Aim Species–area relationships (SARs) are fundamental scaling laws in ecology although their shape is still disputed. At larger areas, power laws best represent SARs. Yet, it remains unclear whether SARs follow other shapes at finer spatial grains in continuous vegetation. We asked which function describes SARs best at small grains and explored how sampling methodology or the environment influence SAR shape. Location Palaearctic grasslands and other non‐forested habitats. Taxa Vascular plants, bryophytes and lichens. Methods We used the GrassPlot database, containing standardized vegetation‐plot data from vascular plants, bryophytes and lichens spanning a wide range of grassland types throughout the Palaearctic and including 2,057 nested‐plot series with at least seven grain sizes ranging from 1 cm2 to 1,024 m2. Using nonlinear regression, we assessed the appropriateness of different SAR functions (power, power quadratic, power breakpoint, logarithmic, Michaelis–Menten). Based on AICc, we tested whether the ranking of functions differed among taxonomic groups, methodological settings, biomes or vegetation types. Results The power function was the most suitable function across the studied taxonomic groups. The superiority of this function increased from lichens to bryophytes to vascular plants to all three taxonomic groups together. The sampling method was highly influential as rooted presence sampling decreased the performance of the power function. By contrast, biome and vegetation type had practically no influence on the superiority of the power law. Main conclusions We conclude that SARs of sessile organisms at smaller spatial grains are best approximated by a power function. This coincides with several other comprehensive studies of SARs at different grain sizes and for different taxa, thus supporting the general appropriateness of the power function for modelling species diversity over a wide range of grain sizes. The poor performance of the Michaelis–Menten function demonstrates that richness within plant communities generally does not approach any saturation, thus calling into question the concept of minimal area.

Similarly to other Mediterranean regions, Italy is expected to experience dramatic climatic changes in the coming decades. Do to their poikilohydric nature, lichens are among the most sensitive organisms to climate change and species requiring temperate-humid conditions may rapidly decline in Italy, such in the case of the epiphytic Lobaria species that are confined to humid forests. Our study, based on ecological niche modelling of occurrence data of three Lobaria species, revealed that in the next decades climate change will impact their distribution range across Italy, predicting a steep gradient of increasing range loss across time slices. Lobaria species are therefore facing a high extinction risk associated with reduction of their range. The current patterns indicate that only L. pulmonaria still has a continuous distribution across Italy, with potential contact between Apennine and Alpine populations. This situation is consistent with the wider climatic niche of this species, still offering a major opportunity for its successful long-term conservation. Results (a) support the inclusion of the three Lobaria species in European conservation policies, such as the Habitat Directive, and (b) warn against an over-estimation of the indicator power of single flagship species to establish conservation priorities for lichens, indicating that even lichens with peculiar and similar climatic envelopes may fail to co-occur within a given forest stand. A multiple indicator approach could provide more useful tools for a community-based conservation strategy for epiphytes.

Aims Understanding fine‐grain diversity patterns across large spatial extents is fundamental for macroecological research and biodiversity conservation. Using the GrassPlot database, we provide benchmarks of fine‐grain richness values of Palaearctic open habitats for vascular plants, bryophytes, lichens and complete vegetation (i.e., the sum of the former three groups). Location Palaearctic biogeographic realm. Methods We used 126,524 plots of eight standard grain sizes from the GrassPlot database: 0.0001, 0.001, 0.01, 0.1, 1, 10, 100 and 1,000 m2 and calculated the mean richness and standard deviations, as well as maximum, minimum, median, and first and third quartiles for each combination of grain size, taxonomic group, biome, region, vegetation type and phytosociological class. Results Patterns of plant diversity in vegetation types and biomes differ across grain sizes and taxonomic groups. Overall, secondary (mostly semi‐natural) grasslands and natural grasslands are the richest vegetation type. The open‐access file ”GrassPlot Diversity Benchmarks” and the web tool “GrassPlot Diversity Explorer” are now available online (https://edgg.org/databases/GrasslandDiversityExplorer) and provide more insights into species richness patterns in the Palaearctic open habitats. Conclusions The GrassPlot Diversity Benchmarks provide high‐quality data on species richness in open habitat types across the Palaearctic. These benchmark data can be used in vegetation ecology, macroecology, biodiversity conservation and data quality checking. While the amount of data in the underlying GrassPlot database and their spatial coverage are smaller than in other extensive vegetation‐plot databases, species recordings in GrassPlot are on average more complete, making it a valuable complementary data source in macroecology.

Summary1. We attempted to elucidate the roles of b-diversity components and similarity in shaping Lobaria pulmonaria lichen communities in Italian forests to provide scientific tools for improving their longterm conservation. 2. A total of 20 sites were selected by stratified random sampling, including five chestnut forests, seven beech-silver fir forests and eight oak forests distributed across 10 administrative regions of Italy. Site selection was based on a national data base including all the available records of L. pulmonaria in Italy. In each forest, four plots were randomly placed, and in each plot, 5-6 trees were randomly selected for lichen sampling. For each forest and plot, meaningful predictors of lichen patterns were quantified. In particular, factors indicative of both geographic conditions and forests structure were considered. The SDR simplex approach was used to estimate the relative importance of similarity (S), relative species replacement (R) and relative richness difference (D) to b-diversity and similarity, while a hierarchical partitioning (HP) method was used to evaluate the relative importance of environmental predictors in explaining their patterns. 3. A total of 201 lichens and three nonlichenized fungi were found, including 51 species of conservation concern. The components of b-diversity and similarity contributed to shaping L. pulmonaria communities at both forest and plot scales across Italy, resulting in nearly random compositions, that is, the species set on each tree was a random sample from the available species pool. Species replacement and similarity were generally associated with forest structure predictors, while richness difference was mainly associated with geographic predictors. The implication of this is that the long-term conservation of L. pulmonaria communities could be promoted by maintaining scattered nodes and appropriate habitat traits, especially in large forested landscapes where species turnover is higher. 4. Synthesis. In this work, we used a new approach for analysing a countrywide data set improving the ecological understanding of the dynamics regulating epiphytic communities. In particular, this study improves the understanding of the contribution of different components of diversity across two spatial scales and evaluates the relative importance of environmental predictors in explaining variation of each diversity component.

Despite the importance for scientific and conservation purposes, the knowledge of the Italian territory is far from exhaustive. New chorological data for 87 vascular taxa regarding the central-southern part of Italy and its two main islands (Sicilia and Sardegna) are presented. Among these taxa, Epilobium nummularifolium, Metrosideros excelsa, and Salvinia minima are recorded as casual aliens for the first time in Europe (excluding Azores and Madeira for M. excelsa), while Cyclamen balearicum and Polygala rupestris are reported for the first time and confirmed for Italian native flora, respectively. Furthermore, several taxa are new or confirmed at regional level. Finally, Lathyrus cirrhosus, Urginea fugax, and Linum tenuifolium are excluded from Italy, continental and peninsular Italy, and Sardegna, respectively.

Marketable yield is the main objective in tomato production, but fair values for quality parameters are also becoming very important. A research project was undertaken for two years to assess the impact of water-saving techniques on yield, fruit quality and water use efficiency (WUE) of processing tomato (cv. Pullrex) in the Mediterranean environment. Additionally, to better understand how irrigation may affect tomato traits, different statistical techniques were applied to the results. Total yield was reduced by 37% on average in both years when half of the crop evapotranspiration (ET) was restored, and maximum marketable tomato yield was obtained under irrigation when 100% of the crop ET was restored. Irrigation cut at tomato veraison (irrigation cutback treatment) did not affect the yield, enhanced fruit quality and maximised WUE, thus contributing to water saving. Through the application of irrigation cutback toward the end of the tomato cycle, there is a possibility to improve tomato quality and, at the same time, save irrigation water. Principal component analysis confirmed that the cutback of irrigation was well correlated with tomato quality

No abstract

In this contribution, new data concerning the distribution of native vascular flora in Italy are presented. It includes new records, confirmations, exclusions, and status changes to the Italian administrative regions for taxa in the genera Ajuga, Chamaemelum, Clematis, Convolvulus, Cytisus, Deschampsia, Eleocharis, Epipactis, Euphorbia, Groenlandia, Hedera, Hieracium, Hydrocharis, Jacobaea, Juncus, Klasea, Lagurus, Leersia, Linum, Nerium, Onopordum, Persicaria, Phlomis, Polypogon, Potamogeton, Securigera, Sedum, Soleirolia, Stachys, Umbilicus, Valerianella, and Vinca. Nomenclatural and distribution updates, published elsewhere, and corrigenda are provided as Suppl. material 1.