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Global Change Biology · 2026 · Vol. 32 · Issue 3 · Wiley
Extensive knowledge exists on plant‐species traits and functions, but we understand less about how population‐ or community‐level emergent traits influence ecosystem functioning. This knowledge gap is important for ecosystems like peatlands, arid drylands, salt marshes, seagrass meadows, and mangroves, where emergent traits of plant communities can create plant‐environment feedbacks that amplify or dampen ecosystem processes....
Ecology Letters · 2026 · Vol. 29 · Issue 3 · Wiley
Metacommunity theory has expanded our understanding of how spatial dynamics and local interactions influence species communities. Different assembly archetypes, reflecting different roles of species differences, habitat differences, and dispersal have been described, but we lack empirical studies specifically in terrestrial habitats testing which archetype is most important. In a replicated design, we experimentally enhanced s...
Plant and Soil · 2025 · Vol. 514 · Issue 1 · Springer
Background and aims Fine roots and their traits determine resource uptake from the soil, thus being fundamental for plant and ecosystem functioning. It has been five years since the concept of the root economics space (RES) has been developed to describe multidimensional fine-root trait coordination. The RES proposed a novel fungal collaboration gradient in addition to the established fast-slow gradient of resource conservatio...
Plant and Soil · 2025 · Vol. 511 · Issue 1-2 · Springer
The number of studies investigating root length has increased, particularly in the context of root length measurements observed through windows such as minirhizotrons and rhizoboxes. However, there are currently two obstacles constraining their broader utility: (1) the absence of standardized terminology or units for root length data, and (2) the translation from two-dimensional (2D) to three-dimensional (3D) data. Here, we de...
Ecology Letters · 2024 · Vol. 27 · Issue 1 · Wiley
Biodiversity–ecosystem functioning (BEF) research has provided strong evidence and mechanistic underpinnings to support positive effects of biodiversity on ecosystem functioning, from single to multiple functions. This research has provided knowledge gained mainly at the local alpha scale (i.e. within ecosystems), but the increasing homogenization of landscapes in the Anthropocene has raised the potential that declining biodiv...
Global Change Biology · 2023 · Vol. 29 · Issue 6 · Wiley
Intensification of land use by humans has led to a homogenization of landscapes and decreasing resilience of ecosystems globally due to a loss of biodiversity, including the majority of forests. Biodiversity–ecosystem functioning (BEF) research has provided compelling evidence for a positive effect of biodiversity on ecosystem functions and services at the local (α‐diversity) scale, but we largely lack empirical evidence on ho...
Plant and Soil · 2020 · Vol. 453 · Issue 1-2 · Springer
Aims Root system responses to the limitation of either nitrogen (N) or phosphorus (P) are well documented, but how the early root system responds to (co-) limitation of one (N or P) or both in a stoichiometric framework is not well-known. In addition, how intraspecific competition alters plant responses to N:P stoichiometry is understudied. Therefore, we aimed to investigate the effects of N:P stoichiometry and competition on...
Oecologia · 2019 · Vol. 191 · Issue 3 · Springer
The exotic South African ragwort ( Senecio inaequidens DC.) rapidly spread across Central Europe after its introduction, but we still do not know to what extent its timing of arrival in a plant community (i.e. before or after natives) and the composition of the native community being invaded affect (1) its capacity to invade a European grassland, (2) the performance of the native species, and (3) the direction and strength of...