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1.
Habitat specificity indices reflect richness (α) and/or distinctiveness (β) components of diversity. The latter may be defined by α and γ (landscape) diversity in two alternative ways: multiplicatively () and additively (). We demonstrate that the original habitat specificity concept of Wagner and Edwards (Landscape Ecol 16:121–131, 2001) consists of three independent components: core habitat specificity (uniqueness of the species composition), patch area and patch species richness. We describe habitat specificity as a family of indices that may include either area or richness components, or none or both, and open for use of different types of mean in calculation of core habitat specificity. Core habitat specificity is a beta diversity measure: the effective number of completely distinct communities in the landscape. Habitat specificity weighted by species number is a gamma diversity measure: the effective number of species that a patch contributes to landscape richness. We compared 12 habitat specificity indices by theoretical reasoning and by use of field data (vascular plant species in SE Norwegian agricultural landscapes). Habitat specificity indices are strongly influenced by weights for patch area and patch species richness, and the relative contribution of rare vs. common species (type of mean). The relevance of properties emphasized by each habitat specificity index for evaluation of patches in a biodiversity context is discussed. Core habitat specificity is emphasized as an ecologically interpretable measure that specifically addresses patch uniqueness while habitat specificity weighted by species number combines species richness and species composition in ways relevant for conservation biological assessment. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.  相似文献   

2.
The importance of the spatial as well as the temporal structure of habitat patches for urban biodiversity has been recognised, but rarely quantified. In dynamic environments the rate of habitat destruction and recreation (i.e. the landscape turnover rate), the minimum amount of potential habitat, its spatial configuration as well as the environmental conditions determining habitat quality are crucial factors for species occurrence. We analysed species responses to environmental parameters and to the spatio-temporal configuration of urban brownfield habitats in a multi-species approach (37 plant and 43 insect species). Species presence/absence data and soil parameters, site age, vegetation structure and landscape context were recorded by random stratified sampling at 133 study plots in industrial areas in the city of Bremen (Germany). Based on the field data, we predicted species occurrences by species distribution models using a multi-model inference approach. Predicted species communities were driven by successional age both at the scale of a single building lot and at the landscape scale. Minimum average succession time of brownfield habitats required to support all and especially regionally rare species depended on the proportion of available open space; the larger the potential habitat area the faster the acceptable turnover. Most plant, grasshopper, and leafhopper species modelled could be maintained at an intermediate turnover rate (mean age of 10–15 years) and a proportion of open sites of at least 40%. Our modelling approach provides the opportunity of inferring optimal spatio-temporal landscape configurations for urban conservation management from patch scale species-environment relationships. The results indicate that urban planning should incorporate land use dynamics into the management of urban biodiversity. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.  相似文献   

3.
Landscape connectivity is important in designing corridor and reserve networks. Combining genetic distances among individuals with least-cost path (LCP) modelling helps to correlate indirect measures of gene flow with landscape connectivity. Applicability of LCP modelling, however, is reduced if knowledge on dispersal pathways or routes is lacking. Therefore, we integrated habitat suitability modelling into LCP analysis to avoid the subjectivity common in LCP analyses lacking knowledge on dispersal pathways or routes. We used presence-only data and ecological niche factor analysis to model habitat suitability for the spiny rat, Niviventer coninga, in a fragmented landscape of western Taiwan. We adapted the resultant habitat suitability map for incorporation into LCP analyses. Slightly increased Mantel correlations indicated that a class-weighted suitability map better explained genetic distances among individuals than did geographical distances. The integration of habitat suitability modelling into LCP analysis can thus generate information on distribution of suitable habitats, on potential routes of dispersal, for placement of corridors, and evaluate landscape connectivity. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.  相似文献   

4.
Habitat fragmentation strongly affects insect species diversity and community composition, but few studies have examined landscape effects on long term development of insect communities. As mobile consumers, insects should be sensitive to both local plant community and landscape context. We tested this prediction using sweep-net transects to sample insect communities for 8 years at an experimentally fragmented old-field site in northeastern Kansas, USA. The site included habitat patches undergoing secondary succession, surrounded by a low turf matrix. During the first 5 years, plant richness and cover were measured in patches. Insect species richness, total density, and trophic diversity increased over time on all transects. Cover of woody plants and perennial forbs increased each year, adding structural complexity to successional patches and potentially contributing to increased insect diversity. Within years, insect richness was significantly greater on transects through large successional patches (5000 m2) than on transects through fragmented arrays of 6 medium-sized (total area 1728 m2) or 15 small (480 m2) patches. However, plant cover did not differ among patch types and was uncorrelated with insect richness within years. Insect richness was strongly correlated with insect density, but trophic and α diversities did not differ among patch types, indicating that patch insect communities were subsets of a common species pool. We argue that differences in insect richness resulted from landscape effects on the size of these subsets, not patch succession rates. Greater insect richness on large patches can be explained as a community-level consequence of population responses to resource concentration.  相似文献   

5.
Wagner  Helene H.  Wildi  Otto  Ewald  Klaus C. 《Landscape Ecology》2000,15(3):219-227
In this paper, we quantify the effects of habitat variability and habitat heterogeneity based on the partitioning of landscape species diversity into additive components and link them to patch-specific diversity. The approach is illustrated with a case study from central Switzerland, where we recorded the presence of vascular plant species in a stratified random sample of 1'280 quadrats of 1 m2 within a total area of 0.23 km2. We derived components of within- and between-community diversity at four scale levels (quadrat, patch, habitat type, and landscape) for three diversity measures (species richness, Shannon index, and Simpson diversity). The model implies that what we measure as within-community diversity at a higher scale level is the combined effect of heterogeneity at various lower levels. The results suggest that the proportions of the individual diversity components depend on the habitat type and on the chosen diversity aspect. One habitat type may be more diverse than another at patch level, but less diverse at the level of habitat type. Landscape composition apparently is a key factor for explaining landscape species richness, but affects evenness only little. Before we can test the effect of landscape structure on landscape species richness, several problems will have to be solved. These include the incorporation of neighbourhood effects, the unbiased estimation of species richness components, and the quantification of the contribution of a landscape element to landscape species richness.  相似文献   

6.
Many amphibian species rely on both aquatic and terrestrial habitats to complete their life cycles. Therefore, processes operating both within the aquatic breeding habitat, and in the surrounding uplands may influence species distributions and community composition. Moreover, changes in land use adjacent to breeding site may degrade aquatic habitats. To assess land use effects on pond-breeding amphibian assemblages, we investigated relationships between land use, breeding habitat conditions, and breeding amphibian use of constructed wetlands in urban environments of the Baltimore metropolitan area, USA. Forest and impervious surface associations with species richness and occurrence occurred at spatial scales ranging from 50 to 1,000 m, with strongest relationships at 500 m. Forest and impervious surface cover within 1,000 m of ponds were also related to water and sediment quality, which in turn were capable of explaining a proportion of the observed variation in species richness and occurrence. Taken together, our results suggest that forest and other land covers within relatively proximal distances to ponds (i.e., within 50–1,000 m) may be influencing species richness directly via the provisioning of upland habitat, and indirectly via influences on within pond habitat quality. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.  相似文献   

7.
Assessing and predicting the species richness of a complex landscape remains a problem because there is no simple scaling function of species richness in a heterogeneous environment. Furthermore, the potential value of an area for biodiversity conservation may depend on which, rather than how many, species the area contains. This paper shows how we can objectively evaluate the contribution of an area, e.g., a habitat patch, to larger-scale plant species richness, e.g., a landscape composed of patches of several habitat types, and how we can test hypotheses that attempt to explain this contribution. We quantified the concept of habitat specificity to assess the proportion of each observed plant population that is concentrated within a given spatial element. A case study of a biodiversity-monitoring program in the Swiss Canton of Aargau showed that the relative contribution of the three main types of land use to the overall species richness differed strongly between higher taxa (vascular plants and molluscs). However, the type of data, i.e., presence-absence or abundance, was not important. Resampling of the plant data suggested that stratification provided an unbiased estimate of relative specificity, whereas unstratified sampling caused bias even for large samples. In a second case study of vascular plants in an agricultural landscape in central Switzerland, we tested whether the type, size or shape of a landscape element can predict its contribution to the species richness of the landscape. Habitat types that were less frequently disturbed contributed more per m2 to landscape species richness than more frequently disturbed ones. Contrary to expectation, patch size was negatively correlated to specificity per m2 for arable fields, whereas patch shape appeared to be unrelated to the specificity per m2 both for arable fields and for meadows. The specificity approach provides a solution to the problem of scaling species richness and is ideally suited for testing hypotheses on the effect of landscape structure on landscape species richness. Specificity scores can easily be combined with measures of other aspects of rarity to assess the contribution of a spatial element to conservation goals formulated at regional, national or global level.  相似文献   

8.

Context

Understanding how landscape patterns affect species diversity is of great importance in the fields of biogeography, landscape ecology and conservation planning, but despite the rapid advance in biodiversity analysis, investigations of spatial effects on biodiversity are still largely focused on species richness.

Objectives

We wanted to know if and how species richness and species composition are differentially driven by the spatial measures dominating studies in landscape ecology and biogeography. As both measures require the same limited presence/absence information, it is important to choose an appropriate diversity measure, as differing results could have important consequences for interpreting ecological processes.

Methods

We recorded plant occurrences on 112 islands in the Baltic archipelago. Species richness and composition were calculated for each island, and the explanatory power of island area and habitat heterogeneity, distance to mainland and structural connectivity at three different landscape sizes were examined.

Results

A total of 354 different plant species were recorded. The influence of landscape variables differed depending on which diversity measure was used. Island area and structural connectivity determined plant species richness, while species composition revealed a more complex pattern, being influenced by island area, habitat heterogeneity and structural connectivity.

Conclusions

Although both measures require the same basic input data, species composition can reveal more about the ecological processes affecting plant communities in fragmented landscapes than species richness alone. Therefore, we recommend that species community composition should be used as an additional standard measure of diversity for biogeography, landscape ecology and conservation planning.
  相似文献   

9.
Semi-natural habitats provide essential resources for pollinators within agricultural landscapes and may help maintain pollination services in agroecosystems. Yet, whether or not pollinators disperse from semi-natural habitat elements into the adjacent agricultural matrix may to a large extent depend on the quality of this matrix and the corresponding pollinator-specific life history traits. To investigate the effects of matrix quality on the distance decay of wild bees and hoverflies, six transects along vegetated field tracks originating at a large semi-natural main habitat and leading into the adjacent agricultural matrix were established in the Wetterau Region, central Hesse, Germany. Species richness of wild bees did not change with distance from the main habitat in landscapes with sufficient grassland cover in the surrounding landscape, but significantly declined when semi-natural grasslands where scarce and isolated in the adjacent agricultural matrix. Abundance of wild bees declined with distance regardless of matrix quality. Species richness of hoverflies did not decline with increasing distance in any landscape. Abundance even increased with distance to the main habitat independently of matrix quality. Thus, our data show that taxa of the pollinator guild may perceive landscapes quite differently. Because of their differing dispersal modes and resource requirements as compared to wild bees, hoverflies may play an important role in maintaining pollination services in agricultural landscapes unsuitable for bee species. Our results highlight the need for considering these taxon-specific differences when predicting the effect of landscape structure on pollinators. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.  相似文献   

10.
We hypothesized that the spatial configuration and dynamics of periurban forest patches in Barcelona (NE of Spain) played a minor role in determining plant species richness and assemblage compared to site conditions, and particularly to both direct (measured at plot level) and potential (inferred from landscape metrics) human-associated site disturbance. The presence of all understory vascular plants was recorded on 252 plots of 100 m2 randomly selected within forest patches ranging in size from 0.25 ha to 218 ha. Species were divided into 6 groups, according to their ecology and conservation status. Site condition was assessed at plot level and included physical attributes, human-induced disturbance and Quercus spp. tree cover. Landscape structure and dynamics were assessed from patch metrics and patch history. We also calculated a set of landscape metrics related to potential human accessibility to forests. Results of multiple linear regressions indicated that the variance explained for non-forest species groups was higher than for forest species richness. Most of the main correlates corresponded to site disturbance variables related to direct human alteration, or to landscape variables associated to indirect human effects on forests: Quercus tree cover (a proxy for successional status) was the most important correlate of non-forest species richness, which decreased when Quercus tree cover increased. Human-induced disturbance was an important correlate of synanthropic and total species richness, which were higher in recently managed and in highly frequented forests. Potential human accessibility also affected the richness of most species groups. In contrast, patch size, patch shape and connectivity played a minor role, as did patch history. We conclude that human influence on species richness in periurban forests takes place on a small scale, whereas large-scale effects attributable to landscape structure and fragmentation are comparatively less important. Implications of these results for the conservation of plant species in periurban forests are discussed.  相似文献   

11.
Agricultural intensification has led to dramatic losses in biodiversity over the past several decades. Many studies have shown the effects of intensification on vegetation or soil communities at field or local scales. However, the functional significance of biodiversity may only appear at larger spatial and temporal scales, due to exchanges among local ecosystems throughout a landscape. To examine how patterns of biodiversity loss are reflected at larger spatial scales, plant and soil biodiversity and associated indicators of ecosystem functions were assessed in riparian areas over a 150 km2 agricultural landscape in the Sacramento Valley of California. Publicly-available GIS data were first used to classify and select sites over the range of soils, topography and plant community types. Representative sites from the landscape were sampled for soil physiochemical properties, as well as microbial, nematode, and plant communities. Higher agricultural intensification, based on field and landscape indices, was negatively correlated with richness and diversity of plant and soil taxa, and was related to indicators of ecosystem functions, such as increased soil nitrate and phosphorus loading, decreased riparian health ratings, and lower soil carbon, soil microbial biomass and soil food web structure. Both field- and landscape-scale factors played important roles in the measured losses. The study area was composed of a wide array of soils, vegetation, and land management, indicating that the observed trends transcended site-specific conditions.  相似文献   

12.
Birds can serve as useful model organisms to investigate community level consequences of forestry practices. In this study we investigated the relationships between wintering bird communities and habitat and landscape characteristics of lowland managed forests in Northern Italy. This area is characterized by the spread of the black locust, an alien species that has been favored by forestry practices at the expense of natural oak forests. Birds were censused in winter by point counts in randomly selected plots of 50 m radius. We first addressed bird community–habitat relationships by means of habitat structure measurements, then we investigated bird community–landscape relationships by using GIS techniques. We used generalized linear models (GLM) to test for the effects of habitat and landscape variables on bird community parameters (namely bird species richness, diversity and abundance). Bird community parameters were influenced by oak biomass and tree age, and by oak area and core area, while the other forest habitat types showed less influence. In forest management terms, the main conclusion is that the retention of native oaks is the keyfactor for the conservation of winter bird diversity in local deciduous woods. At the habitat level black locust harvesting may be tolerated, provided that old, large, native oaks are retained in all local woodlots to preserve landscape connectivity and foraging resources. At the landscape meso-scale, large native oak patches, should be preserved or, where necessary, restored. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.  相似文献   

13.
The effect of environmental heterogeneity on spatial spread of invasive species has received little attention in the literature. Altering landscape heterogeneity may be a suitable strategy to control invaders in man-made landscapes. We use a population-based, spatially realistic matrix model to explore mechanisms underlying the observed invasion patterns of an alien tree species, Prunus serotina Ehrh., in a heterogeneous managed forest. By altering several parameters in the simulation, we test for various hypotheses regarding the role of several mechanisms on invasion dynamics, including spatial heterogeneity, seed dispersers, site of first introduction, large-scale natural disturbances, and forest management. We observe that landscape heterogeneity makes the invasion highly directional resulting from two mechanisms: (1) irregular jumps, which occur rarely via long-distance dispersers and create new founder populations in distant suitable areas, and (2) regular, continuous diffusion toward adjacent cells via short- and mid-distance vectors. At the landscape scale, spatial heterogeneity increases the invasion speed but decreases the final invasion extent. Hence, natural disturbances (such as severe storms) appear to facilitate invasion spread, while forest management can have contrasting effects such as decreasing invasibility at the stand scale by increasing the proportion of light interception at the canopy level. The site of initial introduction influences the invasion process but without altering the final outcome. Our model represents the real landscape and incorporates the range of dispersal modes, making it a powerful tool to explore the interactions between environmental heterogeneity and invasion dynamics, as well as for managing plant invaders. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.  相似文献   

14.
Models describing relationships between landscape features and species distribution patterns often display inter-study inconsistencies. Identifying factors contributing to these inconsistencies is a vital step in clarifying the ecological importance of landscape features and synthesizing an effective knowledge base for use in conservation contexts. We examined the influence of several spatial, temporal, and life history assumptions on the outcomes of distribution versus landscape models (DLMs) relating wetland bird communities at 29 Massachusetts (USA) sites to independent urbanization, wetland, forest, and agricultural landscape gradients. We considered a bird specialization index as well as obligate and facultative species richness as response variables. Landscape gradients were quantified at 10 landscape extents (0–1000 m in 100 m increments) and three time periods (1971, 1985, 2005). Univariate models indicated that our specialization index showed: (1) the strongest response to landscape gradients at small extents (200 m); (2) a negative, threshold response to urbanization was superior to a linear fit; and (3) no evidence of time-lagged effects of landscape change. Interestingly, the form of our model (i.e. linear versus threshold) influenced the extent at which strongest effects were detected. Multivariate models relating the specialization index as well as obligate and facultative species richness to landscape gradients showed evidence of annual variability (i.e. composition, parameter estimates, and variability explained) that did not depend upon an organism’s degree of specialization. Our results provide evidence that violations of common assumptions (e.g. selection of appropriate extent, lack of time-lagged effects, etc.) can impact the outcome of DLMs, which could lead to inter-study inconsistencies.  相似文献   

15.
Andy Millard 《Landscape Ecology》2008,23(10):1231-1241
The species composition of semi-natural vegetation in urban areas is influenced by a diversity of factors operating at a variety of spatial scales. This study investigates relationships at the landscape scale between species numbers of semi-natural plant communities and variations in the nature of designated urban green space. Species’ records were obtained from a survey of tetrads (2 km × 2 km) across a contiguous central area of built-up landscape and nearby satellite settlements in the metropolitan borough of Leeds, northern England. Plant species were categorised into natives, archaeophytes, neophytes, casuals and conservation-designated species. The type and extent of designated urban green space within a tetrad was determined using GIS. There was more built-up and designated green space area in the central urban area than in the satellite settlements. However, this difference was not reflected statistically significantly in plant category species’ numbers. Numbers of native species correlated positively with areas of green space designated for relatively high nature conservation value. Neophytes and casuals correlated positively with semi-natural green space lacking rare native species or high native species richness but designated principally for local community accessibility. The value of such spaces and the importance of their appropriate management, not only for community benefits like individual physical health and mental well-being, but also for overall urban plant biodiversity, is highlighted.  相似文献   

16.
Knowledge of variation in vascular plant species richness and species composition in modern agricultural landscapes is important for appropriate biodiversity management. From species lists for 2201 land-type patches in 16 1-km2 plots five data sets differing in sampling-unit size from patch to plot were prepared. Variation in each data set was partitioned into seven sources: patch geometry, patch type, geographic location, plot affiliation, habitat diversity, ecological factors, and land-use intensity. Patch species richness was highly predictable (75% of variance explained) by patch area, within-patch heterogeneity and patch type. Plot species richness was, however, not predictable by any explanatory variable, most likely because all studied landscapes contained all main patch types – ploughed land, woodland, grassland and other open land – and hence had a large core of common species. Patch species composition was explained by variation along major environmental complex gradients but appeared nested to lower degrees in modern than in traditional agricultural landscapes because species-poor parts of the landscape do not contain well-defined subsets of the species pool of species-rich parts. Variation in species composition was scale dependent because the relative importance of specific complex gradients changed with increasing sampling-unit size, and because the amount of randomness in data sets decreased with increasing sampling-unit size. Our results indicate that broad landscape structural changes will have consequences for landscape-scale species richness that are hard or impossible to predict by simple surrogate variables.  相似文献   

17.
We explored patterns of plant species richness at different spatialscales in 14 habitats in a Swedish rural landscape. Effects of physicalconditions, and relationships between species richness and management historyreaching back to the 17th century were examined, using old cadastralmaps andaerial photographs. The most species-rich habitats were dry open semi-naturalgrasslands, midfield islets and road verges. Alpha diversity (species richnesswithin sites) was highest in habitats on dry substrates (excluding bedrock withsparse pines) and beta diversity (species richness among sites) was highest inmoist to wet habitats. Alpha and beta components of species richness tended tobe inversely related among habitats with similar species richness. Managementhistory influenced diversity patterns. Areas managed as grasslands in the17th and 18th century harboured more species than areasoutside the villages. We also found significant relationships between speciesrichness and soil type. Silt proved to be the most species-rich topsoil(10–20 cm) in addition to thin soils top of on green- orlimestone bedrock. The variation in species richness due to local relief orform of thesite also showed significant relationships, where flat surfaces had the highestnumber of species. In contrast, no significant relationship was found betweenspecies richness and aspect. Our study suggests that present-day diversitypatterns are much influenced by management history, and that small habitat,e.g., road verges and midfield islets, are important for maintaining speciesrichness.This revised version was published online in May 2005 with corrections to the Cover Date.  相似文献   

18.
Modern landscape ecology is based on the patch mosaic paradigm, in which landscapes are conceptualized and analyzed as mosaics of discrete patches. While this model has been widely successful, there are many situations where it is more meaningful to model landscape structure based on continuous rather than discrete spatial heterogeneity. The growing field of surface metrology offers a variety of surface metrics for quantifying landscape gradients, yet these metrics are largely unknown and/or unused by landscape ecologists. In this paper, we describe a suite of surface metrics with potential for landscape ecological application. We assessed the redundancy among metrics and sought to find groups of similarly behaved metrics by examining metric performance across 264 sample landscapes in western Turkey. For comparative purposes and to evaluate the robustness of the observed patterns, we examined 16 different patch mosaic models and 18 different landscape gradient models of landscape structure. Surface metrics were highly redundant, but less so than patch metrics, and consistently aggregated into four cohesive clusters of similarly behaved metrics representing surface roughness, shape of the surface height distribution, and angular and radial surface texture. While the surface roughness metrics have strong analogs among the patch metrics, the other surface components are largely unique to landscape gradients. We contend that the surface properties we identified are nearly universal and have potential to offer new insights into landscape pattern–process relationships. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.  相似文献   

19.
Landscape pattern might be an important determinant of non-native plant invasions because it encompasses components influencing the availability of non-native plant propagules and disturbance regimes. We aimed at exploring the relative role of patch and landscape characteristics, compared to those of habitat type and regional human influence on non-native plant species richness. For this purpose, we identified all non-native plant species in 295 patches of four coastal habitat types across three administrative regions in NE Spain differing in the degree of human influence. For each patch, we calculated several variables reflecting habitat patch geometry (size and shape), landscape composition (distribution of land-cover categories) and landscape configuration (arrangement of patches). The last two groups of variables were calculated at five different spatial extents. Landscape composition was by far the most important group of variables associated with non-native species richness. Natural areas close to diverse and urban landscapes had a high number of non-native species while surrounding agricultural areas could buffer this effect. Regional human influence was also strongly associated with non-native species richness while habitat type was the least important factor. Differences in sensitivity of landscape variables across spatial extents proved relevant, with 100 m being the most influential extent for most variables. These results suggest that landscape characteristics should be considered for performing explicit spatial risk analyses of plant invasions. Consequently, the management of invaded habitats should focus not only at the stand scale but also at the highly influential neighbouring landscape. Prior to incorporate landscape characteristics into management decisions, sensitivity analyses should be taken into account to avoid inconsistent variables.  相似文献   

20.

Context

Protected areas are a cornerstone of the global strategy for conserving biodiversity, and yet their efficacy in comparison to unprotected areas is rarely tested. In the highly fragmented forests of temperate regions, landscape context and forest history may be more important than protection status for plant species diversity.

Objectives

To determine whether there are differences in plant diversity between protected areas and private lands while controlling for landscape context, forest age, and other important factors.

Methods

We used a database of 156 one-hectare forest plots distributed over 120,000 km2 in the fragmented forests of southern Ontario to test whether protected areas and private forests differed in native species richness, relative abundance of exotic species, and the probability of finding species of conservation concern.

Results

Plots with more forest on the surrounding landscape had higher native species richness, lower abundance of exotic species, and greater probability of supporting at least one species of conservation concern. Young forests tended to have higher abundance of exotics, and were less likely to support species of conservation concern. Surprisingly, privately owned forests had greater native species richness and were more likely to support species of conservation concern once these other factors were accounted for. In addition, there were significant interactions between ownership type, forest history, and landscape context.

Conclusions

Our results highlight the importance of privately owned forests in this region, and the need to consider forest history and landscape context when comparing the efficacy of protected areas versus private land for sustaining biodiversity.
  相似文献   

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