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The
Leach cultivars ‘Bikini Island’ and ‘Capistrano’ are good
examples of interspecific rhododendron hybrids that combine the
saturated flower colors of Asian species with cold hardiness
from North American species.
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R.
‘Bikini Island’ |
R. ‘Capistrano’ |
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Under the leadership of plant breeder and
geneticist Dr. Stephen Krebs, the Station maintains its commitment to
developing superior rhododendrons for continental climates (i.e. cold
winters and hot summers). The traditional breeding program is now
complemented by a vigorous research component focused on adaptations of
rhododendrons to biotic and abiotic stresses, such as winter freezing injury
to leaves and buds, summertime ‘bleaching’ of leaves (photoinhibition), and
diseases caused by fungal pathogens (Phytophthora root rot and
powdery mildew). The basic questions being addressed are:
1)
How much natural variation exists among Rhododendron species for tolerance to a particular stress?
2)
What are the genetic and physiological
determinants of this tolerance?
3)
Can stress tolerance be transferred via
conventional or modern techniques to a new generation of hybrids that have
improved landscape performance under stressful conditions?
4)
How is expression of these traits influenced by
other key features of woody plant biology, such as juvenility and dormancy?
Research on these questions is being
conducted on- and off-site, frequently in collaboration with faculty and
graduate students at participating universities.
While
much of the research focus is on a single genus (Rhododendron) at the
whole plant level, our findings are broadly relevant to other woody plant
species or to other levels of investigation (molecular, cellular, or
community). Rhododendrons share many biological features in common with
other members of Ericaceae, the heath family, which includes 120 genera
(2500+
species) that are valued throughout the world as native plants, fruit crops,
and ornamental garden plants.
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Rhododendron root rot is caused
primarily by the soil fungal pathogen Phytophthora cinnamomi.
The fungus colonizes the root vascular system of susceptible hosts,
cuts off water supply to the shoot, and causes a characteristic leaf
wilting and rolling prior to plant mortality. Resistance to the
disease is rare (< 3 % of screened cultivars and species), and we
are using breeding and screening methods to transfer resistance to a
broader array of rhododendron cultivars.

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R.
‘Hindustan’
no inoculum |
R. ‘Hindustan’
+ P. cinnamomi |
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Winter freezing damage can be
observed in a variety of tissues. Floral buds are less cold
hardy than leaves or stems. Field plants showing damage
(browning) to both leaves and buds (A) are less hardy than
plants with buds only affected (B). Breeding selections are made
for plants that have undamaged tissues (C) following winter lows
of –15 to –20F.
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Contact: Stephen Krebs,
skrebs@holdenarb.org
Selected Publications
1)
Wei, H, AL Dhanaraj, LJ Rowland, Y Fu, SL Krebs, and R. Arora (2005).
Comparative analysis of expressed sequence tags from cold-acclimated
and non-acclimated leaves of Rhododendron catawbiense Michx.
Planta 221: 406-416.
2)
Krebs, SL (2005). Loss of winter hardiness in R. ‘Supernova’, an
artificial polyploid.
J. American Rhododendron Society 59: 74-75.
3)
Marian, CO, SL Krebs and R Arora (2004).
Dehydrin variability among
Rhododendron species: a 25- kDa dehydrin is highly conserved and
associated with cold acclimation across diverse species. New Phytologist
161: 773-780.
4)
Krebs, SL and M Wilson
(2002)
Resistance to
Phytophthora root rot among contemporary
rhododendron cultivars. HortScience 37: 790-792.
5)
Lim, CC, SL Krebs, R Arora (1999) A 25 kD dehydrin associated with
genotype- and age-dependent leaf freezing tolerance in Rhododendron:
a genetic marker for cold hardiness? Theoretical and Applied Genetics
99: 912-920
6)
Krebs, SL (1996) Normal segregation of allozyme markers in complex
rhododendron hybrids. Journal of Heredity 87:131-135.