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Dept. of Energy, Biofuels Program
1999-2001
Disease Resistance, its Physiology and Genetics
of Short-Rotation Black Cottonwood
J.D. Johnson
Washington State University - Puyallup, Puyallup,
WA 98371
T.M. Hinckley
Collaborator; Division of Ecosystem Science &
Conservation, College of Forest Resources, Universityof Washington,
Seattle, WA 98195
H.D. Bradshaw
Collaborator; Center for Urban
Horticulture, Universityof Washington,
Seattle, WA 98195
Summary Statement
The genetic improvement of the native black cottonwood (Populus trichocarpa)
and elucidation of components of productivity in this species have
been the primary goals of a nearly three decade long cooperative program
between Washington State University and the University of Washington.
Early recognition of the growth potential of P. trichocarpa (Heilman
et al. 1972), led researchers in 1978 to select this species as focus for
a tree improvement program for short rotation intensive culture (SRIC).
Rapid gains in productivity were made by hybridizing this species with P.
deltoides, resulting in a doubling of yield in four-year rotations (Heilman
and Stettler 1985). The production levels achieved are in the range of
20-25 Mg/ha/yr (~10 dry tons/acre/yr) of dry woody biomass (Stettler et
al. 1988). As a result, SRIC of these fast-growing hybrid poplars has
become an important commercial production system of pulp and wood in the
Pacific Northwest (Abelson, 1991; Zsuffa et al., 1996). Today, the acreage
of hybrid poplar plantations on both sides of the Cascade Range exceeds
25,000 ha, with more than 2,000 clones being tested in 25 field trials
throughout the Pacific Northwest. In addition, many of the clones
developed by the WSU/UW program are physically archived in clone arboreta
located at various farms belonging to WSU-Puyallup and UW Center for Urban
Horticulture. These arboreta represent a unique repository of poplar
germplasm that has been shared with scientists in other regions of the US
as well as around the world.
Introduction of these fast growing hybrid poplar clones developed by
the WSU/UW program into other regions of the US, including the mid-west
and southeast, would allow for significant production of biomass for
energy as well as help counter global warming through carbon dioxide
sequestration. Graham (1994) identified more than 158 million hectares of
non-irrigated land in the contiguous U.S. as suitable for energy crops
such as poplar. Renewable energy consumption in the U.S. increased in 1996
by 8% over 1995 levels. Hydropower generation constitutes 53% of renewable
energy consumption, but biomass is not far behind at 41%, and wood is the
main component of the biomass resource (Renewable Energy Annual, 1997).
Before introducing hybrid poplar into other regions of the US, it is
necessary to control diseases that would otherwise limit the growth
potential of these trees. Breeding for disease resistance is the main
strategy for developing resistant hybrids that will thrive elsewhere.
However, an understanding of host resistance/tolerance mechanisms,
pathogen-host interactions, and pathogen life cycle are required before
breeding efforts can be both successful and efficient (Newcombe, 1996) .
The two most important diseases that limit poplar productivity in the US
are leaf rust, caused by Melampsora spp. and stem canker, caused by
Septoria musiva. Melampsora rust is the major foliar disease
of hybrid poplar globally. Rust can kill young trees and reduce the growth
of older trees by 30 to 40 % (Newcombe, 1996). Septoria canker is
prevalent in the mid-west, aggressively attacking and killing the hybrid
poplars while having little economic impact on the native eastern
cottonwood (P. deltoides). One susceptible clone exhibited a 63%
reduction in biomass due to Septoria canker (Pinon, 1984).
Durability of disease resistance is a critical issue since the hybrids are
grown over large areas and for rotations of from six to twenty or more
years. For example, in western Europe where hybrid poplar culture is of
long standing, clones selected for rust resistance have repeatedly
succumbed in time to new races of Melampsora larici-populina Kleb.
(Pinon, 1995). Similarly, in the Pacific Northwest, it is now apparent
that many new races, or pathotypes, characterize the leaf rust population
(Newcombe, unpublished). It is, therefore, imperative that we begin to
develop an understanding of the mechanisms of how the host tree and
pathogen interact in order to allow us to begin breeding for stable
resistance in the hybrid poplars as well as develop proper cultural
treatments that minimize disease incidence and/or impact. Stable
resistance to these pathogens will ultimately result in higher yields due
to the higher productivity of the WSU/UW hybrids and to lower production
losses resulting from disease. This, coupled with increasing land area put
into SRIC plantations, will substantially increase biofuel feedstock
production in the US.
Importance of hybrid poplar
The WSU/UW poplar researchers recognized the benefits of studying Populus
beyond meeting energy feedstock or regional fiber needs. Many
attributes of Populus--its rapid growth, its suitability for
cloning and tissue culture, its species diversity and the ease with which
it can be bred and hybridized--have also made it an ideal model species
for studies in tree growth and differentiation. Clonal propagation of
specific genotypes permits their study in field, greenhouse and growth
chamber environments. It also allows the simultaneous testing of progenies
with their parents, or even grandparents, to elucidate trait transmission
and expression. Tissue culture allows several techniques of genetic
transformation and capturing of somaclonal variation. The Populus genome
is modest in size (C = 0.5pg, Dhillon, 1987), which facilitates
molecular analysis and speeds up the search for molecular markers
associated with important disease resistance, physiological and
morphological traits. These characteristics coupled with the ability to
cross different Populus species enable us to resolve many phenomena
of disease resistance, and growth and differentiation into their
components and subsequently manipulate them in breeding programs. While
some of the genetic-physiological mechanisms may be unique to Populus,
others are likely to be common to other tree species.
PROPOSED TASKS
Task 1: Tree Breeding and Molecular Genetics
Controlled crosses for the genetic study of disease resistance and
other selected traits
Breeding of known resistance clones, including P. nigra and P.
maximowiczii, infusion of resistance gene(s) by traditional breeding
and molecular biology methods for introduction into commercial hybrids
Task 2: Mechanisms of Disease Resistance
* A. Melampsora rust; develop stable, partial resistance in
commercially important hybrids
B. Septoria canker; understand host/site factors controlling
infection, determine mechanisms of resistance and identify traits/gene(s)
Task 3: Growth and Physiological Impacts of Disease
* A. Changes in carbon and nutrient allocation during symptom
development in known susceptible and resistant clones
B. Physiological compensation to disease development and effects on
tree growth
C. Cultural practices that exacerbate or ameliorate disease incidence
by altering host physiology, including nutrition, spacing and clonal
mixtures.
Task 4: Bio-control Strategies
A. Incidence of myco-parasites and their impact on pathogens
B. Deployment strategies for myco-parasites
Task 5: Maintenance of Genetic Collections
* A. Maintaining clone arboretum, clone banks, stool beds and existing
plantations
Task 6: Database Management
* A. Database on all genetic materials and their pedigrees
* B. Database on field and research records
*Studies ongoing or initiated
REFERENCES TO PROJECT DESCRIPTION
ABELSON, P. 1991. Improved yields of biomass. Science 252:1469.
ANONYMOUS. 1997. Renewable Energy Annual 1997, Volume 1 - Highlights.
Energy Information Administration (EIA) of the Dept. of Energy.
http://www.eia.doe.gov/cneaf/solar.renewable.energy.annual/rea_sum.html.
ARES, A., AND BUTIERREZ, L. 1996. Selection of poplar clones for the
lower valley of the Colorado River, Argentina. Forestry 69:75-82.
BAAS, W.J. 1989. Secondary plant compounds, their ecological significance
and consequences for the carbon budget: Introduction of the Carbon/Nutrient
Cycle theory. Pp. 313-340. In Causes and consequences of Variation in Growth
Rate and Productivity in Higher Plants. H. Lambers, ed. SPB Academic
Publishing bv, the Hague, The Netherlands. 363 p.
BEAVIS, W.D. 1994. The power and deceit of QTL experiments: Lessons from
comparative QTL studies. Proceedings of the Corn and Sorghum Industry
Research Conference, American Seed Trade Association; Washington, D.C., pp.
250-266.
BISOFFI, S., AND GULLBERG, U. 1996. Poplar breeding and selection
strategies. In Biology of Populus and its Implications for
Management and Conservation. Part I, Chapter 6. Edited by R.F.
Stettler, H.D. Bradshaw, Jr., P.E. Heilman, and T.M. Hinckley. NRC Research
Press, National Research Council of Canada, Ottawa, ON. Pp. 139-158.
BRADSHAW, H.D., JR. 1996. Molecular genetics of Populus. In
Biology of Populus and its Implications for Management and
Conservation. Part I, Chapter 8. Edited by R.F. Stettler, H.D.
Bradshaw, Jr., P.E. Heilman, and T.M. Hinckley. NRC Research Press, National
Research Council of Canada, Ottawa, ON. Pp. 183-199.
BRADSHAW, H.D., JR. 1998. Case history in genetics of long-lived plants:
molecular approaches to domestication of a fast-growing forest tree: Populus.
In Molecular Dissection of Complex Traits. Chapter 16. Edited by A.H.
Paterson. CRC Press, Boca Raton, Florida. Pp. 219-228.
BRADSHAW, H.D., JR., VILLAR, M., WATSON, B.D., OTTO, K.G., STEWART, S.,
AND STETTLER, R.F. 1994. Molecular genetics of growth and development in Populus.
III. A genetic linkage map of a hybrid poplar composed of RFLP, STS, and
RAPD markers. Theor. Appl. Genet. 89:167-178.
BROERS, L.H.M., AND DE HAAN, A.A. 1994. Relationship between the origin
of European landraces and the level of partial resistance to wheat leaf
rust. Plant Breeding 113:75-78.
CERVERA, M.T., GUSMÃO, J., STEENACKERS, M., PELEMAN, J., STORME, V.,
VANDEN BROECK, A., VAN MONTAGU, M., AND BOERJAN, W. 1996. Identification of
AFLP molecular markers for resistance against Melampsora larici-populina
in Populus. Theor. Appl. Genet. 93:733-737.
CHAMBERS, P.G.S. AND BORRALHO, N.M.G. 1997. Importance of survival in
short-rotation tree breeding programs. Can. J. For. Res. 27:911-917.
CHRISTIAN, D.P., COLLINS, P.T., HANOWSKI, J.M., AND NIEMI, G.J. 1997.
Bird and small mammal use of short-rotation hybrid poplar plantations. J.
Wildl. Manage. 61:171-182.
CHURCHILL, G.A., AND R.W. DOERGE. 1994. Empirical threshold values for
quantitative trait mapping. Genetics 138: 963-971.
DHILLON, S.S. 1987. In: Cell and Tissue Culture in Forestry; J.M. Bonga
and D.J. Durzan, eds.; Martinus Nijhoff Publishers, Dordrecht, The
Netherlands; Vol. 1:298-313.
DUNLAP, J.M., AND STETTLER, R.F. 1996. Genetic variation and productivity
of Populus trichocarpa and its hybrids. IX. Phenology and Melampsora
rust incidence of native black cottonwood clones from four river valleys in
Washington. Forest Ecology and Management 87:233-256.
EDINGTON, B.R., SHANAHAN, P.E., LEVIN, J., AND RIJKENBERG, F.H.J. 1994.
Inheritance of partial resistance to bean rust in the common bean (Phaseolus
vulgaris L.). Ann. appl. Biol. 125:601-605.
GOULD, S.J., AND VRBA, E.S. 1982. Exaptation - a missing term in the
science of form. Paleobiology 8: 4-15.
GRAHAM, R.L. 1994. An analysis of the potential land base for energy
crops in the coterminous United States. Biomass and Bioenergy 6:175-189.
GUSTAFSSON, L., AND ERIKSSON, I. 1995. Factors of importance for the
epiphytic vegetation of aspen Populus tremula with special emphasis
on bark chemistry and soil chemistry. Journal of Applied Ecology 32:412-424.
HEILMAN, P.E., PEABODY, Jr., D.V., DeBELL, D.S., AND STRAND, R.F. 1972. A
test of close-spaced, short-rotation culture of black cottonwood. Can. J.
For. Res. 2:456-459.
HEILMAN, P.P. AND STETTLER, R.F. 1985. Genetic variation and productivity
of Populus trichocarpa and its hybrids: II. Biomass production in a
4-year plantation. Can. J. For. Res. 15:384-388.
HSIANG, T., AND VAN DER KAMP, B.J. 1985. Variation in rust virulence and
host resistance of Melampsora occidentalis on black cottonwood. Can.
J. Plant Pathol. 7:247-252.
HUANG, N., ANGELES, E.R., DOMINGO, J., MAGPANTAY, G., SINGH, S., ZHANG,
G.,
INGESTAD, T. AND KAHR, M. 1985. Nutrition and growth of coniferous
seedlings at varied relative nitrogen addition rates. Physiol. Plant.
65:109-116
INGESTAD, T. AND AGREN. G. 1995. Plant nutrition and growth: Basic
principles. Plant and Soil 168:15-20.
JOHNSON, R. 1992. Reflections of a plant pathologist on breeding for
disease resistance, with emphasis on yellow rust and eyespot of wheat. Plant
Pathology 41:239-254.
JORDAHL, J.L., FOSTER, L., SCHNOOR, J.L., AND ALVAREZ, P.J.J. 1997.
Effect of hybrid poplar trees on microbial populations important to
hazardous waste bioremediation. Environ. Toxicol. Chem. 16:1318-1321.
KUMARAVADIVEL, N., BENNETT, J., AND KHUSH, G.S. 1997. Pyramiding of
bacterial blight resistance genes in rice: marker-assisted selection using
RFLP and PCR. Theor. Appl. Genet. 95:313-320.
LAMBERS, H., N. FREIJSEN, H. POORTER, T. HIROSE AND A. VAN DER WERF.
1989. Analyses of growth based on net assimilation rate and nitrogen
productivity: Their physiological background. Pp. 1-17. In Causes and
consequences of Variation in Growth Rate and Productivity in Higher Plants.
H. Lambers, ed. SPB Academic Publishing bv, the Hague, The Netherlands. 363
p.
LEFÈVRE, F., GOUÉ-MOURIER, M.C., FAIVRE-RAMPANT, P., AND VILLAR, M.
1998. A single gene cluster controls incompatibility and partial resistance
to various Melampsora larici-populina races in hybrid poplars.
Phytopathology 88:in press.
LEFÈVRE, F., PICHOT, C., AND PINON, J. 1994. Intra- and interspecific
inheritance of some components of the resistance to leaf rust (Melampsora
larici-populina Kleb.) in poplars. Theor. Appl. Genet. 88:501-507.
MOLTZAN, B.D., STACK, R.W., AND MASON, P.A. 1993. First report of Melampsora
occidentalis on Populus trichocarpa in the central United States.
Plant Disease 77:953.
NEWCOMBE, G. 1996. The specificity of fungal pathogens of Populus.
In Biology of Populus and its Implications for Management and
Conservation. Part I, Chapter 10. Edited by R.F. Stettler, H.D.
Bradshaw, Jr., P.E. Heilman, and T.M. Hinckley. NRC Research Press, National
Research Council of Canada, Ottawa, ON. Pp. 223-246.
NEWCOMBE, G. 1998a. Association of Mmd1, major gene for
resistance to Melampsora medusae f.sp. deltoidae, with
quantitative traits in poplar rust. Phytopathology 88: 114-121.
NEWCOMBE, G. 1998b. Exapted resistance to diseases of Populus.
Eur. J. For. Path. 28: in press.
NEWCOMBE, G., BRADSHAW, H.D., JR., CHASTAGNER, G.A, AND STETTLER, R.F.
1996. A major gene for resistance to Melampsora medusae f.sp. deltoidae
in a hybrid poplar pedigree. Phytopathology 86:87-94.
NEWCOMBE, G. and CALLAN, B.E. 1997. First report of Marssonina brunnea
f.sp. brunnea on hybrid poplar in the Pacific Northwest. Plant
Disease 81:231.
NEWCOMBE, G., G.A CHASTAGNER, and S.K. McDONALD. 1994. Additional
coniferous aecial hosts of the poplar leaf rusts, Melampsora
larici-populina and M. medusae f.sp. deltoidae. Plant
Disease 78: 1218.
NYLUND, J-E. AND WALLANDER, H. 1989. Effects of ectomycorrhizae on host
growth and carbon balance in a semi-hydroponic cultivation system. New
Phytol. 112:389-398.
OTT, J. 1985. Analysis of human genetic linkage. Johns Hopkins University
Press, Baltimore; MD, pp. 1-223.
PARLEVLIET, J.E. 1979. Components of resistance that reduce the rate of
epidemic development. Ann. Rev. Phytopathol. 17:203-222.PINON, J. 1984.
Management of diseases of poplars. Eur. J. For. Path. 14:415-425.
PINON, J. 1995. Variability in poplar rusts and evolution of their
populations. Consequences for control strategies. C.R. Acad. Agric. Fr.
81(3):99-109.
PINON, J., AND FREY, P. 1997. Structure of Melampsora larici-populina
populations on wild and cultivated poplar. Eur. J. Pl. Path. 103:159-173.
PRAKASH, C.S. AND HEATHER, W.A. 1989. Inheritance of partial resistance
to two races of leaf rust, Melampsora medusae in eastern cottonwood, Populus
deltoides. Silvae Genetica 38:90-94.
PRAKASH, C.S., AND THIELGES, B.A. 1989. Somaclonal variation in eastern
cottonwood for race-specific partial resistance to leaf rust disease.
Phytopathology 79:805-808.
SCHNEIDER, D. 1998. Burying the problem. Scientific American 278:21-22.
SEDJO, R.A, AND BOTKIN, D. 1997. Using forest plantations to spare
natural forests. Environment 39:14.
SINGH, R.P., AND RAJARAM, S. 1994. Genetics of adult plant resistance to
stripe rust in ten spring bread wheats. Euphytica 72:1-7.
SPIERS, A.G., AND HOPCROFT, D.H. 1994. Comparative studies of the poplar
rusts Melampsora medusae, M. larici-populina and their
interspecific hybrid M. medusae-populina. Mycol. Res. 98:889-903.
STETTLER, R.F., FENN, R.C., HEILMAN, P.E. AND STANTON, B.J. 1988. Populus
trichocarpa x Populus deltoides hybrids for short rotation
culture: variation patterns and four-year field performance. Can. J. For.
Res. 18:745-753.
TIBAYRENC, M., KJELLBERG, F., ARNAUD, J., OURY, B., BRENIERE, S.F.,
DARDE, M.L., AND AYALA, F. 1991. Are eukaryotic microorganisms clonal or
sexual? A population genetics vantage. Proc. Natl. Acad. Sci. USA
88:5129-5133.
VAN OOIJEN, J.W. 1992. Accuracy of mapping quantitative trait loci in
autogamous species. Theor. Appl. Genet. 84: 803-811.
VILLAR, M., LEFÈVRE, F., BRADSHAW, H.D., JR., AND TEISSIER DU CROS, E.
1996. Molecular genetics of rust resistance in poplars (Melampsora
larici-populina Kleb/Populus sp.) by bulked segregant analysis in
a 2x2 factorial mating design. Genetics 143:531-536.
WANG, J., AND VAN DER KAMP, B.J. 1992. Resistance, tolerance, and yield
of western black cottonwood infected by Melampsora rust. Can. J. For.
Res. 22:183-192.
ZENG, Z.-B. 1994. Precision mapping of quantitative trait loci. Genetics
136: 1457-1468.
ZSUFFA, L., GIORDANO, E., PRYOR, L.D., and STETTLER, R.F. 1996. Trends in
poplar culture: some global and regional perspectives. In Biology of Populus
and its implications for management and conservation. Part II, Chapter 19. Edited
by R.F. Stettler, H.D. Bradshaw, Jr., P.E. Heilman, and T.M. Hinckley.
NRC Research Press, National Research Council
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