August Friedrich Schweigger

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.

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.

Non-native (invasive) species offer a unique opportunity to study the geographical distribution and range limits of species, wherein the evolutionary change driven by interspecific interactions between native and non-native closely related species is a key component. The red-eared slider turtle, Tra…

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…

Environmental change can create opportunities for increased rates of lineage diversification, but continued species accumulation has been hypothesized to lead to slowdowns via competitive exclusion and niche partitioning. Such density-dependent models imply tight linkages between diversification and…