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Synthesis of a 13C-Labeled Tracer for Stream DOC: Labeling Tulip Poplar Carbon with 13CO2

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Abstract

Ecosystem tracer-level additions would benefit from a stable isotope-labeled source of complex organic molecules. We tested a method to label tree C with 13C and create a stable isotope tracer for stream dissolved organic carbon (DOC) using tulip poplar (Liriodendron tulipifera L.) seedlings. In 2000, seedlings were grown with 0.82 moles of 13CO2 to assess the distribution and level of 13C enrichment in the tree tissues. In 2001, seedlings were grown with 25 times more 13CO2 to generate tissues with a 13C signal strong enough for a 13C-DOC stream tracer addition. 13C enrichment in the trees varied in each year and by tissue age and type. Tissues formed during labeling (new) were more enriched in 13C than tissues established prior to the 13CO2 injection (old). Stems were most enriched in 13C in both new and old tissues. A higher percentage of 13CO2 was incorporated into seedlings in 2000 (59% ±1) than 2001 (43% ±0). Percent 13C incorporation among tree tissue types paralleled biomass distributions. Although tree C and 13C were equally soluble in both years, a greater percentage of tree C went into solution in 2001 (30%) than 2000 (20%). The water-soluble tree C accounted for approximately 12% of the injected 13CO2 and had both humic and polysaccharide components. Results from a whole-stream 13C-DOC tracer addition demonstrated that tree C could be sufficiently labeled with 13CO2 to create a stream DOC isotope tracer with some polymeric constituents.

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References

  • Abelson PH, Hoering TC. 1961. Carbon isotope fractionation in formation of amino acids by photosynthetic organisms. Proc Natl Acad Sci 47:623–32

    PubMed  Google Scholar 

  • Arndt SK, Wanek W. 2002. Use of decreasing foliar carbon isotope discrimination during water limitation as a carbon tracer to study whole plant carbon allocation. Plant Cell Environ 25:609–16

    Article  Google Scholar 

  • Bader RG. 1956. The lignin fraction of marine sediments. Deep-Sea Res 4:15–22

    Google Scholar 

  • Balatinecz JJ, Forward DF, Bidwell RGS. 1966. Distribution of photoassimilated C14O2 in young jack pine seedlings. Can J Botany 44:362–5

    Google Scholar 

  • Benner R, Fogel ML, Sprague EK, Hodson RE. 1987. Depletion of 13C in lignin and its implications for stable isotope studies. Nature 329:708–10

    Article  Google Scholar 

  • Bottner P, Coûteaux M-M, Anderson JM, Berg B, Billès G, Bolger T, Casabianca H, Romanyá J, Rovira P. 2000. Decomposition of 13C-labelled plant material in a European 65–40° latitudinal transect of coniferous forest soils: simulation of climate change by translocation of soils. Soil Biol Biochem 32:527–43

    Article  Google Scholar 

  • Bower PM, Kelly CA, Fee EJ, Shearer JA, DeClercq DR, Schindler DW. 1987. Simultaneous measurement of primary production by whole-lake and bottle radiocarbon additions. Limnol Oceanogr 32:299–312

    Google Scholar 

  • Broadmeadow MSJ, Griffiths H. 1993. Carbon isotope discrimination and the coupling of CO2 fluxes within forest canopies. In: Ehleringer JR, Hall AE, Farquhar GD, Eds. Stable isotopes and plant carbon – water relations. New York: Academic Press, Inc. p 109–29

    Google Scholar 

  • Cheng X, Kaplan LA. 2001. Improved analysis of dissolved carbohydrates in stream water with HPLC-PAD. Anal Chem 73:458–61

    Article  PubMed  Google Scholar 

  • Cheng X, Kaplan LA. 2003. Simultaneous analyses of neutral carbohydrates and amino sugars in freshwaters with HPLC-PAD. J Chromatogr Sci 41:1–5

    Article  PubMed  Google Scholar 

  • Cole JJ, Carpenter SR, Kitchell JF, Pace ML. 2002. Pathways of organic carbon utilization in small lakes: results from a whole lake 13C addition and coupled model. Limnol Oceanogr 47:1664–75

    Google Scholar 

  • Coûteaux M-M, Bottner P, Anderson JM, Berg B, Bolger T, Casals P, Romanyà J, Thiéry JM, Vallejo VR. 2001. Decomposition of 13C-labelled standard plant material in a latitudinal transect of European coniferous forests: differential impact of climate on the decomposition of soil organic matter compartments. Biogeochemistry 54:147–70

    Article  Google Scholar 

  • Cummins KW, Klug JJ, Wetzel RG, Petersen RC, Suberkropp KF, Manny BA, Wuycheck JC, Howard FO. 1972. Organic enrichment with leaf leachate in experimental lotic ecosystems. BioScience 22:719–22

    Google Scholar 

  • Dickson RE, Nelson EA. 1982. Fixation and distribution of 14C in Populus deltoides during dormancy induction. Physiol Plantarum 54:393–401

    Google Scholar 

  • Downs RJ, Hellmers H. 1975. Environment and the experimental control of plant growth. New York: Academic Press

    Google Scholar 

  • Fernandez I, Mahieu N, Cadisch G. 2003. Carbon isotopic fractionation during decomposition of plant materials of different quality. Global Biogeochem Cyc 17:1–11

    Google Scholar 

  • Feuerstein TP, Ostrom PH, Ostrom NE. 1997. Isotopic biogeochemistry of dissolved organic nitrogen: a new technique and application. Org Geochem 27:363–70

    Article  Google Scholar 

  • Fogel ML, Cifuentes LA. 1993. Isotope fractionation during primary production. In: Engel MH, Macko SA, Eds. Organic geochemistry. New York: Plentum. p 73–98

    Google Scholar 

  • Gandhi H, Wiegner TN, Ostrom PH, Kaplan LA, Ostrom NE. 2004. Isotopic (13C) analysis of dissolved organic carbon in stream water using an elemental analyzer coupled to a stable isotope ratio mass spectrometer. Rapid Communications in Mass Spectrometry. In press

  • Gessner MO, Schwoerbel J. 1989. Leaching kinetics of fresh leaf-litter with implications for the current concept of leaf-processing in streams. Archiv für Hydrobiologie 115:81–90

    Google Scholar 

  • Ghashghaie J, Duranceau M, Badeck FW, Cornic G, Adeline MT, Deléens E. 2001. δ13C of CO2 respired in the dark in relation to δ13C of leaf metabolites: comparison between Nicotiana sylvestris and Helianthus annuus under drought. Plant Cell Environ 24:505–15

    Article  Google Scholar 

  • Hall RO Jr. 1995. Use of a stable carbon isotope addition to trace bacterial carbon through a stream food web. J North Am Benthol Soc 14:269–77

    Google Scholar 

  • Hall RO Jr., Meyer JL. 1998. The trophic significance of bacteria in a detritus-based stream food web. Ecology 79:1995–2012

    Google Scholar 

  • Hansen P. 1967. 14C-studies on apple trees III. The influence of season on storage and mobilization of labeled compounds. Physiol Plantarum 20:1103–11

    Google Scholar 

  • Hedges JI, Keil RG, Benner R. 1997. What happens to terrestrial organic matter in the ocean? Org Geochem 27:195–212

    Article  Google Scholar 

  • Hesslein RH, Broecker WS, Quay PD, Schindler DW. 1980. Whole-lake radiocarbon experiment in an oligotrophic lake in the experimental lakes area, northwestern Ontario. Can J Fish Aquat Sci 37:454–63

    Google Scholar 

  • Holmes RM, Peterson BJ, Deegan LA, Hughes JE, Fry B. 2000. Nitrogen biogeochemistry in the oligohaline zone of a New England estuary. Ecology 81:416–32

    Google Scholar 

  • Hongve D, 1999. Production of dissolved organic carbon in forested catchments. J Hydrol 224:91–9

    Article  Google Scholar 

  • Horwath WR, Pregitzer KS, Paul EA. 1994. 14C allocation in tree-soil systems. Tree Physiol 14:1163–76

    Google Scholar 

  • Hughes JE, Deegan LA, Peterson BJ, Holmes RM, Fry B. 2000. Nitrogen flow through the food web in the oligohaline zone of a New England estuary. Ecology 81:433–52

    Google Scholar 

  • Isebrands JG, Nelson ND. 1983. Distribution of [14C]-labeled photosynthates within intensively cultured Populus clones during the establishment year. Physiol Plantarum 59:9–18

    Google Scholar 

  • Johnston NT, MacDonald JS, Hall KJ, Tschaplinski PJ. 1997. A preliminary study of the role of sockeye salmon (Oncorhynchus nerka) carcasses as carbon and nitrogen sources for benthic insects and fishes in the “Early Stuart” stock spawning streams, 1050 km from the ocean. Fisheries Project Report RD55, British Columbia Ministry of Environment, Lands and Parks, Victoria, British Columbia

  • Kaplan LA. 1992. Comparison of high-temperature and persulfate oxidation methods for determination of dissolved organic carbon in freshwaters. Limnol Oceanogr 37:1119–25

    Google Scholar 

  • Kaplan LA, Newbold JD. 1993. Biogeochemistry of dissolved organic carbon entering streams. In: Ford TE, Ed. Aquatic microbiology: an ecological approach. Boston: Blackwell Scientific Publications. p 139–65

    Google Scholar 

  • Kaplan LA, Newbold JD. 2003. The role of monomers in stream ecosystem metabolism. In: Findlay S, Sinsabaugh RL, Eds. Aquatic ecosystems: interactivity of dissolved organic matter. New York: Academic Press. p 97–119

    Google Scholar 

  • Kuhns MR, Gjerstad DH. 1991. Distribution of 14C-labeled photosynthate in loblolly pine (Pinus taeda) seedlings as affected by season and time after exposure. Tree Physiol 8:259–71

    Google Scholar 

  • Leavitt SW, Long A. 1982. Evidence for 13C/12C fractionation between tree leaves and wood. Nature 298:742–4

    Article  Google Scholar 

  • Leavitt SW, Long A. 1986. Stable-carbon isotope variability in tree foliage and wood. Ecology 67:1002–10

    Google Scholar 

  • Macko SA, Fogel ML, Hare PE, Hoering TC. 1987. Isotopic fractionation of nitrogen and carbon in the synthesis of amino acids by microorganisms. Chem Geol 65:79–92

    Article  Google Scholar 

  • Magill AH, Aber JD. 2000. Dissolved organic carbon and nitrogen relationships in forest litter as affected by nitrogen deposition. Soil Biol Biochem 32:603–13

    Article  Google Scholar 

  • Maillard P, Deléens E, Daudet FA, Lacointe A, Frossard JS. 1994. Carbon and nitrogen partitioning in walnut seedlings during the acquisition of autotrophy through simultaneous 13CO2 and 15NO3 long-term labeling. J Exp Botany 45:203–10

    Google Scholar 

  • McClaugherty CA. 1983. Soluble polyphenols and carbohydrates in throughfall and leaf litter decomposition. Acta Oecolog/Oecolog Generalis 4:375–85

    Google Scholar 

  • McDowell WH, Fisher SG. 1976. Autumnal processing of dissolved organic matter in a small woodland stream ecosystem. Ecology 57:561–9

    Google Scholar 

  • Meyer JL, Wallace JB, Eggert SL. 1998. Leaf litter as a source of dissolved organic carbon in streams. Ecosystems 1:240–9

    Article  Google Scholar 

  • Meyers-Schulte KJ, Hedges JI. 1986. Molecular evidence for a terrestrial component of organic matter dissolved in ocean water. Nature 321:61–3

    Google Scholar 

  • Michener RH, Schell DM. 1994. Stable isotope ratios as tracers in marine aquatic food webs. In: Lajtha K, Michener RH, Eds. Stable isotopes in ecology and environmental science. Boston: Blackwell Scientific Publications. p 138–57

    Google Scholar 

  • Mikan CJ, Zak DR, Kubiske ME. 2000. Combined effects of atmospheric CO2 and N availability on the belowground carbon and nitrogen dynamics of aspen mesocosms. Oecologia 124:432–45

    Google Scholar 

  • Newbold JD, Elwood JW, O’Neill RV, Sheldon AL. 1983. Phosphorus dynamics in a woodland stream ecosystem: a study of nutrient spiralling. Ecology 64:1249–65

    Google Scholar 

  • Nykvist N. 1962. Leaching and decomposition of litter. V. Experiments on leaf litter of Alnus glutinosa, Fagus silvatica, Quercus robur. Oikos 13:232–48

    Google Scholar 

  • Nykvist N. 1963. Leaching and decomposition of soluble organic substances from different types of leaf and needle litter. Studia Forestalia Suecia 3:1–31

    Google Scholar 

  • Opsahl S, Benner R. 1997. Distribution and cycling of terrigenous dissolved organic matter in the ocean. Nature 386:480–2

    Article  Google Scholar 

  • Palmer SM, Hope D, Billett MF, Dawson JJC, Bryant CL. 2001. Sources of organic and inorganic carbon in a headwater stream: evidence from carbon isotope studies. Biogeochemistry 52:321–38

    Article  Google Scholar 

  • Petersen RC, Cummins KW. 1974. Leaf processing in a woodland stream. Freshwater Biol 4:343–68

    Google Scholar 

  • Peterson BJ, Bahr M, Kling GW. 1997. A tracer investigation of nitrogen cycling in a pristine tundra river. Can J Fish Aquat Sci 54:2361–7

    Article  Google Scholar 

  • Peterson BJ, Wollheim WM, Mulholland PJ, Webster JR, Meyer JL, Tank JL, Martí E, Bowden WB, Valett HM, Hershey AE, McDowell WH, Dodds WK, Hamilton SK, Gregory S, Morrall DD. 2001. Control of nitrogen export from watersheds by headwater streams. Science 292:86–90

    Google Scholar 

  • Qualls RG, Haines BL, Swank WT. 1991. Fluxes of dissolved organic nutrients and humic substances in a deciduous forest. Ecology 72:254–66

    Google Scholar 

  • Quinlan JD. 1965. The pattern of distribution of 14carbon in a potted apple rootstock following assimilation of 14carbon dioxide by a single leaf. Rep East Malling Res Station 1964:117–20

    Google Scholar 

  • Schier GA. 1970. Seasonal pathways of 14C-photosynthate in red pine labeled in May, July, and October. Forest Sci 16:1–13

    Google Scholar 

  • Schleser GH. 1992. δ13C pattern in a forest tree as an indicator of carbon transfer in trees. Ecology 73:1922–5

    Google Scholar 

  • Simard SW, Durall DM, Jones MD. 1997. Carbon allocation and carbon transfer between Betula papyrifera and Pseudotsuga menziesii seedlings using a 13C pulse-labeling method. Plant Soil 191:41–55

    Article  Google Scholar 

  • Smith JL, Paul EA. 1988. Use of an in situ labeling technique for the determination of seasonal 14C distribution in Ponderosa pine. Plant Soil 106:221–9

    Google Scholar 

  • Standley LJ, Kaplan LA. 1998. Isolation and analysis of lignin-derived phenols in aquatic humic substances: improvements on the procedures. Org Geochem 28:689–97

    Article  Google Scholar 

  • StreamSolute Workshop. 1990. Concepts and methods for assessing solute dynamics in stream ecosystems. J North Am Benthol Soc 9:95–119

    Google Scholar 

  • Tank JL, Meyer JL, Sanzone DM, Mulholland PJ, Webster JR, Peterson BJ, Wollheim WM, Leonard NE. 2000. Analysis of nitrogen cycling in a forest stream during autumn using a 15N-tracer addition. Limnol Oceanogr 45:1013–29

    Google Scholar 

  • Terwilliger VJ, Huang J. 1996. Heterotrophic whole plant tissue show more 13C enrichment than their carbon sources. Photochemistry 43:1183–8

    Article  Google Scholar 

  • Thurman EM. 1985. Developments in biogeochemistry: organic geochemistry of natural waters. Dordrecht: Martinus Nijhoff/Dr W. Junk Publishers

    Google Scholar 

  • Tranvik L, Kokalj S. 1998. Decreased biodegradability of algal DOC due to interactive effects of UV radiation and humic matter. Aquat Microb Ecol 14:301–7

    Google Scholar 

  • Van Norman RW, Brown AH. 1952. The relative rates of photosynthetic assimilation of isotopic forms of carbon dioxide. Plant Physiol 27:691–709

    Google Scholar 

  • Vivin P, Martin F, Guehl J-M. 1996. Acquisition and within-plant allocation of 13C and 15N in CO2-enriched Quercus robur plants. Physiol Plantarum 98:89–96

    Article  Google Scholar 

  • Webb WL. 1977. Seasonal allocation of photoassimilated carbon in Douglas fir seedlings. Plant Physiol 60:320–2

    Google Scholar 

  • Wetzel RG, Hatcher PG, Bianchi TS. 1995. Natural photolysis by ultraviolet irradiance of recalcitrant dissolved organic matter to simple substrates for rapid bacterial metabolism. Limnol Oceanogr 40:1369–80

    Google Scholar 

  • Wong WW, Clarke LL, Johnson GA, Llaurador M, Klein PD. 1992. Comparison of two elemental-analyzer gas-isotope-ratio mass spectrometer systems in the simultaneous measurement of 13C/12C ratios and carbon content in organic samples. Anal Chem 64:354–8

    Article  Google Scholar 

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Acknowledgements

S. Adams, H. Gandhi, M. Gentile, A. M. Leyman, L.A. Martin, D. Richardson, S. Roberts, K. Rowley, and D. Van Horn assisted with laboratory and field work. D. Tremmel coordinated and oversaw the labeling of the trees at the National Phytotron at Duke University. Comments from two anonymous reviewers and J. Cole helped improve this manuscript. This research is the result of work funded by the National Science Foundation, under grants No. DEB-0109122, DEB-0096276, and IBN-9985877.

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Correspondence to Tracy N. Wiegner.

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Wiegner, T.N., Kaplan, L.A., Newbold, J.D. et al. Synthesis of a 13C-Labeled Tracer for Stream DOC: Labeling Tulip Poplar Carbon with 13CO2. Ecosystems 8, 501–511 (2005). https://doi.org/10.1007/s10021-003-0043-1

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