK, OILJ, PNG, SAZU, SBCE, SBJE, UILJ, UL, UM, UPCLJ, UPUK, ZAGLJ, ZRSKP
10.
The use of photos to investigate ecological change Depauw, Leen; Blondeel, Haben; De Lombaerde, Emiel ...
The Journal of ecology,
June 2022, 2022-06-00, 20220601, Volume:
110, Issue:
6
Journal Article
Peer reviewed
Open access
Global change is causing ecosystems to change at unprecedented rates and the urgency to quantify ecological change is high. We therefore need all possible sources of ecological data to address key ...knowledge gaps.
Ground‐based photos are a form of remote sensing and an unconventional data source with a high potential to improve our understanding of ecological change. They can provide invaluable information on ecological conditions in the past and present at relevant spatiotemporal scales that is very difficult to obtain with other approaches.
Here we review the use of ground‐based photos in a set of relevant ecological research topics, such as biodiversity and community ecology, phenology, global change ecology and landscape ecology. We highlight three main photo‐based methods in ecological research (repeat photography, time‐lapse photography and public archives), alongside which we discuss three case studies to demonstrate novel applications of these methods, to answer fundamental ecological questions.
Synthesis. Photos can significantly support ecological research to improve our understanding of biotic responses in a rapidly changing world. Photos cover relatively large temporal and spatial scales, and can provide large amounts of information with limited time investment. To exploit their full potential, we need to invest not only in technological advances to compile, process and analyse images but also in proper data management.
Photos can significantly support ecological research to improve our understanding of biotic responses in a rapidly changing world. Photos cover relatively large temporal and spatial scales, and can provide large amounts of information with limited time investment. To exploit their full potential, we need to invest not only in technological advances to compile, process and analyse images, but also in proper data management.
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BFBNIB, FZAB, GIS, IJS, KILJ, NLZOH, NUK, OILJ, SAZU, SBCE, SBMB, UL, UM, UPUK