Manizza Manfredi

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Now showing 1 - 6 of 6
  • Article
    The processing and impact of dissolved riverine nitrogen in the Arctic Ocean
    (Springer, 2011-06-11) Tank, Suzanne E. ; Manizza, Manfredi ; Holmes, Robert M. ; McClelland, James W. ; Peterson, Bruce J.
    Although the Arctic Ocean is the most riverine-influenced of all of the world’s oceans, the importance of terrigenous nutrients in this environment is poorly understood. This study couples estimates of circumpolar riverine nutrient fluxes from the PARTNERS (Pan-Arctic River Transport of Nutrients, Organic Matter, and Suspended Sediments) Project with a regionally configured version of the MIT general circulation model to develop estimates of the distribution and availability of dissolved riverine N in the Arctic Ocean, assess its importance for primary production, and compare these estimates to potential bacterial production fueled by riverine C. Because riverine dissolved organic nitrogen is remineralized slowly, riverine N is available for uptake well into the open ocean. Despite this, we estimate that even when recycling is considered, riverine N may support 0.5–1.5 Tmol C year−1 of primary production, a small proportion of total Arctic Ocean photosynthesis. Rapid uptake of dissolved inorganic nitrogen coupled with relatively high rates of dissolved organic nitrogen regeneration in N-limited nearshore regions, however, leads to potential localized rates of riverine-supported photosynthesis that represent a substantial proportion of nearshore production.
  • Preprint
    An analysis of the carbon balance of the Arctic Basin from 1997 to 2006
    ( 2010-06-18) McGuire, A. David ; Hayes, Daniel J. ; Kicklighter, David W. ; Manizza, Manfredi ; Zhuang, Qianlai ; Chen, Min ; Follows, Michael J. ; Gurney, Kevin R. ; McClelland, James W. ; Melillo, Jerry M. ; Peterson, Bruce J. ; Prinn, Ronald G.
    This study used several model-based tools to analyze the dynamics of the Arctic Basin between 1997 and 2006 as a linked system of land-ocean-atmosphere C exchange. The analysis estimates that terrestrial areas of the Arctic Basin lost 62.9 Tg C yr-1 and that the Arctic Ocean gained 94.1 Tg C yr-1. Arctic lands and oceans were a net CO2 sink of 108.9 Tg C yr-1, which is within the range of uncertainty in estimates from atmospheric inversions. Although both lands and oceans of the Arctic were estimated to be CO2 sinks, the land sink diminished in strength because of increased fire disturbance compared to previous decades, while the ocean sink increased in strength because of increased biological pump activity associated with reduced sea ice cover. Terrestrial areas of the Arctic were a net source of 41.5 Tg CH4 yr-1 that increased by 0.6 Tg CH4 yr-1 during the decade of analysis, a magnitude that is comparable with an atmospheric inversion of CH4. Because the radiative forcing of the estimated CH4 emissions is much greater than the CO2 sink, the analysis suggests that the Arctic Basin is a substantial net source of green house gas forcing to the climate system.
  • Article
    Modeling transport and fate of riverine dissolved organic carbon in the Arctic Ocean
    (American Geophysical Union, 2009-10-07) Manizza, Manfredi ; Follows, Michael J. ; Dutkiewicz, Stephanie ; McClelland, James W. ; Menemenlis, Dimitris ; Hill, C. N. ; Townsend-Small, Amy ; Peterson, Bruce J.
    The spatial distribution and fate of riverine dissolved organic carbon (DOC) in the Arctic may be significant for the regional carbon cycle but are difficult to fully characterize using the sparse observations alone. Numerical models of the circulation and biogeochemical cycles of the region can help to interpret and extrapolate the data and may ultimately be applied in global change sensitivity studies. Here we develop and explore a regional, three-dimensional model of the Arctic Ocean in which, for the first time, we explicitly represent the sources of riverine DOC with seasonal discharge based on climatological field estimates. Through a suite of numerical experiments, we explore the distribution of DOC-like tracers with realistic riverine sources and a simple linear decay to represent remineralization through microbial degradation. The model reproduces the slope of the DOC-salinity relationship observed in the eastern and western Arctic basins when the DOC tracer lifetime is about 10 years, consistent with published inferences from field data. The new empirical parameterization of riverine DOC and the regional circulation and biogeochemical model provide new tools for application in both regional and global change studies.
  • Article
    An atmospheric constraint on the seasonal Air-Sea exchange of oxygen and heat in the extratropics
    (American Geophysical Union, 2021-07-22) Morgan, Eric J. ; Manizza, Manfredi ; Keeling, Ralph F. ; Resplandy, Laure ; Mikaloff Fletcher, Sara E. ; Nevison, Cynthia D. ; Jin, Yuming ; Bent, Jonathan D. ; Aumont, Olivier ; Doney, Scott C. ; Dunne, John P. ; John, Jasmin G. ; Lima, Ivan D. ; Long, Matthew C. ; Rodgers, Keith B.
    The air-sea exchange of oxygen (O2) is driven by changes in solubility, biological activity, and circulation. The total air-sea exchange of O2 has been shown to be closely related to the air-sea exchange of heat on seasonal timescales, with the ratio of the seasonal flux of O2 to heat varying with latitude, being higher in the extratropics and lower in the subtropics. This O2/heat ratio is both a fundamental biogeochemical property of air-sea exchange and a convenient metric for testing earth system models. Current estimates of the O2/heat flux ratio rely on sparse observations of dissolved O2, leaving it fairly unconstrained. From a model ensemble we show that the ratio of the seasonal amplitude of two atmospheric tracers, atmospheric potential oxygen (APO) and the argon-to-nitrogen ratio (Ar/O2), exhibits a close relationship to the O2/heat ratio of the extratropics (40–70°). The amplitude ratio, A APO/A ArN2, is relatively constant within the extratropics of each hemisphere due to the zonal mixing of the atmosphere. A APO/A ArN2 is not sensitive to atmospheric transport, as most of the observed spatial variability in the seasonal amplitude of δAPO is compensated by similar variations in δ(Ar/N2). From the relationship between O2/heat and A APO/A ArN2 in the model ensemble, we determine that the atmospheric observations suggest hemispherically distinct O2/heat flux ratios of 3.3 ± 0.3 and 4.7 ± 0.8 nmol J-1 between 40 and 70° in the Northern and Southern Hemispheres respectively, providing a useful constraint for O2 and heat air-sea fluxes in earth system models and observation-based data products.
  • Article
    An assessment of the Atlantic and Arctic sea–air CO2 fluxes, 1990–2009
    (Copernicus Publications on behalf of the European Geosciences Union, 2013-01-29) Schuster, Ute ; McKinley, Galen A. ; Bates, Nicholas R. ; Chevallier, Frédéric ; Doney, Scott C. ; Fay, A. R. ; Gonzalez-Davila, M. ; Gruber, Nicolas ; Jones, S. ; Krijnen, J. ; Landschutzer, Peter ; Lefevre, N. ; Manizza, Manfredi ; Mathis, Jeremy T. ; Metzl, Nicolas ; Olsen, Are ; Rios, Aida F. ; Rodenbeck, C. ; Santana-Casiano, J. M. ; Takahashi, Taro ; Wanninkhof, Rik ; Watson, Andrew J.
    The Atlantic and Arctic Oceans are critical components of the global carbon cycle. Here we quantify the net sea–air CO2 flux, for the first time, across different methodologies for consistent time and space scales for the Atlantic and Arctic basins. We present the long-term mean, seasonal cycle, interannual variability and trends in sea–air CO2 flux for the period 1990 to 2009, and assign an uncertainty to each. We use regional cuts from global observations and modeling products, specifically a pCO2-based CO2 flux climatology, flux estimates from the inversion of oceanic and atmospheric data, and results from six ocean biogeochemical models. Additionally, we use basin-wide flux estimates from surface ocean pCO2 observations based on two distinct methodologies. Our estimate of the contemporary sea–air flux of CO2 (sum of anthropogenic and natural components) by the Atlantic between 40° S and 79° N is −0.49 ± 0.05 Pg C yr−1, and by the Arctic it is −0.12 ± 0.06 Pg C yr−1, leading to a combined sea–air flux of −0.61 ± 0.06 Pg C yr−1 for the two decades (negative reflects ocean uptake). We do find broad agreement amongst methodologies with respect to the seasonal cycle in the subtropics of both hemispheres, but not elsewhere. Agreement with respect to detailed signals of interannual variability is poor, and correlations to the North Atlantic Oscillation are weaker in the North Atlantic and Arctic than in the equatorial region and southern subtropics. Linear trends for 1995 to 2009 indicate increased uptake and generally correspond between methodologies in the North Atlantic, but there is disagreement amongst methodologies in the equatorial region and southern subtropics.
  • Article
    A model of the Arctic Ocean carbon cycle
    (American Geophysical Union, 2011-12-15) Manizza, Manfredi ; Follows, Michael J. ; Dutkiewicz, Stephanie ; Menemenlis, Dimitris ; McClelland, James W. ; Hill, C. N. ; Peterson, Bruce J. ; Key, Robert M.
    A three dimensional model of Arctic Ocean circulation and mixing, with a horizontal resolution of 18 km, is overlain by a biogeochemical model resolving the physical, chemical and biological transport and transformations of phosphorus, alkalinity, oxygen and carbon, including the air-sea exchange of dissolved gases and the riverine delivery of dissolved organic carbon. The model qualitatively captures the observed regional and seasonal trends in surface ocean PO4, dissolved inorganic carbon, total alkalinity, and pCO2. Integrated annually, over the basin, the model suggests a net annual uptake of 59 Tg C a−1, within the range of published estimates based on the extrapolation of local observations (20–199 Tg C a−1). This flux is attributable to the cooling (increasing solubility) of waters moving into the basin, mainly from the subpolar North Atlantic. The air-sea flux is regulated seasonally and regionally by sea-ice cover, which modulates both air-sea gas transfer and the photosynthetic production of organic matter, and by the delivery of riverine dissolved organic carbon (RDOC), which drive the regional contrasts in pCO2 between Eurasian and North American coastal waters. Integrated over the basin, the delivery and remineralization of RDOC reduces the net oceanic CO2 uptake by ~10%.