Your browser doesn't support javascript.
loading
Shifts in the composition of nitrogen deposition in the conterminous United States are discernable in stream chemistry.
Lassiter, Meredith G; Lin, Jiajia; Compton, Jana E; Phelan, Jennifer; Sabo, Robert D; Stoddard, John L; McDow, Stephen R; Greaver, Tara L.
Afiliación
  • Lassiter MG; United States Environmental Protection Agency (U.S. EPA), Office of Research and Development, Center for Public Health and Environmental Assessment, Health and Environmental Effects Assessment Division, 109 T.W. Alexander Dr. Research Triangle Park, NC 27709, United States. Electronic address: lassi
  • Lin J; Oak Ridge Institute for Science and Education, Postdoctoral Participant, Corvallis, OR 97333, United States; U.S. EPA, Office of Research and Development, Center for Public Health and Environmental Assessment, Pacific Ecological Systems Division, 200 SW 35th St., Corvallis, OR 97333, United States.
  • Compton JE; U.S. EPA, Office of Research and Development, Center for Public Health and Environmental Assessment, Pacific Ecological Systems Division, 200 SW 35th St., Corvallis, OR 97333, United States. Electronic address: compton.jana@epa.gov.
  • Phelan J; RTI International, P.O. Box 12194, 3040 Cornwallis Rd., RTP, NC 27709, United States. Electronic address: jenphelan@rti.org.
  • Sabo RD; US EPA Headquarters, Office of Research and Development, Center for Public Health and Environmental Assessment, Health and Environmental Effects Assessment Division, 1200 Penn Ave NW, Mailcode 8623-P, Washington, DC 20460, United States. Electronic address: sabo.robert@epa.gov.
  • Stoddard JL; U.S. EPA, Office of Research and Development, Center for Public Health and Environmental Assessment, Pacific Ecological Systems Division, 200 SW 35th St., Corvallis, OR 97333, United States. Electronic address: stoddard.john@epa.gov.
  • McDow SR; United States Environmental Protection Agency (U.S. EPA), Office of Research and Development, Center for Public Health and Environmental Assessment, Health and Environmental Effects Assessment Division, 109 T.W. Alexander Dr. Research Triangle Park, NC 27709, United States. Electronic address: McDow
  • Greaver TL; United States Environmental Protection Agency (U.S. EPA), Office of Research and Development, Center for Public Health and Environmental Assessment, Health and Environmental Effects Assessment Division, 109 T.W. Alexander Dr. Research Triangle Park, NC 27709, United States. Electronic address: greav
Sci Total Environ ; 881: 163409, 2023 Jul 10.
Article en En | MEDLINE | ID: mdl-37044336
ABSTRACT
Across the conterminous United States (U.S.), the composition of atmospheric nitrogen (N) deposition is changing spatially and temporally. Previously, deposition was dominated by oxidized N, but now reduced N (ammonia [NH3] + ammonium [NH4+]) is equivalent to oxidized N when deposition is averaged across the entire nation and, in some areas, reduced N dominates deposition. To evaluate if there are effects of this change on stream chemistry at the national scale, estimates of N deposition form (oxidized or reduced) from the National Atmospheric Deposition Program Total Deposition data were coupled with stream measurements from the U.S. Environmental Protection Agency (EPA) National Rivers and Streams Assessments (three stream surveys between 2000 and 2014). A recent fine-scaled N input inventory was used to identify watersheds (<1000 km2) where atmospheric deposition is the largest N source (n = 1906). Within these more atmospherically-influenced watersheds there was a clear temporal shift from a greater proportion of sites dominated by oxidized N deposition to a greater proportion of sites dominated by reduced forms of N deposition. We found a significant positive correlation between oxidized N deposition and stream NO3- concentrations, whereas the correlation between reduced N deposition and stream NO3- concentrations were significant but weaker. Sites dominated by atmospheric inputs of reduced N forms had higher stream total organic N and total N despite lower total N deposition on average. This higher stream concentration of total N is mainly driven by the higher concentration of total organic N, suggesting an interaction between elevated reduced N in deposition and living components of the ecosystem or soil organic matter dynamics. Regardless of the proportion of reduced to oxidized N forms in deposition, stream NH4+ concentrations were generally low, suggesting that N deposited in a reduced form is rapidly immobilized, nitrified and/or assimilated by watershed processes.
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Sci Total Environ Año: 2023 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Sci Total Environ Año: 2023 Tipo del documento: Article
...