Landscape Controls on Water‐Energy‐Carbon Fluxes Across Different Ecosystems during the North American Monsoon

Author(s):  
Eli R. Pérez‐Ruiz ◽  
Enrique R. Vivoni ◽  
Enrico A. Yépez ◽  
Julio C. Rodríguez ◽  
David J. Gochis ◽  
...  
Ecohydrology ◽  
2008 ◽  
Vol 1 (3) ◽  
pp. 225-238 ◽  
Author(s):  
Enrique R. Vivoni ◽  
Alex J. Rinehart ◽  
Luis A. Méndez-Barroso ◽  
Carlos A. Aragón ◽  
Gautam Bisht ◽  
...  

2015 ◽  
Vol 15 (12) ◽  
pp. 6943-6958 ◽  
Author(s):  
E. Crosbie ◽  
J.-S. Youn ◽  
B. Balch ◽  
A. Wonaschütz ◽  
T. Shingler ◽  
...  

Abstract. A 2-year data set of measured CCN (cloud condensation nuclei) concentrations at 0.2 % supersaturation is combined with aerosol size distribution and aerosol composition data to probe the effects of aerosol number concentrations, size distribution and composition on CCN patterns. Data were collected over a period of 2 years (2012–2014) in central Tucson, Arizona: a significant urban area surrounded by a sparsely populated desert. Average CCN concentrations are typically lowest in spring (233 cm−3), highest in winter (430 cm−3) and have a secondary peak during the North American monsoon season (July to September; 372 cm−3). There is significant variability outside of seasonal patterns, with extreme concentrations (1 and 99 % levels) ranging from 56 to 1945 cm−3 as measured during the winter, the season with highest variability. Modeled CCN concentrations based on fixed chemical composition achieve better closure in winter, with size and number alone able to predict 82 % of the variance in CCN concentration. Changes in aerosol chemical composition are typically aligned with changes in size and aerosol number, such that hygroscopicity can be parameterized even though it is still variable. In summer, models based on fixed chemical composition explain at best only 41 % (pre-monsoon) and 36 % (monsoon) of the variance. This is attributed to the effects of secondary organic aerosol (SOA) production, the competition between new particle formation and condensational growth, the complex interaction of meteorology, regional and local emissions and multi-phase chemistry during the North American monsoon. Chemical composition is found to be an important factor for improving predictability in spring and on longer timescales in winter. Parameterized models typically exhibit improved predictive skill when there are strong relationships between CCN concentrations and the prevailing meteorology and dominant aerosol physicochemical processes, suggesting that similar findings could be possible in other locations with comparable climates and geography.


2008 ◽  
Vol 35 (22) ◽  
Author(s):  
Enrique R. Vivoni ◽  
Hernan A. Moreno ◽  
Giuseppe Mascaro ◽  
Julio C. Rodriguez ◽  
Christopher J. Watts ◽  
...  

2018 ◽  
Author(s):  
Katja Fennel ◽  
Simone Alin ◽  
Leticia Barbero ◽  
Wiley Evans ◽  
Timotheé Bourgeois ◽  
...  

Abstract. A quantification of carbon fluxes in the coastal ocean and across its boundaries, specifically the air-sea, land-to-coastal-ocean and coastal-to-open-ocean interfaces, is important for assessing the current state and projecting future trends in ocean carbon uptake and coastal ocean acidification, but is currently a missing component of global carbon budgeting. This synthesis reviews recent progress in characterizing these carbon fluxes with focus on the North American coastal ocean. Several observing networks and high-resolution regional models are now available. Recent efforts have focused primarily on quantifying net air-sea exchange of carbon dioxide (CO2). Some studies have estimated other key fluxes, such as the exchange of organic and inorganic carbon between shelves and the open ocean. Available estimates of air-sea CO2 flux, informed by more than a decade of observations, indicate that the North American margins act as a net sink for atmospheric CO2. This net uptake is driven primarily by the high-latitude regions. The estimated magnitude of the net flux is 160 ± 80 Tg C/y for the North American Exclusive Economic Zone, a number that is not well constrained. The increasing concentration of inorganic carbon in coastal and open-ocean waters leads to ocean acidification. As a result conditions favouring dissolution of calcium carbonate occur regularly in subsurface coastal waters in the Arctic, which are naturally prone to low pH, and the North Pacific, where upwelling of deep, carbon-rich waters has intensified and, in combination with the uptake of anthropogenic carbon, leads to low seawater pH and aragonite saturation states during the upwelling season. Expanded monitoring and extension of existing model capabilities are required to provide more reliable coastal carbon budgets, projections of future states of the coastal ocean, and quantification of anthropogenic carbon contributions.


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