Livestock grazing and forest structure regulate the assembly of ecological clusters within plant networks in eastern Australia

Questions

How do changes in grazing intensity by different herbivores and differences in forest structure affect the assembly of ecological clusters within plant ecological networks in dryland plant communities?

Location

Eastern Australia across an area of 0.4 million km².

Methods

We used correlation network analysis and structural equation modelling to examine how changes in grazing intensity, by different herbivores, and differences in forest structure (tree canopy cover, basal area and density) and soil fertility influenced the assembly of ecological clusters of plant communities (i.e. relative abundance of ecological clusters formed by co‐occurring plant species within an ecological network) in three forested communities from eastern Australia.

Results

Livestock grazing and forest structure regulated the relative abundance of ecological clusters within plant networks, but their effects on these plant assemblies were highly dependent on the ecological cluster and forest community type, with no single winner or loser across forest types, conditions or grazing intensities. Thus, the relative abundance of some ecological clusters increased under grazing while others declined, a response that was maintained across different forest structures. The relative importance of grazing, forest structure and soil fertility varied across forest community type. The two eucalypt communities exhibited mixed effects of grazing and forest structure (Eucalyptus largiflorens ) or forest structure only (Eucalyptus camaldulensis ). In the third (Callitris glaucophylla ) community, grazing played a larger role in controlling the plant community assembly. Soil fertility (soil C and P) effects were of a similar magnitude to grazing and forest structure, but the effects differed among clusters.

Conclusions

Livestock grazing and forest structure regulated the relative abundance of ecological clusters within networks of plant communities in forests in eastern Australia. Our study uses a novel approach of ecological clusters to show that differences in grazing and forest structure will always disadvantage some plant ecological clusters. Furthermore, changes in one cluster will ultimately affect other clusters. Any changes in management therefore will have varied effects on different ecological plant clusters.

     

Canopy height and competition explain species segregation in wet heathlands

Questions

What is the general pattern of species co‐occurrence in managed heathlands? Is the pattern consistent among functional groups? Is it ruled by species competition, or by contrasting environments at a fine scale? Does grazing pressure and herbivore species condition species interactions?

Location

Erica mackayana wet heaths, Galicia, NW Iberian Peninsula.

Methods

A null model approach was used to compare species co‐occurrence with generated random matrices from 54 10‐m transects. The C‐score was obtained from the multispecies presence/absence matrix for each transect of shrubs and graminoids recorded at 25‐cm intervals. Differences in canopy height were recorded to assess the importance of the environment compared to inter‐specific competition. Results were linked to different levels of grazing pressure and herbivore species.

Results

Species segregation was the main pattern for all species, but mainly among graminoid species compared to shrubs. Graminoids showed an even proportion of segregated pairs explained by different canopy heights and competition. These differences were mainly species environmental requirements of canopy height. Levels of grazing pressure enhanced species segregation in graminoids but had no effect on shrubs or the total species set.

Conclusions

Competition and canopy height affect the E. mackayana heathland composition, but differently for functional groups. A heterogeneous vegetation profile with shrub mats and open gaps created by light grazing promotes species co‐existence within mats and competition in gaps. I suggest this is an optimum structure for the habitat to be targeted through management.

     

Is intensity of plant root mycorrhizal colonization a good proxy for plant growth rate,dominance and decomposition in nutrient poor conditions?

Questions

Mycorrhizae may be a key element of plant nutritional strategies and of carbon and nutrient cycling. Recent research suggests that in natural conditions, intensity of mycorrhizal colonization should be considered an important plant feature. How are inter‐specific variations in mycorrhizal colonization rate, plant relative growth rate (RGR ) and leaf litter decomposability related? Is (arbuscular) mycorrhizal colonization linked to the dominance of plant species in nutrient‐stressed ecosystems?

Location

Teberda State Biosphere Reserve, northwest Caucasus, Russia.

Methods

We measured plant RGR under mycorrhizal limitation and under natural nutrition conditions, together with leaf litter decomposability and field intensity of mycorrhizal colonization across a wide range of plant species, typical for alpine communities of European mountains. We applied regression analysis to test whether the intensity of mycorrhizal colonization is a good predictor of RGR and decomposition rate, and tested how these traits predict plant dominance in communities.

Results

Forb species with a high level of field mycorrhizal colonization had lower RGR under nutritional and mycorrhizal limitation, while grasses were unaffected. Litter decomposition rate was not related to the intensity of mycorrhizal colonization. Dominant species mostly had a higher level of mycorrhizal colonization and lower RGR without mycorrhizal colonization than subordinate species, implying that they were more dependent on mycorrhizal symbionts. There were no differences in litter decomposability.

Conclusions

In alpine herbaceous plant communities dominated by arbuscular mycorrhizae, nutrient dynamics are to a large extent controlled by mycorrhizal symbiosis. Intensity of mycorrhizal colonization is a negative predictor for whole plant RGR . Our study highlights the importance of mycorrhizal colonization as a key trait underpinning the role of plant species in carbon and nutrient dynamics in nutrient‐limited herbaceous plant communities.

     

Factors influencing above‐ground and soil seed bank vegetation diversity at different scales in a quasi‐Mediterranean ecosystem

Questions

Are factors influencing plant diversity in a fire‐prone Mediterranean ecosystem of southeast Australia scale‐dependent?

Location

Heathy woodland, Otways region, Victoria, southeast Australia

Methods

We measured patterns of above‐ground and soil seed bank vegetation diversity and associated them with climatic, biotic, edaphic, topographic, spatial and disturbance factors at multiple scales (macro to micro) using linear mixed effect and generalized dissimilarity modelling.

Results

At the macro‐scale, we found species richness above‐ground best described by climatic factors and in the soil seed bank by disturbance factors. At the micro‐scale we found species richness best described above‐ground and in the soil seed bank by disturbance factors, in particular time‐since‐last‐fire. We found variance in macro‐scale β‐diversity (species turnover) best explained above‐ground by climatic and disturbance factors and in the soil seed bank by climatic and biotic factors.

Conclusions

Regional climatic gradients interact with edaphic factors and fire disturbance history at small spatial scales to influence species richness and turnover in the studied ecosystem. Current fire management regimes need to incorporate key climatic–disturbance–diversity interactions to maintain floristic diversity in the studied system.

     

Woody plant diversity in relation to environmental factors in a seasonally dry tropical forest landscape

Questions

Water availability is known to be a first‐order driver of plant diversity; yet water also affects fire regimes and soil fertility, which, in turn, affect plant diversity. We examined how precipitation, fire and soil properties jointly determine woody plant diversity. Specifically, we asked how woody plant diversity varies along a sharp precipitation gradient (about 600–1,800 mm mean annual precipitation [MAP ]within a ~45‐km distance) exhibiting considerable variation in long‐term fire burn frequency and soil fertility, in a southern Indian seasonally dry tropical forest (SDTF ) landscape.

Location

Mudumalai, Western Ghats, India.

Methods

Woody plants ≥1‐cm DBH were enumerated in 19 1‐ha permanent plots spanning a range of tropical vegetation types from dry thorn forest, through dry and moist deciduous forest to semi‐evergreen forest. Burn frequencies were derived from annual fire maps. Six measures of surface soil properties – total exchangeable bases (Ca + Mg + K), organic carbon (OC ), total N, pH , plant available P and micronutrients (Fe + Cu + Zn + Mn) were used in the analyses. Five measures of diversity – species richness, Shannon diversity, the rarefied/extrapolated versions of these two measures, and Fisher's α – were modelled as functions of MAP , annual fire burn frequency and the principal components of soil properties.

Results

Most soil nutrients and OC increased with MAP , except in the wettest sites. Woody productivity increased with MAP , while fire frequency was highest at intermediate values of MAP . Woody plant diversity increased with MAP but decreased with increasing fire frequency, resulting in two local diversity maxima along the MAP gradient – in the semi‐evergreen and dry thorn forest – separated by a low‐diversity central region in dry deciduous forest where fire frequency was highest. Soil variables were, on the whole, less strongly correlated with diversity than MAP .

Conclusions

Although woody plant diversity in this landscape, representative of regional SDTF s, is primarily limited by water availability, our study emphasizes the role of fire as a potentially important second‐order driver that acts to reduce diversity in this landscape.

     

The roles of stochasticity and biotic interactions in the spatial patterning of plant species in alpine communities

Questions

Plant community composition can be influenced by multiple biotic, abiotic, and stochastic factors acting on the local species pool to determine their establishment success and abundance and subsequently the diversity of the community. We asked if the influences of biotic interactions on the composition of plant species in communities, as indicated by patterns of plant species spatial associations (independent, positive or negative), vary across a productivity gradient within a single ecosystem type. Do dominant species of communities show spatial patterning suggestive of competitive interactions with interspecific neighbors? Do species that span multiple community types exhibit the same heterospecific interactions with neighbours in each community?

Location

Three alpine communities in the southern Rocky Mountains.

Methods

We measured the occurrence of species in a 1‐cm spatial grid within 2 m × 2 m plots to determine the spatial patterns of species pairs in the three communities. A null model of independent species spatial arrangements was used to determine whether species pairs were positively, negatively or independently associated, and how these patterns differed among the communities across the gradient of resource supply and environmental stress.

Results

Positive associations, indicative of facilitation between species, were most common in the most resource‐poor and least productive community. However negative associations, suggestive of competitive interactions among species, were not more common in the two more resource‐rich, productive communities. The dominant species of these communities did exhibit higher negative than positive associations with neighbours relative to positive patterning. Independent interspecific patterning was equally common relative to positive and negative patterns in all communities. Species that previously were shown to either facilitate other species or compete with neighbours exhibited spatial patterning consistent with the earlier experimental work.

Conclusions

A large number of species exhibit a lack of net biotic interactions, and stochastic factors appear to be as important as competition and facilitation in shaping the structure of the three alpine plant communities we studied.

     

Invasive plants in Minnesota are “joining the locals”: A trait‐based analysis

Questions

Predicting which newly arrived species will establish and become invasive is a problem that has long vexed researchers. In a study of cold temperate oak forest stands, we examined two contrasting hypotheses regarding plant functional traits to explain the success of certain non‐native species. Under the “join the locals” hypothesis, successful invaders are expected to share traits with resident species because they employ successful growth strategies under light‐limited understorey conditions. Instead, under the “try harder” hypothesis, successful invaders are expected to have traits different from native species in order to take advantage of unused niche space.

Location

Minnesota, USA.

Methods

We examined these two theories using 109 native and 11 non‐native plants in 68 oak forest stands. We focused on traits related to plant establishment and growth, including specific leaf area (SLA), leaf carbon‐to‐nitrogen ratio (C:N), wood density, plant maximum height, mycorrhizal type, seed mass and growth form. We compared traits of native and non‐native species using ordinations in multidimensional trait space and compared community‐weighted mean (CWM) trait values across sites.

Results

We found few differences between trait spaces occupied by native and non‐native species. Non‐native species occupied smaller areas of trait space than natives, yet were within that of the native species, indicating similar growth strategies. We observed a higher proportion of non‐native species in sites with higher native woody species CWM SLA and lower CWM C:N. Higher woody CWM SLA was observed in sites with higher soil pH, while lower CWM C:N was found in sites with higher light levels.

Conclusions

Non‐native plants in this system have functional traits similar to natives and are therefore “joining the locals.” However, non‐native plants may possess traits toward the acquisitive end of the native plant trait range, as evidenced by higher non‐native plant abundance in high‐resource environments.

     

New insights into plants co‐existence in species‐rich communities: The pollination interaction perspective

Questions

In animal‐mediated pollination, pollinators can be regarded as a limiting resource for which entomophilous plant species might interact to assure pollination, an event pivotal for their reproduction and population maintenance. At community level, spatially aggregated co‐flowering species can thus be expected to exhibit suitable suites of traits to avoid competition and ensure pollination. We explored the problem by answering the following questions: (1) are co‐flowering species specialized on different guilds of pollinators; (2) do co‐flowering pollinator‐sharing species segregate spatially; and (3) do co‐flowering pollinator‐sharing species that diverge in anther position spatially aggregate more than those that converge in anther position?

Study Site

Euganean Hills, NE Italy.

Methods

Plant composition, flowering phenology and interactions between each entomophilous plant species and pollinating insects were monitored every 15 days in 40 permanent plots placed in an area of 16 ha. We quantified the degree of flowering synchrony, pollinator‐sharing and spatial aggregation between each pair of entomophilous species. We then tested the relationship between the degree of co‐flowering, pollinator‐sharing and spatial aggregation, and between spatial aggregation and anther position.

Results

Entomophilous species converged, at least partially in flowering time, and the phenological synchronization of flowering was significantly associated with the sharing of pollinator guilds. Co‐flowering pollinator‐sharing species segregated spatially. Furthermore, co‐flowering pollinator‐sharing species that diverged in anther position aggregated more than those that converged in anther position.

Conclusions

Reproductive traits that facilitate the co‐existence of co‐flowering species include specialization on different pollinator guilds and a phenological displacement of the flowering time. Furthermore, in circumstances of increased competition due to phenological synchronization, pollinator‐sharing and spatial aggregation, the chance of effective pollination might depend on differences in anther position, resulting in a divergent pollen placement on pollinator bodies. One of the most interesting results we obtained is that the presence of one mechanism does not preclude the operation of others, and each plant species can simultaneously exhibit different strategies. Although more studies are needed, our results can provide additional information about plant–plant interactions and provide new insights into mechanisms allowing the co‐existence of a high number of plant species in local communities.

     

It's a long way to the top: Plant species diversity in the transition from managed to old‐growth forests

Questions

Do vascular plant species richness and beta‐diversity differ between managed and structurally complex unmanaged stands? To what extent do species richness and beta‐diversity relate to forest structural attributes and heterogeneity?

Location

Five national parks in central and southern Italy.

Methods

We sampled vascular plant species composition and forest structural attributes in eight unmanaged temperate mesic forest stands dominated or co‐dominated by beech, and in eight comparison stands managed as high forests with similar environmental features. We compared plant species richness, composition and beta‐diversity across pairs of stands (unmanaged vs managed) using GLMM s. Beta‐diversity was quantified both at the scale of each pair of stands using plot‐to‐plot dissimilarity matrices (species turnover), and across the whole data set, considering the distance in the multivariate species space of individual plots from their centroid within the same stand (compositional heterogeneity). We modelled the relationship between species diversity (richness and beta‐diversity) and forest structural heterogeneity and individual structural variables using GLMM s and multiple regression on distance matrices.

Results

Species composition differed significantly between managed and unmanaged stands, but not richness and beta‐diversity. We found weak evidence that plant species richness increased with increasing levels of structural heterogeneity and canopy diversification. At the scale of individual stands, species turnover was explained by different variables in distinct stands, with variables related to deadwood quantity and quality being selected most often. We did not find support for the hypothesis that compositional heterogeneity varies as a function of forest structural characteristics at the scale of the whole data set.

Conclusions

Structurally complex unmanaged stands have a distinct herb layer species composition from that of mature stands in similar environmental conditions. Nevertheless, we did not find significantly higher levels of vascular plant species richness and beta‐diversity in unmanaged stands. Beta‐diversity was related to patterns of deadwood accumulation, while for species richness the evidence that it increases with increasing levels of canopy diversification was weak. These results suggest that emulating natural disturbance, and favouring deadwood accumulation and canopy diversification may benefit some, but not all, facets of plant species diversity in Apennine beech forests.

     

Broad‐scale patterns in smoke‐responsive germination from the south‐eastern Australian flora

Questions

Fire is a crucial component of many ecosystems. Plants whose seeds germinate in response to smoke may benefit from resource availability in the post‐fire environment. Smoke can influence germination timing and success, as well as seedling vigour, resulting in burgeoning research interest in smoke‐responsive germination. Research in this field has largely focused on four key ‘Mediterranean‐type’ fire‐prone ecosystems: the Mediterranean Basin, South African fynbos, Californian chaparral and Western Australia. There are far fewer studies from south‐eastern Australia, a fire‐prone but not “Mediterranean‐type” region. How does smoke‐responsive germination in this region vary according to ecological, phylogenetic, and methodological variables?

Location

South‐eastern Australia.

Methods

We investigated patterns of smoke‐promoted germination in south‐eastern Australian plants across habitat types, growth forms, fire response strategies, phylogeny, taxonomic levels and smoke application methods. We compiled and interrogated data comprising 303 entries on germination responses to smoke in 233 south‐eastern Australian plant species, from 33 different sources.

Results

Smoke‐responsive germination occurs at a lower rate (~41% of tested species) in south‐eastern Australian flora than it does in fynbos and Western Australian floras, and there is clear patterning within these data. Obligate‐seeding species were more likely to respond, Leguminosae and Rubiaceae were less likely to respond (although we question the generality of these results), while Poaceae were more likely to respond to smoke. Finally, studies using aerosol smoke and studies conducted in situ were most likely to find smoke‐promoted germination.

Conclusions

Obligate seeders and Poaceae may be selected for in habitats with higher fire frequencies, consistent with literature suggesting that short inter‐fire intervals favour grasslands over forests. These findings may be particular to south‐eastern Australia, or more widely applicable; more broad‐scale comparative research will reveal the answer. By synthesizing the south‐eastern Australian smoke germination literature we broaden our understanding beyond the better‐studied Mediterranean‐type floras.

     

Effects of functional diversity and functional dominance on complementary light use depend on evenness

Questions

Does functional diversity play a more important role than species richness in complementary resource use? Is the effect of functional diversity on complementarity greater when species evenness is higher? Does functional dominance play an important role in resource use when species evenness is low?

Location

An arable field in Linhai City, Zhejiang Province, China.

Methods

We assembled experimental plant communities with different species richness (one, two, four, eight and 12 species) and evenness (low and high). In each community, we quantified light interception efficiency (LIE ) and light complementarity index (LC ) to reflect light use. We measured four functional traits related to light capture to quantify functional diversity and functional dominance. We then tested effects of observed species richness, functional diversity and functional dominance on LIE , LC and above‐ground biomass in the low and high evenness communities.

Results

Functional diversity was positively related to LIE , LC and above‐ground biomass in the high evenness communities, but not in the low evenness communities. In contrast, functional dominance was positively related to LIE and negatively related to LC in the low evenness communities, but not in the high evenness communities. Moreover, functional dominance had a larger promotion to above‐ground biomass in the low evenness communities. Observed species richness and evenness had a significant interactive effect on LIE and LC . LIE of a species mixture of the low evenness communities was positively correlated with LIE of the monoculture consisting of the species with the highest initial abundance in the species mixture, while LC of a species mixture of the low evenness communities was negatively correlated with it.

Conclusions

Functional diversity and functional dominance play a crucial role in light complementary use of plant communities, and their effects on light complementarity are mediated by species evenness. Thus, interactions of functional traits and evenness may greatly affect ecosystem functioning.

     

The Holocene history of low altitude Mediterranean Fagus sylvatica forests in southern France

Questions

As the dominant tree in many European forests, Fagus sylvatica functions as an ecosystem engineer, yet its istory remains little understood. Here we ask: (a) are there indications for its presence in southeast France during the last Glacial period; (b) what was the timing of the expansion and decline of F. sylvatica dominated forests; (c) which factors influenced their dynamics and in particular to what extent did past precipitation changes impact upon them; and (d) at which altitudes did these beech forests occur within the region?

Location

Languedoc, the French Mediterranean area.

Method

This article presents a well dated and high‐resolution pollen sequence covering the last 7,800 years from the Palavas Lagoon in the Languedoc together with a review of Fagus charcoal occurrences in the Languedoc and the lower Rhône Valley, and a review of pollen data from a compilation of 69 sites in southeast France.

Results

The Palavas pollen sequence provides a regional summary of F. sylvatica abundance changes near the Mediterranean coast. Around 6,000 years cal BP , an abrupt transition from small beech populations to well‐developed forests is recorded. The maximum development of beech forests occurred between 4,000 and 3,000 years cal BP , while F. sylvatica started to regress after 3,000 years cal BP .

Conclusion

Scattered F. sylvatica populations probably survived throughout southern France during the last Glacial period. F. sylvatica started to spread around 8,000 years cal BP while beech forests never expanded before 6,000 years cal BP . The complex patterns of F. sylvatica expansion in southern France after 6,000 years cal BP suggests that a combination of global (climate change) and local (human impact) factors were responsible for this major change. Recurrent abrupt climate changes, the aridity trend and human deforestation caused beech forests to decline after 3,000 years cal BP .

     

The symmetry of competitive interactions in mixed Norway spruce,silver fir and European beech forests

Questions

We aim for a better understanding of the different modes of intra‐ and inter‐specific competition in two‐ and three‐species mixed‐forests. How can the effect of different modes of competitive interactions be detected and integrated into individual tree growth models? Are species interactions in spruce–fir–beech forests more associated with size‐symmetric or size‐asymmetric competition? Do competitive interactions between two of these species change from two‐ to three‐species mixtures?

Location

Temperate mixed‐species forests in Central Europe (Switzerland).

Methods

We used data from the Swiss National Forest Inventory to fit basal area increment models at the individual tree level, including the effect of ecological site conditions and indices of size‐symmetric and size‐asymmetric competition. Interaction terms between species‐specific competition indices were used to disentangle significant differences in species interactions from two‐ to three‐species mixtures.

Results

The growth of spruce and fir was positively affected by increasing proportions of the other species in spruce–fir mixtures, but negative effects were detected with increasing presence of beech. We found that competitive interactions for spruce and fir were more related to size‐symmetric competition, indicating that species interactions might be more associated with competition for below‐ground resources. Under constant amounts of stand basal area, the growth of beech clearly benefited from the increasing admixture of spruce and fir. For this species, patterns of size‐symmetric and size‐asymmetric competitive interactions were similar, indicating that beech is a strong self‐competitor for both above‐ground and below‐ground resources. Only for silver fir and beech, we found significant changes in species interactions from two‐ to three‐species mixtures, but these were not as prominent as the effects due to differences between intra‐ and inter‐specific competition.

Conclusions

Species interactions in spruce–fir–beech, or other mixed forests, can be characterized depending on the mode of competition, allowing interpretations of whether they occur mainly above or below ground level. Our outcomes illustrate that species‐specific competition indices can be integrated in individual tree growth functions to express the different modes of competition between species, and highlight the importance of considering the symmetry of competition alongside competitive interactions in models aimed at depicting growth in mixed‐species forests.

     

Non‐interacting impacts of fertilization and habitat area on plant diversity via contrasting assembly mechanisms

Aim

The local‐ and regional‐based forms of anthropogenic change reducing grassland diversity are generally identified, but these scale‐dependent processes tend to co‐occur with unclear interactive effects. Here, we explicitly test how common local and regional perturbations simultaneously affect plant alpha and beta diversity in a multiyear community assembly experiment using fragments of grassland habitat of various sizes. We hypothesized that local disturbances and decreasing patch size would interact, suppressing local diversity while homogenizing composition among patches.

Location

North America.

Methods

We conducted a three‐year grassland assembly experiment, factorially manipulating local perturbation (nitrogen addition and mowing) and patch area for 36 patches over 13 ha. We quantified the individual and interactive effects of these local and regional factors on plant alpha and beta diversity within (quadrat scale) and among patches (patch scale). We also used a null model approach to disentangle between stochastic‐ and niche‐based assembly mechanisms.

Results

We detected a gradient of assembly outcomes driven by two non‐interacting factors—the effects of N fertilization on alpha (negative) and beta (positive) diversity regardless of spatial scale and the scale‐dependant effect of increasing patch size on alpha (positive) and beta (positive) diversity. These effects unfolded over time, with the constraints on richness and composition shifting from dispersal‐based during the first sampling year to perturbation‐and size‐based factors at year two and three. Fertilization effects were driven by a mixture of deterministic (i.e., selection at the species level) and stochastic (i.e., random extinctions) processes resulting in a decline in local richness but an increase in spatial heterogeneity in species composition. Area appeared to influence alpha diversity mainly via stochastic “sampling effect”—larger patches represented a larger sample of the regional pool. Niche‐based processes, however, led to convergence in beta diversity among smaller patches driving a positive overall effect of area on beta diversity.

Main conclusion

Our results illustrate how diversity regulation in contemporary grasslands can be simultaneously shaped by local and regional factors acting additively but via contrasting assembly mechanisms that operate at different spatial and temporal scales.

     

Biogeographic variability of coastal perennial grasslands at the European scale

Question

Coastal environments have often been described as azonal. While this characteristic is clear for the foredune system, it seems less evident for more inland fixed dunes, which host habitats of major conservation concern, whose features seem to be more related to local climatic conditions. We hypothesized that, unlike other coastal habitats, dune perennial grasslands differ floristically and structurally across their European range and that patterns of variation are linked to the corresponding climate.

Location

European coasts (Atlantic Ocean, Baltic, Mediterranean, Black Sea).

Methods

We used a large data set of phytosociological relevés, representative of coastal grasslands throughout their European range. The role of climatic variables (temperature, precipitation and continentality) in determining the variability in species composition and vegetation structure (by means of life forms) was investigated through CCA, DCA and GLM. The degree of concentration of species occurrences within groups was calculated through the Phi coefficient.

Results

Through multivariate analyses we identified seven major types of coastal grassland, corresponding to different geographic areas. The groups significantly differed in their climatic envelope, as well as in their species composition and community structure.

Conclusion

Our results confirm the hypothesis that coastal dune perennial grasslands are subjected to local climate, which exerts significant effects on both floristic composition and community structure. As a consequence, coastal grasslands are particularly prone to the effect of possible climate change, which may alter species composition and distribution, and lead to shifts in the distribution of native plant communities.

     

BioTIME: A database of biodiversity time series for the Anthropocene

Motivation

The BioTIME database contains raw data on species identities and abundances in ecological assemblages through time. These data enable users to calculate temporal trends in biodiversity within and amongst assemblages using a broad range of metrics. BioTIME is being developed as a community‐led open‐source database of biodiversity time series. Our goal is to accelerate and facilitate quantitative analysis of temporal patterns of biodiversity in the Anthropocene.

Main types of variables included

The database contains 8,777,413 species abundance records, from assemblages consistently sampled for a minimum of 2 years, which need not necessarily be consecutive. In addition, the database contains metadata relating to sampling methodology and contextual information about each record.

Spatial location and grain

BioTIME is a global database of 547,161 unique sampling locations spanning the marine, freshwater and terrestrial realms. Grain size varies across datasets from 0.0000000158 km² (158 cm²) to 100 km² (1,000,000,000,000 cm²).

Time period and grain

BioTIME records span from 1874 to 2016. The minimal temporal grain across all datasets in BioTIME is a year.

Major taxa and level of measurement

BioTIME includes data from 44,440 species across the plant and animal kingdoms, ranging from plants, plankton and terrestrial invertebrates to small and large vertebrates.

Software format

.csv and .SQL.

     

Projecting potential future shifts in species composition of European urban plant communities

Aim

Urban floras are composed of species of different origin, both native and alien, and with various traits and niches. It is likely that these species will respond to the ongoing climate change in different ways, resulting in future species compositions with no analogues in current European cities. Our goal was to estimate potential shifts in plant species composition in European cities under different scenarios of climate change for the 21st century.

Location

Europe.

Methods

Potential changes in the distribution of 375 species currently growing in 60 large cities in Southern, Central and Western Europe were modelled using generalized linear models and four climate change projections for two future periods (2041–2060 and 2061–2080). These projections were based on two global climate models (CCSM4 and MIROC‐ESM) and two Representative Concentration Pathways (2.6 and 8.5).

Results

Results were similar across all climate projections, suggesting that the composition of urban plant communities will change considerably due to future climate change. However, even under the most severe climate change scenario, native and alien species will respond to climate change similarly. Many currently established species will decline and others, especially annuals currently restricted to Southern Europe, will spread to northern cities. In contrast, perennial herbs, woody plants and most species with temperate continental and oceanic distribution ranges will make up a smaller proportion of future European urban plant communities in comparison with the present communities.

Main conclusions

The projected 21st century climate change will lead to considerable changes in the species composition of urban floras. These changes will affect the structure and functioning of urban plant communities.