Radiocarbon dating suitability of aquatic plant macrofossils
Abstract
Paleolimnological and plant physiological literature were reviewed to determine which types of aquatic plant macrofossils are suitable for radiocarbon dating, with a particular focus on the uptake of reservoir-aged dissolved inorganic carbon (DIC) by emergent plants. Submerged aquatic plants utilize large amounts of DIC and are clearly not suitable for radiocarbon dating. Under certain environmental conditions, some emergent aquatic plants can metabolize DIC in quantities large enough to introduce old-carbon error to radiocarbon dates acquired from their remains (plant macrofossils). Over 300 plant macrofossil images are included in the online resource Tool for Microscopic Identification; http://tmi.laccore.umn.edu) along with guidance on identification and suitability for radiocarbon dating.
Keywords
Radiocarbon dating Lake sediments Plant macrofossils Emergent aquatic plants Submerged aquatic plants Dissolved inorganic carbon (DIC)Notes
Acknowledgments
The authors gratefully acknowledge Dick Baker, Iowa State University, for gracious access to his plant macrofossil reference collection and imaging system; and to Jack Williams for suggesting the "Do not date" list. TMI and this work have been supported by NSF-EAR-1226265 and a University of Minnesota Interdisciplinary Informatics Seed Grant.
References
- Allen MF (1991) The ecology of mycorrhizae. Cambridge University Press, New York 184 pGoogle Scholar
- Bartkov BI, Zvereva G (1974) Raspredelenie assimiliatov v period plodonosheniya bobovykh rastenii. O printcipe dublirovaniya v fitosistemakh. Fiziol i Biokhimiya Kult. Rast. 6:502–505Google Scholar
- Birks HH (2002) Plant macrofossils. In: Smol JP, Birks HJB, Last WM (eds) Tracking Environmental Change Using Lake Sediments, vol 3., Terrestrial, Algal, and Siliceous IndicatorsKluwer Academic Publishers, Dordrecht, pp 49–74CrossRefGoogle Scholar
- Björck S, Wohlfarth B (2002) 14C chronostratigraphic techniques in paleolimnology. In: Smol JP, Birks HJB, Last WM (eds) Tracking Environmental Change Using Lake Sediments, vol 1., Basin Analysis, Coring, and Chronological TechniquesKluwer Academic Publishers, Dordrecht, pp 205–245CrossRefGoogle Scholar
- Brix H (1990) Uptake and photosynthetic utilization of sediment-derived carbon by Phragmites australis (Cav.) Trin. ex Steudel. Aquat Bot 38:377–389CrossRefGoogle Scholar
- Broecker WS, Orr PC (1958) Radiocarbon chronology of Lake Lahontan and Lake Bonneville. Geol Soc Am Bull 69:1009–1032CrossRefGoogle Scholar
- Bruni NC, Young JP, Dengler NC (1996) Leaf developmental plasticity of Ranunculus flabellaris in response to terrestrial and submerged environments. Can J Bot 74:823–837CrossRefGoogle Scholar
- Chivas AR, Garcia A, van der Kaars S, Couapel MJJ, Holt S, Reeves JM, Wheeler DJ, Switzer AD, Murray-Wallace CV, Banerjee D, Price DM, Wang SX, Pearson G, Edgar TN, Beaufort L, de Deckker P, Lawson E, Cecil CB (2001) Sea-level and environmental changes since the last interglacial in the Gulf of Carpentaria, Australia: an overview. Quat Int 83–85:19–46CrossRefGoogle Scholar
- Clarke JT, Warnock RCM, Donoghue PCJ (2011) Establishing a time-scale for plant evolution. New Phytol 192(266):301Google Scholar
- Cole JJ, Caraco NF (2001) Carbon in catchments: connecting terrestrial carbon losses with aquatic metabolism. Mar Environ Res 52:101–110Google Scholar
- Cole JJ, Caraco NF, Kling GW, Kratz TK (1994) Carbon dioxide supersaturation in the surface waters of lakes. Science 265:1568–1570CrossRefGoogle Scholar
- Colmer TD, Pedersen O (2008) Underwater photosynthesis and respiration in leaves of submerged wetland plants: gas films improve CO2 and O2 exchange. New Phytol 177:918–926CrossRefGoogle Scholar
- Constable JVH, Grace JB, Longstreth DJ (1992) High carbon dioxide concentrations in aerynchyma of Typha latifolia. Am J Bot 79:415–418CrossRefGoogle Scholar
- Cronk JK, Fennessy MS (2001) Wetland plants: biology and ecology. Lewis Publishers, Boca Raton, pp 7–12CrossRefGoogle Scholar
- Dacey JWH, Klug MJ (1979) Methane efflux from lake sediments through water lilies. Science 203:1253–1255CrossRefGoogle Scholar
- Dacey JWH, Klug MJ (1982) Tracer studies of gas circulation in Nuphar: 18O2 and 14CO2 transport. Plant Physiol 56:361–366CrossRefGoogle Scholar
- Damon PE, Haynes CV, Long A (1964) Arizona radiocarbon dates V. Radiocarbon 6:91–107Google Scholar
- Deevey ES, Gross MS, Hutchinson GE, Kraybill HL (1954) The natural C14 contents of materials from hard-water lakes. Geology 40:285–288Google Scholar
- Edwards KJ, Schofield JE, Kirby JR, Cook GT (2011) Problematic but promising ponds? Palaeoenvironmental evidence from the Norse Eastern Settlement of Greenland. J. Quat Sci 26:854–865CrossRefGoogle Scholar
- Frost-Christensen H, Sand-Jensen K (1995) Comparative kinetics of photosynthesis in floating and submerged Potamogeton leaves. Aquat Bot 51:121–134CrossRefGoogle Scholar
- Garbey C, Thiebaut G, Muller S (2004) Morphological plasticity of a spreading aquatic macrophyte, Ranunculus peltatus, in response to environmental variables. Plant Ecol 173:125–137CrossRefGoogle Scholar
- Geyh MA, Grosjean M, Núñez L, Schotterer U (1999) Radiocarbon reservoir effect and the timeng of the late-glacial/early Holocene phase in the Atacama Desert (northern Chile). Quat Res 52:143–153CrossRefGoogle Scholar
- Godwin H (1951) Comments on radiocarbon dating for samples from the British Isles. Am J Sci 249:301–307CrossRefGoogle Scholar
- Goslar T, van der Knaap WO, Hicks S, Andric M, Czernik J, Goslar E, Rasanen S, Hyotyla H (2005) Radiocarbon 47:115–134Google Scholar
- Grimm EC (2011) High-resolution age model based on AMS radiocarbon ages for Kettle Lake, North Dakota USA. Radiocarbon 53:39–53Google Scholar
- Hakansson S (1979) Radiocarbon activity in submerged plants from various south Swedish lakes. In: Berger R, and Suess HE (Eds) Radiocarbon dating: proceedings of the Ninth International Conference. University of California Press, pp 433–443Google Scholar
- Hakansson S (1982) University of Lund radiocarbon dates XV. Radiocarbon 24:194–213Google Scholar
- Harley JL, Smith SE (1983) Mycorrhizal symbiosis. Academic Press, New York 483 pGoogle Scholar
- Haynes CV, Damon PE, Grey DC (1966) Arizona radiocarbon dates VI. Radiocarbon 8:1–21Google Scholar
- Heikkinen A, Aikaa O (1977) Geological survey of Finland radiocarbon measurements VII. Radiocarbon 19:263–279Google Scholar
- Higuchi T, Yoda K, Tensho K (1984) Further evidence for gaseous CO2 transport in relation to root uptake of CO2 in rice plant: soil Sci. Plant Nutr 30:125–136CrossRefGoogle Scholar
- Hitchcock CL, Cronquist A, Ownbey M, Thompson JW (1969) Vascular plants of the Pacific Northwest. University of Washington Press, SeattleGoogle Scholar
- Hostrup O, Wiegleb G (1991) Anatomy of leaves of submerged and emergent forms of Littorella uniflora (L.) Ascherson. Aquat Bot 39:195–209CrossRefGoogle Scholar
- Hwang Y, Morris JT (1992) Fixation of inorganic carbon from different sources and its translocation in Spartina alterniflora Loisel. Aquat Bot 43:137–147CrossRefGoogle Scholar
- Keeley JE, Osmond CB, Raven JA (1984) Stylites, a vascular land plant without stomata absorbs CO2 via its roots. Nature 310:694–695CrossRefGoogle Scholar
- Kilian MR, Van Der Plicht J, Van Geel B (1995) Dating raised bogs: new aspects of 14C wiggle matching, a reservoir effect, and climatic change. Quat Sci Rev 14:959–966CrossRefGoogle Scholar
- Larcher W (2003) Physiological plant ecology. Springer, Berlin, pp 149–150CrossRefGoogle Scholar
- Longstreth DJ (1989) Photosynthesis and photorespiration in freshwater emergent and floating plants. Aquat Bot 34:287–299CrossRefGoogle Scholar
- Lowe JJ, Walker MJC, Scott EM, Harkness DD, Bryant CL, Davies SM (2004) A coherent high-precision radiocarbon chronology for the Late-glacial sequence at Sluggan Bog, Co., Antrim. North Irel J Quat Sci 19:147–158CrossRefGoogle Scholar
- Lucassen ECHET, Spierenburg P, Fraaije RGA, Smolders AJP, Roelofs JGM (2009) Alkalinity generation and sediment CO2 uptake influence establishment of Sparganium angustifolium in softwater lakes. Freshw Biol. 54:2300–2314CrossRefGoogle Scholar
- Maberly SC, Madsen TV (1998) Affinity for CO2 in relation to the ability of freshwater macrophytes to use HCO3 −. Func Ecol 12:99–106CrossRefGoogle Scholar
- Maberly SC, Madsen TV (2002) Freshwater angiosperm carbon concentrating mechanisms: processes and patterns. Func Plant Biol 29:393–405CrossRefGoogle Scholar
- Maberly SC, Spence DHN (1989) Photosynthesis and photorespiration in freshwater organisms: amphibious plants. Aquat Bot 34:267–286CrossRefGoogle Scholar
- MacDonald GM, Beukens RP, Kieser WE, Vitt DH (1987) Comparative radiocarbon dating of terrestrial plant macrofossils and aquatic moss from the “ice-free corridor” of western Canada. Geology 15:837–840CrossRefGoogle Scholar
- Madsen TV, Breinolt M (1995) Effects of air contact on growth, inorganic carbon sources, and nitrogen uptake by an amphibious freshwater macrophyte. Plant Physiol 107:149–154Google Scholar
- Marcenko E, Srdoc D, Golubic S, Pezdic J, Head MJ (1989) Carbon uptake in aquatic plants deduced from their natural 13C and 14C content. Radiocarbon 31:785–794Google Scholar
- Miller GH, Mode WN, Wolfe AP, Sauer PE, Bennike O, Forman SL, Short SK, Stafford TK (1999) Stratified interglacial lacustrine sediments from Baffin Island, Arctic Canada: chronology and paleoenvironmental implications. Quat Sci Rev 18:789–810CrossRefGoogle Scholar
- Mommer L, Visser EJW (2005) Underwater photosynthesis in flooded terrestrial plants: a matter of leaf plasticity. Ann Bot 96:581–589CrossRefGoogle Scholar
- Myrbo A, Shapley MD (2006) Seasonal water-column dynamics of dissolved inorganic carbon stable isotopic compositions (δ13CDIC) in small hardwater lakes in Minnesota and Montana. Geochim Cosmochim Acta 70:2699–2714CrossRefGoogle Scholar
- Myrbo A, Morrison A, and McEwan R (2011) Tool for microscopic identification (TMI). http://tmi.laccore.umn.edu. Accessed on 08 Nov 2013
- Nielsen SL (1993) A comparison of aerial and submerged photosynthesis in some Danish amphibious plants. Aquat Bot 45:27–40CrossRefGoogle Scholar
- Nielsen LT, Borum J (2008) Why the free floating macrophyte Stratiotes aloides mainly grows in highly CO2-supersaturated waters. Aquat Bot 89:379–384CrossRefGoogle Scholar
- Olsson IU (1980) Radiocarbon dating of material from different reservoirs. In: Suess HE, Berger R (eds) Radiocarbon dating. UCLA Press, San Diego, pp 613–618Google Scholar
- Olsson IU (1983) Dating non-terrestrial materials. In: Mook WG, and Waterbolk HT (Eds) Proceedings of the International Symposium 14C and Archaeology. PACT v 8, pp 277–294Google Scholar
- Olsson IU (2009) Radiocarbon dating history: early days, questions, and problems met. Radiocarbon 51:1–43Google Scholar
- Oswald WW, Anderson PM, Brown TA, Brubaker LB, Hu FS, Lozhkin AV, Tinner W, Kaltenrieder P (2005) Effects of sample mass and macrofossil type on radiocarbon dating of arctic and boreal lake sediments. Holocene 15:758–767CrossRefGoogle Scholar
- Prins HBA, De Guia MB (1986) Carbon source of the water soldier, Stratiotes aloides L. Aquat Bot 26:225–234CrossRefGoogle Scholar
- Raven JA (1984) Energetics and transport in aquatic plants. Alan R, LissGoogle Scholar
- Raven JA, Edwards D (2001) Roots: evolutionary origins and biogeochemical significance. J Exp Bot 52:381–401CrossRefGoogle Scholar
- Raven JA, Osbourne BA, Johnston AM (1985) Uptake of CO2 by aquatic vegetation. Plant Cell Environ 8:417–425CrossRefGoogle Scholar
- Raven JA, Handley LL, MacFarlane JJ, McInroy S, McKenzie L, Richards JH, Samuelsson G (1988) The role of CO2 uptake by roots and CAM in acquisition of inorganic C by plants of the isoetid life-form: a review, with new data on Eriocaulon decangulare L. New Phytol 108:125–148CrossRefGoogle Scholar
- Richardson K, Griffiths H, Reed ML, Raven JA, Griffiths NM (1984) Inorganic carbon assimilation in the isoetids, Isoetes lacustris L. and Lobelia dortmanna L. Oecologia 61:115–121CrossRefGoogle Scholar
- Robe WE, Griffiths H (1998) Adaptations for amphibious life: changes in leaf morphology, growth rate, carbon and nitrogen investment, and reproduction during adjustment to emersion by the freshwater macrophyte Littorella uniflora. New Phytol 140:9–23CrossRefGoogle Scholar
- Salvucci ME, Bowes G (1982) Photosynthetic and photorespiratory responses of aerial and submerged leaves of Myriophyllum brasiliense. Aquat Bot 13:147–164CrossRefGoogle Scholar
- Sand-Jensen K, Frost-Christensen H (1999) Plant growth and photosynthesis in the transition zone between land and stream. Aquat Bot 63:23–35CrossRefGoogle Scholar
- Sand-Jensen K, Pederson MF, Nielsen SL (1992) Photosynthetic use of inorganic carbon among primary and secondary water plants in streams. Freshwater Biol 27:283–293CrossRefGoogle Scholar
- Singer A, Eshel A, Agami M, Beer S (1994) The contribution of aerenchymal CO2 to the photosynthesis of emergent and submerged culms of Scirpus lacustris and Cyperus papyrus. Aquat Bot 49:107–116CrossRefGoogle Scholar
- Smits AJM, De Lyon MJH, Van Der Velde G, Steentjes PLM, Roelofs JGM (1988) Distribution of three nymphaeid macrophytes (Nymphaea alba L., Nuphar lutea (L.) Sm., and Nymphoides peltata (Gmel.) O. Kuntze) in relation to alkalinity and uptake of inorganic carbon. Aquat Bot 32:45–62CrossRefGoogle Scholar
- Spence DHN, Maberly SC (1985) Occurrence and ecological importance of HCO3 − use among aquatic higher plants. In: Lucas WJ, Berry JA (Eds) Inorganic carbon uptake by aquatic photosynthetic organisms, Proceedings of an International Workshop on Bicarbonate Use in Photosynthesis, pp 125–143Google Scholar
- Stoy V (1965) Photosynthesis, respiration and carbohydrate accumulation in spring wheat in relation to yield. Physiol Plant 4:1–125Google Scholar
- Tornqvist TE, De Jong AFM, Oosterbaan WA, Van Der Borg K (1992) Accurate dating of organic deposits by 14C measurement of macrofossils. Radiocarbon 34:566–577Google Scholar
- Turney CSM, Coope GR, Harkness DD, Lowe JJ, Walker MJC (2000) Implications for the dating of Wisconsian (Weichselian) late-glacial events of systematic radiocarbon age differences between terrestrial plant macrofossils from a site in SW Ireland: Quat Res 53: 114–121Google Scholar
- Vapaavuori EM, Pelkonen P (1985) HCO3 − uptake through the roots and its effect on the productivity of willow cuttings. Plant Cell Environ 8:531–534CrossRefGoogle Scholar
- Vuorinen AH, Vapaavuori EM, Lapinjoki S (1989) Time-course of uptake of dissolved inorganic carbon through willow roots in light and darkness. Physiol Plantarum 77:33–38CrossRefGoogle Scholar
- Wasylikowa K, Walanus A (2004) Timing of aquatic and marsh-plant successions in different parts of Lake Zeribar, Iran, during the Late Glacial and Holocene. Acta Palaeobot 44:129–140Google Scholar
- Weir CE, Dale HM (1960) A developmental study of wild rice, Zizania aquatica L. Can J Bot 38:719–741CrossRefGoogle Scholar
- Wetzel RG (1975) Limnology. Thomson Learning, Michigan 858 ppGoogle Scholar
- Wetzel RG, Brammer ES, Lindstrom K, Forsberg C (1985) Photosynthesis of submersed macrophytes in acidified lakes II. Carbon limitation and utilization of benthic CO2 sources. Aquat Bot 22:107–120CrossRefGoogle Scholar
- Winkel A, Borum J (2009) Use of sediment CO2 by submersed rooted plants. Ann Bot 103:1015–1023CrossRefGoogle Scholar
- Winkel A, Colmer TD, Pedersen O (2011) Leaf gas films of Spartina anglica enhance rhizome and root oxygen during tidal submergence. Plant Cell Environ 34:2083–2092CrossRefGoogle Scholar
- Wium-Andersen S (1971) Photosynthetic uptake of free CO2 by the roots of Lobelia dortmanna. Plant Physiol 25:245–248CrossRefGoogle Scholar