Management intensity affects the relationship between non‐native and native species in subtropical wetlands

Question: Does management intensity affect the association between non‐native and native species and between non‐native species and soil nutrients in wetlands? Location: MacArthur Agro‐Ecology Research Center, Florida, USA. Methods: We evaluated native and non‐native plant richness and relative frequency in 15 1‐m² plots in 40 wetlands across two types of pastures, highly managed (fertilized, ditched, planted, heavily grazed by cattle) and semi‐natural (unfertilized, lightly seasonally grazed). Plant biomass was collected in five 0.25‐m² plots per wetland and sorted to species. Soil cores were collected to analyse soil total nitrogen (N) and phosphorus (P). An information‐theoretic approach was used to compare mixed effects models considering the association of non‐native richness, relative frequency, and biomass with native richness, relative frequency, biomass, C₃ grass relative frequency (a dominant native group), N, P and wetland‐type. Results: Non‐native richness was negatively correlated with native richness in semi‐natural wetlands, but there was no evidence of an association between these variables in highly managed wetlands. Non‐native richness increased with increasing soil N in semi‐natural wetlands, but not in the highly managed wetlands. Soil P was positively related to non‐native frequency in semi‐natural wetlands but negatively related in highly managed wetlands. Non‐native frequency and biomass were negatively related to relative frequency of C₃ grasses in both management types. Conclusions: Our results indicate that management intensity influences relationships between native and non‐native richness. Management intensity interacts with abiotic or biotic factors, such as soil nutrients and composition, in predicting where non‐native species will most likely need control.     

Litter‐dwelling beetles (Insecta: Coleoptera) can survive in clear‐cutting during subsequent soil ploughing

1. A 2‐year study of litter dwelling beetles was conducted in different mature pine stands and clear‐cuts in Lithuania using the litter sifting method. We hypothesized that clear‐cutting and subsequent ploughing would increase species diversity and the abundance of beetles, and also would encourage the immediate appearance of early‐successional beetle species replacing late successional species in the clear‐cuts.
2. We did not confirm a hypothesis regarding increase in the number of species and abundance of beetles in clear‐cuts.
3. Our hypothesis regarding the immediate appearance of early successional species and disappearance of late‐successional species in clear‐cuts was confirmed.
4. We also revealed that subsequent soil ploughing in clear‐cuts did not accelerate this process, which was linked to the possibility of late successional species surviving in the undisturbed spaces between the strips of ploughed soil.
5. The present study shows that late‐successional forest litter‐dwelling coleopteran species of old pine forests have a better chance of survival in a ploughed clear‐cut, at least in northern Europe, than has been reported in other studies.

     

Determinants of community organization of a South African mesic grassland

Abstract. Question: What is the long‐term influence of nutrient availability, productivity and soil pH on grassland community organization? Location: Ukulinga research farm, KwaZulu‐Natal, South Africa. Methods: The influence of fertilization on soil pH, nitrogen (N) and phosphorus (P) on variation in plant traits, community composition and species richness were examined in a 50‐year grassland fertilization experiment. Results: Averaged over 30 years, above‐ground net primary production (ANPP) was 337, 428 and 518 g.m^‐2 in sites not fertilized, fertilized with N, and fertilized with N plus P respectively. ANPP depended directly on N‐fertilization but not on P‐fertilization or liming, and responded positively to the interaction of N (first limiting nutrient) and P (second limiting nutrient). Short narrow‐leaved grass species —Themeda triandra, Tristachya leucothrix and Setaria nigrirostris— dominated sites of lowest ANPP where N was limiting (unfertilized, P‐fertilized or limed sites). A tall narrow‐leaved species, Eragrostis curvula, dominated sites of intermediate ANPP where P was limiting (N‐fertilized sites). By contrast, a tall broad‐leaved species, Panicum maximum, dominated the most productive sites where neither N nor P were limiting (N‐ and P‐fertilized sites). Certain species responded to liming and type of N‐fertilizer apparently because of their effects on soil pH. N‐fertilization reduced the density of herbaceous dicots (forbs) from 14 (unfertilized) to two (high N, no P, no lime) and five species per m² (high N, no P, limed). This effect was attributed to increased ANPP and a decrease in soil pH from 4.6 (KCl) in unfertilized sites to 3.49 (high N, no lime) and 4.65 (high N and lime). Soil acidification had no effect on grass species richness but influenced the abundance of certain species. Conclusions: Grassland community organization is determined not only by the influence of N availability, but also by the hierarchical interaction of N and P availability, in part through their compounded effect on ANPP, and by individualistic species responses to soil pH.     

Importance of assemblage‐level thinning: A field experiment in an alpine meadow on the Tibet plateau

Question: Which fraction of the decrease in species richness under fertilization can be explained by assemblage‐level thinning? Location: An alpine meadow on the eastern Tibet plateau. Methods: 60‐m² plots were randomly assigned to a control or one of four levels of ammonium phosphate fertilizer. Treatments were repeated for three years. The effect of as semblage‐level thinning was decided based on similarity in quadrats within and between fertilizing levels, bootstrap simulation based on random thinning of the high density (low production, low fertility) quadrats and correlation of species’ biomass in low fertility and high fertility. Results: Fertilization increased production, reduced species richness and reduced density of individuals. Heavily fertilized quadrats are more similar in species composition in 2000 but less similar in 2001 and 2002. Rarefaction showed that a decrease in density can account for 32.3‐42.9% decrease of species richness, but the simulated species richness is always significantly higher than the observed one. When production and species richness are similar at two levels of fertilization, species biomass in the higher fertility treatment is positively correlated with biomass at lower fertility. When the two fertilizer levels differed in production and species richness, there was no evidence of correlation in species biomass, suggesting that assemblage level thinning cannot explain all the loss of species. Conclusion: Although a decrease in density could explain much of the decrease (up to 42.9%) in species richness when this alpine meadow was fertilized, other important mechanisms such as interspecific competition cannot be ignored. Future studies should investigate the effect of assemblage level thinning on species diversity, and search for mechanisms responsible for a decrease in diversity.     

A conceptual model of plant community changes following cessation of cultivation in semi‐arid grassland

Question: Can vegetation changes that occur following cessation of cultivation for cereal crop production in semi‐arid native grasslands be described using a conceptual model that explains plant community dynamics following disturbance? Location: Eighteen native grasslands with varying time‐since‐last cultivation across northern Victoria, Australia. Methods: We examined recovery of native grasslands after cessation of cultivation along a space for‐ time chronosequence. By documenting floristic composition and soil properties of grasslands with known cultivation histories, we established a conceptual model of the vegetation states that occur following cessation of cultivation and inferred transition pathways for community recovery. Results: Succession from an exotic‐dominated grassland to native grassland followed a linear trajectory. These changes represent an increase in richness and cover of native forbs, a decrease in cover of exotic annual species and little change in native perennial graminoids and exotic perennial forbs. Using a state‐and‐transition model, two distinct vegetation states were evident: (1) an unstable, recently cultivated state, dominated by exotic annuals, and (2) a more diverse, stable state. The last‐mentioned state can be divided into two further states based on species composition: (1) a never‐cultivated state dominated by native perennial shrubs and grasses, and (2) a long‐uncultivated state dominated by a small number of native perennial and native and exotic annual species that is best described as a subset of the never‐cultivated state. Transitions between these states are hypothesized to be dependent upon landscape context, seed availability and soil recovery. Conclusions: Legacies of past land use on soils and vegetation of semi‐arid grasslands are not as persistent as in other Australian communities. Recovery appears to follow a linear, directional model of post‐disturbance regeneration which may be advanced by overcoming dispersal barriers hypothesised to restrict recovery.     

Long‐term effects of plant diversity and composition on plant stoichiometry

Plant elemental composition can indicate resource limitation, and changes in key elemental ratios (e.g. plant C:N ratios) can influence rates including herbivory, nutrient recycling, and pathogen infection. Although plant stoichiometry can influence ecosystem‐level processes, very few studies have addressed whether and how plant C:N stoichiometry changes with plant diversity and composition. Here, using two long‐term experimental manipulations of plant diversity (Jena and Cedar Creek), we test whether plant richness (species and functional groups) or composition (functional group proportions) affects temporal trends and variability of community‐wide C:N stoichiometry. Site fertility determined the initial community‐scale C:N ratio. Communities growing on N‐poor soil (Cedar Creek) began with higher C:N ratios than communities growing on N‐rich soil (Jena). However, site‐level plant C:N ratios converged through time, most rapidly in high diversity plots. In Jena, plant community C:N ratios increased. This temporal trend was stronger with increasing richness. However, temporal variability of C:N decreased as plant richness increased. In contrast, C:N decreased over time at Cedar Creek, most strongly at high species and functional richness, whereas the temporal variability of C:N increased with both measures of diversity at this site. Thus, temporal trends in the mean and variability of C:N were underlain by concordant changes among sites in functional group proportions. In particular, the convergence of community‐scale C:N over time at these very different sites was mainly due to increasing proportions of forbs at both sites, replacing high mean C:N (C4 grasses, Cedar Creek) or low C:N (legumes, Jena) species. Diversity amplified this convergence; although temporal trends differed in sign between the sites, these trends increased in magnitude with increasing species richness. Our results suggest a predictive mechanistic link between trends in plant diversity and functional group composition and trends in the many ecosystem rates that depend on aboveground community C:N. Synthesis We compared the effect of plant diversity on the temporal dynamics of community stoichiometry in two long‐term grassland diversity experiments: the Cedar Creek and Jena Experiments. Changes in community C:N ratios were accelerated by increasing diversity at both sites, but in opposite directions depending on soil fertility. Stoichiometry changes were driven by shifts of functional group composition differing in their elemental compositions, the identity of the functional groups depending on the site. Thus, we highlighted that community turnover constrained the effect of diversity on plant stoichiometry at both sites     

Open‐cut mining impacts on soil abiotic and bacterial community properties as shown by restoration chronosequence

Open‐cut mining severely disrupts landforms and soils, preventing or impeding the restoration of preexisting or functional ecosystems because essential properties of the original soils cannot immediately or easily be reinstated. We examined the soil physicochemical and bacterial characteristics of 21 coal‐mined sites in subtropical Queensland, Australia, 3–23 years after establishment of native plant species relative to nonmined analogue sites. Soil disturbance significantly decreased total nitrogen, nitrate nitrogen, and especially total carbon (TC). The TC is projected to take 36 years to recover. Bacterial communities assessed by 16S ribosomal RNA sequencing showed greater species richness and evenness in rehabilitated as compared with nonmined soils, regardless of rehabilitation age. However, bacterial species composition was associated significantly with soil electrical conductivity, the plant density, and total stem cross‐sectional area of woody vegetation. The bacterial communities on rehabilitated sites became progressively more similar to those of nonmined analogue sites over time. This work demonstrates that if topsoils are conserved carefully during mining and supplemented by inorganic fertilizer addition, vigorous plant growth and changes in bacterial community composition can occur soon after plant establishment. This will mitigate the effects of soil disturbance and accelerate the return to the chemical and biological attributes of nonmined analogue soils.     

Gall‐forming insect species richness along a non‐scleromorphic vegetation rainfall gradient in South Africa: The importance of plant community composition

Abstract Currently there is no single accepted hypothesis to explain gall‐forming insect species richness at a particular locality. Hygrothermal stress, soil nutrient availability, plant species richness, plant structural complexity, plant family or genus size, and host plant geographical range size have all been implicated in the determination of gall‐forming insect species richness. Previous studies of such richness at xeric sites have included predominantly scleromorphic vegetation, usually on nutrient‐poor soils. This study is the first to investigate gall‐forming insect species richness of xeric, non‐scleromorphic vegetation. Two habitat types were sampled at each of five localities across a rainfall gradient in the savanna biome of South Africa. The habitat types differed with respect to plant species composition and topography. Gall‐forming insect species richness did not increase with increasing hygrothermal stress or decreasing soil fertility. Rather, gall‐forming insect species richness was largely dependent on the presence of Terminalia sericea as well as other members of the Combretaceae and Mimosaceae. Plots where all these taxa were present had the highest gall‐forming insect species richness, up to 15 species, whereas plots with none of these taxa had a maximum of four galling‐insect species. Despite herb, shrub and tree strata not differing in gall‐forming insect species richness, insect galls were more common on woody than non‐woody plants. Also, stem galls were more frequent than apical or leaf galls. An alternative hypothesis to explain local gall‐forming insect species richness is suggested: galling insects may preferentially select those plant species with characteristics such as chemical toxicity, mechanical strength, degree of lignification or longevity that can be manipulated to benefit the galler. Thus plant community composition should be considered when attempting to explain gall‐forming insect species richness patterns.     

Species co‐occurrence networks show reptile community reorganization under agricultural transformation

Agricultural transformation represents one of the greatest threats to biodiversity, causing degradation and loss of habitat, leading to changes in the richness and composition of communities. These changes in richness and composition may, in turn, lead to altered species co‐occurrence, but our knowledge of this remains limited. We used a novel co‐occurrence network approach to examine the impact of agricultural transformation on reptile community structure within two large (> 172 000 km²; 224 sites) agricultural regions in southeastern Australia. We contrasted assemblages from sites surrounded by intact and modified landscapes and tested four key hypotheses that agricultural transformation leads to (H1) declines in species richness, (H2) altered assemblages, (H3) declines in overall co‐occurrence, and (H4) complex restructuring of pairwise associations. We found that modified landscapes differed in composition but not richness compared with intact sites. Modified landscapes were also characterized by differences in co‐occurrence network structure; with species sharing fewer sites with each other (reduced co‐occurrence connectance), fewer highly‐connected species (truncation of the frequency distribution of co‐occurrence degree) and increased modularity of co‐occurrence networks. Critically, overall loss of co‐occurrence was underpinned by complex changes to the number and distribution of pair‐wise co‐occurrence links, with 41–44% of species also gaining associations with other species. Change in co‐occurrence was not correlated with changes in occupancy, nor by functional trait membership, allowing a novel classification of species susceptibility to agricultural transformation. Our study reveals the value of using co‐occurrence analysis to uncover impacts of agricultural transformation that may be masked in conventional studies of species richness and community composition.     

Effects of long‐term cutting in a grassland system: perspectives for restoration of plant communities on nutrient‐poor soils

Abstract. The upper courses of brook valley systems harbour Nardo‐Galion saxatilis communities characteristic of oligo‐trophic soils under low‐intensity farming. Most of these communities have disappeared under intensified farming i.e. application of fertilizers. We studied the possibilities of restoration i.e. re‐establishment of the former plant community by adopting various cutting regimes after the cessation of fertilization in 1972. The various cutting regimes revealed different effects after 25 yr. Regimes with cutting every second year with or without removal of the swath, and complete abandonment deviated from the other regimes that included annual haymaking with different frequency and timing. The latter group of cutting regimes came closer to the community of an adjacent field where fertilization stopped in 1967. This field in turn harboured several Nardo‐Galion species after 25 yr of annual cutting, and showed more resemblance with a local reference community (at a distance of 500 m) that had not been fertilized since the 1940s. The local reference still does not match poorly developed Nardo‐Galion saxatilis communities found in the region of ca. 50 km around the study area, and is far from well developed Nardo‐Galion communities in the same region. The study site still harbours several species characteristic of eutrophic soil and few species characteristic of oligotrophic soil after 25 yr of annual cutting and removal of the swath. The soil seed bank harbours only few target species. Although species characteristic of oligotrophic soil are present in an adjacent field and Nardo‐Galion saxatilis species occur at 500 m, they have not (yet) established in the target area.     

Effects of long‐term fire exclusion and frequent fire on plant community composition: A case study from semi‐arid shrublands

Time since last fire and fire frequency are strong determinants of plant community composition in fire‐prone landscapes. Our study aimed to establish the influence of time since last fire and fire frequency on plant community composition and diversity of a south‐west Australian semi‐arid shrubland. We employed a space‐for‐time approach using four fire age classes: ‘young’, 8–15 years since last fire; ‘medium’, 16–34; ‘old’, 35–50; and ‘very old’, 51–100; and three fire frequency classes: burnt once, twice and three times within the last 50 years. Species diversity was compared using one‐way ANOVA and species composition using PERMANOVA. Soil and climatic variables were included as covariables to partition underlying environmental drivers. We found that time since last fire influenced species richness, diversity and composition. Specifically, we recorded a late successional transition from woody seeders to long‐lived, arid‐zone, resprouting shrub species. Fire frequency did not influence species richness and diversity but did influence species composition via a reduction in cover of longer‐lived resprouter species – presumably because of a reduced ability to replenish epicormic buds and/or sufficient starch stores. The distinct floristic composition of old and very old habitat, and the vulnerability of these areas to wildfires, indicate that these areas are ecologically important and management should seek to preserve them.     

Forest plant community as a driver of soil biodiversity: experimental evidence from collembolan assemblages through large‐scale and long‐term removal of oak canopy trees Quercus petraea

Plant–soil interactions are increasingly recognized to play a major role in terrestrial ecosystems functioning. However, few studies to date have focused on slow dynamic ecosystems such as forests. As they are vertically stratified by multiple vegetation strata, canopy tree removal by thinning operations could alter forest plant community through tree canopy opening. Very little is known about cascading effects on soil biodiversity. We conducted a large‐scale, multi‐site assessment of collembolan assemblage response to long‐term canopy tree removal in sessile oak Quercus petraea temperate forests. A total of 33 experimental plots were studied covering a large gradient of canopy tree basal area, stand age and local abiotic contexts. Collembolan abundance strongly declined with canopy tree removal in early forest successional stage and this was mediated by negative effect of understory plant community composition changes, i.e. shift from moss and forb to tree seedling, fern, shrub and grass species. Negative effect of this composition shift on collembolan species richness was largely offset by positive effect of the increase in understory plant species richness. This gives support to both the plant mass‐ratio and functional diversity hypotheses. Collembolan functional groups had contrasting response patterns, which were mediated by different ecological factors. Epedaphic (r‐strategist) abundance and species richness increased with canopy tree removal in relation with the increase in understory plant species richness. In contrast, euedaphic (K‐strategist) abundance and species richness declined with canopy tree removal in early forest successional stage in relation with changes in understory plant community composition and species richness, as well as microclimatic conditions. Overall, our study provides experimental evidence that forest plant community can be a strong driver of collembolan assemblages. It also emphasizes the role of trees as foundation species of forest ecosystems that can shape soil biodiversity through their regulation of understory plant community and ecosystem abiotic conditions.     

Nutrient limitation and nutrient‐driven shifts in plant species composition in a species‐rich fen meadow

Question: We studied the development and persistence of the effects of nutrient pulses on biomass production and species composition in a fen meadow. Location: Nature reserve, central Netherlands, 5 m a.s.l. Methods: Single pulse fertilization with N and P in a factorial design on an undrained central and a drained margin site in a species‐rich fen meadow (Cirsio dissecti‐Molinietum). Biomass production and species composition were monitored during four years. Results: At the central site, N addition boosted biomass production, but only during one year. The species composition was not changed. P fertilization increased the biomass production and changed the species composition from a vegetation dominated by Carex panicea to a grassland community with abundant Holcus lanatus, but not before the second year. At the margin site, P fertilization changed the species composition in a similar way, but biomass production was not increased. N fertilization had no effect. At both sites the P induced shift in species composition persisted for four years although the P effect declined during the experiment. Conclusions: The biomass responses show that N was limiting in the central site. Another nutrient, besides N and P (probably K) must have been limiting in the marginal site. The fast decline of the N effect on biomass is ascribed to increased denitrification and biomass removal. The delay in the P effect on biomass and species composition and the persistence of the P effect on species composition are ascribed to fast immobilisation and subsequent slow release of fertilizer P in the peat soil. Recurrence of the P pulses is expected to cause permanent changes in species composition.     

Short‐term effect of selection cutting in boreal balsam fir forest on cerambycid and scolytid beetles

The ecology and management of boreal forest ecosystems are drawing greater attention worldwide as their importance is being increasingly recognized for carbon sequestration or for harbouring the world's largest remaining intact forests. Selection cuts have been introduced as a more socially acceptable silvicultural method to improve the maintenance of habitat structure and functions as they mimic aspects of boreal forest succession dynamics. Many studies have shown that selection cutting helps maintaining arthropod communities in mature forests, but few have examined the increased risks of damage by bark‐ and wood‐boring insects in boreal forests of eastern North America. We used multidirectional flight‐interception traps to quantify the response of these beetles to 25 and 40% selection cutting in a balsam fir–white birch forest of Québec, Canada. The abundance and species number of both cerambycid and scolytid beetles were 5–6 times larger in selectively cut stands than in controls the year following treatments. Analyses revealed that bark‐ and wood‐boring beetles’ response was mostly associated with increased canopy openness in selectively cut stands (and sun‐exposed locations within them) and residual tree injuries caused by harvesting operations. These conditions attracted beetles such as Trypodendron lineatum (Scolytinae) and Rhagium inquisitor (Cerambycidae), two species known for their ability to attack weakened, dying and dead hosts. Most species were more abundant in selection cuts, except for Evodinus m. monticola (Cerambycidae) whose abundance was strongly reduced after treatment. Some beetles can have detrimental effects on residual trees and thus could reduce timber value, but most species found in treated stands do not represent a high risk for healthy trees. Thus, selection cuts do not seem favourable to the establishment of tree‐killing beetles. However, as they were found more active/abundant after selection cutting, it would be wise to further study their population dynamics over mid‐ and long‐term periods, along with the ecological and economic implications associated with this silvicultural treatment.     

Dispersal,diversity and distribution patterns in pioneer vegetation: The role of river‐floodplain connectivity

Question: Are there changes in dispersal patterns in floodplain pioneer vegetation with effects on seedling number, species richness and species composition along a gradient of declining river‐floodplain connectivity? Location: Middle Elbe river floodplain, Germany. Methods: An experiment with five treatments was set up along a gradient of declining river‐floodplain connectivity, partitioning seedlings into three groups: (1) emerging solely from water dispersed seeds, (2) from wind/animal dispersed seeds and (3) from the soil diaspore bank. Two controls were established: without any manipulation and exclusion of all seeds. The results were compared with those of vegetation and soil sampling to evaluate the representativeness of the experimental sites in terms of species composition, diversity, seedling number and soil parameters. Results: Water dispersal and the soil diaspore bank were the major dispersal strategies shaping floodplain pioneer vegetation at the Middle Elbe river. The number of seedlings, species richness and the variation in species composition in these habitats depend on the degree of connectivity. The seedling number and species richness is highest in sites of permanent or almost permanent exchange with the main channel, where water dispersal additionally contributes to the number of seedlings grown from the soil seed bank. Conclusion: The results underline the importance of river‐floodplain ecotones as sink habitats for water‐dispersed seeds. Considering the strongly reduced river‐floodplain interactions due to dykes and other engineering structures, management strategies are necessary to improve connectivity and the renewal of fluvial land forms.     

Plant functional traits along environmental gradients in seasonally dry and fire‐prone ecosystem

Questions: How does the abundance and richness of plant assemblages with different functional (regeneration and nutrient acquisition) traits vary with fire regime, moisture availability and substrate fertility? What is the role of different functional traits in maintaining plant diversity under changing environmental conditions in seasonally dry and fire‐prone environments? Location: Southwest Western Australia. Methods: Plant species abundance and soil nutrients were determined at 16 forest sites with variable fire histories across an aridity gradient. All plant species were classified based on their functional traits as (1) perennial or annual, (2) ectomycorrhizal, arbuscular mycorrhizal, ericoid mycorrhizal, orchid mycorrhizal, proteoid or other non‐mycorrhizal, (3) resprouters or seeder, and (4) nitrogen fixer or non‐fixer. We used a multivariate (fourth‐corner) technique to simultaneously test the significance and direction of the relationship between each of these traits and fire frequency, fire interval length, aridity, and soil N, P and C fractions. Results: The functional response of the vegetation to fire regime was minor and restricted to annual species, which comprised only ～4% of taxa. Proteoid and ectomycorrhizal species dominated over species with arbuscular and orchid mycorrhizal roots, N‐fixers dominated over non‐fixers, and seeders dominated over resprouters when N fertility was low but organic labile P was high. Further, proteoid and ectomycorrhizal species richness increased with aridity, while arbuscular mycorrhizal species richness decreased. Conclusions: While the functional composition of southwest Australian vegetation is largely insensitive to changes in fire regime, nutrient acquisition and, to a lesser extent, regeneration traits provide mechanisms for the vegetation community to adjust to changes in resource availability. Thus, diversity responses to environmental change in seasonally dry and fire‐prone ecosystems are likely to be primarily mediated by the composition of nutrient acquisition traits in the vegetation community.     

Seed bank,seed dispersal and vegetation cover: Colonization along a newly‐created river channel

Question : What is the relative importance of the initial seed bank and subsequent seed dispersal for floristic composition of bank vegetation two years after creation of a newly‐cut reach of a river channel? Location : River Cole, West Midlands, United Kingdom. Methods : We took bank and bed sediment samples from a 0.5‐km reach of a new river channel cut into intact flood‐plain. After river diversion, seed samples deposited on artificial turf mats placed on the river banks and flood‐plain edge were taken in summer and winter 2002 and 2003. Seed rain samples from funnel traps were taken during summer 2002 and 2003. We undertook greenhouse germination trials to assess viable seed species within these samples. In summer 2004, we surveyed river bank vegetation. Agglomerative cluster analysis was used to investigate floristic similarity between seed bank, seed rain, seed deposition samples and final bank vegetation cover. DCA was used to explore contrasts between the samples and to assess whether these reflected interpretable environmental gradients. Results : Seed rain samples contained a small subset of species in the summer depositional samples. 38 species were found within the final vegetation, the seed bank, and at least one of the four sets of depositional samples; a further 30 species not present in the seed‐bank samples were present in at least one of the four sets of depositional samples and the final vegetation. Floristic composition of the vegetation was most similar to the depositional samples from winter 2002 and 2003 and summer 2003. DCA axis 1 reflected a time sequence from seed‐bank samples through depositional samples to the final vegetation. Conclusions : Newly cut river banks were colonized rapidly. Seed remobilization and hydrochorous transport from the upstream catchment are important for colonization. Species richness was highest in samples deposited during winter when high river flows can remobilize and transport viable seeds from upstream. This process would also have enhanced the species richness of seed production along the banks during the second summer (2003).     

Land‐use and isolation interact to affect wetland plant assemblages

Different management regimes imposed on similar habitat types provide opportunities to investigate mechanisms driving community assembly and changes in species composition. We investigated the effect of pasture management on vegetation composition in wetlands with varying spatial isolation on a Florida cattle ranch. We hypothesized that increased pasture management intensity would dampen the expected negative effect of wetland isolation on native species richness due to a change from dispersal‐driven community assembly to niche‐driven assembly by accentuated environmental tolerance. We used native plant richness, exotic plant richness and mean coefficient of conservatism (CC) to assess wetland plant assemblage composition. Sixty wetlands were sampled, stratified by three levels of isolation across two pasture management intensities; semi‐native (less intensely managed; mostly native grasses, never fertilized) and agronomically improved (intensely managed, planted with exotic grasses, and fertilized). Improved pasture wetlands had lower native richness and CC scores, and greater total soil phosphorus and exotic species coverage compared to semi‐native pasture wetlands. Increased wetland isolation was significantly associated with decreases in native species richness in semi‐native pasture wetlands but not in improved pasture wetlands. Additionally, the species–area relationship was stronger in wetlands in improved pastures than semi‐native pastures. Our results indicate that a) native species switch from dispersal‐based community assembly in semi‐native pastures to a species‐sorting process in improved pastures, and b) recently‐introduced exotic species already sorted for more intensive management conditions are primarily undergoing dispersal‐based community assembly. That land‐use may alter the relative importance of assembly processes and that different processes drive native and exotic richness has implications for both ecosystem management and restoration planning.     

Biodiversity of semi‐arid Mediterranean grasslands: Impact of grazing and afforestation

Question: What is the impact of grazing and/or afforestation on grassland diversity, species composition and cover parameters? Location: Semi‐arid Mediterranean grasslands of Jordan. Methods: Vegetation, litter, bare soil and rock cover were compared among four management types – free grazing and protected from grazing with three levels of tree cover. Species composition, plant cover, species richness and evenness were used to evaluate differences in vegetation among management types. Species composition differences among management types were also investigated. Results: Semi‐arid Mediterranean grasslands harbour appreciable levels of plant biodiversity. Grazing did not affect plant diversity, indicating the high resilience against and adaptation to grazing; however,grazing affected species composition and cover parameters. Afforestation seems to protect soil through higher litter cover but its impact on plant biodiversity was negative and markedly affected species composition. Conclusions: Neither protection from grazing or massive afforestation alone are sufficient for conserving biodiversity in this system. A management model is suggested where the landscape should be maintained as a mosaic of four management types: complete protection from grazing, grazing rotation, planting sparse trees in eroded areas and revegetating degraded areas using native, herbaceous and grazing tolerant species.     

Species richness–environment relationships within coastal sclerophyll and mesophyll vegetation in Ku‐ring‐gai Chase National Park,New South Wales,Australia

Abstract Patterns in species richness from a wide range of plant communities in Ku‐ring‐gai Chase National Park, New South Wales, Australia, were examined in relation to a number of environmental variables, including soil physical and chemical characteristics. Total species richness and richness of three growth‐form types (trees, shrubs and ground cover) were determined in duplicate 500‐m² quadrats from 50 sites on two geological substrata: Hawkesbury Sandstone and Narrabeen shales and sandstones. Generalized linear models (GLM) were used to determine the amount of variation in species richness that could be significantly explained by the measured environmental variables. Seventy‐three per cent of the variation in total species richness was explained by a combination of soil physical and chemical variables and site attributes. The environmental variables explained 24% of the variation in tree species richness, 67% of the variation in shrub species richness and 62% of the variation in ground cover species richness. These results generally support the hypothesis of an environmental influence on patterns in total species richness and richness of shrubs and ground cover species. However, tree species richness was not adequately predicted by any of the measured environmental variables; the present environment exerts little influence on the richness of this growth‐form type. Historical factors, such as fire or climatic/environmental conditions at time of germination or seedling establishment, may be important in determining patterns in tree species richness at the local scale.