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Titel:Ecological effects of willow and poplar invasions at the Río Negro in northern Patagonia, Argentina
Autor:Thomas, Lisa
Weitere Beteiligte: Leyer, Ilona (Prof. Dr.)
Veröffentlicht:2015
URI:https://archiv.ub.uni-marburg.de/diss/z2015/0396
DOI: https://doi.org/10.17192/z2015.0396
URN: urn:nbn:de:hebis:04-z2015-03963
DDC: Biowissenschaften, Biologie
Titel (trans.):Ökologische Auswirkungen von invasiven Weiden und Pappeln am Río Negro in Nordpatagonien, Argentinien
Publikationsdatum:2015-11-30
Lizenz:https://rightsstatements.org/vocab/InC-NC/1.0/

Dokument

Schlagwörter:
Salix humboldtiana, floodplain forest, Biologie, succession, riparian landscapes, riparian vegetation, Invasion <Biologie>, Humboldt-Weide

Summary:
Species of the Salicaceae family, particularly Salix species and their hybrids, are typical invaders of river systems throughout the world with severe consequences for native ecosystems. Along Patagonian streams, riparian softwood forests structured by dominant invasive Salicaceae are increasing significantly in abundance, area and species diversity. The region of the Río Negro in northern Patagonia has been invaded by several woody plant species with a dramatical increase in the recent decades. The most dominant taxa are willows of the Salix alba L. - Salix fragilis L. complex, a hybrid of this complex and Salix babylonica L. and Populus spp. Additionally, Elaeagnus angustifolia Willd. and Tamarix spp. have been spreading aggressively in recent years. This thesis provides information on the possible consequences of these invasions for Salix humboldtiana Willd., the only native woody species along the Río Negro, due to interspecific competition and invasion development. Vegetative reproduction is especially for S. fragilis and its hybrids of great importance for the colonisation of new habitats and probably is the most important reason for their invasion success. In the first study (Chapter 2), a greenhouse experiment was conducted in order to assess the vegetative reproduction capacities of native and invasive Salicaceae (S. humboldtiana, S. × rubens Schrank, a S. babylonica hybrid and Populus spec.) under various soil composition and moisture gradients. The invasive willow hybrids showed better vegetative re-sprouting capacities and performed sinificantly better than S. humboldtiana and Populus spec. They developed more living cuttings as well as more and longer sprouts under all treatment combinations and they generated significantly higher above- and belowground biomass. After completely removing the shoot and root biomass of the cuttings re-sprouting capacities were evaluated in a second experiment. Again, the invasive willows had a superior re-sprouting ability and growth performance. These results demonstrate that invasive willows are able to establish more successfully by vegetative reproduction than the native willow and that they have a higher re-sprouting potential after disturbances. This ability in combination with the advantages of vegetative reproduction compared to generative reproduction seems to be the key factor for invasive success and, simultaneously, a potential threat for S. humboldtiana through out-competition. In a further approach (Chapter 3), age structure analyses were carried out which revealed that mixed adult forest stands are the results of joint establishment events with all Salicaceae taxa involved. The analysed 20 stands on islands had low mean ages <15 years. Investigation on growth performance (basal area, crown diameter, tree hight and crown base hight) of adult stands revealed that non-native willows and poplars are able to actively displace the native S. humboldtiana by competitive strength: A significant better growth performance with e.g. higher basal area and crown diameter was found for the non-native willows in adult life stage. Furthermore, adult S. humboldtiana was more frequent at the middle river stretch, while invasive willow hybrids showed an opposing pattern suggesting a downstream directed invasion process. In order to evaluate the competition potential of invasive alien woody plants (Salicaceae, Elaeagnus and Tamarix) for S. humboldtiana, habitat distribution models for different life stages (seedling, juvenile, adult) were developed (Chapter 4). The objective was to identify ecological niches and relationships between species occurrence and different abiotic factors. Data on species (presence/ absence) and explanatory environmental variables were gathered in the field on 167 plots using a grid-based, stratified-randomized sampling design. The environmental variables flood duration, the amount of gravel and the location (upper or middle river valley) proved to be the best explanatory variables to describe the occurrence of the species. For all life stages, a strong niche overlap could be observed for S. humboldtiana and invasive taxa, particularly Salicaceae, with no remaining exclusive habitat for the native willow. Additionally, investigations on vegetation change offer insights into invasion development (Chapter 5). Multispectral satellite images from the years 1986 and 2003 of the upper Río Negro were used to detect land cover changes. This study demonstrated that during this time period floodplain forests expanded considerably their distribution area by almost 150%, probably due to the explosive spread of non-native species. The results of this thesis can be summarized as follows: Invasive willows have significant better vegetative reproduction and re-sprouting capacities, better growth performances in the adult life stage and exhibit a strong niche overlap with the native willow species. These findings indicate a high competition potential of invasive Salicaceae with, consequently, a possible out-competition and suppression of S. humboldtiana.

Bibliographie / References

  1. Adair R, Sagliocco J-L, Bruzzese E (2006) Strategies for the biological control of invasive willows (Salix spp.) in Australia. Aust J Entomol 45:259–267.
  2. Holland-Clift S, O'Dowd DJ, Mac Nally R (2011) Impacts of an invasive willow (Salix × rubens) on riparian bird assemblages in south-eastern Australia. Austral Ecol 36:511–520.
  3. Chavez, PS (1996) Image-based atmospheric corrections revisited and improved. Photogramm Eng Rem S 62:1025-1036.
  4. Isebrands JG, Richardson J (2014) Poplars and Willows: Trees for Society and the Environment. CABI, Oxfordshire, UK
  5. Gut B (2008) Trees in Patagonia. Birkhäuser Verlag AG, Basel.
  6. Gut B (2008) Trees in Pataonia, 1 st ed. Birkhäuser, Basel
  7. Stohlgren TJ, Binkley D, Chong GW, et al (1999) Exotic plant species invade hot spots of native plant diversity. Ecol Monogr 69:25–46.
  8. Corenblit D, Steiger J, González E, et al (2014) The biogeomorphological life cycle of poplars during the fluvial biogeomorphological succession: a special focus on Populus nigra L. Earth Surf Process Landforms 39:546– 563. doi: 10.1002/esp.3515
  9. Hultine KR, Bush SE (2011) Ecohydrological consequences of non-native riparian vegetation in the southwestern United States: A review from an ecophysiological perspective. Water Resour Res. 47:W07542, doi: 10.1029/2010WR010317 References 127
  10. Gurnell A (2014) Plants as river system engineers. Earth Surf Process Landforms 39:4–25.
  11. Barsoum N (2002) Relative contributions of sexual and asexual regeneration strategies in Populus nigra and Salix alba during the first years of establishment on a braided gravel bed river. Evol Ecol 15:255–279.
  12. Moggridge H, Gurnell A (2009) Controls on the sexual and asexual regeneration of Salicaceae along a highly dynamic, braided river system. Aquat Sci 71:305–317. References 128
  13. Shah JJF, Harner MJ, Tibbets TM (2010) Elaeagnus angustifolia Elevates Soil Inorganic Nitrogen Pools in Riparian Ecosystems. Ecosystems 13:46-61.
  14. Mineau M, Baxter C, Marcarelli A (2011) A non-native riparian tree (Elaeagnus angustifolia) changes nutrient dynamics in streams. Ecosystems 14:353–365.
  15. Renöfält BM, Jansson R, Nilsson C (2005) Spatial patterns of plant invasiveness in a riparian corridor. Landsc Ecol 20:165–176.
  16. Stokes KE (2008) Exotic invasive black willow (Salix nigra) in Australia: influence of hydrological regimes on population dynamics. Plant Ecol 197:91–105.
  17. Akasheh OZ, Neale CMO, Jayanthi, H. (2008) Detailed mapping of riparian vegetation in the middle Rio Grande River using high resolution multi-spectral airborne remote sensing. J Arid Environ 72:1734-1744.
  18. Natale E, Zalba SM, Oggero A, Reinoso H (2010) Establishment of Tamarix ramosissima under different conditions of salinity and water availability: Implications for its management as an invasive species. J Arid Environ 74:1399–1407.
  19. Speziale KL, Ezcurra C (2011) Patterns of alien plant invasions in northwestern Patagonia, Argentina. J Arid Environ 75:890–897.
  20. Friedl MA, Brodley CE (1997) Decision tree classification of land cover from remotely sensed data. Remote Sens Environ 61:399-409.
  21. Kolar CS, Lodge DM (2001) Progress in invasion biology: predicting invaders. Trends Ecol Evol 16:199–204.
  22. Tockner K, Stanford JA (2002) Riverine flood plains: present state and future trends. Environ Conserv 29:308– 330.
  23. Speziale K, Lambertucci S (2010) A call for action to curb invasive species in South America. Nature 467:153.
  24. Karrenberg S, Edwards PF, Kollmann J (2002) The life history of Salicaceae living in the active zone of flood plains. Freshw Biol 47:733-748.
  25. Planty-Tabacchi AM, Tabacchi E, Naiman RJ, et al (1996) Invasibility of species-rich communities in riparian zones. Conserv Biol 10:598–607.
  26. Karrenberg S, Kollmann J, Edwards PJ, et al (2003b) Patterns in woody vegetation along the active zone of a near- natural Alpine river. Basic Appl Ecol 4:157–166.
  27. Goettlicher D, Obregon A, Homeier J, Rollenbeck R, Nauss T, Bendix J (2009) Land-cover classification in the Andes of southern Ecuador using Landsat ETM plus data as a basis for SVAT modelling. Int J Remote Sens 30:1867-1886.
  28. Beismann H, Wilhelmi H, Baillères H, et al (2000) Brittleness of twig bases in the genus Salix: fracture mechanics and ecological relevance. J Exp Bot 51:617–33.
  29. Richardson DM, Rejmánek M (2011) Trees and shrubs as invasive alien species -a global review. Divers Distrib 17:788–809.
  30. Mack RN, Simberloff D, Lonsdale WM, et al (2000) Biotic invasions: causes, epidemiology, global consequences, and control. Ecol Appl 10:689–710.
  31. Sher AA, Marshall DL, Taylor JP (2002) Establishment patterns of native Populus and Salix in the presence of invasive nonnative Tamarix. Ecol Appl 12:760-772.
  32. Friedman JM, Lee VJ (2002) Extreme floods, channel change, and riparian forests along ephemeral streams. Ecol Monogr 72:409–425.
  33. Civille JC, Sayce K, Smith SD, Strong DR (2005) Reconstructing a century of Spartina alterniflora invasion with historical records and contemporary remote sensing. Ecoscience 12:330-338.
  34. Thomas LK, Tölle L, Ziegenhagen B, Leyer I (2012) Are Vegetative Reproduction Capacities the Cause of Widespread Invasion of Eurasian Salicaceaein Patagonian River Landscapes? PLoS ONE 7, doi10.1731/journal.pone.0050652.
  35. Vilà M, Espinar JL, Hejda M, Hulme PE, Jarošík V, Maron JL, Pergl J, Schaffner U, Sun Y, Pyšek P. (2011) Ecological impacts of invasive alien plants: a meta-analysis of their effects on species, communities and ecosystems. Ecol Lett 14:702–708.
  36. Vilà M, Ibanez I (2011) Plant invasions in the landscape. Landscape Ecol 26:461-472.
  37. Parolin P, Oliveira AC, Piedade MTF, et al (2002) Pioneer trees in Amazonian floodplains: three key species form monospecific stands in different habitats. Folia Geobot 37:225–238.
  38. Speziale K, Carrete M, Lambertucci S, Tella JL (2012) Dealing with non-native species: what makes the difference in South America? Biol Invasions 14:1609–1621.
  39. Albright TP, Ode DJ (2011) Monitoring the dynamics of an invasive emergent macro-phyte community using operational remote sensing data. Hydrobiologia 661:469-474.
  40. Serra MN, Albariño R, Díaz Villanueva V (2013) Invasive Salix fragilis alters benthic invertebrate communities and litter decomposition in northern Patagonian streams. Hydrobiologia 701:173–188.
  41. Garau AM, Caccia FD, Guarnaschelli AB (2008) Impact of standing vegetation on early establishment of willow cuttings in the flooded area of the Parana River Delta (Argentina). New For 36:79–91.
  42. Casco SL, Neiff JJ, Neiff AP (2010) Ecological responses of two pioneer species to a hydrological connectivity gradient in riparian forests of the lower Paraná River. Plant Ecol 209:167–177.
  43. Thomas LK, Leyer I (2012) Age structure, growth performance and composition of native and invasive Salicaceae in Patagonia. Plant Ecol 215:1045-1056.
  44. Stohlgren T, Bull K, Otsuki Y, et al (1998) Riparian zones as havens for exotic plant species in the central grasslands. Plant Ecol 138:113–125.
  45. Zalba, SM, Villamil, CB (2002) Woody Plant Invasion in Relictual Grasslands. Biol Invasions 4:55-72. References References
  46. Peri PL, Bloomberg M (2002) Windbreaks in southern Patagonia, Argentina : A review of research on growth models, windspeed reduction, and effects on crops. Agrofor Syst 56:129–144.
  47. Katz GL, Shafroth PB (2003) Biology, ecology and management of Eleagnus angustifolia L. (Russian Olive) in Western North America. Wetlands 23:763–777.
  48. Decant JP (2008) Russian Olive, Elaeagnus angustifolia, Alters Patterns in Soil Nitrogen Pools Along the Rio Grande River, New Mexico, USA. Wetlands 28:896-904.
  49. Cohen J (1960) A Coefficient of Agreement for Nominal Scales. Educational and Psychological Measurement 20:37-46.
  50. Ayesa JA, López CR, Bran DE, Umaña FJ, Lagorio PA (2002) Cartografia biofísica de la Patagonia norte. INTA Bariloche, San Carlos de Bariloche, Argentina.
  51. Ares A, Nacional U, Palihue A (2002) Changes through time in traits of poplar clones in selection trials. New For 23:105–119.
  52. Naumann M (1996) Das nordpatagonische Seengebiet Nahuel Huapi (Argentinien). Biogeographische Struktur, Landnutzung seit dem 17. Jahrhundert und aktuelle Degradationsprozesse. University of Marburg, Marburger Geographische Schriften, Heft 131
  53. Reynolds L V, Cooper DJ, Hobbs NT (2014) Drivers of riparian tree invasion on a desert stream. River Res Appl 30:60–70.
  54. Borodowski ED, Suárez RO (2004) El cultivo de álamos y sauces: su historia en el Delta del Paraná. SAGPyA For 32:5–13.
  55. Correa MN (1984) Flora Patagonica -Dicotyledones dialipétalas (Salicaceae a Cruciferae), Colección científica del INTA, Buenos Aires References 126
  56. Catford JA, Downes BJ, Gippel CJ, Vesk PA (2011) Flow regulation reduces native plant cover and facilitates exotic invasion in riparian wetlands. J Appl Ecol 48:432–442.
  57. Datri LA, Paramo F, Canzutti A, Guichal A (2010) Fluctuaciones de la racionalidad económica y cambios en el neoecosistema de la confluencia de los ríos Limay y Neuquén. In: Cambios de uso de la tierra. Causas, consecuencias y mitigación, Revista de la Asociación Argentina de Ecología de Paisajes 1:143-158. Asociación Argentina de Ecología de Paisajes.
  58. Bendix J, Hupp CR (2000) Hydrological and geomorphological impacts on riparian plant communities. Hydrol Process 14:2977–2990.
  59. Justice CO, Townshend JRG (1981) Integrating ground data with remote sensing. Terrain Analysis and Remote Sensing (ed J. R. G. Townshend), pp. 38-58. Allen & Unwin, London.
  60. Reinhart KO, Gurnee J, Tirado R, Callaway RM (2006) Invasion through quantitative effects: Intense shade drives native decline ans invasive success. Ecol Appl 16:1821–1831.
  61. Hauman L, Burkhart A, Parodi LR, Cabrera AL (1947) La vegetation de la Argentina. Sociedad argentina de estudios geograficos, Buenos Aires
  62. Rouse JW, Haas RH, Schell JA, Deering DW (1973) Monitoring Vegetation Systems in the Great Plains with ERTS. 3rd ERTS Symposium 1:48-62.
  63. Guisan A, Zimmermann NE (2000) Predictive habitat distribution models in ecology. Ecol Modell 135:147–186.
  64. Liotta J (2001) Rasgos biológicos de Salix humboldtiana Willd. y régimen de pulso de inundación. Interciencia 26:397–403.
  65. Cushing CE, Cummins KW, Minshall GW (2006) River and Stream Ecosystems of the World. University of California Press, Berkeley and Los Angeles, California
  66. Hunziker JH (1992) The Origin of the Hybrid Triploid Willows Cultivated in Argentina. Silvae Genet 11:151–153.
  67. Lamarque LJ, Delzon S, Lortie CJ (2011) Tree invasions: a comparative test of the dominant hypotheses and functional traits. Biol Invasions 13:1969–1989.
  68. Budde KB, Gallo L, Marchelli P, Mosner E, Liepelt S, Ziegenhagen B, Leyer I (2011) Wide spread invasion without sexual reproduction? A case study on European willows in Patagonia, Argentina. Biol Invasions 13:45- 54.
  69. Stromberg JC, Lite SJ, Dixon MD (2010) Effects of stream flow patterns on riparian vegetation of a semiarid river: implications for a changing climate. River Res Appl 26:712–729.
  70. Asaeda T, Gomes PIA, Sakamoto K, Rashid H (2011) Tree colonization trends on a sediment bar after a major flood. River Res Appl 27:976–984.
  71. Hughes FMR, Adams WM, Muller E, et al (2001) The importance of different scale processes for the restoration of floodplain woodlands. Regul Rivers Res Manag 17:325–345.
  72. Ward JV, Tockner K, Arscott DB, Claret C (2002) Riverine landscape diversity. Freshw Biol 47:517-539.
  73. Karrenberg S, Blaser S, Kollmann J, et al (2003a) Root anchorage of saplings and cuttings of woody pioneer species in a riparian environment. Funct Ecol 17:170–177.
  74. Giljohann KM, Hauser CE, Williams NSG, Moore JL (2011) Optimizing invasive species control across space: willow invasion management in the Australian Alps. J Appl Ecol 48:1286–1294.
  75. Richardson DM, Holmes PM, Esler KJ, et al (2007) Riparian vegetation: degradation, alien plant invasions, and restoration prospects. Divers Distrib 13:126–139.
  76. Van Splunder I, Coops H, Voesenek LACJ, Blom CWPM (1995) Establishment of alluvial forest species in floodplains: the role of dispersal timing, germination characteristics and water level fluctuations. Acta Bot Neerl 44:269–278.
  77. Gallien L, Douzet R, Pratte S, Zimmermann NE, Thuiller, W (2012) Invasive species distribution models – how violating the equilibrium assumption can create new insights. Glob Ecol Biogeogr 21:1126–1136.
  78. Shafroth PB, Beauchamp VB, Briggs MK, et al (2008) Planning Riparian Restoration in the Context of Tamarix Control in Western North America. Restor Ecol 16:97–112. References 129
  79. Stromberg JC, Chew MK, Nagler PL, Glenn EP (2009) Changing Perceptions of Change: The Role of Scientists in Tamarix and River Management. Restor Ecol 17:177–186.
  80. Datri LA, Maddio R. (2008) Geometrías fluviales en la definición del daisaje de la Colonia Valentina sur (Neuquén) y balsa Las Perlas (Río Negro). Calidad de vida 5:141-157.
  81. Karrenberg S, Suter M (2003) Phenotypic trade-offs in the sexual reproduction of Salicaceae from flood plains. Am J Bot 90:749–754.
  82. Leyer I (2006) Dispersal, diversity and distribution patterns in pioneer vegetation: The role of river-floodplain connectivity. J Veg Sci 17:407-416.
  83. Kollmann J, Vieli M, Edwards PJ, et al (1999) Interactions between vegetation development and island formation in the Alpine river Tagliamento. Appl Veg Sci 2:25–36.
  84. Baker HG (1974) The evolution of weeds. Annu Rev Ecol Syst 5:1–24.
  85. Selequist CA, Scott ML, Auble GT (1993) Establishment of Populus deltoides under simulated alluvial groundwater declines. Am Midl Nat 130:274–285.
  86. Shafroth PB, Scott ML, Friedman JM, Laven RD (1994) Establishment, Sex Structure and Breeding System of An Exotic Riparian Willow, Salix x rubens. Am Midl Nat 132:159-172.
  87. Naiman R, Décamps H (1997) The ecology of interfaces: riparian zones. Annu Rev Ecol Syst 28:621–658.
  88. Di Tomaso JM (1998) Impact, biology, and ecology of saltcedar (Tamarix spp.) in the Southwestern United States. Weed Technol 12:326–336.
  89. Pyšek P, Richardson DM, Rejmánek M, et al (2004) Alien plants in checklists and floras : towards better communication between taxonomists and ecologists. Taxon 53:131–143.
  90. Huang CY, Asner GP (2009) Applications of Remote Sensing to Alien Invasive Plant Studies. Sensors 9:4869-4889.
  91. Argus GW (1974) An experimental study of hybridization and pollination in Salix (willow). Can J Bot 52:1613– 1619.
  92. Braatne JH, Jamieson R, Gill M, Rood SB (2007) Instream flows and the decline of riparian cottonwoods along the Yakima River, Washington, USA. River Res Applic 23:247–267.
  93. Thiebault J (1998) Nuclear DNA amount in pure species and hybrid willows (Salix): a flow cytrometric investigation. Can J Bot 76:157–165.
  94. Baldi G, Paruelo JM (2008) Land-Use and Land Cover Dynamics in South American Temperate Grasslands. Ecol Soc 13.
  95. Barbosa FG, Schneck F, Melo AS (2012) Use of ecological niche models to predict the distribution of invasive species: a scientometric analysis. Braz J Biol 72:821–829.
  96. Natale ES, Tamarix E, Gaskin J, et al (2008) Especies del género Tamarix (Tamaricaceae) invadiendo ambientes naturales y seminaturales en Argentina Introducción. Bol Soc Argent Bot 43:137–146.
  97. Hupp CR, Osterkamp WR (1996) Riparian vegetation and fluvial geomorphic processes. Geomorphology 14:277– 295.
  98. Klich MG (2000) Leaf variations in Elaeagnus angustifolia related to environmental heterogeneity. Environ Exp Bot 44:171–183.
  99. Glenn EP, Nagler PL (2005) Comparative ecophysiology of Tamarix ramosissima and native trees in western US riparian zones. J Arid Environ 61:419-446.
  100. Abd El-Kawy OR, Rod JK, Ismail HA, Suliman AS (2011) Land use and land cover change detection in the western Nile delta of Egypt using remote sensing data. Appl Geogr 31:483-494.
  101. Osterkamp WR, Hupp CR (2010) Fluvial processes and vegetation — Glimpses of the past, the present, and perhaps the future. Geomorphology 116:274–285.
  102. Diaz B, Murace M, Peri P, et al (2003) Natural and preservative-treated durability of Populus nigra cv Italica timber grown in Santa Cruz Province, Argentina. Int Biodeterior Biodegradation 52:43–47.
  103. Glova GJ, Sagar PM (1994) Comparison of Fish and Macroinvertebrate Standing Stocks in Relation to Riparian Willows (Salix spp.) in 3 New-Zealand Streams. N Z J Mar Freshw Res 28:255-266.
  104. Lester PJ, Mitchell SF, Scott D (1994) Effects of riparian willow trees (Salix fragilis) on macroinvertebrate densities in two small Central Otago , New Zealand , streams. New Zeal J Mar Freshw Res 28:267–276.
  105. Henderson L (1991) Alien Invasive Salix spp. (Willows) in the Grassland Biome of South Africa. S Afr For J 157:91-95.
  106. Hansen MC, Defries RS, Townshend JRG, Sohlberg R (2000) Global land cover classification at 1km spatial resolution using a classification tree approach. Int J Remote Sens 21:1331-1364.
  107. Singh, A (1989) Digital Change Detection Techniques Using Remotely-Sensed Data. Int J Remote Sens 10:989-03.
  108. Steiger J, Tabacchi E, Dufour S, et al (2005) Hydrogeomorphic processes affecting riparian habitat within alluvial channel-floodplain river systems: a review for the temperate zone. River Res Appl 21:719–737.
  109. Francis RA, Gurnell AM (2006) Initial establishment of vegetative fragments within the active zone of a braided gravel-bed river (River Tagliamento, NE Italy). Wetlands 26:641–648.


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