Fritz Knoll

Anthropogenic changes drive shifts in species' geographic distributions and increase the occurrence of leading or trailing‐edge marginal populations. Theoretical predictions and empirical observations indicate substantial changes in life‐history traits in marginal populations, often involving dispersal and reproductive abilities. Using a common garden experiment, we studied the variation of life‐history traits of populations sampled on spatial gradients extending from range‐core to range‐edge habitats for three expanding (miner's lettuce Claytonia perfoliata, Danish scurvygrass Cochlearia danica and rock samphire Crithmum maritimum) and one receding plant species (dune pansy Viola tricolor subs. curtisii). We monitored life‐history traits related to dispersal, phenology, survival, reproductive output and selfing ability. Significant shifts in life‐history traits between central and marginal populations strongly differed among species. Marginal populations of the three expanding species displayed modified seed weight in natura, suggesting increased dispersal abilities in leading‐edge populations. Discarding unassessed maternal effects, this trait modification can be due to phenotypic plasticity or to genetic differentiation. In miner's lettuce, marginal expanding populations show advanced phenology and higher reproductive output, that may potentially influence their colonization ability. In rock samphire, life‐history traits showed large intra‐ and inter‐population variability that did not follow a core‐to‐edge geographic trend, except for seed size. Finally, the receding populations of the dune pansy displayed a shift towards a plant architecture maximizing survival but reducing individual reproductive success. Altogether, our results indicated a common trend for increased dispersal abilities in marginal populations of expanding species. However, shifts in species' distributions may drive idiosyncratic changes in other life‐history traits, for which we observed no general evolutionary syndrome at range edges. These findings go along a stochastic view of trait evolution during range expansion, and question how to draw predictive projections of species' distribution shifts under current global change.

The genus Viola (Violaceae) is among the 40–50 largest genera among angiosperms, yet its taxonomy has not been revised for nearly a century. In the most recent revision, by Wilhelm Becker in 1925, the then-known 400 species were distributed among 14 sections and numerous unranked groups. Here, we provide an updated, comprehensive classification of the genus, based on data from phylogeny, morphology, chromosome counts, and ploidy, and based on modern principles of monophyly. The revision is presented as an annotated global checklist of accepted species of Viola, an updated multigene phylogenetic network and an ITS phylogeny with denser taxon sampling, a brief summary of the taxonomic changes from Becker’s classification and their justification, a morphological binary key to the accepted subgenera, sections and subsections, and an account of each infrageneric subdivision with justifications for delimitation and rank including a description, a list of apomorphies, molecular phylogenies where possible or relevant, a distribution map, and a list of included species. We distribute the 664 species accepted by us into 2 subgenera, 31 sections, and 20 subsections. We erect one new subgenus of Viola (subg. Neoandinium, a replacement name for the illegitimate subg. Andinium), six new sections (sect. Abyssinium, sect. Himalayum, sect. Melvio, sect. Nematocaulon, sect. Spathulidium, sect. Xanthidium), and seven new subsections (subsect. Australasiaticae, subsect. Bulbosae, subsect. Clausenianae, subsect. Cleistogamae, subsect. Dispares, subsect. Formosanae, subsect. Pseudorupestres). Evolution within the genus is discussed in light of biogeography, the fossil record, morphology, and particular traits. Viola is among very few temperate and widespread genera that originated in South America. The biggest identified knowledge gaps for Viola concern the South American taxa, for which basic knowledge from phylogeny, chromosome counts, and fossil data is virtually absent. Viola has also never been subject to comprehensive anatomical study. Studies into seed anatomy and morphology are required to understand the fossil record of the genus.

Aims Human-induced pressures such as deforestation cause anthropogenic range contractions (ARCs). Such contractions present dynamic distributions that may engender data misrepresentations within species distribution models. The temporal bias of occurrence data—where occurrences represent distributions before (past bias) or after (recent bias) ARCs—underpins these data misrepresentations. Occurrence–habitat mismatching results when occurrences sampled before contractions are modelled with contemporary anthropogenic variables; niche truncation results when occurrences sampled after contractions are modelled without anthropogenic variables. Our understanding of their independent and interactive effects on model performance remains incomplete but is vital for developing good modelling protocols. Through a virtual ecologist approach, we demonstrate how these data misrepresentations manifest and investigate their effects on model performance. Location Virtual Southeast Asia. Methods Using 100 virtual species, we simulated ARCs with 100-year land-use data and generated temporally biased (past and recent) occurrence datasets. We modelled datasets with and without a contemporary land-use variable (conventional modelling protocols) and with a temporally dynamic land-use variable. We evaluated each model's ability to predict historical and contemporary distributions. Results Greater ARC resulted in greater occurrence–habitat mismatching for datasets with past bias and greater niche truncation for datasets with recent bias. Occurrence–habitat mismatching prevented models with the contemporary land-use variable from predicting anthropogenic-related absences, causing overpredictions of contemporary distributions. Although niche truncation caused underpredictions of historical distributions (environmentally suitable habitats), incorporating the contemporary land-use variable resolved these underpredictions, even when mismatching occurred. Models with the temporally dynamic land-use variable consistently outperformed models without. Main conclusions We showed how these data misrepresentations can degrade model performance, undermining their use for empirical research and conservation science. Given the ubiquity of ARCs, these data misrepresentations are likely inherent to most datasets. Therefore, we present a three-step strategy for handling data misrepresentations: maximize the temporal range of anthropogenic predictors, exclude mismatched occurrences and test for residual data misrepresentations.

Biological communities are reshuffling owing to species range shifts in response to climate change. This process inherently leads to novel assemblages of interacting species. Yet, how climatic change and local dynamics in biotic interactions jointly affect range shifts is still poorly understood.We combine a unique long‐term transplant competition‐exclusion experiment with species distribution models (SDMs) to test the effects of biotic interactions on understorey species range shifts under climate change in European temperate forests. Using a time‐series of 18 years of individual‐level demographic data of four common understorey plant species transplanted beyond their cold range edge to plots with and without interspecific competition, we built integral projection models (IPMs) and analysed the effects of competition on five key vital rates and population growth. We assessed the results of the transplant experiment in the context of the modelled species’ current and future potential distributions.We find that species’ population performances in the transplant experiment decreased with lower predicted habitat suitability from the SDMs. The population performance at the transplant sites was mediated by biotic interactions with the local plant community: for two species with intermediate levels of predicted habitat suitability at the transplant sites, competition effects could explicitly differentiate between net population growth (λ > 1) or shrinkage (λ < 1).Synthesis: Our findings contest the long‐standing idea that at cold range edges, mainly abiotic factors structure species’ distributions. We conclude that biotic interactions, through acting on local population dynamics, may impact species distributions at the continental scale. Hence, predicting climate‐change impacts on biodiversity redistributions ultimately requires us to also integrate dynamics in biotic interactions.

The Qinghai-Tibetan Plateau (QTP) harbors abundant and diverse plant life owing to its high habitat heterogeneity. However, the distribution pattern of biodiversity hotspots and their conservation status remain unclear. Based on 148,283 high-resolution occurrence coordinates of 13,450 seed plants, w…

Identifying physical and ecological boundaries that limit where species can occur is important for predicting how those species will respond to global change. The island of Borneo encompasses a wide range of habitats that support some of the highest richness on Earth, making it an ideal location for…

The Eurasian and Mediterranean Selaginella helvetica group is one of the taxonomically challenging groups in the cosmopolitan lycophyte genus Selaginella. Species of the S. helvetica group are all small plants with lax strobili composed of more or less isomorphic sporophylls (isosporophylls) that ar…

The description of a new species is a key step in cataloguing the World’s flora. However, this is only a preliminary stage in a long process of understanding what that species represents. We investigated how long the species discovery process takes by focusing on three key stages: 1, the collection …

Background The knowledge of distributional dynamics of living organisms is a prerequisite for protecting biodiversity and for the sustainable use of biotic resources. Clematis sect. Fruticella s. str. is a small group of shrubby, yellow-flowered species distributed mainly in arid and semi-arid areas…