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Catastrophic Dieback of Cyperus Papyrus in Response to Geochemical Changes in an East Mediterranean Altered Wetland

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Abstract

Catastrophic vegetation dieback is a common phenomenon that has occurred in many wetland habitats worldwide. Different mechanisms have been proposed to explain these occurrences. We tested two published models proposed as potential mechanisms for the catastrophic dieback of Cyperus papyrus in the Hula Nature Reserve (HNR), Israel. Sulfide toxicity and P limitation models were tested using lysimeters. The sulfide toxicity was tested by redox-suppression simulation, while the P deficiency was evaluated using N/P ratio index. The sulfide toxicity model was not accepted as a viable mechanism because papyrus stands did not show any sign of stress, even when growing with sulfide concentration threefold that reported during the cattail dieback in a nearby wetland or values reported in the literature. The P limitation model was not supported by the N/P index that indicated N limitation rather than P limitation. Next, we tested two alternative mechanisms that link the dieback to N cycles and depletion in the HNR system or to a sequential stressor cascade that caused major N limitation. We concluded that the N deficiency hypothesis is a better explanation for the observed dieback and the current health status of C. papyrus in this East Mediterranean ecosystem.

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References

  • APHA (2000) Standard methods for the examination of water and wastewater, 31st edn. American Public Health Association, Washington DC

    Google Scholar 

  • Armstrong J, Armstrong W (2001) An overview of the effects of phytotoxins on Phragmites australis in relation to die-back. Aquatic Botany 69:251–268

    Article  CAS  Google Scholar 

  • Armstrong J, Armstrong W, Van der Putten WH (1996a) Phragmites die-back: bud and root death, blockages within the aeration and vascular systems and the possible role of phytotoxins. New Phytology 133:399–414

    Article  CAS  Google Scholar 

  • Armstrong J, Afreen-Zobayed F, Armstrong W (1996b) Phragmites die-back: sulphide- and acetic acid-induced bud and root death, lignifications, and blockages with the aeration and vascular systems. New Phytology 134:601–614

    Article  CAS  Google Scholar 

  • Ashkenazi S, Markel D, Kaplan D (1999) The catastrophic decline of cattail Typha domingensis in Lake Agmon: possible mechanisms and remedial measures. Journal Mediterranean Ecology 1:85–100

    Google Scholar 

  • Avisar D, Fox A (2006) Chemical evolution and vegetation response in an altered wetland ecosystem, Hula Valley, Israel (1988–2004). Final report submitted to Hula Nature Reserve

  • Bakker C, de Graaf HF, Ernst WHO, van Bodegom PM (2005) Does the seed bank contribute to restoration of species rich vegetation in wet dune slacks? Applied Vegetation. Science 8:39–48

    Google Scholar 

  • Boar RR, Harper DM, Adams CS (1999) Biomass allocation in Cyperus papyrus in a tropical wetland, Lake Naivasha, Kenya. Biotropica 31(3):411–421

    Article  Google Scholar 

  • Chapin FS III (1980) The mineral nutrition of wild plants. Annual Review Ecological System 11:233–260

    Article  CAS  Google Scholar 

  • Davis SM, Ogden JC (1994) Everglades: the ecosystem and its restoration. St. Lucie Press, Delray Beach

    Google Scholar 

  • Department of Agriculture (1986) The Hula: a soil survey report (in Hebrew). Israel Ministry of Agriculture/Water Commissioner, Dept Soil Conservation and Drainage, Lake Kinneret Authority, Zemach

    Google Scholar 

  • Deverel SL, Wang B, Rojstaczer S (1998) Subsidence of organic soils, Sacramento-San Joaquin delta, California. In: Borchers JW (ed) Land subsidence case studies and current research, special publication no. 8. Denver: Association of Engineering Geologists, pp 489–502

  • Dimentman C, Bromley HJ, Por FD (1992) Lake Hula: Reconstruction of the fauna and hydrobiology of a lost lake. The Israel Academy of Sciences and Humanities, Jerusalem

    Google Scholar 

  • Dixon JB (1989) In: Weed SB (ed) Minerals in soil environments, 2nd edn. Soil Sci Soc Am, Madison, Wisconsin, USA, pp 305–308

  • Erwin KL (2009) Wwetlands and global climate change: the role of wetland restoration in a changing world. Wetlands Ecological Management 17:71–84

    Article  Google Scholar 

  • Gale PM, Reddy KR, Graetz DA (1995) Phosphorus retention by wetland soils used for treated wastewater disposal. Journal of Environmental Quality 23:370–377

    Article  Google Scholar 

  • Ganzert C, Pfadenhauer J (1986) Seasonal dynamics of shoot nutrients in Schoenus ferrugineus (Cyperaceae). Holarctic Ecology 9:137–142

    Google Scholar 

  • Geurts JM, Sarneel JM, Willers BJC, Roelofs JGM, Verhoeven JTA, Lamers LPM (2009) Interacting effects of sulphate pollution, sulphide toxicity and eutrophication on vegetation development in fens: a mesocosm experiment. Environmental Pollution 157(7):2072–2081

    Article  PubMed  CAS  Google Scholar 

  • Golan R (2009) Biogeochemical performance of the Hula Nature Reserve system. Report GSI/08/2009 (In Hebrew with English summary). The Ministry of National Infrastructures, Geological Survey of Israel, Jerusalem, Israel

  • Galatowitsch SM, van der Valk AG (1996) Vegetation and environmental conditions in recently restored wetlands in the prairie pothole region of the USA. Vegetatio 126:89–99

    Google Scholar 

  • Gophen M (2000) Nutrient and plant dynamics in Lake Agmon Wetlands (Hula Valley, Israel): a review with emphasis on Typha domingensis (1994–1999). Hydrobiologia 441:25–36

    Article  Google Scholar 

  • Gorsuch TT (1976) Dissolution of organic matter. In: LaFluer PD (ed) Accuracy in trace analysis. sampling, sample handling, analysis, vol 1, special publication 422. National Bureau of Standards, Washington DC, pp 491–508

    Google Scholar 

  • Güsewell S, Koerselman W (2002) Variation in nitrogen and phosphorus concentrations of wetland plants. Plant Ecology, Evolution and Systematics 5(1):37–61

    Article  Google Scholar 

  • Güsewell S, Koerselman W, Verhoeven JTA (2003) Biomass N:P ratios as indicators of nutrient limitation for plant populations in wetlands. Journal of Applied Ecology 13:372–384

    Article  Google Scholar 

  • Gustafsson JP (2009) Visual MINTEQ, Version 2.61. Department of Land and Water Resources Engineering, KTH, Stockholm

    Google Scholar 

  • Harper DM, Mavuti KM (2004) Lake Naivasha, Kenya: ecohydrology to guide the management of a tropical protected area. Ecohydrology and Hydrobiology 4:287–305

    Google Scholar 

  • Holden J, Burt TP (2003) Hydrological studies on blanket peat: the significance of the acrotelm-catotelm model. Journal of Ecology 91:86–102

    Article  Google Scholar 

  • Jones MB, Muthuri FM (1985) The canopy structure and microclimate of papyrus (Cyperus papyrus) swamps. Journal of Ecology 73:481–491

    Article  Google Scholar 

  • Kansiime F, Saunders MJ, Loiselle SA (2007) Functioning and dynamics of wetland vegetation of Lake Victoria: an overview. Wetlands Ecological Management 15:443–451

    Article  Google Scholar 

  • Keddy PA (2002) Wetland ecology, 2nd edn. Cambridge University Press, New York

    Google Scholar 

  • Koch MS, Mendelsshon IA, McKee KL (1990) Mechanism for the hydrogen sulfide-induced growth limitation in wetland macrophytes. Limnology and Oceanography 35:399–408

    Article  CAS  Google Scholar 

  • Koch MS, Schopmeyer SA, Nielsen OI, Kyhn-Hansen C, Madden CJ (2007) Conceptual model of seagrass die-off in Florida Bay: links to biogeochemical processes. Journal of Experimental Marine Biology and Ecology 350:73–88

    Article  CAS  Google Scholar 

  • Koerselman W, Meuleman AFM (1996) The vegetation N:P ratio: a new tool to detect the nature of nutrient limitation. Journal of Applied Ecology 33:1441–1450

    Article  Google Scholar 

  • Li S, Mendelssohn IA, Chen H, Orem WM (2009) Does sulphate enrichment promote the expansion of Typha domingensis (cattail) in the Florida Everglades? Freshwater Biology 54:1909–1923

    Article  CAS  Google Scholar 

  • Lindsay WL (1979) Chemical equilibria in soils. Wiley, New York

    Google Scholar 

  • Macek P, Rejmánková E, Lepš J (2010) Dynamics of Typha domingensis spread in Eleocharis dominated oligotrophic tropical wetlands following nutrient enrichment. Evolutionary Ecology 24:1505–1519

    Article  Google Scholar 

  • Marlies EW, van der Welle J, Roelofs GM, Lamers PM (2008) Multi-level effects of sulphur–iron interactions in freshwater wetlands in The Netherlands. Science of the Total Environment 406:426–429

    Article  Google Scholar 

  • Markel D, Sas E, Lazar B, Bein A (1998) Biogeochemical evolution of a sulfur-iron rich aquatic system in reflooded wetland environment (Lake Agmon, northern Israel). Wetlands Ecological Management 6:103–120

    Article  CAS  Google Scholar 

  • Marschner H (1995) Mineral nutrition of higher plants, 2nd edn. Academic, London

    Google Scholar 

  • Mendelssohn IA, McKee KL (1988) Spartina alternifloradie-back in Louisiana: time-course investigation of soil waterlogging effects. Journal of Ecology 76:509–521

    Article  Google Scholar 

  • Mitsch WJ, Gosselink JG (2000) Wetlands, 3rd edn. Van Nostrand Reinhold, New York

    Google Scholar 

  • Montegrossi G, Tassi F, Vasellia O, Bidini E, Minissale A (2006) A new, rapid and reliable method for the determination of reduced sulphur (S2−) species in natural water discharges. Applied Geochemistry 21(5):849–857

    Article  CAS  Google Scholar 

  • Moran R (1982) Formulation for determination of chlorophyllous pigments extracted with N, N-dimethylformamide. Plant Physiology 69:1376–1381

    Article  PubMed  CAS  Google Scholar 

  • Murphy J, Riley JP (1962) A modified single solution method for determination of phosphate in natural waters. Analytica Chimica Acta 27:31–36

    Article  CAS  Google Scholar 

  • Muthuri FM, Jones MB (1997) Nutrient distribution in a papyrus swamp: Lake Naivasha, Kenya. Aquatic Botany 56:35–50

    Article  CAS  Google Scholar 

  • Pezeshki SR, Pan SZ, DeLaune RD, Patrick WH Jr (1988) Sulfide-induced toxicity: inhibition of carbon assimilation in Spartina alterniflora. Photosynthetica 22:437–442

    CAS  Google Scholar 

  • Qualls RG, Richardson CJ (2000) Phosphorus enrichment affects litter decomposition, immobilization, and soil microbial phosphorus in wetland mesocosms. Soil Science Society of America Journal 64:799–808

    Article  CAS  Google Scholar 

  • Richardson CJ (1985) Mechanisms controlling phosphorus retention capacity in freshwater wetlands. Science 228:1424–1426

    Article  PubMed  CAS  Google Scholar 

  • Richardson CJ, Reiss P, Hussain NA, Alwash AJ, Pool DJ (2005) The restoration potential of the Mesopotamian marshes of Iraq. Science 307:1307–1311

    Article  PubMed  CAS  Google Scholar 

  • Romero JA, Brix H, Comin FA (1999) Interactive effects of N and P on growth, nutrient allocation and NH4 uptake kinetics by Phragmites australis. Aquatic Botany 64:369–380

    Article  CAS  Google Scholar 

  • Sederias J, Colman B (2009) Inhibition of Chara vulgaris oospore germination by sulfidic sediments. Aquatic Botany 91:273–278

    Article  CAS  Google Scholar 

  • Sharpley AN, Rekolainen S (1997) Phosphorus in agriculture and its environmental implications. In: Tunney H et al (eds) Phosphorus loss from soil to water. CAB International, Wallingford, pp 1–53

    Google Scholar 

  • SPSS (2002) SigmaPlot 2002 for Windows, version 17. SPSS, Chicago

    Google Scholar 

  • Stephens JC, Allen LH, Chen A (1984) Organic soil subsidence. Reviews in Engineering Geology 6:107–122

    Article  Google Scholar 

  • Stookey LL (1970) Ferrozine—a new spectrophotometric reagent for iron. Analytical Chemistry 42(7):779–781

    Article  CAS  Google Scholar 

  • Sutula M, Day JW, Cable J, Rudnick D (2001) Hydrological and nutrient budgets of freshwater and estuarine wetlands of Taylor Slough in Southern Everglades, Florida (USA). Biogeochemistry 56:287–310

    Article  Google Scholar 

  • Tsipris J, Meron M (1998) Climatic and hydrological aspects of the Hula restoration project. Wetlands Ecology and Management 6:91–100

    Article  Google Scholar 

  • Tunney H, Carton OT, Brooks PC, Johnston AE (1997) Phosphorus loss from soil and water. CAB International, New York

    Google Scholar 

  • Tylova-Munzarova E, Lorenzen B, Brix H, Votrubova O (2005) The effects of NH4+ and NO3− on growth, resource allocation and nitrogen uptake kinetics of Phragmites australis and Glyceria maxima. Aquatic Botany 81:326–342

    Article  CAS  Google Scholar 

  • van Eck WH, van de Steeg JM, Blom HM, de Kroon H (2004) Is tolerance to summer flooding corre-lated with distribution patterns in river floodplains? A comparative study of 20 terrestrial grassland species. Oikos 107:393–405

    Article  Google Scholar 

  • Van Bodegom PM, Grootjans AP, Sorrell BK, Bekker RM, Bakker C, Ozinga WA (2006) Plant traits in response to raising groundwater levels in wetland restoration: Evidence from three case studies. Applied Vegetation Science 9:251–260

    Google Scholar 

  • Venterink OH, Wassen JM, Verkroost AWM, Ruiter PC (2003) Species richness-productivity patterns differ between N-, P-, and K-limited wetlands. Ecology 84(8):2191–2199

    Article  Google Scholar 

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Acknowledgments

This research was partially supported by the Israeli National Park Authority. Further support was given by the GLOWA-Jordan River Project funded by the German Ministry of Science and Education (BMBF), in collaboration with the Israeli Ministry of Science and Technology (MOST).

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Correspondence to M. Iggy Litaor.

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Simhayov, R., Litaor, M.I., Barnea, I. et al. Catastrophic Dieback of Cyperus Papyrus in Response to Geochemical Changes in an East Mediterranean Altered Wetland. Wetlands 33, 747–758 (2013). https://doi.org/10.1007/s13157-013-0434-9

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  • DOI: https://doi.org/10.1007/s13157-013-0434-9

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