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  • 1
    Publication Date: 2024-01-27
    Keywords: DEPTH, water; DO20150330; DO20150330-track; Dongfanghong 2; LATITUDE; LONGITUDE; Nitrate; Nitrogen, organic, dissolved; Underway water sampling; UWS; δ15N, dissolved organic nitrogen; δ15N, nitrate
    Type: Dataset
    Format: text/tab-separated-values, 155 data points
    Location Call Number Limitation Availability
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  • 2
    Publication Date: 2024-01-27
    Keywords: Ammonium; Date/Time of event; Date/Time of event 2; DO20140317; DO20140317_NWPO#1; DO20140317_NWPO#10; DO20140317_NWPO#11; DO20140317_NWPO#12; DO20140317_NWPO#13; DO20140317_NWPO#14; DO20140317_NWPO#15; DO20140317_NWPO#16; DO20140317_NWPO#17; DO20140317_NWPO#18; DO20140317_NWPO#19; DO20140317_NWPO#2; DO20140317_NWPO#20; DO20140317_NWPO#21; DO20140317_NWPO#22; DO20140317_NWPO#23; DO20140317_NWPO#24; DO20140317_NWPO#25; DO20140317_NWPO#26; DO20140317_NWPO#27; DO20140317_NWPO#28; DO20140317_NWPO#29; DO20140317_NWPO#3; DO20140317_NWPO#30; DO20140317_NWPO#31; DO20140317_NWPO#32; DO20140317_NWPO#33; DO20140317_NWPO#34; DO20140317_NWPO#35; DO20140317_NWPO#36; DO20140317_NWPO#37; DO20140317_NWPO#38; DO20140317_NWPO#39; DO20140317_NWPO#4; DO20140317_NWPO#40; DO20140317_NWPO#41; DO20140317_NWPO#42; DO20140317_NWPO#43; DO20140317_NWPO#44; DO20140317_NWPO#5; DO20140317_NWPO#6; DO20140317_NWPO#7; DO20140317_NWPO#8; DO20140317_NWPO#9; DO20150330; DO20150330_NWPO#1; DO20150330_NWPO#10; DO20150330_NWPO#11; DO20150330_NWPO#12; DO20150330_NWPO#13; DO20150330_NWPO#14; DO20150330_NWPO#15; DO20150330_NWPO#16; DO20150330_NWPO#17; DO20150330_NWPO#18; DO20150330_NWPO#19; DO20150330_NWPO#2; DO20150330_NWPO#20; DO20150330_NWPO#21; DO20150330_NWPO#22; DO20150330_NWPO#23; DO20150330_NWPO#24; DO20150330_NWPO#25; DO20150330_NWPO#26; DO20150330_NWPO#27; DO20150330_NWPO#28; DO20150330_NWPO#29; DO20150330_NWPO#3; DO20150330_NWPO#30; DO20150330_NWPO#31; DO20150330_NWPO#32; DO20150330_NWPO#33; DO20150330_NWPO#34; DO20150330_NWPO#35; DO20150330_NWPO#36; DO20150330_NWPO#37; DO20150330_NWPO#38; DO20150330_NWPO#4; DO20150330_NWPO#5; DO20150330_NWPO#6; DO20150330_NWPO#7; DO20150330_NWPO#8; DO20150330_NWPO#9; Dongfanghong 2; Event label; Latitude of event; Latitude of event 2; Longitude of event; Longitude of event 2; MULT; Multiple investigations; Nitrate; Nitrogen, total, water soluble; δ15N, nitrate; δ15N, water soluble total nitrogen
    Type: Dataset
    Format: text/tab-separated-values, 408 data points
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  • 3
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    In:  Supplement to: Luo, Li; Kao, Shuh-Ji; Bao, Hongyan; Xiao, Huayun; Xiao, Hongwei; Yao, Xiaohong; Gao, Huiwang; Li, Jiawei; Lu, Yangyang (2018): Sources of reactive nitrogen in marine aerosol over the Northwest Pacific Ocean in spring. Atmospheric Chemistry and Physics, 18(9), 6207-6222, https://doi.org/10.5194/acp-18-6207-2018
    Publication Date: 2024-01-27
    Description: Atmospheric deposition of long-range transport of anthropogenic reactive nitrogen (Nr, mainly comprised of NHx , NOy and water-soluble organic nitrogen, WSON) from continents may have profound impact on marine biogeochemistry. However, surface ocean dissolved organic nitrogen (DON) may also contribute to aerosol WSON in the overlying atmosphere. Despite the importance of off-continent dispersion and Nr interactions at the atmosphere–ocean boundary, our knowledge of the sources of various nitrogen species in the atmosphere over the open ocean remains limited due to insufficient observations. We conducted two cruises in the spring of 2014 and 2015 from the coast of China through the East China seas (ECSs, i.e. the Yellow Sea and East China Sea) to the open ocean (i.e. the north-western Pacific Ocean, NWPO). Concentrations of water-soluble total nitrogen (WSTN), NO3- and [NH4]+ , as well as the 15N of WSTN and NO3- in marine aerosol, were measured during both cruises. In the spring of 2015, we also analysed the concentrations and 15N of [NO3]- and the DON of surface seawater (SSW; at a depth of 5m) along the cruise track. Aerosol [NO3]- , [NH4]+ and WSON decreased logarithmically (1–2 orders of magnitude) with distance from the shore, reflecting strong anthropogenic emission sources of [NO3]-, [NH4]+ and WSON in China. Average aerosol [NO3]- and [NH4]+ concentrations were significantly higher in 2014 (even in the remote NWOP) than in 2015 due to the stronger wind field in 2014, underscoring the role of the Asian winter monsoon in the seaward transport of anthropogenic [NO3]- and [NH4]+ . However, the background aerosol WSON over the NWPO in 2015 (13.3±8.5 nmol/m3 was similar to that in 2014 (12.2±6.3 nmol/m3, suggesting an additional non-anthropogenic WSON source in the open ocean. Obviously, marine DON emissions should be considered in model and field assessments of net atmospheric WSON deposition in the open ocean. This study contributes information on parallel isotopic marine DON composition and aerosol Nr datasets, but more research is required to explore complex Nr sources and deposition processes in order to advance our understanding of anthropogenic influences on the marine nitrogen cycle and nitrogen exchange at land–ocean and atmosphere–ocean interfaces.
    Type: Dataset
    Format: application/zip, 2 datasets
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  • 4
    Publication Date: 2016-01-07
    Description: Suspended particles from the lower Changjiang were collected monthly from 2003 to 2011, which corresponds to the three construction periods of the Three Gorges Dam. Organic carbon (%OC), organic carbon to total nitrogen molar ratio, stable carbon isotope, and terrestrial biomarkers were examined. Rating curve studies were applied for the temporal trend analysis. The composition of particulate lignin phenols exhibited clear annual and periodic variations but only minor seasonal changes. Lignin phenol ratios (vanillyl/syringyl and cinnamyl/vanillyl) indicated that the terrigenous organic matter (OM) was primarily composed of woody and nonwoody tissue derived from angiosperm plants. The low-lignin phenol yields (Λ8) in combination with higher acid to aldehyde ratios reflected a substantial contribution fromsoil OM to the particle samples or modifications during river transport. The temporal shift of the lignin phenol vegetation index with the sediment load during the flood seasons revealed particulate organic matter (POM) erosion from soils and the impact of hydrodynamic processes. The dam operations affected the seasonal variability of terrigenous OM fluxes, although the covariation of lignin and sediment loads with discharged water implies that unseasonal extreme conditions and climate changemost likely had larger influences, because decreases in the sediment load and lignin flux alter the structure and composition of particulate OM (POM) on interannual time scales, indicating that they may be driven by climate variability. The modification of the composition and structure of POM will have significant impacts on regional carbon cycles and marine ecosystems.
    Repository Name: EPIC Alfred Wegener Institut
    Type: Article , isiRev
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  • 5
    Publication Date: 2022-10-26
    Description: © The Author(s), 2021. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Eglinton, T. I., Galy, V. V., Hemingway, J. D., Feng, X., Bao, H., Blattmann, T. M., Dickens, A. F., Gies, H., Giosan, L., Haghipour, N., Hou, P., Lupker, M., McIntyre, C. P., Montluçon, D. B., Peucker-Ehrenbrink, B., Ponton, C., Schefuß, E., Schwab, M. S., Voss, B. M., Wacker, L., Wu, Y., & Zhao, M. Climate control on terrestrial biospheric carbon turnover. Proceedings of the National Academy of Sciences of the United States of America, 118(8), (2021): e2011585118, htps://doi.org/ 10.1073/pnas.2011585118.
    Description: 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.
    Description: This work was supported by grants from the US NSF (OCE-0928582 to T.I.E. and V.V.G.; OCE-0851015 to B.P.-E., T.I.E., and V.V.G.; and EAR-1226818 to B.P.-E.), Swiss National Science Foundation (200021_140850, 200020_163162, and 200020_184865 to T.I.E.), and National Natural Science Foundation of China (41520104009 to M.Z.).
    Keywords: Radiocarbon ; Plant biomarkers ; Carbon turnover times ; Fluvial carbon ; Carbon cycle
    Repository Name: Woods Hole Open Access Server
    Type: Article
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  • 6
    Publication Date: 2022-09-23
    Description: Understanding the biogeochemical transformation of dissolved organic matter (DOM) across fluvial networks will ultimately help to predict anthropogenic influences. To date, few studies have evaluated the anthropogenic impact on the spatial and temporal changes of DOM composition in large river systems. Here, FT-ICR-MS combined with excitation-emission matrix spectroscopy (EEMs) and biomarkers were applied to resolve chemical differences of DOM collected from the Changjiang basin at different hydrological and environmental conditions. PCA and cluster analysis illustrated that samples collected from lake systems and northern and southern tributaries differed from the two batches of main stream samples, particularly due to higher contribution of nitrogen and sulfur containing compounds. Correlation of land-use information along the tributaries with different PCA loadings indicated that agricultural, forest and wetland areas and wastewater discharge control the composition of DOM within these subregions. Higher heteroatom content (especially CHONx) in the low discharge period (2009) may be contributed by paddy soil leaching into groundwater. The relative peak magnitude of sulfur containing formulas was elevated during flood season (2010), which may be related to pollutions in areas of high population density. In addition, lignin phenol concentrations were higher in the flood season because of elevated soil erosion. Consequently, land use and human activities can strongly alter the quality and composition of DOM in watersheds flowing through densely populated regions, which may also impact or influence the riverine carbon flux in anthropogenically disturbed river systems.
    Repository Name: EPIC Alfred Wegener Institut
    Type: Article , isiRev
    Format: application/pdf
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