Search

The UN Decade on Ecosystem Restoration calls for upscaling restoration efforts, but many terrestrial restoration projects are constrained by seed availability. To overcome these constraints, wild plants are increasingly propagated on farms to produce seeds for restoration projects. During on-farm propagation, the plants face non-natural conditions with different selection pressures, and they might evolve adaptations to cultivation that parallel those of agricultural crops, which could be detrimental to restoration success. To test this, we compared traits of 19 species grown from wild-collected seeds to those from their farm-propagated offspring of up to four cultivation generations, produced by two European seed growers, in a common garden experiment. We found that some plants rapidly evolved across cultivated generations towards increased size and reproduction, lower within-species variability, and more synchronized flowering. In one species, we found evolution towards less seed shattering. These trait changes are typical signs of the crop domestication syndrome, and our study demonstrates that it can also occur during cultivation of wild plants, within only few cultivated generations. However, there was large variability between cultivation lineages, and the observed effect sizes were generally rather moderate, which suggests that the detected evolutionary changes are unlikely to compromise farm-propagated seeds for ecosystem restoration. To mitigate the potential negative effects of unintended selection, we recommend to limit the maximum number of generations the plants can be cultivated without replenishing the seed stock from new wild collections.

Several larger vertebrate species have recovered from dramatic bottlenecks caused by overhunting and habitat destruction. One of the most notable comebacks concerns the Eurasian beaver (Castor fiber L.), which has increased its range by natural dispersal from both relict populations and populations established through translocations. Genetic methods have recently been used to study beavers at several locations. However, owing to a lack of reference samples from relict populations and alternative names of mitochondrial DNA haplotypes, the ancestry of re-established beaver populations remains obscure. Here, we focus on the genetic characterization of several newly established populations. Unlike previous studies, we also used microsatellite genotypes of reference samples from all relict populations. Our analysis was fully capable of tracing the origin of the nuclear and mitochondrial genome to relict populations. Although we confirmed an extraordinarily low genetic diversity in relict populations, our analysis showed restored diversity in newly established populations resulting from translocations. Recent expansions and stochastic effects have created a strong but complicated population structure, with neighbouring populations differing significantly in genetic composition. We conclude that this restored genetic diversity very likely contributes to the viability and ongoing expansion of the newly established populations.

Plants must continuously respond to environmental changes, and a timely question is whether and how populations respond to ongoing global warming and increased drought frequencies and intensities. Plants can either respond through migration or through phenotypic plasticity or their populations can adapt evolutionarily, which encompasses the evolution of trait means and of trait plasticity. One way to detect such evolutionary changes within plant populations is through historical comparisons where plants grown from seeds collected in the past (“ancestors”) are compared to freshly collected seeds from the same populations (“descendants”) in common garden experiments. We used 21- to 26-year-old seeds stored in seed banks for two multi-species experiments that investigated changes in phenotypic traits and their plasticity conferring drought tolerance in early life stages of European plant species. In the first experiment, we used seedlings of four Mediterranean species, ceased watering and recorded their day of mortality. In the second experiment, we studied phenotypic responses to drought in juvenile plants of nine species originating from temperate regions in Europe. In one of four species in the first experiment, descendants survived significantly longer without watering and were smaller than their ancestors. In the second experiment, descendant plants were generally taller under well-watered conditions but smaller under drought than their ancestors, thus showing stronger plasticity. Our historical comparisons suggest that some populations have likely evolved through changes in trait means and plasticity in ways consistent with adaptation to increased drought. Using seed bank material for historical comparisons has several weaknesses, such as unknown sampling protocols or invisible fractions. However, we show how accurately sampled and stored seed bank collections can be used similar to the resurrection approach for investigating rapid evolutionary processes in early life stages of plants under climate change.

Addressing global biodiversity loss requires an expanded focus on multiple dimensions of biodiversity. While most studies have focused on the consequences of plant interspecific diversity, our mechanistic understanding of how genetic diversity within plant species affects plant productivity remains limited. Here, we use a tree species × genetic diversity experiment to disentangle the effects of species diversity and genetic diversity on tree productivity, and how they are related to tree functional diversity and trophic feedbacks. We found that tree species diversity increased tree productivity via increased tree functional diversity, reduced soil fungal diversity, and marginally reduced herbivory. The effects of tree genetic diversity on productivity via functional diversity and soil fungal diversity were negative in monocultures but positive in the mixture of the four tree species tested. Given the complexity of interactions between species and genetic diversity, tree functional diversity and trophic feedbacks on productivity, we suggest that both tree species and genetic diversity should be considered in afforestation.Biodiversity, the richness of species in a given ecosystem, is essential for maintaining ecological functions. This is supported by many long-term biodiversity experiments where researchers manipulated the numbers of tree species they planted in a forest and then evaluated both its productivity (how much biological material the forest produced in a given timeframe) and the health of its trees. This work contributed to our understanding of forest ecology and paved the way for better reforestation approaches. The most important observation was that diverse forests, which contain several tree species, are more productive and healthier than monocultures where a single tree species dominates. However, it remained unclear what the role of genetic diversity within individual tree species is in determining productivity and health of forests. Tang, Zhang et al. set out to improve on previous studies on tree genetic diversity and community productivity by looking at two possible mechanisms that might affect the productivity of a forest ecosystem using publicly available data. First, they looked at the diversity of traits found within a tree population, which determines what resources in the ecosystem the trees can exploit; for example, trees with varied specific leaf areas (that is the ratio between a leaf’s area and its dry mass) have more access to different intensities of sunlight for photosynthesis, allowing the whole forest to gain more biomass. Second, they considered interactions with other organisms such as herbivore animals and soil fungi that affect tree growth by either consuming their leaves or competing for the same resources. Tang, Zhang et al. used a mathematical model to interpret a complex dataset that includes multiple parameters for each of four types of forest: a forest with a single tree species seeded from a single parent tree (which will have low species and genetic diversity), a forest with a single tree species seeded from several parent trees (low species diversity and high genetic diversity, due to the diversity of parents), a forest with four tree species each seeded from a single parent tree (high species diversity and low genetic diversity), and a forest with four tree species each seeded from several parent trees (high species and genetic diversity). Using their model, Tang, Zhang et al. determined that species diversity promotes productivity because the increased diversity of traits allows trees to exploit more of the surrounding resources. Genetic diversity, on the other hand, did not seem to have a direct effect on overall productivity. However, greater genetic diversity did coincide with an increase in the diversity of traits in forests with a single tree species, which led to a decrease in damage to tree leaves by herbivores. This suggests that high genetic diversity in species-rich forests is likely also beneficial as herbivores are less able to damage tree foliage. As expected, in single-species forests with both low and high genetic diversity, higher soil fungi diversity was associated with a loss in productivity. Interestingly, in forests that had high species and genetic diversity, this effect was reversed, and higher genetic diversity reduced the loss of productivity caused by soil fungi, resulting in higher productivity overall. These results should be considered in reforestation projects to promote genetic diversity of trees on top of species diversity when replanting. How genetic diversity leads to downstream mechanisms that benefit community productivity is not fully understood and future research could look at what specific genetic features matter most to help select the ideal mixture of trees to maximize productivity and increase the land’s ecological and economic value.

Projections of global climate models suggest that ongoing human-induced climate change will lead to an increase in the frequency of severe droughts in many important agricultural regions of the world. Eco-hydrological models that integrate current understanding of the interacting processes governing soil water balance and plant growth may be useful tools to predict the impacts of climate change on crop production. However, the validation status of these models for making predictions under climate change is still unclear, since few suitable datasets are available for model testing. One promising approach is to test models using data obtained in “space-for-time” substitution experiments, in which samples are transferred among locations with contrasting current climates in order to mimic future climatic conditions. An important advantage of this approach is that the soil type is the same, so that differences in soil properties are not confounded with the influence of climate on water balance and crop growth. In this study, we evaluate the capability of a relatively simple eco-hydrological model to reproduce 6 years (2013–2018) of measurements of soil water contents, water balance components and grass production made in weighing lysimeters located at two sites within the TERENO-SoilCan network in Germany. Three lysimeters are located at an upland site at Rollesbroich with a cool, wet climate, while three others had been moved from Rollesbroich to a warmer and drier climate on the lower Rhine valley floodplain at Selhausen. Four of the most sensitive parameters in the model were treated as uncertain within the framework of the GLUE (generalized likelihood uncertainty estimation) methodology, while the remaining parameters in the model were set according to site measurements or data in the literature. The model satisfactorily reproduced the measurements at both sites, and some significant differences in the posterior ranges of the four uncertain parameters were found. In particular, the results indicated greater stomatal conductance as well an increase in dry-matter allocation below ground and a significantly larger maximum root depth for the three lysimeters that had been moved to Selhausen. As a consequence, the apparent water use efficiency (above-ground harvest divided by evapotranspiration) was significantly smaller at Selhausen than Rollesbroich. Data on species abundance on the lysimeters provide one possible explanation for the differences in the plant traits at the two sites derived from model calibration. These observations showed that the plant community at Selhausen had changed significantly in response to the drier climate, with a significant decrease in the abundance of herbs and an increase in the proportion of grass species. The differences in root depth and leaf conductance may also be a consequence of plasticity or acclimation at the species level. Regardless of the reason, we may conclude that such adaptations introduce significant additional uncertainties into model predictions of water balance and plant growth in response to climate change.

BackgroundOpen cast lignite mines, sand pits and military training areas represent human-made, secondary habitats for specialized xerothermophilous and psammophilous species. Rare species, including the earwigLabidurariparia,are found in high population densities in such sites. However, it is unknown from which sources colonisation took place and how genetic variation compares to that of ancient populations on natural sites.MethodsUsing nine microsatellite markers, we analysed genetic variation and population structure ofL. ripariain 21 populations in NE Germany both from secondary habitats such as lignite-mining sites, military training areas and a potassium mining heap, and rare primary habitats, such as coastal and inland dunes.ResultsGenetic variation was higher in populations from post-mining sites and former military training areas than in populations from coastal or inland dune sites. Overall population differentiation was substantial (FST = 0.08;FʹST = 0.253), with stronger differentiation among primary (FST = 0.196;FʹST = 0.473) than among secondary habitats (FST = 0.043;FʹST = 0.147). Differentiation followed a pattern of isolation by distance. Bayesian structure analysis revealed three gene pools representing primary habitats on a coastal dune and two different inland dunes. All populations from secondary habitats were mixtures of the two inland dune gene pools, suggesting multiple colonization of post-mining areas from different source populations and hybridisation among source populations.DiscussionPopulations ofL. ripariafrom primary habitats deserve special conservation, because they harbour differentiated gene pools. The majority of theL. ripariapopulations, however, thrive in secondary habitats, highlighting their role for conservation.Implications for insect conservationA dual strategy should be followed of conserving both remaining natural habitat harbouring particular intraspecific gene pools and secondary habitat inhabited by large admixed and genetically highly variable populations.

Environmental monitoring involves the quantification of microscopic cells and particles such as algae, plant cells, pollen, or fungal spores. Traditional methods using conventional microscopy require expert knowledge, are time-intensive and not well-suited for automated high throughput. Multispectral imaging flow cytometry (MIFC) allows measurement of up to 5000 particles per second from a fluid suspension and can simultaneously capture up to 12 images of every single particle for brightfield and different spectral ranges, with up to 60x magnification. The high throughput of MIFC has high potential for increasing the amount and accuracy of environmental monitoring, such as for plant-pollinator interactions, fossil samples, air, water or food quality that currently rely on manual microscopic methods. Automated recognition of particles and cells is also possible, when MIFC is combined with deep-learning computational techniques. Furthermore, various fluorescence dyes can be used to stain specific parts of the cell to highlight physiological and chemical features including: vitality of pollen or algae, allergen content of individual pollen, surface chemical composition (carbohydrate coating) of cells, DNA- or enzyme-activity staining. Here, we outline the great potential for MIFC in environmental research for a variety of research fields and focal organisms. In addition, we provide best practice recommendations.

Land use change, by disrupting the co-evolved interactions between plants and their pollinators, could be causing plant reproduction to be limited by pollen supply. Using a phylogenetically controlled meta-analysis on over 2200 experimental studies and more than 1200 wild plants, we ask if land use intensification is causing plant reproduction to be pollen limited at global scales. Here we report that plants reliant on pollinators in urban settings are more pollen limited than similarly pollinator-reliant plants in other landscapes. Plants functionally specialized on bee pollinators are more pollen limited in natural than managed vegetation, but the reverse is true for plants pollinated exclusively by a non-bee functional group or those pollinated by multiple functional groups. Plants ecologically specialized on a single pollinator taxon were extremely pollen limited across land use types. These results suggest that while urbanization intensifies pollen limitation, ecologically and functionally specialized plants are at risk of pollen limitation across land use categories., An insufficient amount of pollen transfer by pollinators (pollen limitation) could reduce plant reproduction in human-impacted landscapes. Here the authors conduct a global meta-analysis and find that pollen limitation is high in urban environments and depends of plant traits such as pollinator dependency.

Ensuring ecosystem resilience is an intuitive approach to safeguard the functioning of ecosystems and hence the future provisioning of ecosystem services (ES). However, resilience is a multi-faceted concept that is difficult to operationalize. Focusing on resilience mechanisms, such as diversity, network architectures or adaptive capacity, has recently been suggested as means to operationalize resilience. Still, the focus on mechanisms is not specific enough. We suggest a conceptual framework, resilience trinity, to facilitate management based on resilience mechanisms in three distinctive decision contexts and time-horizons: i) reactive, when there is an imminent threat to ES resilience and a high pressure to act, ii) adjustive, when the threat is known in general but there is still time to adapt management, and iii) provident, when time horizons are very long and the nature of the threats is uncertain, leading to a low willingness to act. Resilience has different interpretations and implications at these different time horizons, which also prevail in different disciplines. Social ecology, ecology, and engineering are often implicitly focussing on provident, adjustive, or reactive resilience, respectively, but these different notions and of resilience and their corresponding social, ecological, and economic trade-offs need to be reconciled. Otherwise, we keep risking unintended consequences of reactive actions, or shying away from provident action because of uncertainties that cannot be reduced. The suggested trinity of time horizons and their decision contexts could help ensuring that longer-term management actions are not missed while urgent threats to ES are given priority.

Ongoing global warming, coupled with increased drought frequencies, together with other biotic drivers may have resulted in complex evolutionary adaptation. The resurrection approach, comparing ancestors raised from stored seeds with their contemporary descendants under common conditions, is a powerful method to test for recent evolution in plant populations. We used 21-26-yr-old seeds of four European plant species - Matthiola tricuspidata, Plantago crassifolia, Clinopodium vulgare and Leontodon hispidus - stored in seed banks together with re-collected seeds from their wild populations. To test for evolutionary changes, we conducted a glasshouse experiment that quantified heritable changes in plant responses to drought and simulated insect herbivory. In three out of the four studied species, we found evidence that descendants had evolved shorter life cycles through faster growth and flowering. Shifts in the osmotic potential and leaf dry matter content indicated that descendants also evolved increased drought tolerance. A comparison of quantitative genetic differentiation (Q

A growing number of restoration projects require large amounts of seeds. As harvesting natural populations cannot cover the demand, wild plants are often propagated in large-scale monocultures. There are concerns that this cultivation process may cause genetic drift and unintended selection, which would alter the genetic properties of the cultivated populations and reduce their genetic diversity. Such changes could reduce the pre-existing adaptation of restored populations, and limit their adaptability to environmental change.We used single nucleotide polymorphism (SNP) markers and a pool-sequencing approach to test for genetic differentiation and changes in gene diversity during cultivation in 19 wild grassland species, comparing the source populations and up to four consecutive cultivation generations grown from these sources. We then linked the magnitudes of genetic changes to the species’ breeding systems and seed dormancy, to understand the roles of these traits in genetic change.The propagation of native seeds for ecosystem restoration changed the genetic composition of the cultivated generations only moderately. The genetic differentiation we observed as a consequence of cultivation was much lower than the natural genetic differentiation between different source regions, and the propagated generations harbored even higher gene diversity than wild-collected seeds. Genetic change was stronger in self-compatible species, probably as a result of increased outcrossing in the monocultures.Synthesis and applicationsOur study indicates that large-scale seed production maintains the genetic integrity of natural populations. Increased genetic diversity may even increase the adaptive potential of propagated seeds, which makes them especially suitable for ecological restoration. However, we have been working with seeds from Germany and Austria, where the seed production is regulated and certified. Whether other seed production systems perform equally well remains to be tested.

Plant diversity loss can alter higher trophic -level communities via non -random species interactions, which in turn may cascade to affect key ecosystem func-tions. These non -random linkages might be best captured by patterns of phyloge-netic diversity, which take into account co -evolutionary dependencies. However,lack of adequate phylogenetic data of higher trophic levels hampers our mecha-nistic understanding of biodiversity relationships in species-rich ecosystems.2. We used DNA barcoding to generate data on the phylogenetic diversity of lepi-dopteran caterpillars in a large- scale forest biodiversity experiment in subtropicalChina. We analysed how different metrics of lepidopteran phylogenetic diversity(Faith's PD, MPD, MNTD) and taxonomic diversity were influenced by multiple components of tree diversity (taxonomic, functional, phylogenetic).3. Our data from six sampling periods represent 7,204 mitochondrial cytochrome c oxidase subunit I (COI) sequences of lepidopteran larvae, clustered into 461 mo-lecular operational taxonomic units. Lepidopteran abundance, the effective num-ber of species (irrespective of the focus on rare or common species) and Faith's PD and MPD (reflecting basal evolutionary splits), but not MNTD (reflecting re-cent evolutionary splits), significantly increased with experimentally manipulated ree species richness. Lepidopteran MNTD decreased with increasing tree MNTD. Path analyses showed that tree phylogenetic and functional diversity explained part, but not all of the effects of tree species richness on lepidopteran diversity. Importantly, tree diversity effects on lepidopteran diversity were to a large extent indirect, operating via changes in lepidopteran abundance. 4. Synthesis. Our study shows that evolutionary dependencies determine the response of herbivore communities to changes in host plant diversity. Incorporating a wider range of diversity metrics both at the level of producers and consumers can thus help to develop a more comprehensive understanding of the functional consequences of biodiversity change across trophic levels. Moreover, the dependence of trophic linkages on herbivore abundances underlines the need to address the consequences of current declines in insect abundances for ecosystem structure and functioning. peerReviewed

Plant diversity begets diversity at other trophic levels. While species richness is the most commonly used measure for plant diversity, the number of evolutionary lineages (i.e. phylogenetic diversity) could theoretically have a stronger influence on the community structure of co-occurring organisms. However, this prediction has only rarely been tested in complex real-world ecosystems. Using a comprehensive multitrophic dataset of arthropods and fungi from a species-rich subtropical forest, we tested whether tree species richness or tree phylogenetic diversity relates to the diversity and composition of organisms. We show that tree phylogenetic diversity but not tree species richness determines arthropod and fungi community composition across trophic levels and increases the diversity of predatory arthropods but decreases herbivorous arthropod diversity. The effect of tree phylogenetic diversity was not mediated by changed abundances of associated organisms, indicating that evolutionarily more diverse plant communities increase niche opportunities (resource diversity) but not necessarily niche amplitudes (resource amount). Our findings suggest that plant evolutionary relatedness structures multitrophic communities in the studied species-rich forests and possibly other ecosystems at large. As global change non-randomly threatens phylogenetically distinct plant species, far-reaching consequences on associated communities are expected. A free Plain Language Summary can be found within the Supporting Information of this article.

Description, A global dataset shows that animal pollinators are crucial for reproduction in half of wild flowering plants., Despite evidence of pollinator declines from many regions across the globe, the threat this poses to plant populations is not clear because plants can often produce seeds without animal pollinators. Here, we quantify pollinator contribution to seed production by comparing fertility in the presence versus the absence of pollinators for a global dataset of 1174 plant species. We estimate that, without pollinators, a third of flowering plant species would produce no seeds and half would suffer an 80% or more reduction in fertility. Pollinator contribution to plant reproduction is higher in plants with tree growth form, multiple reproductive episodes, more specialized pollination systems, and tropical distributions, making these groups especially vulnerable to reduced service from pollinators. These results suggest that, without mitigating efforts, pollinator declines have the potential to reduce reproduction for most plant species, increasing the risk of population declines.

Aims: Floral traits are frequently studied in population biology and evolutionary ecology but are rarely considered in functional trait-based studies focusing on the assembly of communities. We address this gap in trait-based community assembly by synthesizing the existing literature on processes driving floral and pollination-related trait patterns at community scales. We highlight limitations of the field due to lack of data and suggest potential directions of future research. Methods: We conducted a systematic literature search collating studies that investigated floral traits in the context of plant community assembly, which allowed us to synthesize the current state of the art and point out important gaps in our knowledge. Conclusions: The literature review shows that including pollination-related traits in community assembly studies can shed new light on species coexistence patterns not accounted for by other types of traits. The synthesis presented here shows the diversity of approaches and existing techniques which can generate a step forward in this open field of research. What currently seems to hinder comprehensive analyses of floral traits at community levels is the lack of data, particularly in existing large repositories for traits worldwide, as well as a gap in linking modern coexistence theory with floral traits., Akademie Věd České Republiky. Grant Number: RVO 67985939 Grantová Agentura České Republiky. Grant Number: GACR 16‐15012S

Climate change and land‐use changes are among the major threats to biodiversity as they alter global and local environmental conditions in unprecedented dimensions. Therefore, the investigation of the ability of species and communities to cope with rapidly changing environments as well as the comprehensive understanding of possible evolutionary adaptation processes is urgently needed for their sustainable management and the maintenance of associated ecosystem processes. Here, seminatural grasslands receive special attention, because they are among the most species‐rich ecosystems in Central Europe, which are threatened by global change and land‐use intensification already since the beginning of the twentieth century. Hence, understanding their potential to respond to rapidly changing environments is important for future management. Here, the Global Change Experimental Facility (GCEF) is an opportunity to investigate the role of microevolution in response to climate change. Two of the land‐use regimes in the GCEF are seminatural, extensively used species‐rich meadow and pasture grasslands established by sowing common, native, and regionally typical grassland species in 2014. In view of ecological restoration, for each species a seed mixture of up to seven source populations was sown aiming to establish high levels of intraspecific variation from the regional gene pool. Here, we present the first evaluation of genetic and trait variation of source populations and of their establishment in the GCEF two years after sowing for six grassland species. Using AFLP markers, we assessed genetic variation of source populations and tested whether the source gene pools have established in the experiment. Additionally, we investigated phenotypic variation of source populations and performed PST‐FST comparisons to test whether trait differentiation is adaptive. Our study revealed that genetic and phenotypic differentiation of source populations is widespread in the grassland species studied, even on small geographic scales. The GCEF populations are highly diverse due to the mixture of the different, often genetically and phenotypically differentiated source populations. They represent a genetically diverse source for both selection among existing and evolution of new genotypes. Thus, the GCEF can be used as experiment to study evolutionary processes in response to the climate change and land‐use scenarios.

Land-use intensification is a major driver of biodiversity declines, and it is known to decrease species numbers and alter community composition of managed grasslands. An open question is whether similar impacts occur within species, i.e. whether grassland management affects also the genetic diversity of plant populations and alters their genetic composition, possibly reflecting adaptation to land use. To address these questions, we sampled 61 populations of the common grassland herb Plantago lanceolata that covered a broad range of land use intensities in the German Biodiversity Exploratories, and we grew their offspring in a common environment to quantify variation in plant size, architecture, reproduction, and leaf economy. All measured traits harboured substantial heritable variation, and six out of nine traits showed population differentiation. Interestingly, several traits were significantly correlated with land use intensity, but with opposing trends for mowing versus grazing: Increased mowing intensity was associated with larger plant size and lower specific leaf area (SLA), which may reflect evolutionary responses to increased light competition and a lesser need for resource conservation in highly productive meadows. In contrast, increased grazing intensity tended to be associated with smaller plant size and higher SLA, a phenotype syndrome known from grazing lawns. Moreover, we found that land-use intensification also affected genetic diversity, again with opposing effects for mowing versus grazing: while increased mowing was associated with decreased levels of intrapopulation phenotypic variation, the opposite was true for increased grazing intensity. In summary, land use intensification has not only already caused rapid evolutionary changes in these grassland populations, it also affects their future evolutionary potential.

The growing number of restoration projects worldwide increases the demand for seed material of native species. To meet this demand, seeds are often produced through large-scale cultivation on specialised farms, using wild-collected seeds as the original sources. However, during cultivation, plants experience novel environmental conditions compared to those in natural populations, and there is a danger that the plants in cultivation are subject to unintended selection and lose their adaptation to natural habitats. Although the propagation methods are usually designed to maintain as much natural genetic diversity as possible, the effectiveness of these measures have never been tested. We obtained seed of five common grassland species from one of the largest native seed producers in Germany. For each species, the seeds were from multiple generations of seed production. We used AFLP markers and a common garden experiment to test for genetic and phenotypic changes during cultivation of these plants. The molecular markers detected significant evolutionary changes in three out of the five species and we found significant phenotypic changes in two species. The only species that showed substantial genetic and phenotypic changes was the short-lived and predominantly selfing Medicago lupulina, while in the other, mostly perennial and outcrossing species, the observed changes were mostly minor. Agricultural propagation of native seed material for restoration can cause evolutionary changes, at least in some species. We recommend caution, particularly in selfing and short-lived species, where evolution may be more rapid and effects may thus be more severe.

Interactions between species of different trophic levels have long been recognized as fundamental processes in ecology. Although mounting evidence indicates that plant species diversity (PSD) or plant genetic diversity (PGD) can influence the plant-associated arthropod community, these two fundamental levels of biodiversity are not often manipulated simultaneously to assess their effects on species interactions. We used a large tree diversity experiment (BEF-China), which manipulates PSD and PGD in a crossed design to test individual and combined effects of PSD and PGD on multitrophic interaction networks and interaction partner species richness and occurrence. We focused on two tree species, on which sap-sucking Hemiptera and interacting ant species commonly occur. This tri-trophic interaction can be divided into the antagonistic plant–Hemiptera interaction and the mutualistic Hemiptera–ant interaction, known as trophobioses. Qualitative evaluation of tri-trophic interaction networks at different PSD and PGD combinations showed increased interaction partner redundancy at high PSD and PGD. This was supported by increased Hemiptera species richness at high PSD and PGD. Furthermore, the data indicate higher occurrence of Hemiptera and trophobioses and higher trophobiotic ant species richness with increasing PSD and PGD. As no plant diversity component alone caused an effect we conclude that the combined effect of high PGD and high PSD might be additive. In summary, as plant genetic diversity, especially at low species richness, seems to increase the interaction partner redundancy in interaction networks and the diversity of interacting communities, we suggest that genetic diversity should be considered in forest conservation and restoration programs.

Aims Genetic variation in plant traits represents the raw material for future adaptive evolution. Its extent can be estimated as heritability based on the performance of experimental plants of known relatedness, such as maternal half-sib seed families. While there is considerable heritability information for herbaceous plants and commercially important trees, little is known for woody species of natural subtropical forest. Moreover, it is open whether heritability is higher for species with r- or K-strategies, for more common species with larger distribution ranges than for rarer ones, or for populations closer to the centres of distributional ranges. Methods For 14 woody species in Chinese subtropical forest, we collected 13–38 maternal seed families, assessed seed size, grew replicates of each seed family in one more and one less benign nursery environment and measured stem diameter and plant height after 7 months. Important findings For the different species, plants grew 1.8–8.1 times taller in the more benign environment. For all 14 species, variation between seed families (and thus heritability) was significant (with very few exceptions at the P < 0.001 level) for seed size and for stem diameter and plant height in both nurseries. Moreover, significant seed family by nursery interactions for stem diameter and plant height for all species (P < 0.001) indicated significant heritability for plasticity in these traits. Multiple regression analysis suggests that heritabilities were higher for species with higher age at reproduction and higher wood density (traits indicating a K strategy) but also for species with higher specific leaf area (a trait rather indicating an r strategy). Furthermore, heritabilities were higher for species with larger range sizes, while there was no significant relationship between heritabilities and the distance of the study area to the range margins of our study species. In conclusion, the detected large heritability estimates suggest considerable potential for the evolution of plant performance and its plasticity for trees of subtropical forest. Moreover, our study shows that the simple method of comparing plants of different maternal seed families is valuable to address evolutionary ecological questions for so far understudied species.

Aims Positive plant diversity–ecosystem function relations are ultimately driven by variation in functional traits among individuals that form a community. To date, research has largely focused on the role of species diversity for ecosystem functioning. However, substantial intraspecific trait variation is common and a significant part of this variation caused by genetic differences among individuals. Here, we studied the relative importance of species diversity and seed family (SF) diversity within species for growth and herbivory in experimental subtropical tree assemblages. Methods In 2010, we set up a field experiment in subtropical China, using four species from the local species pool. Trees were raised from seeds, with seeds from the same mother tree forming an SF. We established 23 plots containing one or four species (species diversity treatment) and one or four SFs per species (SF diversity treatment). Tree growth (stem diameter, plant height and crown expansion) and herbivory (percentage leaf loss due to leaf chewers) were monitored annually from 2011 to 2013. Important findings Tree species richness promoted growth but had no effect on herbivory. In contrast, SF diversity reduced growth and increased herbivory but only so in species mixtures. Most of the observed effects were time dependent, with the largest effect found in 2013. Our results suggest that biodiversity can affect plant performance directly via tree species–species interactions, or context dependent, via potential effects on inter-trophic interactions. Two important conclusions should be drawn from our findings. Firstly, in future studies regarding biodiversity and ecosystem functioning (BEF) relationships, intraspecific genetic diversity should be given similar weight as species diversity as it has often been neglected and its effects are not well understood. Secondly, we demonstrate opposite effects of biodiversity among and within species, stressing the importance to consider the effects of multiple levels of biodiversity simultaneously.

Aims Changing biodiversity can affect ecosystem functioning. However, the role of genetic diversity within species, relative to the one of species diversity, has hardly been addressed. Methods To address the effects of both genetic diversity and species diversity during the important stage of early tree life, we used eight seed families (SF) taken from each of 12 evergreen and deciduous tree species of subtropical forest to perform a factorial experiment. We established 264 communities of 16 trees each. Each community had a species diversity of either one or four species and a genetic diversity of either one, two or four SF per species. We measured plant survival, growth rate, final biomass and herbivory 20 months after sowing. Important Findings Species differed from each other in biomass, growth rate, herbivory and survival (P < 0.001). Deciduous species tended to have much higher biomass (P < 0.1) and experienced higher herbivory (P < 0.05) than evergreen species. Species diversity affected the performance of different species differently (species diversity by species interaction, P

Vegetative reproduction and spread through clonal growth plays an important role in arctic-alpine ecosystems with short cool growing seasons. Local variation in winter snow accumulation leads to discrete habitat types that may provide divergent conditions for sexual and vegetative reproduction. Therefore, we studied variation in clonal structure of a dominant, evergreen, dwarf shrub (Empetrum nigrum s.l. with the two taxa E. nigrum L. s.s. and E. hermaphroditum Hagerup) along a snow cover gradient and compared clonal diversity and spatial genetic structure between habitats.We studied 374 individual shoots using 105 polymorphic AFLP markers and analyses based on hierarchical clustering, clonal diversity indices, and small-scale spatial genetic structure with pairwise kinship coefficient. We used two approaches to define a threshold of genotypic distance between two samples that are considered the same clone. Clonality was examined among three habitats (exposed ridges, sheltered depressions, birch forest) differing in snow conditions replicated in four study regions in Norway and Sweden.Clonality of E. hermaphroditum differed between habitats with an increase in clonal diversity with decreasing snow depth. Small-scale spatial genetic structure increased with decreasing clonal diversity and increasing clone size. In three study regions, E. hermaphroditum was the only species, whereas in one region E. nigrum also occurred, largely confined to exposed ridges.Our results demonstrated that snow cover in conjunction with associated habitat conditions plays an important role for the mode of propagation of the dwarf shrub E. hermaphroditum.

In plant conservation and ecosystem restoration, plants are often translocated to ensure or enhance plant survival and performance. While the effects of ecotype origin on the performance of translocated plants are increasingly acknowledged among researchers and practitioners, ecotype effects on associated communities and ecosystems have hardly been studied. This is critical because plants also constitute the habitat for a large number of interacting organisms, and many of them might be influenced by plant ecotype characteristics. Here, we studied different ecotypes of Centaurea jacea L., a plant species commonly used in grassland restoration, and their effects on seed herbivores and their parasitoids. We grew eight C. jacea ecotypes originating from different regions in Germany in a common garden and found that the ecotypes differed up to three-fold in the frequencies of seed herbivores. These differences appeared to be mainly driven by ecotype differences in flowering phenology. We also found that there were up to four-fold differences in the frequencies of parasitoids, and even up to nine-fold differences in the abundances of parasitoids among ecotypes. In summary, plants from different origins substantially differed in their effects on interacting organisms, potentially reflecting coevolutionary relationships across trophic levels. The introduction of foreign ecotypes in restoration projects may thus not only affect the plants themselves, but it may also disrupt the balance of their biotic interactions.

Biodiversity-ecosystem functioning experiments found that productivity generally increases with species richness, but less is known about effects of within-species genetic richness and potential interactions between the two. While functional differences between species can explain species richness effects, empirical evidence regarding functional differences between genotypes within species and potential consequences for productivity is largely lacking. We therefore measured within- and among-species variation in functional traits and growth and determined stand-level tree biomass in a large forest experiment factorially manipulating species and genetic richness in subtropical China. Within-species variation across genetic seed families, in addition to variation across species, explained a substantial amount of trait variation. Furthermore, trait responses to species and genetic richness varied significantly within and between species. Multivariate trait variation was larger among individuals from species mixtures than those from species monocultures, but similar among individuals from genetically diverse vs genetically uniform monocultures. Correspondingly, species but not genetic richness had a positive effect on stand-level tree biomass. We argue that identifying functional diversity within and among species in forest communities is necessary to separate effects of species and genetic diversity on tree growth and community productivity.