Biocomplexity Grant Progress report: May 2003: UCR group DEB

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Biocomplexity Grant Progress report: May 2003: UCR group DEB 9981548 Progress During this year, we continued experiments evaluating four topic areas within the context of the overall collaboration of the study of Common Mycorrhizal Networks (CMN). Our focal region is the southern end of the oak study, the coast live oak (Quercus agrifolia), and with linkages for synthesizing overall data with the UC Davis and southern Oregon University groups. The four areas are (1) assessing diversity of mycorrhizal fungi, (2) evaluating the spatial structure of mycorrhizal fungi, and (3) evaluating movement of resources between roots and mycorrhizal fungi through the CMN, and 4) synthesizing the complex array of results. a) Diversity. We found that α diversity is very high. However, it is not infinite. In further analysis, we found that the species increment curve follows a broken stick model rather than a smooth curve. What this means is that in EM, β diversity continues to remain positive. b) Vertical structure continues to be a focal point in understanding the spatial structure. We have now demonstrated that mycorrhizal fungal hyphae extend into the granite matrix below the thin soil layer. Oaks extend along the hillsides and hilltops as well as in the valley bottoms. Along the hillsides and higher elevations, we demonstrated that mycorrhizal root tips extend deep into granite materials using faults in the geologic bedrock (>4 m deep). Importantly, we have demonstrated that the fractures and granitic matrix have little of value to the plant nutritionally. However, we have determined that there is not enough water in the soil layers to maintain the evergreen oaks through the extended summer and autumn drought. However, there is an annual re-charge of water into the granite matrix. But, flow through this material is unsaturated, and therefore too slow to account for water use by the plant. However, mycorrhizal hyphae can transport water along depletion gradients. We are currently completing measurement of the soil moisture and nutrient gradients in this granite matrix, fractures, and in the soil. Our goal for the next year is to determine if mycorrhizal hyphae can account for additional use of the granite matrix water. c) We have continued evaluation of the role of hydraulic lift in sustaining mycorrhizal activity. In greenhouse studies, we have demonstrated that water is transferred from fungus to plant during the daytime, when the driver is transpirational demand. During the night, horizontal gradients in the soil surface creates the demand and water moves from saturated deep roots through surface roots, into mycorrhizae and out the CMN. This water is used to aid in nutrient absorption by the fungi, and re-distribution through the CMN to the plants. In the valley bottoms where deep roots reach groundwater, surface mycorrhizae are comprised of a high diversity of fungal taxa and include many mesic species. These can be found active and hydrated, even into severe drought (<-5MPa). Isotopic signatures show that much of this water is derived from groundwater. Alternatively, in higher elevations where roots cannot reach the groundwater, drought tolerant fungi (Glomus, Cenococcum) predominate and the amounts of mycorrhizae are much lower than in areas where hydraulic lift can occur.

d) Synthesizing all of these data is one of the largest tasks of the program. We have initiated efforts linking variability among fungal species, and temporal dynamics of these interactions using a stoichiometric modeling framework. We are undertaking experiments and accumulated literature demonstrating a range in growth responses of plants to different fungal species and combinations of species. We have organized these into functional group categories. Subsequently, we recently started to model these using stoichiometric relationships to predict complex outcomes depending on the interactions. We will continue developing this approach to understanding the common mycorrhizal network. Larger Society Implications Our results are important to management of Conservation Reserves in California and elsewhere. While oaks and other trees are important to creating aboveground architecture for birds, reptiles and insects, their role as connectors of below-above ground linkages has not been integrated into conservation and restoration planning and management. As we have shown, individual species of these symbiotic fungi are not ubiquitous. They are diverse, with many different functions. The importance of microbial biodiversity has only recently been recognized and our work contributes to this effort. The work has been highlighted in two recent instances. First, the work is one of the cornerstones of the diversity issues for reserve design in the western Riverside County Multiple Species Conservation plan. Second, our research plots are being further utilized in restoration studies linking belowground and insect diversity, and community structure. For this work, Allen received the Academic Leadership Award from the Inland Empire Section of the American Planning Association. Secondly, we have supported undergraduate and graduate students as well as post-docs on this project. Many have gone on in both academia and in private industry. This includes several under-represented students and post-docs. A list is provided below. Participants Undergraduate students New students Completed or Continuing: Andersen, Hally Dang, Minh * Despas, Frantz* Dhillon, Amy Fleming, Kathleen Gaddis, LaQuasha* Kamal, Nazia* Lamb, Kelly Lee, Moon* Lepe Robert* Olivares, Elaine*

Potter, Samantha Tea, Vinh* Graduate students New Rodrigo Vargas Continuing Bornyasz, Margaret Lansing, Jennifer Completed Lindahl, Amy Post-doctoral New Swenson, William Petra Prouzova-Kucerova Completed Treseder, Kathleen (NSF post-doctoral fellowship) Querejeta, Jose Ignacio (Fulbright Fellow, from Spain) Snyder, Season Egerton-Warburton, Louise Staff Veronique Rorive Doljanin, Christina Tennant, Tracy Publications: Updates: Lindahl, A. 2002. Ecto- and arbuscular mycorrhizal fungi in transplanted oak seedlings in a southern California Oak (Quercus agrifolia: Fagaceae)-grassland ecosystem. M.S. Thesis, University of California. Allen, M.F., W. Swenson, J.I. Querejeta, L.M. Egerton-Warburton, and K.K. Treseder. In press. Ecology of mycorrhizae: A conceptual framework for complex interactions among plants and fungi. Annual Review of Phytopathology. Querejeta, J.I, J.M. Barea, M.F. Allen. F. Caravaca, and A. Roldan. In press. Differential response of δ 13 C and water use efficiency to arbuscular mycorrhizal infection in two aridland woody plant species. Oecologia. Crocker, T.L., R. L. Hendrick, R. Ruess, K. S. Pregitzer, A. J. Burton, M. F. Allen, J. Shan and L. A. Morris. In press. Substituting root numbers for length: Improving the use of minirhizotrons to study fine root dynamics. Applied Soil Ecology. Egerton-Warburton, L.M., R.C. Graham, and K.R. Hubbert. 2003. Spatial variability in mycorrhizal hyphae and nutrient and water availability in a soil-weathered bedrock profile. Plant and Soil 249: 331-342.

Querejeta, J. I., L. Egerton-Warburton and M. F. Allen. 2003. Direct nocturnal water transfer from oaks to their mycorrhizal symbionts during severe soil drying. Oecologia 134: 55-64. Treseder, K. K. and M. F. Allen. 2002. Evidence for direct N and P limitation of arbuscular mycorrhizal fungi. New Phytologist 155: 507-515. Allen, M.F., L. Egerton-Warburton, K. Treseder, C. Cario, A. Lindahl, J. Lansing, I. Querejeta, O. Karen, S. Harney and T. Zink. accepted. Biodiversity and mycorrhizal fungi in southern California: Harbingers of regional environmental change? In: B. Kus, J. Beyers and R. Fisher, Planning for Biodiversity: Bringing research and management together. USDA Forest Service Publication No---. Allen, M.F. D.A. Jasper, and J.C. Zak. 2002. Chapter 14. Micro-organisms. Pp 257-278. In A.J. Davy and M. Perrow. Handbook of Ecological Restoration Volume 1. Principles of restoration, Part 4. Manipulation of the biota. Cambridge University Press. Egerton-Warburton, L.M., E.B. Allen and M.F. Allen. 2002. Mycorrhizal fungal communities: their organization, role and conservation in ecosystems under elevated atmospheric CO 2 and anthropogenic nitrogen deposition. Pp. 19-43. In: K. Sivasithamparam, K.W. Dixon, and R.L. Barrett (eds). Microorganisms in Plant Conservation and Biodiversity. Kluwer Academic Press. Renker C, Zobel M, Öpik M, Allen MF, Allen EB, Vosátka M, Rydlová J, Buscot F. In press. Structure, dynamics and restoration of plant communities: does arbuscular mycorrhiza matter? In: Temperton V, Nuttle T, Hobbs R, Halle S (eds): Assembly rules and restoration ecology ˆ bridging the gap between theory and practice. Island Press. Rillig, M.C., K.K. Treseder and M.F. Allen. 2002. Global change and mycorrhizal fungi. In M.van der Heijden and I. Sanders. Mycorrhizal Ecology. Springer-Verlag, NY. Treseder, K. K., S. J. Morris, and M. F. Allen. In press. The contribution of root exudates, symbionts, and detritus to carbon sequestration in the soil. In: Roots and soil management-- Interactions between roots and soil. S. F. Wright and R. Zobel, eds. Soil Science Society of America monograph. Already entered Egerton,-Warburton, L.M., R.C. Graham, E.B. Allen, and M.F. Allen. 2001. Reconstruction of historical changes in mycorrhizal fungal communities under anthropogenic nitrogen deposition. Proceedings of the Royal Society of London, Series B. 268: 2479-2484. Allen, M.F., J. Lansing, and E.B. Allen. 2001. The role of mycorrhizal fungi in composition and dynamics of plant communities: A scaling issue. Progress in Botany 63:344-367. Allen, M.F. 2002. Mycorrhizae: Arbuscular mycorrhizae. Pp. 2120-2124, In: Encyclopedia of Environmental Microbiology. John Wiley & Sons. Allen, M.F. 2001. Modeling arbuscular mycorrhizal infection: is % infection an appropriate variable? Mycorrhiza 10:255-258. Egerton-Warburton, L.M. and M.F. Allen. 2001. Endo- and ectomycorrhizae in Quercus agrifolia Nee. (Fagaceae): patterns of root colonization and effects on seedling growth. Mycorrhiza 11: 283-290.

Rillig, M.C., K.K. Treseder and M.F. Allen. 2002. Global change and mycorrhizal fungi. In M.van der Heijden and I. Sanders. Mycorrhizal Ecology. Springer-Verlag, NY. Allen, E.B., J.S. Brown and M.F. Allen. 2001. Restoration of animal, plant, and microbial diversity. In: Encyclopedia of Biodiversity, volume 5. S. Levin, ed. Academic Press, San Diego. Pp 185-202. Treseder, K.K. and M.F. Allen. 2000. Black boxes and missing sinks: Fungi in global change research. Mycological Research 104: 1282-1283. Treseder, K.K. and M.F. Allen. 2000. Mycorrhizal fungi have a potential role in soil carbon storage under elevated CO 2 and nitrogen deposition. New Phytologist 147: 189-200. Allen, M.F. 2000. Book Review: Current advances in mycorrhizae research. Mycological Research 104: 1535-1536. Allen, M.F. 2000. Mycorrhizae. in M. Alexander (ed.). Encyclopedia of Microbiology, 2nd edition. Pp 328-336. Academic Press, San Diego.