Global phosphorus retention by river damming |
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Authors: | Taylor Maavara Christopher T. Parsons Christine Ridenour Severin Stojanovic Hans H. Dürr Helen R. Powley Philippe Van Cappellen |
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Affiliation: | aEcohydrology Research Group, Water Institute, University of Waterloo, Waterloo, ON, Canada, N2L 3G1;;bDepartment of Earth and Environmental Sciences, University of Waterloo, Waterloo, ON, Canada, N2L 3G1 |
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Abstract: | More than 70,000 large dams have been built worldwide. With growing water stress and demand for energy, this number will continue to increase in the foreseeable future. Damming greatly modifies the ecological functioning of river systems. In particular, dam reservoirs sequester nutrient elements and, hence, reduce downstream transfer of nutrients to floodplains, lakes, wetlands, and coastal marine environments. Here, we quantify the global impact of dams on the riverine fluxes and speciation of the limiting nutrient phosphorus (P), using a mechanistic modeling approach that accounts for the in-reservoir biogeochemical transformations of P. According to the model calculations, the mass of total P (TP) trapped in reservoirs nearly doubled between 1970 and 2000, reaching 42 Gmol y−1, or 12% of the global river TP load in 2000. Because of the current surge in dam building, we project that by 2030, about 17% of the global river TP load will be sequestered in reservoir sediments. The largest projected increases in TP and reactive P (RP) retention by damming will take place in Asia and South America, especially in the Yangtze, Mekong, and Amazon drainage basins. Despite the large P retention capacity of reservoirs, the export of RP from watersheds will continue to grow unless additional measures are taken to curb anthropogenic P emissions.The systematic damming of rivers began with the onset of the Industrial Revolution and peaked in the period from 1950 to 1980 (1, 2). After slowing down during the 1990s, the pace of dam building has recently risen again sharply (3). As a consequence, the number of hydroelectric dams with generating capacity >1 MW is expected to nearly double over the next two decades (2). The current surge in dam construction will increase the proportion of rivers that are moderately to severely impacted by flow regulation from about 50% at the end of the 20th century to over 90% by 2030 (3). Homogenization of river flow regimes resulting from damming is a growing, worldwide phenomenon and has been invoked as one of the reasons for the decline in freshwater biodiversity (4).Another major global driver of environmental change of river systems is enrichment by anthropogenic nutrients, in particular phosphorus (P) (5, 6). Fertilizer use, soil erosion, and the discharge of wastewater have more than doubled the global P load to watersheds compared with the inferred natural baseline (7–10). Because P limits or colimits primary productivity of many aquatic ecosystems, increased river fluxes of P have been identified as a main cause of eutrophication of surface water bodies, including lakes and coastal marine environments (6, 11, 12). River damming and P enrichment are interacting anthropogenic forcings, because sediments accumulating in reservoirs trap P and, thus, reduce the downstream transfer of P along the river continuum (13–15). This raises the question to what extent P retention by dams may offset anthropogenic P enrichment of rivers.The number of published studies from which P retention efficiencies in dam reservoirs can be obtained is small: an extensive literature search only yields useable data for 155 reservoirs (Dataset S1), that is, less than 0.2% of the ∼75,000 dam reservoirs larger than 0.1 km2 (16). The existing data nonetheless clearly show that even a single dam can significantly alter the flow of P along a river. For example, dam-impounded Lake Kariba (Zambezi River), Lake Diefenbaker (South Saskatchewan River), and Lac d’Orient (Seine River) sequester ∼87%, 94%, and 71% of their total P inflows, respectively (17–19). For the 1 million km2 Lake Winnipeg watershed, 28 reservoirs and lakes accumulate over 90% of the total P load (18). The global retention of P by dams, however, remains poorly constrained (20, 21). Previous estimations have simply applied a correction factor to river P loads to represent retention by dams (22–24). This approach does not distinguish between the various chemical forms of P, nor does it account for differences in reservoir hydraulics or provide information about uncertainties on retention estimates.Here, we follow a mass balance modeling approach developed previously to calculate the global retention of nutrient silicon by dams (25). The mass balance model represents the key biogeochemical processes controlling P cycling in reservoirs (). The model separates total P (TP) into the following pools: total dissolved P (TDP); particulate organic P (POP); exchangeable P (EP); and unreactive particulate P (UPP). UPP consists mostly of crystalline phosphate minerals that are inert on reservoir-relevant timescales (≤100 y); TDP comprises inorganic and organic forms of P, whereas EP includes orthophosphate and organic P molecules sorbed to or coprecipitated with oxides, clay minerals, and organic matter. Reactive P (RP) is defined as the sum of TDP, EP, and POP; RP represents the potentially bioavailable fraction of TP.Open in a separate windowMass balance model used to estimate retention of P in reservoirs. Fin,i is the influx of the ith P pool into the reservoir, Fi,out is the corresponding efflux out of the reservoir, F12 represents P fixation by primary productivity, F21 represents mineralization of POP, F13 and F31 are the sorption and desorption rates of dissolved P, and Fi,bur is the permanent burial flux of the ith particulate P pool in the reservoir’s sediments.Global predictive relationships for the retention of TP and RP in reservoirs are derived from a Monte Carlo analysis of the model, which accounts for parameter variability within expected ranges. The relationships are applied to the reservoirs in the Global Reservoirs and Dams (GRanD) database (16), to estimate the sequestration of TP and RP by dams in each of the major river basins of the world. Throughout, P retention efficiencies in a reservoir are defined as[1]where RX is the fractional retention of TP or RP, and Xin and Xout are the input and output fluxes of TP or RP in units of mass per unit time. Annual amounts of TP and RP retained in a reservoir are then calculated by multiplying the RX values with the corresponding TP and RP input fluxes from the dam’s upstream watershed. The latter are obtained from the Global-NEWS-HD model, which estimates emission yields for dissolved inorganic P (DIP), dissolved organic P (DOP), and particulate P (PP), of which 20% is assumed to be reactive (7, 26). The Global-NEWS-HD yield estimates are based on the biogeophysical characteristics, population density, socioeconomic status, land use, and climatic conditions within the drainage basin (20).Because the biogeochemical mass balance model explicitly represents the in-reservoir transformations between the different forms of P, it allows us to estimate how dams modify both the total and reactive fluxes of P along rivers. With the proposed approach, we reconstruct global TP and RP retentions by dams in 1970 and 2000 and make projections for 2030. For the latter, we apply the nutrient P loading trends developed for the four Millennium Ecosystem Assessment (MEA) scenarios (27). The results illustrate the evolving role of damming in the continental P cycle and, in particular, the ongoing geographical shift in P retention resulting from the current boom in dam construction. |
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Keywords: | phosphorus river damming biogeochemical cycles nutrient retention eutrophication |
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