Analyzing
drought resistance and suggesting a physiological selection criterion for
drought resistance
– The need to consider cause and effect
Chlorophyll
fluorescence was evaluated as a phenotypic marker for drought resistance in
drought-stressed pot-grown barley varieties by using polyphasic OJIP
fluorescence transient of photosystem II (PSII) in response to leaf drying
(Oukarroum et al., 2007). The measurement and analysis is not simple and it was
repeated over time with considerable replications. A numerical drought factor
index (DFI) was developed as a final indicator of PSII response over time to
leaf drying in terms of its fluorescence transient components. It was found
that there was a relationship between the field response to drought of certain
varieties and their DFI in this experiment indicating that DFI expressed their
drought resistance. Relative water content (RWC) at peak drought stress was
also measured in the experiment. In the discussion the authors mention that the
highest and lowest varieties for DFI were also highest and lowest in their RWC.
They concluded that DFI should be used to select barley for drought resistance
since it is related to their field performance and their RWC in the pot
experiment. Using the data in the report one can develop a regression of DFI
over RWC (not done by the authors). It can be seen (Figure) that the
association is solid. Evidently DFI is largely a function of leaf water status
and varieties that maintain high RWC under stress sustain a higher DFI and
lower injury to PSII performance. Therefore the conclusion from this study is
that RWC and not DFI (chlorophyll fluorescence) should be used as a
selection criterion in barley, for two reasons:
1.
Variations in RWC among varieties are the main cause of the variations in PSII
and DFI. These varieties differ in their dehydration avoidance (the ability to
maintain high leaf water status under drought stress) and PSII activity as
measured here is a reflection of that.
2.
RWC is much simpler, faster and cheaper to measure than polyphasic OJIP
fluorescence transient of PSII, which is an important consideration in
selection work.

Abdallah
Oukarroum, Saïd El Madidi, Gert Schansker, Reto J. Strasser. 2007. Probing
the responses of barley cultivars (Hordeum vulgare L.) by chlorophyll a
fluorescence OLKJIP under drought stress and re-watering. Environ.
Exp. Bot. 60:438-446.
Abstract
The main objective of this study was to
evaluate the effects of drought and re-watering on 10 varieties of barley
(Hordeum vulgare L.) originating from Morocco. Five varieties obtained from the
National Institute of Agricultural Research (INRA) of Morocco and five
landraces (local varieties defined by high stress tolerance, high yield
stability, an intermediate yield and low-input demand) collected at five
localities in the south of Morocco were used in the present study. After 2
weeks of growth, drought stress was initiated by withholding water for 2 weeks
followed by 1 week of re-watering. The polyphasic OJIP fluorescence transient was
used to evaluate photosystem II (PSII) criteria at the end of the first week of
drought stress (moderate drought), at the end of the second week (severe
drought) and the end of the recovery phase. Drought and re-watering had little
effect on the maximum quantum yield of primary photochemistry ?Po(=FV/FM). The
photosynthetic performance index (PI) is the product of an antenna, reaction
center and electron transport dependent parameter. It revealed differences
between varieties as a function of drought and re-watering. For the screening
for drought stress tolerance, changes in the PI during a 2-week drought stress
treatment were analysed and a new parameter was defined: the drought factor
index (DFI) = log(PIweek 1/PIcontrol) + 2 log(PIweek 2/PIcontrol). The DFI of
the tested varieties correlated with their drought tolerance. Another parameter
that was analysed was the relative water content. It decreased during the
drought stress treatment varying between 61% and 78.2% at the end of the
drought period. During the subsequent recovery period, it increased in a
species-dependent manner (65.1–94.1%). A third parameter studied were changes
in the initial fluorescence rise. The fluorescence rise during the first 300 ?s
(L-band) can give information on the energetic connectivity between PSII units
whereas changes in the rise during the first 2 ms (K-band) offer information on
developing limitations on the donor side of PSII. Changes in respectively the L
and K-bands of the fluorescence transients OJIP were shown to have predictive
value with respect to the vitality of leaves and the tolerance of the varieties
to drought stress.
UPDATE:
Same
conclusion as above can be reached for the paper by Hu et al. (2009)*. They
found that Bermudagrass cv. Tifway had higher net photosynthesis than cv C299
under drought stress, owing to a respective difference in photosystem metabolic
activity under stress. However the two cultivars also differed in their RWC.
This was not considered at all by the authors. When the reader will normalized
for RWC (as above), it will be seen that there is no difference in net
photosynthesis between the two cultivars for the same level of leaf
dehydration. Hence, The difference between the two cultivars was in their
capacity for dehydration avoidance rather than their capacity for photosynthesis
in the dehydrated state.
(*)
Longxing Hu, Zhaolong Wang and Bingru Huang. 2009. Photosynthetic Responses of
Bermudagrass to Drought Stress Associated with Stomatal and Metabolic
Limitations. Crop Sci.49:1902-1909.