Jump to content

File:Where carbon goes when water flows.jpg

Page contents not supported in other languages.
This is a file from the Wikimedia Commons
From Wikipedia, the free encyclopedia

Original file (737 × 719 pixels, file size: 596 KB, MIME type: image/jpeg)

Summary

Description
English: Where carbon goes when water flows

(1) Atmospheric particles act as cloud-condensing nuclei, promoting cloud formation (Kerminen et al., 2000; Riipinen et al., 2011). (2) Raindrops absorb organic and inorganic carbon through particle scavenging and adsorption of organic vapors while falling toward earth (Waterloo et al., 2006; Neu et al., 2016). (3) Burning and volcanic eruptions produce highly condensed polycyclic aromatic molecules (i.e., black carbon) that is returned to the atmosphere along with greenhouse gases such as CO2 (Baldock et al., 2004; Myers-Pigg et al., 2016). (4) Terrestrial plants fix atmospheric CO2 through photosynthesis, returning a fraction back to the atmosphere through respiration (Field et al., 1998). Lignin and celluloses represent as much as 80% of the OC in forests and 60% in pastures (Martens et al., 2004; Bose et al., 2009). (5) Litterfall and root OC mix with sedimentary material to form organic soils where plant-derived and petrogenic OC is both stored and transformed by microbial and fungal activity (Schlesinger and Andrews, 2000; Schmidt et al., 2011; Lehmann and Kleber, 2015). (6) Water absorbs plant and settled aerosol-derived DOC and DIC as it passes over forest canopies (i.e., throughfall) and along plant trunks/stems (i.e., stemflow) (Qualls and Haines, 1992). Biogeochemical transformations take place as water soaks into soil solution and groundwater reservoirs (Grøn et al., 1992; Pabich et al., 2001) and overland flow occurs when soils are completely saturated (Linsley et al., 1975) or rainfall occurs more rapidly than saturation into soils (Horton, 1933). (7) Organic carbon derived from the terrestrial biosphere and in situ primary production is decomposed by microbial communities in rivers and streams along with physical decomposition (i.e., photo-oxidation), resulting in a flux of CO2 from rivers to the atmosphere that are the same order of magnitude as the amount of carbon sequestered annually by the terrestrial biosphere (Richey et al., 2002; Cole et al., 2007; Raymond et al., 2013). Terrestrially-derived macromolecules such as lignin (Ward et al., 2013) and black carbon (Myers-Pigg et al., 2015) are decomposed into smaller components and monomers, ultimately being converted to CO2, metabolic intermediates, or biomass. (8) Lakes, reservoirs, and floodplains typically store large amounts of OC and sediments, but also experience net heterotrophy in the water column, resulting in a net flux of CO2 to the atmosphere that is roughly one order of magnitude less than rivers (Tranvik et al., 2009; Raymond et al., 2013). Methane production is also typically high in the anoxic sediments of floodplains, lakes, and reservoirs (Bastviken et al., 2004). (9) Primary production is typically enhanced in river plumes due to the export of fluvial nutrients (Cooley et al., 2007; Subramaniam et al., 2008). Nevertheless, estuarine waters are a source of CO2 to the atmosphere, globally (Cai, 2011). (10) Coastal marshes both store and export “blue carbon” (Odum et al., 1979; Dittmar et al., 2001; Moore et al., 2011). Marshes and wetlands are suggested to have an equivalent flux of CO2 to the atmosphere as rivers, globally (Wehrli, 2013). (11) Continental shelves and the open ocean typically absorb CO2 from the atmosphere (Cai, 2011), sequestering a small fraction of the fixed CO2 as organic carbon in (12) marine sediments due to the “biological pump” (Moran et al., 2016).

References...

  • Kerminen, V. M., Virkkula, A., Hillamo, R., Wexler, A. S., and Kulmala, M. (2000). Secondary organics and atmospheric cloud condensation nuclei production. J. Geophys. Res. Atmosph. 105, 9255–9264. doi: 10.1029/1999JD901203
  • Riipinen, I., Pierce, J. R., Yli-Juuti, T., Nieminen, T., Hakkinen, S., Ehn, M., et al. (2011). Organic condensation: a vital link connecting aerosol formation to cloud condensation nuclei (CCN) concentrations. Atmosph. Chem. Phys. 11, 3865. doi: 10.5194/acp-11-3865-2011
  • Waterloo, M. J., Oliveira, S. M., Drucker, D. P., Nobre, A. D., Cuartas, L. A., Hodnett, M. G., et al. (2006). Export of organic carbon in run-off from an amazonian rainforest blackwater catchment. Hydrol. Process. 20, 2581–2259. doi: 10.1002/hyp.6217
  • Neu, V., Ward, N. D., Krusche, A. V., and Neill, C. (2016). Dissolved organic and inorganic carbon flow paths in an Amazonian transitional forest. Front. Mar. Sci. 3:114. doi: 10.3389/fmars.2016.00114
  • Baldock, J. A., Masiello, C. A., Gelinas, Y., and Hedges, J. I. (2004). Cycling and composition of organic matter in terrestrial and marine ecosystems. Mar. Chem. 92, 39–64. doi: 10.1016/j.marchem.2004.06.016
  • Myers-Pigg, A. N., Griffin, R. J., Louchouarn, P., Norwood, M. J., Sterne, A., and Karakurt Cevik, B. (2016). Signatures of biomass burning aerosols in the plume of a saltmarsh wildfire in South Texas. Environ. Sci. Technol. 50, 9308–9314. doi: 10.1021/acs.est.6b02132
  • Field, C. B., Behrenfeld, M. J., Randerson, J. T., and Falkowski, P. (1998). Primary production of the biosphere: integrating terrestrial and oceanic components. Science. 281, 237–240. doi: 10.1126/science.281.5374.237
  • Martens, D., Reedy, T., and Lewis, D. (2004). Soil organic carbon content and composition of 130-year crop, pasture and forest land-use managements. Global Change Biol. 10, 65–78. doi: 10.1046/j.1529-8817.2003.00722.x
  • Bose, S. K., Francis, R. C., Govender, M., Bush, T., and Spark, A. (2009). Lignin content versus syringyl to guaiacyl ratio amongst poplars. Bioresour. Technol. 100, 1628–1633 doi: 10.1016/j.biortech.2008.08.046
  • Schlesinger, W. H., and Andrews, J. A. (2000). Soil respiration and the global carbon cycle. Biogeochemistry 48, 7–20. doi: 10.1023/A:1006247623877
  • Schmidt, M. W., Torn, M. S., Abiven, S., Dittmar, T., Guggenberger, G., Janssens, I. A., et al. (2011). Persistence of soil organic matter as an ecosystem property. Nature 478, 49–56. doi: 10.1038/nature10386
  • Lehmann, J., and Kleber, M. (2015). The contentious nature of soil organic matter. Nature 528, 60–68. doi: 10.1038/nature16069
  • Qualls, R. G., and Haines, B. L. (1992). Biodegradability of dissolved organic matter in forest throughfall, soil solution, and stream water. Soil Sci. Soc. Am. J. 56, 578–586. doi: 10.2136/sssaj1992.03615995005600020038x
  • Grøn, C., Tørsløv, J., Albrechtsen, H. J., and Jensen, H. M. (1992). Biodegradability of dissolved organic carbon in groundwater from an unconfined aquifer. Sci. Total Environ. 117, 241–251. doi: 10.1016/0048-9697(92)90091-6
  • Pabich, W. J., Valiela, I., and Hemond, H. F. (2001). Relationship between DOC concentration and vadose zone thickness and depth below water table in groundwater of Cape Cod, USA. Biogeochemistry 55, 247–268. doi: 10.1023/A:1011842918260
  • Linsley, J.r., R. K., Kohler, M. A., and Paulhus, J. L. H. (1975). Hydrology for Engineers. New York, NY: McGraw-Hill Book Co., Inc.
  • Horton, R. E. (1933). The role of infiltration in the hydrologic cycle. Trans. Am. Geophys. Union 14, 446–460. doi: 10.1029/TR014i001p00446
  • Richey, J. E., Melack, J. M., Aufdenkampe, A. K., Ballester, V. M., and Hess, L. L. (2002). Carbon dioxide evasion from central Amazonian wetlands as a significant source of atmospheric CO2 in the tropics. Nature 416, 617–620. doi: 10.1038/416617a
  • Cole, J. J., Prairie, Y. T., Caraco, N. F., McDowell, W. H., Tranvik, L. J., Striegl, R. G., et al. (2007). Plumbing the global carbon cycle: integrating inland waters into the terrestrial carbon budget. Ecosystems 10, 172–185. doi: 10.1007/s10021-006-9013-8
  • Raymond, P. A., Hartmann, J., Lauerwald, R., Sobek, S., McDonald, C., Hoover, M., et al. (2013). Global carbon dioxide emissions from inland waters. Nature 503, 355–359. doi: 10.1038/nature12760
  • Ward, N. D., Keil, R. G., Medeiros, P. M., Brito, D. C., Cunha, A. C., Dittmar, T., et al. (2013). Degradation of terrestrially derived macromolecules in the Amazon River. Nat. Geosci. 6, 530–533. doi: 10.1038/ngeo1817
  • Myers-Pigg, A. N., Louchouarn, P., Amon, R. M., Prokushkin, A., Pierce, K., and Rubtsov, A. (2015). Labile pyrogenic dissolved organic carbon in major Siberian Arctic rivers: implications for wildfire-stream metabolic linkages. Geophys. Res. Lett. 42, 377–385. doi: 10.1002/2014GL062762
  • Tranvik, L. J., Downing, J. A., Cotner, J. B., Loiselle, S. A., Striegl, R. G., Ballatore, T. J., et al. (2009). Lakes and reservoirs as regulators of carbon cycling and climate. Limnol. Oceanogr. 54, 2298–2314. doi: 10.4319/lo.2009.54.6_part_2.2298
  • Bastviken, D., Cole, J., Pace, M., and Tranvik, L. (2004). Methane emissions from lakes: dependence of lake characteristics, two regional assessments, and a global estimate. Global Biogeochem. Cycles 18:GB4009. doi: 10.1029/2004GB002238
  • Cooley, S. R., Coles, V. J., Subramaniam, A., and Yager, P. L. (2007). Seasonal variations in the Amazon plume-related atmospheric carbon sink. Global Biogeochem. Cycles 21, 1–15. doi: 10.1029/2006GB002831
  • Subramaniam, A., Yager, P. L., Carpenter, E. J., Mahaffey, C., Björkman, K., Cooley, S., et al. (2008). Amazon River enhances diazotrophy and carbon sequestration in the tropical North Atlantic Ocean. Proc. Natl. Acad. Sci. U.S.A. 105, 10460–10465. doi: 10.1073/pnas.0710279105
  • Cai, W. J. (2011). Estuarine and coastal ocean carbon paradox: CO2 sinks or sites of terrestrial carbon incineration? Ann. Rev. Mar. Sci. 3, 123–145. doi: 10.1146/annurev-marine-120709-142723
  • Odum, W. E., Fisher, J. S., and Pickral, J. C. (1979). “Factors controlling the flux of particulate organic carbon from estuarine wetlands,” in Ecological Processes in Coastal and Marine Systems, ed R. J. Livingston (New York, NY: Springer). 69–80.
  • Dittmar, T., Lara, R. J., and Kattner, G. (2001). River or mangrove? Tracing major organic matter sources in tropical Brazilian coastal waters. Mar. Chem. 73, 253–271. doi: 10.1016/s0304-4203(00)00110-9...
Date
Source [1] doi:10.3389/fmars.2017.00007
Author Nicholas D. Ward, Thomas S. Bianchi, Patricia M. Medeiros, Michael Seidel, Jeffrey E. Richey, Richard G. Keil and Henrique O. Sawakuchi

Licensing

w:en:Creative Commons
attribution share alike
This file is licensed under the Creative Commons Attribution-Share Alike 4.0 International license.
You are free:
  • to share – to copy, distribute and transmit the work
  • to remix – to adapt the work
Under the following conditions:
  • attribution – You must give appropriate credit, provide a link to the license, and indicate if changes were made. You may do so in any reasonable manner, but not in any way that suggests the licensor endorses you or your use.
  • share alike – If you remix, transform, or build upon the material, you must distribute your contributions under the same or compatible license as the original.

Captions

Where carbon goes when water flows

Items portrayed in this file

depicts

29 November 2016

image/jpeg

File history

Click on a date/time to view the file as it appeared at that time.

Date/TimeThumbnailDimensionsUserComment
current23:47, 4 November 2020Thumbnail for version as of 23:47, 4 November 2020737 × 719 (596 KB)EpipelagicUploaded a work by Nicholas D. Ward, Thomas S. Bianchi, Patricia M. Medeiros, Michael Seidel, Jeffrey E. Richey, Richard G. Keil and Henrique O. Sawakuchi from [https://www.frontiersin.org/articles/10.3389/fmars.2017.00007/full] {{doi|10.3389/fmars.2017.00007}} with UploadWizard

The following 3 pages use this file:

Global file usage

The following other wikis use this file:

Metadata