Vascular Plant Species Richness Research Articles

Spatial patterns of vascular plant species richness in Poland: Relations among species group richness and hot spot distribution

Knowledge of spatial patterns of species richness (SR) is highly relevant for theoretical research in ecology and the development of conservation plans. In Poland, despite a long tradition of botanical surveys, vascular plant SR has not been mapped, nor have the correlations in richness among different plant species groups been explored at the entire country scale. Here, we used a recently published data set to examine spatial patterns and relationships among the joined SR of vascular plant species, including native species, archaeophytes, neophytes, and species with high conservation value (i.e., red-list species). The basic spatial unit employed was a 10 × 10 km grid from the Atlas of Distribution of Vascular Plants in Poland (ATPOL). We found that SR of native species and archaeophytes, neophytes, and red-list species were positively correlated. The main patterns of SR and the percentage of particular groups in the joined SR were based on three components: (1) gradient of overall SR, (2) invasion level, and (3) peculiarity of flora in some regions resulting from the high number and proportion of rare species that often have high conservation value (red-list species). In general, northeastern Poland was species-poor, while the Carpathian Mountain range, the uplands in southern Poland, and some parts of Wisła River valley had the highest SR concentrations. e location of SR hotspots usually did not overlap with the existing national parks system. The correlations among native SR, high conservation value species, and neophyte SR suggest that biological invasions are among the most important threats to vascular plant diversity in Poland. Finally, despite likely biases in SR assessments, we demonstrated that the presented maps seem to reflect general ecological gradients influencing vascular plant distribution in Poland.

Ash Treatment Promotes the Revegetation of Abandoned Extracted Peatlands

Treating peat with nutrient-rich ash significantly increases the content of different nutrients in the substrate. Such ash treatment promotes the revegetation of abandoned extracted peatlands. The aim of this study is to analyze the effect of wood ash (WA15 = 15 t ha−1 and WA10 = 10 t ha−1), oil shale ash (OSA8 = 8 t ha−1), and a mixture of wood ash and oil shale ash (WA10 + OSA8) on the revegetation (vascular plants and bryophytes) of the Puhatu abandoned extracted peatland in NE Estonia. The following results were obtained: (1) The MRPP tests indicate that there are compositional differences between the treatments. (2) Altogether, 23 vascular plant and 3 bryophyte species were recorded in the treatment areas. (3) Nine years after these ash treatments, the highest mean vascular plant species richness was recorded for WA15 (3.8 ± 0.3) and the lowest for OSA8 (2.0 ± 0.3). (4) A greater number of vascular plant species was observed in the WA15 area. (5) Mixed ash and wood ash had a significant effect on the amount of biomass in vascular plants. Treating with either wood ash or a mixture of ash ensured the rapid formation of vascular plants and bryophyte layers, contributing to the restoration of the abandoned peatland ecosystem.

Plant species richness (PSR) along island biogeographical gradients in inhabited islands of Shinan-gun, Republic of Korea

The objective of this study is assess the influences of 8 environmental factors, population, coastline length, island area, vegetated area, highest peak, distance to the mainland, longitude, latitude on vascular plant species richness (PSR) of 10 inhabited islands of Shinan-gun, South Korea. In simple regression, the relationships between PSR and distance to the mainland, longitude and latitude were significant at the 5% level. When distance increases, longitude and latitude decrease, plant species richness increases. The relationship between PSR and coastline length, island area and highest peak were not significant at 5% level. But coastline length, island area and vegetated area showed negative relation with plant species richness and highest peak showed positive relation. Relationship between population and PSR was not statistically significant and showed negative relation. This may indicate PSR decrease by the effects of human dynamics, but further research is needed. In stepwise regression method three variables, distance, longitude and latitude, explained 98.0% of the variation in PSR.

Association between wild vascular plant species richness and preterm birth in urban areas: a retrospective cohort study in Southern California

Association between wild vascular plant species richness and preterm birth in urban areas: a retrospective cohort study in Southern California

Close to the edge: Spatial variation in plant diversity, biomass and floral resources in conventional and agri‐environment cereal fields

Abstract Non‐crop (segetal) plants in arable systems are commonly perceived simply as ‘weeds’, that is, harmful at worst and undesirable at best. The increase in management intensity in European arable systems has vastly reduced the populations of all but the most disturbance‐tolerant plant species, negatively impacting the whole agricultural food web. In recent years, efforts have been made to promote agricultural biodiversity through measures such as flower strips and unsprayed field margins. However, studies of their impacts on the arable flora have rarely considered their spatial variation within the crop field. We investigated the spatial distribution of vascular plant species richness and their contribution to the food web via biomass and flower units in conventional and agri‐environment cereal fields in six regions of Germany. We studied two types of in‐crop measures (extensive cereals without pesticides or fertiliser, and with or without intercropping with flowering species) and one adjacent measure (neighbouring flower strip), recording at 1‐m intervals from the field edge to the interior. These results were then extrapolated to illustrate the effects of these measures on resource provision at the field scale. Species richness and plant biomass dropped off sharply after the first metre in the conventional treatments, regardless of the adjacent habitat. The ‘extensive’ treatments maintained a much higher level of diversity and resource provision in the field interior. At the field level, this can mean more than a 60‐fold difference in the provision of flowering resources between conventional management (1900 flower units/ha) and agri‐environment measures (AEMs) (127,000 units/ha for extensive cereals). Synthesis and applications. The strong edge effects we found in conventional cultivation support the premise that reducing field sizes could play a role in promoting in‐crop biodiversity. However, incorporating extensive field margins as an AEM would be more efficient at maximising the diversity of generalists whilst maintaining high yields.

Permaculture enhances carbon stocks, soil quality and biodiversity in Central Europe

Permaculture is proposed as a tool to design and manage agroecological systems in response to the pressing environmental challenges of soil degradation, climate change and biodiversity loss. However, scientific evidence on the effects of permaculture is still scarce. In this comprehensive study on a wide range of soil and biodiversity indicators, we examined nine farms utilizing permaculture and paired control fields with locally predominant agriculture in Central Europe. We found 27% higher soil carbon stocks on permaculture sites than on control fields, while soil bulk density was 20% lower and earthworm abundance was 201% higher. Moreover, concentrations of various soil macro- and micronutrients were higher on permaculture sites indicating better conditions for crop production. Species richness of vascular plants, earthworms and birds was 457%, 77% and 197% higher on permaculture sites, respectively. Our results suggest permaculture as effective tool for the redesign of farming systems towards environmental sustainability.

Current and future patterns of vascular plant species richness across a forest–grassland–desert transect in East Asia

AbstractQuestionsRapid climate change has profoundly altered the spatial distribution of terrestrial plants especially in arid and semi‐arid biomes. However, it remains poorly documented how climate shapes the current and future patterns of plant diversity within and across these vulnerable vegetation types.LocationParts of Mongolia, southeastern Russia, and northern China (94.78°–126.78°E, 34.60°–54.27°N).MethodsUsing a random forest model trained by a comprehensively compiled database on vascular plant species richness (i.e., the number of species within a defined plot area) and corresponding climate variables, soil conditions and vegetation types (forest, grassland, desert), we assessed the current pattern of vascular plant species richness across a typical forest–grassland–desert transect in East Asia. We further predicted future changes in vascular plant species richness under three climate scenarios (SSP1‐2.6, SSP3‐7.0, and SSP5‐8.5).ResultsVascular plant species richness generally showed a decrease from northeast to southwest across the transect, mainly explained by spatial variations in growing‐season precipitation and the minimum temperature of the coldest month. More than half of the transect area will likely experience a loss in vascular plant species richness in 2041–2070 under all three scenarios. The decrease in vascular plant species richness will likely occur in a smaller area under the low‐emission scenario (SSP1‐2.6). We also predict distinct changes in vascular plant species richness for different vegetation types, including a slight increase in forests but an overall decrease in both grasslands and deserts.ConclusionsOur findings suggest a dominant role of growing‐season precipitation in shaping the spatiotemporal patterns of vascular plant species richness across the forest–grassland–desert transect and highlight a risk of plant diversity loss in the regional dryland ecosystems in response to future climate change.

Poor transferability of richness models: Predicting plot-scale plant diversity in the Waterberg, South Africa

Modelling measures of biodiversity for understudied taxa or regions is one method to address taxonomic and geographic biases in biodiversity data. However, modelling biodiversity metrics, such as species richness, to unsampled areas is only useful if predictions are reliable. As a result, testing the transferability of richness models is necessary for assessing the potential for models to predict to unsampled areas. Here we test the transferability of plant richness models between two reserves to examine if the richness-environment relationship from one reserve can accurately estimate richness patterns in the other reserve, using the vascular plant species richness of the Waterberg region (savanna biome; northern South Africa) as a model system. Six richness response variables (total species, grass species, herb species, woody species, genus, and family richness) and a set of 16 predictor variables were analysed with three modelling approaches and two statistical techniques to build: (1) models comprising all available predictor variables, (2) models using a subset of predictor variables chosen based on model performance, and (3) models using a subset of predictor variables that reduce the difference in the environmental conditions between the two reserves. The models’ performance in the training area varied considerably, but soil variables were consistently the most important predictors of plant richness. However, the transferability of all the models was consistently poor across all modelling approaches and both techniques, possibly reflecting the degree to which each reserve contains novel environments absent from the other reserve (despite being separated by only c. 60 km and sharing vegetation types). Due to the poor performance of these richness models, they are currently not useful for predicting richness to other areas in the vicinity of the reserves or in the broader region. However, in areas, like the Waterberg region, that have high plant diversity and are poorly sampled, there may be value in continued development of richness models to address biodiversity gaps, thereby providing better data to inform conservation decisions.

Distribution of native plants and birds on 27 remote Tuamotu atolls (South Pacific Ocean): a contribution to the Island species-area relationship

ABSTRACT Island species-area relationship (ISAR) is the most documented pattern in island biogeography. Different hypotheses were advanced to explain this pattern. In this study, I selected 27 remote Tuamotu atolls in the South Pacific Ocean with complete surveys of native species richness of birds and vascular plants to test the influence of four abiotic predictors on species richness (atoll emerged area, habitat diversity, mean elevation, and number of islets). Linear regressions were used to assess the relative influence of predictors on native species richness while stepwise regression was then used to identify the best model. Atoll area was a significant predictor to explain native bird and plant species richness, attesting ISAR on the remote surveyed atolls. Stepwise model demonstrated that both habitat diversity and atoll area explained bird species richness, whereas atoll area and mean elevation were the best predictors for native plants. These results suggest that ISAR can be related to different hypotheses, depending on the taxon studied. Among hypotheses, the simple “target-area” hypothesis was a suitable framework to explain ISAR of native birds, while the “disturbance” hypothesis was relevant to support ISAR of native plants observed on the atolls.

Maintaining habitat diversity at small scales benefits wild bees and pollination services in mountain apple orchards

Abstract Landscape context influences wild bee abundance and diversity, alongside pollination‐related services. Growing evidence supports the positive effects of landscape heterogeneity on bee diversity and fruit production for pollination‐dependent crops in flatlands. However, little remains known about these relationships in mountainous environments where the landscape matrix surrounding crops is often more complex than in lowlands. We conducted our study in apple orchards in South Tyrol, an Alpine region in Italy, using pan‐traps, direct observations of visitation frequency and a pollinator exclusion experiment. We investigated the scale‐dependent effects of landscape heterogeneity and other parameters on wild bee assemblages and the related pollination service they provide at five spatial scales (radius 100–2000 m). We found that landscape heterogeneity positively affected the abundance and richness of wild bees, with the strongest effect at 500 m. We calculated a multidiversity index, reflecting the land‐use intensity based on the species richness of vascular plants, grasshoppers, butterflies, birds and bats. We identified a positive relationship between this multidiversity index and wild bee richness. Additionally, we found that visitation rate of wild bees was negatively affected by crop cover and that abundance of honeybees did not influence wild bee visitation rate or reproductive success. Finally, reproductive success was positively related to semi‐natural habitat cover. Landscape heterogeneity should be maintained in apple orchards to continue to reap the benefits of vital pollination‐related services. Diversification strategies should be implemented to promote habitat diversity at small scales, even in regions with more than 80% of (semi‐)natural habitats.

Topographic Complexity Is a Principal Driver of Plant Endemism in Mediterranean Islands.

The frequency of endemism in the flora of Mediterranean Islands does not follow a straightforward species-area relationship, and the determinants of endemism are several and complex. The aim of this study was to estimate the explanatory power of a small number of variables on the species richness of vascular plants on selected Mediterranean islands and archipelagos, and on the proportion of narrow endemism in each. We used a novel approach whereby the topographic complexity and isolation of an island were estimated through more detailed methods than those utilised previously. These parameters, along with island area and human population density, were used in a number of regression models with the number of taxa or proportion of endemics as the dependent variables. The results demonstrated that 'topography', a factor that was not specifically included in previous models for Mediterranean islands, exerted a consistent, statistically significant effect on both the number of taxa as well as the proportion of endemic taxa, in all models tested. The 'isolation' factor was not a significant predictor of the number of taxa in any of the models but was a statistically significant predictor of the proportion of endemic taxa in two of the models. The results can be used to make broad predictions about the expected number of taxa and endemics on an island, enabling the categorisation of islands as 'species-poor' or 'species-rich', potentially aiding conservation efforts.

Geodiversity data for Europe.

Geodiversity is an essential part of nature's diversity. However, geodiversity is insufficiently understood in terms of its spatial distribution and its relationship to biodiversity over large spatial extents. Here, we present European geodiversity data at resolutions of 1 km and 10 km. We assess terrestrial geodiversity quantitatively as a richness variable (georichness) using a commonly employed grid-based approach. The data incorporate aspects of geological, pedological, geomorphological and hydrological diversity, which are also available as separate richness variables. To evaluate the data, we correlated European georichness with empirically tested national georichness data from Finland, revealing a positive correlation at both 1 km (rp = 0.37, p < 0.001) and 10 km (rp = 0.59, p < 0.001) resolutions. We also demonstrate potential uses of the European data by correlating georichness with vascular plant species richness in two contrasting example areas: Finland and Switzerland. The positive correlations between georichness and species richness in Finland (rp = 0.34, p < 0.001) and Switzerland (rp = 0.26, p < 0.001) further support the use of our data in geodiversity-biodiversity research. Moreover, there is great potential beyond geodiversity-biodiversity questions, as the data can be exploited across different regions, ecosystems and scales. These geodiversity data provide an insight on abiotic diversity in Europe and establish a quantitative large-scale geodiversity assessment method applicable worldwide. This article is part of the Theo Murphy meeting issue 'Geodiversity for science and society'.

Vascular plant communities and biocrusts act as controlling factors in mitigating soil erosion on the Great Wall in a semi-humid area of Northwestern China

The Great Wall, a World Heritage Site and a vertical wall habitat, is under threat of soil erosion. The role of vascular plants and biocrust in controlling soil erosion has attracted attention, yet our knowledge of the underlying mechanism is limited, and there is a lack of systematic strategies for erosion prevention and control. In this study, we quantified the vascular plant community functional composition (including species diversity, functional diversity, and community-weighted mean), biocrust coverage, and soil erosion levels associated with seven different zones (lower, middle, and upper zones on East and West faces, plus wall crest) of the Great Wall. We then employed a combination of linear regression analysis, random forest model, and structural equation model to evaluate the individual and combined effects, as well as the direction and relative importance of these factors in reducing soil erosion. The results indicated that the vascular plant species richness, species diversity, functional richness, community-weighted mean, and moss crust coverage decreased significantly from the crest to the lower zone of the Great Wall (P < 0.05), and were negatively correlated with the soil erosion area and depth on both sides of the Great Wall (P < 0.05). This suggests that higher zones on the wall favored the colonization and growth of biocrusts and vascular plants and that biocrusts and vascular plants reduced soil erosion on the wall. Based on these findings, we propose a “restoration framework” for managing soil erosion on walls, based on biocrust and vascular plant communities (namely target species selection, plant community construction, biocrust inoculation, and maintenance of community stability), which aims to address the urgent need for more effective soil erosion prevention and control strategies on the Great Wall and provide practical methods that practitioners can utilize.

Effect of the rotation frequency in the eucalypt plantations

In the last century, eucalypt plantations are increasing all over the world. Concretely, in the Basque Country (northern Iberian Peninsula), 7% of pine plantations have been recently substituted by eucalypt plantations, where little is known about their ecological impact on soil and plant diversity. However, the most relevant impact is due to forest management, as Eucalyptus globulus Labill. plantations have a short harvesting cycle, 12–15 years rotations. In fact, the species is able to regenerate from stumps; therefore, those plantations are replanted after 3–4 rotations. This type of invasive and frequent management could lead to further adverse effects on the ecosystem. The aim of this study was to characterise and compare the eucalypt plantations newly established (New: never been harvested) with older ones (Old: several times harvested and grown from stumps), having been established for at least 35 years, and to identify the primary factors that could influence the richness and diversity of vascular plant species in those plantations. The results indicated that both plantations exhibited comparable characteristics with respect to deadwood (volume and decay stage) and tree size and density. However, the Old plantations exhibited higher forest heterogeneity, pH, and higher shrub and herb richness and diversity. Overall, generalist and invasive species were found in the New plantations, while in the Old plantations, typical species of the native forests were also observed. The factor that influenced plant diversity was the volume of deadwood. Regarding life forms, higher altitude and proximity to watercourses favoured tree diversity; and lower canopy cover, shrub diversity. In conclusion, the longer the plantation has been established, the greater the number of species that are able to survive and adapt. This is probably due to the fact that management disturbance is specific and not sufficient to remove the already established plants and the soil seed bank.

Cut stumps vs broken stumps: Does it make any difference in the maintenance of plant and lichen biodiversity in Central European mountain forests?

Excessive forest exploitation significantly contributes to land degradation and the creation of human-made deadwood. Stumps are sometimes ignored in studies on the biodiversity of coarse woody debris. We investigated whether the type of stump, i.e. broken stumps (naturally created) and cut stumps (formed during forestry operations) had an impact on the species composition and species diversity as well as due to this fact they can be characterized by plant indicators. The research covered 728 spruce stumps (287 broken and 441 cut stumps) that were inhabited by lichens, liverworts, mosses and vascular plants in mountain forest belt (Karkonosze Mts., Poland). The following types of microhabitats were included in the research: the upper surface and the lateral surface of a stump with both bark and wood. There are statistically significant compositional differences between the two types of stumps, which was demonstrated by ordination analyses and indicator species analysis. According to the generalized linear models, the probability of occurrence increases in cut stumps in case of liverworts and vascular plants and also along the decomposition stages. The generalized linear mixed-effects model showed that there was a higher species richness of liverworts, mosses and vascular plants on the cut stumps and less drier but the reverse situation was in lichens. The generalized additive models for their cover showed similar trends. Almost all of the taxonomic groups were affected by altitude both in terms of species composition and total cover on the stumps. We concluded that cut stumps are an important type of deadwood for biodiversity and provide a convenient habitat, especially for many lichens and bryophytes.

Wealth of Vascular Plants of Avani Seeds Vidhya Sankul, Mehsana, Dist. Mehsana, North Gujarat, India

The present study was aimed at determining the vascular plant species richness of the Avani seeds vidhya-sankul, Mehsana campus. For this, the species richness data was obtained by both secondary sources and intensive surveys from 2020-2022. Campus is extended over 8 acres of land. The campus area are the representative of climax vegetation and exhibit the diversity of species such as trees, shrubs, herbs, climbers and other shade loving herbs. Botanical gardens have valuable medicinal and other plants having high economic value. The data from the primary and secondary sources resulted in the documentation of 284 species belonging to 239 genera under 86 families. Leguminosae and Poaceae were the dominant dicotyledonous and monocotyledonous families respectively. 96% species are belonging angiosperms plants and Zemia pygmea Sims is a rare plants belonging gymnosperms in campus.

How diverse are the mountain karst forests of Mexico?

Tropical forests on karstic relief (tropical karst forest) are among the most species-rich biomes. These forests play pivotal roles as global climate regulators and for human wellbeing. Their long-term conservation could be central to global climate mitigation and biodiversity conservation. In Mexico, karst landscapes occupy 20% of the total land surface and are distributed mainly in the southeast of the country, along the eastern slope, and in the Yucatan Peninsula. Within each of these areas, the following types of karst occur: coastal karst, plain karst, hill karst, and mountain karst (low, medium, high). Mountain karst cover 2.07% of Mexico's land surface and are covered by tropical rainforests, montane cloud forests, and tropical deciduous forests. These are probably one of the most diverse biomes in Mexico. However, the mountain karst forests of Mexico have received little attention, and very little is known about their diversity. Here, we evaluated the vascular plant species richness within the mountain karst forests of Mexico. We assembled the first, largest, and most comprehensive datasets of Mexican mountain karst forest species, from different public databases (CONABIO, GBIF, IBdata-UNAM), which included a critical review of all data. We compiled a list of the families, genera, and species present within the mountain karst forests of Mexico. Taxa that best characterize these forests were identified based on their spatial correlation with this biome. We explored biodiversity patterns, identifying areas with the highest species richness, endemism centers, and areas of relatively low sampling intensity. We found that within the mountain karst forests of Mexico there are representatives of 11,771 vascular plant species (253 families and 2,254 genera), ca. 50% of the Mexican flora. We identified 372 species endemic to these forests. According to preliminary IUCN red list criteria, 2,477 species are under some category of conservation risk, of which 456 (3.8%) are endangered. Most of the Mexican mountain karst forests have been extensively explored and six allopatric, species-rich areas were identified. Compared to other regions in the world, the mountain karst forests of Mexico are one of the most diverse biomes. They contain more species than some entire montane systems in Mexico such as Sierra Madre Oriental, and Sierra Madre del Sur. Also, the mountain karst forests of Mexico are most diverse than similar forests of South America and Asia, even if considering the effect of different sampling areas. The fact that mountain karst forests are embedded in areas of high biotic diversity, probably contributes to their great floristic diversity. Thus, the mountain karst forests of Mexico are an important source of diversity and shelters a large percentage of the Mexican flora.

Rapid functional but slow species diversity recovery of steppe vegetation on former arable fields in southern Ukraine

AbstractQuestionsEuropean steppes are among the most threatened ecosystems in the Palaearctic region, mainly because of conversion to arable land. Abandonment may allow for the passive recovery of steppes. We made use of an exceptional old‐field succession chronosequence of nearly 100 years to answer the following questions: (a) Are the plant species composition, species richness and functional characteristics typical of virgin grass steppes able to self‐restore during ca. 100 years after abandonment? (b) Do the rates of recovery of the above vegetation characteristics differ over the studied chronosequence? (c) Do topsoil carbon and nitrogen content change over the succession chronosequence, leading to concentrations similar to that of virgin steppes?LocationSouthern Ukraine.MethodsWe sampled vegetation and soil in a virgin grass steppe and in old fields abandoned for 6, 15, 31, 50 and ca. 97 years. We subjected the composition data to multivariate analysis. To test whether species richness, functional and soil characteristics of the old fields diverge from those of the virgin steppe, we used one‐way analysis of variance with Tukey's honestly significant difference (HSD) statistic to create 90% confidence intervals.ResultsThe vegetation composition of the three most recently abandoned old fields differed significantly from that of the virgin steppe. The species richness of vascular plants was lower in old fields than in the virgin steppe. The share of steppe habitat specialists was similar to the virgin steppe only in the field abandoned for ca. 97 years. Functional characteristics were significantly different from the virgin steppe only in the most recently abandoned old field. Contents of Corg and Ntot in fields abandoned for ≤50 years were lower compared with the virgin steppe.ConclusionsThe functional characteristics of steppe vegetation seem to recover much faster than its biodiversity. However, based on our results, 100 years can be enough time for the spontaneous re‐establishment of typical steppe vegetation.

How does understory vegetation diversity and composition differ between monocultures and mixed plantations of hybrid poplar and spruce?

Although monocultures are important for timber production, they are often associated with lower biological diversity than mixtures. Thus, mixed plantations have been suggested as a way to enhance biodiversity because of their inherent compositional diversity. However, the effects of monocultures versus mixtures on understory diversity and composition can vary in different ecosystems. The objective of this study was to assess how monocultures and mixed plantations influence understory vegetation diversity and composition in the boreal forest region of southern Quebec. We sampled plantations established with deciduous Populus trichocarpa Torrey & A. Gray × balsamifera L. and P. maximowiczii Henry × balsamifera L. and coniferous Picea abies (L.) Karst. and Picea glauca (Moench) species planted in monocultures and in mixed plantations on abandoned farmlands and a forest site. We assessed understory vegetation diversity and composition in each canopy type (coniferous, deciduous, mixed) and in each plantation type. We evaluated bryophyte and lichen diversity and composition specifically in tree microhabitats: soil, tree bases, and tree trunks. We found that vascular plant and lichen species richness was similar in all plantation types, while bryophyte species richness was higher in spruce monocultures and in mixed plantations compared to poplar monocultures. Our results also highlight how land-use history influenced vascular plant composition as abandoned farmland sites were composed of more ruderal vascular plants, while the previously forested site was composed of species found in natural forests. In the context of reforestation and plantations, our study suggests mixing spruce with poplars to maximize understory vegetation diversity as the addition of spruce in mixed plantations promoted the establishment of terrestrial bryophytes, while poplars favored the establishment of epiphytic lichens.

Spatial patterns of phylogenetic and species diversity of Fennoscandian vascular plants in protected areas

Protected areas are one of the main strategic means for conserving biodiversity. Yet, the design of protected areas usually neglects phylogenetic diversity, an important diversity measure. In this paper we assess the phylogenetic diversity and species richness of vascular plants in Fennoscandian protected areas. We evaluate how much species richness and phylogenetic diversity is found within and outside protected areas, and the differences in plant diversity between different categories of protected areas. We also assess the differences in the diversity-area relationship of the different protected area categories in terms of both species richness and phylogenetic diversity. We build a multi-locus phylogeny of 1,519 native vascular plants of Norway, Sweden, and Finland. We estimate the phylogenetic diversity and species richness by combining the phylogeny with publicly available occurrence data and the currently protected area system of Fennoscandia. Our results indicate that protected areas in Fennoscandia hold more plant diversity when larger, and that phylogenetic diversity increases faster with area than species richness. We found evidence for more plant diversity outside of protected areas of the different countries of Fennoscandia than inside of protected areas, but no evidence for plant diversity differences between areas with different protection status. Hence, our results indicate that the current protected area system in Fennoscandia is no more effective in conserving phylogenetic diversity and species richness of vascular plants than a random selection of localities. Our results also indicate that planning conservation strategies around phylogenetic diversity, rather than species richness, might be a first step to protect vascular plant diversity more effectively.