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1.

Context

In modern agricultural landscapes, fragmentation of partial habitats is a significant filter for multi-habitat users, reducing local taxonomic and functional diversity. There is compelling evidence that small species are more susceptible than large species. The impact of habitat fragmentation on intraspecific body-size distribution, however, is yet unexplored.

Objectives

We tested habitat fragmentation, a major driver of pollinator loss, for its impact on intraspecific body-size distributions of solitary wild-bee species. Subsequently, we tested individual body size for its impact on pollination services.

Methods

We sampled 1272 individuals of the four most common Andrena wild bee species in 22 newly established flowering fields (0.21–0.41 ha) in Hessen, Central Germany, over two consecutive years. Study sites were located in a ca. 80 ha landscape context of increasing habitat fragmentation. We analysed the pollen loads of the most abundant species.

Results

Body size within local populations of the two medium-sized bees increased with fragmentation, suggesting intraspecific selection for higher dispersal capacity. Pollen analysis carried out for the most common species revealed that larger individuals visited a significantly smaller plant spectrum. Habitat fragmentation may thus alter pollination services without necessarily affecting species richness or composition.

Conclusions

Systematic body-size variation at the population level thus explains the considerable variability between simple community measures and ecosystem functioning. Filtering processes at the individual level require increased understanding for targeting pollination services under current and future land-use change.
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2.

Context

Identifying the drivers shaping biological assemblages in fragmented tropical landscapes is critical for designing effective conservation strategies. It is still unclear, however, whether tropical biodiversity is more strongly affected by forest loss, by its spatial configuration or by matrix composition across different spatial scales.

Objectives

Assessing the relative influence of forest patch and landscape attributes on dung beetle assemblages in the fragmented Lacandona rainforest, Mexico.

Methods

Using a multimodel inference approach we tested the relative impact of forest patch size and landscape forest cover (measures of forest amount at the patch and landscape scales, respectively), patch shape and isolation (forest configuration indices at the patch scale), forest fragmentation (forest configuration index at the landscape scale), and matrix composition on the diversity, abundance and biomass of dung beetles.

Results

Patch size, landscape forest cover and matrix composition were the best predictors of dung beetle assemblages. Species richness, beetle abundance, and biomass decreased in smaller patches surrounded by a lower percentage of forest cover, and in landscapes dominated by open-area matrices. Community evenness also increased under these conditions due to the loss of rare species.

Conclusions

Forest loss at the patch and landscape levels and matrix composition show a larger impact on dung beetles than forest spatial configuration. To preserve dung beetle assemblages, and their key functional roles in the ecosystem, conservation initiatives should prioritize a reduction in deforestation and an increase in the heterogeneity of the matrix surrounding forest remnants.
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3.

Context

Landscape modification is an important driver of biodiversity declines, yet we lack insight into how ongoing landscape change and legacies of historical land use together shape biodiversity.

Objectives

We examined how a history of agricultural land use and current forest fragmentation influence the abundance of red-backed salamanders (Plethodon cinereus). We hypothesized that historical agriculture and fragmentation cause changes in habitat quality and landscape structure that limit abundance.

Methods

We measured salamander abundance at 95 forested sites in New York, USA, and we determined whether sites were agricultural fields within the last five decades. We used a structural equation model to estimate relationships between historical agriculture and salamander abundance mediated by changes in forest vegetation, microclimate, and landscape structure.

Results

Historical agriculture affected salamander abundance by altering forest vegetation at a local scale and forest cover at a landscape scale. Abundance was lowest at post-agricultural sites with low woody vegetation, leaf litter depth, and canopy cover. Post-agricultural sites had limited forest cover in the surrounding landscape historically, and salamander abundance was positively related to historical forest cover, suggesting that connectivity to source populations affects colonization of regenerating forests. Abundance was also negatively related to current forest fragmentation.

Conclusions

Historical land use can have legacy effects on animal abundance on par with effects of ongoing landscape change. We showed that associations between animal abundance and historical land use can be driven by altered site conditions and surrounding habitat area, indicating that restoration efforts should consider local site conditions and landscape context.
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4.

Context

Urbanisation places increasing stress on ecosystem services; however existing methods and data for testing relationships between service delivery and urban landscapes remain imprecise and uncertain. Unknown impacts of scale are among several factors that complicate research. This study models ecosystem services in the urban area comprising the towns of Milton Keynes, Bedford and Luton which together represent a wide range of the urban forms present in the UK.

Objectives

The objectives of this study were to test (1) the sensitivity of ecosystem service model outputs to the spatial resolution of input data, and (2) whether any resultant scale dependency is constant across different ecosystem services and model approaches (e.g. stock- versus flow-based).

Methods

Carbon storage, sediment erosion, and pollination were modelled with the InVEST framework using input data representative of common coarse (25 m) and fine (5 m) spatial resolutions.

Results

Fine scale analysis generated higher estimates of total carbon storage (9.32 vs. 7.17 kg m?2) and much lower potential sediment erosion estimates (6.4 vs. 18.1 Mg km?2 year?1) than analyses conducted at coarser resolutions; however coarse-scale analysis estimated more abundant pollination service provision.

Conclusions

Scale sensitivities depend on the type of service being modelled; stock estimates (e.g. carbon storage) are most sensitive to aggregation across scales, dynamic flow models (e.g. sediment erosion) are most sensitive to spatial resolution, and ecological process models involving both stocks and dynamics (e.g. pollination) are sensitive to both. Care must be taken to select model data appropriate to the scale of inquiry.
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5.

Context

Despite decades of research, there is an intense debate about the consistency of the hump-shaped pattern describing the relationship between diversity and disturbance as predicted by the intermediate disturbance hypothesis (IDH). Previous meta-analyses have not explicitly considered interactive effects of disturbance frequency and intensity of disturbance on plant species diversity in terrestrial landscapes.

Objective

We conducted meta-analyses to test the applicability of IDH by simultaneously examining the relationship between species richness, disturbance frequency (quantified as time since last disturbance as originally proposed) and intensity of disturbance in forest landscapes.

Methods

The effects of disturbance frequency, intensity, and their interaction on species richness was evaluated using a mixed-effects model.

Results

We found that species richness peaks at intermediate frequency after both high and intermediate disturbance intensities, but the richness-frequency relationship differed between intensity classes.

Conclusions

Our study highlights the need to measure multiple disturbance components that could help reconcile conflicting empirical results on the effect of disturbance on plant species diversity.
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6.

Context

In heterogeneous landscapes, habitat complementation is a key process underlying the distribution of mobile species able to exploit non-substitutable resources over large home ranges. For instance, insectivorous bats need to forage in a diversity of habitat patches offering varied compositions and structures within forest landscape mosaics to fulfill their life cycle requirements.

Objectives

We aimed at analyzing the effects of forest structure and composition measured at the stand and landscape scales on bat species richness, abundance and community composition in pine plantation forests of south-western France.

Methods

We sampled bat communities at different periods of the summer season using automatic ultrasound recorders along a tree composition gradient from pine monocultures to pure oak stands. We analyzed bat species activity (as a proxy for bat abundance) and species richness with linear mixed models. Distance-based constrained ordinations were used to partition the spatio-temporal variation in bat communities.

Results

Deciduous tree cover increased bat activity and modified community composition at both stand and landscape scales. Changes in bat communities were mostly driven by landscape-scale variables while bat activity responded more to stand-scale predictors.

Conclusions

The maintenance of deciduous trees at both stand and landscape scales is likely critical for bat communities living in fast-growing conifer plantations, by increasing the availability and diversity of prey and roosting sites. Our study suggests that bats respond to forest composition at both stand and landscape scales in mosaic plantation landscapes, mainly through a resource complementation process.
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7.

Context

The anthropocene is characterised by global landscape modification, and the structure of remnant habitats can explain different patterns of species richness. The most pervasive processes of degradation include habitat loss and fragmentation. However, a recovery of modified landscape is occurring in some areas.

Objectives

The main goal is to know how lichen and bryophyte epiphytic richness growing on Mediterranean forests is influenced not only by fragments characteristics but also by the structure of the landscape. We introduce a temporal dimension in order to evaluate if the historical landscape structure is relevant for current epiphytic communities.

Methods

40 well-preserved forest fragments were selected in a landscape with a large habitat loss over decades, but with a recovery of forest surface in the last 55 years. The most relevant fragment and landscape-scale attributes were considered. Some of the variables were measured in three different years to incorporate a temporal framework.

Results

The results showed that variables at fragment scale had a higher influence, whereas variables at the landscape scale were irrelevant. Among all the historical variables analyzed, only the shift in forest fragment size had influence on species richness.

Conclusions

Mediterranean forests had suffered fragmentation along centuries. Their epiphytic communities also suffer the hard conditions of Mediterranean climate. Our results indicate that Mediterranean epiphytic communities may be in a threshold since it they will never be similar to those communities existing previous fragmentation process even a recovery habitat occur or, they may require more time to response to this habitat recovery.
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8.

Context

Anthropogenic landscape simplification and natural habitat loss can negatively affect wild bees. Alternatively, anthropogenic land-use change may diversify landscapes, creating complementary habitats that maintain overall resource continuity and diversity.

Objectives

We examined the effects of landscape composition, including land-cover diversity and percent semi-natural habitat, on wild bee abundance and species richness within apples, a pollinator-dependent crop. We also explored whether different habitats within diverse landscapes can provide complementary floral resources for bees across space and time.

Methods

We sampled bees during apple bloom over 2 years within 35 orchards varying in surrounding landscape diversity and percent woodland (the dominant semi-natural habitat) at 1 km radii. To assess habitat complementarity in resource diversity and temporal continuity, we sampled flowers and bees within four unique habitats, including orchards, woodlands, semi-natural grasslands, and annual croplands, over three periods from April–June.

Results

Surrounding landscape diversity positively affected both wild bee abundance and richness within orchards during bloom. Habitats in diverse landscapes had different flower communities with varying phenologies; flowers were most abundant within orchards and woodlands in mid-spring, but then declined over time, while flowers within grasslands marginally increased throughout spring. Furthermore, bee communities were significantly different between the closed-canopy habitats, orchards and woodlands, and the open habitats, grasslands and annual croplands.

Conclusions

Our results suggest that diverse landscapes, such as ones with both open (grassland) and closed (woodland) semi-natural habitats, support spring wild bees by providing flowers throughout the entire foraging period and diverse niches to meet different species’ requirements.
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9.

Context

Edge effects due to habitat loss and fragmentation have pervasive impacts on many natural ecosystems worldwide.

Objective

We aimed to explore whether, in tandem with the resource-based model of edge effects, species feeding-guild and flight-capacity can help explain species responses to an edge.

Methods

We used a two-sided edge gradient that extended from 1000 m into native Eucalyptus forest to 316 m into an exotic pine plantation. We used generalised additive models to examine the continuous responses of beetle species, feeding-guild species richness and flight-capable group species richness to the edge gradient and environmental covariates.

Results

Phytophagous species richness was directly related to variation in vegetation along the edge gradient. There were more flight-capable species in Eucalyptus forest and more flightless species in exotic pine plantation. Many individual species exhibited multiple-peaked edge-profiles.

Conclusions

The resource based model for edge effects can be used in tandem with traits such as feeding-guild and flight-capacity to understand drivers of large scale edge responses. Some trait-groups can show generalisable responses that can be linked with drivers such as vegetation richness and habitat structure. Many trait-group responses, however, are less generalisable and not explained by easily measured habitat variables. Difficulties in linking traits with resources along the edge could be due to unmeasured variation and indirect effects. Some species’ responses reached the limits of the edge gradient demonstrating the need to examine edge effects at large scales, such as kilometres.
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10.

Context

An ecosystem service approach for land-use or conservation decisions normally uses economic or biophysical assessments for valuating nature’s services. In contrast, even though ecosystem services are required for human well-being, the actual use of services by differing stakeholder groups are rarely considered in typical ecosystem service assessments, especially the more intangible, cultural ecosystem services.

Objectives

The aim of this research was to quantify different uses for 15 cultural and provisioning ecosystem service indicators across seven stakeholder groups in a watershed proposed with large hydroelectric dam development.

Methods

We used a large-scale survey to quantify use and frequency of use for ecosystem services.

Results

We demonstrate that different stakeholder groups use ecosystem services differently, both in terms of specific ecosystem service indicators, as well as for frequency of ecosystem service use. Across all stakeholder groups, specific cultural ecosystem services were consistently more important to participants when compared to provisioning ecosystem services, especially aesthetic/scenic values.

Conclusions

This work is of global importance as it highlights the importance of considering cultural ecosystem services (e.g. aesthetic/scenic, sense-of-place values) along with multiple stakeholder groups to identify the trade-offs and synergies during decision-making processes for land-use or conservation initiatives.
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11.

Context

Urbanization has altered many landscapes around the world and created novel contexts and interactions, such as the rural–urban interface.

Objectives

We sought to address how a forest patch’s location in the rural–urban interface influences which avian species choose to occur within the patch. We predicted a negative relationship between forest bird richness and urbanization surrounding the patch, but that it would be ameliorated by the area of tree cover in the patch and matrix, and that total tree-cover area would be more influential on forest bird species richness than area of tree cover in the focal patch alone.

Methods

We conducted bird surveys in 44 forest patches over 2 years in Southeast Michigan and evaluated bird presence and richness relative to patch and matrix tree cover and development density.

Results

We observed 43 species, comprised of 21 Neotropical migrants, 19 residents, and three short-distance migrants. Focal-patch tree-cover area and the matrix tree-cover area were the predominant contributors to a site’s overall forest-bird species richness at the rural–urban interface, but the addition of percent of over-story vegetation and percentage of deciduous tree cover influenced the ability of the patches to support forest species, especially Neotropical migrants. Development intensity in the matrix was unrelated to species richness and only had an effect in four species models.

Conclusions

Although small forest patches remain an important conservation strategy in developed environments, the influence of matrix tree cover suggests that landscape design decisions in surrounding matrix can contribute conservation value at the rural–urban interface.
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12.

Context

Mediterranean forests have been fragmented intensively over time, thereby yielding small and isolated forest remnants. They host a rich variety of epiphytes, which may be affected by landscape structure. Previous studies have analyzed the influence of habitat quality on these epiphytic communities, but there is little knowledge of the effects of other fragment features.

Objectives

We evaluated the impacts of forest loss and fragmentation on epiphytic communities (lichens and bryophytes) at plot and fragment scales after controlling the variation in forest structure and management.

Methods

We considered 40 fragments of dense oak forests in a human-modified landscape. We quantified their spatial attributes (size and shape), the quality of the surrounding matrix and the forest stand structure. We modeled community traits, and the presence and abundance of species at fragment and plot scales.

Results

Fragment size, shape, and the quality of the surrounding matrix were key factors that affected epiphytic richness and diversity. Larger and more regularly shaped fragments hosted the richest and most diverse communities, possibly offering a larger core area and thus favoring the entry of typical forest species. A high-contrast matrix was only favorable in small fragments, probably allowing the arrival of propagules. The species-level response was highly variable.

Conclusions

Landscape structure provides powerful explanations of the richness and diversity losses among epiphytes. Forest management should ensure the retention of the largest possible continuous forests. The management strategy of the matrix will depend on the conservation goal, since we observed different effects related with quality and fragment size.
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13.

Context

Habitat destruction is the leading threat to terrestrial biodiversity, isolating remnant habitat in a matrix of modified vegetation.

Objectives

Our goal was to determine how species richness in several broad taxonomic groups from remnant forest was influenced by matrix quality, which we characterized by comparing plant biomass in forest and the surrounding matrix.

Methods

We coupled data on species-area relationships (SARs) in forest remnants from 45 previously published studies with an index of matrix quality calculated using new estimates of plant biomass derived from satellite imagery.

Results

The effect size of SARs was greatest in landscapes with low matrix quality and little forest cover. SARs were generally stronger for volant than for non-volant species. For the terrestrial taxa included in our analysis, matrix quality decreased as the proportion of water, ice, or urbanization in a landscape increased.

Conclusions

We clearly demonstrate that matrix quality plays a major role in determining patterns of species richness in remnant forest. A key implication of our work is that activities that increase matrix quality, such as active and passive habitat restoration, may be important conservation measure for maintaining and restoring biodiversity in modified landscapes.
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14.

Context

Landscape and habitat filters are major drivers of biodiversity of small habitat islands by influencing dispersal and extinction events in plant metapopulations.

Objectives

We assessed the effects of landscape and habitat filters on the species richness, abundance and trait composition of grassland specialist and generalist plants in small habitat islands. We studied traits related to functional spatial connectivity (dispersal ability by wind and animals) and temporal connectivity (clonality and seed bank persistence) using model selection.

Methods

We sampled herbaceous plants, landscape (local and regional isolation) and habitat filters (inclination, woody encroachment and disturbance) in 82 grassland islands in Hungary.

Results

Isolation decreased the abundance of good disperser specialist plants due to the lack of directional vectors transferring seeds between suitable habitat patches. Clonality was an effective strategy, but persistent seed bank did not support the survival of specialist plants in isolated habitats. Generalist plants were unaffected by landscape filters due to their wide habitat breadth and high propagule availability. Clonal specialist plants could cope with increasing woody encroachment due to their high resistance against environmental changes; however, they could not cope with intensive disturbance. Steep slopes providing environmental heterogeneity had an overall positive effect on species richness.

Conclusions

Specialist plants were influenced by the interplay of landscape filters influencing their abundance and habitat filters affecting species richness. Landscape filtering by isolation influenced the abundance of specialist plants by regulating seed dispersal. Habitat filters sorted species that could establish and persist at a site by influencing microsite availability and quality.
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15.

Context

Agroforestry systems in temperate Europe are known to provide both, provisioning and regulating ecosystem services (ES). Yet, it is poorly understood how these systems affect ES provision at a landscape scale in contrast to agricultural practises.

Objectives

This study aimed at developing a novel, spatially explicit model to assess and quantify bundles of provisioning and regulating ES provided by landscapes with and without agroforestry systems and to test the hypothesis that agroforestry landscapes provide higher amounts of regulating ES than landscapes dominated by monocropping.

Methods

Focussing on ES that are relevant for agroforestry and agricultural practices, we selected six provisioning and regulating ES—“biomass production”, “groundwater recharge”, “nutrient retention”, “soil preservation”, “carbon storage”, “habitat and gene pool protection”. Algorithms for quantifying these services were identified, tested, adapted, and applied in a traditional cherry orchard landscape in Switzerland, as a case study. Eight landscape test sites of 1 km?×?1 km, four dominated by agroforestry and four dominated by agriculture, were mapped and used as baseline for the model.

Results

We found that the provisioning ES, namely the annual biomass yield, was higher in landscape test sites with agriculture, while the regulating ES were better represented in landscape test sites with agroforestry. The differences were found to be statistically significant for the indicators annual biomass yield, groundwater recharge rate, nitrate leaching, annual carbon sequestration, flowering resources, and share of semi-natural habitats.

Conclusions

This approach provides an example for spatially explicit quantification of provisioning and regulating ES and is suitable for comparing different land use scenarii at landscape scale.
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16.

Context

We address the issue of adapting landscapes for improved insect biodiversity conservation in a changing climate by assessing the importance of additive (main) and synergistic (interaction) effects of land cover and land use with climate.

Objectives

We test the hypotheses that ant richness (species and genus), abundance and diversity would vary according to land cover and land use intensity but that these effects would vary according to climate.

Methods

We used a 1000 m elevation gradient in eastern Australia (as a proxy for a climate gradient) and sampled ant biodiversity along this gradient from sites with variable land cover and land use.

Results

Main effects revealed: higher ant richness (species and genus) and diversity with greater native woody plant canopy cover; and lower species richness with higher cultivation and grazing intensity, bare ground and exotic plant groundcover. Interaction effects revealed: both the positive effects of native plant canopy cover on ant species richness and abundance, and the negative effects of exotic plant groundcover on species richness were greatest at sites with warmer and drier climates.

Conclusions

Impacts of climate change on insect biodiversity may be mitigated to some degree through landscape adaptation by increasing woody native vegetation cover and by reducing land use intensity, the cover of exotic vegetation and of bare ground. Evidence of synergistic effects suggests that landscape adaptation may be most effective in areas which are currently warmer and drier, or are projected to become so as a result of climate change.
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17.

Context

According to the trophic-rank hypothesis, species may be differentially affected by habitat isolation due to their trophic position in the food chain, i.e. high-order trophic levels may be more negatively affected than low-order levels.

Objectives

The aim of this paper is to study how species richness, abundance and composition of saproxylic beetle communities are affected by patch (=tree) quality and small-scale patch connectivity. Following the trophic-rank hypothesis, we expected predators to be more negatively affected by patch isolation than wood-feeding beetles.

Methods

We studied the beetle community, patch connectivity and patch quality on 28 large oaks. Different connectivity measures were calculated using 50 m-buffers around trees and using distances to the five nearest trees.

Results

Beetle species richness increased with the diameter of oaks, i.e. patch quality. No evidence of the trophic-rank hypothesis was found for species richness patterns. In accordance with the trophic-rank hypothesis, abundance of predatory beetles increased with patch connectivity but lower trophic levels were unaffected or even decreased with patch connectivity.

Conclusions

The structure of invertebrate communities on trees changes with small-scale patch connectivity due to a differential response of low-order and high-order trophic levels. Isolated trees are more exposed to the sun than the more connected trees, which may affect the beetles; however, it was impossible to distinguish the microclimatic from the spatial effects. Although scattered trees generally have a higher conservation value than trees in forests, we conclude that forest trees may be more important for certain trophic levels.
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18.

Context

Understanding the factors contributing to maintaining biodiversity is crucial to mitigate the impact of anthropogenic disturbances. Representing large proportions of green area in highly modified landscapes, residential gardens are often seen as local habitats that can contribute to larger networks of suitable environments at the landscape scale.

Objectives

We investigated the impact of the landscape context on butterfly communities observed in residential gardens, taking into account garden characteristics, land-use types and presence of linear features in the surrounding landscape. We examined how species traits affected butterflies’ response to landscape context and habitat quality.

Methods

We performed a cross-scale study, based on citizen science data documenting butterfly species composition and abundance in 920 gardens across France. We examined the effect of garden quality, the area of different land-use types and the length of linear elements measured at three scales within the surrounding landscape. Species were grouped according to their habitat preference and mobility.

Results

Urbanization negatively affected total species richness and the abundance of butterfly in each group. This was related to declining habitat quality and reduced area of suitable habitat in the surrounding landscape. The magnitude of this effect, however, was negatively correlated with mobility, a trait related to habitat preference. The spatial scale at which landscape context best explained variation in butterfly abundance changed with species’ habitat preference.

Conclusions

This study highlights the importance of preserving high quality habitats in altered landscapes and considering species’ mobility and habitat preference when assessing the impact of landscapes on butterfly communities.
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19.

Context

An increasing number of studies have investigated the impact of environmental heterogeneity on faunal assemblages when measured at multiple spatial scales. Few studies, however, have considered how the effects of heterogeneity on fauna vary with the spatial scale at which the response variable is characterised.

Objectives

We investigated the relationship between landscape properties in a region characterised by diverse fire mosaics, and the structure and composition of avian assemblages measured at both the site- (1 ha) and landscape-scale (100 ha).

Methods

We surveyed birds and calculated spatial landscape properties in sub-tropical woodlands of central Queensland, Australia.

Results

Environmental heterogeneity, as measured by topographic complexity, was consistently important for bird species richness and composition. However, the explanatory power of topographic complexity varied depending on the spatial scale and the component of diversity under investigation. We found different correlates of richness within particular foraging guilds depending on the scale at which richness was measured. Extent of long-unburnt habitat (>10 years since fire) was the most important variable for the landscape-scale richness of frugivores, insectivores and canopy feeders, whereas environmental heterogeneity in the surrounding landscape was more important for site-scale richness of these foraging guilds.

Conclusions

The response of species richness to landscape characteristics varies among scales, and among components of diversity. Thus, depending on the scale at which a biodiversity conservation goal is conceptualised—maximising richness at a site, or across a landscape—different landscape management approaches may be preferred.
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20.

Context

The variation in spatial distribution between ecosystem services can be high. Hence, there is a need to spatially identify important sites for conservation planning. The term ‘ecosystem service hotspot’ has often been used for this purpose, but definitions of this term are ambiguous.

Objectives

We review and classify methods to spatially delineate hotspots. We test how spatial configuration of hotspots for a set of ecosystem services differs depending on the applied method. We compare the outcomes to a heuristic site prioritisation approach (Marxan).

Methods

The four tested hotspot methods are top richest cells, spatial clustering, intensity, and richness. In a conservation scenario we set a target of conserving 10 % of the quantity of five regulating and cultural services for the forest area of Telemark county, Norway.

Results

Spatial configuration of selected areas as retrieved by the four hotspots and Marxan differed considerably. Pairwise comparisons were at the lower end of the scale of the Kappa statistic (0.11–0.27). The outcomes also differed considerably in mean target achievement, cost-effectiveness in terms of land-area needed per unit target achievement and compactness in terms of edge-to-area ratio.

Conclusions

An ecosystem service hotspot can refer to either areas containing high values of one service or areas with multiple services. Differences in spatial configuration among hotspot methods can lead to uncertainties for decision-making. This also has consequences for analysing the spatial co-occurrence of hotspots of multiple services and of services and biodiversity.
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