McIntyre Cameron P.

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Cameron P.

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  • Article
    Climate control on terrestrial biospheric carbon turnover
    (National Academy of Sciences, 2021-02-23) Eglinton, Timothy I. ; Galy, Valier ; Hemingway, Jordon D. ; Feng, Xiaojuan ; Bao, Hongyan ; Blattmann, Thomas M. ; Dickens, Angela F. ; Gies, Hannah ; Giosan, Liviu ; Haghipour, Negar ; Hou, Pengfei ; Lupker, Maarten ; McIntyre, Cameron P. ; Montlucon, Daniel B. ; Peucker-Ehrenbrink, Bernhard ; Ponton, Camilo ; Schefuß, Enno ; Schwab, Melissa S. ; Voss, Britta M. ; Wacker, Lukas ; Wu, Ying ; Zhao, Meixun
    Terrestrial vegetation and soils hold three times more carbon than the atmosphere. Much debate concerns how anthropogenic activity will perturb these surface reservoirs, potentially exacerbating ongoing changes to the climate system. Uncertainties specifically persist in extrapolating point-source observations to ecosystem-scale budgets and fluxes, which require consideration of vertical and lateral processes on multiple temporal and spatial scales. To explore controls on organic carbon (OC) turnover at the river basin scale, we present radiocarbon (14C) ages on two groups of molecular tracers of plant-derived carbon—leaf-wax lipids and lignin phenols—from a globally distributed suite of rivers. We find significant negative relationships between the 14C age of these biomarkers and mean annual temperature and precipitation. Moreover, riverine biospheric-carbon ages scale proportionally with basin-wide soil carbon turnover times and soil 14C ages, implicating OC cycling within soils as a primary control on exported biomarker ages and revealing a broad distribution of soil OC reactivities. The ubiquitous occurrence of a long-lived soil OC pool suggests soil OC is globally vulnerable to perturbations by future temperature and precipitation increase. Scaling of riverine biospheric-carbon ages with soil OC turnover shows the former can constrain the sensitivity of carbon dynamics to environmental controls on broad spatial scales. Extracting this information from fluvially dominated sedimentary sequences may inform past variations in soil OC turnover in response to anthropogenic and/or climate perturbations. In turn, monitoring riverine OC composition may help detect future climate-change–induced perturbations of soil OC turnover and stocks.
  • Article
    Isotopic evidence for sources of dissolved carbon and the role of organic matter respiration in the Fraser River basin, Canada
    (Springer, 2022-07-10) Voss, Britta M. ; Eglinton, Timothy I. ; Peucker-Ehrenbrink, Bernhard ; Galy, Valier ; Lang, Susan Q. ; McIntyre, Cameron P. ; Spencer, Robert G. M. ; Bulygina, Ekaterina ; Wang, Zhaohui Aleck ; Guay, Katherine A.
    Sources of dissolved and particulate carbon to the Fraser River system vary significantly in space and time. Tributaries in the northern interior of the basin consistently deliver higher concentrations of dissolved organic carbon (DOC) to the main stem than other tributaries. Based on samples collected near the Fraser River mouth throughout 2013, the radiocarbon age of DOC exported from the Fraser River does not change significantly across seasons despite a spike in DOC concentration during the freshet, suggesting modulation of heterogeneous upstream chemical and isotopic signals during transit through the river basin. Dissolved inorganic carbon (DIC) concentrations are highest in the Rocky Mountain headwater region where carbonate weathering is evident, but also in tributaries with high DOC concentrations, suggesting that DOC respiration may be responsible for a significant portion of DIC in this basin. Using an isotope and major ion mass balance approach to constrain the contributions of carbonate and silicate weathering and DOC respiration, we estimate that up to 33 ± 11% of DIC is derived from DOC respiration in some parts of the Fraser River basin. Overall, these results indicate close coupling between the cycling of DOC and DIC, and that carbon is actively processed and transformed during transport through the river network.
  • Article
    Temporal and spatial variability of particle transport in the deep Arctic Canada Basin
    (John Wiley & Sons, 2015-04-11) Hwang, Jeomshik ; Kim, Minkyoung ; Manganini, Steven J. ; McIntyre, Cameron P. ; Haghipour, Negar ; Park, Jong Jin ; Krishfield, Richard A. ; Macdonald, Robie W. ; McLaughlin, Fiona A. ; Eglinton, Timothy I.
    To better understand the current carbon cycle and potentially detect its change in the rapidly changing Arctic Ocean, we examined sinking particles collected quasi-continuously over a period of 7 years (2004–2011) by bottom-tethered sediment trap moorings in the central Canada Basin. Total mass flux was very low (<100 mg m−2 d−1) at all sites and was temporally decoupled from the cycle of primary production in surface waters. Extremely low radiocarbon contents of particulate organic carbon and high aluminum contents in sinking particles reveal high contributions of resuspended sediment to total sinking particle flux in the deep Canada Basin. Station A (75°N, 150°W) in the southwest quadrant of the Canada Basin is most strongly influenced while Station C (77°N, 140°W) in the northeast quadrant is least influenced by lateral particle supply based on radiocarbon content and Al concentration. The results at Station A, where three sediment traps were deployed at different depths, imply that the most likely mode of lateral particle transport was as thick clouds of enhanced particle concentration extending well above the seafloor. At present, only 1%–2% of the low levels of new production in Canada Basin surface waters reaches the interior basin. Lateral POC supply therefore appears to be the major source of organic matter to the interior basin. However, ongoing changes to surface ocean boundary conditions may influence both lateral and vertical supply of particulate material to the deep Canada Basin.
  • Article
    Tectonically-triggered sediment and carbon export to the Hadal zone
    (Nature Publishing Group, 2018-01-09) Bao, Rui ; Strasser, Michael ; McNichol, Ann P. ; Haghipour, Negar ; McIntyre, Cameron P. ; Wefer, Gerold ; Eglinton, Timothy I.
    Sediments in deep ocean trenches may contain crucial information on past earthquake history and constitute important sites of carbon burial. Here we present 14C data on bulk organic carbon (OC) and its thermal decomposition fractions produced by ramped pyrolysis/oxidation for a core retrieved from the >7.5 km-deep Japan Trench. High-resolution 14C measurements, coupled with distinctive thermogram characteristics of OC, reveal hemipelagic sedimentation interrupted by episodic deposition of pre-aged OC in the trench. Low δ13C values and diverse 14C ages of thermal fractions imply that the latter material originates from the adjacent margin, and the co-occurrence of pre-aged OC with intervals corresponding to known earthquake events implies tectonically triggered, gravity-flow-driven supply. We show that 14C ages of thermal fractions can yield valuable chronological constraints on sedimentary sequences. Our findings shed new light on links between tectonically driven sedimentological processes and marine carbon cycling, with implications for carbon dynamics in hadal environments.