Ashley A. Coble
University of New Hampshire
Network
Latest external collaboration on country level. Dive into details by clicking on the dots.
Publication
Featured researches published by Ashley A. Coble.
Global Biogeochemical Cycles | 2016
Adam S. Wymore; Ashley A. Coble; Bianca Rodríguez-Cardona; William H. McDowell
Considering recent increases in anthropogenic N loading, it is essential to identify the controls on N removal and retention in aquatic ecosystems because the fate of N has consequences for water quality in streams and downstream ecosystems. Biological uptake of nitrate (NO3−) is a major pathway by which N is removed from these ecosystems. Here we used data from the second Lotic Intersite Nitrogen eXperiment (LINX II) in a multivariate analysis to identify the primary drivers of variation in NO3− uptake velocity among biomes. Across 69 study watersheds in North America, dissolved organic carbon:NO3− ratios and photosynthetically active radiation were identified as the two most important predictor variables in explaining NO3− uptake velocity. However, within a specific biome the predictor variables of NO3− uptake velocity varied and included various physical, chemical, and biological attributes. Our analysis demonstrates the broad control of elemental stoichiometry on NO3− uptake velocity as well as the importance of biome-specific predictors. Understanding this spatial variation has important implications for biome-specific watershed management and the downstream export of NO3−, as well as for development of spatially explicit global models that describe N dynamics in streams and rivers.
Journal of Geophysical Research | 2016
Ashley A. Coble; Amy Marcarelli; Evan S. Kane; David Toczydlowski; Robert Stottlemyer
Dissolved organic matter (DOM) composition may be an important determinant of its fate in freshwaters, but little is known about temporal variability in DOM composition and the biodegradability of DOM in northern temperate watersheds. We measured biodegradable dissolved organic carbon (BDOC) via incubation assays and DOM composition using optical indices on 11 dates in three Lake Superior tributaries. Percent BDOC (%BDOC) and BDOC concentrations were seasonally synchronous across these watersheds, despite that they vary in size by orders of magnitude (1.7 to 3400 km2). Relative to %BDOC, BDOC concentrations were more tightly constrained among sites on any given date. BDOC also varied within seasons; for example, %BDOC on two different dates in winter were among the highest (29% and 54%) and lowest (0%) values observed for each site (overall %BDOC range: 0 to 72%). DOM composition varied the most among tributaries during a summer storm event when BDOC (both as percent and concentration) was elevated but was remarkably similar among tributaries during fall, spring, and winter. Multivariate models identified humic-like and tryptophan-like fluorophores as predictors of %BDOC, but DOM composition only described 21% of the overall variation in %BDOC. Collectively, these three rivers exported ~18 Gg C yr−1 as DOC and ~2 Gg C yr−1 as BDOC, which corresponded to 9 to 17% of annual DOC exported in biodegradable form. Our results suggest much of the C exported from these northern temperate watersheds may be biodegradable within 28 days and that large pulses of labile DOM can be exported during storm events and spring snowmelt.
Journal of The American Water Resources Association | 2018
Amy Marcarelli; Ashley A. Coble; Karl M. Meingast; Evan S. Kane; Colin Brooks; Ishi Buffam; Sarah A. Green; Casey J. Huckins; David Toczydlowski; Robert Stottlemyer
Lake Superior receives inputs from approximately 2,800 tributaries that provide nutrients and dissolved organic matter (DOM) to the nearshore zone of this oligotrophic lake. Here, we review the magnitude and timing of tributary export and plume formation in Lake Superior, how these patterns and interactions may shift with global change, and how emerging technologies can be used to better characterize tributary–lake linkages. Peak tributary export occurs during snowmelt-driven spring freshets, with additional pulses during raindriven storms. Instream processing and transformation of nitrogen, phosphorus, and dissolved organic carbon (DOC) can be rapid but varies seasonally in magnitude. Tributary plumes with elevated DOC concentration, higher turbidity, and distinct DOM character can be detected in the nearshore during times of high runoff, but plumes can be quickly transported and diluted by in-lake currents and mixing. Understanding the variability in size and load of these tributary plumes, how they are transported within the lake, and how long they persist may be best addressed with environmental sensors and remote sensing using autonomous and unmanned vehicles. The connections between Lake Superior and its tributaries are vulnerable to climate change, and understanding and predicting future changes to these valuable freshwater resources will require a nuanced and detailed consideration of tributary inputs and interactions in time and space.
Journal of Great Lakes Research | 2015
Ashley A. Coble; Amy Marcarelli; Evan S. Kane
Biogeochemistry | 2016
Ashley A. Coble; Amy Marcarelli; Evan S. Kane; Casey J. Huckins
Journal of Geophysical Research | 2018
Ashley A. Coble; Adam S. Wymore; Michelle D. Shattuck; Jody D. Potter; William H. McDowell
Biogeochemistry | 2018
Sujay S. Kaushal; Arthur J. Gold; Susana Bernal; Tammy A. Newcomer Johnson; Kelly Addy; Amy J. Burgin; Douglas A. Burns; Ashley A. Coble; Eran Hood; Yuehan Lu; Paul M. Mayer; Elizabeth C. Minor; Andrew W. Schroth; Philippe Vidon; Henry F. Wilson; Marguerite A. Xenopoulos; Thomas R. Doody; Joseph G. Galella; Phillip Goodling; Katherine Haviland; Shahan Haq; Barret M. Wessel; Kelsey L. Wood; Norbert A. Jaworski; Kenneth T. Belt
Archive | 2017
Ashley A. Coble; Amy Marcarelli; Evan S. Kane; Casey J. Huckins
Journal of Geophysical Research | 2016
Ashley A. Coble; Amy Marcarelli; Evan S. Kane; David Toczydlowski; Robert Stottlemyer
Global Biogeochemical Cycles | 2016
Adam S. Wymore; Ashley A. Coble; Bianca Rodríguez-Cardona; William H. McDowell