A Review on Landscape Factors for Biodiversity Performance Enhancement in Urban Parks
Abstract
:1. Introduction
- To review landscape factors that have been shown to impact biodiversity performance in urban parks.
- To provide scientific evidence for assessing urban parks from the perspective of biodiversity conservation during design and management periods.
2. Review Methods
2.1. Literature Search
2.2. Reference Screening
2.3. Organizing the Key References
3. Biodiversity in Urban Parks
3.1. Common Methods to Assess Biodiversity in Urban Parks
3.2. Relations Between Landscape Factors and Biodiversity
3.2.1. Shape and Size of Urban Parks
Category | Landscape Factors | Summary of Findings | Study Sites | References |
---|---|---|---|---|
Shape and size | Size of the urban park (+) * | Park area best predicted breeding bird richness (38.8% variance explained), with smaller parks showing food limitation effects. | A total of 54 urban parks in the city of Oulu in northern Finland and their surrounding 9 ha areas. | [33] |
Urban park area significantly predicts species diversity and occupancy probabilities, demonstrating critical habitat size effects. | Review articles | [47] | ||
Higher nest predation in small patches predicts greater open-nester abundance in large, magpie-free habitats, highlighting patch-size effects. | A total of 48 woodland patches within a 15 km2 farmland area around the village of Kraghede, Denmark. | [52] | ||
Urban green space size positively correlates with insectivore guild richness seasonally, driven by food resource availability. | A 250 m buffer around 18 urban green spaces in Dehradun city, Uttarakhand, India. | [36] | ||
Patch area predominantly predicts bird functional group abundances and species richness, demonstrating area-sensitive responses. | A total of 44 small forest patches (0.5–20.0 ha) embedded in an urbanized landscape in Seoul. | [49] | ||
Small green spaces’ edge-dominated, resource-poor conditions drive avian population decline through exposure risks and reduced carrying capacity. | A total of 12 green projects in Boston, USA. | [59] | ||
Urban park area and perimeter positively correlate with plant richness, peaking at 30 ha. | A total of 33 typical urban parks in Changchun, China. | [46] | ||
Woodland size emerged as the primary driver of avian species richness, demonstrating area-dependent biodiversity thresholds. | A total of 32 woodlands in Springfield, MA, USA. | [48] | ||
Urban park size positively predicts herpetofauna richness, with larger areas disproportionately supporting rare species. | A total of 10 urban areas and 165 urban parks in the eastern United States. | [45] | ||
The shape of park (−) * | Park shape complexity nonlinearly reduces plant richness, demonstrating edge-driven diversity constraints. | A total of 33 typical urban parks in Changchun, China. | [46] | |
Compact-shaped woodlands in xeric conditions drove avian diversity metrics, not species counts, revealing habitat-metric dependencies. | A total of 32 woodlands in Springfield, MA, USA. | [48] | ||
Park geometries minimizing edge-to-core ratios enhance biodiversity through micro-climate stabilization and pathogen resistance, prioritizing compact spatial designs. | A large-scale replicated habitat corridor experiment located at the Savannah River Site, a National Environmental Research Park south of New Ellenton, South Carolina, USA. | [60] |
3.2.2. Vegetation Composition in Urban Parks
Category | Landscape Factors | Summary of Findings | Study Sites | References |
---|---|---|---|---|
Vegetation composition | Vegetation coverage (+) * | Larger green spaces in parks significantly affect bird presence positively. | A total of 26 urban parks within Beijing city, China. | [19] |
Nest predation rates are similar or higher in artificial habitats rather than in habitats with a high vegetation coverage rate. | A total of 100 randomly selected urban 1 km squares in a British urban area. | [42] | ||
Tree coverage (+) * | Tree coverage is positively correlated with bird species richness due to increased resource availability and tree diversity, which enhance food and micro-habitat diversity. | Four kinds of urban green space in Local Government Areas (LGAs) of south-east Queensland, Australia. | [64] | |
Increased forest cover in parks is linked to higher amphibian species richness. | A total of 10 urban areas and 165 urban parks in the eastern United States. | [45] | ||
Increasing tree cover in the urban matrix is the most promising and efficient measure to enhance bird species richness and diversity. | A total of 96 sample sites (urban green space) in three cities in Swiss. | [65] | ||
Shrub coverage (+) * | Shrub cover is especially important, with areas containing dense shrubs attracting more birds. | Four small community parks in Beijing: Nanguan Park, Dongdan Park, Shuangxiu Park, and Madian Park in China. | [21] | |
Well-developed shrub layers promote higher bird species richness and diversity. | A total of 32 woodlands in Springfield, MA, USA. | [48] | ||
Natural, unmanaged shrubbed woodland patches are preferred by small mammals. | A total of 11 cells in Milan, 18 in Florence, and 12 in Rome in Italy | [67] | ||
Grass coverage (−) * | Over-managed lawns reduce the biodiversity value of park grasslands compared with that of meadows. | Review article | [68] | |
Newly established habitat patches where human activities take place affect the distribution of ground-feeding species. | Seoul and surrounding cities in Gyeonggi Province, South Korea. | [49] | ||
Coverage of habitat with two or more layers (+) * | Vertical vegetation diversity has a slight positive impact on bird species richness during breeding. | A 250 m buffer around 18 urban green spaces in Dehradun city, Uttarakhand, India. | [36] | |
More vegetation layers and vertical structures attract a wider range of bird species. | Four small community parks in Beijing: Nanguan Park, Dongdan Park, Shuangxiu Park, and Madian Park in China | [21] | ||
More complex vegetation structures increase bird species richness and abundance, particularly for migrants and ground nesters. | Seoul and surrounding cities in Gyeonggi Province, South Korea. | [49] | ||
Vegetation diversity (+) * | Complex vegetation structures are linked to higher bird diversity. | A total of 12 shrines and temples, 9 urban parks, and 3 historic parks from among the green spaces in Bunkyo ward, Tokyo, Japan. | [69] | |
Greater plant diversity, particularly trees and flowers, boosts bee populations and diversity. | A total of 16 sites (areas from 200 m2 to 8.0 km2) in urban and suburban green spaces (parks, preserves, and other natural areas) in the Fox Cities region of northeastern Wisconsin, USA. | [43] | ||
Enhancing vegetation diversity and structure in urban areas supports greater bird species richness. | A total of 100 randomly selected urban 1 km squares in British urban. | [42] | ||
Larger urban green spaces with rich plant communities increase bird richness via structural diversity. | A 250 m buffer around 18 urban green spaces in Dehradun city, Uttarakhand, India. | [36] | ||
Invertebrates benefit from rough vegetation and floral diversity, and bird species richness responds positively to increased woody plant species. | Review article | [15] | ||
Omnivorous and tree-nesting birds thrive with increased plant species richness, both herbaceous and woody. | A total of 26 urban parks within Beijing city, China. | [19] | ||
A higher diversity of tree species enhances the capacity of small urban green spaces (SPUGSs) to harbor diverse bird populations. | A total of 28 SPUGS in an urban area, Tio Claro, Brazil. | [70] | ||
Diverse vegetation provides food and shelter for different bird species. | Four small community parks in Beijing: Nanguan Park, Dongdan Park, Shuangxiu Park, and Madian Park in China. | [21] |
3.2.3. Artificial Components in Urban Parks
Category | Landscape Factors | Summary of Findings | Study Sites | References |
---|---|---|---|---|
Artificial components | Impermeable surface (−) * | An impervious surface cover negatively impacts bird and bat populations across various metrics. | Three types of urban green spaces in south-east Melbourne, including (1) golf courses, (2) public parks, and (3) residential neighborhoods. | [32] |
An impervious surfaces reduce overall bird richness and the richness of functional groups. | Campo Grande municipality (20°27′53″ S; 54°36′58″ W), central-west Brazil | [7] | ||
Landscapes with less impervious surface areas tend to have greater biodiversity than urbanized areas with limited green spaces. | A total of 16 sites (areas from 200 m2 to 8.0 km2) in urban and suburban green spaces (parks, preserves, and other natural areas) in the Fox Cities region of northeastern Wisconsin, USA. | [43] | ||
More impervious surfaces in urban parks are linked to lower species richness. | A total of 10 urban areas and 165 urban parks in the eastern USA. | [45] | ||
An impervious surface is one of the main drivers that reduce species abundance and richness through direct changes in resources and habitats. | Review article | [73] | ||
Water body (+) * | Various wetland types in urban parks increase amphibian species richness. | A total of 10 urban areas and 165 urban parks in the eastern USA. | [45] | |
Higher water surface ratios are positively correlated with greater bird species richness. | Four small community parks in Beijing: Nanguan Park, Dongdan Park, Shuangxiu Park, and Madian Park in China. | [21] | ||
Ground-nesting and other bird species are significantly more likely to be found near water, emphasizing the importance of water for bird diversity. | In four parks in Vancouver and Burnaby, Canada. | [35] | ||
Pathway (−) * | Higher pedestrian traffic is associated with lower species richness and reduced habitat occupation for 16 species during breeding seasons. | In three large parks of Madrid: Moro (18 ha), Oeste (98 ha), and Retiro (110 ha), in Spain. | [76] | |
Bird species diversity and abundance decrease near trails. | A total of 32 woodlands in Springfield, MA, USA. | [48] | ||
Artificial surface edge (−) * | The shape of the curving trails limits the variety and number of birds. | A total of 32 woodlands in Springfield, MA, USA | [48] |
3.2.4. Landscape Patterns in Urban Parks
Category | Landscape Factors | Summary of Findings | Study Sites | References |
---|---|---|---|---|
Landscape pattern | Habitat patch edge (+) * | Habitat fragmentation drives predation surges via edge-mediated effects and matrix-derived predator incursions. | A total of 48 woodland patches within a 15 km2 farmland area around the village of Kraghede, Denmark. | [52]. |
Edge-mediated abiotic fluxes drive micro-climate fluctuations in fragmented habitats, demonstrating edge-driven ecological instability. | Review article | [54] | ||
Edge effects amplify predation in small habitat islands through edge-dominated configurations and matrix-forced predator spillover. | A total of 10 forest tracts in central Maryland (3.8–905 ha) and one in southeastern Tennessee, USA. | [84] | ||
Aggregation of the habitat patch (+) * | Habitat aggregation enhances propagule establishment in suitable patches yet only partially offsets habitat deficits through spatial configuration. | Review article | [80] | |
High-quality habitat aggregation enhances metapopulation stability in fragmented landscapes by sustaining source habitats where quality surpasses size/isolation effects. | All the potential habitat patches in central southern England. | [78] | ||
Habitat aggregation moderately enhances butterfly (less so plant) diversity in fragmented grasslands, though area effects dominate. | A total of 62 calcareous grasslands were selected as study sites in ‘Fränkische Schweiz’, located in the vicinity of the town Bayreuth in southern Germany. | [79] | ||
Multi-scale habitat aggregation enhances avian biodiversity through broadleaf–conifer gradients and connectivity, mitigating fragmentation while optimizing structural habitat quality. | A total of 126 1 ha plots in the forest landscape of the Black Forest, southwest Germany. | [85] |
3.2.5. Surrounding Land Use of Urban Parks
Category | Landscape Factors | Summary of Findings | Study Sites | References |
---|---|---|---|---|
Surrounding land use | Building (−) | Adjacent building density and proximity significantly suppress avian species richness (S) and diversity (H′) through edge-driven disturbance. | A total of 32 woodlands in Springfield, MA, USA. | [48] |
Avian attraction to urban parks elevates collision risks from adjacent buildings through edge-mediated structural hazards. | Bryant Park located in the Midtown neighborhood of Manhattan, NJ, USA. | [86] | ||
Building density inversely predicts avian species richness and densities, demonstrating urban infrastructure’s biodiversity suppression. | A total of 100 randomly selected urban 1 km squares in British urban. | [42] | ||
Traffic lines (−) | Road zones exhibited 40% reduced male productivity per hectare due to noise-driven habitat degradation suppressing reproductive success. | A nature reserve, ‘Bolgerijen-Autena’, is located in the center of the Netherlands. | [89] | |
Road density suppresses spotted flycatcher distribution, while close park proximity enhances it, revealing urban spatial thresholds. | A total of 54 urban parks in the city of Oulu in northern Finland and their surrounding 9 ha areas. | [33] | ||
Green space (+) | Contiguous urban green spaces enhance bee communities through area-dependent habitat benefits. | A total of 16 sites (areas from 200 m2 to 8.0 km2) in urban and suburban green spaces (parks, preserves, and other natural areas) in the Fox Cities region of northeastern Wisconsin, USA. | [43] | |
Proximal green spaces (≤200 m) enhance avian richness by breeding resource provisioning around urban parks. | A total of 26 urban parks within Beijing city, China. | [19] | ||
Landscape metrics (500 m forest cover and park area) enhance avian occurrence predictions by amplifying local habitat feature efficacy. | Four parks in Vancouver and Burnaby, Canada. | [35] | ||
Park area and vegetation complexity drive avian richness, with nest boxes offsetting small-park (<0.75 ha) limitations under urban matrix pressures. | In the city of Oulu in northern Finland. | [33] | ||
Connected parks and forested habitats sustain greater unique species richness than isolated counterparts through enhanced habitat connectivity. | A total of 10 parks in the urban area of the city of Rio de Janeiro, Brazil. | [71] |
4. Additional Landscape Strategies to Enhance Biodiversity of Urban Parks
4.1. Enhance the Networking of the Urban Green Spaces and Parks
4.2. Preserve Old Trees in Urban Park
4.3. Enhance Vertical Structure Complexity of Habitat Patches
4.4. Enhance the Habitat Spatial Arrangement
5. Challenges and Future Directions
6. Conclusions
Author Contributions
Funding
Institutional Review Board Statement
Informed Consent Statement
Data Availability Statement
Acknowledgments
Conflicts of Interest
Abbreviations
SDGs | Sustainable Development Goals |
FRAC | Fractal Dimension Index |
PARA | Mean Perimeter Area Ratio |
PAFRAC | Perimeter-Area Fractal Dimension |
CV | coefficient of variation |
FHD | foliage height diversity |
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Ye, Q.; Wang, X.; Liang, L.; Qiu, J.-W.; Tsim, S.-T. A Review on Landscape Factors for Biodiversity Performance Enhancement in Urban Parks. Diversity 2025, 17, 262. https://doi.org/10.3390/d17040262
Ye Q, Wang X, Liang L, Qiu J-W, Tsim S-T. A Review on Landscape Factors for Biodiversity Performance Enhancement in Urban Parks. Diversity. 2025; 17(4):262. https://doi.org/10.3390/d17040262
Chicago/Turabian StyleYe, Qiting, Xiuzhi Wang, Lingzi Liang, Jian-Wen Qiu, and Siu-Tai Tsim. 2025. "A Review on Landscape Factors for Biodiversity Performance Enhancement in Urban Parks" Diversity 17, no. 4: 262. https://doi.org/10.3390/d17040262
APA StyleYe, Q., Wang, X., Liang, L., Qiu, J.-W., & Tsim, S.-T. (2025). A Review on Landscape Factors for Biodiversity Performance Enhancement in Urban Parks. Diversity, 17(4), 262. https://doi.org/10.3390/d17040262