1) Urbanization may lead to changes in local richness (alpha diversity) or in community composition (beta diversity), although the direction of change can be challenging to predict.
For instance, introduced species may offset the loss of native specialist taxa, leading to no change in alpha diversity in urban areas, but decreased beta diversity (i.e., more homogenous community structure). Alternatively, because urban areas can have low connectivity and high environmental heterogeneity between sites, they may support distinct communities from one another over small geographic distances.
2) Wetlands and ponds provide critical ecosystem services and support diverse communities, making them important systems in which to understand consequences of urbanization. To determine how urban development shapes pond community structure, we surveyed 68 ponds around Madison, Wisconsin, USA, which were classified as urban, greenspace, or rural based on surrounding land use. We evaluated the influence of local abiotic factors, presence of nonnative fishes, and landscape characteristics on alpha diversity of aquatic plants, macroinvertebrates, and vertebrates. We also analyzed whether surrounding land cover was associated with changes in community composition and/or the presence of specific taxa.
3) We found a 23% decrease in mean richness (alpha diversity) from rural to urban pond sites, and a 15% decrease in richness from rural to urban greenspace pond sites. Among landscape factors, observed pond richness was negatively correlated with adjacent developed land and mowed lawns, as well as greater distances to other waterbodies. Among pond level factors, habitat complexity was associated with increased richness, while the presence of invasive fish was associated with decreased richness.
4) Beta diversity was relatively high for all ponds due to turnover in composition between sites. Urban ponds supported more introduced species, lacked a subset of native species found in rural ponds, and had slightly higher beta diversity than greenspace and rural ponds.
5) Synthesis and Applications: Integrating ponds into connected greenspaces comprised of native vegetation (rather than mowed grass), preventing nonnative fish introductions, and promoting habitat complexity may mitigate negative effects of urbanization on aquatic richness. The high beta diversity of distinct pond communities emphasizes their importance to biodiversity support in urban environments, despite being small in size and rarely incorporated into urban conservation planning.
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Survey of pond habitats and aquatic diversity of Madison, Wisconsin from May to Aug 2019 and 2020 Data Set
1) Urbanization may lead to changes in local richness (alpha diversity) or in community composition (beta diversity), although the direction of change can be challenging to predict. For instance, introduced species may offset the loss of native specialist taxa, leading to no change in alpha diversity in urban areas, but decreased beta diversity (i.e., more homogenous community structure). Alternatively, because urban areas can have low connectivity and high environmental heterogeneity between sites, they may support distinct communities from one another over small geographic distances. 2) Wetlands and ponds provide critical ecosystem services and support diverse communities, making them important systems in which to understand consequences of urbanization. To determine how urban development shapes pond community structure, we surveyed 68 ponds around Madison, Wisconsin, USA, which were classified as urban, greenspace, or rural based on surrounding land use. We evaluated the influence of local abiotic factors, presence of nonnative fishes, and landscape characteristics on alpha diversity of aquatic plants, macroinvertebrates, and vertebrates. We also analyzed whether surrounding land cover was associated with changes in community composition and/or the presence of specific taxa. 3) We found a 23% decrease in mean richness (alpha diversity) from rural to urban pond sites, and a 15% decrease in richness from rural to urban greenspace pond sites. Among landscape factors, observed pond richness was negatively correlated with adjacent developed land and mowed lawns, as well as greater distances to other waterbodies. Among pond level factors, habitat complexity was associated with increased richness, while the presence of invasive fish was associated with decreased richness. 4) Beta diversity was relatively high for all ponds due to turnover in composition between sites. Urban ponds supported more introduced species, lacked a subset of native species found in rural ponds, and had slightly higher beta diversity than greenspace and rural ponds. 5) Synthesis and Applications: Integrating ponds into connected greenspaces comprised of native vegetation (rather than mowed grass), preventing nonnative fish introductions, and promoting habitat complexity may mitigate negative effects of urbanization on aquatic richness. The high beta diversity of distinct pond communities emphasizes their importance to biodiversity support in urban environments, despite being small in size and rarely incorporated into urban conservation planning.
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- Award ID(s):
- 2025982
- NSF-PAR ID:
- 10397281
- Publisher / Repository:
- Environmental Data Initiative
- Date Published:
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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Abstract Urbanization can influence local richness (alpha diversity) and community composition (beta diversity) in numerous ways. For instance, reduced connectivity and land cover change may lead to the loss of native specialist taxa, decreasing alpha diversity. Alternatively, if urbanization facilitates nonnative species introductions and generalist taxa, alpha diversity may remain unchanged or increase, while beta diversity could decline due to the homogenization of community structure. Wetlands and ponds provide critical ecosystem services and support diverse communities, making them important systems in which to understand the consequences of urbanization. To determine how urban development shapes pond community structure, we surveyed 68 ponds around Madison, Wisconsin, USA, which were classified as urban, greenspace, or rural based on surrounding land use. We evaluated how landscape and local pond factors were correlated with the alpha diversity of aquatic plants, macroinvertebrates, and aquatic vertebrates. We also analyzed whether surrounding land use was associated with changes in community composition and the presence of specific taxa. We found a 23% decrease in mean richness (alpha diversity) from rural to urban pond sites and a 15% decrease from rural to greenspace pond sites. Among landscape factors, adjacent developed land, mowed lawn cover, and greater distances to other waterbodies were negatively correlated with observed pond richness. Among pond level factors, habitat complexity was associated with increased richness, while nonnative fishes were associated with decreased richness. Beta diversity was relatively high for all ponds due to turnover in composition between sites. Urban ponds supported more nonnative species, lacked a subset of native species found in rural ponds, and had slightly higher beta diversity than greenspace and rural ponds. Our results suggest that integrating ponds into connected greenspaces, maintaining riparian vegetation, preventing nonnative fish introductions, and promoting habitat complexity may mitigate the negative effects of urbanization on aquatic richness. While ponds are small in size and rarely incorporated into urban conservation planning, the high beta diversity of distinct pond communities emphasizes their importance for supporting urban biodiversity.
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Abstract Global tropical forests have been modified and fragmented by commodity agroforests, leading to significant alterations in ecological communities. Nevertheless, these production landscapes offer secondary habitats that support and sustain local biodiversity. In this study, we assess community level and species‐specific responses of amphibians to land management in areca, coffee and rubber, three of the largest commodity agroforests in the Western Ghats.
A total of 106 agroforests across a 30,000‐km2landscape were surveyed for amphibians using a combination of visual and auditory encounter surveys. We used a Bayesian multi‐species occupancy modelling framework to examine patterns of species richness, beta diversity, dominance structure and individual species occupancies. The influence of biogeographic variables such as elevation and latitude as well as microhabitat availability of streams, ponds and unpaved plantation roads was tested on amphibian species occupancy.
Coffee agroforests had the highest species richness and lowest dominance when compared to areca and rubber. Beta diversity was highest in areca for within agroforest measures. Compared across agroforests, coffee had highest beta diversity with areca and rubber. Both elevation and latitude showed an overall positive association with amphibian occupancy, although species‐specific responses varied considerably.
Microhabitat availability was one of the strongest predictors of amphibian occupancy, with mean community response being positive with presence of water bodies and roads. Pond presence increased species richness per site by 34.7% (species‐specific responses in occupancy ranged from –2.7% to 327%). Stream presence alone did not change species richness but species‐specific response ranged from –59% to 273%. Presence of plantation roads also increased species richness by 21.5% (species‐specific response ranged from –82% to 656%). Being unpaved with little vehicular traffic, plantation roads seem to provide additional habitats for amphibians. Presence of all three microhabitats at a site increased species richness by 75%.
Our study highlights the importance of land management strategies that maintain diverse native canopy and freshwater bodies and other microhabitats in sustaining amphibian fauna. Market‐driven land‐use change from coffee to other agroforest types will have detrimental effects on amphibian communities and their long‐term sustainability in the Western Ghats.
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The Baltimore Ecosystem Study (BES) has established a network of long-term permanent biogeochemical study plots. These plots will provide long-term data on vegetation, soil and hydrologic processes in the key ecosystem types within the urban ecosystem. The current network of study plots includes eight forest plots, chosen to represent the range of forest conditions in the area, and four grass plots. These plots are complemented by a network of 200 less intensive study plots located across the Baltimore metropolitan area. Plots are currently instrumented with lysimeters (drainage and tension) to sample soil solution chemistry, time domain reflectometry probes to measure soil moisture, dataloggers to measure and record soil temperature and trace gas flux chambers to measure the flux of carbon dioxide, nitrous oxide and methane from soil to the atmosphere. Measurements of in situ nitrogen mineralization, nitrification and denitrification were made at approximately monthly intervals from Fall 1998 - Fall 2000. Detailed vegetation characterization (all layers) was done in summer 1998. Data from these plots has been published in Groffman et al. (2006, 2009) and Groffman and Pouyat (2009). In November of 1998 four rural, forested plots were established at Oregon Ridge Park in Baltimore County northeast of the Gwynns Falls Watershed. Oregon Ridge Park contains Pond Branch, the forested reference watershed for BES. Two of these four plots are located on the top of a slope; the other two are located midway up the slope. In June of 2010 measurements at the mid-slope sites on Pond Branch were discontinued. Monuments and equipment remain at the two plots. These plots were replaced with two lowland riparian plots; Oregon upper riparian and Oregon lower riparian. Each riparian sites has four 5 cm by 1-2.5 meter depth slotted wells laid perpendicular to the stream, four tension lysimeters at 10 cm depth, five time domain reflectometry probes, and four trace gas flux chambers in the two dominant microtopographic features of the riparian zones - high spots (hummocks) and low spots (hollows). Four urban, forested plots were established in November 1998, two at Leakin Park and two adjacent to Hillsdale Park in west Baltimore City in the Gwynns Falls. One of the plots in Hillsdale Park was abandoned in 2004 due to continued vandalism. In May 1999 two grass, lawn plots were established at McDonogh School in Baltimore County west of the city in the Gwynns Falls. One of these plots is an extremely low intensity management area (mowed once or twice a year) and one is in a low intensity management area (frequent mowing, no fertilizer or herbicide use). In 2009, the McDonogh plots were abandoned due to management changes at the school. Two grass lawn plots were established on the campus of the University of Maryland, Baltimore County (UMBC) in fall 2000. One of these plots is in a medium intensity management area (frequent mowing, moderate applications of fertilizer and herbicides) and one is in a high intensity management area (frequent mowing, high applications of fertilizer and herbicides). Literature Cited Bowden R, Steudler P, Melillo J and Aber J. 1990. Annual nitrous oxide fluxes from temperate forest soils in the northeastern United States. J. Geophys. Res.-Atmos. 95, 13997 14005. Driscoll CT, Fuller RD and Simone DM (1988) Longitudinal variations in trace metal concentrations in a northern forested ecosystem. J. Environ. Qual. 17: 101-107 Goldman, M. B., P. M. Groffman, R. V. Pouyat, M. J. McDonnell, and S. T. A. Pickett. 1995. CH4 uptake and N availability in forest soils along an urban to rural gradient. Soil Biology and Biochemistry 27:281-286. Groffman PM, Holland E, Myrold DD, Robertson GP and Zou X (1999) Denitrification. In: Robertson GP, Bledsoe CS, Coleman DC and Sollins P (Eds) Standard Soil Methods for Long Term Ecological Research. (pp 272-290). Oxford University Press, New York Groffman PM, Pouyat RV, Cadenasso ML, Zipperer WC, Szlavecz K, Yesilonis IC,. Band LE and Brush GS. 2006. Land use context and natural soil controls on plant community composition and soil nitrogen and carbon dynamics in urban and rural forests. Forest Ecology and Management 236:177-192. Groffman, P.M., C.O. Williams, R.V. Pouyat, L.E. Band and I.C. Yesilonis. 2009. Nitrate leaching and nitrous oxide flux in urban forests and grasslands. Journal of Environmental Quality 38:1848-1860. Groffman, P.M. and R.V. Pouyat. 2009. Methane uptake in urban forests and lawns. Environmental Science and Technology 43:5229-5235. DOI: 10.1021/es803720h. Holland EA, Boone R, Greenberg J, Groffman PM and Robertson GP (1999) Measurement of Soil CO2, N2O and CH4 exchange. In: Robertson GP, Bledsoe CS, Coleman DC and Sollins P (Eds) Standard Soil Methods for Long Term Ecological Research. (pp 258-271). Oxford University Press, New York Robertson GP, Wedin D, Groffman PM, Blair JM, Holland EA, Nadelhoffer KJ and. Harris D. 1999. Soil carbon and nitrogen availability: Nitrogen mineralization, nitrification and carbon turnover. In: Standard Soil Methods for Long Term Ecological Research (Robertson GP, Bledsoe CS, Coleman DC and Sollins P (Eds) Standard Soil Methods for Long Term Ecological Research. (pp 258-271). Oxford University Press, New York Savva, Y., K. Szlavecz, R. V. Pouyat, P. M. Groffman, and G. Heisler. 2010. Effects of land use and vegetation cover on soil temperature in an urban ecosystem. Soil Science Society of America Journal 74:469-480."more » « less
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