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Mycorrhizal presentation, Megan McLin, Hubbard Brook REU talks

  1. The effect of nitrogen on mycorrhizal colonization associated with Populus grandidentata Megan McLin Bartlett Experimental Forest MELNHE Project
  2. Bartlett, NH
  3. The MELHNE project -studying N and P acquisition and limitation through a series of nutrient manipulations in northern hardwood forests
  4. Mycorrhizal Fungi
  5. Background: Mycorrhiza the root fungus • Symbiotic Fungi • Crucial link between root system and soil • Creates surface area • Releases enzymes in soil to to break down nutrients Egli, S.; Brunner, I. (2011): Mykorrhiza. Eine faszinierende Lebensgemeinschaft im Wald. 3. Aufl. Merkbl. Prax. 35 8 S
  6. Nitrogen Deposition
  7. Nitrogen Deposition: Questions? • Will nitrogen exceed the nutritional needs of the ecosystem causing a decrease in mycorrhizal abundance? • Studies have shown that ecosystems have been susceptible to decline in response to nitrogen deposition. (Bevege, 102)
  8. Arbuscular vs Ecto Mycorrhizae
  9. Arbuscular vs Ecto Mycorrhizae • Ecto can be seen within the naked eye or dissecting microscope 10x-50x magnification • Arbuscular can be seen with high magnification 200x magnification • In spite of their profound morphological and taxonomic differences,some of the effects of AM fungi and ECM fungi on host physiology are similar (Tinker, Jones & Durall,1992).
  10. Bigtooth Aspen
  11. Methods • Mycorrhizal colonization will be measured by directly collecting Populus grandidentata roots. Both AM and EM mycorrhizal colonization will be quantified on each root with a microscope and staining techniques.
  12. Field Methods • The collection of the roots came from nitrogen plot. • Three treatment trees and three control trees were sampled • Control trees were sampled outside buffer and also on same slope • Organic horizon depth was used to root trace
  13. Field Methods cont. • Tree DBH was taken for trees as well as nearby neighbors • Four Cardinal directions for root tracing • Tree roots were placed in corresponding test tubes
  14. Lab Methods: Ectomycorrhizal • Roots were separated from soil. • Cut into 5 mm sections • Examined under dissecting microscope • The portion of ectomycorrhizal root tips were calculated
  15. Lab Methods: Ectomycorrhizal Gridline intersect method (Figure 4.5A in Brundrett et al. 1996).
  16. Lab Methods: Arbuscular
  17. Figure 4.4B in Brundrett et al. 1996). Figure 4.4B in Brundrett et al. 1996).
  18. Results
  19. Data Control Ecto Quantifying Treatment Ecto Quantifying
  20. Data cont.
  21. Conclusion • Nitrogen decreases mycorrhizal colonization • Control showed more mycorrhizal activity • Treatment trees showed more DSE hyphae • Different staining technique
  22. Future Work • Continue work with senior thesis • Molecular work • Trying different staining techniques
  23. Cited sources Bevege DI. 1968. A rapid technique for clearing tannins and staining intact roots for detection of mycorrhizas caused by Endogone spp. and some records of infection in Australasian plants. Transactions of the British Mycological Society 51: 808- 810. Cripps, C. L. 2001. Mycorrhizae of Aspen Forests: ecology and potential application. In: Sustaining Aspen in Western Landscapes: Proceedings of the Symposium on Western Aspen Forests, Grand Junction, CO, June 2000. pp. 285- 298.
  24. Acknowledgments The Shoestring crew Ruth Yanai Craig See Adam Wild Franklin Diggs Tougaloo College
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