The Pladias (Plant Diversity Analysis and Synthesis) Database of the Czech Flora and Vegetation was developed by the Pladias project team in 2014-2018 and has been continuously updated since then. The flora section of the database contains critically revised information on the Czech vascular flora, including 13.6 million plant occurrence records, which are dynamically displayed in maps, and data on 120 plant characteristics (traits, environmental associations and other information), divided into the sections: (1) Habitus and growth type, (2) Leaf, (3) Flower, (4) Fruit, seed and dispersal, (5) Belowground organs and clonality, (6) Trophic mode, (7) Karyology, (8) Taxon origin, (9) Ecological indicator values, (10) Habitat and sociology, (11) Distribution and frequency, and (12) Threats and protection. The vegetation section of the database contains information on Czech vegetation types extracted from the monograph Vegetation of the Czech Republic. The data are supplemented by national botanical bibliographies, electronic versions of the standard national flora and vegetation monographs, a database of more than 19,000 pictures of plant taxa and vegetation types, and digital maps (shapefiles) with botanical information. The data from the database are available online on a public portal www.pladias.cz, which also provides download options for various datasets and online identification keys to the species and vegetation types of the Czech Republic. In this paper, we describe the general scope, structure and content of the database, and details of the data on plant characteristics. To illustrate the data and describe the main geographic patterns in selected plant characteristics, we provide maps of mean values of numerical characteristics or proportions of categories for categorical characteristics on the map of the country in a grid of 5 longitudinal × 3 latitudinal minutes (approximately 6.0 km × 5.5 km). We also summarize the main variation patterns in the functional traits in the Czech flora using the principal component analysis.

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SummaryPolyploidy is widely recognized as a major mechanism of sympatric speciation in plants, yet little is known about its effects on interactions with other organisms. Mycorrhizal fungi are among the most common plant symbionts and play an important role in plant nutrient supply. It remains to be understood whether mycorrhizal associations of ploidy-variable plants can be ploidy-specific.We examined mycorrhizal associations in three cytotypes (2x, 3x, 4x) of the Gymnadenia conopsea group (Orchidaceae), involving G. conopsea s.s. and G. densiflora, at different spatial scales and during different ontogenetic stages. We analysed: adults from mixed-and single-ploidy populations at a regional scale; closely spaced adults within a mixed-ploidy site; and mycorrhizal seedlings.All Gymnadenia cytotypes associated mainly with saprotrophic Tulasnellaceae (Basidiomycota). Nonetheless, both adults and seedlings of diploids and their autotetraploid derivatives significantly differed in the identity of their mycorrhizal symbionts. Interploidy segregation of mycorrhizal symbionts was most pronounced within a site with closely spaced adults.This study provides the first evidence that polyploidization of a plant species can be associated with a shift in mycorrhizal symbionts. This divergence may contribute to niche partitioning and facilitate establishment and co-existence of different cytotypes.

SummaryRoot hemiparasites are green photosynthetic plants, which parasitically acquire resources from host xylem. Mineral nutrients and water, two principal below-ground abiotic resources, were assumed to affect the interaction between hemiparasites and their hosts. The shape of these effects and the underlying physiological mechanisms have, however, remained unclear.We conducted a glasshouse experiment with root-hemiparasitic Rhinanthus alectorolophus, in which we manipulated the availability of mineral nutrients and water. Biomass production and Chl fluorescence of the hemiparasites and hosts were recorded, together with proportion of host-derived carbon in hemiparasite biomass.The abiotic resources had profound interactive effects on the performance of both the hemiparasite and the hosts, as well as the balance of above-ground biomass between them. These effects were mainly based on an increase of growth and photosynthetic efficiency under high nutrient concentrations, on the hemiparasite's ability to induce strong water stress on the hosts if water is limiting, and on release of the host from parasitism by simultaneous abundance of both resources.Hemiparasitism is a highly variable interaction, in which environmental conditions affect both the parasitic and autotrophic (and thus competitive) components. A hemiparasite's own photosynthesis plays a crucial role in the assimilation of parasitized mineral resources and their transformation into growth and fitness.

Rhinanthoid Orobanchaceae form a monophyletic lineage that include the hemiparasitic genera Euphrasia, Melampyrum, Tozzia, Bartsia, Nothobartsia, Odontites (s.l.), Rhinanthus, Rhynchocorys, Parentucellia, Hedbergia and holoparasitic Lathraea. In this study, we aimed to reconstruct the phylogeny, evolution of life-history traits (life cycle and seed size) and explain the extant biogeographical patterns in this group. For phylogenetic reconstruction, we used molecular data obtained by sequencing the nuclear ITS region and the chloroplast trnT-trnL intergenic spacer and matK+trnK regions. The genus Melampyrum was found to occupy the sister position to the rest of the group. The other genera were assembled in the sister Rhinanthus-Rhynchocorys-Lathraea and Bartsia-Euphrasia-Odontites subclades. The reconstruction of life-cycle evolution yielded ambiguous results suggesting nonetheless a substantially higher likelihood of perenniality compared to annuality in most ancestor lineages. Seed size varied across two orders of magnitude (average weight per seed: 0.02-7.22 mg) and tended to decrease in the Bartsia-Euphrasia-Odontites subclade compared to the rest of the group. Seed-size evolution was correlated with life-history evolution in the group if the generally small-seeded Bartsia-Euphrasia-Odontites subclade is excluded. We formulated hypotheses relating the extant biogeographical affinities of individual genera to the geological history of the Euro-Caucasian diversity center of the group. Notable dispersal events in Euphrasia and Bartsia were hypothesized to be allowed or at least facilitated by a specific combination of the life-history traits.

Summary Heterotrophic acquisition of substantial amounts of organic carbon by hemiparasitic plants was clearly demonstrated by numerous studies. Many hemiparasites are, however, also limited by competition for light preventing the establishment of their populations on highly productive sites. In a growth‐chamber experiment, we investigated the effects of competition for light, simulated by shading, on growth and heterotrophic carbon acquisition by the hemiparasite Rhinanthus alectorolophus attached to C3 and C4 hosts using analyses of biomass production and stable isotopes of carbon. Shading had a detrimental effect on biomass production and vertical growth of the hemiparasites shaded from when they were seedlings, while shading imposed later caused only a moderate decrease of biomass production and had no effect on the height. Moreover, shading increased the proportion of host‐derived carbon in hemiparasite biomass (up to 50% in shaded seedlings). These results demonstrate that host‐derived carbon can play a crucial role in carbon budget of hemiparasites, especially if they grow in a productive environment with intense competition for light. The heterotrophic carbon acquisition can allow hemiparasite establishment in communities of moderate productivity, helping well‐attached hemiparasites to escape from the critical seedling stage.

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Abbreviations g(r) or PCF = pair correlation function; j mm (r) = mark correlation function; j id (r) = distance decay (similarity) function; c(r) = mark variogram; NM = null model. NomenclatureFull names of species are in Table S1. AbstractQuestions: How do spatial patterns of tree distribution and species co-occurrence differ between primary and secondary tropical rain forests? What signatures of ecological processes might be discerned by comparing the spatial patterns of trees between primary and secondary forest plots?Location: Tropical rain forest vegetation, lowlands of Papua New Guinea.Methods: All trees over 5 cm DBH were surveyed in two non-replicated 1-ha plots situated in primary and secondary forest. Grid location, DBH, height and species identity were recorded for all surveyed trees. Analysis of the spatial pattern and the autocorrelation of tree sizes and identities were used to assess the structure of the forest found within the plots. Functions combining Ripley's K and the individual species-area relationship were applied to study the spatial distribution of trees and species diversity.Results: The spatial distribution of common species, and all stems collectively, was aggregated in the secondary forest plot but not different from random in the primary forest plot. Diameter and height were also strongly spatially auto-correlated in the secondary forest plot but not in the primary forest plot. Conspecific aggregations were more common in the secondary forest plot. Finally, the secondary forest plot was characterized by the presence of diversity-repelling species and lower diversity than the primary forest plot, where diversityaccumulating species were present. Conclusions:We attribute the weaker autocorrelation of tree size in the primary forest to the development of size hierarchies throughout the course of stand aging. The conspecific aggregation and low local diversity within the secondary forest plot are likely caused by dispersal limitation during a brief period of establishment after disturbance. The higher local diversity of the primary forest can be explained by the reduction of species aggregation through increased mortality of conspecifics. This is caused by strong intraspecific competition, supporting the spatial segregation hypothesis (interspecific spatial segregation).