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1.

Context

Native vegetation is often used as a proxy for habitat to estimate habitat availability in landscapes. This approach may lead to incorrect estimates of the impacts of habitat loss and fragmentation on species, which have not been thoroughly quantified so far.

Objectives

We quantified to what extent the loss of native vegetation reflect actual habitat loss by native species in landscapes. We tested the hypothesis that habitat availability declines at greater rates than native vegetation and thus is overestimated when it is quantified on the basis of native vegetation.

Methods

Using simulations, we quantified how the loss of native vegetation in artificial and real landscapes affects habitat availability for species with different habitat requirements. We contrasted a generalist species, which uses all native vegetation, with 10 habitat-specialist species classified into three categories (interior, patchy and riparian species).

Results

Habitat availability generally declined at greater rates than native vegetation for all specialist species. This pattern was apparent for different specialist species in a broad range of landscape types. Interior species always lost habitat availability more rapidly than the generalist species. Most riparian species lost habitat availability more rapidly than the generalist species. Responses of patchy species were more complex, depending on their dispersal abilities and landscape structure.

Conclusions

Habitat availability is likely to be overestimated when native vegetation is used as proxy for habitat, because habitat availability will generally decline at greater rates than native vegetation. Therefore, a species-centered approach should be adopted when estimating habitat availability in landscapes.
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2.

Context

The history of the landscape directly affects biotic assemblages, resulting in time lags in species response to disturbances. In highly fragmented environments, this phenomenon often causes extinction debts. However, few studies have been carried out in urban settings.

Objectives

To determine if there are time lags in the response of temperate natural grasslands to urbanization. Does it differ for indigenous species and for species indicative of disturbance and between woody and open grasslands? Do these time lags change over time? What are the potential landscape factors driving these changes? What are the corresponding vegetation changes?

Methods

In 1995 and 2012 vegetation sampling was carried out in 43 urban grassland sites. We calculated six urbanization and landscape measures in a 500 m buffer area surrounding each site for 1938, 1961, 1970, 1994, 1999, 2006, and 2010. We used generalized linear models and model selection to determine which time period best predicted the contemporary species richness patterns.

Results

Woody grasslands showed time lags of 20–40 years. Contemporary open grassland communities were, generally, associated with more contemporary landscapes. Altitude and road network density of natural areas were the most frequent predictors of species richness. The importance of the predictors changed between the different models. Species richness, specifically, indigenous herbaceous species, declined from 1995 to 2012.

Conclusions

The history of urbanization affects contemporary urban vegetation assemblages. This indicates potential extinction debts, which have important consequences for biodiversity conservation planning and sustainable future scenarios.
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3.

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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4.

Context

In agricultural landscapes, small woodland patches can be important wildlife refuges. Their value in maintaining biodiversity may, however, be compromised by isolation, and so knowledge about the role of habitat structure is vital to understand the drivers of diversity. This study examined how avian diversity and abundance were related to habitat structure in four small woods in an agricultural landscape in eastern England.

Objectives

The aims were to examine the edge effect on bird diversity and abundance, and the contributory role of vegetation structure. Specifically: what is the role of vegetation structure on edge effects, and which edge structures support the greatest bird diversity?

Methods

Annual breeding bird census data for 28 species were combined with airborne lidar data in linear mixed models fitted separately at (i) the whole wood level, and (ii) for the woodland edges only.

Results

Despite relatively small woodland areas (4.9–9.4 ha), bird diversity increased significantly towards the edges, being driven in part by vegetation structure. At the whole woods level, diversity was positively associated with increased vegetation above 0.5 m and especially with increasing vegetation density in the understorey layer, which was more abundant at the woodland edges. Diversity along the edges was largely driven by the density of vegetation below 4 m.

Conclusions

The results demonstrate that bird diversity was maximised by a diverse vegetation structure across the wood and especially a dense understorey along the edge. These findings can assist bird conservation by guiding habitat management of remaining woodland patches.
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5.

Context

Environmental processes and dispersal are primary determinants of metacommunity dynamics. The relative importance of these effects may vary between species of different abundance classes, given variation in life history traits. Under high disturbance conditions, rare species may be more easily eliminated from their optimal habitats and their distribution may therefore be more heavily dependent upon dispersal from nearby habitat patches than common species.

Objectives

We tested if metacommunity dynamics vary between abundance classes in a high disturbance environment.

Methods

Standardized butterfly sampling was conducted in the urban parks of Hong Kong. To estimate the strength of environmental processes, we measured an array of environmental variables for all sampled parks. Spatial predictors were generated to estimate the effect of dispersal.

Results

For shaping common species compositions, we found environmental processes (and specifically environmental variables including floral density and surrounding woody plant cover) slightly more important than spatial processes. For rare species, only spatial processes were significant while environmental processes were insignificant. Our result contrasts previous studies in natural metacommunities, which have shown that both common and rare species compositions are shaped by environmental processes and similar variables.

Conclusions

Our results demonstrate that high disturbance conditions may inhibit rare species establishment and persistence in urban landscapes. Local habitat management may not be sufficient in conserving rare species in urban environments—spatial context and configuration should be considered in planning for biodiversity. We also highlight the utility of community deconstruction analysis in providing insights into rare species metacommunity dynamics.
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6.

Context

Woodland and agricultural expansion are major causes of grassland fragmentation. Fire and rainfall play important roles in maintaining grasslands, however, fire activity has been reduced in fragmented landscapes.

Objectives

Quantify the degree to which basic landscape fragmentation metrics could be used as drivers of woody cover potential.

Methods

Woody plant percent cover was calculated between 2004 and 2008 at?>?2000 sites. At each site, we calculated these fragmentation metrics for grassland cover type (classified by the National Land Cover Database); # patches, landscape proportion, edge density, largest patch index, effective mesh size and patch cohesion index within 3 circular areas (10 km2, 360 km2 and 3600 km2) surrounding the sampling site. A quantile regression was performed to identify which metrics were useful at predicting the 25th, 50th, 75th or 95th quantile of woody cover distribution.

Results

Grassland proportion and edge density were significant predictors of the woody plant potential (75th and 95th quantile). Woody cover potential was positively associated with edge density suggesting that fragmented areas (i.e., areas with high number of edges) maintained higher woody cover, while grassland proportion was negatively associated with woody plant potential.

Conclusion

We propose that in addition to a lack of fire, fragmented landscapes may facilitate further woodland expansion by reducing natural land and restricting grasslands to smaller, less connected patches, which can maintain higher woody cover. Given current trends in woodland expansion, special attention should be given to areas that are found within a fragmented landscape and climatically prone to woodland expansion.
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7.

Context

With global change, microclimates become important refuges for temperature-sensitive, range-restricted organisms. In African savannas, woody vegetation on Macrotermes mounds create widely-dispersed microclimates significantly cooler than the surrounding matrix, which buffer against elevated temperatures at the finer scale of mounds, allowing species to persist at the landscape scale. Termite colonies cultivate symbiotic fungi to digest lignin, but the fungi require temperatures between 29 and 32 °C, which termites strive to maintain. Mound-associated vegetation is a hot-spot for elephant herbivory, so removal of woody species cover by elephants could influence mound-associated microclimates, impacting temperature regulation by termites.

Objectives

We explored the interaction between two prominent ecosystem engineers (termites and elephants) to ascertain whether elephant removal of mound woody cover affects (1) external mound-associated microclimate and (2) internal mound temperature.

Methods

We surveyed 44 mounds from three sites in Kruger National Park, South Africa, during an El Niño/Southern Oscillation-induced drought and heatwave, recording whether sub-canopy, external, mound-surface and internal mound temperatures varied with vegetation removal by elephant.

Results

Elephant damage to mound-associated vegetation reduces the fine-scale microclimate effect provided by vegetation on Macrotermes mounds. Despite this, termites were able to regulate internal mound temperatures, whereas internal temperatures of abandoned mounds increased with elevated surface temperatures.

Conclusions

Termites can persist despite loss of mound-associated microclimates, but the loss likely increases energetic costs of mound thermoregulation. Since mound vegetation buffers against drought, loss of widely-dispersed, fine-scale microclimates could increase as megaherbivores remain constrained to protected areas, impacting climate-sensitive organisms and ecosystem function at a range of scales.
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8.
9.

Context

Species are expected to shift their distributions in response to global environmental changes and additional protected areas are needed to encompass the corresponding changes in the distributions of their habitats. Conservation policies are likely to become obsolete unless they integrate the potential impacts of climate and land-use change on biodiversity.

Objectives

We identify conservation priority areas for current and future projected distributions of Iberian bird species. We then investigate the extent to which global change informed priority areas are: (i) covered by existing protected area networks (national protected areas and Natura 2000); (ii) threatened by agricultural or urban land-use changes.

Methods

We use outputs of species distributions models fitted with climatic data as inputs in spatial prioritization tools to identify conservation priority areas for 168 bird species. We use projections of land-use change to then discriminate between threatened and non-threatened priority areas.

Results

19% of the priority areas for birds are covered by national protected areas and 23% are covered by Natura 2000 sites. The spatial mismatch between protected area networks and priority areas for birds is projected to increase with climate change. But there are opportunities to improve the protection of birds under climate change, as half of the priority areas are currently neither protected nor in conflict with urban or agricultural land-uses.

Conclusions

We identify critical areas for bird conservation both under current and climate change conditions, and propose that they could guide the establishment of new conservation areas across the Iberian Peninsula complementing existing protected areas.
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10.

Context

Urban landscapes are a mixture of built structures, human-altered vegetation, and remnant semi-natural areas. The spatial arrangement of abiotic and biotic conditions resulting from urbanization doubtless influences the establishment and spread of non-native species in a city.

Objectives

We investigated the effects of habitat structure, thermal microclimates, and species coexistence on the spread of a non-native lizard (Anolis cristatellus) in the Miami metropolitan area of South Florida (USA).

Methods

We used transect surveys to estimate lizard occurrence and abundance on trees and to measure vegetation characteristics, and we assessed forest cover and impervious surface using GIS. We sampled lizard body temperatures, habitat use, and relative abundance at multiple sites.

Results

At least one of five Anolis species occupied 79 % of the 1035 trees surveyed in primarily residential areas, and non-native A. cristatellus occupied 25 % of trees. Presence and abundance of A. cristatellus were strongly associated with forest patches, dense vegetation, and high canopy cover, which produced cooler microclimates suitable for this species. Presence of A. cristatellus was negatively associated with the ecologically similar non-native A. sagrei, resulting in reduced abundance and a shift in perch use of A. cristatellus.

Conclusions

The limited spread of A. cristatellus in Miami over 35 years is due to the patchy, low-density distribution of wooded habitat, which limits dispersal by diffusion. The presence of congeners may also limit spread. Open habitats—some parks, yards and roadsides—contain few if any A. cristatellus, and colonization of isolated forest habitat appears to depend on human-mediated dispersal.
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11.

Context

Climate change alters the vegetation composition and functioning of ecosystems. Measuring the magnitude, direction, and rate of changes in vegetation composition induced by climate remains a serious and unmet challenge. Such information is required for a predictive capability of how individual ecosystem will respond to future climates.

Objectives

Our objectives were to identify the relationships between 20 climate variables and 39 ecosystems across the southwestern USA. We sought to understand the magnitude of relationships between variation in vegetation composition and bioclimatic variables as well as the amount of ecosystem area expected to be affected by future climate changes.

Methods

Bioclimatic variables best explaining the plant species composition of each ecosystem were identified. The strength of relationships between beta turnover and bioclimate gradients was calculated, the spatial concordance of ecosystem and bioclimate configurations was shown, and the area of suitable climate remaining within the boundaries of contemporary ecosystems under future climate projections was measured.

Results

Across the southwestern USA, four climate variables account for most of the climate related variation in vegetation composition. Twelve ecosystems are highly sensitive to climate change. By 2070, two ecosystems lose about 4000 (15 %) and 7000 (31 %) km2 of suitable climate area within their current boundaries (the Western Great Plains Sandhill Steppe and Sonora-Mojave Creosotebush-White Bursage Desert Scrub ecosystems, respectively). The climatic areas of riparian ecosystems are expected to be reduced by half.

Conclusions

Results provide specific climate and vegetation parameters for anticipating how, where and when ecosystem vegetation transforms with climate change. Projecting the loss of suitable climate for the vegetation composition of ecosystems is important for assessing ecosystem threats from climate change and for setting priorities for ecosystem conservation and restoration across the southwestern USA.
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12.

Context

Encroachment of woody vegetation represents a significant global threat to biodiversity in grasslands, but practices used to reverse encroachment are rarely evaluated comprehensively. Several factors may drive encroachment, such as land use history, alteration of disturbance regimes, and local environment, but their relative importance is poorly understood. Another complicating factor is that encroachment may proceed via positive feedbacks that result in thresholds, beyond which its reversal is difficult.

Objectives

We ask what impact reintroducing frequent fire has on encroachment relative to the influences of landscape context and historical vegetation. We investigate whether woody cover frequency distributions suggest that feedbacks reinforce encroachment after a threshold of woody cover is surpassed.

Methods

We analyze aerial photos in glade grasslands in Missouri, USA, to assess encroachment patterns over a 75-year period. Fire was excluded from this landscape for the first 45 years, and then reintroduced at varying frequencies in the last 30 years.

Results

Woody vegetation cover increased sevenfold from 1939 to 2014 overall. After the reintroduction of prescribed fire, woody cover stayed approximately constant in burned glades, but continued increasing in unburned glades. Woody cover followed bimodal frequency distributions in burned areas. Fire-tolerant vegetation tended to encroach near historically wooded areas, while fire-sensitive vegetation responded more to fire history.

Conclusions

Altered disturbance regimes, in addition to numerous recognized drivers, can cause ecosystem state changes associated with losses to biodiversity. Conducting management early in the encroachment process and restoring grasslands at broad landscape scales may help counteract local feedbacks that promote encroachment.
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13.

Context

Understanding how rare species are distributed can be difficult due to heterogeneity between landscape units. Lack of statistical replication of landscapes can make it difficult to carry out testing. Model systems may be a solution.

Objectives

We test whether lichen thalli along the trunk of a tree are analogous to habitat patches in a kilometers-extent landscape and hence can function as a model system. This model system allows for increased statistical power. We use this system to test whether landscapes with rare species are different from those without.

Methods

We sampled macrolichen diversity along the trunk of 24 balsam fir trees in a stand on the Avalon Peninsula, Newfoundland, Canada, along with microclimate variables. We analysed difference in pattern by aspect and along the gradient of 1 m up the trunk as well as between trees containing the rare Erioderma pedicellatum and those without.

Results

We found no difference in total patch richness or abundance between the micro-landscapes. We found significantly consistent patterns in lichen patches along the trunk. These patterns were similar on the trees with the rare species. Lichen species richness did not differ between trees containing the rare species versus those that did not.

Conclusions

Lichen patch pattern is statistically similar between trees and as such, these can be considered as replicate landscape units. Thus, landscape ecologists can use micro-landscapes as model systems to conduct observational and manipulative experiments to test questions about spatial pattern and process, such as those concerning distribution of rare species.
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14.

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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15.

Context

Interactions among disturbances, climate, and vegetation influence landscape patterns and ecosystem processes. Climate changes, exotic invasions, beetle outbreaks, altered fire regimes, and human activities may interact to produce landscapes that appear and function beyond historical analogs.

Objectives

We used the mechanistic ecosystem-fire process model FireBGCv2 to model interactions of wildland fire, mountain pine beetle (Dendroctonus ponderosae), and white pine blister rust (Cronartium ribicola) under current and future climates, across three diverse study areas.

Methods

We assessed changes in tree basal area as a measure of landscape response over a 300-year simulation period for the Crown of the Continent in north-central Montana, East Fork of the Bitterroot River in western Montana, and Yellowstone Central Plateau in western Wyoming, USA.

Results

Interacting disturbances reduced overall basal area via increased tree mortality of host species. Wildfire decreased basal area more than beetles or rust, and disturbance interactions modeled under future climate significantly altered landscape basal area as compared with no-disturbance and current climate scenarios. Responses varied among landscapes depending on species composition, sensitivity to fire, and pathogen and beetle suitability and susceptibility.

Conclusions

Understanding disturbance interactions is critical for managing landscapes because forest responses to wildfires, pathogens, and beetle attacks may offset or exacerbate climate influences, with consequences for wildlife, carbon, and biodiversity.
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16.

Context

Competitive interactions potentially play an important role in structuring bird communities. It is unclear how differences in functional traits influence the niche dimensions of highly mobile waterbird species, particularly when they co-exist in spatiotemporally heterogeneous communities.

Objectives

We investigated the inter-relationships between waterbird trait groupings (movement, dietary and foraging habitat) and environmental variable groupings (rainfall, land cover, vegetation structure and water quality). Specifically, we tested whether the scale of environmental variables filtered movement traits and whether these traits operated in conjunction with dietary and foraging habitat traits to form distinct ecological niches in waterbirds.

Methods

We conducted waterbird and environmental variable surveys in 60 sites, sampled seven times each at bimonthly intervals, in KwaZulu-Natal, South Africa. Trait-environment relationships were tested using a combination of RLQ and fourth-corner analyses.

Results

Several significant trait-environment relationships emerged in bivariate correlations and multivariate ordination space. Movement traits correlated with the scale of environmental variables; migrant and nomadic species responded to broad scale environmental variables. Vegetation structure and land cover were particularly important in explaining the abundance of species foraging in emergent vegetation. Three groups emerged along a gradient in multivariate ordination space providing evidence for ecological niche separation of waterbirds with different movement traits.

Conclusions

Our findings suggest that the scale of landscape resources can act as a filter of movement traits, and that in conjunction with dietary and foraging traits, waterbirds with different movement traits occupy distinct ecological niches.
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17.

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.
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18.

Context

Spatial variation in abundance is influenced by local- and landscape-level environmental variables, but modeling landscape effects is challenging because the spatial scales of the relationships are unknown. Current approaches involve buffering survey locations with polygons of various sizes and using model selection to identify the best scale. The buffering approach does not acknowledge that the influence of surrounding landscape features should diminish with distance, and it does not yield an estimate of the unknown scale parameters.

Objectives

The purpose of this paper is to present an approach that allows for statistical inference about the scales at which landscape variables affect abundance.

Methods

Our method uses smoothing kernels to average landscape variables around focal sites and uses maximum likelihood to estimate the scale parameters of the kernels and the effects of the smoothed variables on abundance. We assessed model performance using a simulation study and an avian point count dataset.

Results

The simulation study demonstrated that estimators are unbiased and produce correct confidence interval coverage except in the rare case in which there is little spatial autocorrelation in the landscape variable. Canada warbler abundance was more highly correlated with site-level measures of NDVI than landscape-level NDVI, but the reverse was true for elevation. Canada warbler abundance was highest when elevation in the surrounding landscape, defined by an estimated Gaussian kernel, was between 1300 and 1400 m.

Conclusions

Our method provides a rigorous way of formally estimating the scales at which landscape variables affect abundance, and it can be embedded within most classes of statistical models.
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19.

Context

Habitat loss and habitat fragmentation negatively affect amphibian populations. Roads impact amphibian species through barrier effects and traffic mortality. The landscape variable ‘accessible habitat’ considers the combined effects of habitat loss and roads on populations.

Objectives

The aim was to test whether accessible habitat was a better predictor of amphibian species richness than separate measures of road effects and habitat loss. I assessed how accessible habitat and local habitat variables determine species richness and community composition.

Methods

Frog and tadpole surveys were conducted at 52 wetlands in a peri-urban area of eastern Australia. Accessible habitat was delineated using a highway. Regressions were used to examine relationships between species richness and eleven landscape and local habitat variables. Redundancy analysis was used to examine relationships between community composition and accessible habitat and local habitat variables.

Results

Best-ranked models of species richness included both landscape and local habitat variables. There were positive relationships between species richness and accessible habitat and distance to the highway, and uncertain relationships with proportion cover of native vegetation and road density. There were negative relationships between species richness and concreted wetlands and wetland electrical conductivity. Four species were positively associated with accessible habitat, whereas all species were negatively associated with wetland type.

Conclusions

Barrier effects caused by the highway and habitat loss have negatively affected the amphibian community. Local habitat variables had strong relationships with species richness and community composition, highlighting the importance of both availability and quality of habitat for amphibian conservation near major roads.
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20.

Context

North American grassland songbird populations have declined significantly due to habitat loss and fragmentation. Understanding the influence of the surrounding landscape on prairie fragment occupancy is vital for predicting the fate of grassland birds in these heavily altered landscapes.

Objectives

We examined the relative importance of local and landscape variables on grassland bird occupancy of prairie fragments using a focal-patch study. We also investigated the spatial scale at which landscape variables were most influential.

Methods

We surveyed birds on 29 unplowed prairie fragments in western Minnesota and eastern North and South Dakota. We quantified local habitat on the fragment using vegetation surveys and aerial photographs and the landscape surrounding the fragment out to 4 km using aerial photographs. We analyzed occupancy using multi-model approaches applied to multiple logistic regression.

Results

Of 38 species encountered, nine were neither too rare nor too abundant to be analyzed. Predictors of patch occupancy were unique for each bird species, yet general patterns emerged. For eight species, landscape variables were more important than local variables. Mostly, those landscape variables measured configuration (e.g., edge density) and not composition (e.g., percent cover of a particular matrix element). Landscape effects were mostly from variables measured at the greatest extents from the prairie fragment.

Conclusions

Using a focal-patch study design we demonstrated the importance of the surrounding landscape, often out to 4 km from the fragment edge, on prairie occupancy by grassland birds. Effective management of grassland songbirds will require attention to the landscape context of prairie fragments.
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