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PHYSIOLOGICAL CHARACTERISTICS LEADING TO DIFFERENCES IN DROUGHT TOLERANCE IN PHASEOLUS VULGARIS AND P.
ACUTIFOLIUS
Jesse Riaz Traub James Kelly Wayne Loescher Plant Breeding, Genetics, and Biotechnology Michigan State University East Lansing, Michigan USA
We have assessed numerous common bean genotypes with varying degrees of stress tolerance, including tepary (P. acutifolius), to identify traits correlated with drought tolerance. Techniques included: Metabolomics – untargeted and targeted LC/MS Biochemical assays – conventional methodologies Gas exchange – Li-Cor 6400XT equipment Fluorescence parameters – with new, inexpensive, and field appropriate equipment
Metabolomic studies showed most components little changed with drought stress, but leaf concentrations of certain soluble carbohydrates increased with drought, sometimes dramatically, especially in more tolerant genotypes, suggesting correlations with tolerance and observed leaf water potentials.
0
100
200
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600
Jaguar SER Tepary Zorro
umol
all
suga
r / g
dry
leaf
tiss
ue
Total micromoles of osmotica in leaf tissue
d
Note: targeted LC/MS showed no significant differences in ABA levels
Drought affected numerous photosynthetic traits. Assimilation versus CO2 concentration analyses (A/Ci curves) did not indicate parameters related to drought tolerance, but rubisco carboxylation and electron transport rates were clearly related to general productivity
Lower stomatal conductances were invariably associated with drought tolerance regardless of water treatment.
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0.6
0.8
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1.2
1.4
0 1 2 3 4 5 6
Stom
atal
Con
duct
ance
(mol
H2O
m-2
s-1)
Day
Conductance JaguarSER16TeparyZorroJaguarSER 16TeparyZorro
71% 28% 21% 13% Pot capacity:
Grafting showed that stomatal conductance and tolerance were primarily controlled by shoot factors, not roots.
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0.8
0.9
1
0 1 2 3 4 5
Stom
atal
Con
duct
ance
(mol
H2O
m-2
s-1)
Days after watering
Conductance
jag/jag
jag/tep
tep/jag
tep/tep
Increasing temperatures showed no effects until 45°C when gas exchange, fluorescence, oxidative stress, and visual assessments indicated distinct genotypic differences. Fluorescence methods were useful for heat tolerance screening, and were correlated with field observations of drought tolerance.
CO2 assimilation measured with Li-Cor 6400
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0.2
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0.6
0.8
1
1.2
tep fuj 544 zor 549 553 538 539 548 546 545 jag ser 550 541
Stom
atal
Con
duct
ance
(mol
H2O
m-2
s-1)
Genotype
Stomatal Conductance via Li-Cor 6400
35 C
40 C
45 C
0.4
0.45
0.5
0.55
0.6
0.65
0.7
0.75
0.8
tep ser 549 zor 538 539 jag fuj 550 544 541 548 546 545 553
Phot
osys
tem
II e
ffic
ency
Genotype
Photosystem II efficiency via PhotosynQ 35 C40 C45 C
0
0.2
0.4
0.6
0.8
1
tep 544 jag zor ser 538 545 553 fuj 539 549 546 550 548 541
Non
-pho
toch
emic
al q
uenc
hing
Genotype
Non-photochemical quenching via PhotosynQ
35 C40 C45 C
20
25
30
35
40
45
50
0
5
10
15
20
25
0 2 4 6 8 10
Tem
pera
ture
(°C)
Phot
osyn
thes
is (u
mol
CO
2 m
-2 s-
1)
Day
Photosynthesis via Li-Cor 6400
538 541 553
jag tep temp
Conclusions: 1. Plant breeders can easily use new, inexpensive and convenient methods* to supplement or bolster field data and characterize stress tolerance of bean lines. 2. Most importantly, to improve drought tolerance in bean germplasm, our data emphasize the need to select for: a. lower stomatal conductance b. and higher heat tolerance
* ‘PhotosynQ’ <- New Old - >