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This dataset presents comprehensive and easy-to-use information on 29 functional traits of clonal growth, bud banks, and lifespan of members of the Central European flora. The source data were compiled from a number of published sources (see the reference file) and the authors' own observations or studies. In total, 2,909 species are included (2,745 herbs and 164 woody species), out of which 1,532 (i.e., 52.7% of total) are classified as possessing clonal growth organs (1,480, i.e., 53.9%, if woody plants are excluded). This provides a unique, and largely unexplored, set of traits of clonal growth that can be used in studies on comparative plant ecology, plant evolution, community assembly, and ecosystem functioning across the large flora of Central Europe. It can be directly imported into a number of programs and packages that perform trait-based and phylogenetic analyses aimed to answer a variety of open and pressing ecological questions.

Below-ground bud banks have experienced much recent interest due to discoveries that they (1) account for the majority of seasonal population renewal in many communities, (2) are crucial to regeneration following disturbance, and (3) have important consequences for plant population dynamics and plant and ecosystem function across a number of habitats. This review presents an overview of the role of bud banks in plant population renewal, examines bud bank life history, summarizes bud bank traits and their potential ecological implications, synthesizes the response of bud banks to disturbance, and highlights gaps to guide future research. The characteristics and life history of buds, including their natality, dormancy, protection and longevity, provide a useful framework for advancing our understanding of bud banks. The fate of buds depends on their age, size, type, location, and biotic and abiotic factors that collectively regulate bud bank dynamics. A bud bank can provide a demographic storage effect stabilizing population dynamics, and also confer resistance to disturbance and invasion. Regeneration capacity following disturbance is determined by interactions among the rates of bud natality, depletion and dormancy (meristem limitation), and the resources available to support the regeneration process. The resulting response of plants and their bud banks to disturbances such as fire, herbivory and anthropogenic sources determines the community's regenerative capacity. Vegetation responses to environmental change may be mediated through changes in bud bank dynamics and phenology. Environmental change that depletes the bud bank or prohibits its formation likely results in a loss of vegetation resilience and plant species diversity. Standardization of bud sampling, examination of bud banks in more ecosystems and their response to environmental variation and disturbance regimes, employment of stage-structured bud bank modelling and evaluation of the cost of bud bank construction and maintenance will benefit this expanding field of research.

Despite long-time awareness of the importance of the location of buds in plant biology, research on belowground bud banks has been scant. Terms such as lignotuber, xylopodium and sobole, all referring to belowground bud-bearing structures, are used inconsistently in the literature. Because soil efficiently insulates meristems from the heat of fire, concealing buds below ground provides fitness benefits in fire-prone ecosystems. Thus, in these ecosystems, there is a remarkable diversity of bud-bearing structures. There are at least six locations where belowground buds are stored: roots, root crown, rhizomes, woody burls, fleshy swellings and belowground caudexes. These support many morphologically distinct organs. Given their history and function, these organs may be divided into three groups: those that originated in the early history of plants and that currently are widespread (bud-bearing roots and root crowns); those that also originated early and have spread mainly among ferns and monocots (nonwoody rhizomes and a wide range of fleshy underground swellings); and those that originated later in history and are strictly tied to fire-prone ecosystems (woody rhizomes, lignotubers and xylopodia). Recognizing the diversity of belowground bud banks is the starting point for understanding the many evolutionary pathways available for responding to severe recurrent disturbances.

• Perennials have a complex shoot architecture with axillary meristems organized in zones of differential bud activity and fate. This includes zones of buds maintained dormant for multiple seasons and used as reservoirs for potential growth in case of damage. The shoot of Arabis alpina, a perennial relative of Arabidopsis thaliana, consists of a zone of dormant buds placed between subapical vegetative and basal flowering branches. This shoot architecture is shaped after exposure to prolonged cold, required for flowering. • To understand how vernalization ensures the maintenance of dormant buds, we performed physiological and transcriptome studies, followed the spatiotemporal changes of auxin, and generated transgenic plants. • Our results demonstrate that the complex shoot architecture in A. alpina is shaped by its flowering behavior, specifically the initiation of inflorescences during cold treatment and rapid flowering after subsequent exposure to growth-promoting conditions. Dormant buds are already formed before cold treatment. However, dormancy in these buds is enhanced during, and stably maintained after, vernalization by a BRC1-dependent mechanism. Post-vernalization, stable maintenance of dormant buds is correlated with increased auxin response, transport, and endogenous indole-3-acetic acid levels in the stem. • Here, we provide a functional link between flowering and the maintenance of dormant buds in perennials.

Recent analyses of plant traits across large sets of species have revolutionized our understanding of plant functional differentiation. However, understanding of ecological relevance of this differentiation is contingent upon knowledge of environmental preferences of species, namely along gradients of disturbance and productivity for which no quantitative data were available until recently. We examined the relationships of key functional traits (life‐history categories, leaf‐height‐seed (LHS) traits, clonal growth and bud bank traits) in the herb‐dominated flora of Central Europe to species niche positions along the gradients of disturbance frequency, disturbance severity and productivity. Life‐history categories and bud bank size showed the strongest response to disturbance and productivity, whereas relationship of LHS traits was much weaker. A number of traits, including clonal growth form and bud bank size, showed a significantly unimodal response to disturbance frequency. Responses of many traits to disturbance frequency were different from their responses to disturbance severity. Our findings support the notions that disturbance and productivity are key gradients of species functional differentiation and that disturbance severity and frequency select for different trait suites. Furthermore, the data indicate that in a predominantly herbaceous flora, the traits of life span, clonal growth and resprouting show stronger relationship with the environment than the LHS traits, which are more important in floras with high proportions of woody species. Since most previous trait analyses are based on woody‐plant‐dominated floras, patterns revealed in a herb‐dominated flora deepen our understanding of the full range of variation within the plant kingdom. A plain language summary is available for this article. Plain Language Summary

Resprouting as a response to disturbance is now widely recognized as a key functional trait among woody plants and as the basis for the persistence niche. However, the underlying mechanisms that define resprouting responses to disturbance are poorly conceptualized. Resprouting ability is constrained by the interaction of the disturbance regime that depletes the buds and resources needed to fund resprouting, and the environment that drives growth and resource allocation. We develop a buds-protection-resources (BPR) framework for understanding resprouting in fire-prone ecosystems, based on bud bank location, bud protection, and how buds are resourced. Using this framework we go beyond earlier emphases on basal resprouting and highlight the importance of apical, epicormic and below-ground resprouting to the persistence niche. The BPR framework provides insights into: resprouting typologies that include both fire resisters (i.e. survive fire but do not resprout) and fire resprouters; the methods by which buds escape fire effects, such as thick bark; and the predictability of community assembly of resprouting types in relation to site productivity, disturbance regime and competition. Furthermore, predicting the consequences of global change is enhanced by the BPR framework because it potentially forecasts the retention or loss of above-ground biomass.

• It remains uncertain how perennial grasses with different photosynthetic pathways respond to fire, and how this response varies with stress at the time of burning. Resprouting after fire was examined in relation to experimentally manipulated pre-fire watering frequencies. We asked the following questions: are there response differences to fire between C₃ and C₄ grasses? And, how does post-fire resprouting vary with pre-fire drought stress? • Fifty-two perennial Australian grasses (37 genera, 13 tribes) were studied. Three watering frequencies were applied to simulate increasing drought. Pre-fire tiller number, tiller density, specific leaf area and leaf dry matter content were measured as explanatory variables to assess response. • Most species (90%) and individuals (79%) resprouted following experimental burning. C₄ grasses had higher probabilities of surviving fire relative to C₃ grasses. Responses were not related to phylogeny or tribe. High leaf dry matter content reduced the probability of dying, but also reduced the re-emergence of tillers. • Post-fire tiller number increased with increasing drought, regardless of photosynthetic type, suggesting that drought plays a role in the ability of grasses to recover after fire. This has implications for understanding the persistence of species in landscapes where fire management is practiced.