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  • Carbon cycle
  • American Geophysical Union  (20)
  • Massachusetts Institute of Technology and Woods Hole Oceanographic Institution  (4)
  • American Chemical Society
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  • 1
    Publication Date: 2022-05-25
    Description: Author Posting. © American Geophysical Union, 2009. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Global Biogeochemical Cycles 23 (2009): GB4028, doi:10.1029/2009GB003519.
    Description: Nitrogen cycle dynamics have the capacity to attenuate the magnitude of global terrestrial carbon sinks and sources driven by CO2 fertilization and changes in climate. In this study, two versions of the terrestrial carbon and nitrogen cycle components of the Integrated Science Assessment Model (ISAM) are used to evaluate how variation in nitrogen availability influences terrestrial carbon sinks and sources in response to changes over the 20th century in global environmental factors including atmospheric CO2 concentration, nitrogen inputs, temperature, precipitation and land use. The two versions of ISAM vary in their treatment of nitrogen availability: ISAM-NC has a terrestrial carbon cycle model coupled to a fully dynamic nitrogen cycle while ISAM-C has an identical carbon cycle model but nitrogen availability is always in sufficient supply. Overall, the two versions of the model estimate approximately the same amount of global mean carbon uptake over the 20th century. However, comparisons of results of ISAM-NC relative to ISAM-C reveal that nitrogen dynamics: (1) reduced the 1990s carbon sink associated with increasing atmospheric CO2 by 0.53 PgC yr−1 (1 Pg = 1015g), (2) reduced the 1990s carbon source associated with changes in temperature and precipitation of 0.34 PgC yr−1 in the 1990s, (3) an enhanced sink associated with nitrogen inputs by 0.26 PgC yr−1, and (4) enhanced the 1990s carbon source associated with changes in land use by 0.08 PgC yr−1 in the 1990s. These effects of nitrogen limitation influenced the spatial distribution of the estimated exchange of CO2 with greater sink activity in high latitudes associated with climate effects and a smaller sink of CO2 in the southeastern United States caused by N limitation associated with both CO2 fertilization and forest regrowth. These results indicate that the dynamics of nitrogen availability are important to consider in assessing the spatial distribution and temporal dynamics of terrestrial carbon sources and sinks.
    Description: We also acknowledge the financial support of the National Aeronautics and Space Administration Land Cover and Land Use Change Program (NNX08AK75G).
    Keywords: Nitrogen cycle ; Carbon cycle ; ISAM
    Repository Name: Woods Hole Open Access Server
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  • 2
    Publication Date: 2022-05-25
    Description: Author Posting. © American Geophysical Union, 2011. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Geophysical Research Letters 38 (2011): L09804, doi:10.1029/2011GL047238.
    Description: Atmospheric mixing ratios of CO2 are strongly seasonal in the Arctic due to mid-latitude transport. Here we analyze the seasonal influence of moist synoptic storms by diagnosing CO2 transport from a global model on moist isentropes (to represent parcel trajectories through stormtracks) and parsing transport into eddy and mean components. During winter when northern plants respire, warm moist air, high in CO2, is swept poleward into the polar vortex, while cold dry air, low in CO2, that had been transported into the polar vortex earlier in the year is swept equatorward. Eddies reduce seasonality in mid-latitudes by ∼50% of NEE (∼100% of fossil fuel) while amplifying seasonality at high latitudes. Transport along stormtracks is correlated with rising, moist, cloudy air, which systematically hides this CO2 transport from satellites. We recommend that (1) regional inversions carefully account for meridional transport and (2) inversion models represent moist and frontal processes with high fidelity.
    Description: This research is supported by the National Aeronautics and Space Administration contracts NNX08AT77G, NNX06AC75G, and NNX08AM56G.
    Keywords: Atmospheric transport ; Carbon cycle ; Inversion ; Isentropic coordinates ; Synoptic weather ; Tracer modeling
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  • 3
    Publication Date: 2022-05-25
    Description: Author Posting. © American Geophysical Union, 2011. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Global Biogeochemical Cycles 25 (2011): GB3018, doi:10.1029/2010GB003813.
    Description: Studies indicate that, historically, terrestrial ecosystems of the northern high-latitude region may have been responsible for up to 60% of the global net land-based sink for atmospheric CO2. However, these regions have recently experienced remarkable modification of the major driving forces of the carbon cycle, including surface air temperature warming that is significantly greater than the global average and associated increases in the frequency and severity of disturbances. Whether Arctic tundra and boreal forest ecosystems will continue to sequester atmospheric CO2 in the face of these dramatic changes is unknown. Here we show the results of model simulations that estimate a 41 Tg C yr−1 sink in the boreal land regions from 1997 to 2006, which represents a 73% reduction in the strength of the sink estimated for previous decades in the late 20th century. Our results suggest that CO2 uptake by the region in previous decades may not be as strong as previously estimated. The recent decline in sink strength is the combined result of (1) weakening sinks due to warming-induced increases in soil organic matter decomposition and (2) strengthening sources from pyrogenic CO2 emissions as a result of the substantial area of boreal forest burned in wildfires across the region in recent years. Such changes create positive feedbacks to the climate system that accelerate global warming, putting further pressure on emission reductions to achieve atmospheric stabilization targets.
    Description: This study was supported through grants provided as part of the Arctic System Science Program (NSF OPP‐ 0531047), the North American Carbon Program (NASA NNG05GD25G), and the Bonanza Creek Long‐Term Ecological Program (funded jointly by NSF grant DEB‐0423442 and USDA Forest Service, Pacific Northwest Research Station grant PNW01‐JV11261952‐231).
    Keywords: Carbon cycle ; High-latitude ecosystems ; Modeling
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  • 4
    Publication Date: 2022-05-25
    Description: Author Posting. © American Geophysical Union, 2011. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Global Biogeochemical Cycles 25 (2011): GB3022, doi:10.1029/2010GB003892.
    Description: The North Atlantic Ocean accounts for about 25% of the global oceanic anthropogenic carbon sink. This basin experiences significant interannual variability primarily driven by the North Atlantic Oscillation (NAO). A suite of biogeochemical model simulations is used to analyze the impact of interannual variability on the uptake and storage of contemporary and anthropogenic carbon (Canthro) in the North Atlantic Ocean. Greater winter mixing during positive NAO years results in increased mode water formation and subsequent increases in subtropical and subpolar Canthro inventories. Our analysis suggests that changes in mode water Canthro inventories are primarily due to changes in water mass volumes driven by variations in water mass transformation rates rather than local air-sea CO2 exchange. This suggests that a significant portion of anthropogenic carbon found in the ocean interior may be derived from surface waters advected into water formation regions rather than from local gas exchange. Therefore, changes in climate modes, such as the NAO, may alter the residence time of anthropogenic carbon in the ocean by altering the rate of water mass transformation. In addition, interannual variability in Canthro storage increases the difficulty of Canthro detection and attribution through hydrographic observations, which are limited by sparse sampling of subsurface waters in time and space.
    Description: We would like to acknowledge funding from the NOAA Climate Program under the Office of Climate Observations and Global Carbon Cycle Program (NOAA‐NA07OAR4310098), NSF (OCE‐0623034), NCAR, the WHOI Ocean Climate Institute, a National Defense Science and Engineering Graduate Fellowship and an Environmental Protection Agency STAR graduate fellowship. NCAR is sponsored by the National Science Foundation.
    Keywords: North Atlantic Oscillation ; Anthropogenic carbon ; Carbon cycle ; Climate change ; Global climate model ; Mode waters
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  • 5
    Publication Date: 2022-05-25
    Description: Author Posting. © American Geophysical Union, 2007. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Global Biogeochemical Cycles 21 (2007): GB2026, doi:10.1029/2006GB002900.
    Description: We investigate the interannual variability in the flux of CO2 between the atmosphere and the Southern Ocean on the basis of hindcast simulations with a coupled physical-biogeochemical-ecological model with particular emphasis on the role of the Southern Annular Mode (SAM). The simulations are run under either pre-industrial or historical CO2 concentrations, permitting us to separately investigate natural, anthropogenic, and contemporary CO2 flux variability. We find large interannual variability (±0.19 PgC yr−1) in the contemporary air-sea CO2 flux from the Southern Ocean (〈35°S). Forty-three percent of the contemporary air-sea CO2 flux variance is coherent with SAM, mostly driven by variations in the flux of natural CO2, for which SAM explains 48%. Positive phases of the SAM are associated with anomalous outgassing of natural CO2 at a rate of 0.1 PgC yr−1 per standard deviation of the SAM. In contrast, we find an anomalous uptake of anthropogenic CO2 at a rate of 0.01 PgC yr−1 during positive phases of the SAM. This uptake of anthropogenic CO2 only slightly mitigates the outgassing of natural CO2, so that a positive SAM is associated with anomalous outgassing in contemporaneous times. The primary cause of the natural CO2 outgassing is anomalously high oceanic partial pressures of CO2 caused by elevated dissolved inorganic carbon (DIC) concentrations. These anomalies in DIC are primarily a result of the circulation changes associated with the southward shift and strengthening of the zonal winds during positive phases of the SAM. The secular, positive trend in the SAM has led to a reduction in the rate of increase of the uptake of CO2 by the Southern Ocean over the past 50 years.
    Description: This work was supported by NASA headquarters under the Earth System Science Fellowship Grant NNG05GP78H to N. S. L. and grants NAG5-12528 and NNG04GH53G to N. G. Both S. C. D. and I. D. L. were supported by NSF/ONR NOPP (N000140210370) and NASA (NNG05GG30G).
    Keywords: Southern Ocean ; Carbon cycle ; Southern Annular Mode
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  • 6
    Publication Date: 2022-05-25
    Description: Author Posting. © American Geophysical Union, 2010. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Journal of Geophysical Research 115 (2010): C11015, doi:10.1029/2010JC006152.
    Description: The concentration of inert gases and their isotopes in the deep ocean are useful as tracers of air-sea gas exchange during deepwater formation. ΔKr/Ar, ΔN2/Ar, and δ40Ar were measured in deep profiles of samples collected in the northwest Pacific, subtropical North Pacific and tropical Atlantic oceans. For the ocean below 2000 m, we determined a mean ΔKr/Ar composition of −0.96% ± 0.16%, a mean ΔN2/Ar of 1.29% ± 0.21% relative to equilibrium saturation, and for δ40Ar a value of 1.188‰ ± 0.055‰ relative to air. These data are used to constrain high-latitude ventilation processes in the framework of three-box and seven-box ocean models. For the three-box model tracer data, we constrain the appropriate surface area of the high-latitude region in both models to be 3.6% (+2.5%, −1.7%) of ocean surface area and the bubble air injection rate to be 22.7 (+8.8, −7.3) mol air m−2 yr−1. Results for the seven-box model were similar, with a high-latitude area of 3.3% (+2.2%, −1.3%). Our results provide geochemical support for suggestions that the effective area of high-latitude ventilation is much smaller than the region of elevated preformed nutrients and demonstrate that noble gases strongly constrain the ocean solubility pump. Reducing high-latitude surface area weakens the CO2 solubility pump in the box models and limits communication between the atmosphere and deep ocean. These tracers should be useful constraints on high-latitude ventilation and the strength of the solubility pump in more complex ocean general circulation models.
    Description: Funding was provided by NSF‐OCE‐0647979.
    Keywords: Noble gases ; Ventilation ; Carbon cycle ; Solubility pump ; Gas exchange
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  • 7
    Publication Date: 2022-05-25
    Description: Author Posting. © American Geophysical Union, 2011. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Journal of Geophysical Research 116 (2011): C11019, doi:10.1029/2010JC006509.
    Description: The advance and retreat of sea ice produces seasonal convection and stratification, dampens surface waves and creates a separation between the ocean and atmosphere. These are all phenomena that can affect the air-sea gas transfer velocity (k660), and therefore it is not straightforward to determine how sea ice cover modulates air-sea flux. In this study we use field estimates k660 to examine how sea ice affects the net gas flux between the ocean and atmosphere. An inventory of salinity, 3He, and CFC-11 in the mixed layer is used to infer k660 during the drift of Ice Station Weddell in 1992. The average of k660 is 0.11 m d−1 across nearly 100% ice cover. In comparison, the only prior field estimates of k660 are disproportionately larger, with average values of 2.4 m d−1 across 90% sea ice cover, and 3.2 m d−1 across approximately 70% sea ice cover. We use these values to formulate two scenarios for the modulation of k660 by the fraction of sea ice cover in a 1-D transport model for the Southern Ocean seasonal ice zone. Results show the net CO2 flux through sea ice cover represents 14–46% of the net annual air-sea flux, depending on the relationship between sea ice cover and k660. The model also indicates that as much as 68% of net annual CO2 flux in the sea ice zone occurs in the springtime marginal ice zone, which demonstrates the need for accurate parameterizations of gas flux and primary productivity under partially ice-covered conditions.
    Description: Support for this work was provided by the Climate Center at the Lamont‐Doherty Earth Observatory, an NSF IGERT Fellowship and a NOAA Climate and Global Change Postdoctoral Fellowship to BL, and NSF grant OPP 01‐25523/ANT 04‐40825 (PS).
    Description: 2012-05-15
    Keywords: CO2 ; Southern Ocean ; Carbon cycle ; Gas exchange ; Sea ice
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  • 8
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    Massachusetts Institute of Technology and Woods Hole Oceanographic Institution
    Publication Date: 2022-05-25
    Description: Submitted in partial fulfillment of the requirements for the degree of Doctor of Philosophy at the Massachusetts Institute of Technology and the Woods Hole Oceanographic Institution February 2011
    Description: The sinking flux of particulate matter into the ocean interior is an oceanographic phenomenon that fuels much of the metabolic demand of the subsurface ocean and affects the distribution of carbon and other elements throughout the biosphere. In this thesis, I use a new suite of observations to study the dynamics of marine particulate matter at the contrasting sites of the subtropical Sargasso Sea near Bermuda and the waters above the continental shelf of the Western Antarctic Peninsula (WAP). An underwater digital camera system was employed to capture images of particles in the water column. The subsequent analysis of these images allowed for the determination of the particle concentration size distribution at high spatial, depth, and temporal resolutions. Drifting sediment traps were also deployed to assess both the bulk particle flux and determine the size distribution of the particle flux via image analysis of particles collected in polyacrylamide gel traps. The size distribution of the particle concentration and flux were then compared to calculate the average sinking velocity as a function of particle size. I found that the average sinking velocities of particles ranged from about 10-200 m d-1 and exhibited large variability with respect to location, depth, and date. Particles in the Sargasso Sea, which consisted primarily of small heterogeneous marine snow aggregates, sank more slowly than the rapidly sinking krill fecal pellets and diatom aggregates of the WAP. Moreover, the average sinking velocity did not follow a pattern of increasing velocities for the larger particles, a result contrary to what would be predicted from a simple formulation of Stokes’ Law. At each location, I derived a best-fit fractal correlation between the flux size distribution and the total carbon flux. The use of this relationship and the computed average sinking velocities enabled the estimation of particle flux from measurements of the particle concentration size distribution. This approach offers greatly improved spatial and temporal resolution when compared to traditional sediment trap methods for measuring the downward flux of particulate matter. Finally, I deployed specialized in situ incubation chambers to assess the respiration rates of microbes attached to sinking particles. I found that at Bermuda, the carbon specific remineralization rate of sinking particulate matter ranged from 0.2 to 1.1 d-1, while along the WAP, these rates were very slow and below the detection limit of the instruments. The high microbial respiration rates and slow sinking velocities in the Sargasso Sea resulted in the strong attenuation of the flux with respect to depth, whereas the rapid sinking velocities and slow microbial degradation rates of the WAP resulted in nearly constant fluxes with respect to depth.
    Description: The Scurlock Bermuda Biological Station for Research Fund provided travel support to and from Bermuda. A grant from the National Science Foundation (NSF) Carbon and Water Program (06028416) enabled all the Sargasso Sea research as well as the opportunity to develop and test much of the methodology presented in this thesis. Internal awards from the WHOI Rinehart Access to the Sea Program and the WHOI Coastal Oceans Institute provided early funding that supported my first season of research in Antarctica and were instrumental in securing the larger external NSF Office of Polar Programs (OPP) Western Antarctic Peninsula Flux Project (OPP 0838866) grant for a second year of science in the region. The NSF OPP Palmer Long-Term Ecological Research Project and the Food for Benthos on the Antarctic Continental Shelf Project provided logistical support in the region. Phoebe Lam and Scott Doney’s grant from the WHOI Ocean Carbon and Climate Institute supported a semester of my time. The Henry G. Houghton Fund and the MIT Student Assistance Fund subsidized educational costs, textbooks, equipment, and travel expenses to conferences. In my first year I was supported by funding from Scott Doney’s NSF grant (OCCE-0312710).
    Keywords: Sediment transport ; Carbon cycle ; Laurence M. Gould (Ship) Cruise LMG0901 ; Laurence M. Gould (Ship) Cruise LMG0902 ; Laurence M. Gould (Ship) Cruise LMG1001 ; Nathaniel B. Palmer (Ship) Cruise NBP1002
    Repository Name: Woods Hole Open Access Server
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  • 9
    Publication Date: 2022-05-25
    Description: Author Posting. © American Geophysical Union, 2012. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Geophysical Research Letters 39 (2012): L19703, doi:10.1029/2012GL052883.
    Description: Carbon cycling studies focusing on transport and transformation of terrigenous carbon sources toward marine sedimentary sinks necessitate separation of particulate organic carbon (OC) derived from many different sources and integrated by river systems. Much progress has been made on isolating and characterizing young biologically-formed OC that is still chemically intact, however quantification and characterization of old, refractory rock-bound OC has remained troublesome. Quantification of both endmembers of riverine OC is important to constrain exchanges linking biologic and geologic carbon cycles and regulating atmospheric CO2 and O2. Here, we constrain petrogenic OC proportions in suspended sediment from the headwaters of the Ganges River in Nepal through direct measurement using ramped pyrolysis radiocarbon analysis. The unique results apportion the biospheric and petrogenic fractions of bulk particulate OC and characterize biospheric OC residence time. Compared to the same treatment of POC from the lower Mississippi-Atchafalaya River system, contrast in age spectra of the Ganges tributary samples illustrates the difference between small mountainous river systems and large integrative ones in terms of the global carbon cycle.
    Description: This work was partially supported by U.S. National Science Foundation (NSF) Cooperative Agreement OCE-228996 to NOSAMS and NSF grants OCE-0851015 & OCE-0928582 to VG.
    Description: 2013-04-03
    Keywords: Ganges ; Himalaya ; Mississippi ; POC ; Carbon cycle ; Radiocarbon
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  • 10
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    Massachusetts Institute of Technology and Woods Hole Oceanographic Institution
    Publication Date: 2022-05-25
    Description: Submitted in partial fulfillment of the requirements for the degree of Master of Science at the Massachusetts Institute of Technology and Woods Hole Oceanographic Institution August 1994
    Description: The work presented here consists of a literature review and calculations to estimate the importance of photochemistry to carbon cycling in the oceans, followed by a photophysical study of a series of stable nitroxide radical probes that have been used for the quantitative detection of individual carbon-centered radicals and reducing species in natural waters. Two appendices follow. The first contains preliminary experiments utilizing one of the nitroxide probes in an investigation of hydroxyl radical production rates and steadystate concentrations in seawater. The second consists of an investigation of the singlet lifetimes of humic acids (HA), in order to aid in understanding their photochemical cycling and nt1uence on other compounds. The impact of photochemical reactions on global oceanic carbon cycling was calculated from literature values. The results indicate that between 1 and 13% of all dissolved organic carbon in the oceans is oxidized photochemically. This is a significant flux term, much larger than that of riverine input for example. A photophysical study of nitroxide radical probes was undertaken. For all of the compounds studied, steady-state absorption and fluorescence spectra were identical to those of the parent fluorophores. A decrease in fluorescence lifetime and quantum yield of tens- to hundreds-fold was observed for the paramagnetic compounds relative to their diamagnetic counterparts. Very rapid fluorescence quenching rates (3 to 80 x 1010 s-1) were calculated for the fluorescamine moiety of the paramagnetic nitroxide compounds in a variety of solvents. Calculated energy minimized geometries were very similar for all compounds which implies that geometric differences are not responsible for the variations found m fluorescence lifetimes and quantum yields between compounds. Calculated Forster and Dexter overlap integrals do not support deexcitation by these mechanisms. Time-resolved absorption measurements resulted in no evidence for transient species due to either intersystem crossing to the triplet state or charge transfer. Of the mechanisms considered, direct internal conversion to the ground state, is most likely given our results. An investigation of the utility of 3-(aminomethyl)-2,2,5,5-tetramethyl-1- pyrrolidinyloxy free radical (3-amp) for detection and quantification of hydroxyl radicals in natural waters found that the addition of primary probe compounds resulted in the generation of secondary carbon-centered radicals that were successfully trapped by 3-amp. Competition kinetics experiments with dimethyl sulfoxide resulted in a natural scavenger rate constant that matched previous literature results for coastal seawater. As expected, the addition of formate resulted in decreases, and the addition of nitrite in increases, in the hydroxyl radical trapping rate by this method. The resulting quantum yield values were about an order of magnitude higher than previous literature results. However, probably due to the use of different latitudes at which to estimate the incident solar radiation at the sea surface, hydroxyl radical production rate and steady-state concentrations calculated were about an order of magnitude lower than literature results. One experiment showed no increase in the hydroxyl radical production rate from Milli-Q water to oligotrophic and coastal seawater although the sample absorption coefficients increase by a factor of more than 20. However a single experiment comparing three different coastal seawater samples did show a correlation between absorption and hydroxyl radical production rate. More detailed work is needed to recognize the full potential of this method. Marine HA fluorescence lifetime measurements utilizing time-resolved single photon counting revealed a large portion of chromophores with very short (20-60 ps) lifetimes and low quantum yields. At least three distinct lifetimes could be distinguished by iterative deconvolution, although they probably result from the grouping of a multitude of individual chromophores. The theory of calculating the quantum yields of individual chromophores measured in a mixture is developed and calculations are made, although from an incomplete data set. Shorter fluorescent lifetimes for a given chromophore center within HA result in smaller quantum yields and are thought to be caused by very rapid competing intramolecular dark pathways such as energy or electron transfer Preliminary work investigating changes in time-resolved fluorescent lifetimes due to different sources of HA (Orinoco vs. Suwanee Rivers) and solution types (seawater vs. standard buffer) showed little variability.
    Description: This material is based upon work supported under a National Science Foundation Graduate Research Fellowship.
    Keywords: Photochemistry ; Carbon cycle ; Argo Maine (Ship) Cruise ; Weatherbird II (Ship) Cruise
    Repository Name: Woods Hole Open Access Server
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